JP2015536997A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2015536997A5 JP2015536997A5 JP2015542015A JP2015542015A JP2015536997A5 JP 2015536997 A5 JP2015536997 A5 JP 2015536997A5 JP 2015542015 A JP2015542015 A JP 2015542015A JP 2015542015 A JP2015542015 A JP 2015542015A JP 2015536997 A5 JP2015536997 A5 JP 2015536997A5
- Authority
- JP
- Japan
- Prior art keywords
- optionally substituted
- alkyl
- compound
- compound according
- item
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 150000001875 compounds Chemical class 0.000 claims description 57
- -1 nitro, hydroxy Chemical group 0.000 claims description 22
- 229910052736 halogen Inorganic materials 0.000 claims description 19
- 150000002367 halogens Chemical class 0.000 claims description 19
- 125000002252 acyl group Chemical group 0.000 claims description 17
- 125000001072 heteroaryl group Chemical group 0.000 claims description 16
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 16
- 125000000217 alkyl group Chemical group 0.000 claims description 15
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 15
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 14
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 14
- PWEGVZDXTQLFLQ-UHFFFAOYSA-N dioxidoboron Chemical class [O-][B][O-] PWEGVZDXTQLFLQ-UHFFFAOYSA-N 0.000 claims description 14
- 125000001841 imino group Chemical group [H]N=* 0.000 claims description 14
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims description 14
- 125000005328 phosphinyl group Chemical group [PH2](=O)* 0.000 claims description 14
- 125000005499 phosphonyl group Chemical group 0.000 claims description 14
- 125000005017 substituted alkenyl group Chemical group 0.000 claims description 14
- 125000005415 substituted alkoxy group Chemical group 0.000 claims description 14
- 125000004426 substituted alkynyl group Chemical group 0.000 claims description 14
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims description 14
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 14
- 125000003107 substituted aryl group Chemical group 0.000 claims description 12
- 125000003739 carbamimidoyl group Chemical group C(N)(=N)* 0.000 claims description 8
- 208000008589 Obesity Diseases 0.000 claims description 5
- 235000020824 obesity Nutrition 0.000 claims description 5
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 4
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- 239000011780 sodium chloride Substances 0.000 claims description 4
- 210000001519 tissues Anatomy 0.000 claims description 4
- 206010012601 Diabetes mellitus Diseases 0.000 claims description 3
- 125000005354 acylalkyl group Chemical group 0.000 claims description 3
- 125000005349 heteroarylcycloalkyl group Chemical group 0.000 claims description 3
- 210000000577 Adipose Tissue Anatomy 0.000 claims description 2
- 208000007082 Alcoholic Fatty Liver Diseases 0.000 claims description 2
- 206010003211 Arteriosclerosis coronary artery Diseases 0.000 claims description 2
- 210000004556 Brain Anatomy 0.000 claims description 2
- 208000007342 Diabetic Nephropathy Diseases 0.000 claims description 2
- 206010061835 Diabetic nephropathy Diseases 0.000 claims description 2
- 206010058108 Dyslipidaemia Diseases 0.000 claims description 2
- 206010016262 Fatty liver alcoholic Diseases 0.000 claims description 2
- 206010061227 Lipid metabolism disease Diseases 0.000 claims description 2
- 208000008338 Non-alcoholic Fatty Liver Disease Diseases 0.000 claims description 2
- 108009000135 Nonalcoholic fatty liver disease Proteins 0.000 claims description 2
- 239000000654 additive Substances 0.000 claims description 2
- 230000000996 additive Effects 0.000 claims description 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 2
- 201000009846 fatty liver disease Diseases 0.000 claims description 2
- 201000005569 gout Diseases 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 125000002757 morpholinyl group Chemical group 0.000 claims description 2
- 230000002093 peripheral Effects 0.000 claims description 2
