PE20060316A1 - Derivados de prolina como inhibidores de dipeptidil peptidasa-iv - Google Patents
Derivados de prolina como inhibidores de dipeptidil peptidasa-ivInfo
- Publication number
- PE20060316A1 PE20060316A1 PE2005000515A PE2005000515A PE20060316A1 PE 20060316 A1 PE20060316 A1 PE 20060316A1 PE 2005000515 A PE2005000515 A PE 2005000515A PE 2005000515 A PE2005000515 A PE 2005000515A PE 20060316 A1 PE20060316 A1 PE 20060316A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- compounds
- diabetic
- inhibitors
- difluoropyrrolidin
- Prior art date
Links
- 229940124213 Dipeptidyl peptidase 4 (DPP IV) inhibitor Drugs 0.000 title 1
- ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Chemical class OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 title 1
- 239000003603 dipeptidyl peptidase IV inhibitor Substances 0.000 title 1
- -1 AZETIDINYL Chemical class 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 206010012601 diabetes mellitus Diseases 0.000 abstract 2
- 101000790711 Chlamydomonas reinhardtii Uncharacterized membrane protein ycf78 Proteins 0.000 abstract 1
- 208000002249 Diabetes Complications Diseases 0.000 abstract 1
- 206010012655 Diabetic complications Diseases 0.000 abstract 1
- 102000004190 Enzymes Human genes 0.000 abstract 1
- 108090000790 Enzymes Proteins 0.000 abstract 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical class O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 abstract 1
- 229940124639 Selective inhibitor Drugs 0.000 abstract 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- WSFSSNUMVMOOMR-BJUDXGSMSA-N methanone Chemical compound O=[11CH2] WSFSSNUMVMOOMR-BJUDXGSMSA-N 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Classifications
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- 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
- C07D207/14—Nitrogen atoms not forming part of a nitro radical
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/14—Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
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- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/08—Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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- A61P25/10—Antiepileptics; Anticonvulsants for petit-mal
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D275/00—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
- C07D275/04—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems
- C07D275/06—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems with hetero atoms directly attached to the ring sulfur atom
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- 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
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- 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
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- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
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- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
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- 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
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- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Diabetes (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Physical Education & Sports Medicine (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Obesity (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Cardiology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Ophthalmology & Optometry (AREA)
- Heart & Thoracic Surgery (AREA)
- Reproductive Health (AREA)
- Emergency Medicine (AREA)
- Urology & Nephrology (AREA)
- Addiction (AREA)
- Psychiatry (AREA)
- Immunology (AREA)
- Pregnancy & Childbirth (AREA)
- Hospice & Palliative Care (AREA)
- Vascular Medicine (AREA)
- Nutrition Science (AREA)
- Child & Adolescent Psychology (AREA)
Abstract
SE REFIERE A COMPUESTOS DE FORMULA (I), EN DONDE R1 ES ALQUILO(C1-C6), ARILO, HETEROARILO, OPCIONALMENTE SUSTITUIDO CON 1 A 3 CIANO, HALOGENO, NITRO, CF3, ALQUILO(C1-C6), ALCOXI(C1-C6), CICLOALQUILO(C3-C6) O FENILO; R2 Y R3 SON INDEPENDIENTEMENTE H, ALQUILO(C1-C6), ENTRE OTROS, Q ES UN ENLACE COVALENTE, -C(O)-, O -S(O)2-; HET ES HETEROCICLOALQUILO TAL COMO AZETIDINILO, PIPERAZINILO, PIPERIDINILO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: (3,3-DIFLUOROPIRROLIDIN-1-IL)-((2S,4S)-4-(4-(PIRIMIDIN-2-IL)PIPERAZIN-1-IL)PIRROLIDIN-2-IL)METANONA, ((2S,4S)-4-(3-(TRIFLUOROMETIL)-5,6-DIHIDRO-[1,2,4]TRIAZOLO[4,3-a]PIRAZIN-7(8H)-IL)PIRROLIDIN-2-IL)-(3,3-DIFLUOROPIRROLIDIN-1-IL)METANONA, ENTRE OTROS. TAMBIEN SE REFIERE A UNA COMPOSICION FARMACEUTICA. ESTOS COMPUESTOS SON INHIBIDORES SELECTIVOS DE LA ENZIMA DIPEPTIDIL PEPTIDASA-IV (DPP-IV), POR LO QUE SON UTILES PARA TRATAR COMPLICACIONES DIABETICAS, NEFROPATIA DIABETICA, MICROANGIOPATIA DIABETICA Y SIMILARES
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US57030004P | 2004-05-12 | 2004-05-12 | |
| US66430505P | 2005-03-21 | 2005-03-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20060316A1 true PE20060316A1 (es) | 2006-05-08 |
Family
ID=34966115
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2005000515A PE20060316A1 (es) | 2004-05-12 | 2005-05-09 | Derivados de prolina como inhibidores de dipeptidil peptidasa-iv |
Country Status (36)
| Country | Link |
|---|---|
| US (4) | US7291618B2 (es) |
| EP (2) | EP2116541B1 (es) |
| JP (1) | JP4227660B2 (es) |
| KR (1) | KR100869616B1 (es) |
| AP (1) | AP2320A (es) |
| AR (1) | AR049894A1 (es) |
| AT (1) | ATE437870T1 (es) |
| AU (1) | AU2005247684B2 (es) |
| BR (1) | BRPI0510284A (es) |
| CA (1) | CA2566108C (es) |
| CR (1) | CR8744A (es) |
| CY (1) | CY1109322T1 (es) |
| DE (1) | DE602005015699D1 (es) |
| DK (1) | DK1753748T3 (es) |
| EA (1) | EA011086B9 (es) |
| EC (1) | ECSP066985A (es) |
| ES (1) | ES2327857T3 (es) |
| GE (1) | GEP20084421B (es) |
| HR (1) | HRP20090471T1 (es) |
| IL (1) | IL178339A (es) |
| MA (1) | MA28578B1 (es) |
| MX (1) | MXPA06013114A (es) |
| MY (1) | MY139805A (es) |
| NL (1) | NL1029015C2 (es) |
| NO (1) | NO20064400L (es) |
| NZ (1) | NZ550229A (es) |
| PA (1) | PA8632701A1 (es) |
| PE (1) | PE20060316A1 (es) |
| PL (1) | PL1753748T3 (es) |
| PT (1) | PT1753748E (es) |
| RS (1) | RS51106B (es) |
| SI (1) | SI1753748T1 (es) |
| SV (1) | SV2006002110A (es) |
| TW (1) | TWI347322B (es) |
| UY (1) | UY28892A1 (es) |
| WO (1) | WO2005116014A1 (es) |
Families Citing this family (121)
| Publication number | Priority date | Publication date | Assignee | Title |
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| SI1757606T1 (sl) * | 2001-02-24 | 2009-10-31 | Boehringer Ingelheim Pharma | Ksantinski derivati za uporabo kot zdravila kot tudi postopek za njihovo pripravo |
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