PE20231379A1 - Agonista de receptor de melanocortina-4 amorfo - Google Patents
Agonista de receptor de melanocortina-4 amorfoInfo
- Publication number
- PE20231379A1 PE20231379A1 PE2023001493A PE2023001493A PE20231379A1 PE 20231379 A1 PE20231379 A1 PE 20231379A1 PE 2023001493 A PE2023001493 A PE 2023001493A PE 2023001493 A PE2023001493 A PE 2023001493A PE 20231379 A1 PE20231379 A1 PE 20231379A1
- Authority
- PE
- Peru
- Prior art keywords
- compound
- amorphous
- melanocortin
- receptor agonist
- pyrrolidin
- Prior art date
Links
- 102000001796 Melanocortin 4 receptors Human genes 0.000 title 1
- 108010021436 Type 4 Melanocortin Receptor Proteins 0.000 title 1
- 239000000018 receptor agonist Substances 0.000 title 1
- 229940044601 receptor agonist Drugs 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 5
- WFKAJVHLWXSISD-UHFFFAOYSA-N isobutyramide Chemical compound CC(C)C(N)=O WFKAJVHLWXSISD-UHFFFAOYSA-N 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 208000010228 Erectile Dysfunction Diseases 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
- 206010061218 Inflammation Diseases 0.000 abstract 1
- 208000008589 Obesity Diseases 0.000 abstract 1
- 102000003827 Plasma Kallikrein Human genes 0.000 abstract 1
- 108090000113 Plasma Kallikrein Proteins 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 206010012601 diabetes mellitus Diseases 0.000 abstract 1
- -1 heteroaromatic carboxamide Chemical class 0.000 abstract 1
- 201000001881 impotence Diseases 0.000 abstract 1
- 230000004054 inflammatory process Effects 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 229940047889 isobutyramide Drugs 0.000 abstract 1
- 235000020824 obesity Nutrition 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
-
- 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
- C07D403/06—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 carbon chain containing only aliphatic carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/10—Drugs for genital or sexual disorders; Contraceptives for impotence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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
- C07D207/16—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Diabetes (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Child & Adolescent Psychology (AREA)
- Epidemiology (AREA)
- Emergency Medicine (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Gynecology & Obstetrics (AREA)
- Reproductive Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyrane Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Referido a un compuesto amorfo de formula 1, o una sal farmaceuticamente aceptable del mismo, caracterizado porque R1 es alquilo de C2-C5. Este compuesto derivado de carboxamida heteroaromatica es inhibidor de la calicreina plasmatica. En donde dicho compuesto es clorhidrato de N-((3S,5S)-1-((3S,4R)-1-(ter-butil)-4-5 (4-cloro-fenil)pirrolidin-3-carbonil)-5-(morfolin-4-carbonil)-pirrolidin-3-il)-N-((1s,4R)-4-metilciclohexil)isobutiramida. Tambien se refiere a un metodo para preparar dicho compuesto amorfo o la sal farmaceuticamente aceptable del mismo, una composicion farmaceutica que comprende dicho compuesto, y su uso para prevenir o tratar obesidad, diabetes, inflamacion o disfuncion erectil.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR20200142399 | 2020-10-29 | ||
PCT/KR2021/015467 WO2022092908A1 (ko) | 2020-10-29 | 2021-10-29 | 무정형의 멜라노코르틴-4 수용체 작용제 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20231379A1 true PE20231379A1 (es) | 2023-09-07 |
