WO1996040115A1 - Method and compositions for inhibition of adaptor protein/tyrosine kinase interactions - Google Patents
Method and compositions for inhibition of adaptor protein/tyrosine kinase interactions Download PDFInfo
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- WO1996040115A1 WO1996040115A1 PCT/US1996/008741 US9608741W WO9640115A1 WO 1996040115 A1 WO1996040115 A1 WO 1996040115A1 US 9608741 W US9608741 W US 9608741W WO 9640115 A1 WO9640115 A1 WO 9640115A1
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- quinone
- indol
- dihydroxy
- methylbut
- methyl
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/14—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
Definitions
- the present invention relates to methods and compositions for the inhibition of adaptor protein/phosphotyrosine interactions, especially wherein those interactions involve a protein tyrosine kinase capable of complexing with a member an the SH2 domain-containing 0 family of adaptor proteins associated with a cell proliferative disorder.
- the present invention relates to particular organic compounds, and methods utilizing such compounds.
- a central feature of this process is the reversible phosphorylation of certain proteins.
- the phosphorylation or dephosphorylation of amino acid residues triggers conformational changes in regulated proteins that alter their biological properties. Proteins are phosphorylated by protein kinases and are dephosphorylated by protein phosphatases.
- Protein kinases and phosphatases are classified according to the amino acid residues they act on, with one class being serine-threonine kinases and phosphatases (reviewed in Scott, J.D. and Soderling, T.R., 1992, 2 . :289-295) , which act on serine and threonine residues, and the other class being the tyrosine kinases and phosphatases (reviewed in Fischer, E.H. et al . , 1991 Science 253 :401-406; Schlessinger, J. and Ullrich, A., 1992, Neuron 9_:383-391; Ullrich, A. and Schlessinger, J.
- the protein kinases and phosphatases may be further defined as being receptors, i.e., the enzymes are an integral part of a transmembrane, ligand-binding molecule, or as non-receptors, meaning they respond to an extracellular molecule indirectly by being acted upon by a ligand-bound receptor.
- Phosphorylation is a dynamic process involving competing phosphorylation and dephosphorylation reactions, and the level of phosphorylation at any given instant reflects the relative activities, at that instant, of the protein kinases and phosphatases that catalyze these reactions.
- Protein tyrosine kinases comprise a large family of proteins, including many growth factor receptors and potential oncogenes, which share ancestry with, but nonetheless differ from, serine/threonine-specific protein kinases (Hanks et al . , 1988, Science 241:42-52) .
- Receptor-type protein tyrosine kinases having a transmembrane topology have been studied extensively. The binding of a specific ligand to the extracellular domain of a receptor protein tyrosine kinase is thought to induce receptor dimerization and phosphorylation of their own tyrosine residues.
- cytoplasmic domains of receptors may serve as specific binding sites that interact with a host of cytoplasmic signalling molecules, thereby activating various signal transduction pathways (Ullrich, A. and Schlessinger, J. , 1990, Cell £1:203-212) .
- the intracellular, cytoplasmic, non-receptor protein tyrosine kinases may be broadly defined as those protein tyrosine kinases which do not contain a hydrophobic, transmembrane domain.
- the known cytoplasmic protein tyrosine kinases into eleven distinct morphotypes, including the SRC family (Martinez, R. et al. , 1987, Science 2J37 :411-414; Sukegawa, J. et al.. 1987, Mol. Cell. Biol., 2:41-47; Yamanishi, Y. et al. , 1987, 2.237-243; Marth, J.D. et al.
- cytoplasmic protein tyrosine kinases have been linked to certain phases of the cell cycle (Morgan, D.O. et al. , 1989, Cell 57: 775-786; Kipreos, E.T. et al. , 1990, Science 248 : 217-220; Weaver et al. , 1991, Mol. Cell. Biol. 1JL:4415-4422) / and cytoplasmic protein tyrosine kinases have been implicated in neuronal development (Maness, P., 1992, Dev. Neurosci 14 . :257-270) . Deregulation of kinase activity through mutation or overexpression is a well- established mechanism underlying cell transformation (Hunter et al. , 1985, supra; Ullrich et al. , supra) .
- Adaptor proteins are intracellular proteins having characteristic conserved peptide domains (SH2 and/or SH3 domains, as described below) which are critical to the signal transduction pathway. Such adaptor proteins serve to link protein tyrosine kinases, especially receptor-type protein tyrosine kinases to downstream intracellular signalling pathways such as the RAS signalling pathway. It is thought that such adaptor proteins may be involved in targeting signal transduction proteins to the correct site in the plasma membrane or subcellular compartments, and may also be involved in the regulation of protein movement within the cell. Such adaptor proteins are among the protein substrates of the receptor-type protein tyrosine kinases, and have in common one or two copies of an approximately 100 amino acid long motif.
- SH2 domain Src homology 2 domain.
- SH2-containing polypeptides may otherwise, however, be structurally and functionally distinct from one another (Koch, CA. et al. ,
- SH2 domains directly recognize phosphorylated tyrosine amino acid residues.
- the peptide domains also have independent sites for the recognition of amino acid residues surrounding the phosphotyrosine residue (s) .
- SH3 domains function, in part, as protein-binding domains that act to link signals transmitted from the cell surface to downstream effector genes such as ras (Pawson, T. and Schlessinger, J., 5 1993 Current Biology, 2:434-442) .
- G-proteins Simon, M.I. et al . , 1991, Science 252 :802-808; Kaziro, Y. et al..
- Ras activation is also required for transformation by viral oncogenic tyrosine kinases (Smith, M.R. et al.. 1986, Nature 320:540-43) .
- Ras activity is regulated by the opposing actions of the
- GAPs GTPase-activating proteins
- guanine nucleotide exchange factors 25 GTPase-activating proteins (GAPs) and guanine nucleotide exchange factors, with GAPs stimulating the slow intrinsic rate of GTP hydrolysis on Ras and exchange factors stimulating the basal rate of exchange of GDP for GTP on Ras.
- GAPs act as negative regulators of Ras function, while
- the GRB-2 SH2 domain binds to specific tyrosine phosphorylated sequences in receptor tyrosine kinases while the GRB-2 SH3 domains bind to proline- rich sequences present in the Sos exchange factor. Binding of GRB-2 to the receptor kinases, therefore, allows for the recruitment of Sos to the plasma membrane, where Ras is located (Schlessinger, J., 1993, TIBS 18:273-275) .
- Grb2 has been shown to be associated with CSF-1 receptor (vanderGeer and Hunter, 1993, EMBO J. 12 (13) :5161-5172) , PDGF receptor (Li et al. , 1994, MCB 14 (1) :509-517) , EGF-R (Matuoka et al., 1993, EMBO J. 12 (9) :3467-3475; Lowenstein et al. , 1992, Cell 70:431-442) and Fak (Schlaepfer et al. , 1994, Nature 372:786-791), amongst other proteins.
