US20050096473A1

US20050096473A1 - Thiourea and urea liquid-phase combinatorial libraries: synthesis and apoptosis induction

Info

Publication number: US20050096473A1
Application number: US10/947,049
Authority: US
Inventors: Zhaohai Zhu; Chen Mao; Rama Narla; Fatih Uckun
Original assignee: Parker Hughes Institute
Current assignee: Parker Hughes Institute
Priority date: 1999-03-19
Filing date: 2004-09-21
Publication date: 2005-05-05
Also published as: CA2367857A1; EP1163195A1; AU3891300A; JP2002540086A; WO2000056681A1; US20020103380A1; US6794541B2; WO2000056681A9

Abstract

This invention provides combinatorial chemistry libraries containing thiourea and urea compounds. In addition, the invention relates to methods for constructing combinatorial chemistry libraries containing thiourea and urea compounds. Furthermore, this invention relates to methods for the identification of bioactive thiourea and urea compounds as well as compositions and therapeutic methods for treating cancer.

Description

PRIORITY OF THE INVENTION

This application is a continuation application of international application number PCT/US00/06989 filed on 19 Mar. 2000 claiming priority under 35 U.S.C. 119 (a)-(e) to U.S. Provisional Application Number 60/125,146 filed on 19 Mar. 1999; the international application was published under PCT Article 21(2) in English as WO 00/56681.

FIELD OF THE INVENTION

This invention relates to combinatorial chemistry libraries containing thiourea and urea compounds. In addition, the invention relates to methods for constructing combinatorial chemistry libraries containing thiourea and urea compounds. Furthermore, this invention relates to methods for the identification of bioactive thiourea and urea compounds as well as compositions and therapeutic methods for treating cancer.

BACKGROUND OF THE INVENTION

A common method of drug discovery is to first delineate a biochemical pathway that is involved in a targeted pathological process. The biological pathway is analyzed so as to determine crucial elements which, if obstructed, restrained or otherwise adversely modified could inhibit the pathological process. Generally, an assay can be developed that is indicative of the functional ability of an element of the biochemical pathway. The assay can then be performed in the presence of a number of different molecules. The researcher can then determine the molecules that have the desired effect on the pathway, and that molecule or molecules can be used in treatment or can be further modified to augment and enhance the desired effect.
As the assays that are indicative of these pathways become faster, and more easily automated, the rate determining step regarding molecular screening becomes the production of the molecules to be tested. Thus, the development of techniques to rapidly and systematically synthesize large numbers of molecules possessing diverse structural properties has grown in importance. On such technique for rapidly and systematically synthesizing large numbers of molecules possessing diverse structural properties is the construction of combinatorial libraries. Combinatorial chemistry employing solution-phase combinatorial synthesis plays and increasingly important role in drug discovery efforts.
Combinatorial libraries are typically formed via a multistep synthetic procedure employing either solution-phase or solid-phase methods. The procedure typically includes mixtures of different subunits which are added stepwise to growing oligomers until a desired oligomer size is reached. Alternatively, the subunits can be combined in one synthetic step to produce a random array of oligomers or a combination of the two procedures may be employed. The result is the rapid synthesis of a large, diverse group of chemical compounds that can be screened with the predictive assay developed with regard to the targeted pathological process. Since the chance of finding useful molecules increases with the size of the combinatorial library, it is desirable to generate libraries composed of large numbers of oligomers which vary in their subunit sequence.
Apoptosis is a biochemical process that is an important part of a number of diseases. Apoptosis is a common mode of eukaryotic cell death which is triggered by an inducible cascade of biochemical events leading to activation of endonucleases that cleave the nuclear DNA into oligonucleosome-length fragments. Several of the biochemical events that contribute to apoptotic cell death as well as both positive and negative regulators of apoptosis have recently been identified (Whyllie A., et al. (1980) Int. Rev. Cytol. 68, 251-305; Steller H., (1995) Science 267, 1445-1449; Fraser, A., Evan, G. (1996) Cell 85, 781-784; and Korsmeyer, S. J. (1995). Trends Genet. 11, 101-105). Apoptosis plays a pivotal role in the development and maintenance of a functional immune system by ensuring the timely self-destruction of autoreactive immature and mature lymphocytes as well as any emerging target neoplastic cells by cytotoxic T cells.
In addition to the beneficial effects associated with apoptosis, inappropriate apoptosis contributes to the pathogenesis and drug resistance of human leukemias and lymphomas (Cohen, J. J., et al. (1992)Annu. Rev. Immunol. 10, 267-293; Linette, G. P., Korsmeyer, S. J. (1994) Curr. Opin. Cell Biol. 6, 809-815; and Thompson, C. B. (1995)Science 367, 1456-1462). Thus, agents that are useful to modulate apoptosis are potentially useful as therapeutic agents for treating diseases in which inappropriate apoptosis is implicated. As a result, there is a considerable amount of ongoing research devoted to the identification of molecular regulators of apoptosis, and there is currently a need for novel agents (e.g. chemical or biological), and novel therapeutic methods, that are useful for modulating apoptosis. Such agents and methods may be useful for treating cancer (e.g. leukemias and lymphomas) or immune disorders in mammals. They may also be useful as pharmacological tooIs for use in in vitro or in vivo studies to enhance the understanding of the molecular basis of apoptosis (e.g. the pro-apoptotic versus the anti-apoptotic regulatory signal), as well as the pathogenesis of human lymphoid malignancies.
Novel thiourea and urea compounds have been found to be potent cytotoxic agents with potent activity against cancer cells. For example, certain thiourea and urea compounds exhibit potent cytotoxic activity, particularly against human leukemic cell lines. Additionally, thiourea and urea compounds have been found to be nonnucleoside inhibitors of HIV reverse transcriptase. Currently the production of thiourea and urea compounds however, is limited to the small scale synthesis of individual molecules. Thus, a method for the rapid and systematic synthesis of large numbers of thiourea and urea compounds possessing diverse structural properties is desirable.

