RU2003127367A - Бензимидазоловые соединения для модулирования ige и ингибирования клеточной пролиферации - Google Patents
Бензимидазоловые соединения для модулирования ige и ингибирования клеточной пролиферации Download PDFInfo
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- RU2003127367A RU2003127367A RU2003127367/15A RU2003127367A RU2003127367A RU 2003127367 A RU2003127367 A RU 2003127367A RU 2003127367/15 A RU2003127367/15 A RU 2003127367/15A RU 2003127367 A RU2003127367 A RU 2003127367A RU 2003127367 A RU2003127367 A RU 2003127367A
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- Russia
- Prior art keywords
- substituted
- alkyl
- group
- heteroaryl
- salt
- Prior art date
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- 230000035407 negative regulation of cell proliferation Effects 0.000 title claims 2
- 150000001556 benzimidazoles Chemical class 0.000 title 1
- 125000001072 heteroaryl group Chemical group 0.000 claims 42
- 150000001875 compounds Chemical class 0.000 claims 41
- 125000000217 alkyl group Chemical group 0.000 claims 28
- 150000003839 salts Chemical class 0.000 claims 28
- 239000008194 pharmaceutical composition Substances 0.000 claims 27
- 229910052739 hydrogen Inorganic materials 0.000 claims 24
- 125000001624 naphthyl group Chemical group 0.000 claims 20
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 20
- 125000006763 (C3-C9) cycloalkyl group Chemical group 0.000 claims 16
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 16
- 125000005842 heteroatom Chemical group 0.000 claims 16
- 125000000547 substituted alkyl group Chemical group 0.000 claims 16
- 239000000126 substance Substances 0.000 claims 15
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 claims 12
- 239000004615 ingredient Substances 0.000 claims 10
- 125000001931 aliphatic group Chemical group 0.000 claims 9
- 125000003367 polycyclic group Chemical group 0.000 claims 9
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 8
- 125000003545 alkoxy group Chemical group 0.000 claims 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 8
- -1 camphoril Chemical group 0.000 claims 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 8
- 229910052736 halogen Inorganic materials 0.000 claims 8
- 150000002367 halogens Chemical class 0.000 claims 8
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 8
- 229910052757 nitrogen Inorganic materials 0.000 claims 8
- 229910052760 oxygen Inorganic materials 0.000 claims 8
- 239000001301 oxygen Substances 0.000 claims 8
- 125000001424 substituent group Chemical group 0.000 claims 8
- 125000005415 substituted alkoxy group Chemical group 0.000 claims 8
- 229910052717 sulfur Inorganic materials 0.000 claims 8
- 239000011593 sulfur Substances 0.000 claims 8
- 206010020751 Hypersensitivity Diseases 0.000 claims 6
