RU2008143179A - Органические соединения - Google Patents
Органические соединения Download PDFInfo
- Publication number
- RU2008143179A RU2008143179A RU2008143179/04A RU2008143179A RU2008143179A RU 2008143179 A RU2008143179 A RU 2008143179A RU 2008143179/04 A RU2008143179/04 A RU 2008143179/04A RU 2008143179 A RU2008143179 A RU 2008143179A RU 2008143179 A RU2008143179 A RU 2008143179A
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- disease
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- 150000002894 organic compounds Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract 22
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 14
- 239000001257 hydrogen Substances 0.000 claims abstract 14
- 229910052736 halogen Inorganic materials 0.000 claims abstract 13
- 150000002367 halogens Chemical group 0.000 claims abstract 13
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract 8
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract 7
- 150000002431 hydrogen Chemical class 0.000 claims abstract 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract 6
- 125000001424 substituent group Chemical group 0.000 claims abstract 6
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract 6
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract 5
- 229930195733 hydrocarbon Natural products 0.000 claims abstract 5
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract 5
- 125000000217 alkyl group Chemical group 0.000 claims abstract 4
- -1 amino, hydroxy Chemical group 0.000 claims abstract 4
- 229910052799 carbon Inorganic materials 0.000 claims abstract 4
- 125000004043 oxo group Chemical group O=* 0.000 claims abstract 4
- 125000003118 aryl group Chemical group 0.000 claims abstract 3
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract 3
- 125000003545 alkoxy group Chemical group 0.000 claims abstract 2
- 125000004429 atom Chemical group 0.000 claims abstract 2
- 125000004452 carbocyclyl group Chemical group 0.000 claims abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 2
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract 2
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract 2
- 229910052760 oxygen Inorganic materials 0.000 claims abstract 2
- 125000003003 spiro group Chemical group 0.000 claims abstract 2
- 229910052717 sulfur Inorganic materials 0.000 claims abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 7
- 239000000651 prodrug Substances 0.000 claims 6
- 229940002612 prodrug Drugs 0.000 claims 6
- 150000003839 salts Chemical class 0.000 claims 6
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims 6
- 201000010099 disease Diseases 0.000 claims 5
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 4
- 206010020880 Hypertrophy Diseases 0.000 claims 4
- 102000007330 LDL Lipoproteins Human genes 0.000 claims 4
- 208000017169 kidney disease Diseases 0.000 claims 4
- 208000031226 Hyperlipidaemia Diseases 0.000 claims 3
- 208000022559 Inflammatory bowel disease Diseases 0.000 claims 3
- 208000001132 Osteoporosis Diseases 0.000 claims 3
- 230000001771 impaired effect Effects 0.000 claims 3
- 208000015122 neurodegenerative disease Diseases 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 208000011580 syndromic disease Diseases 0.000 claims 3
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 2
- 208000024827 Alzheimer disease Diseases 0.000 claims 2
- 201000001320 Atherosclerosis Diseases 0.000 claims 2
- 206010004446 Benign prostatic hyperplasia Diseases 0.000 claims 2
- 208000024172 Cardiovascular disease Diseases 0.000 claims 2
- 206010009900 Colitis ulcerative Diseases 0.000 claims 2
