CN101516860B - 可用作janus激酶抑制剂的苯并*唑和*唑并吡啶 - Google Patents
可用作janus激酶抑制剂的苯并*唑和*唑并吡啶 Download PDFInfo
- Publication number
- CN101516860B CN101516860B CN2007800339907A CN200780033990A CN101516860B CN 101516860 B CN101516860 B CN 101516860B CN 2007800339907 A CN2007800339907 A CN 2007800339907A CN 200780033990 A CN200780033990 A CN 200780033990A CN 101516860 B CN101516860 B CN 101516860B
- Authority
- CN
- China
- Prior art keywords
- phenyl
- methyl
- amino
- morpholine
- benzo azoles
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- WPODTHCWPDTNCY-UHFFFAOYSA-N CCN(CC)C(c(cc1)c(C)cc1Nc1nc2cccc(-c3cc(F)c(CN4CCOCC4)c(F)c3)c2[o]1)=O Chemical compound CCN(CC)C(c(cc1)c(C)cc1Nc1nc2cccc(-c3cc(F)c(CN4CCOCC4)c(F)c3)c2[o]1)=O WPODTHCWPDTNCY-UHFFFAOYSA-N 0.000 description 1
- NBJSVVQVQLOIMW-UHFFFAOYSA-N CCN(CC1)CCN1c(c(C)c1)ccc1Nc1nc(cccc2-c3ccc(C(N4CCOCC4)=O)c(F)c3)c2[o]1 Chemical compound CCN(CC1)CCN1c(c(C)c1)ccc1Nc1nc(cccc2-c3ccc(C(N4CCOCC4)=O)c(F)c3)c2[o]1 NBJSVVQVQLOIMW-UHFFFAOYSA-N 0.000 description 1
- UQZKVIPZBBHCRB-UHFFFAOYSA-N CCN(CC1)CCN1c(cc1)c(C)cc1Nc1nc(cccc2-c3ccc(CN4CCOCC4)c(F)c3)c2[o]1 Chemical compound CCN(CC1)CCN1c(cc1)c(C)cc1Nc1nc(cccc2-c3ccc(CN4CCOCC4)c(F)c3)c2[o]1 UQZKVIPZBBHCRB-UHFFFAOYSA-N 0.000 description 1
- ZUIVNYCUKBVSNF-UHFFFAOYSA-N CN(CC1)CCN1C(c(cc1)ccc1-c1c2[o]c(Nc(cc3OC)cc(OC)c3OC)nc2ccc1)=O Chemical compound CN(CC1)CCN1C(c(cc1)ccc1-c1c2[o]c(Nc(cc3OC)cc(OC)c3OC)nc2ccc1)=O ZUIVNYCUKBVSNF-UHFFFAOYSA-N 0.000 description 1
- ZETRKABEMXPMMZ-UHFFFAOYSA-N CN(CC1)CCN1c(cc1)ccc1Nc1nc(cccc2-c3ccc(C(N(CC4)CCS4(=O)=O)=O)c(F)c3)c2[o]1 Chemical compound CN(CC1)CCN1c(cc1)ccc1Nc1nc(cccc2-c3ccc(C(N(CC4)CCS4(=O)=O)=O)c(F)c3)c2[o]1 ZETRKABEMXPMMZ-UHFFFAOYSA-N 0.000 description 1
- XZUACEBPSMDTSG-UHFFFAOYSA-N COc(cc(cc1OC)Nc2nc(cccc3-c4cc(NS(C)(=O)=O)ccc4)c3[o]2)c1OC Chemical compound COc(cc(cc1OC)Nc2nc(cccc3-c4cc(NS(C)(=O)=O)ccc4)c3[o]2)c1OC XZUACEBPSMDTSG-UHFFFAOYSA-N 0.000 description 1
- QYNMYGHYYZOWHP-UHFFFAOYSA-N Cc1cc(-c2cccc3c2[o]c(Nc(cc2)ccc2N2CCN(C)CC2)n3)ccc1C(N1CC=[O]CC1)=O Chemical compound Cc1cc(-c2cccc3c2[o]c(Nc(cc2)ccc2N2CCN(C)CC2)n3)ccc1C(N1CC=[O]CC1)=O QYNMYGHYYZOWHP-UHFFFAOYSA-N 0.000 description 1
- TXELIJASPTUHBS-UHFFFAOYSA-N Cc1cc(-c2cccc3c2[o]c(Nc(cc2C)ccc2N2CCN(CCN(C)C)CC2)n3)ccc1C(N1CC=[O]CC1)=O Chemical compound Cc1cc(-c2cccc3c2[o]c(Nc(cc2C)ccc2N2CCN(CCN(C)C)CC2)n3)ccc1C(N1CC=[O]CC1)=O TXELIJASPTUHBS-UHFFFAOYSA-N 0.000 description 1
- CCYLXRZCCYTEPD-UHFFFAOYSA-N Cc1cc(Nc2nc3cccc(-c4cc(F)c(CN5CCOCC5)c(F)c4)c3[o]2)ccc1C(NCCCN(C)C)=O Chemical compound Cc1cc(Nc2nc3cccc(-c4cc(F)c(CN5CCOCC5)c(F)c4)c3[o]2)ccc1C(NCCCN(C)C)=O CCYLXRZCCYTEPD-UHFFFAOYSA-N 0.000 description 1
- MJOXOVWTFNXARD-UHFFFAOYSA-N Nc(c(N1CCOCC1)c1)ccc1Nc1nc(cccc2-c3cc(F)c(CN4CCOCC4)c(F)c3)c2[o]1 Chemical compound Nc(c(N1CCOCC1)c1)ccc1Nc1nc(cccc2-c3cc(F)c(CN4CCOCC4)c(F)c3)c2[o]1 MJOXOVWTFNXARD-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