- 241000124008 Mammalia Species 0.000 claims 6
- 208000030961 allergic reaction Diseases 0.000 claims 6
- 238000000034 method Methods 0.000 claims 6
- 125000004176 4-fluorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1F)C([H])([H])* 0.000 claims 4
- 239000000048 adrenergic agonist Substances 0.000 claims 4
- 238000005576 amination reaction Methods 0.000 claims 4
- 125000003118 aryl group Chemical group 0.000 claims 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 4
- 229910052799 carbon Inorganic materials 0.000 claims 4
- 230000000737 periodic effect Effects 0.000 claims 4
- 208000024891 symptom Diseases 0.000 claims 4
- 230000004663 cell proliferation Effects 0.000 claims 3
- 239000003814 drug Substances 0.000 claims 3
- 230000002401 inhibitory effect Effects 0.000 claims 3
- 239000002574 poison Substances 0.000 claims 3
- 231100000614 poison Toxicity 0.000 claims 3
- HEMGYNNCNNODNX-UHFFFAOYSA-N 3,4-diaminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1N HEMGYNNCNNODNX-UHFFFAOYSA-N 0.000 claims 2
- 229940121948 Muscarinic receptor antagonist Drugs 0.000 claims 2
- 229940099471 Phosphodiesterase inhibitor Drugs 0.000 claims 2
- GUGOEEXESWIERI-UHFFFAOYSA-N Terfenadine Chemical compound C1=CC(C(C)(C)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 GUGOEEXESWIERI-UHFFFAOYSA-N 0.000 claims 2
- 230000010933 acylation Effects 0.000 claims 2
- 238000005917 acylation reaction Methods 0.000 claims 2
- 230000001387 anti-histamine Effects 0.000 claims 2
- 239000000739 antihistaminic agent Substances 0.000 claims 2
- 208000006673 asthma Diseases 0.000 claims 2
- 230000037396 body weight Effects 0.000 claims 2
- 239000000812 cholinergic antagonist Substances 0.000 claims 2
- 239000003246 corticosteroid Substances 0.000 claims 2
- 239000003085 diluting agent Substances 0.000 claims 2
- 230000002757 inflammatory effect Effects 0.000 claims 2
- 239000003112 inhibitor Substances 0.000 claims 2
- 239000003199 leukotriene receptor blocking agent Substances 0.000 claims 2
- 239000002571 phosphodiesterase inhibitor Substances 0.000 claims 2
- 230000002265 prevention Effects 0.000 claims 2
- 150000003919 1,2,3-triazines Chemical class 0.000 claims 1
- 150000003920 1,2,4-triazines Chemical class 0.000 claims 1
- 150000000182 1,3,5-triazines Chemical class 0.000 claims 1
- GOUHYARYYWKXHS-UHFFFAOYSA-M 4-formylbenzoate Chemical compound [O-]C(=O)C1=CC=C(C=O)C=C1 GOUHYARYYWKXHS-UHFFFAOYSA-M 0.000 claims 1
- BXRFQSNOROATLV-UHFFFAOYSA-N 4-nitrobenzaldehyde Chemical compound [O-][N+](=O)C1=CC=C(C=O)C=C1 BXRFQSNOROATLV-UHFFFAOYSA-N 0.000 claims 1
- 102000003915 DNA Topoisomerases Human genes 0.000 claims 1
- 108090000323 DNA Topoisomerases Proteins 0.000 claims 1
- 102000007537 Type II DNA Topoisomerases Human genes 0.000 claims 1
- 108010046308 Type II DNA Topoisomerases Proteins 0.000 claims 1