SUMMARY OF THE INVENTION

Generally, the present invention relates to a combinatorial library including compounds of the Formula I

wherein X is S or O;

- R and R₁are individually
  
  where Ar is aryl; R₂is H or C₁to C₆alkyl; n is 0-3 and where the aryl moiety is optionally substituted from 1 to 7 times with any combination of H, halo, alkyl, haloalkyl, arylalkyl, alkoxy, haloalkoxy, and aralkoxy. One embodiment is a combinatorial library of claim 1, wherein R and R₁are individually
  
  where R₂is H or C₁to C₆alkyl; n is 0-3 and where the phenyl moiety is optionally substituted from 1 to 5 times with any combination of R₃R₄, R₅, R₆, R₇, R₈, R₉, R₁₀, R₁₁, R₁₂, R₁₃, R₁₄, R₁₅, R₁₆, R₁₇, R₁₈, R₁₉, R₂₀, R₂₁, R₂₂, R₂₃, R₂₄, R₂₅, R₂₆, and R₂₇; and where R₃is H, R₄is 2-methyl, R₅is 2-trifluoromethyl, R₆is 2-fluoro, R₇2chloro, R₈is 2-methoxy, R₉is 2-ethoxy, R₁₀3-methyl, R₁₁is 3-trifluoromethyl, R₁₂is 3-fluoro, R₁₃is 3-chloro, R₁₄is 3-iodo, R₁₅is 3-methoxy, R₁₆is 4-methyl, R₁₇is 4-trifluoromethyl, R₁₈is 4-fluoro, R₁₉is 4-chloro, R₂₀is 4-bromo, R₂₁is 4-methoxy, R₂₂is 5-trifluoromethyl, R₂₃is 5-fluoro, R₂₄is 6-fluoro, R₂₅is 5-methoxy, R₂₆is 3-benzyloxy, and R₂₇is 4-benzyloxy.

Another embodiment is a method for synthesizing a combinatorial library including compounds of the Formula I:

where X is S or O;

- R and R₁are individually
  
  where Ar is aryl; R₂is H or C₁to C₆alkyl; n is 0-3 and where the aryl moiety is optionally substituted from 1 to 7 times with any combination of H, halo, alkyl, haloalkyl, arylalkyl, alkoxy, haloalkoxy, and aralkoxy, including the step of contacting a subunit selected from the group consisting of urea and thiourea with an amine in a suitable carrier.

Yet another embodiment is composition for determining possible apoptosis induction agents for a biological substrate, comprising a combinatorial library or compounds generated therefrom.
A further embodiment of the present invention is a method of killing a cancer cell by contacting the cancer cell with a combinatorial library or compounds generated therefrom.
Another embodiment of the invention includes a kit for determining possible apoptosis induction agents for a biological substrate.
The above summary of the present invention is not intended to describe each disclosed embodiment or every implementation of the present invention. The Figures and the detailed description which follow more particularly exemplify these embodiments.

BRIEF DESCRIPTION OF THE DRAWINGS

The invention may be more completely understood in consideration of the following detailed description of various embodiments of the invention in connection with the accompanying drawings, in which:
FIG. 1A and B: are FAB mass spectrum of Combinatorial Library 1.
FIG. 2A and B: are ESI mass spectrum (FIG. 4A) and a computer-generated MS spectrum (FIG. 4B) of Combinatorial Library 34.
FIG. 3A and B: are ESI mass spectrum of CL35 (FIG. 3A) and a computer generated mass spectrum (FIG. 3B) of CL35 for comparison.
While the invention is amenable to various modifications and alternative forms, specifics thereof have been shown by way of example in the drawings and will be described in detail. It should be understood, however, that the intention is not to limit the invention to the particular embodiments described. On the contrary, the intention is to cover all modifications, equivalents, and alternatives falling within the spirit and scope of the invention.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

The present invention is believed to be applicable to combinatorial chemistry libraries containing thiourea and urea compounds. In particular, the present invention is directed to combinatorial chemistry libraries containing thiourea and urea compounds, methods for constructing these libraries and methods for the identification of bioactive thiourea and urea compounds. While the present invention is not so limited, an appreciation of various aspects of the invention will be gained through a discussion of the examples provided below.
The term “combinatorial library” refers to an intentionally created collection of differing molecules which can be prepared synthetically and screened for biological activity. A combinatorial library consists of at least two compounds.
The term “combinatorial chemistry” refers to the synthesis of compounds from sets of subunit and chemical reactions used in one or more reaction steps.
The term “alkyl” refers to straight or branched hydrocarbon radicals, such as methyl, ethyl, propyl, butyl, octyl, isopropyl, tert-butyl, sec-pentyl, and the like. Alkyl groups can either be unsubstituted or substituted with one or more substituents, e.g., halogen, alkoxy, aryl, arylalkyl, aralkoxy and the like. Typically, alkyl groups include 1 to 8 carbon atoms, preferably 1 to 5, and more preferably 1 to 3 carbon atoms.
The term “halo” refers to fluoride, chloride, bromide, and iodide radicals.
The term “aryl” refers to monovalent unsaturated aromatic carbocyclic radicals having a single ring, such as phenyl, or multiple condensed rings, such as naphthyl or anthryl, which can be optionally substituted by substituents such as halogen, alkyl, arylalkyl, alkoxy, aralkoxy, and the like.
The term “haloalkyl” refers to an alkyl group substituted with a halo radical as defined above.
The term “alkoxy” refers to an oxygen atom substituted with an alkyl radical as defined above. Typical alkoxy groups include methoxy, ethoxy, propoxy, iopropoxy, and the like. Preferable alkoxy groups include methoxy and ethoxy.
The term “arylalkyl” refers to an alkyl radical defined as above substituted with an aryl radical as defined above. Typical arylalkyl groups include phenethyl, benzyl, and naphthethyl. Preferable alylalkyl groups include phenethyl and benzyl.
The term “aralkoxy” refers to an alkoxy group as defined above where the alkyl group is substituted with an aryl radical as defined above.
The term “haloalkoxy” refers to an alkoxy group as defined above where the alkyl group is substituted with a halo radical as defined above.
The term bioactive refers to a molecule that exhibits anti-cancer, anti-microbial, or anti-viral activity.
Thiourea and Urea Combinatorial Libraries
The present invention provides combinatorial libraries that include thiourea and urea compounds represented by the Formula I:

where X is S or O;

- R and R₁are individually
  
  where Ar is aryl; R₂is H or C₁to C₆alkyl; n is 0-3 and where the aryl moiety is optionally substituted from 1 to 7 times with any combination of H, halo, alkyl, haloalkyl, arylalkyl, alkoxy, haloalkoxy, and aralkoxy. In addition, R and R₁include

In one embodiment R₁and R₂are individually

where R₂is H or C₁to C₆alkyl; n is 0-3 and where the phenyl moiety is optionally substituted from 1 to 5 times with any combination of R₃R₄, R₅, R₆, R₇, R₈, R₉, R₁₀, R₁₁, R₁₂, R₁₃, R₁₄, R₁₅, R₁₆, R₁₇, R₁₈, R₁₉, R₂₀, R₂₁, R₂₂, R₂₃, R₂₄, R₂₅, R₂₆, and R₂₇; and where R₃is H, R₄is 2-methyl, R₅is 2-trifluoromethyl, R₆is 2-fluoro, R₇2-chloro, R₈is 2-methoxy, R₉is 2-ethoxy, R₁₀3-methyl, R₁₁is 3-trifluoromethyl, R₁₂is 3-fluoro, R₁₃is 3-chloro, R₁₄is 3-iodo, R₁₅is 3-methoxy, R₁₆is 4-methyl, R₁₇is 4-trifluoromethyl, R₁₈is 4-fluoro, R₁₉is 4-chloro, R₂₀is 4-bromo, R₂₁is 4-methoxy, R₂₂is 5-trifluoromethyl, R₂₃is 5-fluoro, R₂₄is 6-fluoro, R₂₅is 5-methoxy, R₂₆is 3-benzyloxy, and R₂₇is 4-benzyloxy.
In a preferred embodiment the combinatorial libraries include compounds of Formula I where R₁and R₂are independently selected from the group

