PE20210671A1 - Triazolobenzazepinas como antagonistas del receptor v1a de la vasopresina - Google Patents
Triazolobenzazepinas como antagonistas del receptor v1a de la vasopresinaInfo
- Publication number
- PE20210671A1 PE20210671A1 PE2020000640A PE2020000640A PE20210671A1 PE 20210671 A1 PE20210671 A1 PE 20210671A1 PE 2020000640 A PE2020000640 A PE 2020000640A PE 2020000640 A PE2020000640 A PE 2020000640A PE 20210671 A1 PE20210671 A1 PE 20210671A1
- Authority
- PE
- Peru
- Prior art keywords
- compounds
- 4alkyl
- ring
- receptor
- group
- Prior art date
Links
- 102000004136 Vasopressin Receptors Human genes 0.000 title abstract 2
- 108090000643 Vasopressin Receptors Proteins 0.000 title abstract 2
- 239000005557 antagonist Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 5
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 238000002360 preparation method Methods 0.000 abstract 2
- WAYZQLIRXHPOCN-UHFFFAOYSA-N 5,6-dihydro-4h-[1,2,4]triazolo[4,3-a][1]benzazepine Chemical compound C1CCC2=NN=CN2C2=CC=CC=C21 WAYZQLIRXHPOCN-UHFFFAOYSA-N 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 239000002207 metabolite Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 238000011321 prophylaxis Methods 0.000 abstract 1
- 239000002464 receptor antagonist Substances 0.000 abstract 1
- 229940044551 receptor antagonist Drugs 0.000 abstract 1
- 102000005962 receptors Human genes 0.000 abstract 1
- 108020003175 receptors Proteins 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- -1 tert-butyl [8-chloro-1- [1- (pyridin-2-yl) piperidin-4-yl] -5,6-dihydro-4H- [1,2,4] triazolo [4, 3-a] [1] benzazepin-5-yl] carbamate Chemical class 0.000 abstract 1
- 238000011282 treatment Methods 0.000 abstract 1
- QDEVEJYEXBFIJD-UHFFFAOYSA-N triazolo[4,5-i][1]benzazepine Chemical class C1=CC2=CC=CC=NC2=C2C1=NN=N2 QDEVEJYEXBFIJD-UHFFFAOYSA-N 0.000 abstract 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
- A61K31/4196—1,2,4-Triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
- C07D223/02—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D223/06—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
- C07D223/02—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D223/06—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D223/08—Oxygen atoms
- C07D223/10—Oxygen atoms attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
- C07D223/14—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D223/16—Benzazepines; Hydrogenated benzazepines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
-
- 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
- C07D413/14—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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
- C07D487/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
- C07D487/20—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D491/12—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 three hetero rings
- C07D491/20—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