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 claims 1
- 239000002168 alkylating agent Substances 0.000 claims 1
- 229940100198 alkylating agent Drugs 0.000 claims 1
- 150000008064 anhydrides Chemical class 0.000 claims 1
- 239000003242 anti bacterial agent Substances 0.000 claims 1
- 230000000843 anti-fungal effect Effects 0.000 claims 1
- 239000002260 anti-inflammatory agent Substances 0.000 claims 1
- 230000003110 anti-inflammatory effect Effects 0.000 claims 1
- 230000000340 anti-metabolite Effects 0.000 claims 1
- 229940088710 antibiotic agent Drugs 0.000 claims 1
- 229940121375 antifungal agent Drugs 0.000 claims 1
- 239000002256 antimetabolite Substances 0.000 claims 1
- 229940100197 antimetabolite Drugs 0.000 claims 1
- 239000002246 antineoplastic agent Substances 0.000 claims 1
- 229940111121 antirheumatic drug quinolines Drugs 0.000 claims 1
- 239000003443 antiviral agent Substances 0.000 claims 1
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzenecarboxaldehyde Natural products O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 claims 1
- 239000011230 binding agent Substances 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 150000001907 coumarones Chemical class 0.000 claims 1
- ARUKYTASOALXFG-UHFFFAOYSA-N cycloheptylcycloheptane Chemical group C1CCCCCC1C1CCCCCC1 ARUKYTASOALXFG-UHFFFAOYSA-N 0.000 claims 1
- 150000002240 furans Chemical class 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 150000002461 imidazolidines Chemical class 0.000 claims 1
- 150000002537 isoquinolines Chemical class 0.000 claims 1
- 150000003854 isothiazoles Chemical class 0.000 claims 1
- 150000002545 isoxazoles Chemical class 0.000 claims 1
- 150000002780 morpholines Chemical class 0.000 claims 1
- 125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 claims 1
- 150000002916 oxazoles Chemical class 0.000 claims 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 claims 1
- 125000004309 pyranyl group Chemical class O1C(C=CC=C1)* 0.000 claims 1
- 150000003216 pyrazines Chemical class 0.000 claims 1
- 150000003217 pyrazoles Chemical class 0.000 claims 1
- 150000003218 pyrazolidines Chemical class 0.000 claims 1
- 150000004892 pyridazines Chemical class 0.000 claims 1
- 150000003222 pyridines Chemical class 0.000 claims 1
- 150000003230 pyrimidines Chemical class 0.000 claims 1
- 150000003233 pyrroles Chemical class 0.000 claims 1
- 150000003235 pyrrolidines Chemical class 0.000 claims 1
- 150000003248 quinolines Chemical class 0.000 claims 1
- 150000003557 thiazoles Chemical class 0.000 claims 1
- 150000004886 thiomorpholines Chemical class 0.000 claims 1
- 229930192474 thiophene Natural products 0.000 claims 1
- 150000003577 thiophenes Chemical class 0.000 claims 1
