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
-
- 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)
- Diabetes (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Obesity (AREA)
- Emergency Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Child & Adolescent Psychology (AREA)
- Epidemiology (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) | EP2292228A1 (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) | PE20120355A1 (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) |
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| CN101312951A (zh) | 2005-11-21 | 2008-11-26 | 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 |
| JP4671369B2 (ja) | 2007-05-18 | 2011-04-13 | 塩野義製薬株式会社 | I型11βヒドロキシステロイド脱水素酵素阻害活性を有する含窒素複素環誘導体 |
| WO2009010416A2 (en) | 2007-07-17 | 2009-01-22 | F. Hoffmann-La Roche Ag | Inhibitors of 11b-hydroxysteroid dehydrogenase |
| CN101969946A (zh) * | 2008-02-04 | 2011-02-09 | 阿斯利康(瑞典)有限公司 | 4-[4-(2-金刚烷基氨基甲酰基)-5-叔丁基-吡唑-1-基]苯甲酸的新晶型 |
| EP2271629A1 (en) * | 2008-04-22 | 2011-01-12 | AstraZeneca AB | Substituted pyrimidin-5-carboxamides 281 |
| JP2012516327A (ja) * | 2009-01-30 | 2012-07-19 | アストラゼネカ アクチボラグ | カルボキシ含有ピラゾールアミド化合物を製造するための新規な方法 |
| 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 |
| EP2582709B1 (de) | 2010-06-18 | 2018-01-24 | Sanofi | Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen |
| 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 |
| 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 |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, 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 |
| 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 |
| WO2012176717A1 (ja) | 2011-06-22 | 2012-12-27 | セントラル硝子株式会社 | ピラゾール化合物の製造方法 |
| 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 |
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| KR101346902B1 (ko) | 2005-07-09 | 2014-01-02 | 아스트라제네카 아베 | 당뇨병 치료에 있어 glk 활성화제로서 사용하기 위한헤테로아릴 벤즈아미드 유도체 |
| WO2007017649A1 (en) | 2005-08-09 | 2007-02-15 | Astrazeneca Ab | Heteroarylcarbamoylbenzene derivatives for the treatment of diabetes |
| CA2627813A1 (en) | 2005-11-01 | 2007-05-10 | Janssen Pharmaceutica 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 |
| CN101312951A (zh) * | 2005-11-21 | 2008-11-26 | 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 |
| TW200804341A (en) | 2006-01-31 | 2008-01-16 | Incyte Corp | Amido compounds and their use as pharmaceuticals |
| RS54216B1 (sr) | 2006-03-22 | 2015-12-31 | F. Hoffmann-La Roche Ag. | Pirazoli kao 11-beta-hsd-1 |
| US8053447B2 (en) | 2006-04-07 | 2011-11-08 | High Point Pharmaceuticals, Llc | 11β-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 |
| WO2008012532A2 (en) | 2006-07-27 | 2008-01-31 | Astrazeneca Ab | : 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 |
| JP4671369B2 (ja) | 2007-05-18 | 2011-04-13 | 塩野義製薬株式会社 | I型11βヒドロキシステロイド脱水素酵素阻害活性を有する含窒素複素環誘導体 |
| WO2009010416A2 (en) | 2007-07-17 | 2009-01-22 | F. Hoffmann-La Roche Ag | Inhibitors of 11b-hydroxysteroid dehydrogenase |
| CA2703781A1 (en) | 2007-11-06 | 2009-05-14 | Astrazeneca Ab | 4-[4-(2-adamantylcarbamoyl)-5-tert-butyl-pyrazol-1-yl]benzoic acid - 465 |
| CN101969946A (zh) | 2008-02-04 | 2011-02-09 | 阿斯利康(瑞典)有限公司 | 4-[4-(2-金刚烷基氨基甲酰基)-5-叔丁基-吡唑-1-基]苯甲酸的新晶型 |
| EP2271629A1 (en) | 2008-04-22 | 2011-01-12 | AstraZeneca AB | Substituted pyrimidin-5-carboxamides 281 |