Combinatorial Synthesis
Combinatorial library synthesis is typically performed ether on a solid support, such as peptide synthesis resins, or in liquid phase. For solid support synthesis of combinatorial libraries a large number of beads or particles are suspended in a suitable carrier, such as a solvent, in an initial reaction vessel. The beads, for example, are provided with a functionalized point of attachment for a chemical subunit. The beads are then divided and placed in various separate reaction vessels. The first chemical subunit is attached to the bead, providing a variety of differently substituted solid supports. The beads are washed to remove excess reagents and recombined. The beads are again divided into separate reaction vessels and the second chemical subunit is coupled to the chemical module. This recombining and division synthetic process can be repeated until each of a number of selected chemical subunits have been incorporated onto the molecule attached to the solid support.
Solid-phase synthesis makes it easier to conduct multistep reactions and to drive reactions to completion, because excess reagents can be added and then easily washed away after each reaction step. But a much wider range of organic reactions is available for liquid-phase synthesis, the technology used traditionally by most synthetic organic chemists, and products in solution can be more easily identified and characterized. Liquid phase synthesis of combinatorial libraries typically involves combining all the desired chemical subunits in a suitable carrier, such as a solvent, and applying reactions conditions which facilitate the combining of the various chemical subunits in a random fashion to produce an array of final molecules. Alternatively, the total number of chemical subunits can be split into various grouping. These groupings can be added stepwise to the reaction vessel containing a suitable carrier and another grouping of chemical subunits thereby producing an array of final molecules in a less-random, more systematic and controlled fashion. Thus, the synthesis of compounds of a combinatorial library can take place through several sequential reaction steps in which the same or different sets of subunits and chemical reactions are used, as well as the reaction of multiple subunits in one reaction step to form multicomponent compounds.
Combinatorial library synthesis can be performed either manually or through the use of an automated process. For the manual construction of a combinatorial library, an individual would perform the carious chemical manipulations. For the construction of a combinatorial library through an automated process, the various chemical manipulations will typically be performed robotically.
Combinatorial library synthesis of the present invention is typically performed in liquid phase. The desired chemical subunits (e.g. thioureas, ureas, and amine as defined below) are combined and contacted with each other in a suitable carrier, such as a solvent, at a suitable temperature. Examples of suitable solvents include ethers, such as diethyl ether (Et₂O), chlorinated solvents, such as methylene chloride (CH₂Cl₂), chloroform, or dichloroethane, aromatics, such as toluene, or acetonitrile. Preferably, the organic solvent is acetonitrile. Suitable reaction temperatures are those which allow the desired reaction to proceed to completion in a minimum amount of time while producing the desired products in high yield and purity. Typically, reaction temperatures are such that the carrier used refluxes. The resulting crude reaction mixture is concentrated, diluted in a suitable solvent, such as a halogenated solvent, washed with an aqueous acid solution and then neutralized. The crude reaction mixture can be concentrated by a variety of methods known to those of skill in the art such as distillation, or evaporation at elevated temperatures or reduced pressure or both. Suitable halogenated solvents used to dilute the concentrated crude reaction mixture include, for example, CH₂Cl₂, chloroform, and dichloromethane. Preferable halogenated solvents include chloroform. Aqueous acid solutions useful in the present invention are known to those of skill in the art and include, for example, aqueous solutions of hydrochloric acid or acetic acid. Neutralization agents useful in the present invention are known to those of skill in the art and include, for example, alkaline salts such as CaO, NaOH, KOH and NaHCO₃.
The present method typically employs a molar ratio of the various chemical subunits of about 1:1. It shall be understood however, that the molar ratio among the various chemical subunits can be varied to as to affect the final composition of the desired combinatorial library. For example, one subgroup may be added in excess so as to produce a combinatorial library with an excess of compounds which include that particular subgroup.
Typical chemical subunits include ureas and thioureas. Preferable ureas and thioureas include, for example, those that undergo alkylamino, arylamino, and arylalkylamino de-amination. Examples of most preferred ureas and thioureas include1,1′-thiocarbonyldiimidizole (TCDI), and 1,1′-carbonyldiimidizole (CDI).
Additional chemical subunits include compounds of Formula II

where Ar is aryl; R₂is H or C₁to C₆alkyl; n is 0-3 and where the aryl moiety is optionally substituted from 1 to 7 times with any combination of H, halo, alkyl, haloalkyl, arylalkyl, alkoxy, haloalkoxy, and aralkoxy.
Preferred subunits include compounds of Formula III

where R₂is H or C₁to C₆alkyl; n is 0-3 and where the phenyl moiety is optionally substituted from 1 to 5 times with any combination of R₃R₄, R₅, R₆, R₇, R₈, R₉, R₁₀, R₁₁, R₁₂, R₁₃, R₁₄, R₁₅, R₁₆, R₁₇, R₁₈, R₁₉, R₂₀, R₂₁, R₂₂, R₂₃, R₂₄, R₂₅, R₂₆, and R₂₇; and where R₃is H, R₄is 2-methyl, R₅is 2-trifluoromethyl, R₆is 2-fluoro, R₇2-chloro, R₈is 2-methoxy, R₉is 2-ethoxy, R₁₀3-methyl, R₁₁is 3-trifluoromethyl, R₁₂is 3-fluoro, R₁₃is 3-chloro, R₁₄is 3-iodo, R₁₅is 3-methoxy, R₁₆is 4-methyl, R₁₇is 4-trifluoromethyl, R₁₈is 4-fluoro, R₁₉is 4-chloro, R₂₀is 4-bromo, R₂₁is 4-methoxy, R₂₂is 5-trifluoromethyl, R₂₃is 5-fluoro, R₂₄is 6-fluoro, R₂₅is 5-methoxy, R₂₆is 3-benzyloxy, and R₂₇is 4-benzyloxy.
Most preferred subunits include the following compounds