- IVGIZAJFMSXYMU-UHFFFAOYSA-N C=C(C(C(CCCC1)C1=C)=O)c1ccc2[nH]c(-c(cc3)ccc3C(NC(CC3)CCC3=C)=O)nc2c1 Chemical compound C=C(C(C(CCCC1)C1=C)=O)c1ccc2[nH]c(-c(cc3)ccc3C(NC(CC3)CCC3=C)=O)nc2c1 IVGIZAJFMSXYMU-UHFFFAOYSA-N 0.000 description 1
- SSCVYUJJLOSEJZ-UHFFFAOYSA-N C=C(C(c(cc1)cc(Cl)c1Cl)=O)c1ccc2[nH]c(-c(cc3)ccc3C(Nc3ccccc3)=O)nc2c1 Chemical compound C=C(C(c(cc1)cc(Cl)c1Cl)=O)c1ccc2[nH]c(-c(cc3)ccc3C(Nc3ccccc3)=O)nc2c1 SSCVYUJJLOSEJZ-UHFFFAOYSA-N 0.000 description 1
- OTQNLZLSDPHWQD-UHFFFAOYSA-N C=C(C1CCCCCC1)C(c1ccc2[nH]c(-c(cc3)ccc3NC(C3=CCCCC3)=O)nc2c1)=O Chemical compound C=C(C1CCCCCC1)C(c1ccc2[nH]c(-c(cc3)ccc3NC(C3=CCCCC3)=O)nc2c1)=O OTQNLZLSDPHWQD-UHFFFAOYSA-N 0.000 description 1
- NAKAOWDHZPTVEH-UHFFFAOYSA-N CC(C(c1ccc2[nH]c(-c(cc3)ccc3C(Nc3ccccc3)=O)nc2c1)=C)=O Chemical compound CC(C(c1ccc2[nH]c(-c(cc3)ccc3C(Nc3ccccc3)=O)nc2c1)=C)=O NAKAOWDHZPTVEH-UHFFFAOYSA-N 0.000 description 1
- FUOIMOCLJQZQAS-UHFFFAOYSA-N CC(C)(C(CC1)C2)C1(C)C2NC(c1ccc2[nH]c(-c(cc3)ccc3NC(c(cc3)ccc3Cl)=O)nc2c1)=O Chemical compound CC(C)(C(CC1)C2)C1(C)C2NC(c1ccc2[nH]c(-c(cc3)ccc3NC(c(cc3)ccc3Cl)=O)nc2c1)=O FUOIMOCLJQZQAS-UHFFFAOYSA-N 0.000 description 1
- 0 CC(CC1)CCC1C(**c1ccc2[n]c(-c(cc3)ccc3C(NC3[C@](C)CCCC3)=O)nc2c1)=O Chemical compound CC(CC1)CCC1C(**c1ccc2[n]c(-c(cc3)ccc3C(NC3[C@](C)CCCC3)=O)nc2c1)=O 0.000 description 1
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- UCSVEEFUIBENRY-UHFFFAOYSA-N CC(CC1)CCC1NC(c1ccc2[nH]c(-c(cc3)ccc3C(NC3(CC(C4)C5)CC5CC4C3)=O)nc2c1)=O Chemical compound CC(CC1)CCC1NC(c1ccc2[nH]c(-c(cc3)ccc3C(NC3(CC(C4)C5)CC5CC4C3)=O)nc2c1)=O UCSVEEFUIBENRY-UHFFFAOYSA-N 0.000 description 1
- TUPXGQAAAVKSMD-UHFFFAOYSA-N CC(CCCC1)C1NC(c(cc1)ccc1-c1nc2cc(C(C(C3CCCCCC3)=C)=O)ccc2[nH]1)=O Chemical compound CC(CCCC1)C1NC(c(cc1)ccc1-c1nc2cc(C(C(C3CCCCCC3)=C)=O)ccc2[nH]1)=O TUPXGQAAAVKSMD-UHFFFAOYSA-N 0.000 description 1
- LHSDEXSYNZTFOH-UHFFFAOYSA-N CC(CCCC1)C1NC(c(cc1)ccc1-c1nc2cc(C(NC3CCCCC3)=O)ccc2[nH]1)=O Chemical compound CC(CCCC1)C1NC(c(cc1)ccc1-c1nc2cc(C(NC3CCCCC3)=O)ccc2[nH]1)=O LHSDEXSYNZTFOH-UHFFFAOYSA-N 0.000 description 1
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- KTZHJGGYMVYLLS-UHFFFAOYSA-N O=C(c(cc1)ccc1-c1nc2cc(C(NC3CCCCC3)=O)ccc2[nH]1)NC1C(CC2)CC2C1 Chemical compound O=C(c(cc1)ccc1-c1nc2cc(C(NC3CCCCC3)=O)ccc2[nH]1)NC1C(CC2)CC2C1 KTZHJGGYMVYLLS-UHFFFAOYSA-N 0.000 description 1
- KNNALUKZJGKHEC-UHFFFAOYSA-N O=C(c(cc1)ccc1-c1nc2cc(C(Nc(cc3)ccc3F)=O)ccc2[nH]1)NC1C(CC2)CC2C1 Chemical compound O=C(c(cc1)ccc1-c1nc2cc(C(Nc(cc3)ccc3F)=O)ccc2[nH]1)NC1C(CC2)CC2C1 KNNALUKZJGKHEC-UHFFFAOYSA-N 0.000 description 1
- FOTVARABJJKAND-UHFFFAOYSA-N O=C(c(cc1)ccc1-c1nc2cc(C(Nc3ccccc3)=O)ccc2[nH]1)Nc(cc1)ccc1Cl Chemical compound O=C(c(cc1)ccc1-c1nc2cc(C(Nc3ccccc3)=O)ccc2[nH]1)Nc(cc1)ccc1Cl FOTVARABJJKAND-UHFFFAOYSA-N 0.000 description 1
