AR065300A1 - Compuestos quimicos derivados de 1,2-pirazol - Google Patents
Compuestos quimicos derivados de 1,2-pirazolInfo
- Publication number
- AR065300A1 AR065300A1 ARP080100584A ARP080100584A AR065300A1 AR 065300 A1 AR065300 A1 AR 065300A1 AR P080100584 A ARP080100584 A AR P080100584A AR P080100584 A ARP080100584 A AR P080100584A AR 065300 A1 AR065300 A1 AR 065300A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- optionally substituted
- independently selected
- cyano
- halo
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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
- C07D231/18—One oxygen or sulfur atom
-
- 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
- A61K31/415—1,2-Diazoles
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- 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
-
- 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
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/38—Drugs for disorders of the endocrine system of the suprarenal hormones
- A61P5/46—Drugs for disorders of the endocrine system of the suprarenal hormones for decreasing, blocking or antagonising the activity of glucocorticosteroids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
- A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Diabetes (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Epidemiology (AREA)
- Child & Adolescent Psychology (AREA)
- Emergency Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Compuestos utiles en la inhibicion de 11betaHSD1; procesos para su elaboracion y composiciones farmacéuticas que los comprenden. Reivindicacion 1: Un compuesto de la formula (1): donde: Q es O, S o un enlace simple; R1 es alquilo C1-6, alquenilo C2- 6, alquinilo C2-6, cicloalquilo C3-7, heterociclilo, aril-alquiIoC1-3, heteroariI-alquiloC1-3, cicloalquilC3-7-alquiloC1-3, cicloalquilC3-7-alqueniloC2-3 o cicloalquilC3-7-alquiniloC2-3 [donde cada sin esta opcionalmente sustituido con 1, 2 o 3 sustituyentes seleccionados de manera independiente de alquilo C1-3, hidroxi, halo, oxo, ciano, trifluormetilo, alcoxi C1-3, alquiloC1-3S(O)n- (donde n es 0, 1, 2 o 3), R5CON(R5')-, (R5)(R5'')NC(O)-, R5'C(O)O-, R5'OC(O)-, (R5')(R5'')NC(O)N(R5ö')-, R5SO2N(R5'')- y (R5')(R5ö)NSO2- (donde R5 es alquilo C1-3 opcionalmente sustituido con 1, 2 o 3 sustituyentes seleccionados de hidroxilo, halo o ciano; y R5' y R5''se seleccionan de manera independiente de hidrogeno y alquilo C1-3 opcionalmente sustituido con 1, 2 o 3 sustituyentes seleccionados de manera independiente de hidroxilo, halo, alcoxi C1-3, carboxi y ciano; o R5' y R5'' junto con el átomo de nitrogeno al cual están unidos forman un anillo saturado de 4 a 7 miembros )]; R2 se selecciona de heterociclilo, cicloalquiloC3-7(CH2)m-, y policicloalquiloC6-12(CH2)m- (donde m es 0, 1 o 2, y los anillos están opcionalmente sustituidos con 1, 2 o 3 sustituyentes seleccionados de manera independiente de R6); R3 se selecciona de