- Growth factors and their receptors are crucial for normal development but can also act as oncogenes leading to cell transformation, oncogenesis, and cell proliferative disorders, including cancer.
- Activation of the oncogenic potential of normal cellular proteins such as protein tyrosine kinases may, for example, occur by alteration of the proteins' corresponding enzymatic activities, their inappropriate binding to other cellular components, or both.
- Philadelphia chromosome-positive human leukemias it is known that the BCR-ABL oncoprotein is involved in the pathenogenesis of such leukemias.
- BCR-ABL exhibits deregulated tyrosine kinase activity. It has recently been demonstrated (Pendergast, A.M. et al.
- BCR-ABL binds the SH2/SH3 domain- containing GRB-2 adaptor protein. Further, it has been demonstrated that BCR-ABL/GRB-2 binding is mediated by the direct interaction the GRB-2 SH2 domain and a tyrosine- phosphorylated region of the BCR-ABL protein, and that this interaction is required for the activation of the Ras signaling pathway.
- cell proliferative disorders such as the form of leukemia described above.
- One approach to the treatment of oncogenenic, cell proliferative disorders would be to attempt to "short circuit" abnormal signal transduction events which contribute to the appearance of such disorders, by interfering with one or more of these requisite events.
- the amelioration of an abnormal kinase activity may be interfered with by targeting and directly inhibiting the enzymatic activity of the kinase involved in the cell proliferative disorder. It has been proposed that certain compounds may have such anti-tyrosine kinase activity. See, for example, Levitzki and Gazit, 1995, Science 267:1782-1788. wherein certain quinazoline derivatives are proposed to directly inhibit receptor tyrosine kinase enzymatic activity. In instances wherein the signal transduction event of interest involves an adaptor protein/protein tyrosine kinase interaction, the inhibition of such interactions may lead to the amelioration of cell proliferative disorder symptoms.
- the present invention relates to methods and compositions for the inhibition of adaptor protein/protein tyrosine kinase protein interactions, especially wherein those interactions involving a protein tyrosine kinase capable of complexing with a member of the SH2-and/or SH3- containing family of adaptor proteins are associated with a cell proliferative disorder.
- the present invention relates to particular organic compounds and methods utilizing such compounds.
- PTK Protein tyrosine kinase
- PTK Protein tyrosine kinase
- PTK may refer to either a transmembrane, receptor-type protein tyrosine kinase or a cytoplasmic protein tyrosine kinase, unless otherwise indicated.
- the compounds of the invention inhibit PTK/adaptor protein interactions, especially PTK/adaptor protein interactions wherein the PTK is, for example, an epidermal growth factor receptor (EGF-R) protein tyrosine kinase molecule, a platelet derived growth factor receptor (PDGF-R) protein tyrosine kinase molecule, or an insulin growth factor-like receptor tyrosine kinase molecule (IGF- 1R) .
- EGF-R epidermal growth factor receptor
- PDGF-R platelet derived growth factor receptor
- IGF- 1R insulin growth factor-like receptor tyrosine kinase molecule
- Rl and R2 are independently H, acetate or aryl, alkylaryl and higher alkyl acid ester; R3 to R14 are independently H, alkyl, alkenyl, alkynyl, OH, hydroxyalkyl, alkoxy, nitro, halo, trihalomethyl, amide, carboxamide, carboxy, sulfonyl, sulfonamide, amino, and mercapto which can be substituted or substituted where appropriate.
- Rl and R2 of the formula can be as listed in Table I following the formula. Illustrative preparations or isolations of these compounds are found in the working examples.
- R1-R12 of the formula can be as listed in Table II following the formula. Illustrative preparations or isolations of these compounds are found in the working examples.
- R3-R10 hydrogen
- alkyl as used herein is meant a straight or branched chain saturated hydrocarbon group having from 1 to 20 carbons such as methyl, ethyl, isopropyl, n-butyl, s- butyl, t-butyl, n-amyl, isoamyl, n-hexyl, n-octyl and n- decyl;
- alkenyl and “alkynyl” are used to mean straight or branched chain hydrocarbon groups having from 2 to 10 carbons and unsaturated by a double or triple bond respectively, such as vinyl, allyl, propargyl, 1-methylvinyl, but-1-enyl, but-2- enyl, but-2-ynyl, 1 methylbut-2-enyl, pent-1-enyl, pent-3- enyl, 3-methylbut-l-ynyl, 1, 1-dimethylallyl, hex-2-enyl and 1-methyl
- substituted means that the group in question may bear one or more substituents including but not limited to halogen, hydroxy, cyano, alkyl, aryl, alkenyl, alkynyl, amino, nitro, mercapto, carboxy and other substituents known to those skilled in the art.
- substituents including but not limited to halogen, hydroxy, cyano, alkyl, aryl, alkenyl, alkynyl, amino, nitro, mercapto, carboxy and other substituents known to those skilled in the art.
- Preferred compounds of the present invention include the following:
- the present invention encompasses a pharmaceutical composition comprising a compound of the invention, and methods for using a compound or pharmaceutical composition of the invention in an animal, particularly a human, to ameliorate symptoms of cell proliferative disorders involving protein tyrosine kinase/adaptor protein interactions.
- This invention is based, in part, on the discovery that the disclosed compounds, while exhibiting no inhibitory effect on protein tyrosine kinase enzymatic activity, act to inhibit the binding of an SH2-containing peptide to a tyrosine phosphorylated EGF receptor.
- the data representing this discovery is presented in the Examples in Sections 6, 7 and 8, below.
- the present invention represents the first instance whereby compounds have been discovered which directly inhibit the interaction between adaptor proteins and protein tyrosine kinase molecules.
- Rl and R2 are independently H, acetate or aryl, alkylaryl and higher alkyl acid ester;
- R3 to R14 are independently H, alkyl, alkenyl, alkynyl, hydroxyalkyl, OH, alkoxy, nitro, halo, trihalomethyl, amide, carboxamide, carboxy, sulfonyl, sulfonamide, amino, and mercapto which can be substituted or substituted where appropriate.
- alkyl groups of the compounds of the present invention may be substituted where appropriate with one or more carboxy or aryl groups.
- Alkenyl groups of compounds of the present invention may be substituted where appropriate with one or more carboxy groups.
- Rl and R2 are each independently hydrogen, lower alkyl, acetyl, aryl, alkylaryl or higher alkyl acid ester, and wherein at least one of Rl and R2 is other than hydrogen;
- R3 to R12 are each independently H, alkyl, alkylcarboxy, alkenyl, alkenylcarboxy, aryl, alkylaryl, OH, alkoxy, nitro, halo, trihalomethyl, amide, carboxamide, carboxy, sulfonyl, sulfonamide, amino, mercapto or 2-methylbut-2- en-4-yl; and wherein at least one of Rll and R12 is 2- methylbut-2-en-4-yl.
- Groups R1-R12 may be substituted or unsubstituted where appropriate.