- 239000008194 pharmaceutical composition Substances 0.000 claims description 2
- 125000004076 pyridyl group Chemical group 0.000 claims description 2
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 2
- 229910052711 selenium Inorganic materials 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims 7
- 125000001309 chloro group Chemical group Cl* 0.000 claims 3
- 206010016654 Fibrosis Diseases 0.000 claims 1
- 206010022489 Insulin resistance Diseases 0.000 claims 1
- 125000006448 cycloalkyl cycloalkyl group Chemical group 0.000 claims 1
- 230000004761 fibrosis Effects 0.000 claims 1
- 201000007270 liver cancer Diseases 0.000 claims 1
- 150000003573 thiols Chemical class 0.000 claims 1
- 210000002356 Skeleton Anatomy 0.000 description 4
- 102000005962 receptors Human genes 0.000 description 4
- 108020003175 receptors Proteins 0.000 description 4
- 230000001225 therapeutic Effects 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000000883 anti-obesity agent Substances 0.000 description 2
- 239000003472 antidiabetic agent Substances 0.000 description 2
- 239000002246 antineoplastic agent Substances 0.000 description 2
- 125000000717 hydrazino group Chemical group [H]N([*])N([H])[H] 0.000 description 2
- 230000001404 mediated Effects 0.000 description 2
- 230000035592 Brain Concentration Effects 0.000 description 1
- 230000037289 Plasma half life Effects 0.000 description 1
- 230000037240 Plasma half-life Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000036470 plasma concentration Effects 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261725949P | 2012-11-13 | 2012-11-13 | |
| US61/725,949 | 2012-11-13 | ||
| PCT/US2013/069686 WO2014078309A1 (en) | 2012-11-13 | 2013-11-12 | Cannabinoid receptor mediating compounds |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015536997A JP2015536997A (ja) | 2015-12-24 |
| JP2015536997A5 true JP2015536997A5 (US07794700-20100914-C00152.png) | 2016-12-28 |
| JP6272626B2 JP6272626B2 (ja) | 2018-01-31 |
Family
ID=49725346
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015542015A Active JP6272626B2 (ja) | 2012-11-13 | 2013-11-12 | カンナビノイド受容体媒介性化合物 |
Country Status (7)
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IN2015DN03733A (US07794700-20100914-C00152.png) * | 2012-11-13 | 2015-09-18 | Us Health | |
| US11155521B2 (en) * | 2012-11-13 | 2021-10-26 | The United States Of America As Represented By The Secretary, Department Of Health And Human Services | Cannabinoid receptor mediating compounds |
| US10329259B2 (en) | 2014-05-09 | 2019-06-25 | The United States Of America, As Represented By The Secretary, Department Of Health & Human Services | Pyrazole derivatives and their use as cannabinoid receptor mediators |
| US20180273485A1 (en) * | 2015-06-04 | 2018-09-27 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Serv | Cannabinoid receptor mediating compounds |
| EP3423448A1 (en) * | 2016-03-04 | 2019-01-09 | The U.S.A. as represented by the Secretary, Department of Health and Human Services | Cannabinoid receptor mediating compounds |
| RU2703484C1 (ru) * | 2018-05-22 | 2019-10-17 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Саратовский государственный аграрный университет имени Н.И. Вавилова" | Способ производства безоболочных колбасок для функционального питания |
| AU2021242808A1 (en) * | 2020-03-24 | 2022-10-06 | Novo Nordisk A/S | Solid dispersions of amorphous 3, 4-diphenyl-4, 5-dihydro- 1H-pyrazole derivatives, compositions comprising them and uses thereof as cannabinoid CB1 receptor inhibitors |
| AU2021253263A1 (en) * | 2020-04-07 | 2022-10-13 | Novo Nordisk A/S | Process for producing 4,5-dihydro-1H-pyrazoles and intermediates |
| WO2023159317A1 (en) * | 2022-02-24 | 2023-08-31 | Inversago Pharma Inc. | Methods for treating subjects with abdominal obesity hypertriglyceridemia and/or impaired glucose |
| WO2023177568A1 (en) * | 2022-03-14 | 2023-09-21 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Cannabinoid receptor modulating compounds |
