CN102245607B - 吗啉代嘌呤衍生物 - Google Patents
吗啉代嘌呤衍生物 Download PDFInfo
- Publication number
- CN102245607B CN102245607B CN200980151585.4A CN200980151585A CN102245607B CN 102245607 B CN102245607 B CN 102245607B CN 200980151585 A CN200980151585 A CN 200980151585A CN 102245607 B CN102245607 B CN 102245607B
- Authority
- CN
- China
- Prior art keywords
- compound
- morpholin
- group
- purin
- amine
- 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
- 0 CC1c(nc(nc2N3CC(C)(*)COCC3)Cl)c2N=C[C@]1* Chemical compound CC1c(nc(nc2N3CC(C)(*)COCC3)Cl)c2N=C[C@]1* 0.000 description 9
- XINDIUOJBNUZMM-UHFFFAOYSA-N C(c1ccccc1)N1CC2(CC2)NCC1 Chemical compound C(c1ccccc1)N1CC2(CC2)NCC1 XINDIUOJBNUZMM-UHFFFAOYSA-N 0.000 description 1
- GLUUGHFHXGJENI-UHFFFAOYSA-N C1NCCNC1 Chemical compound C1NCCNC1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 1
- YNAVUWVOSKDBBP-UHFFFAOYSA-N C1NCCOC1 Chemical compound C1NCCOC1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 1
- APCBTRDHCDOPNY-SSDOTTSWSA-N CC(C)(C)OC(N(CC1)C[C@@H]1O)=O Chemical compound CC(C)(C)OC(N(CC1)C[C@@H]1O)=O APCBTRDHCDOPNY-SSDOTTSWSA-N 0.000 description 1
- NOILJADDRQDQEN-QMMMGPOBSA-N CC(C)(C)O[NH+](N(CC1)C[C@H]1[n]1c2nc(Cl)nc(Cl)c2nc1)[O-] Chemical compound CC(C)(C)O[NH+](N(CC1)C[C@H]1[n]1c2nc(Cl)nc(Cl)c2nc1)[O-] NOILJADDRQDQEN-QMMMGPOBSA-N 0.000 description 1
- CSBSQWMQXKAAGI-UHFFFAOYSA-N CC(C)C[n]1c(Cl)nc2c(N3CCOCC3)nc(-c3cnc(N)nc3)nc12 Chemical compound CC(C)C[n]1c(Cl)nc2c(N3CCOCC3)nc(-c3cnc(N)nc3)nc12 CSBSQWMQXKAAGI-UHFFFAOYSA-N 0.000 description 1
- ZSZQYYBPHBSCKM-KRWDZBQOSA-N CC(C)C[n]1c(Cl)nc2c(N3[C@@H](C)COCC3)nc(-c3cnc(N(C(OC(C)(C)C)=O)C(OC(C)(C)C)=O)nc3)nc12 Chemical compound CC(C)C[n]1c(Cl)nc2c(N3[C@@H](C)COCC3)nc(-c3cnc(N(C(OC(C)(C)C)=O)C(OC(C)(C)C)=O)nc3)nc12 ZSZQYYBPHBSCKM-KRWDZBQOSA-N 0.000 description 1
- RHQXYBYIDZQMDN-UHFFFAOYSA-N CC(C)C[n]1c(N(CC2)CCN2S(C)(=O)=O)nc2c(N3CCOCC3)nc(-c3cnc(N)nc3)nc12 Chemical compound CC(C)C[n]1c(N(CC2)CCN2S(C)(=O)=O)nc2c(N3CCOCC3)nc(-c3cnc(N)nc3)nc12 RHQXYBYIDZQMDN-UHFFFAOYSA-N 0.000 description 1