hidrogeno, aIquilo C1-4, cicloalquilo C3-5 y cicloalquilmetilo C3-5 (donde cada uno está opcionalmente sustituido con 1, 2 o 3 átomos de fluor); R2 y R3 junto con el átomo de nitrogeno al cual están unidos forman un sistema de anillo monocíclico, bicíclico o puenteado, saturado, que, en forma opcional, contiene 1 o 2 heteroátomos de anillo adicionales seleccionados de nitrogeno, oxígeno y azufre, y que está opcionalmente fusionado a un anillo monocíclico saturado, parcialmente saturado o insaturado, donde el sistema de anillo resultante está opcionalmente sustituido con 1, 2 o 3 sustituyentes seleccionados de modo independiente de R7; R6 y R7 se seleccionan de manera independiente de hidroxilo, halo, oxo, carboxi, ciano, trifluormetilo, R9, R9O-, R9CO-, R9C(O)O-, R9CON(R9')-, (R9')(R9'')NC(O)-, (R9')(R9ö)N-, R9S(O)a- donde a es 0 a 2, R9'OC(O)-, (R9')(R9ö)NSO2-, R9SO2N(R9)-, (R9')(R9ö)NC(O)N(R9'')-, fenilo y heteroarilo [donde los grupos fenilo y heteroarilo están opcionalmente fusionados a un fenilo, heteroarilo o un anillo de 5 o 6 miembros saturado o parcialmente saturado que, en forma opcional, contiene 1, 2 o 3 heteroátomos seleccionados de manera independiente de nitrogeno, oxígeno y azufre, donde el sistema de anillo resultante está opcionalmente sustituido con 1, 2 o 3 sustituyentes seleccionados de modo independiente de alquilo C1-4, hidroxilo, ciano, trifluormetilo, trifluormetoxi, halo, alcoxi C1-4, alcoxiC1-4-alquiloC1-4, amino, N- alquilaminoC1-4, di-N,N-(alquilo C1-4)amino, N-alquilcarbamoiloC1-4, di-N,N-(alquilo C1-4)carbamoilo, alquilC1-4S(O)r-, alquilC1-4S(O)alquiIoC1-4 (donde r es 0, 1 u 2)]; R9 se selecciona de manera independiente de alquilo C1-3 opcionalmenle sustituido con hidroxilo, hato, alcoxi C1-4, carboxi o ciano; R9', R9ö y R9''' se seleccionan de manera independiente de hidrogeno y alquilo C1-3 opcionalmente sustituido con 1, 2, o 3 sustituyentes seleccionados de manera independiente de hidroxilo, halo, alcoxi C1-4, carboxi y ciano; A es un anillo fenilo o heteroarilo (donde el anillo fenilo o heteroarilo está opcionalmente sustituido en átomos de carbono del anillo, con 1, 2 u 3 grupos R10, y en un nitrogeno de anillo disponible en un grupo heteroarilo, con R11); R10 se selecciona de manera independiente de alquilo C1-4, hidroxilo, ciano, trifluormetilo, trifluormetoxi, halo, alcoxi C1-4, alcoxiC1-4-alquiloC1-4, amino, N-alquilaminoC1-4, di-N,N-(alquilo C1-4)amino, N- alquilcarbamoíloC1-4, di-N,N-(alquilo C1-4)carbamoílo, aIquiloC1-4S(O)s-, alquiloC1-4S(O)salquiloC1-4 (donde s es 0, 1 o 2)]; R11 es, de manera independiente, alquilo C1-3 opcionalmente sustituido con 1, 2 o 3 átomos de fluor; X es un enlace directo, cicloalcanodiílo C3-4, cicloalcanilideno C3-4, -C(R12)(R13)-, -C(R12)(R13)C(R14)(R15)-, -CH2O- o -CH2S(O)t- (donde t es 0, 1 o 2): Y es un enlace directo, cicloalcanodiílo C3-4, cicloalcanilideno C3-4, -C(R16)(R17)- o - C(R18)(R19)C(R20)(R21)-; donde R12, R13, R14, R15, R16, R17, R18, R19, R20 y R21se seleccionan de manera independiente de hidrogeno y metilo; o una de sus sales aceptables para uso farmacéutico.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US88933607P | 2007-02-12 | 2007-02-12 | |