- C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurosurgery (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Referido a compuestos derivados de 5,6-dihidro-4H-[1,2,4]triazolo[4,3- a][1]benzazepina, de formula I, caracterizado por: el anillo A es un grupo cicloalquilo o heterociclilo; Y es -O-, -C(O)-, -CH2-, -NH-, -C1-4alquil-N(R18)- o enlace si el anillo B esta presente, entre otros; el anillo B es un gupo heteroarilo, arilo o heterociclilo opcionalmente sustituido; R1 es H, halogeno, C1-4alquilo, entre otros; R2 es un grupo hidrogeno o C1-4alquilo; R3 es a NR4R5, grupo OR6 o halogeno; entre otros; sus sales, isomeros, metabolitos biologicamente activos, entre otros. Un compuesto preferido es ter-butil [8-cloro-1-[1-(piridin-2-il)piperidin-4-il]-5,6-dihidro-4H-[1,2,4]triazolo[4,3-a][1]benzazepin-5-il] carbamato. Estos compuestos triazolobenzazepinas son moduladores del receptor V1a de la vasopresina que actuan central y/o perifericamente, particularmente antagonistas del receptor V1a. Tambien se refiere a un proceso para la preparacion de los compuestos, compuestos intermediarios para el proceso de preparacion, composiciones farmaceuticas que contienen los compuestos en combinacion con uno o mas principios activos adicionales, y el uso de las mismas en el tratamiento y/o profilaxis de una enfermedad o afeccion asociada con la funcion del receptor V1a.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU1700521A HU231206B1 (hu) | 2017-12-15 | 2017-12-15 | Triazolobenzazepinek |
PCT/IB2018/060077 WO2019116324A1 (en) | 2017-12-15 | 2018-12-14 | Triazolobenzazepines as vasopressin v1a receptor antagonists |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20210671A1 true PE20210671A1 (es) | 2021-04-05 |
Family
ID=89992589
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2020000640A PE20210671A1 (es) | 2017-12-15 | 2018-12-14 | Triazolobenzazepinas como antagonistas del receptor v1a de la vasopresina |
Country Status (22)
Country | Link |
---|---|
US (1) | US11298363B2 (es) |
EP (1) | EP3724192B1 (es) |
JP (1) | JP7428647B2 (es) |
KR (1) | KR20200100111A (es) |
CN (1) | CN111479813B (es) |
AR (1) | AR113933A1 (es) |
AU (1) | AU2018385724B2 (es) |
BR (1) | BR112020011880A2 (es) |
CA (1) | CA3085562A1 (es) |
CL (1) | CL2020001564A1 (es) |
CU (1) | CU24630B1 (es) |
EA (1) | EA202091344A1 (es) |
HU (1) | HU231206B1 (es) |
IL (1) | IL275084B2 (es) |
JO (1) | JOP20200149B1 (es) |
MX (1) | MX2020006204A (es) |
PE (1) | PE20210671A1 (es) |
PH (1) | PH12020500548A1 (es) |
SG (1) | SG11202005299VA (es) |
TN (1) | TN2020000083A1 (es) |
TW (1) | TWI826406B (es) |
WO (1) | WO2019116324A1 (es) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW202202495A (zh) | 2020-03-26 | 2022-01-16 | 匈牙利商羅特格登公司 | 作為gamma-胺基丁酸A受體次單元alpha 5受體調節劑之㖠啶及吡啶并〔3,4-c〕嗒𠯤衍生物 |
TWI804119B (zh) * | 2020-12-21 | 2023-06-01 | 大陸商上海濟煜醫藥科技有限公司 | 三氮唑類三并環衍生物及其製備方法和應用 |
HUP2100338A1 (hu) | 2021-09-29 | 2023-04-28 | Richter Gedeon Nyrt | GABAA ALFA5 receptor modulátor hatású biciklusos aminszármazékok |
WO2023164710A1 (en) * | 2022-02-28 | 2023-08-31 | The Trustees Of Columbia University In The City Of New York | Avpr1a blockade to reduce social isolation-induced anxiety in females |
Family Cites Families (45)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DK0382185T3 (da) | 1989-02-10 | 1994-07-04 | Otsuka Pharma Co Ltd | Carbostyrilderivater |
FR2679903B1 (fr) | 1991-08-02 | 1993-12-03 | Elf Sanofi | Derives de la n-sulfonyl indoline portant une fonction amidique, leur preparation, les compositions pharmaceutiques en contenant. |
EP1097920B1 (en) | 1993-07-21 | 2004-09-22 | Yamanouchi Pharmaceutical Co. Ltd. | Intermediate for condensed benzazepine derivatives |
CN1104418C (zh) | 1994-06-15 | 2003-04-02 | 大塚制药株式会社 | 苯并杂环衍生物 |