- compounds of the present invention are described by formula (III) above, and pharmaceutically acceptable salts thereof, wherein: Rl and R2 are both H;
- R3 to RIO are each independently H, alkyl, alkylcarboxy, alkenyl, alkenylcarboxy, aryl, alkylaryl, OH, alkoxy, nitro, halo, trihalomethyl, amide, carboxamide, carboxy, sulfonyl, sulfonamide, amino, mercapto or 2-methylbut-2- en-4-yl; and
- Rll and R12 are each independently H or 2-methylbut-2- en-4-yl, wherein at least one of Rll and R12 is 2- methylbut-2-en-4-yl;
- R3 to RIO is other than H.
- Rl and R2 are each independently aryl, alkylaryl and higher alkyl acid ester
- R3 to R12 are each independently H, alkyl, alkylcarboxy, alkenyl, alkenylcarboxy, aryl, alkylaryl, OH, alkoxy, nitro, fluoro, chloro, iodo, trihalomethyl, amide, carboxamide, carboxy, sulfonyl, sulfonamide, amino, or mercapto.
- Rl, R2, Rll and R12 are H;
- R3 to RIO are each independently H, alkyl, alkylcarboxy, alkenyl, alkenylcarboxy, aryl, alkylaryl, alkoxy, hydroxy, nitro, halo, trihalomethyl, amide, carboxamide, carboxy, sulfonyl, sulfonamide, amino, or mercapto, wherein at least one of R3 to RIO is other than H;
- R3 when R4-R10 are each H, R3 may not be 2- methylbut-2-en-4-yl or 2-hydroxy-2-methylbut- 4-yl;
- R4-R6 and R8-R10 are each H, R3 and R7 may not simultaneously be 2-methylbut-2-en-4- yi;
- R5 and R9 may not simultaneously be 2-methylbut-2-en-4-yl or
- R4 and R8 may not both be 2-methylbut-2-en-4-yl or 2- methylbut-1, 4-dien-4-yl, and R4 and R8 may not be 2-methylbut-2-en-4-yl and 2-methylbut-l, 4- dien-4-yl .
- the present invention also encompasses compounds of formula (III) above, and pharmaceutically acceptable salts thereof, wherein R3-R5 and R7-R9 are H and either or both of R6 and RIO are 2-methylbut-2-en-4-yl .
- Rl and R2 are acetyl
- Rll and R12 are H
- R3 to RIO are each independently H, alkyl, alkylcarboxy, alkenyl, alkenylcarboxy, aryl, alkylaryl, OH, alkoxy, nitro, halo, trihalomethyl, amide, carboxamide, carboxy, sulfonyl, sulfonamide, amino, and mercapto, wherein: (a) when both Rl and R2 are acetyl; or when one of
- Rl and R2 is acetyl and R3-R4, R6-R8 and R10- R12 are H; R5 and R9 may not simultaneously be 2-methylbut-2-en-4-yl;
- R3 and R7 may not simultaneously be 2-methylbut-2-en-4-yl
- R4 and R8 may not simultaneously be 2-methylbut-2-en-4-yl .
- Rl and R2 are lower alkyl
- Rll and R12 are H
- R3 to RIO are each independently H, alkyl, alkylcarboxy, alkenyl, alkenylcarboxy, aryl, alkylaryl, OH, alkoxy, nitro, halo, trihalomethyl, amide, carboxamide, carboxy, sulfonyl, sulfonamide, amino, and mercapto, wherein:
- R3 when both Rl and R2 are methyl, and R4-R10 are H, R3 may not be 2-methylbut-2-en-4-yl;
- R5 and R9 may not simultaneously be 2-methylbut-2-en-4-yl .
- the present invention also includes compounds of formula (III) above, and pharmaceutically acceptable salts thereof,
- R4 is 2-methylbut-2-en-4-yl and R3 and R5-R10 are H; or R5 is 2-methylbut-2-en-4-yl and R3-R4 and R6-R10 are H;
- R6 is 2-methylbut-2-en-4-yl, and R3-R5 and R7-R10 are H.
- Rl and R2 are each independently hydrogen, lower alkyl, acetyl, aryl, alkylaryl or higher alkyl acid ester,
- R3 to RIO are each independently H, alkyl, alkylcarboxy, aryl, alkylaryl, alkenyl, alkenylcarboxy, OH, alkoxy, nitro, halo, trihalomethyl, amide, carboxyamide, carboxy, sulfonyl, sulfonamide, amino, mercapto, 4- methylphenylsulfonylamino, or 2-methylbut-2-en-4-yl; and
- Rll and R12 are selected from the group consisting of hydrogen, methyl, ethyl, propyl, butyl, aryl, alkylaryl, alkylcarboxy, alkenylcarboxy, but-l-en-4-yl, 2- methylbut-l-en-4-yl, 4-methyl-n-pentyl, 2-phenylethyl, 2-methylpent-2-en-4-yl, and 4-carboxy-n-butyl, wherein at least one of Rll and R12 is other than hydrogen.
- Rl and R2 are each independently hydrogen, lower alkyl, acetyl, aryl, alkylaryl or higher alkyl acid ester,
- R3 to RIO are each independently H, alkyl, alkylcarboxy, aryl, alkylaryl, alkenyl, alkenylcarboxy, OH, alkoxy, nitro, halo, trihalomethyl, amide, carboxyamide, carboxy, sulfonyl, sulfonamide, amino, mercapto, 4- methylphenylsulfonylamino, or 2-methylbut-2-en-4-yl; and
- Rll and R12 are both 3-methyl-n-butyl .
- Rl and R2 are each independently hydrogen, lower alkyl, acetyl, aryl, alkylaryl or higher alkyl acid ester,
- R3 to RIO are each independently H, alkyl, alkylcarboxy, aryl, alkylaryl, alkenyl, alkenylcarboxy, OH, alkoxy, nitro, halo, trihalomethyl, amide, carboxyamide, carboxy, sulfonyl, sulfonamide, amino, mercapto, 4- methylphenylsulfonylamino, or 2-methylbut-2-en-4-yl and wherein at least one of R3 to RIO is other than hydrogen; and
- Rll and R12 are each independently hydrogen or 3-methyl ⁇ n-butyl
- the invention encompasses the compounds described above as well as pharmaceutically acceptable salts thereof.
- the compounds of the present invention can either be synthesized or isolated as described herein.
- the compounds of the present invention can be synthesized in accordance with standard organic chemistry techniques using readily available starting materials. Alternatively, the compounds can be isolated as described in Section 5.2, below. Chemical synthesis and isolation methods are provided herein solely for illustration. Variation of these methods will be apparent to those skilled in the art.
- the present Example employed a fungus culture (PenLabs Inc. #592), and the following fermentation conditions: medium yeast malt extract plus trace elements at 22°C
- the seed medium consisted of mannitol 60.0 g; soybean meal 12.5 g, citric acid 2.5 g, yeast extract 0.5 g, and H 2 0 to 1 liter.