US98573507P | 2007-11-06 | 2007-11-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR065300A1 true AR065300A1 (es) | 2009-05-27 |
Family
ID=39438215
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP080100584A AR065300A1 (es) | 2007-02-12 | 2008-02-11 | Compuestos quimicos derivados de 1,2-pirazol |
Country Status (23)
Country | Link |
---|---|
US (2) | US7816391B2 (es) |
EP (2) | EP2124937A1 (es) |
JP (1) | JP2010518063A (es) |
KR (1) | KR20090108726A (es) |
CN (1) | CN102503891A (es) |
AR (1) | AR065300A1 (es) |
AU (1) | AU2008215976B2 (es) |
BR (1) | BRPI0808450A2 (es) |
CA (1) | CA2676154A1 (es) |
CL (1) | CL2008000422A1 (es) |
CO (1) | CO6220949A2 (es) |
EC (1) | ECSP099571A (es) |
IL (1) | IL200047A0 (es) |
MX (1) | MX2009008506A (es) |
NZ (1) | NZ578568A (es) |
PE (2) | PE20090649A1 (es) |
RU (2) | RU2462456C2 (es) |
SA (1) | SA08290055B1 (es) |
SG (1) | SG177892A1 (es) |
TW (1) | TW200836719A (es) |
UY (1) | UY30912A1 (es) |
WO (1) | WO2008099145A1 (es) |
ZA (1) | ZA201000838B (es) |
Families Citing this family (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102659659B (zh) | 2005-11-21 | 2014-07-23 | 盐野义制药株式会社 | 具有I型11β羟基类固醇脱氢酶抑制活性的杂环化合物 |
TW200827346A (en) | 2006-11-03 | 2008-07-01 | Astrazeneca Ab | Chemical compounds |
TW200836719A (en) | 2007-02-12 | 2008-09-16 | Astrazeneca Ab | Chemical compounds |
CA2689659C (en) | 2007-05-18 | 2012-10-23 | Shionogi And Co., Ltd. | Nitrogen-containing heterocyclic derivative having 11.beta.-hydroxysteroid dehydrogenase type 1 inhibitory activity |
EP2178845B1 (en) | 2007-07-17 | 2013-06-19 | F. Hoffmann-La Roche AG | Inhibitors of 11b-hydroxysteroid dehydrogenase |
AU2009211215B2 (en) * | 2008-02-04 | 2011-11-03 | Astrazeneca Ab | Novel crystalline forms of 4- [4- (2-adamantylcarbam0yl) -5-tert-butyl-pyrazol-1-yl] benzoic acid |
AU2009239794A1 (en) * | 2008-04-22 | 2009-10-29 | Astrazeneca Ab | Substituted pyrimidin-5-carboxamides 281 |
CN102300851A (zh) * | 2009-01-30 | 2011-12-28 | 阿斯利康(瑞典)有限公司 | 制备含羧基的吡唑酰氨基化合物597的新方法 |
EP2243479A3 (en) | 2009-04-20 | 2011-01-19 | Abbott Laboratories | Novel amide and amidine derivates and uses thereof |
US8871208B2 (en) * | 2009-12-04 | 2014-10-28 | Abbvie Inc. | 11-β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitors and uses thereof |
WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
GB201004301D0 (en) * | 2010-03-15 | 2010-04-28 | Syngenta Participations Ag | Process |
US8933024B2 (en) | 2010-06-18 | 2015-01-13 | Sanofi | Azolopyridin-3-one derivatives as inhibitors of lipases and phospholipases |
US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
TW201215387A (en) | 2010-07-05 | 2012-04-16 | Sanofi Aventis | Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament |
JP5605104B2 (ja) * | 2010-09-10 | 2014-10-15 | セントラル硝子株式会社 | ピラゾール化合物の製造方法 |
JP5915004B2 (ja) * | 2011-06-22 | 2016-05-11 | セントラル硝子株式会社 | ピラゾール化合物の製造方法 |
US9012657B2 (en) | 2011-06-22 | 2015-04-21 | Central Glass Company, Limited | Method for producing pyrazole compound |
WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
EP2760862B1 (en) | 2011-09-27 | 2015-10-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
JP2015129094A (ja) * | 2012-04-16 | 2015-07-16 | 大日本住友製薬株式会社 | アリールアミノピラゾール誘導体 |
WO2019042267A1 (zh) * | 2017-08-28 | 2019-03-07 | 中国医学科学院药物研究所 | 吡咯-2-甲酰胺类化合物及其制备方法和用途 |
Family Cites Families (49)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GR66581B (es) | 1978-02-21 | 1981-03-27 | Delalande Sa | |
US4816391A (en) * | 1984-02-29 | 1989-03-28 | Syntex (U.S.A.) Inc. | Amine stabilized aminoglycoside formulations |
CA1307786C (en) | 1984-12-14 | 1992-09-22 | Keiichi Yokoyama | Quinazoline derivatives and antihypertensive preparations containing same as effective components |
MY123528A (en) | 1999-09-16 | 2006-05-31 | Mitsubihsi Tanabe Pharma Corp | Aromatic nitrogen-containing 6-membered cyclic compounds. |
US7273868B2 (en) | 2000-04-28 | 2007-09-25 | Tanabe Seiyaku Co., Ltd. | Pyrazine derivatives |
WO2002020463A2 (en) | 2000-09-05 | 2002-03-14 | Tularik Inc. | Fxr modulators |
IL155202A0 (en) | 2000-10-20 | 2003-11-23 | Biocryst Pharm Inc | Biaryl compounds as serine protease inhibitors |
SE0102764D0 (sv) | 2001-08-17 | 2001-08-17 | Astrazeneca Ab | Compounds |
JP2005528395A (ja) | 2002-04-05 | 2005-09-22 | ザ ユニバーシティ オブ エディンバラ | 組成物 |
TW200503994A (en) | 2003-01-24 | 2005-02-01 | Novartis Ag | Organic compounds |
US7432287B2 (en) | 2003-02-26 | 2008-10-07 | Banyu Pharmeceutical Co., Ltd. | Heteroarylcarbamoylbenzene derivative |
JP4629657B2 (ja) | 2003-04-11 | 2011-02-09 | ハイ・ポイント・ファーマスーティカルズ、エルエルシー | 11β−ヒドロキシステロイドデヒドロゲナーゼ1型化活性化合物 |
CN1832741A (zh) | 2003-08-07 | 2006-09-13 | 默克公司 | 作为11-β-羟甾类脱氢酶-1抑制剂的吡唑甲酰胺类 |
SG146624A1 (en) | 2003-09-11 | 2008-10-30 | Kemia Inc | Cytokine inhibitors |
GB0327761D0 (en) | 2003-11-29 | 2003-12-31 | Astrazeneca Ab | Compounds |
KR20060101772A (ko) | 2003-12-19 | 2006-09-26 | 화이자 인코포레이티드 | 당뇨병 및 비만을 치료하기 위한,11-베타-하이드록시스테로이드 데하이드로게나제 유형1(11-베타-hsd-1)의 저해제로서의벤젠설폰일아미노-피리딘-2-일 유도체 및 관련 화합물 |
BRPI0510623A (pt) | 2004-05-06 | 2007-10-30 | Pfizer | compostos de derivados de prolina e morfolina |
TW200600086A (en) | 2004-06-05 | 2006-01-01 | Astrazeneca Ab | Chemical compound |
PT1763517E (pt) | 2004-06-28 | 2011-07-01 | Hoffmann La Roche | Derivados de pirimidina como inibidores 11beta-hsd1 |
WO2006048750A2 (en) | 2004-11-02 | 2006-05-11 | Pfizer Inc. | Novel compounds of substituted and unsubstituted adamantyl amides |
WO2006050476A2 (en) | 2004-11-03 | 2006-05-11 | Vertex Pharmaceuticals Incorporated | Pyrimidine derivatives as ion channel modulators and methods of use |
KR101496206B1 (ko) | 2005-01-05 | 2015-02-27 | 애브비 인코포레이티드 | 11-베타-하이드록시스테로이드 데하이드로게나제 타입 1 효소의 억제제로서의 아다만틸 유도체 |