Family
ID=81384115
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2023001493A PE20231379A1 (es) | 2020-10-29 | 2021-10-29 | Agonista de receptor de melanocortina-4 amorfo |
Country Status (13)
Country | Link |
---|---|
EP (1) | EP4219471A4 (es) |
JP (1) | JP2023548162A (es) |
KR (1) | KR20220057469A (es) |
CN (1) | CN116419757A (es) |
AU (1) | AU2021370071B2 (es) |
CA (1) | CA3195214A1 (es) |
CL (1) | CL2023001221A1 (es) |
CO (1) | CO2023006514A2 (es) |
IL (1) | IL302425A (es) |
MX (1) | MX2023004654A (es) |
PE (1) | PE20231379A1 (es) |
WO (1) | WO2022092908A1 (es) |
ZA (1) | ZA202305591B (es) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2022139441A1 (ko) * | 2020-12-22 | 2022-06-30 | 주식회사 엘지화학 | 무정형의 멜라노코르틴 수용체 작용제 및 이의 제조방법 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU766191B2 (en) * | 1999-06-04 | 2003-10-09 | Merck & Co., Inc. | Substituted piperidines as melanocortin-4 receptor agonists |
CA2433025A1 (en) * | 2001-01-23 | 2002-08-01 | Chaoyu Xie | Substituted piperidines/piperazines as melanocortin receptor agonists |
AR044510A1 (es) | 2003-04-14 | 2005-09-14 | Merck & Co Inc | Procedimiento e intermedios para preparar acidos carboxilicos de pirrolidina |
KR100661118B1 (ko) * | 2003-11-12 | 2006-12-26 | 주식회사 엘지생명과학 | 멜라노코틴 수용체의 항진제 |
TWI332501B (en) * | 2006-07-14 | 2010-11-01 | Lg Life Sciences Ltd | Melanocortin receptor agonists |
UA99555C2 (en) * | 2008-11-12 | 2012-08-27 | Элджи Лайф Саенсез Лтд. | Melanocortin receptor agonists |
MX2019009463A (es) | 2017-02-08 | 2019-12-16 | Tilray Inc | Metodo y aparatos para procesamiento de canabis a traves de energia radiante de baja presion. |
MX2021014074A (es) * | 2019-11-07 | 2021-12-10 | Lg Chemical Ltd | Agonistas de receptor de melanocortina-4. |
-
2021
- 2021-10-29 AU AU2021370071A patent/AU2021370071B2/en active Active
- 2021-10-29 IL IL302425A patent/IL302425A/en unknown
- 2021-10-29 PE PE2023001493A patent/PE20231379A1/es unknown
- 2021-10-29 JP JP2023526433A patent/JP2023548162A/ja active Pending
- 2021-10-29 EP EP21886902.2A patent/EP4219471A4/en active Pending
- 2021-10-29 CA CA3195214A patent/CA3195214A1/en active Pending
- 2021-10-29 CN CN202180072880.1A patent/CN116419757A/zh active Pending
- 2021-10-29 MX MX2023004654A patent/MX2023004654A/es unknown
- 2021-10-29 WO PCT/KR2021/015467 patent/WO2022092908A1/ko active Application Filing
- 2021-10-29 KR KR1020210146187A patent/KR20220057469A/ko active IP Right Grant
-
2023
- 2023-04-27 CL CL2023001221A patent/CL2023001221A1/es unknown
- 2023-05-17 CO CONC2023/0006514A patent/CO2023006514A2/es unknown
- 2023-05-24 ZA ZA2023/05591A patent/ZA202305591B/en unknown
Also Published As
Publication number | Publication date |
---|---|
AU2021370071B2 (en) | 2024-01-11 |
JP2023548162A (ja) | 2023-11-15 |
EP4219471A1 (en) | 2023-08-02 |
EP4219471A4 (en) | 2024-03-13 |
CN116419757A (zh) | 2023-07-11 |
AU2021370071A1 (en) | 2023-06-01 |
IL302425A (en) | 2023-06-01 |
CL2023001221A1 (es) | 2023-11-03 |
CA3195214A1 (en) | 2022-05-05 |
KR20220057469A (ko) | 2022-05-09 |
ZA202305591B (en) | 2024-09-25 |
WO2022092908A1 (ko) | 2022-05-05 |
CO2023006514A2 (es) | 2023-07-31 |
MX2023004654A (es) | 2023-05-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PE20220766A1 (es) | Agonistas de receptor de melanocortina-4 | |
RU2424240C2 (ru) | Антибактериальные производные пиперидина | |