Screening
The present invention is directed toward the generation of thiourea and urea combinatorial libraries. These libraries can be used to select one or more urea or thiourea species that demonstrate biological activity such as, for example, apoptotic activity. Apoptosis plays a pivotal role in the development and maintenance of a functional immune system by ensuring the timely self-destruction of autoreactive immature and mature lymphocytes as well as any emerging target neoplastic cells by cytotoxic T cells. In addition to the beneficial effects associated with apoptosis, inappropriate apoptosis contributes to the pathogenesis and drug resistance of human leukemias and lymphomas.
Several methods have been developed to screen libraries of compounds to identify those compounds having the desired biological activity. Such methods are well known to those of skill in the art. For example, a cellular or enzyme solution may be combined with at solution of the compounds of a particular combinatorial library under conditions favorable to elicit a biological response such as inhibition of an enzyme or regulation of a cellular pathway. The biological activity of library compounds may be detected by any of the numerous biological assays which are well known in the art such as, for example, the MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide) assay (Boehringer Mannheim Corp., Indianapolis, Ind.) or the in apoptosis/TUNEL assay (Zhu D et al., Clinical Cancer Research 4:2967-2976, 1998). In cases where the compounds of a given combinatorial library demonstrate biological activity by binding to a biological target such as an enzyme the compound/biological target complex can be separated from other assay components using various methods known to those of skill in the art such as size-exclusion chromatography. The compound/biological target complex can then be denatured to release the compound which can then be isolated using various methods known to those of skill in the art, such as HPLC, and subjected to mass spectrometry for identification.
An alternative manner of identifying biologically active compounds is iterative synthesis and screening to deconvolute the combinatorial library. Iterative synthesis/screeing involves the synthesis of compounds in such a manner that a combinatorial library results that is not directly resolvable to determine the identity of discrete biologically active compounds, but that instead is resolvable to determine the identity of a specific compound in any mixture that shows biological activity when assayed. A new sublibrary is then synthesized based on this information and assayed, and the identity of the next specific subunit determined. The iterative process is continued until the identity of a complete, active molecule is determined. Iterative synthesis/screeing has several characteristics including diminishing library size as the iterations proceed, ending with the last step which involves the synthesis and assaying of the individual compound. Various methods of deconvolution fall within the iteration definition and will be considered as a form of iterative synthesis/screening.

EXAMPLES

Example 1

Synthesis of N,N′-Bis(2-phenylethyl)thiourea Combinatorial Libraries, Deconvolution and Identification of Biologically Active Species

The reaction is accomplished by phenethylamine substitution of imidazoles in thiocarbonyldiimidazole (TCDI) in solvent acetonitrile under reflux. The reaction is carried out in equimolar ratio. After the reaction is completed, the substituted imidazole is protonated with dilute aqueous acid and separated during solvent/solvent extraction.
Stage (I): synthesis of compound 1 in Scheme 1.
The synthesis of compound 1 was carried out by adding an equimolar amount of p-chlorophenethylamine into a solution of TCDI in acetonitrile at 0° C., followed by reflux for 1 h. Thin-layer chromatography (TLC) indicated the completion of the reaction. The concentrated reaction mixture was re-dissolved in CHCl₃. The substituted imidazole from TCDI was washed out with dilute hydrochloric acid (0.65 M) during liquid/liquid extraction. After neutralization (saturated NaHCO₃solution), drying (MgSO₄) and concentration; a white powder (m.p. 126° C.) was obtained as the desired product (1) with 90% yield and 99% purity by HPLC.
The structure of compound 1 was confirmed with ¹H NMR, ¹³C NMR, MALDI-TOF MS, and elemental analysis:
1,3-Bisp-chlorophenethyl)-2-thiourea (compound 1). ¹H NMR (300 MHz, CDCl₃, TMS) d 7.28 (d, ³J(H,H)=8.4 Hz, 4H, Ar), 7.11 (d, ³J(H,H)=8.4 Hz, 4H, Ar), 5.58 (bs, 2H, NH), 3.62 (bs, 4H, α-CH₂), 2.84 (t, ³J(H,H)=6.9 Hz, 4H, β-CH₂); ¹³C NMR d 181.6, 136.6, 132.4, 130.0, 128.7, 45.2, 34.4; MS: m/z (MALDI-TOF) 353.3 (C₁₇H₁₈C₁₂N₂S requires 353.3); UV/Vis (CH₃CN) I_max194, 224, and 249 nm; HPLC retention time 15.9 min with the following conditions: HP 1100 Series with a LiChrospher 100 RP-18 (5 mm) column (Part #799250D-584, 250-4), mobile phase: water/acetonitrile=50/50, flow rate: 1.5 mL/min, injection volume: 30 mL, wavelength: 225 nm. Anal. Calcd for C, 57.79; H, 5.13; Cl, 20.07; N, 7.93; S, 9.07. Found: C, 57.90; H, 5.13; Cl, 20.02; N, 7.88; S, 9.03.
A two-step one-pot procedure was also developed to substitute one imidazole on TCDI for each step. First, one molar equivalent of p-chlorophenethylamine was allowed to react with TCDI under 0° C. followed by reflux for 1 h. The mono-substituted thiocarbonyl intermediate was less polar as indicated by TLC (R_f0.76) vs. the di-substituted compound 2 (R_f0.46). After the completion of the first substitution by p-chlorophenethylamine, one molar equivalent of phenethylamine was added at the room temperature, followed by reflux for 1 h. After work-up, a yellow wax was obtained as product with a quantitative yield.
The structure of compound 2 was confirmed with ¹H NMR, ¹³C NMR, MALDI-TOF MS and elemental analysis:
1-(p-Chlorophenethyl)-3-phenethyl-2-thiourea (Compound 2). ¹H NMR (300 MHz, CDCl₃, TMS) d 7.33-7.09 (m, 9H, Ar), 5.62 and 5.55 (2 bs, 2, NH), 3.62 (bs, 4H, α-CH₂), 2.87 (t, ³J(H,H)=6.9 Hz, 2H, β-CH₂), 2.83 (t, ³J(H,H)=6.6 Hz, 2H, b-CH₂); ¹³C NMR d 181.5, 138.1, 136.7, 132.3, 130.0, 128.7, 128.6, 126.6, 45.3, 35.0, 34.4; MS: m/z (MALDI-TOF) 320.5 (C₁₇H₁₉CIN₂S requires 318.9); UV/Vis l_max192, 212 (shoulder), and 249 nm; HPLC retention time 10.3 min. Anal. Calcd for C₁₇H₁₉ClN₂S: C, 64.04; H, 6.01; Cl, 11.12; N, 8.79; S, 10.06. Found: C, 64.00; H, 6.07; Cl, 11.00; N, 8.87; S, 10.11.
Stage (II): synthesis of a small mixture library (SML) containing only three members (1, 2 and 3 in Scheme 2) as a model, starting from an equimolar mixture of phenethylamine and p-chlorophenethylamine in acetonitrile. The same procedure was followed as in stage (I). The library was obtained as a white powder with a quantitative yield.