ES2369389T3 (es) | 2005-04-05 | 2011-11-30 | F. Hoffmann-La Roche Ag | 1h-pirazol-4-carboxamidas, su preparación y su empleo como inhibidores de 11-beta- hidroxiesteroide dehidrogenasa. |
RU2404164C2 (ru) | 2005-04-06 | 2010-11-20 | Ф.Хоффманн-Ля Рош Аг | Производные пиридин-3-карбоксамида в качестве обратных агонистов св1 |
WO2006106423A2 (en) | 2005-04-07 | 2006-10-12 | Pfizer Inc. | Amino sulfonyl derivatives as inhibitors of human 11-.beta.-hydrosysteroid dehydrogenase |
EP1879881A2 (en) | 2005-04-14 | 2008-01-23 | Bristol-Myers Squibb Company | Inhibitors of 11-beta hydroxysteroid dehydrogenase type i |
US20110059941A1 (en) | 2005-05-24 | 2011-03-10 | Peter William Rodney Caulkett | 2-phenyl substituted imidazol [4,5b] pyridine/pyrazine and purine derivatives as glucokinase modulators |
EP1894919B1 (en) | 2005-06-07 | 2012-03-28 | Shionogi & Co., Ltd. | Heterocyclic compound having type i 11 beta hydroxysteroid dehydrogenase inhibitory activity |
KR100970294B1 (ko) * | 2005-06-08 | 2010-07-15 | 니뽄 다바코 산교 가부시키가이샤 | 복소환 화합물 |
AU2006257646A1 (en) | 2005-06-16 | 2006-12-21 | Pfizer Inc. | N-(pyridin-2-YL)-sulfonamide derivatives |
BRPI0622262A2 (pt) | 2005-07-09 | 2011-08-09 | Astrazeneca Ab | composto, composição farmacêutica, uso de um composto ou um sal farmaceuticamente aceitável do mesmo, e, processo para a preparação de um composto |
WO2007017649A1 (en) | 2005-08-09 | 2007-02-15 | Astrazeneca Ab | Heteroarylcarbamoylbenzene derivatives for the treatment of diabetes |
US8680122B2 (en) | 2005-11-01 | 2014-03-25 | Janssen Pharmacetica N.V. | Substituted pyrrolones as allosteric modulators of glucokinase |
WO2007052843A1 (ja) | 2005-11-04 | 2007-05-10 | Takeda Pharmaceutical Company Limited | 複素環アミド化合物およびその用途 |
CN102659659B (zh) * | 2005-11-21 | 2014-07-23 | 盐野义制药株式会社 | 具有I型11β羟基类固醇脱氢酶抑制活性的杂环化合物 |
WO2007089683A1 (en) | 2006-01-31 | 2007-08-09 | Incyte Corporation | Amido compounds and their use as pharmaceuticals |
WO2007107470A2 (en) * | 2006-03-22 | 2007-09-27 | F. Hoffmann-La Roche Ag | Pyrazoles as 11-beta-hsd-1 |
CA2648074A1 (en) | 2006-04-07 | 2007-10-18 | High Point Pharmaceuticals, Llc | 11.beta.-hydroxysteroid dehydrogenase type 1 active compounds |
WO2007125049A1 (en) | 2006-04-27 | 2007-11-08 | Solvay Pharmaceuticals Gmbh | Use of cbx cannabinoid receptor modulators as potassium channel modulators |
US20100022589A1 (en) | 2006-07-27 | 2010-01-28 | Mccoull William | Pyridine-3-carboxamide compounds and their use for inhibiting 11-beta-hydroxysteroid dehydrogenase |
TW200827346A (en) | 2006-11-03 | 2008-07-01 | Astrazeneca Ab | Chemical compounds |
TW200836719A (en) | 2007-02-12 | 2008-09-16 | Astrazeneca Ab | Chemical compounds |
CA2689659C (en) | 2007-05-18 | 2012-10-23 | Shionogi And Co., Ltd. | Nitrogen-containing heterocyclic derivative having 11.beta.-hydroxysteroid dehydrogenase type 1 inhibitory activity |