- YQIDHDLKUQOZRR-UHFFFAOYSA-N O=C(c(cc1)ccc1-c1nc2cc(NC(c(cc3)cc(Cl)c3Cl)=O)ccc2[nH]1)NC1(CC(C2)C3)CC3CC2C1 Chemical compound O=C(c(cc1)ccc1-c1nc2cc(NC(c(cc3)cc(Cl)c3Cl)=O)ccc2[nH]1)NC1(CC(C2)C3)CC3CC2C1 YQIDHDLKUQOZRR-UHFFFAOYSA-N 0.000 description 1
- UXUNAEZJRDMDRT-UHFFFAOYSA-N O=C(c(cc1)ccc1-c1nc2cc(NC(c(cc3)cc(Cl)c3Cl)=O)ccc2[nH]1)NC1CCCCCC1 Chemical compound O=C(c(cc1)ccc1-c1nc2cc(NC(c(cc3)cc(Cl)c3Cl)=O)ccc2[nH]1)NC1CCCCCC1 UXUNAEZJRDMDRT-UHFFFAOYSA-N 0.000 description 1
- MEIGEXAHFSESNQ-UHFFFAOYSA-N O=C(c(cc1)ccc1-c1nc2cc(NC(c3ccccc3)=O)ccc2[nH]1)NC1CCCCC1 Chemical compound O=C(c(cc1)ccc1-c1nc2cc(NC(c3ccccc3)=O)ccc2[nH]1)NC1CCCCC1 MEIGEXAHFSESNQ-UHFFFAOYSA-N 0.000 description 1
- LLSIPXQFQJOVAM-UHFFFAOYSA-N O=C(c(cc1)ccc1Cl)Nc(cc1)ccc1-c1nc2cc(C(Nc3ccccc3)=O)ccc2[nH]1 Chemical compound O=C(c(cc1)ccc1Cl)Nc(cc1)ccc1-c1nc2cc(C(Nc3ccccc3)=O)ccc2[nH]1 LLSIPXQFQJOVAM-UHFFFAOYSA-N 0.000 description 1
- HBUPFFLHEBPLQK-UHFFFAOYSA-N O=C(c1ccc2[nH]c(-c(cc3)ccc3C(Nc(cc3)ccc3F)=O)nc2c1)NC1C(CC2)CC2C1 Chemical compound O=C(c1ccc2[nH]c(-c(cc3)ccc3C(Nc(cc3)ccc3F)=O)nc2c1)NC1C(CC2)CC2C1 HBUPFFLHEBPLQK-UHFFFAOYSA-N 0.000 description 1
- WPPJSMHCHJSXGW-UHFFFAOYSA-N O=C(c1ccc2[nH]c(-c(cc3)ccc3C(Nc(cc3Cl)ccc3Cl)=O)nc2c1)NC1C(CC2)CC2C1 Chemical compound O=C(c1ccc2[nH]c(-c(cc3)ccc3C(Nc(cc3Cl)ccc3Cl)=O)nc2c1)NC1C(CC2)CC2C1 WPPJSMHCHJSXGW-UHFFFAOYSA-N 0.000 description 1
- DPDIEZVLGBAPDC-UHFFFAOYSA-N O=C(c1ccc2[nH]c(-c(cc3)ccc3C(Nc3ccccc3)=O)nc2c1)NC1CCCCC1 Chemical compound O=C(c1ccc2[nH]c(-c(cc3)ccc3C(Nc3ccccc3)=O)nc2c1)NC1CCCCC1 DPDIEZVLGBAPDC-UHFFFAOYSA-N 0.000 description 1
- ZKKRIDDFYDRBCR-UHFFFAOYSA-N O=C(c1ccc2[nH]c(-c(cc3)ccc3C(Nc3cnccc3)=O)nc2c1)NC1CCCCCC1 Chemical compound O=C(c1ccc2[nH]c(-c(cc3)ccc3C(Nc3cnccc3)=O)nc2c1)NC1CCCCCC1 ZKKRIDDFYDRBCR-UHFFFAOYSA-N 0.000 description 1
- WMQZMWJOOVWSPK-UHFFFAOYSA-N O=C(c1ccc2[nH]c(-c(cc3)ccc3NC(c(c(F)c(c(F)c3F)F)c3F)=O)nc2c1)NC1CCCCC1 Chemical compound O=C(c1ccc2[nH]c(-c(cc3)ccc3NC(c(c(F)c(c(F)c3F)F)c3F)=O)nc2c1)NC1CCCCC1 WMQZMWJOOVWSPK-UHFFFAOYSA-N 0.000 description 1
- XJMSGDZIYVQREZ-UHFFFAOYSA-N O=C(c1ccc2[nH]c(-c(cc3)ccc3NC(c(cc3)cc(Cl)c3Cl)=O)nc2c1)NC1CCCCC1 Chemical compound O=C(c1ccc2[nH]c(-c(cc3)ccc3NC(c(cc3)cc(Cl)c3Cl)=O)nc2c1)NC1CCCCC1 XJMSGDZIYVQREZ-UHFFFAOYSA-N 0.000 description 1
- JQDQWEHZRGQUKL-UHFFFAOYSA-N O=C(c1ccccc1)Nc(cc1)ccc1-c1nc2cc(C(Nc3ccccc3)=O)ccc2[nH]1 Chemical compound O=C(c1ccccc1)Nc(cc1)ccc1-c1nc2cc(C(Nc3ccccc3)=O)ccc2[nH]1 JQDQWEHZRGQUKL-UHFFFAOYSA-N 0.000 description 1
- NERNEOQIBFRCKA-UHFFFAOYSA-N [O-][NH+](c(cc1)ccc1-c1nc2cc(C(Cc(cc3)ccc3F)=O)ccc2[nH]1)c(c(F)c(c(F)c1F)F)c1F Chemical compound [O-][NH+](c(cc1)ccc1-c1nc2cc(C(Cc(cc3)ccc3F)=O)ccc2[nH]1)c(c(F)c(c(F)c1F)F)c1F NERNEOQIBFRCKA-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
- A61K31/422—Oxazoles not condensed and containing further heterocyclic rings
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/18—Benzimidazoles; Hydrogenated benzimidazoles with aryl radicals directly attached in position 2