SCHEME 2

Synthesis of a small mixture library (SML)

Compound R R′ Ratio

1 H H 1

2 Cl Cl 1

3 H Cl 2
The composition of SML was confirmed with ¹H NMR, LC-MS and elemental analysis:
SML. ¹H NMR (300 MHz, CDCl₃, TMS) d 7.35-7.08 (m, 9H, Ar), 5.62 (bs, 2H, NH), 3.62 (bs, 4H, α-CH₂), 2.84 (quintet, 4H, β-CH₂). LC-MS retention time 7.4 min corresponds to m/z 285.0 Da, 9.4 min to 319.0 Da, and 12.2 min to 353.0 Da; calcd mass of 284.4 (3), 318.9 (2) and 353.3 (1). Anal. Calcd for 1/2/3=1/2/1: C, 64.42; H, 6.05; Cl, 10.58; N, 8.84; S, 10.11. Found: C, 64.06; H, 6.02; Cl, 11.10; N, 8.84; S, 10.08.
Stage (III), a main library (CL1) was synthesized (Chart 1) utilizing the same method as that given in Stage II above, and started with an equimolar solution of 15 amines. The number of members in a combinatorial library can be predicted based on the following formula that takes into account the number of differing substituents, and the number of possible positions. $\begin{matrix} Number of members in library = n + C (n, r) \\ = n + n! / [(n - r)! X r!] \\ Number of members in library = 15 + 15! / [(15 - 2)! \times 2!] = 120. \end{matrix}$
The main library, CL1, that was synthesized had 15 possible substituents at two different possible positions, leading to 120 members in the combinatorial library.
The composition of CL1 was confirmed with ¹H NMR and MS:
CL1. ¹H NMR (300 MHz, CDCl₃, TMS) d 7.42-6.70 (m, rel. intensity 16, Ar), 5.75 (br, rel. intensity 3.5, NH), 5.12 (2 peaks, rel. intensity 1, OCH₂-Ph), 3.86-3.61 (m, rel. intensity 15, a-CH₂and OCH₃), 2.84 (m, rel. intensity 10, b-CH₂), 2.32 (s, rel. intensity 1, CH₃-Ph).
FIG. 1A shows the FAB MS spectrum of CL1. The mass range 284-709 corresponds to the 34 different molecular weights out of 120 members in CL1. To assist visual comparison, a theoretical mass spectrum of CL1 was generated manually with a DeltaGraph Program (FIG. 1B, which displays primary peaks only (isotopes not considered.). The mass distribution can generally be viewed as three groups: 284-422, 497-566, and 709. The FAB MS in FIG. 1A matches the theoretical mass spectrum profile in FIG. 1B.
Stage (4): deconvolution and re-synthesis were guided by an iterative screening procedure during which the cytotoxic anti-cancer activities of the individual sub-libraries were measured against the human leukemia cell lines NALM-6 and MOLT-3 using MTT assays. In general, whenever feasible, an active library was evenly splitted into two sub-libraries and upon biologic testing the more active one of the two sub-libraries was selected for further iteration. However, this is not always true when even-splitting was not possible or some special consideration. For example, library CL1 was discovered to be active and was primarily split to two uneven libraries (CL3 with 55 members, and CL4 with 64 members, Chart 2 and Chart 3). Another special example is the small 10-member sublibrary CL2. Since fluorinated compounds may possess enhanced activities and since fluorine has similar atomic radius with hydrogen, CL2 (10 members, Chart 2) was constructed with fluorine-substituted phenethylamines and phenethylamine.

CL2 is significantly more potent than CL3 and CL4. However, at this stage, we could not exclude the possibility that dilution in CL3 and CIA played a function since they contain more members. Thus, one of these two sublibraries, CL3, was split to CL5 (28 members) and CL6 (27 members, Chart 4). CL6 displayed higher potency, being split to CL7 (15 members) and CL8 (14 members, two members were overlapping in CL7 and CL8). Library CL8 is more active in the MTT assay, it was split to CL11 (6 members) and CL12 (8 members). The eight members in CL12 were synthesized individually. At this stage, since the difference between CL8 and CL7 was not significant, CL7 was also split to CL9 and CL10. And the members of CL10 were synthesized individually. The splitting process is summarized in Chart 3. The activity data are shown in Table 1. The most active CL10 compound was CL10b. The most active CL12 compounds were CL12a and CL12b.

TABLE 1


Structure and Activity of Libraries CL2, CL10 and CL12.

				IC₅₀
Structure	Rⁱ	R^j	MW	Nalm6	(MTT) Molt3

CL1				13.1	37.7
CL2				0.9	3.7
CL2a	H	H	284.4	18.2	17.4
CL2b	H	2-F	302.4	21.3	21.1
CL2c	H	3-F	302.4	17.6	12.1
CL2d	H	4-F	302.4	17.5	13.8
CL2e	2-F	2-F	320.4	19.8	19.8
CL2f	2-F	3-F	320.4	17.0	13.0
CL2g	2-F	4-F	320.4	13.9	11.2
CL2h	3-F	3-F	320.4	14.7	12.7
CL2i	3-F	4-F	320.4	18.2	12.9

CL2j

4-F

320.4

unstable compound

CL3				92.5	52.6
CL4				84.0	98.8
CL5				21.4	32.4
CL6				4.9	10.0
CL7				18.7	13.3
CL8				7.7	8.4
CL9				45.6	50.0
CL10				26.2	26.2
CL10a	4-F	2,5-(MeO)₂	362.5	29.2	28.5
CL10b	4-F	2,4-Cl₂	371.3	14.8	26.3
CL10c	4-Cl₂	2,5-(MeO)₂	378.9	33.6	29.0
CL10d	4-Cl	2,4-Cl₂	487.8	22.0	29.7
CL10e	4-F	3,4-(BnO)₂	514.7	>100	>51.4
CL10f	4-Cl	3,4-(BnO)₂	531.1	>100	>100
CL11				71.6	42.7
CL12a	2-MeO	2,5-(MeO)₂	374.5	17.4	10.9
CL12b	2-MeO	2,4-Cl₂	383.3	17.1	11.6
CL12c	2,5-(MeO)₂	2,5-(MeO)₂	404.5	28.9	39.8
CL12d	2,5-(MeO)₂	2,4-Cl₂	413.4	40.9	34.1
CL12e	2-MeO	3,4-(BnO)₂	526.7	58.1	76.7
CL12f	2,5-(MeO)₂	3,4-(BnO)₂	556.7	27.4	37.2
CL12g	2,4-Cl₂	3,4-(BnO)₂	565.6	>100	21.8
CL12h	3,4-(BnO)₂	3,4-(BnO)₂	708.9	47.8	73.3