FR2740136B1 (fr) | 1995-10-24 | 1998-01-09 | Sanofi Sa | Derives d'indolin-2-one, procede pour leur preparation et les compositions pharmaceutiques les contenant |
PL359340A1 (en) | 2000-05-19 | 2004-08-23 | Triazole derivatives | |
DK1307430T3 (da) | 2000-07-05 | 2006-01-30 | Ortho Mcneil Pharm Inc | Ikke-peptidsubstituerede spirobenzoazepiner som vasopressin-antagonister |
US7056910B2 (en) | 2000-11-28 | 2006-06-06 | Astellas Pharma Inc. | 1,4,5.6-tetrahydroimidazo[4,5-d]diazepine derivatives or salts thereof |
MXPA04003358A (es) | 2001-10-12 | 2004-07-08 | Serenix Pharmaceuticals Llc | Antagonistas de vasopresina v1a de ?-lactamilo. |
JP2005104838A (ja) | 2003-01-09 | 2005-04-21 | Tanabe Seiyaku Co Ltd | 縮合フラン化合物 |
EP1597260B1 (en) * | 2003-02-19 | 2006-12-27 | Pfizer Limited | Triazole compounds useful in therapy |
GB0303852D0 (en) * | 2003-02-19 | 2003-03-26 | Pfizer Ltd | Triazole compounds useful in therapy |
GB0325021D0 (en) * | 2003-10-27 | 2003-12-03 | Pfizer Ltd | Therapeutic combinations |
OA13347A (en) | 2003-12-22 | 2007-04-13 | Pfizer | Triazole derivatives as vasopressin antagonists. |
GB0400700D0 (en) * | 2004-01-13 | 2004-02-18 | Pfizer Ltd | Compounds useful in therapy |
EP1632494A1 (en) | 2004-08-24 | 2006-03-08 | Ferring B.V. | Vasopressin v1a antagonists |
MX2007002248A (es) * | 2004-08-25 | 2008-10-02 | Pfizer | Triazolobenzodiazepinas y su uso como antagonistas de vasopresina. |
EP1831197A2 (de) | 2004-12-31 | 2007-09-12 | Abbott GmbH & Co. KG | Substituierte oxindol-derivate, diese enthaltende arzneimittel und deren verwendung |
CA2602194A1 (en) | 2005-03-24 | 2006-09-28 | Abbott Gmbh & Co. Kg | Substituted oxindol derivatives, drugs containing said derivatives and the use thereof |
RU2007146444A (ru) | 2005-05-13 | 2009-06-20 | Лексикон Фармасьютикалз, Инк. (Us) | Полициклические соединения и способы их применения |
BRPI0612988A2 (pt) | 2005-07-14 | 2010-12-14 | Hoffmann La Roche | derivados de indol-3-il-carbonil-espiro-piperidina como antagonistas de receptor v1a |
DK1912976T3 (da) | 2005-07-21 | 2009-01-26 | Hoffmann La Roche | Indol-3-YL-carbonyl-piperidin-benzoimidazolderivater som V1A-receptorantagonister |
AU2006274884B2 (en) | 2005-07-29 | 2012-04-05 | F. Hoffmann-La Roche Ag | Indol-3-yl-carbonyl-piperidin and piperazin derivatives |
DE102006051796A1 (de) * | 2006-11-03 | 2008-05-08 | Merck Patent Gmbh | Triaza-benzo[e]azulenderivate |
WO2008092887A1 (en) | 2007-02-01 | 2008-08-07 | Glaxo Group Limited | I-oxa-3-azaspiro (4.5) decan-2-one and 1-oxa-3, 8-diazaspiro (4.5) decan-2-one derivatives for the treatment of eating disorders |
TWI459947B (zh) | 2007-06-26 | 2014-11-11 | Otsuka Pharma Co Ltd | 苯并氮呯化合物及藥學製劑 |
ES2431279T3 (es) | 2008-11-28 | 2013-11-25 | F. Hoffmann-La Roche Ag | Arilciclohexiléteres de dihidro-tetraazabenzoazulenos para uso como antagonistas del receptor V1A de la vasopresina |
GB0903493D0 (en) | 2009-02-27 | 2009-04-08 | Vantia Ltd | New compounds |
TW201103907A (en) | 2009-03-20 | 2011-02-01 | Lundbeck & Co As H | Amide derivatives as neuropeptide Y5 receptor ligands |
EP2495236A4 (en) | 2009-10-26 | 2013-03-27 | Otsuka Pharma Co Ltd | BENZAZEPINE COMPOUND |
GB201004677D0 (en) | 2010-03-19 | 2010-05-05 | Vantia Ltd | New salt |
US8461151B2 (en) | 2010-04-13 | 2013-06-11 | Hoffmann-La Roche Inc. | Aryl-/heteroaryl-cyclohexenyl-tetraazabenzo[e]azulenes |