- the pH of the seed medium was adjusted to 7.0 before autoclaving.
- 30mL seed medium were dispensed per 250 ml flask (6 days 28°C) , which was then inoculated with 1 ml of spore/mycelium homogenate suspension (2 days) .
- Stock cultures were maintained frozen at -80°C in spore storage solutions.
- the fermentation mixture (mycelium and broth) was homogenized and filtered through cheesecloth by suction filtration. The filtrate was extracted three times with 0.5 v/v of ethyl acetate. The ethyl acetate layers were combined and the solvent removed by rotary evaporation. The mycelium was extracted twice with 0.4 v/v of ethyl acetate. The ethyl acetate layers were combined and the solvent removed by rotary evaporation. The oily residues both containing the asterriquinones were combined and dried on a vacuum pump overnight.
- the crude extract obtained above underwent CPC fractionation on a PC Inc. high speed countercurrent chromatograph (HSCC) containing a "tripple" coil column.
- HSCC high speed countercurrent chromatograph
- a 1:3:3:3 v/v/v/v of n-hexane, ethyl acetate, methanol and water was mixed and allowed to settle overnight.
- the lower layer was pumped into HSCC column as the stationary phase.
- the upper layer was used as the mobile phase. After two hours, the lower and upper layer were switched.
- the HSCC run was completed after four hours.
- the crude metabolites eluted from 8 to 12 minutes.
- the active fractions were pooled and evaporated under reduced pressure to dryness.
- the pooled HSCC fraction (8-12) was subjected to semi- preparative HPLC (Water HPLC system with a Water 996 photodioarray detector using Millennium software) fractionations using the following conditions:
- Mass spectra were recorded on PE Sciex LC-MS model API III (Ion Spray) , exact mass measurements were performed at high resolution (HR-FAB) . Mass spectral analysis for compound I gave a molecular ion of 507 (M+H) + (molecular weight: 506) . The molecular formula C 32 H 31 N 2 0 4 (M + +H) : 507.2289; found 507.2291) . 1 H NMR spectra of compound I were recorded in CDCl 3 at 500 MHz on a Brucker DRX-500. Chemical shifts are given in ppm relative to TMS at zero ppm using the solvent peak at 7.26 ppm (CDC1 3 ) as an internal standard.
- 2,3,5,6- tetrabromo-1,4-quinone reacts with excess indole in the presence of potassium carbonate and aluminum oxide in dimethylformamide or dimethylsulfoxide at 100°C to produce the substituted 2, 5-dibromo-3, 6- (3-indolyl) -1,4-quinone which can react with base such as sodium hydroxide to give the substituted 2, 5-dihydroxy-3, 6- (3-indolyl) -1,4-quinone (Hoerher, J. ; Schwenner, E.; Franck, B., Liebigs Ann . Chem. 1986, 10: 1765-1771) .
- Example 1 Methylation of Example 1 with methyl iodide and potassium carbonate in dimethylforamide followed by purification produced the title compound.
- This compound could also be prepared by heating 2, 5-dibromo-3, 6-di [2- (2-methylbut-2-en-4- yl) indol-3-y] 1,4-quinone in methanol in the presence of powdered.potassium carbonate.
- Example 33 Preparation of 2,5-Dihydroxy-3, 6-di- [2- (4-methyl-n-pentyl) indol-3-yl] -1,4-quinone Refer to Example 28 using 2- (4-methyl-n-pentyl) indole as the starting indole.
- Example 28 using 2- (4-carboxy-n-butyl) indole as the starting indole.
- 39a) Preparation of 2- (4-carboxy-3-buten-l-yl) indole Refer to 28a) using 4-bromo-2-butenoic acid as the alkylating agent.
- Example 28 using 2- (3-methyl-n-butyl) -5- (4- methylphenylsulfonylamino) indole as the starting indole.
- 47a) Preparation of 2- (3-methyl-n-butyl) -5- (4- methylphenylsulfonylamino) indole Refer to 45a) using 5-amino-2- (3-methyl-n-butyl) indole.
- the PTK/adaptor protein complexes which may be disrupted by the methods and compositions of the invention comprise at least one member of the PTK family of proteins and at least one member of the adaptor family of proteins, as described below. Under standard physiological conditions, the components of such complexes are capable of forming stable, non-covalent attachments with one or more of the other PTK/adaptor protein complex components.
- the compounds of he invention inhibit PTK/adaptor protein complexes wherein the PTK component is an epidermal growth factor receptor (EGF-R) protein tyrosine kinase molecule, a platelet derived growth factor receptor (PDGF-R) protein tyrosine kinase molecule or an insulin growth factor-like receptor tyrosine kinase molecule (IGF-1R) .
- EGF-R epidermal growth factor receptor
- PDGF-R platelet derived growth factor receptor
- IGF-1R insulin growth factor-like receptor tyrosine kinase molecule
- Intracellular, cytoplasmic PTK components of the PTK/adaptor protein complexes may include, for example, members of the Src family, such molecules as src, yes, fgr, fyn, lyn, hck, lck, and blk; members of the Fes family, such as fes and fer; members of the Abl family, such as abl and arg; and members of the Jak family, such as jakl and jak2.
- Transmembrane, receptor PTK components of the PTK/adaptor protein complexes may include, for example, such molecules as members of the FGF receptor, Sevenless/ROS, Insulin receptor, PDGF receptor, and EGF receptor family of growth factor 5 receptors.
- the adaptor protein components of the PTK/adaptor protein complexes comprise one or more SH2 and/or one or more SH3 non-catalytic domains.
- the SH2 and SH3 domains which may be a part of the adaptor proteins are as described, above,
- Adaptor proteins which may be components of the PTK/adaptor protein complexes may include, for example, p85, c-Crk, SHC, Nek, ISGF3 ⁇ , guanine triphosphatase activator protein (GAP) , and members of the GRB subfamily of proteins, such as GRB1, GRB-2, GRB-3, GRB-4,
- the invention may be used for the treatment of cell proliferative disorders, such as oncogenic disorders, involving a PTK capable of complexing with a member of the SH2- and/or SH3-containing family of adaptor proteins.
- the compounds of the invention may be
- PTK component is EGF-R, PDGF-R, MCT or IGF-1R.
- the compounds of the invention are, for example, BCR-ABL- associated cancers (such as, for example, chronic myelogenous and acute lymphocytic leukemias) , gliomas, glioblastomas, melanoma, human ovarian cancers, human breast cancers (especially HER-2/GRB-7-associated human breast cancers) , and
- Disruption is meant to refer not only to a physical separation of PTK/adaptor protein complex components, but is also meant to refer to a perturbation of the activity of the PTK/adaptor complexes, regardless of whether or not such complexes remain able, physically, to 0 form.
- Activity refers to the function the PTK/adaptor protein complex in the signal transduction cascade of the cell in which such a complex is formed, i.e..