Cytotoxic Activity Assay

The cytotoxic activity of the CL2 library compounds was investigated via apoptosis/TUNEL assay. TUNEL assay allows the detection of exposed 3 hydroxyl groups in fragmented DNA. The CL2 compounds prepared as described above, were tested, along with DMSO as a control.
The cytotoxicity assay of various CL2 compounds against human tumor cell lines was performed using the MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide) assay (Boehringer Mannheim Corp., Indianapolis, Ind.). Briefly, exponentially growing tumor cells were seeded into a 96-well plate at a density of 2.5×10⁴cells/well and incubated for 36 hours at 37° C. prior to compound exposure. On the day of treatment, culture medium was carefully aspirated from the wells and replaced with fresh medium containing the CL2 compounds at concentrations ranging from 0.0 to 100 μM. Triplicate wells were used for each treatment.
Human cell lines were obtained from American Type Culture Collection (Rockville, Md.) and maintained as a continuous cell line in Dulbecco's modified Eagles' medium supplemented with 10% fetal bovine serum and antibiotics. Cells used in this study include human leukemia cells (NALM-6 and MOLT-3).
The cells were incubated with the various compounds for 24-36 hours at 37° C. in a humidified 5% CO₂atmosphere. To each well, 10 μl of MTT (0.5 mg/ml final concentration) was added and the plates were incubated at 37° C. for 4 hours to allow MTT to form formazan crystals by reacting with metabolically active cells. The formazan crystals were solubilized overnight at 37° C. in a solution containing 10% SDS in 0.01 M HCl. The absorbance of each well was measured in a microplate reader (Labsystems) at 540 nm and a reference wavelength of 690 nm. To translate the OD₅₄₀values into the number of live cells in each well, the OD₅₄₀values were compared to those on standard OD₅₄₀—versus—cell number curves generated for each cell line. The percent survival was calculated using the formula: $% Survival = \frac{live cell number [test]}{live cell number [control]} \times 100$
The IC₅₀values were calculated by non-linear regression analysis.
The demonstration of apoptosis was performed by the in situ nick-end-labeling method using ApopTag in situ detection kit (Oncor, Gaithersburg, Md.) according to the manufacturer's recommendations. Exponentially growing cells were seeded in 6-well tissue culture plates at a density of 50×10⁴cells/well and cultured for 36 hours at 37° C. in a humidified 5% CO₂atmosphere. The supernatant culture medium was carefully aspirated and replaced with fresh medium containing unconjugated EGF or EGF-P154 at a concentration of 10, 25, or 50 Tg/ml. After a 36 hour incubation at 37° C. in a humidified 5% CO₂incubator, the supernatants were carefully aspirated and the cells were treated for 1-2 minutes with 0.1% trypsin. The detached cells were collected into a 15 ml centrifuge tube, washed with medium and pelleted by centrifugation at 1000 rpm for 5 minutes. Cells were resuspended in 50 Tl of PBS, transferred to poly-L-lysine coated coverslips and allowed to attach for 15 minutes. The cells were washed once with PBS and incubated with equilibration buffer for 10 minutes at room temperature.
After removal of the equilibration buffer, cells were incubated for 1 hour at 37° C. with the reaction mixture containing terminal deoxynucleotidyl transferase (TdT) and digoxigenin-11-UTP for labeling of exposed 3′-hydroxyl ends of fragmented nuclear DNA. The cells were washed with PBS and incubated with anti-digoxigenin antibody conjugated to FITC for 1 hour at room temperature to detect the incorporated dUTP. After washing the cells with PBS, the coverslips were mounted onto slides with Vectashield containing propidium iodide (Vector Labs, Burlingame, Calif.) and viewed with a confocal laser scanning microscope. Non-apoptotic cells do not incorporate significant amounts of dUTP due to lack of exposed 3-hydroxyl ends, and consequently have much less fluorescence than apoptotic cells which have an abundance of exposed 3′-hydroxyl ends. In control reactions, the TdT enzyme was omitted from the reaction mixture.
The cytotoxic activities of CL1 and CL3 library compounds were also investigated via apoptosis/TUNEL assay described above. Combinatorial libraries 1, 2, and 3 all caused apoptosis of NALM-6 leukemia cells in a concentration-dependent fashion.

Example 2

Synthesis of Combinatorial Thiourea Mixture Libraries in Solution Phase

A mixture containing 1830 components was synthesized in solution phase in one step from thiocarbonyldiimidazole and 60 commercially-available amines. Subsequently, 60 positional scanning deconvolution libraries were synthesized for the identification of the active components. Several individual compounds were synthesized and tested for biologic activity. Among them, 1,3-bis(1,2-diphenylethyl)-2-thiourea and 1-(1,2-diphenylethyl)-3-(diphenylmethyl)-2-thiourea are the most potent with IC₅₀values below 10 μg/ml in MTT assays.
The parent library containing 1830 members was assembled in one synthetic step using Scheme 3. The number of the members in CL34 is calculated as: 60+C(60,2)=60+60!/(2×58!)=60+60×59/2=1830.

A mixture of equimolar 60 amines (Table 2) substituted the imidazole moiety in TCDI under reflux. Specifically, a solution of 60 amines (1 mmol each, Table 2) in acetonitrile (60 mL) was added into a solution of TCDI (5.35 g, 30 mmol) in acetonitrile (100 mL) dropwise at 0° C., followed by reflux for 1 h. The completion of the reaction was monitored with TLC. The same work-up was followed as described in Example 1. A yellow gel was obtained as the desired library in 70% yield. ¹H NMR included all peaks observable with the individual compound and SML.

TABLE 2


The 60 building blocks used to assemble the parent library.