- 208000011231 Crohn disease Diseases 0.000 claims 2
- 208000032928 Dyslipidaemia Diseases 0.000 claims 2
- 206010056438 Growth hormone deficiency Diseases 0.000 claims 2
- 102000015779 HDL Lipoproteins Human genes 0.000 claims 2
- 206010019280 Heart failures Diseases 0.000 claims 2
- 206010020772 Hypertension Diseases 0.000 claims 2
- 206010022489 Insulin Resistance Diseases 0.000 claims 2
- 208000007177 Left Ventricular Hypertrophy Diseases 0.000 claims 2
- 208000017170 Lipid metabolism disease Diseases 0.000 claims 2
- 206010027476 Metastases Diseases 0.000 claims 2
- 206010028980 Neoplasm Diseases 0.000 claims 2
- 208000008589 Obesity Diseases 0.000 claims 2
- 208000004403 Prostatic Hyperplasia Diseases 0.000 claims 2
- 208000000924 Right ventricular hypertrophy Diseases 0.000 claims 2
- MUMGGOZAMZWBJJ-DYKIIFRCSA-N Testostosterone Chemical compound O=C1CC[C@]2(C)[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 MUMGGOZAMZWBJJ-DYKIIFRCSA-N 0.000 claims 2
- 201000006704 Ulcerative Colitis Diseases 0.000 claims 2
- 210000001367 artery Anatomy 0.000 claims 2
- 206010003246 arthritis Diseases 0.000 claims 2
- 238000006243 chemical reaction Methods 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
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- 239000003814 drug Substances 0.000 claims 2
- 230000002526 effect on cardiovascular system Effects 0.000 claims 2
- 208000007565 gingivitis Diseases 0.000 claims 2
- 230000004153 glucose metabolism Effects 0.000 claims 2
- 230000003054 hormonal effect Effects 0.000 claims 2
- 201000001421 hyperglycemia Diseases 0.000 claims 2
- 208000006575 hypertriglyceridemia Diseases 0.000 claims 2
- 208000002551 irritable bowel syndrome Diseases 0.000 claims 2
- 150000002632 lipids Chemical class 0.000 claims 2
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- 239000000932 sedative agent Substances 0.000 claims 2
- 230000001624 sedative effect Effects 0.000 claims 2
- 230000008719 thickening Effects 0.000 claims 2
- 238000011282 treatment Methods 0.000 claims 2
- 230000002792 vascular Effects 0.000 claims 2
- 210000005166 vasculature Anatomy 0.000 claims 2
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims 1
- 108091005477 5-HT3 receptors Proteins 0.000 claims 1
- 108091005482 5-HT4 receptors Proteins 0.000 claims 1
- PQSUYGKTWSAVDQ-ZVIOFETBSA-N Aldosterone Chemical compound C([C@@]1([C@@H](C(=O)CO)CC[C@H]1[C@@H]1CC2)C=O)[C@H](O)[C@@H]1[C@]1(C)C2=CC(=O)CC1 PQSUYGKTWSAVDQ-ZVIOFETBSA-N 0.000 claims 1
- PQSUYGKTWSAVDQ-UHFFFAOYSA-N Aldosterone Natural products C1CC2C3CCC(C(=O)CO)C3(C=O)CC(O)C2C2(C)C1=CC(=O)CC2 PQSUYGKTWSAVDQ-UHFFFAOYSA-N 0.000 claims 1
- 206010002329 Aneurysm Diseases 0.000 claims 1
- 102000005666 Apolipoprotein A-I Human genes 0.000 claims 1
- 108010059886 Apolipoprotein A-I Proteins 0.000 claims 1
- 208000028698 Cognitive impairment Diseases 0.000 claims 1
- 208000032781 Diabetic cardiomyopathy Diseases 0.000 claims 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims 1
- 208000002705 Glucose Intolerance Diseases 0.000 claims 1
- 208000035150 Hypercholesterolemia Diseases 0.000 claims 1
- 206010033645 Pancreatitis Diseases 0.000 claims 1
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- 206010036049 Polycystic ovaries Diseases 0.000 claims 1
- 208000017442 Retinal disease Diseases 0.000 claims 1
- 206010038923 Retinopathy Diseases 0.000 claims 1
- 229940122388 Thrombin inhibitor Drugs 0.000 claims 1
- 229960002478 aldosterone Drugs 0.000 claims 1
- 230000001195 anabolic effect Effects 0.000 claims 1