EP2178845B1 (en) | 2007-07-17 | 2013-06-19 | F. Hoffmann-La Roche AG | Inhibitors of 11b-hydroxysteroid dehydrogenase |
MX2010005048A (es) | 2007-11-06 | 2010-07-28 | Astrazeneca Ab | Acido 4-[4-(2-adamantilcarbamoil)-5-terc-butil-pirazol-1-il]benzoi c-465. |
AU2009211215B2 (en) | 2008-02-04 | 2011-11-03 | Astrazeneca Ab | Novel crystalline forms of 4- [4- (2-adamantylcarbam0yl) -5-tert-butyl-pyrazol-1-yl] benzoic acid |
AU2009239794A1 (en) | 2008-04-22 | 2009-10-29 | Astrazeneca Ab | Substituted pyrimidin-5-carboxamides 281 |
CN102300851A (zh) | 2009-01-30 | 2011-12-28 | 阿斯利康(瑞典)有限公司 | 制备含羧基的吡唑酰氨基化合物597的新方法 |
TW201118085A (en) | 2009-10-20 | 2011-06-01 | Astrazeneca Ab | Adamantyl iminocarbonyl-substituted pyrimidines as inhibitors of 11-β-HSD1 |
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- 2008-02-11 PE PE2012000020A patent/PE20120355A1/es not_active Application Discontinuation
- 2008-02-11 WO PCT/GB2008/000454 patent/WO2008099145A1/en active Application Filing
- 2008-02-11 EP EP08702088A patent/EP2124937A1/en not_active Withdrawn
- 2008-02-11 MX MX2009008506A patent/MX2009008506A/es not_active Application Discontinuation
- 2008-02-11 CA CA002676154A patent/CA2676154A1/en not_active Abandoned
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- 2008-02-11 JP JP2009548741A patent/JP2010518063A/ja active Pending
- 2008-02-11 KR KR1020097018195A patent/KR20090108726A/ko not_active Application Discontinuation
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- 2008-02-11 BR BRPI0808450-5A patent/BRPI0808450A2/pt not_active IP Right Cessation
- 2008-02-11 CN CN2011102665044A patent/CN102503891A/zh active Pending
- 2008-02-11 AR ARP080100584A patent/AR065300A1/es not_active Application Discontinuation
- 2008-02-11 AU AU2008215976A patent/AU2008215976B2/en not_active Ceased
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Also Published As
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IL200047A0 (en) | 2010-04-15 |
CN102503891A (zh) | 2012-06-20 |
CO6220949A2 (es) | 2010-11-19 |
WO2008099145A1 (en) | 2008-08-21 |
RU2012125372A (ru) | 2013-12-27 |
EP2292228A1 (en) | 2011-03-09 |
TW200836719A (en) | 2008-09-16 |
BRPI0808450A2 (pt) | 2014-08-12 |
SG177892A1 (en) | 2012-02-28 |
US7816391B2 (en) | 2010-10-19 |
RU2462456C2 (ru) | 2012-09-27 |
US20090221663A1 (en) | 2009-09-03 |
ZA201000838B (en) | 2010-10-27 |
PE20120355A1 (es) | 2012-05-17 |
ECSP099571A (es) | 2009-09-29 |
KR20090108726A (ko) | 2009-10-16 |
AU2008215976B2 (en) | 2011-11-24 |
RU2009133259A (ru) | 2011-03-20 |
JP2010518063A (ja) | 2010-05-27 |
US8344016B2 (en) | 2013-01-01 |
PE20090649A1 (es) | 2009-06-26 |
MX2009008506A (es) | 2009-10-12 |
SA08290055B1 (ar) | 2012-09-26 |
US20110224273A1 (en) | 2011-09-15 |
UY30912A1 (es) | 2008-09-30 |
EP2124937A1 (en) | 2009-12-02 |
AU2008215976A1 (en) | 2008-08-21 |
NZ578568A (en) | 2012-01-12 |
CA2676154A1 (en) | 2008-08-21 |
CL2008000422A1 (es) | 2009-01-02 |
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