- compositions of the invention do not, however, directly interfere with (i.e. , inhibit or enhance) the enzymatic activity of the protein tyrosine kinase of interest.
- in vitro complex _ formation may be assayed by, first, immobilizing one component, or a functional portion thereof, of the complex of interest to a solid support. Second, the immobilized complex component may be exposed to a compound such as one identified as above, and to the second component, or a functional 0 portion thereof, of the complex of interest. Third, it may be determined whether or not the second component is still capable of forming a complex with the immobilized component in the presence of the compound.
- in vivo complex formation may be assayed 5 by utilizing co-immunoprecipitation techniques well known to those of skill in the art. Briefly, a cell line capable of forming a PTK/adaptor complex of interest may be exposed to one or more of the compounds of the invention, and a cell lysate may be*, prepared from this exposed cell line. An antibody raised against one of the components of the complex of interest may be added to the cell lysate, and subjected to standard immunoprecipitation techniques. In cases where a complex is still formed, the immunoprecipitation will precipitate the complex, whereas in cases where the complex has been disrupted, only the complex component to which the antibody is raised will be precipitated.
- a compound of the invention on the transformation capability of the PTK/adaptor protein of interest may be directly assayed.
- one or more of the compounds of the invention may be administered to a cell such as a fibroblast or hematopoietic cell capable of forming a PTK/adaptor complex which, in the absence of a compound of the invention, would lead to the cell's transformation (Muller, A.J. et al.. 1991, Mol. Cell. Biol. 11:1785-1792; McLaughlin, J. et al . , 1987, Proc. Natl. Acad. Sci. USA M:6558-6562) .
- the transformation state of the cell may then be measured in vitro, by monitoring, for example, its ability to form colonies in soft agar (Lugo and Witte, 1989, Mol. Cell. Biol. 1:1263-1270; Gishizky, M.L. and Witte, O.N., 1992, Science 256:836-839) .
- a cell's transformation state may be monitored in vivo by determining its ability to form tumors in immunodeficient nude or severe combined immunodeficiency (SCID) mice (Sawyers, CL. et al .
- Section 5.1 may be administered to a patient at therapeutically effective doses to treat or ameliorate cell proliferative disorders involving PTK/adaptor protein interactions.
- a therapeutically effective dose refers to that amount of the compound sufficient to result in amelioration of symptoms of a cell proliferative disorder.
- Described, below, in Section 5.4.2.1 are methods for determining the effective dosage of the compounds of the invention for the treatment of cell proliferative disorders.
- Further, described, below, in Section 5.4.2.2 are methods for formulations and pharmaceutical compositions comprising the compounds of the invention, and methods for the administration of such compounds, formulations, and compositions.
- EFFECTIVE DOSE Toxicity and therapeutic efficacy of the compounds of the invention can be determined by standard pharmaceutical procedures in cell cultures or experimental animals, e.g.. for determining the LD 50 (the dose lethal to 50% of the population) and the ED 50 (the dose therapeutically effective in 50% of the population) .
- the dose ratio between toxic and therapeutic effects is the therapeutic index and it can be expressed as the ratio LD 50 /ED 50 .
- Compounds which exhibit large therapeutic indices are preferred. While compounds that exhibit toxic side effects may be used, care should be taken to design a delivery system that targets such compounds to the site of affected tissue in order to minimize potential damage to uninfected cells and, thereby, reduce side effects.
- the data obtained from the cell culture assays and animal studies can be used in formulating a range of dosage for use in humans.
- the dosage of such compounds lies preferably within a range of circulating concentrations that include the ED 50 with little or no toxicity.
- the dosage may vary within his range depending upon the dosage form employed and the route of administration utilized.
- the therapeutically effective dose can be estimated initially from cell cu_ture assays.
- a dose may be formulated in animal models to achieve a circulating plasma concentration range that includes the IC 50 (i.e. , the concentration of the test compound which achieves a half-maximal inhibition of symptoms) as determined in cell culture.
- IC 50 i.e. , the concentration of the test compound which achieves a half-maximal inhibition of symptoms
- levels in plasma may be measured, for example, by high performance liquid chromatography.
- Dosage amount and interval may be adjusted individually to provide plasma levels of the active moiety which are sufficient to maintain inhibition of adaptor protein/protein tyrosine kinase interactions, or minimal effective concentration (MEC) .
- MEC minimal effective concentration
- the MEC will vary for each compound but can be estimated from in vi tro data, e . g. , the interactions using the assays described herein. Dosages necessary to achieve the MEC will depend on individual characteristics and route the administration. However, HPLC assays or bioassays can be used to determine plasma concentrations.
- Dosage intervals can also be determined using the MEC value.
- Compounds should be administered using a regimen which maintains plasma levels above the MEC for 10-90% of the time, preferably between 30-90% and most preferably between 50-90%.
- adaptor proteins are intracellular proteins.
- PTK/adaptor protein interactions are intracellular, regardless of whether the PTK of interest is of the transmembrane or the intracellular type. Therefore, the compounds of the invention act intracellularly to interfere with the formation and/or activity of the PTK/adaptor complexes .
- a variety of methods are known to those of skill in the art for administration of compounds which act intracellularly, as, for example, discussed in this Section.
- Pharmaceutical compositions for use in accordance with the compounds of the present invention may be formulated in conventional manner using one or more physiologically acceptable carriers or excipients.
- the compounds and their physiologically acceptable salts and solvates may be formulated for administration by inhalation or insufflation (either through the mouth or the nose) or oral, buccal, parenteral or rectal administration.
- the pharmaceutical compositions may take the form of, for example, tablets or capsules prepared by conventional means with pharmaceutically acceptable excipients such as binding agents (e.g. , pregelatinised maize starch, polyvinylpyrrolidone or hydroxypropyl methylcellulose) ; fillers (e.g.. lactose, microcrystalline cellulose or calcium hydrogen phosphate) ; lubricants (e.g. , magnesium stearate, talc or silica) ; disintegrants (e.g. , potato starch or sodium starch glycolate) ; or wetting agents (e.g. , sodium lauryl sulphate) .
- binding agents e.g. , pregelatinised maize starch, polyvinylpyrrolidone or hydroxypropyl methylcellulose
- fillers e.g.. lactose, microcrystalline cellulose or calcium hydrogen phosphate
- lubricants e.g. , magnesium stearate, talc or si
- Liquid preparations for oral administration may take the form of, for example, solutions, syrups or suspensions, or they may be presented as a dry product for constitution with water or other suitable vehicle before use.
- Such liquid preparations may be prepared by conventional means with pharmaceutically acceptable additives such as suspending agents (e.g.. sorbitol syrup, cellulose derivatives or hydrogenated edible fats) ; emulsifying agents (e.g. , lecithin or acacia) ; non-aqueous vehicles (e.g.. almond oil, oily esters, ethyl alcohol or fractionated vegetable oils) ; and preservatives (e.g. , methyl or propyl-p-hydroxybenzoates or sorbic acid) .