- 239000000883 anti-obesity agent Substances 0.000 claims 1
- 239000003472 antidiabetic agent Substances 0.000 claims 1
- 229940125708 antidiabetic agent Drugs 0.000 claims 1
- 239000002220 antihypertensive agent Substances 0.000 claims 1
- 229940030600 antihypertensive agent Drugs 0.000 claims 1
- 239000003524 antilipemic agent Substances 0.000 claims 1
- 239000002246 antineoplastic agent Substances 0.000 claims 1
- 229940125710 antiobesity agent Drugs 0.000 claims 1
- 229940127218 antiplatelet drug Drugs 0.000 claims 1
- 230000000949 anxiolytic effect Effects 0.000 claims 1
- 230000036528 appetite Effects 0.000 claims 1
- 235000019789 appetite Nutrition 0.000 claims 1
- 230000001925 catabolic effect Effects 0.000 claims 1
- 230000015556 catabolic process Effects 0.000 claims 1
- 230000001906 cholesterol absorption Effects 0.000 claims 1
- 229940127089 cytotoxic agent Drugs 0.000 claims 1
- 206010012601 diabetes mellitus Diseases 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 239000003623 enhancer Substances 0.000 claims 1
- 229940011871 estrogen Drugs 0.000 claims 1
- 239000000262 estrogen Substances 0.000 claims 1
- 239000008103 glucose Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 201000010066 hyperandrogenism Diseases 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 claims 1
- 229940126601 medicinal product Drugs 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 230000000626 neurodegenerative effect Effects 0.000 claims 1
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- 201000010065 polycystic ovary syndrome Diseases 0.000 claims 1
- 230000002980 postoperative effect Effects 0.000 claims 1
- 201000009104 prediabetes syndrome Diseases 0.000 claims 1
- XOFYZVNMUHMLCC-ZPOLXVRWSA-N prednisone Chemical compound O=C1C=C[C@]2(C)[C@H]3C(=O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 XOFYZVNMUHMLCC-ZPOLXVRWSA-N 0.000 claims 1
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- 0 *C(CC(Nc1nnc(cc2CN)[n]1cc2-c(c(Cl)c1)ccc1Cl)=O)C1CCCC1 Chemical compound *C(CC(Nc1nnc(cc2CN)[n]1cc2-c(c(Cl)c1)ccc1Cl)=O)C1CCCC1 0.000 description 1
- JIKSZIPJKTWEDU-UHFFFAOYSA-N CC(C)COc1c(CN)c(-c(c(Cl)c2)ccc2Cl)c[n]2c1ncc2C(N1CCOCC1)=O Chemical compound CC(C)COc1c(CN)c(-c(c(Cl)c2)ccc2Cl)c[n]2c1ncc2C(N1CCOCC1)=O JIKSZIPJKTWEDU-UHFFFAOYSA-N 0.000 description 1
- FIATUNXLTSBECJ-UHFFFAOYSA-N CCCCNc1c(CN)c(-c(c(Cl)c2)ccc2Cl)c[n]2c1ncc2 Chemical compound CCCCNc1c(CN)c(-c(c(Cl)c2)ccc2Cl)c[n]2c1ncc2 FIATUNXLTSBECJ-UHFFFAOYSA-N 0.000 description 1
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- OIRJUPRDPAYWPR-UHFFFAOYSA-N CCOC(CN(C)c1cnc(cc2CN)[n]1cc2-c(c(Cl)c1)ccc1Cl)=O Chemical compound CCOC(CN(C)c1cnc(cc2CN)[n]1cc2-c(c(Cl)c1)ccc1Cl)=O OIRJUPRDPAYWPR-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
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| US10669271B2 (en) | 2018-03-30 | 2020-06-02 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| LT3790877T (lt) | 2018-05-11 | 2023-05-10 | Incyte Corporation | Tetrahidro-imidazo[4,5-c]piridino dariniai kaip pd-l1 imunomoduliatoriai |
| BR112021001709A2 (pt) | 2018-08-01 | 2021-05-04 | Araxes Pharma Llc | compostos espiro heterocíclicos e métodos de uso dos mesmos para o tratamento de câncer |
| WO2020047198A1 (en) | 2018-08-31 | 2020-03-05 | Incyte Corporation | Salts of an lsd1 inhibitor and processes for preparing the same |
| US12419865B2 (en) | 2018-12-06 | 2025-09-23 | Arisan Therapeutics Inc. | Compounds for the treatment of arenavirus infection |
| TW202115059A (zh) | 2019-08-09 | 2021-04-16 | 美商英塞特公司 | Pd—1/pd—l1抑制劑之鹽 |
| CN114555596B (zh) | 2019-09-30 | 2025-02-25 | 詹森药业有限公司 | 放射性标记的mgl pet配体 |