-
- 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
- C07D401/02—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
- C07D401/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
-
- 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
- C07D403/12—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 chain containing hetero atoms as chain links
-
- 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
- C07D403/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pulmonology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US27526001P | 2001-03-12 | 2001-03-12 | |
| US60/275,260 | 2001-03-12 | ||
| US10/090,044 US6759425B2 (en) | 1999-10-21 | 2002-02-27 | Benzimidazole compounds for modulating IgE and inhibiting cellular proliferation |
| US10/090,044 | 2002-02-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RU2003127367A true RU2003127367A (ru) | 2005-03-20 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2003127367/15A RU2003127367A (ru) | 2001-03-12 | 2002-02-28 | Бензимидазоловые соединения для модулирования ige и ингибирования клеточной пролиферации |
Country Status (20)
| Country | Link |
|---|---|
| US (2) | US7282518B2 (enExample) |
| EP (1) | EP1368028B1 (enExample) |
| JP (1) | JP2004528304A (enExample) |
| CN (1) | CN1496257A (enExample) |
| AR (1) | AR034023A1 (enExample) |
| AT (1) | ATE369853T1 (enExample) |
| BR (1) | BR0208010A (enExample) |
| CA (1) | CA2441177A1 (enExample) |
| CZ (1) | CZ20032691A3 (enExample) |
| DE (1) | DE60221804T2 (enExample) |
| DK (1) | DK1368028T3 (enExample) |
| ES (1) | ES2291455T3 (enExample) |
| HU (1) | HUP0303460A3 (enExample) |
| MX (1) | MXJL03000027A (enExample) |
| NZ (1) | NZ528835A (enExample) |
| PL (1) | PL364230A1 (enExample) |
| PT (1) | PT1368028E (enExample) |
| RU (1) | RU2003127367A (enExample) |
| WO (1) | WO2002072090A1 (enExample) |
| ZA (1) | ZA200307916B (enExample) |
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| US6919366B2 (en) * | 1998-05-22 | 2005-07-19 | Avanir Pharmaceuticals | Benzimidazole derivatives as modulators of IgE |
| US6911462B2 (en) * | 1998-05-22 | 2005-06-28 | Avanir Pharmaceuticals | Benzimidazole compounds for regulating IgE |
| JP2004528304A (ja) * | 2001-03-12 | 2004-09-16 | アバニール・ファーマシューティカルズ | IgEを調節し、細胞増殖を阻害するためのベンゾイミダゾール化合物 |
| US8354397B2 (en) * | 2001-07-27 | 2013-01-15 | Curis, Inc. | Mediators of hedgehog signaling pathways, compositions and uses related thereto |
| TW200304820A (en) * | 2002-03-25 | 2003-10-16 | Avanir Pharmaceuticals | Use of benzimidazole analogs in the treatment of cell proliferation |
| EP1388535A1 (en) * | 2002-08-07 | 2004-02-11 | Aventis Pharma Deutschland GmbH | Acylated arylcycloalkylamines and their use as pharmaceuticals |