- the preparations may also contain buffer salts, flavoring, coloring and sweetening agents as appropriate.
- Preparations for oral administration may be suitably formulated to give controlled release of the active compound.
- the compositions may take the form of tablets or lozenges formulated in conventional manner.
- the compounds for use according to the present invention are conveniently delivered in the form of an aerosol spray presentation from pressurized packs or a nebuliser, with the use of a suitable propellant, e.g. , dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas.
- a suitable propellant e.g. , dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas.
- a pressurized aerosol the dosage unit may be determined by providing a valve to deliver a metered amount.
- Capsules and cartridges of e.g. gelatin for use in an inhaler or insufflator may
- the compounds may be formulated for parenteral administration by injection, e.g. , by bolus injection or continuous infusion.
- Formulations for injection may be presented in unit dosage form, e.g.. in ampoules or in multi- dose containers, with an added preservative.
- the compositions may take such forms as suspensions, solutions or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilizing and/or dispersing agents.
- the active ingredient may be in powder form for constitution with a suitable vehicle, e.g. , sterile pyrogen-free water, before use.
- the compounds may also be formulated in rectal compositions such as suppositories or retention enemas, e.g. , containing conventional suppository bases such as cocoa butter or other glycerides.
- the compounds may also be formulated as a depot preparation. Such long acting formulations may be administered by implantation (for example subcutaneously or intramuscularly) or by intramuscular injection.
- the compounds may be formulated with suitable polymeric or hydrophobic materials (for example as an emulsion in an acceptable oil) or ion exchange resins, or as sparingly soluble derivatives, for example, as a sparingly soluble salt.
- suitable polymeric or hydrophobic materials for example as an emulsion in an acceptable oil
- ion exchange resins for example as sparingly soluble derivatives, for example, as a sparingly soluble salt.
- the compositions may, if desired, be presented in a pack or dispenser device which may contain one or more unit dosage forms containing the active ingredient.
- the pack may for example comprise metal or plastic foil, such as a blister pack.
- the pack or dispenser device may be accompanied by instructions for administration.
- Adaptor-GST fusion protein The adaptor-GST (glutathione-S-transferase) fusion proteins used herein were GRB-2-GST fusion proteins prepared by expression in E. coli transformed with GRB-2/pGEX constructs. The GRB-2 portions of these fusion proteins consisted of only the SH2 domain of 0 the GRB-2 protein. Transformed cells are grown in Luria broth (LB) supplemented with ampicillin. After reaching an optical density (OD) at 600 nm of 0.3, the cells are induced for 6 hours with isopropyl -D-thiogalactopyranoside (IPTG) in order to express the fusion protein.
- LB Luria broth
- IPTG isopropyl -D-thiogalactopyranoside
- the cells are precipitated, pelleted at 10,000 x g for 10 minutes at 4°C, washed, and resuspended in phosphate buffered saline (PBS) .
- PBS phosphate buffered saline
- the cells are lysed by sonication (6 strokes, 5 seconds per stroke) .
- Insoluble material is removed by centrifugation ⁇ at 10,000 x g for 10 minutes at 4°C, and the supernatant is passed over a Glutathion-Sepharose column.
- Bound GRB-2-GST fusion protein is eluted off the column with 5 mM reduced glutathion, then dialyzed against PBS.
- EGF-R Epidermal growth factor receptor tyrosine kinase
- EGF-R Epidermal growth factor receptor tyrosine kinase
- EGF-R protein was isolated from the cell lysates by immobilization onto microtiter plates, as described below. EGF-R was subsequently phosphorylated in vitro, as explained below.
- the EGF-R molecule was immobilized onto microtiter plates.
- Microtiter plates were prepared by first coating the wells of the plate, overnight at 4°C, with an anti-EGF-R monoclonal antibody directed against the extracellular domain of EGFR (UBI, #05-101) at a concentration of 0.5 ⁇ g (in PBS) per microtiter well, at a final volume of 150 ⁇ l per well.
- the coating solution was removed from the microtiter wells, and replaced with blocking buffer (5% dry milk in PBS) for 30 minutes at room temperature, after which the blocking buffer is removed and the wells were washed 4 times with TBST buffer (150 mM NaCl, 50 mM Tris-HCl, pH 7.2, 0.1% Triton X-100) .
- blocking buffer 5% dry milk in PBS
- TBST buffer 150 mM NaCl, 50 mM Tris-HCl, pH 7.2, 0.1% Triton X-100
- EGF-R-expressing cells were added to each well, in 150 ⁇ l of PBS, incubated 30 minutes at room temperature, with shaking. Unbound EGF-R was removed by washing wells 5 times with TBST buffer. Approximately 50-100 ng of EGF-R protein was bound per well.
- EGF-R overexpressing cell line which exhibits a high endogenous phosphatase activity, such as the A431 cell line used herein. This is because during lysis and incubation with the immobilized antibody, the phosphatases remove phosphate groups from the EGF-R molecules, thus prohibiting endogenous adaptor proteins, such as GRB proteins, to bind EGFR, which could potentially lead to artifactual results. Alternatively, cells may be starved before lysis, if the cell line utilized may be readily starved. Preparation of autophophorylated EGF-R: The following in vitro kinase reaction yielded autophosphorylated EGF-R.
- the kinase reaction was initiated by the addition of 15 ⁇ l of ATP/Mn 2+ mix (in 50 mM MnCl 2 , final concentration of 10 ⁇ M ATP, for a total volume of 150 ⁇ l.
- the plate was incubated for 5 minutes at room temperature, shaking, the supernatant was aspirated, and the plates were then washed 5 times with TBST.
- Assay procedure Either 30 ng GRB-2-GST fusion proteins (i.e. a 1:1 ratio of EGF-R:GRB-2 proteins) or 5 ng GRB-2-GST fusion proteins (i.e. a 4:1 ratio of EGF-R:GRB-2 proteins) were added to the phosphorylated EGF-R coated microtiter wells in incubation buffer (0.1 M potassium phosphate buffer, pH 6.5) for 30 minutes, at room temperature, in the presence of Compound I. Control wells were incubated with GRB-2-GST fusion proteins in the absence of Compound I.
- incubation buffer 0.1 M potassium phosphate buffer, pH 6.5
- GRB-2-GST fusion protein bound to the immobilized EGF-R is then preferably determined by with a purified rabbit antiserum against the GST-moiety of the fusion protein (AMRAD, New Victoria, Australia; Catalog No. 00001605) . Incubations were for 30 minutes at room temperature. After incubation, antibody was removed and the wells are washed extensively with TBST. For visualization, wells were next incubated with a TAGO goat-anti-rabbit peroxidase antibody at room temperature for 30 minutes. After incubation, the antibody was removed, the wells were washed with tap water, and then with TBST.
- EL-6 or EL-12 may be utilized to assay fusion protein binding.
