HRP20020475B1 - Novi derivati benzoimidazola korisni kao sredstvaprotiv proliferacije - Google Patents
Novi derivati benzoimidazola korisni kao sredstvaprotiv proliferacijeInfo
- Publication number
- HRP20020475B1 HRP20020475B1 HR20020475A HRP20020475A HRP20020475B1 HR P20020475 B1 HRP20020475 B1 HR P20020475B1 HR 20020475 A HR20020475 A HR 20020475A HR P20020475 A HRP20020475 A HR P20020475A HR P20020475 B1 HRP20020475 B1 HR P20020475B1
- Authority
- HR
- Croatia
- Prior art keywords
- cr4r5
- aryl
- groups
- cycloalkyl
- alkyl
- Prior art date
Links
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical class C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 title 1
- 230000001028 anti-proliverative effect Effects 0.000 title 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 12
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 9
- 125000000041 C6-C10 aryl group Chemical group 0.000 abstract 8
- 125000000217 alkyl group Chemical group 0.000 abstract 6
- 125000003118 aryl group Chemical group 0.000 abstract 4
- 229910052799 carbon Inorganic materials 0.000 abstract 4
- 125000004434 sulfur atom Chemical group 0.000 abstract 3
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 abstract 2
- 125000005865 C2-C10alkynyl group Chemical group 0.000 abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 2
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
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- A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
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- A61P17/00—Drugs for dermatological disorders
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- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
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- A61P17/04—Antipruritics
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- A61P19/00—Drugs for skeletal disorders
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- A61P5/14—Drugs for disorders of the endocrine system of the thyroid hormones, e.g. T3, T4
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
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- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
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- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
Abstract
Spoj formule,ili njegova farmaceutski prihvatljiva sol, predlijek ili solvat, naznačen time štoX jeCH ili N; R1 se bira između -(CR4R5)tC(O)OR3, -(CR4R5)tC(O)NR3R4, -(CR4R5)tOR3, -(CR4R5)tC(O)(C3-C10 cikloalkil), -(CR4R5)tC(O)(C6-C10 aril), -(CR4R5)tC(O)(4- do 10- člani heterocikl), -(CR4R5)t(C3-C10 cikloalkil), -(CR4R5)t(C6-C10 aril) i -(CR4R5)t(4- do 10- člani heterocikl), gdje svaki t je, nezavisno, cijeli broj od 0 do 5; spomenuti cikloalkilni, arilni i heterociklički R1 ostaci izborno su spojeni sa benzenskim prstenom, C5-C8 cikloalkilnom skupinom, ili 4- do 10- članom heterocikličkom skupinom; -(CR4R5)t- ostaci prethodnih R1 skupina izborno obuhvaćaju dvostruku ili trostruku vezu ugljik-ugljik, gdje t je cijeli broj od 2 do 5; svakaod prethodnih R1 skupina je izborno supstituiranas 1 ili 2 skupine koje se nezavisno biraju između-NR3R4, -OR3, C1-C10 alkila, C2-C10 alkenila i C2-C10 alkinila, pri čemu su spomenute alkilne, alkenilne i alkinilne skupine supstituirane s 1 ili 2 skupine koje se nezavisno biraju između -NR3R4 i -OR3; i prethodne R1 skupine su izborno supstituirane s 1 do 3 R2 skupina; svaki R2 se, nezavisno, bira između H, C1-C10 alkila, C2-C10 alkenil, C2-C10alkinila, C3-C10 cikloalkila, okso, halogen, cijano, nitro, trifluormetila, difluormetoksi, trifluormetoksi, azido, -OR3, -C(O)R3, -C(O)OR3, ?NR4C(O)OR6, -OC(O)R3, -NR4SO2R6, -SO2NR3R4, -NR4C(O)R3, -C(O)NR3R4, -NR5C(O)NR3R4, -NR3R4, ?S(O)j(CR4R5)m(C6-C10 aril), -S(O)j(C1-C6 alkil), gdje j je cijelibroj od 0 do 2, -(CR4R5)m(C6-C10 aril), ?O(CR4R5)m(C6-C10 aril), -NR4(CR4R5)m(C6-C10 aril), -O(CR4R5)m(4- do 10- člani heterocikl), ?NR4(CR4R5)m(4- do 10- člani heterocikl), -(CR4R5)m(4- do 10- članiheterocikl) i -(CR4R5)m(C3-C10 cikloalkil), gdje svaki m je, nezavisno, cijeli broj od 0 do 4; spomenute alkilne, alkenilne i alkinilne skupine izborno sadrže 1 do 2 hetero ostatka koji se biraju između O, -S(O)j, gdje j je cijeli broj od 0 do 2, i -N(R3)-, pod uvjetom da dva atoma O, dva atoma S, ili O i S atomi nisu direktno vezani jedan za drugi, i pod uvjetom da svaki O atom, S atom ili N atom nije direktno