- C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
- C07D263/58—Benzoxazoles; Hydrogenated benzoxazoles 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 in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- 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
-
- 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
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- 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
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- 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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Immunology (AREA)
- Dermatology (AREA)
- Obesity (AREA)
- Neurosurgery (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Oncology (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP06120733.8 | 2006-09-15 | ||
| EP06120733A EP1900729A1 (en) | 2006-09-15 | 2006-09-15 | Benzoxazoles and oxazolopyridines being useful as Janus kinases inhibitors |
| PCT/EP2007/007983 WO2008031594A1 (en) | 2006-09-15 | 2007-09-13 | Benzoxazoles and oxazolopyridines being useful as janus kinases inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101516860A CN101516860A (zh) | 2009-08-26 |
| CN101516860B true CN101516860B (zh) | 2012-06-27 |
Family
ID=37717673
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2007800339907A Expired - Fee Related CN101516860B (zh) | 2006-09-15 | 2007-09-13 | 可用作janus激酶抑制剂的苯并*唑和*唑并吡啶 |
Country Status (30)
| Country | Link |
|---|---|
| US (1) | US8629168B2 (https=) |
| EP (2) | EP1900729A1 (https=) |
| JP (1) | JP5325105B2 (https=) |
| KR (1) | KR20090064389A (https=) |
| CN (1) | CN101516860B (https=) |
| AR (1) | AR062786A1 (https=) |
| AT (1) | ATE532774T1 (https=) |
| AU (1) | AU2007296916B2 (https=) |
| BR (1) | BRPI0716841A2 (https=) |
| CA (1) | CA2660987A1 (https=) |
| CL (1) | CL2007002669A1 (https=) |
| CO (1) | CO6150142A2 (https=) |
| CR (1) | CR10639A (https=) |
| EA (1) | EA200900388A1 (https=) |
| ES (1) | ES2377148T3 (https=) |
| GT (1) | GT200900056A (https=) |
| IL (1) | IL196860A0 (https=) |
| MA (1) | MA30723B1 (https=) |
| MX (1) | MX2009002812A (https=) |
| NO (1) | NO20091469L (https=) |
| PA (1) | PA8748101A1 (https=) |
| PE (1) | PE20080842A1 (https=) |
| PL (1) | PL2066647T3 (https=) |
| PT (1) | PT2066647E (https=) |
| SM (1) | SMP200900023B (https=) |
| TN (1) | TN2009000070A1 (https=) |
| TW (1) | TW200819444A (https=) |
| UY (1) | UY30587A1 (https=) |
| WO (1) | WO2008031594A1 (https=) |
| ZA (1) | ZA200900477B (https=) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2467670B (en) | 2007-10-04 | 2012-08-01 | Intellikine Inc | Chemical entities and therapeutic uses thereof |
| US8993580B2 (en) | 2008-03-14 | 2015-03-31 | Intellikine Llc | Benzothiazole kinase inhibitors and methods of use |