- the epitopes recognized by such antibodies map on the SH2 domain of GRB-2, but do not interfere with GRB-2 binding to phosphorylated EGFR. Binding of these antibodies is then determined by using a streptavidin-biotinylated horseradish peroxidase reactant.
- binding of the fusion protein to the immobilized EGFR may be assayed by incubating w..th 1 mM l-chloro-2,4 dinitrobenzene (CDNB) and 1.54 mg/ml reduced glutathion in incubation buffer. The OD is then measured at 340 nm. This reaction is linear up to OD 1.0, and can be stopped with competitive GST inhibitors, as described in Mannervik and Danielson (Mannervik, B. and Danielson, U.H., 1988, CRC Critical Reviews in Biochemistry 23_:238) .
- Compound I proves to be a potent inhibitor of GRB-2/SH2 binding, having an IC 50 of 2.9 ⁇ M. (IC 50 , as used herein, return to the concentration of test compound required to inhibit one-half of GRB-2/SH2 binding relative to the amount of binding which occurs in the absence of test compound.)
- 32D cl.3 murine lymphoblastoid cell, IL-3 dependent .
- 32D bcr/abl 32D over expressing bcr/abl kinase, pooled, IL-3 independent.
- 32D cl.3 RPMI + 10% FBS + 1 ng/ml IL-3 + 2 mM Glutamine.
- 32D cl.3 J2/leuk RPMI + 10% FBS + 2 mM Glutamine.
- 32D bcr/abl RPMI + 10% FBS + 2 mM Glutamine.
- IL-3 Interleukin-3, mouse (UBI Cat. # 01-374)
- Acetic Acid Glacial, Fisher Cat. #A38. working solution: Dissolve 200 g SDS- in 250 ml warm H 2 0 and 500 ml DMF, stir in low heat. When SDS is almost solubilized, add 25 ml 80% acetic acid and 25 ml IN HCL to solution. Adjust volume to 1000 ml'.
- 6.2 PROCEDURE All of the following steps were conducted at room temperature unless specifically indicated. 6.2.1 CELL SEEDING (1) The cells were grown in tissue culture dish (10 cm, Corning 25020-100) to about lxlO 6 cell/ml, subculture every 2- 3 days at 1:10 (1:20 for 32D bcr/abl line) . (2) Viable cells were counted with trypan blue according to standard procedure.
- 32D cl.3 seeding medium should contain 2 ng/ml IL-3.
- Compound I drug stock (10 mM in DMSO) was diluted 1:50. 1:2 serial dilutions were performed for the remaining 8 wells in each line of the tissue culture plate. 50 ⁇ l were added to each well. Control wells received medium alone. Cells were incubated with drugs in 5% C0 2 at 37° for 15 hrs.
- Compound I on bcr/abl function was tested using the cell growth assay described, above, in Section 6.1. Briefly, three cell lines were used in this assay. First, an IL-3 dependent cell line (32D cl.3) was used, which requires the presence of the IL-3 cytokine for survival. Next, two IL-3 independent cell lines were used, including 32D cl.3 J2/leuk, which consists of the 32D cl.3 cell line transformed with raf and myc, and 32D bcr/abl, which consists of the 32D cl.3 cell line transformed with bcr/abl.
- 32D cl.3 J2/leuk which consists of the 32D cl.3 cell line transformed with raf and myc
- 32D bcr/abl which consists of the 32D cl.3 cell line transformed with bcr/abl.
- MCF-7SRB Growth Assay MCF-7 (ATCC# HTB 22) cells (H+B22) were seeded at 2000 cells/well in a 96-well flat bottom plate in normal growth media, which was 10% FBS/RPMI supplemented with 2 mM Glutamine. The plate of cells was incubated for about 24 hours at 37°C after which it received an equal volume of compound dilution per well making the total volume per well 200 ⁇ l . The compound was prepared at 2 times the desired highest final concentration and serially diluted in the normal growth media in a 96-well round bottom plate and then transferred to plate of cells. DMSO serves as the vector control up to 0.2% as final concentration.
- the cells were then incubated at 37°C in a humidified 5% C0 2 incubator. Four days following dosing of compound, the media was discarded and 200 ⁇ l/well of ice-cold 10% TCA (Trichloroacetic Acid) was added to fix cells. After 60 minutes at 4°C, the TCA was discarded and the plate was rinsed 5 times with water. The plate was then air-dried and 100 ⁇ l/well of 0.4% SRB (Sulforhodamine B from Sigma) 20 in 1% Acetic Acid was added to stain cells for 10 minutes at room temperature. The SRB was discarded and the plate was rinsed 5 times with 1% Acetic Acid.
- TCA Terichloroacetic Acid
- SRB counterion binding dye sulforhodamine B
- C6 cells In assays using C6 cells (CCL 107) , compounds (100 ⁇ l) were added to 96-well plates containing attached cellular monolayers (2000 cells/well in 100 ⁇ l) .
- C6 (ATCC# CCL 107) cells were maintained in Ham's F10 supplemented with 5% fetal bovine serum (FBS) and 2 mM glutamine (GL ⁇ ) . After 4 days (37°C, 5% C0 2 ) the monolayers were washed 3 times with PBS and fixed with 200 ⁇ l ice-cold 10% TCA (Fisher Scientific) , and kept at 4°C for 60 min.
- FBS fetal bovine serum
- GL ⁇ 2 mM glutamine
- the TCA was removed and the fixed monolayers were washed 5 times with tap water and allowed to dry completely at room temperature on absorbent paper.
- the cellular protein was stained for 10 min with 100 ⁇ l 0.4% SRB dissolved in 1% acetic acid. After 5 washes with tap water, the dye was solubilized in 10 mM Tris base (100 ⁇ l per well) and absorbance read at 570 nm on a Dynatech plate reader model MR5000. Growth inhibition data were expressed as a percentage of absorbance detected in control wells which were treated with 0.4% DMSO alone. DMSO controls were not different from cells grown in regular growth medium. IC 50 values were determined using a four parameter curve fit 5 function.
- Assay 3 MCF-7/HER-2B Growth Assay.
- the protocol used herein is essentially similar to that described above (for 5 the MCF-7 Growth Assay) except that immediately before
- Compound I was added, the normal growth media was removed and 0.5% FBS/RPMI supplemented with 2 mM Glutamine is added onto the cells. The compound was also prepared in this 0.5% serum media. The plate of cells was incubated for four days and 0 developed as per standard techniques.
- Assay 4 A431/SRB Growth Assay.
- A431 ATCC# CRL 1555 cells were tested essentially according to the protocol described, above, for the MCF-7/HER-2B growth assay.
- MCF7-HER 2 6 IC 50 refers to the concentration of test compound required to inhibit cell proliferation to 50% of the level seen in the same cell line which has not been contacted to test compound (in this case, Compound I) .
- test compound in this case, Compound I
- results depicted in this Section demonstrate that Compound I acts to inhibit cell proliferation.