vezan za trostruku vezu ili nearomatičnu dvostruku vezu; spomenute cikloalkilne, arilne i heterocikličke R2 skupine su izborno spojenesa C6-C10 arilnom skupinom, C5-C8 cikloalkilnom skupinom, ili sa 4- do 10- članom heterocikličkom skupinom; a spomenute alkilne, cikloalkilne, arilnei heterocikličke R2 skupine su izborno supstituirane s 1 do 5 supstituenata koji se nezavisno biraju između okso (=O), halogen, cijano, nitro, trifluormetila, difluormetoksi, trifluormetoksi, azido, -NR4SO2R6, -SO2NR3R4, -C(O)R3, -C(O)OR3, -OC(O)R3,-NR4C(O)OR6, -NR4C(O)R3, -C(O)NR3R4, ?NR3R4, -OR3, C1-C10 alkila, -(CR4R5)m(C6-C10 aril) i -(CR4R5)m(4- do 10- člani heterocikl), gdje svaki m je, nezavisno, cijeli broj od 0 do 4; svaki R3 se, nezavisno, bira između H, C1-C10 alkila, -(CR4R5)m(C6-C10 aril) i -(CR4R5)m(4- do 10- člani heterocikl), gdje svaki m je, nezavisno, cijeli broj od 0 do 4;spomenuta a
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US16821799P | 1999-11-30 | 1999-11-30 | |
PCT/IB2000/001636 WO2001040217A1 (en) | 1999-11-30 | 2000-11-10 | Novel benzoimidazole derivatives useful as antiproliferative agents |
Publications (2)
Publication Number | Publication Date |
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HRP20020475A2 HRP20020475A2 (en) | 2005-10-31 |
HRP20020475B1 true HRP20020475B1 (hr) | 2007-06-30 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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HR20020475A HRP20020475B1 (hr) | 1999-11-30 | 2002-05-29 | Novi derivati benzoimidazola korisni kao sredstvaprotiv proliferacije |
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Families Citing this family (113)
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UA75055C2 (uk) * | 1999-11-30 | 2006-03-15 | Пфайзер Продактс Інк. | Похідні бензоімідазолу, що використовуються як антипроліферативний засіб, фармацевтична композиція на їх основі |
EP1415987B1 (en) | 2000-10-20 | 2007-02-28 | Eisai R&D Management Co., Ltd. | Nitrogenous aromatic ring compounds as anti cancer agents |
US20100074949A1 (en) | 2008-08-13 | 2010-03-25 | William Rowe | Pharmaceutical composition and administration thereof |
PL209872B1 (pl) | 2002-03-27 | 2011-10-31 | Glaxo Group Ltd | Pochodna chinolinowa, sposób jej wytwarzania i jej zastosowanie oraz zawierająca ją farmaceutyczna kompozycja |
US6989392B2 (en) | 2002-06-18 | 2006-01-24 | Abbott Laboratories | 2-Aminoquinolines as melanin concentrating hormone receptor antagonists |
WO2003105850A1 (en) * | 2002-06-18 | 2003-12-24 | Abbott Laboratories | 2-aminoquinolines as melanin concentrating hormone receptor antagonists |
PA8580301A1 (es) * | 2002-08-28 | 2005-05-24 | Pfizer Prod Inc | Nuevos derivados de benzoimidazol utiles como agentes antiproliferativos |
PT1585743E (pt) | 2002-12-19 | 2007-07-12 | Pfizer | Compostos de 2- (1h-indazol-6-ilamin)-benzamida como inibidores de proteína-cinases úteis para o tratamento de doenças aftálmicas. |
JP2007516168A (ja) * | 2003-06-24 | 2007-06-21 | ファイザー・プロダクツ・インク | 1−[2−(ベンゾイミダゾル−1−イル)キノリン−8−イル]−ピペリジン−4−イルアミン誘導体の製造方法 |
DE602004000260T2 (de) | 2003-07-22 | 2006-08-24 | Arena Pharmaceuticals, Inc., San Diego | Diaryl- und arylheteroarylharnstoffderivate als modulatoren des 5-ht2a-serotoninrezeptors, die sich zur prophylaxe und behandlung von damit im zusammenhang stehenden erkrankungen eignen |
AP2006003549A0 (en) * | 2003-08-21 | 2006-04-30 | Osi Pharm Inc | N-substituted benzimidazolyl C-kit inhibitors. |
CN101337930B (zh) | 2003-11-11 | 2010-09-08 | 卫材R&D管理有限公司 | 脲衍生物的制备方法 |
RU2006121990A (ru) | 2003-11-21 | 2007-12-27 | Эррэй Биофарма Инк. (Us) | Ингибиторы протеинкиназ акт |
AU2011265309B2 (en) * | 2003-11-21 | 2014-06-05 | Array Biopharma, Inc. | AKT protein kinase inhibitors |
GB0411421D0 (en) * | 2004-05-21 | 2004-06-23 | Glaxo Group Ltd | Novel compounds |
ME02970B (me) | 2004-06-24 | 2018-07-20 | Vertex Pharma | Modulatori atp-vezujućih kasetnih transportera |
US8354427B2 (en) | 2004-06-24 | 2013-01-15 | Vertex Pharmaceutical Incorporated | Modulators of ATP-binding cassette transporters |
BRPI0513915A (pt) * | 2004-08-26 | 2008-05-20 | Pfizer | compostos aminoeteroarila enantiomericamente puros como inibidores de proteìna quinase |
EP1797881B1 (en) | 2004-09-17 | 2009-04-15 | Eisai R&D Management Co., Ltd. | Medicinal composition with improved stability and reduced gelation properties |
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