| TWI276631B (en) | 2002-09-12 | 2007-03-21 | Avanir Pharmaceuticals | Phenyl-aza-benzimidazole compounds for modulating IgE and inhibiting cellular proliferation |
| AU2003270426A1 (en) * | 2002-09-12 | 2004-04-30 | Avanir Pharmaceuticals | PHENYL-INDOLE COMPOUNDS FOR MODULATING IgE AND INHIBITING CELLULAR PROLIFERATION |
| US20050239844A1 (en) * | 2002-11-02 | 2005-10-27 | Kyung-Lim Lee | Composition fo preventing secretion of immunoglobulin e-dependent histamine releasing factor |
| ATE363905T1 (de) * | 2003-04-17 | 2007-06-15 | Janssen Pharmaceutica Nv | 2-phenyl-benzimidazol und 2-phenyl-imidazo-4,5)- pyridin-derivate als checkpoint-kinase-cds1 (chk2)-hemmer zur behandlung von krebs |
| AU2004263190A1 (en) * | 2003-08-08 | 2005-02-17 | Avanir Pharmaceuticals | Selective pharmacologic inhibition of protein trafficking and related methods of treating human diseases |
| US7485658B2 (en) * | 2003-08-21 | 2009-02-03 | Osi Pharmaceuticals, Inc. | N-substituted pyrazolyl-amidyl-benzimidazolyl c-Kit inhibitors |
| BRPI0413785A (pt) | 2003-08-21 | 2006-11-07 | Osi Pharm Inc | composto, composição, e, método de tratamento de distúrbio hiperproliferativo |
| DE602005027739D1 (de) | 2004-06-30 | 2011-06-09 | Janssen Pharmaceutica Nv | Arylsubstituiertes benzimidazol- und imidazopyridinether als wirkstoffe gegen krebs |
| CN101300251B (zh) * | 2005-09-06 | 2011-08-03 | 史密丝克莱恩比彻姆公司 | 作为plk抑制剂的苯并咪唑噻吩化合物 |
| JP2009001495A (ja) * | 2005-10-13 | 2009-01-08 | Taisho Pharmaceutical Co Ltd | 2−アリール−ベンゾイミダゾール−5−カルボキサミド誘導体 |
| ATE533485T1 (de) | 2005-10-31 | 2011-12-15 | Merck Sharp & Dohme | Cetp-inhibitoren |
| AU2006311914C1 (en) * | 2005-11-03 | 2013-10-24 | Chembridge Corporation | Heterocyclic compounds as tyrosine kinase modulators |
| GB0606774D0 (en) * | 2006-04-03 | 2006-05-10 | Novartis Ag | Organic compounds |
| AR063311A1 (es) | 2006-10-18 | 2009-01-21 | Novartis Ag | Compuestos organicos |
| WO2008128968A1 (en) * | 2007-04-19 | 2008-10-30 | Novartis Ag | Nicotinic acid derivatives as modulators of metabotropic glutamate receptor-5 |
| WO2009043784A1 (en) | 2007-10-04 | 2009-04-09 | F. Hoffmann-La Roche Ag | Cyclopropyl aryl amide derivatives and uses thereof |
| WO2009112445A1 (en) * | 2008-03-10 | 2009-09-17 | Novartis Ag | Method of increasing cellular phosphatidyl choline by dgat1 inhibition |
| CN103288803B (zh) * | 2013-05-17 | 2017-10-31 | 郎恒元 | 苯并咪唑酰胺类化合物及其制备方法和应用 |
| CN104208701A (zh) * | 2013-05-29 | 2014-12-17 | 天津金耀集团有限公司 | 含有抗真菌药物的复方吸入制剂 |
| CN110234640B (zh) * | 2016-09-20 | 2023-04-07 | 利昂贝拉尔中心 | 作为抗癌剂的苯并咪唑衍生物 |
| EP3810117A4 (en) * | 2018-06-01 | 2022-03-02 | Merck Sharp & Dohme Corp. | NEW [3.3.1] BICYCLO COMPOUNDS AS INDOLAMINE-2,3-DIOXYGENASE INHIBITORS |
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| JPH06263993A (ja) | 1991-01-21 | 1994-09-20 | Konica Corp | アゾメチン系染料、インドアニリン系染料及びインドフェノール系染料の製造法 |