A1



A2



A3



A4



A5



A6



A7



A8



A9



A10



A11



A12



A13



A14



A15



A16



A17



A18



A19



A20



A21



A22



A23



A24



A25



A26



A27



A28



A29



A30



A31



A32



A33



A34



A35



A36



A37



A38



A39



A40



A41



A42



A43



A44



A45



A46



A47



A48



A49



A50



A51



A52



A53



A54



A55



A56



A57



A58



A59



A60

The product mixture was purified by aqueous acid wash/extraction. The reaction and purification conditions employed were the same as described for SML. The collected yield was 70%. The ESI-MS spectrum is shown in FIG. 2A and a computer-generated MS spectrum is shown in FIG. 2B for comparison.
The IC₅₀value of the CL34 parent library in MTT assays was 70 μg/ml. After the parent mixture library was discovered to be active, 60 positional scanning deconvolution libraries (Boger, D. L.; Jiang, W.; Goldberg, J. J. Org. Chem. 1999, 64, 7094-7100; (b) Dooley, C. T.; Houghten, R. A. Life Sci. 1993, 52, 1509; (c) Pinilla, C.; Appel, J. R.; Blanc, P.; Houghten, R. A. Biotechniques, 1992, 13, 901) were assembled in order to identify those building blocks essential for an active thiourea library as shown in Scheme 4.
Each of the sublibraries is comprised of thiourea compounds that share an identical N substitution on one end and differ from each other by the variant N′ substitution on the other end representing one of the 60 different building blocks shown in Table 2.
The solution phase combinatorial synthesis was accomplished using the Argonaut Quest 205 synthesizer, which can carry out 10 reactions in parallel. All of the reaction conditions used for glass flasks were readily adapted for the synthesizer, except reflux was replaced with temperature control at 81° C. (bp of acetonitrile) in sealed reaction vessels. Specifically, anhydrous acetonitrile (20 mL for each reaction vessel) was loaded in parallel in reaction vessels of Quest 205 synthesizer, which consists of 10 reaction vessels with 100-mL capacity each, followed by loading of TCDI (1.069 g, 6 mmol each reaction vessel). The reaction vessels were cooled down to 5° C. with circulating ice-water. Amines A1-A10 (Table 2) were dissolved in 20-mL anhydrous acetonitrile each separately, and added into the TCDI solutions dropwise, separately. The reaction vessels were heated up and maintained at 81° C. for 1 h in closed nitrogen-gas environment. The completion of the first substitution can be monitored with TLC. A stock solution of amines A1-A60 (Table 2) (1 mmol each) were dissolved in 200-mL acetonitrile. The amine mixture solution (20 mL each time) was added into every reaction vessel sequentially via syringes. The reaction vessels were heated up and maintained at 81° C. for 1 h. The same work-up was followed as in Example 1. A yellow gel was obtained with a 68-100% yield.

The biologic activity of the sublibraries was examined in standard MTT assays. The results, expressed as the IC₅₀values (in μg/ml) are shown in Table 3.

TABLE 3


MTT Assay Results and Yields of Synthesis of the
Deconvolution Libraries

IC₅₀, μg/mL

	Sublibrary	Nalm6	Molt3	Yield, %

CL34A1	41.05	51.2	94
CL34A2	5.6	63.8	96
CL34A3	8.7	28.4	100
CL34A4	7.9	26.3	100
CL34A5	19.0	8.6	92
CL34A6	15.7	41.9	100
CL34A7	52.9	45.4	93
CL34A8	48.3	39.1	100
CL34A9	17.8	22.2	100
CL34A10	31.6	29.3	78
CL34A11	38.3	35.6	81
CL34A12	33.4	49.6	91
CL34A13	43.7	42.0	100
CL34A14	78.6	72.5	81
CL34A15	76.3	95.7	83
CL34A16	78.6	97.4	84
CL34A17	41.3	76.8	83
CL34A18	74.2	46.2	78
CL34A19	41.5	40.5	73
CL34A20	33.7	40.6	61
CL34A21	37.0	39.1	100
CL34A22	38.6	45.9	93
CL34A23	60.2	98.5	91
CL34A24	92.1	85.3	92
CL34A25	44.7	29.2	84
CL34A26	56.3	>100	91
CL34A27	25.9	20.5	90
CL34A28	55.5	50.3	92
CL34A29	44.2	45.6	71
CL34A30	58.6	>100	94
CL34A31	56.3	>100	89
CL34A32	53.4	>100	92
CL34A33	44.8	64.5	89
CL34A34	54.4	>100	95
CL34A35	93.1	99.3	99
CL34A36	62.1	>100	90
CL34A37	45.3	>100	96
CL34A38	61.6	46.3	93
CL34A39	49.5	53.6	94
CL34A40	36.4	>100	84
CL34A41	73.2	>100	91
CL34A42	78.3	>100	99
CL34A43	84.8	98.4	100
CL34A44	70.3	91.6	98
CL34A45	20.8	21.0	94
CL34A46	88.4	89.6	78
CL34A47	>100	>100	68
CL34A48	89.6	83.6	78
CL34A49	97.4	95.6	93
CL34A50	91.9	>100	90
CL34A51	95.6	>100	31
CL34A52	78.4	89.8	85
CL34A53	67.8	88.2	89
CL34A54	70.8	71.6	88
CL34A55	75.9	85.1	91
CL34A56	10.6	32.0	99
CL34A57	11.6	15.6	64
CL34A58	48.3	91.5	98
CL34A59	62.1	71.5	86
CL34A60	63.3	57.6	85

The results in Table 2 indicate that sublibraries CL34A2, CL34A3, CL34A4, and CL34A5, containing 60 compounds each, have significant cytotoxic activity with IC50 values <10 μg/ml. Sublibraries CL34A56 and CL34A57 were also cytotoxic, with slightly higher IC50 values. 21 individual compounds (6 symmetrical and 15 asymmetrical compounds) using the active building blocks of these 6 sublibraries were synthesized (Chart 4).
Specifically, anhydrous acetonitrile (10 mL for each reaction vessel) was loaded in parallel in reaction vessels of Quest 205 synthesizer, followed by loading of TCDI (0.535 g, 3 mmol each reaction vessel). The reaction vessels were cooled down to 5° C. with circulating ice-water. Amines A2, A3, A5, A56 and A57 (6 mmol each) were dissolved in 20-mL anhydrous acetonitrile each separately, and added into #1-#5 of the TCDI solutions, separately. Amine A2 (3 mmol each in three round-bottomed flasks) was dissolved in anhydrous acetonitrile (10-mL each) separately, and added into TCDI solutions in reaction vessels #6-#8 dropwise at 5° C. Amine A3 (3 mmol each in two round-bottomed flasks) was dissolved in anhydrous acetonitrile (10-mL each) separately, and added into TCDI solutions in reaction vessels #9 and #10 dropwise at 5° C. The reaction vessels #6-#10 were heated up to and maintained at 81° C. for one hour (The temperature of the two banks, #1-#5 and #6-#10, can be controlled separately). Amines A3, A4 and A5 were dissolved in 10-mL acetonitrile each in three round-bottomed flasks, and added into reaction vessels #6-#8 dropwise at 5° C. Amines A4 and A5 were dissolved in 10-mL acetonitrile each in two round-bottomed flasks, and added into reaction vessels #9 and #10 separately at 5° C. The reaction vessels were heated up to and maintained at 81° C. for one hour. The same work-up was followed as in Example 1.

These 21 compounds were tested for cytotoxic activity against Nalm6 leukemia cell line using MTT assays. The results are presented in Table 4. The most active compounds were L34ASA5 (1,3-bis(1,2-diphenylethyl)-2-thiourea) and L34A3AS (1-(1,2-diphenylethyl)-3-(diphenylmethyl)-2-thiourea). L34A2A5 and L34A3A56 ranked second best.