| JP5788316B2 (ja) | 2008-07-08 | 2015-09-30 | インテリカイン， エルエルシー | キナーゼインヒビターおよび使用方法 |
| EP2318415B1 (en) * | 2008-07-15 | 2013-02-20 | Sanofi | Oxazolopyrimidines as edg-1 receptor agonists |
| TW201010977A (en) * | 2008-08-12 | 2010-03-16 | Takeda Pharmaceutical | Amide compound |
| US8476431B2 (en) | 2008-11-03 | 2013-07-02 | Itellikine LLC | Benzoxazole kinase inhibitors and methods of use |
| WO2010061971A1 (ja) | 2008-11-28 | 2010-06-03 | 興和株式会社 | ピリジン－３－カルボキシアミド誘導体 |
| EP2518054A1 (en) | 2009-12-24 | 2012-10-31 | Takeda Pharmaceutical Company Limited | Amide compound |
| AR079980A1 (es) * | 2010-01-13 | 2012-03-07 | Sanofi Aventis | Derivados de oxazolopirimidina sustituida en 2,5,7 |
| US9295673B2 (en) | 2011-02-23 | 2016-03-29 | Intellikine Llc | Combination of mTOR inhibitors and P13-kinase inhibitors, and uses thereof |
| US8907093B2 (en) * | 2011-07-07 | 2014-12-09 | Sanofi | Carboxylic acid derivatives having an oxazolo[4,5-c]pyridine ring |
| US8580816B2 (en) * | 2011-07-07 | 2013-11-12 | Sanofi | Carboxylic acid derivatives having an oxazolo[5,4-b]pyridine ring |
| CN103102359B (zh) * | 2011-11-15 | 2016-11-09 | 江苏先声药业有限公司 | 嘧啶类化合物及其应用 |
| EP4556010A3 (en) | 2011-11-30 | 2025-07-23 | Emory University | Jak inhibitors for use in the prevention or treatment of a viral disease caused by a coronaviridae |
| WO2014075318A1 (zh) * | 2012-11-19 | 2014-05-22 | 江苏先声药业有限公司 | 嘧啶类化合物及其应用 |
| WO2014153509A1 (en) | 2013-03-22 | 2014-09-25 | Millennium Pharmaceuticals, Inc. | Combination of catalytic mtorc 1/2 inhibitors and selective inhibitors of aurora a kinase |
| CN103664759A (zh) * | 2013-12-06 | 2014-03-26 | 常熟市联创化学有限公司 | 一种3-羟基-2-硝基吡啶的制备方法 |
| WO2015117146A1 (en) | 2014-02-03 | 2015-08-06 | Quadriga Biosciences, Inc. | Beta-substituted gamma-amino acids and analogs as chemotherapeutic agents |
| ES2896882T3 (es) | 2014-02-03 | 2022-02-28 | Quadriga Biosciences Inc | Beta-aminoácidos beta sustituidos y análogos como agentes quimioterapéuticos |
| WO2016047678A1 (ja) * | 2014-09-25 | 2016-03-31 | 武田薬品工業株式会社 | 複素環化合物 |
| CN108026026B (zh) | 2015-08-03 | 2021-02-09 | 夸德里加生物科学公司 | 作为化疗剂的β-取代的β-氨基酸和类似物及其应用 |
| CN114761013A (zh) | 2019-09-27 | 2022-07-15 | 迪斯克医药公司 | 治疗骨髓纤维化和相关病症的方法 |
| WO2021231798A1 (en) | 2020-05-13 | 2021-11-18 | Disc Medicine, Inc. | Anti-hemojuvelin (hjv) antibodies for treating myelofibrosis |
| TW202307005A (zh) | 2021-05-28 | 2023-02-16 | 美商邊際分析公司 | 以核醣體蛋白質S6激酶α-1 (RSK1)及核醣體蛋白質S6激酶α-3 (RSK2)之調節劑治療神經病症之方法 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1409712A (zh) * | 1999-12-10 | 2003-04-09 | 辉瑞产品公司 | 吡咯并[2,3－d]嘧啶化合物 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE0301373D0 (sv) * | 2003-05-09 | 2003-05-09 | Astrazeneca Ab | Novel compounds |
| DE10344223A1 (de) * | 2003-09-24 | 2005-04-21 | Merck Patent Gmbh | 1,3-Benzoxazolylderivate als Kinase-Inhibitoren |