| EP4037773A1 (en) | 2019-09-30 | 2022-08-10 | Incyte Corporation | Pyrido[3,2-d]pyrimidine compounds as immunomodulators |
| PE20230407A1 (es) | 2019-11-11 | 2023-03-07 | Incyte Corp | Sales y formas cristalinas de un inhibidor de pd-1/pd-l1 |
| WO2022099071A1 (en) | 2020-11-06 | 2022-05-12 | Incyte Corporation | Process for making a pd-1/pd-l1 inhibitor and salts and crystalline forms thereof |
| US11780836B2 (en) | 2020-11-06 | 2023-10-10 | Incyte Corporation | Process of preparing a PD-1/PD-L1 inhibitor |
| WO2022099075A1 (en) | 2020-11-06 | 2022-05-12 | Incyte Corporation | Crystalline form of a pd-1/pd-l1 inhibitor |
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| US5559158A (en) | 1993-10-01 | 1996-09-24 | Abbott Laboratories | Pharmaceutical composition |
| SE9500051D0 (sv) * | 1995-01-09 | 1995-01-09 | Frode Rise | Antioxidants, tissue- and/or neuroprotectants |
| GB2351081A (en) * | 1999-06-18 | 2000-12-20 | Lilly Forschung Gmbh | Pharmaceutically active imidazoline compounds and analogues thereof |
| CN100415744C (zh) * | 2001-02-20 | 2008-09-03 | 阿斯特拉曾尼卡有限公司 | 用于治疗与gsk3有关的病症的2-芳基氨基-嘧啶 |
| SE0100567D0 (sv) * | 2001-02-20 | 2001-02-20 | Astrazeneca Ab | Compounds |
| CA2452803A1 (en) * | 2001-08-10 | 2003-02-20 | Altana Pharma Ag | Tricyclic imidazopyridines |
| ES2345096T3 (es) | 2002-02-13 | 2010-09-15 | F. Hoffmann-La Roche Ag | Nuevos derivados de piridina y pirimidina. |
| ATE309988T1 (de) | 2002-02-13 | 2005-12-15 | Hoffmann La Roche | Neue pyridin- und quinolin-derivate |
| MY139563A (en) * | 2002-09-04 | 2009-10-30 | Bristol Myers Squibb Co | Heterocyclic aromatic compounds useful as growth hormone secretagogues |
| EP1753730A1 (en) * | 2004-06-04 | 2007-02-21 | Takeda Pharmaceutical Company Limited | Dipeptidyl peptidase inhibitors |
| GB0413605D0 (en) * | 2004-06-17 | 2004-07-21 | Addex Pharmaceuticals Sa | Novel compounds |
| WO2006019965A2 (en) | 2004-07-16 | 2006-02-23 | Takeda San Diego, Inc. | Dipeptidyl peptidase inhibitors |
-
2007
- 2007-03-29 CN CNA2007800112382A patent/CN101410397A/zh active Pending
- 2007-03-29 US US12/295,549 patent/US8097617B2/en not_active Expired - Fee Related
- 2007-03-29 RU RU2008143179/04A patent/RU2008143179A/ru not_active Application Discontinuation
- 2007-03-29 MX MX2008012617A patent/MX2008012617A/es not_active Application Discontinuation
- 2007-03-29 KR KR1020087023759A patent/KR20080104351A/ko not_active Withdrawn
- 2007-03-29 CA CA002644963A patent/CA2644963A1/en not_active Abandoned
- 2007-03-29 JP JP2009502104A patent/JP2009531390A/ja active Pending
- 2007-03-29 AU AU2007233709A patent/AU2007233709A1/en not_active Abandoned
- 2007-03-29 WO PCT/EP2007/053064 patent/WO2007113226A1/en not_active Ceased
- 2007-03-29 EP EP07727536A patent/EP2004643A1/en not_active Withdrawn
- 2007-03-29 BR BRPI0710110-4A patent/BRPI0710110A2/pt not_active IP Right Cessation
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2011
- 2011-12-06 US US13/311,949 patent/US20120077787A1/en not_active Abandoned
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|---|---|
| US20120077787A1 (en) | 2012-03-29 |
| EP2004643A1 (en) | 2008-12-24 |
| JP2009531390A (ja) | 2009-09-03 |
| WO2007113226A1 (en) | 2007-10-11 |
| CN101410397A (zh) | 2009-04-15 |
| MX2008012617A (es) | 2008-10-10 |
| KR20080104351A (ko) | 2008-12-02 |
| CA2644963A1 (en) | 2007-10-11 |
| US20090253689A1 (en) | 2009-10-08 |
| US8097617B2 (en) | 2012-01-17 |
| BRPI0710110A2 (pt) | 2011-08-02 |
| AU2007233709A1 (en) | 2007-10-11 |
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