- 3T3 CELLULAR PROLIFERATION INHIBITION ASSAY The following protocol describes the procedures used to determine the ability of the compounds to inhibit cellular proliferation in 3T3 engineered cell lines that over expressing EGFr, IGFlr, or PDGFr.
- IGF1 Ligand human, recombinant; G511, Promega Corp, USA.
- PDGF Ligand human PDGF B/B; 1276-956, Boehringer Mannheim, Germany.
- SRB sulfohodamine B; S-9012, Sigma Chemical Co., USA.
- Tris Base Buffer 10 mM tris base (BP152-5, Fisher Scientific, USA) .
- N-1H 3T3 (ATCC# 1658) engineered cell liens: 3T3- EGFr, 3T3-IGFlr, 3T3-PDGFr.
- the ligands are prepared in the serum free DMEM with 0.1% bovine albumin.
- the negative control cells receive the serum free DMEM with 0.1% bovine albumin only; the positive control cells receive the ligands (EGF, IGF1, or PDGF) but no drugs.
- the drugs are prepared in the serum free DMEM in a 96 well plate, and a serial dilution is taken the place. A total of lO ⁇ l/well medium of the diluted drugs are added into the cells. The total volume of each well is 200 ⁇ L. Quadruplicates (wells) and 11 concentration points are applied to each drug tested.
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EP96917126A EP0831809A4 (en) | 1995-06-07 | 1996-06-05 | Method and compositions for inhibition of adaptor protein/tyrosine kinase interactions |
BR9609353A BR9609353A (en) | 1995-06-07 | 1996-06-05 | Pharmaceutical composition suitable for administration in humans to improve symptoms of a cell proliferative disorder and compounds |
JP9501241A JPH11506770A (en) | 1995-06-07 | 1996-06-05 | Methods and compositions for inhibiting adapter protein / tyrosine kinase interactions |
MX9709442A MX9709442A (en) | 1995-06-07 | 1996-06-05 | Method and compositions for inhibition of adaptor protein/tyrosine kinase interactions. |
AU59799/96A AU697120C (en) | 1995-06-07 | 1996-06-05 | Method and compositions for inhibition of adaptor protein/tyrosine kinase interactions |
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- 1996-06-05 CN CN96196106A patent/CN1192680A/en active Pending
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- 1996-06-05 EP EP96917126A patent/EP0831809A4/en not_active Withdrawn
- 1996-06-05 IL IL12242796A patent/IL122427A0/en unknown
- 1996-06-05 WO PCT/US1996/008741 patent/WO1996040115A1/en not_active Application Discontinuation
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US6376529B1 (en) | 1995-06-07 | 2002-04-23 | Peng Cho Tang | Mono- and bis-indolylquinones and prophylactic and therapeutic uses thereof |
US6750240B2 (en) | 1996-11-13 | 2004-06-15 | Sugen, Inc. | Methods of using bis-indolylquinones |
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EP0959881A1 (en) * | 1996-11-13 | 1999-12-01 | Sugen, Inc. | Synthetic methods for the preparation of indolylquinones and mono- and bis-indolylquinones prepared therefrom |
US6660763B2 (en) | 1996-11-13 | 2003-12-09 | Sugen, Inc. | Bis-indolylquinone compounds |
US7135320B2 (en) | 1996-12-03 | 2006-11-14 | New York University | Adaptor protein FRS2 and related products and methods |
US6310181B1 (en) | 1996-12-03 | 2001-10-30 | New York University Medical Center | Adaptor protein FRS2 and related products and methods |
WO1998024902A1 (en) * | 1996-12-03 | 1998-06-11 | Sugen, Inc. | Adaptor protein frs2 and related products and methods |
US6051597A (en) * | 1997-06-13 | 2000-04-18 | Merck & Co., Inc. | Indolylquinones as antidiabetic agents |
US6943191B1 (en) | 1998-02-27 | 2005-09-13 | The United States Of America As Represented By The Department Of Health And Human Services | Disubstituted lavendustin A analogs and pharmaceutical composition comprising the analogs |
US6077849A (en) * | 1998-04-02 | 2000-06-20 | Merck & Co., Inc. | Antidiabetic agents |
WO2001021589A3 (en) * | 1999-09-24 | 2002-01-17 | Sugen Inc | Mono- and bis-indolylquinones and prophylactic and therapeutic uses thereof |
WO2001021589A2 (en) * | 1999-09-24 | 2001-03-29 | Sugen, Inc. | Mono- and bis-indolylquinones and prophylactic and therapeutic uses thereof |
US7057052B2 (en) | 2002-09-26 | 2006-06-06 | Duke University | Heterocyclic quinones as pharmaceutical agents |
US8501780B2 (en) | 2004-06-24 | 2013-08-06 | Glaxosmithkline Llc | Indazole carboxamides and their use |
FR2878849A1 (en) * | 2004-12-06 | 2006-06-09 | Aventis Pharma Sa | New substituted indole derivatives, useful for treatment of cancer, are kinase inhibitors |
WO2006061493A1 (en) * | 2004-12-06 | 2006-06-15 | Aventis Pharma S.A. | Substituted indoles, compositions containing them, method for the production thereof and their use |
US7566736B2 (en) | 2004-12-06 | 2009-07-28 | Aventis Pharma S.A. | Substituted indoles, compositions containing them, method for the production thereof and their use |
EA012613B1 (en) * | 2004-12-06 | 2009-10-30 | Авентис Фарма С.А. | Substituted indoles, compositions containing them, method for the production thereof and their use |
US8354406B2 (en) | 2005-06-30 | 2013-01-15 | Glaxosmithkline Llc | Chemical compounds |
US8372875B2 (en) | 2007-03-23 | 2013-02-12 | GlaxoSmithKline, LLC | Indole carboxamides as IKK2 inhibitors |
US8063071B2 (en) | 2007-10-31 | 2011-11-22 | GlaxoSmithKline, LLC | Chemical compounds |
US8354539B2 (en) | 2009-03-10 | 2013-01-15 | Glaxo Group Limited | Indole derivatives as IKK2 inhibitors |
Also Published As
Publication number | Publication date |
---|---|
US20020016353A1 (en) | 2002-02-07 |
BR9609353A (en) | 1999-05-11 |
US6090838A (en) | 2000-07-18 |
EP0831809A1 (en) | 1998-04-01 |
MX9709442A (en) | 1998-02-28 |
US5780496A (en) | 1998-07-14 |
CA2224103A1 (en) | 1996-12-19 |
AU5979996A (en) | 1996-12-30 |
EP0831809A4 (en) | 2001-11-28 |
JPH11506770A (en) | 1999-06-15 |
US6239161B1 (en) | 2001-05-29 |
IL122427A0 (en) | 1998-06-15 |
AR003140A1 (en) | 1998-07-08 |
KR19990022369A (en) | 1999-03-25 |
CN1192680A (en) | 1998-09-09 |
AU697120B2 (en) | 1998-09-24 |
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