| GB0402140D0 (en) * | 2004-01-30 | 2004-03-03 | Smithkline Beecham Corp | Novel compounds |
| EP1674467A1 (en) * | 2004-12-22 | 2006-06-28 | 4Sc Ag | 2,5- and 2,6-disubstituted benzazole derivatives useful as protein kinase inhibitors |
| ATE497959T1 (de) * | 2005-09-02 | 2011-02-15 | Hoffmann La Roche | Benzoxazol-, oxazolopyridin-, benzothiazol- und thiazolopyridinderivate |
| MX2009000769A (es) * | 2006-07-21 | 2009-01-28 | Novartis Ag | Compuestos de 2,4-di(arilaminio)-pirimidin-5-carboxamida como inhibidores de cinasas jak. |
-
2006
- 2006-09-15 EP EP06120733A patent/EP1900729A1/en not_active Ceased
-
2007
- 2007-09-12 UY UY30587A patent/UY30587A1/es not_active Application Discontinuation
- 2007-09-13 WO PCT/EP2007/007983 patent/WO2008031594A1/en not_active Ceased
- 2007-09-13 AU AU2007296916A patent/AU2007296916B2/en not_active Ceased
- 2007-09-13 PL PL07802300T patent/PL2066647T3/pl unknown
- 2007-09-13 PE PE2007001237A patent/PE20080842A1/es not_active Application Discontinuation
- 2007-09-13 KR KR1020097005248A patent/KR20090064389A/ko not_active Withdrawn
- 2007-09-13 ES ES07802300T patent/ES2377148T3/es active Active
- 2007-09-13 JP JP2009527741A patent/JP5325105B2/ja not_active Expired - Fee Related
- 2007-09-13 PT PT07802300T patent/PT2066647E/pt unknown
- 2007-09-13 CN CN2007800339907A patent/CN101516860B/zh not_active Expired - Fee Related
- 2007-09-13 EA EA200900388A patent/EA200900388A1/ru unknown
- 2007-09-13 AR ARP070104060A patent/AR062786A1/es unknown
- 2007-09-13 MX MX2009002812A patent/MX2009002812A/es active IP Right Grant
- 2007-09-13 CA CA002660987A patent/CA2660987A1/en not_active Abandoned
- 2007-09-13 BR BRPI0716841-1A2A patent/BRPI0716841A2/pt not_active IP Right Cessation
- 2007-09-13 AT AT07802300T patent/ATE532774T1/de active
- 2007-09-13 EP EP07802300A patent/EP2066647B1/en active Active
- 2007-09-13 US US12/440,298 patent/US8629168B2/en not_active Expired - Fee Related
- 2007-09-14 TW TW096134606A patent/TW200819444A/zh unknown
- 2007-09-14 CL CL200702669A patent/CL2007002669A1/es unknown
- 2007-09-14 PA PA20078748101A patent/PA8748101A1/es unknown
-
2009
- 2009-01-21 ZA ZA200900477A patent/ZA200900477B/xx unknown
- 2009-02-02 IL IL196860A patent/IL196860A0/en unknown
- 2009-02-26 CR CR10639A patent/CR10639A/es not_active Application Discontinuation
- 2009-02-27 TN TN2009000070A patent/TN2009000070A1/fr unknown
- 2009-03-10 CO CO09024347A patent/CO6150142A2/es unknown
- 2009-03-11 GT GT200900056A patent/GT200900056A/es unknown
- 2009-03-30 MA MA31738A patent/MA30723B1/fr unknown
- 2009-04-09 SM SM200900023T patent/SMP200900023B/it unknown
- 2009-04-15 NO NO20091469A patent/NO20091469L/no not_active Application Discontinuation
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1409712A (zh) * | 1999-12-10 | 2003-04-09 | 辉瑞产品公司 | 吡咯并[2,3－d]嘧啶化合物 |
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