US8492376B2 (en) * | 2010-04-21 | 2013-07-23 | Hoffmann-La Roche Inc. | Heteroaryl-cyclohexyl-tetraazabenzo[e]azulenes |
US8513238B2 (en) | 2010-05-10 | 2013-08-20 | Hoffmann-La Roche Inc. | Heteroaryl-cyclohexyl-tetraazabenzo[E]azulenes |
TW201206939A (en) | 2010-05-11 | 2012-02-16 | Sanofi Aventis | Substituted phenyl cycloalkyl pyrrolidine (piperidine) spirolactams and amides, preparation and therapeutic use thereof |
WO2012068149A1 (en) * | 2010-11-15 | 2012-05-24 | Agenebio, Inc. | Benzodiazepine derivatives, compositions and methods for treating cognitive impairment |
EP2900672B1 (de) * | 2012-09-28 | 2017-02-22 | Bayer Pharma Aktiengesellschaft | Bet-proteininhibitorische 5-aryl-triazolo-azepine |
CA2901577A1 (en) | 2013-02-18 | 2014-08-21 | The Scripps Research Institute | Modulators of vasopressin receptors with therapeutic potential |
RS62227B1 (sr) | 2014-12-09 | 2021-09-30 | Bayer Ag | 1,3-tiazol-2-il supstituisani benzamidi |
US10532995B2 (en) | 2015-02-27 | 2020-01-14 | Verseon Corporation | Substituted pyrazole compounds as serine protease inhibitors |
WO2017007756A1 (en) | 2015-07-06 | 2017-01-12 | Rodin Therapeutics, Inc | Hetero-halo inhibitors of histone deacetylase |
CN106349241B (zh) * | 2015-07-15 | 2020-04-21 | 上海翰森生物医药科技有限公司 | 具有hsp90抑制活性的***衍生物及其制备方法和应用 |
US9988367B2 (en) | 2016-05-03 | 2018-06-05 | Bayer Pharma Aktiengesellschaft | Amide-substituted pyridinyltriazole derivatives and uses thereof |
US10526314B2 (en) | 2016-05-03 | 2020-01-07 | Bayer Aktiengesellschaft | Hydroxyalkyl-substituted heteroaryltriazole derivatives and uses thereof |
UY37221A (es) | 2016-05-03 | 2017-11-30 | Bayer Pharma AG | Derivados de feniltriazol sustituidos con amida y usos de estos |
-
2017
- 2017-12-15 HU HU1700521A patent/HU231206B1/hu unknown
-
2018
- 2018-12-12 TW TW107144774A patent/TWI826406B/zh active
- 2018-12-13 AR ARP180103643A patent/AR113933A1/es unknown
- 2018-12-14 SG SG11202005299VA patent/SG11202005299VA/en unknown
- 2018-12-14 CU CU2020000048A patent/CU24630B1/es unknown
- 2018-12-14 KR KR1020207020172A patent/KR20200100111A/ko not_active Application Discontinuation
- 2018-12-14 JO JOP/2020/0149A patent/JOP20200149B1/ar active
- 2018-12-14 TN TNP/2020/000083A patent/TN2020000083A1/en unknown
- 2018-12-14 CA CA3085562A patent/CA3085562A1/en active Pending
- 2018-12-14 PE PE2020000640A patent/PE20210671A1/es unknown
- 2018-12-14 CN CN201880080932.8A patent/CN111479813B/zh active Active
- 2018-12-14 BR BR112020011880-0A patent/BR112020011880A2/pt unknown
- 2018-12-14 EA EA202091344A patent/EA202091344A1/ru unknown
- 2018-12-14 EP EP18836400.4A patent/EP3724192B1/en active Active
- 2018-12-14 MX MX2020006204A patent/MX2020006204A/es unknown
- 2018-12-14 AU AU2018385724A patent/AU2018385724B2/en active Active
- 2018-12-14 US US16/954,085 patent/US11298363B2/en active Active
- 2018-12-14 JP JP2020532928A patent/JP7428647B2/ja active Active
- 2018-12-14 WO PCT/IB2018/060077 patent/WO2019116324A1/en active Application Filing
-
2020
- 2020-06-03 IL IL275084A patent/IL275084B2/en unknown
- 2020-06-09 PH PH12020500548A patent/PH12020500548A1/en unknown
- 2020-06-11 CL CL2020001564A patent/CL2020001564A1/es unknown
Also Published As
Publication number | Publication date |
---|---|
CU20200048A7 (es) | 2021-03-11 |
CN111479813B (zh) | 2023-03-21 |
US20210260072A1 (en) | 2021-08-26 |
CN111479813A (zh) | 2020-07-31 |