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| US5322847A (en) | 1992-11-05 | 1994-06-21 | Pfizer Inc. | Azabenzimidazoles in the treatment of asthma, arthritis and related diseases |
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-
2002
- 2002-02-28 JP JP2002571049A patent/JP2004528304A/ja active Pending
- 2002-02-28 NZ NZ528835A patent/NZ528835A/en unknown
- 2002-02-28 PT PT02715052T patent/PT1368028E/pt unknown
- 2002-02-28 RU RU2003127367/15A patent/RU2003127367A/ru not_active Application Discontinuation
- 2002-02-28 PL PL02364230A patent/PL364230A1/xx unknown
- 2002-02-28 CA CA002441177A patent/CA2441177A1/en not_active Abandoned
- 2002-02-28 BR BR0208010-9A patent/BR0208010A/pt not_active IP Right Cessation
- 2002-02-28 CZ CZ20032691A patent/CZ20032691A3/cs unknown
- 2002-02-28 DE DE60221804T patent/DE60221804T2/de not_active Expired - Fee Related
- 2002-02-28 HU HU0303460A patent/HUP0303460A3/hu unknown
- 2002-02-28 CN CNA028064860A patent/CN1496257A/zh active Pending
- 2002-02-28 EP EP02715052A patent/EP1368028B1/en not_active Expired - Lifetime
- 2002-02-28 DK DK02715052T patent/DK1368028T3/da active
- 2002-02-28 ES ES02715052T patent/ES2291455T3/es not_active Expired - Lifetime
- 2002-02-28 AT AT02715052T patent/ATE369853T1/de not_active IP Right Cessation
- 2002-02-28 WO PCT/US2002/006801 patent/WO2002072090A1/en not_active Ceased
- 2002-02-28 MX MXJL03000027A patent/MXJL03000027A/es not_active Application Discontinuation
- 2002-03-11 AR ARP020100869A patent/AR034023A1/es unknown
-
2003
- 2003-10-10 ZA ZA200307916A patent/ZA200307916B/en unknown
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2004
- 2004-03-05 US US10/795,006 patent/US7282518B2/en not_active Expired - Fee Related
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2007
- 2007-04-27 US US11/741,702 patent/US20070202133A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| EP1368028A1 (en) | 2003-12-10 |
| BR0208010A (pt) | 2004-12-21 |
| DE60221804D1 (de) | 2007-09-27 |
| DE60221804T2 (de) | 2008-05-15 |
| NZ528835A (en) | 2005-05-27 |
| ZA200307916B (en) | 2004-09-03 |
| CN1496257A (zh) | 2004-05-12 |
| JP2004528304A (ja) | 2004-09-16 |
| US20070202133A1 (en) | 2007-08-30 |
| ES2291455T3 (es) | 2008-03-01 |
| ATE369853T1 (de) | 2007-09-15 |
| AR034023A1 (es) | 2004-01-21 |
| US7282518B2 (en) | 2007-10-16 |
| MXJL03000027A (es) | 2004-04-30 |
| US20040214821A1 (en) | 2004-10-28 |
| PT1368028E (pt) | 2007-11-26 |
| EP1368028B1 (en) | 2007-08-15 |
| CA2441177A1 (en) | 2002-09-19 |
| DK1368028T3 (da) | 2007-12-27 |
| PL364230A1 (en) | 2004-12-13 |
| WO2002072090A1 (en) | 2002-09-19 |
| CZ20032691A3 (en) | 2004-04-14 |
| HUP0303460A3 (en) | 2004-07-28 |
| HUP0303460A2 (hu) | 2004-03-01 |
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