Family Cites Families (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4675189A (en) | 1980-11-18 | 1987-06-23 | Syntex (U.S.A.) Inc. | Microencapsulation of water soluble active polypeptides |
| JPS60100516A (ja) | 1983-11-04 | 1985-06-04 | Takeda Chem Ind Ltd | 徐放型マイクロカプセルの製造法 |
| CA1256638A (en) | 1984-07-06 | 1989-06-27 | Motoaki Tanaka | Polymer and its production |
| JP2551756B2 (ja) | 1985-05-07 | 1996-11-06 | 武田薬品工業株式会社 | ポリオキシカルボン酸エステルおよびその製造法 |
| DZ3335A1 (fr) | 2000-03-23 | 2001-09-27 | Solvay Pharm Bv | Derives de 4,5-dihydro-1h-pyrazole ayant une activite antagoniste de cb1 |
| ATE284872T1 (de) * | 2001-03-22 | 2005-01-15 | Solvay Pharm Bv | 4,5-dihydro-1h-pyrazolderivate mit cb1- antagonistischer wirkung |
| PL368441A1 (en) * | 2001-09-21 | 2005-03-21 | Solvay Pharmaceuticals B.V. | Novel 4,5-dihydro-1h-pyrazole derivatives having cb1-antagonistic activity |
| HUP0402113A3 (en) | 2001-09-21 | 2012-05-29 | Solvay Pharm Bv | 4,5-dihydro-1h-pyrazole derivatives having cb1-antagonistic activity, preparation and use thereof |
| US20050239859A2 (en) * | 2003-09-03 | 2005-10-27 | Solvay Pharmaceuticals Gmbh | Novel medical uses of 4,5-dihydro-1h-pyrazole derivatives having cb1- antagonistic activity |
| CN100563651C (zh) | 2004-01-30 | 2009-12-02 | 索尔瓦药物有限公司 | 具有cb1-拮抗活性的1,3,5-三取代的4,5-二氢-1h-吡唑衍生物 |
| EP1574211A1 (en) * | 2004-03-09 | 2005-09-14 | Inserm | Use of antagonists of the CB1 receptor for the manufacture of a composition useful for the treatment of hepatic diseases |
| WO2006060192A2 (en) * | 2004-11-30 | 2006-06-08 | Bayer Pharmaceuticals Corporation | Pyrazole derivatives |
| CA2651385C (en) | 2006-05-05 | 2015-02-03 | John F. Mcelroy | Cannabinoid receptor antagonists/inverse agonists useful for treating metabolic disorders, including obesity and diabetes |
| US7655685B2 (en) | 2007-11-02 | 2010-02-02 | Jenrin Discovery, Inc. | Cannabinoid receptor antagonists/inverse agonists useful for treating metabolic disorders, including obesity and diabetes |
| KR20100091255A (ko) | 2007-12-10 | 2010-08-18 | 7티엠 파마 에이/에스 | 카나비노이드 수용체 조절자 |
| WO2010111573A1 (en) | 2009-03-27 | 2010-09-30 | Abbott Laboratories | Compounds as cannabinoid receptor ligands |
| US8217038B2 (en) | 2009-10-07 | 2012-07-10 | Jenrin Discovery, Inc. | Cannabinoid receptor antagonists/inverse agonists useful for treating metabolic disorders, including obesity and diabetes |
| JP5946192B2 (ja) * | 2010-11-18 | 2016-07-05 | ジェンリン ディスカバリーＪｅｎｒｉｎ Ｄｉｓｃｏｖｅｒｙ | 肥満症及び糖尿病を含む代謝性疾患の処置に有用なカンナビノイド受容体拮抗薬／逆作動薬 |
| US11155521B2 (en) * | 2012-11-13 | 2021-10-26 | The United States Of America As Represented By The Secretary, Department Of Health And Human Services | Cannabinoid receptor mediating compounds |
| IN2015DN03733A (US07794700-20100914-C00152.png) | 2012-11-13 | 2015-09-18 | Us Health | |
| US10329259B2 (en) | 2014-05-09 | 2019-06-25 | The United States Of America, As Represented By The Secretary, Department Of Health & Human Services | Pyrazole derivatives and their use as cannabinoid receptor mediators |
| US20180273485A1 (en) * | 2015-06-04 | 2018-09-27 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Serv | Cannabinoid receptor mediating compounds |
-
2013
- 2013-11-12 IN IN3733DEN2015 patent/IN2015DN03733A/en unknown
- 2013-11-12 CN CN201380069389.9A patent/CN104884057B/zh active Active
- 2013-11-12 WO PCT/US2013/069686 patent/WO2014078309A1/en active Application Filing
- 2013-11-12 CA CA2889697A patent/CA2889697C/en active Active
- 2013-11-12 EP EP13802153.0A patent/EP2919779B1/en active Active
- 2013-11-12 US US14/442,383 patent/US9765031B2/en active Active
- 2013-11-12 JP JP2015542015A patent/JP6272626B2/ja active Active
-
2017
- 2017-08-10 US US15/674,365 patent/US10683270B2/en active Active
- 2017-08-10 US US15/674,333 patent/US10787419B2/en active Active
-
2020
- 2020-05-08 US US16/870,093 patent/US11485709B2/en active Active
-
2022
- 2022-09-29 US US17/956,313 patent/US20230202983A1/en not_active Abandoned
-
2023
- 2023-02-10 US US18/108,264 patent/US11939297B2/en active Active