PE20161342A1 (es) | Combinaciones de inhibidores de histona desacetilasa y farmacos inmunomoduladores | |
PH12019501707A1 (en) | N-[4-fluoro-5-[[(2s,4s)-2-methyl-4-[(5-methyl-1,2,4-oxadiazol-3-yl)methoxy]-1-piperidyl]methyl]thiazol-2-yl]acetamide as oga inhibitor | |
MX2022011365A (es) | Derivados de biarilo como inhibidores de la interaccion proteina-proteina de yap/taz-tead. | |
PE20110367A1 (es) | DERIVADOS DE 4-CIANO-4-FENIL-PIRROLIDIN-2-CARBOXAMIDAS SUSTITUIDAS COMO INHIBIDORES DE LA INTERACCION p53-MDM2 | |
PE20061373A1 (es) | Composicion farmaceutica que contiene 'n-(2-cloro-6-metilfenil)-2-[[6-[4-(2-hidroxietil)-1-piperazinil]-2-metil-4-pirimidinil]amino]-5-tiazolcarboxamida | |
PE20231379A1 (es) | Agonista de receptor de melanocortina-4 amorfo | |
TW200716644A (en) | Aspartyl protease inhibitors | |
MX2009006493A (es) | Compuestos inhibidores activos, citoesqueleticos, de la quinasa de rho, composiciones y usos. | |
AR061873A1 (es) | Derivados de pirrolotriazina inhibidores de tirosinquinasas, composiciones farmaceuticas que los contienen utiles para el tratamiento de enfermedades proliferativas. | |
ECSP078003A (es) | Inhibidores de aspartil proteasas | |
PE20050772A1 (es) | Piperidinilcarbonil-pirrolidinas como agonistas de melanocortina | |
CO6140054A2 (es) | Compuestos de dialquilfenilo con actividad agonista del receptor beta2 adrenergico y antagonista del receptor muscarinico | |
CO6270285A2 (es) | Derivados de 4-[(4-amino-1, 3, 5-triazin-2-il)amino]-n-arilmetilcicloalquilcarboxamida | |
CA2409741A1 (en) | Tnf-.alpha. production inhibitors | |
PH12020552244A1 (en) | Heterocyclic compounds as trk inhibitors | |
MX2024009925A (es) | Composiciones y metodos para tratar trastornos del snc. | |
PE20190106A1 (es) | Inhibidores del potenciador del homologo zeste 2 | |
PE20212067A1 (es) | Forma cristalina de 1-(1-oxo-1,2-dihidroisoquinolin-5-il)-5-(trifluorometil)-n-(2- (trifluorometil)piridin-4-il)-1h-pirazol-4-carboxamida monohidratada | |
PH12021550687A1 (en) | Pharmaceutical composition for oral administration comprising aminopyrimidine derivative or its salt | |
PE20061418A1 (es) | Composiciones farmaceuticas de 4-[(ciclopropanocarbonilamino)metil]-2-(2,6-dioxopiperidin-3-il)isoindol-1,3-diona para el tratamiento o prevencion de lupus cutaneo | |
BR112013031121A2 (pt) | composto de acordo com a fórmula i a v, ou um sal farmaceuticamente aceitável, solvato, polimorfo, ou pró-droga do mesmo; composto; polimorfo de sal cloridrato de 2-morfolino-n-(3-(4-(5-(pirrolidina-1-carbonil)-1h-pirrol-3-il)tiazol-2-il)acetamida (fórmula i); ingrediente ativo constituído do mesmo; composição farmacêutica; polimorfo de 2-morfolino-n-(3-(4-(5-(pirrolidina-1-carbonil)1h-pirrol-3-il)tiazol-2-il)fenil)acetamida (fórmula i); ingrediente ativo constituído do mesmo; uso de um composto ou sal farmaceuticamente aceitável, solvato, polimorfo ou pró-droga do mesmo e uso de um polimorfo ou ingrediente ativo de sal cloridrato de 2-morfolino-n-(3-(4-(5-(pirrolidina-1-carbonil)-1h-pirrol-3-il)tiazol-2il)tiazol-2-il)fenil)acetamida (fórmula i) e uso de um polimorfo ou ingrediente ativo de 2-morfolino-n-(3-(4-(5-(pirrolidina-1-carbonil)-1h1pirrol-3-il)tiazol-2-il)fenil)acetamida(fórmula i) na fabricação de um medicamento | |
PE20221630A1 (es) | Derivado de amino arilo novedoso util como inhibidor de diacilglicerol aciltransferasa 2 y uso del mismo | |
CA3156340A1 (en) | N-(1H-IMIDAZOL-2-YL)BENZAMIDE COMPOUND AND PHARMACEUTICAL COMPOSITION COMPRISING IT AS ACTIVE SUBSTANCE |