| JP2012516327A (ja) | 2009-01-30 | 2012-07-19 | アストラゼネカ アクチボラグ | カルボキシ含有ピラゾールアミド化合物を製造するための新規な方法 |
| TW201118085A (en) | 2009-10-20 | 2011-06-01 | Astrazeneca Ab | Adamantyl iminocarbonyl-substituted pyrimidines as inhibitors of 11-β-HSD1 |
-
2008
- 2008-02-05 TW TW097104688A patent/TW200836719A/zh unknown
- 2008-02-08 CL CL2008000422A patent/CL2008000422A1/es unknown
- 2008-02-09 SA SA8290055A patent/SA08290055B1/ar unknown
- 2008-02-11 RU RU2009133259/04A patent/RU2462456C2/ru not_active IP Right Cessation
- 2008-02-11 JP JP2009548741A patent/JP2010518063A/ja active Pending
- 2008-02-11 KR KR1020097018195A patent/KR20090108726A/ko not_active Ceased
- 2008-02-11 BR BRPI0808450-5A patent/BRPI0808450A2/pt not_active IP Right Cessation
- 2008-02-11 WO PCT/GB2008/000454 patent/WO2008099145A1/en not_active Ceased
- 2008-02-11 PE PE2012000020A patent/PE20120355A1/es not_active Application Discontinuation
- 2008-02-11 CA CA002676154A patent/CA2676154A1/en not_active Abandoned
- 2008-02-11 CN CN2011102665044A patent/CN102503891A/zh active Pending
- 2008-02-11 EP EP10183055A patent/EP2292228A1/en not_active Withdrawn
- 2008-02-11 SG SG2011091865A patent/SG177892A1/en unknown
- 2008-02-11 EP EP08702088A patent/EP2124937A1/en not_active Withdrawn
- 2008-02-11 AR ARP080100584A patent/AR065300A1/es not_active Application Discontinuation
- 2008-02-11 PE PE2008000295A patent/PE20090649A1/es not_active Application Discontinuation
- 2008-02-11 AU AU2008215976A patent/AU2008215976B2/en not_active Ceased
- 2008-02-11 MX MX2009008506A patent/MX2009008506A/es not_active Application Discontinuation
- 2008-02-11 NZ NZ578568A patent/NZ578568A/en not_active IP Right Cessation
- 2008-02-12 UY UY30912A patent/UY30912A1/es not_active Application Discontinuation
- 2008-10-28 US US12/259,562 patent/US7816391B2/en not_active Expired - Fee Related
-
2009
- 2009-07-23 IL IL200047A patent/IL200047A0/en unknown
- 2009-08-11 EC EC2009009571A patent/ECSP099571A/es unknown
- 2009-08-12 CO CO09084454A patent/CO6220949A2/es not_active Application Discontinuation
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2010
- 2010-02-04 ZA ZA2010/00838A patent/ZA201000838B/en unknown
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-
2012
- 2012-06-20 RU RU2012125372/04A patent/RU2012125372A/ru not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| ZA201000838B (en) | 2010-10-27 |
| AU2008215976B2 (en) | 2011-11-24 |
| AU2008215976A1 (en) | 2008-08-21 |
| JP2010518063A (ja) | 2010-05-27 |
| RU2009133259A (ru) | 2011-03-20 |
| MX2009008506A (es) | 2009-10-12 |
| US7816391B2 (en) | 2010-10-19 |
| IL200047A0 (en) | 2010-04-15 |
| CL2008000422A1 (es) | 2009-01-02 |
| KR20090108726A (ko) | 2009-10-16 |
| US20090221663A1 (en) | 2009-09-03 |
| CN102503891A (zh) | 2012-06-20 |
| EP2124937A1 (en) | 2009-12-02 |
| NZ578568A (en) | 2012-01-12 |
| SG177892A1 (en) | 2012-02-28 |
| CA2676154A1 (en) | 2008-08-21 |
| PE20090649A1 (es) | 2009-06-26 |
| UY30912A1 (es) | 2008-09-30 |
| US20110224273A1 (en) | 2011-09-15 |
| WO2008099145A1 (en) | 2008-08-21 |
| ECSP099571A (es) | 2009-09-29 |
| TW200836719A (en) | 2008-09-16 |
| BRPI0808450A2 (pt) | 2014-08-12 |
| PE20120355A1 (es) | 2012-05-17 |
| EP2292228A1 (en) | 2011-03-09 |
| SA08290055B1 (ar) | 2012-09-26 |
| CO6220949A2 (es) | 2010-11-19 |
| RU2462456C2 (ru) | 2012-09-27 |
| RU2012125372A (ru) | 2013-12-27 |
| US8344016B2 (en) | 2013-01-01 |
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