TABLE 4


MTT Assay Results and Yields for the Lead Compounds

	ED₅₀, μg/mL
Compounds	Nalm6	Yield, %

Group 1
L34A2A2	50	76
L34A3A3	>100	78
L34A4A4	30	67
L34A5A5	<10	68
L34A2A3	50	67
L34A2A4	50	80
L34A2A5	25	68
L34A3A4	>50	82
L34A3A5	<10	85
L34A4A5	50	97
Group 2
L34A56A56	50	78
L34A57A57	30	75
L34A2A56	>50	85
L34A2A57	>50	82
L34A3A56	25	82
L34A3A57	30	81
L34A4A56	50	72
L34A4A57	30	63
L34A5A56	50	82
L34A5A57	30	82
L34A56A57	>50	92

The physicochemical data for the two most active compounds are as follows:
1,3-Bis(1,2-diphenylethyl)-2-thiourea (L34A5A5). A white powder (0.887 g, 68% yield) was obtained as the desired product. ¹H NMR (CDCl₃, 300 MHz) d 7.31-6.80 (m, 20H), 6.08 (bs, 2H), 5.08 (bs, 2H), 3.00 (d, J=6.6 Hz, 4H); ¹³C NMR (CDCl₃, 75 MHz) d 180., 140.0, 136.1, 129.3, 129.1, 128.7, 128.4, 128.2, 126.5, 126.2, 107.2, 60.0, 59.3, 43.1; m/z (MALDI-TOF) 437.1 (C₂₉H₂₈N₂S+H⁺ requires 437.6); UV-vis l_max202, 208, 253 nm; HPLC retention time 37.7 min, purity 98%.
1-(1,2-Diphenylethyl)-3-(diphenylmethyl)-2-thiourea (L34A3A5). A white powder (0.981 g, 77% yield) was obtained as the desired product. ¹H NMR (CDCl₃, 300 MHz) d 7.35-7.15 (m, 15H), 6.91 (m, 5H), 6.16 (m, 3H), 5.22 (bs, 1H), 3.04 (m, 2H); m/z (MALDI-TOF) 422.4 (C₂₈H₂₆N₂S⁺ requires 422.6); UV-vis l_max202, 206, 253 nm; HPLC retention time 33.3 min, purity 92%.

Example 3

Synthesis of Urea Mixture Libraries

A mixture containing 1830 urea compounds was synthesized in one step depicted in Scheme 5 from carbonyldiimidazole and 60 commercially-available amines shown in FIG. 3, as described for thiourea compounds in Example 2. Sixty positional scanning deconvolution libraries were synthesized for the identification of active components. FIG. 3A shows the ESI-MS spectrum of CL35. FIG. 3B shows a computer-generated MS spectrum of CL35 for comparison.

The MTT assay results for these sublibraries are shown in Table 5.

TABLE 5


MTT Assay Results of the Deconvolution Libraries

IC₅₀, μg/mL

	Sublibrary	Nalm6	Molt3

CL35A1	>100	>100
CL35A2	>100	>100
CL35A3	>100	>100
CL35A4	36.9	24.1
CL35A5	20.6	22.9
CL35A6	33.3	26.2
CL35A7	95.6	>100
CL35A8	90.2	91.3
CL35A9	37.9	31.8
CL35A10	81.4	96.4
CL35A11	65.3	95.1
CL35A12	74.4	57.9
CL35A13	24.8	36.7
CL35A14	60.3	64.1
CL35A15	86.2	>100
CL35A16	81.5	>100
CL35A17	71.2	96.1
CL35A18	84.2	90.5
CL35A19	81.2	95.6
CL35A20	62.5	68.2
CL35A21	70.1	66.3
CL35A22	68.3	66.2
CL35A23	88.2	81.5
CL35A24	70.6	95.4
CL35A25	58.1	56.2
CL35A26	60.4	66.2
CL35A27	23.4	23.6
CL35A28	45.8	71.5
CL35A29	47.8	50.3
CL35A30	85.6	>100
CL35A31	70.2	62.5
CL35A32	66.3	60.5
CL35A33	48.1	60.2
CL35A34	37.2	46.5
CL35A35	66.3	>100
CL35A36	90.5	91.2
CL35A37	49.6	96.5
CL35A38	42.5	70.2
CL35A39	36.2	48.9
CL35A40	70.2	94.0
CL35A41	49.2	37.9
CL35A42	70.5	78.2
CL35A43	75.6	79.1
CL35A44	73.6	70.5
CL35A45	44.7	32.3
CL35A46	53.2	55.8
CL35A47	>100	>100
CL35A48	>100	>100
CL35A49	98.1	92.6
CL35A50	96.8	90.2
CL35A51	18.9	38.3
CL35A52	25.8	48.3
CL35A53	27.1	29.7
CL35A54	62.5	60.4
CL35A55	56.8	50.6
CL35A56	53.4	55.9
CL35A57	42.6	52.6
CL35A58	43.4	40.2
CL35A59	66.8	70.2
CL35A60	>100	>100

Sublibraries CL35A2, CL35A3, CL35A4, and CL35A5, containing 60 compounds each, were the most biologically active.

The present invention should not be considered limited to the particular examples described above, but rather should be understood to cover all aspects of the invention as fairly set out in the attached claims. Various modifications, equivalent processes, as well as numerous structures to which the present invention may be applicable will be readily apparent to those of skill in the art to which the present invention is directed upon review of the instant specification.
The content of all publications, patents, and patent documents described and cited herein is incorporated by reference as if fully set forth. The invention described herein may be modified to include alternative embodiments. All such obvious alternatives are within the spirit and scope of the invention, as claimed below.

Claims

1. A process comprising:

reacting a compound of formula I:

with an amine selected from:

2. A process comprising:

reacting a compound of formula I:

with amines of formula:

3. A process comprising:

reacting a compound of formula I:

with an amine selected from:

4. A process comprising:

reacting a compound of formula I:

with amines of formula:

5. A product produced by the process of claim 2.

6. The product of claim 5, wherein the product includes a library of 1830 members.

7. A product produced by the process of claim 4.

8. The product of claim 7, wherein the product includes a library of 1830 members.

9 A compound selected from the group of:

10. A method of killing a cancer cell by contacting the cancer cell with the product of claim 5.

11. A method of killing a cancer cell by contacting the cancer cell with the product of claim 7.

12. A method comprising administering to a cancer patient an effective cancer cell killing amount of a compound of Formula I

wherein X is S or O;

R and R₁are individually

wherein Ar is aryl; R₂is H or C₁to C₆alkyl; n is 0-3 and where the aryl moiety is optionally substituted from 1 to 7 times with any combination of H, halo, alkyl, haloalkyl, arylalkyl, alkoxy, haloalkoxy, and aralkoxy.

13. The method of claim 12, wherein R and R₁are individually selected from the group of:

14. The method of claim 12, wherein the compound is:

14. The method of claim 12, wherein the cancer patient has leukemia.

15. The method of claim 10, wherein the cancer cell is a leukemia cell.

16. The method of claim 11, wherein the cancer cell is a leukemia cell.

17. A kit for determining possible apoptosis induction agents for a biological substrate comprising the product of claim 5.

18. A kit for determining possible apoptosis induction agents for a biological substrate comprising the product of claim 7.