WO2019116324A1 (en) | 2019-06-20 |
AR113933A1 (es) | 2020-07-01 |
SG11202005299VA (en) | 2020-07-29 |
JOP20200149A1 (ar) | 2020-06-10 |
CA3085562A1 (en) | 2019-06-20 |
EP3724192A1 (en) | 2020-10-21 |
TW201938170A (zh) | 2019-10-01 |
MX2020006204A (es) | 2020-08-27 |
EP3724192B1 (en) | 2022-08-03 |
HU231206B1 (hu) | 2021-10-28 |
PH12020500548A1 (en) | 2021-01-25 |
CU24630B1 (es) | 2022-12-12 |
HUP1700521A2 (en) | 2019-06-28 |
JP7428647B2 (ja) | 2024-02-06 |
EA202091344A1 (ru) | 2020-09-09 |
IL275084A (en) | 2020-07-30 |
BR112020011880A2 (pt) | 2020-11-24 |
JOP20200149B1 (ar) | 2022-10-30 |
TN2020000083A1 (en) | 2022-01-06 |
AU2018385724B2 (en) | 2023-05-25 |
CL2020001564A1 (es) | 2020-11-06 |
TWI826406B (zh) | 2023-12-21 |
JP2021506821A (ja) | 2021-02-22 |
AU2018385724A1 (en) | 2020-07-09 |
US11298363B2 (en) | 2022-04-12 |
IL275084B2 (en) | 2023-06-01 |
KR20200100111A (ko) | 2020-08-25 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PE20210671A1 (es) | Triazolobenzazepinas como antagonistas del receptor v1a de la vasopresina | |
PE20221628A1 (es) | Compuestos inhibidores de rip1 y metodos para hacer y utilizar los mismos | |
PE20230249A1 (es) | Compuestos de heteroarilo biciclicos y usos de estos | |
MX2020004405A (es) | Compuestos biciclicos en puente como moduladores del receptor farnesoide x. | |
PE20180462A1 (es) | Moduladores cot y metodos de uso de los mismos | |
PE20161251A1 (es) | Compuestos heteroarilo o arilo biciclicos fusionados y su uso como inhibidores de irak4 | |
UY28526A1 (es) | Miméticos de glucocorticoides, métodos de preparación composiciones farmacéuticas y usos de los mismos | |
CO6321245A2 (es) | Mimeticos de glucocorticoides metodos para su fabricacion cpomposiciones farmaceuticas y uso de los mismos | |
CO2021017504A2 (es) | Derivados de benzisoxazol sulfonamida | |
PE20181487A1 (es) | Heteroarilhidroxipirimidinonas como agonistas del receptor de apelina (apj) | |
ECSP034428A (es) | Ciclopentanoindoles, composiciones conteniendo tales compuestos y su uso | |
PA8614301A1 (es) | Derivados de tropano | |
AR049706A1 (es) | Moduladores del receptor de progesterona que comprenden derivados de pirrol-oxindol y sus usos | |
ECSP056097A (es) | Antagonistas del receptor cgrp | |
PE20160589A1 (es) | Heteroaril-ciclohexil-tetraazabenzo[e]azulenos como antagonistas de los receptores de vasopresina v1a | |
UY31881A (es) | Derivados sustituidos de imidazo[1,5-a]pirrolo[2,3-e]pirazinas e imidazo[1,2-a]pirrolo[2,3-e]pirazinas, sus sales, prodrogas, metabolitos biológicalmente activos, estereoisómeros e isómeros farmacéuticamente aceptables. | |
UY27752A1 (es) | Derivados del tropano útiles en terapia | |
PE20080263A1 (es) | Compuestos de pirrolo-pirimidina y sus usos | |
UY29197A1 (es) | Compuestos de n-sulfonilaminobencil-2-fenoxiacetamida sustituidos | |
CL2020001817A1 (es) | Moduladores del receptor c5a | |
PE20091194A1 (es) | Derivados de heterociclicos como moduladores del receptor m1 | |
MX2020004400A (es) | Compuestos espirociclicos como moduladores del receptor farnesoide x. | |
CO2021013166A2 (es) | Compuestos de hexahidro-1h-pirazino[1,2-a]pirazina para el tratamiento de una enfermedad autoinmunitaria | |
UY38707A (es) | Nuevos antagonistas cíclicos del receptor b2 de bradiquinina | |
PE20220944A1 (es) | Inhibidor de irak y metodo de preparacion para el mismo y uso del mismo |