- OHTWTCMDFHFQOY-UHFFFAOYSA-N CC(C)C[n]1c(N(CCN2C(C)=O)CC2=C)nc2c(N3CCOCC3)nc(C3=CN=C(N)NC3)nc12 Chemical compound CC(C)C[n]1c(N(CCN2C(C)=O)CC2=C)nc2c(N3CCOCC3)nc(C3=CN=C(N)NC3)nc12 OHTWTCMDFHFQOY-UHFFFAOYSA-N 0.000 description 1
- KBDQYYDPHNMVNZ-UHFFFAOYSA-N CC(C)C[n]1c(N2CCNCC2)nc2c(N3CCOCC3)nc(-c3cnc(N)nc3)nc12 Chemical compound CC(C)C[n]1c(N2CCNCC2)nc2c(N3CCOCC3)nc(-c3cnc(N)nc3)nc12 KBDQYYDPHNMVNZ-UHFFFAOYSA-N 0.000 description 1
- GVYLZZWPZPJRQZ-HNNXBMFYSA-N CC(C)C[n]1c(N2C[C@H](C)NCC2)nc2c(N3CCOCC3)nc(-c3cnc(N)nc3)nc12 Chemical compound CC(C)C[n]1c(N2C[C@H](C)NCC2)nc2c(N3CCOCC3)nc(-c3cnc(N)nc3)nc12 GVYLZZWPZPJRQZ-HNNXBMFYSA-N 0.000 description 1
- ZZSFJJXXKQZFAJ-AKEULKHASA-N CC(C)C[n]1c(NCCN)nc2c1NC(/C(/C=N\CN)=C/NC)N=C2N1CCOCC1 Chemical compound CC(C)C[n]1c(NCCN)nc2c1NC(/C(/C=N\CN)=C/NC)N=C2N1CCOCC1 ZZSFJJXXKQZFAJ-AKEULKHASA-N 0.000 description 1
- DEMAOQGGZHKNKW-AWEZNQCLSA-N CC(C)C[n]1c(NCCNC(C)=O)nc2c(N3[C@@H](C)COCC3)nc(-c3cnc(N)nc3)nc12 Chemical compound CC(C)C[n]1c(NCCNC(C)=O)nc2c(N3[C@@H](C)COCC3)nc(-c3cnc(N)nc3)nc12 DEMAOQGGZHKNKW-AWEZNQCLSA-N 0.000 description 1
- ONIYTJSMFYZZHG-UHFFFAOYSA-N CC(C)C[n]1c(NCCNC=O)nc2c(N3CCOCC3)nc(-c3cnc(N)nc3)nc12 Chemical compound CC(C)C[n]1c(NCCNC=O)nc2c(N3CCOCC3)nc(-c3cnc(N)nc3)nc12 ONIYTJSMFYZZHG-UHFFFAOYSA-N 0.000 description 1
- LJAPUPVIMIHMIH-LBPRGKRZSA-N CC(C)C[n]1c2nc(-c3cnc(N)nc3)nc(N3[C@@H](C)COCC3)c2nc1 Chemical compound CC(C)C[n]1c2nc(-c3cnc(N)nc3)nc(N3[C@@H](C)COCC3)c2nc1 LJAPUPVIMIHMIH-LBPRGKRZSA-N 0.000 description 1
- DFAXHFMCZXCSTQ-UHFFFAOYSA-N CC(C)C[n]1c2nc(Cl)nc(N3CCOCC3)c2nc1 Chemical compound CC(C)C[n]1c2nc(Cl)nc(N3CCOCC3)c2nc1 DFAXHFMCZXCSTQ-UHFFFAOYSA-N 0.000 description 1
- NVJWSEFUVKAWRZ-MJZZXOEVSA-N CC/C(/CC(C)=C)=C(\N)/N=C\C Chemical compound CC/C(/CC(C)=C)=C(\N)/N=C\C NVJWSEFUVKAWRZ-MJZZXOEVSA-N 0.000 description 1
- NVNLTQRPMREFLU-UHFFFAOYSA-N CCC(CC(N1CCOCC1)=C1N=CNC1=N1)=C1Cl Chemical compound CCC(CC(N1CCOCC1)=C1N=CNC1=N1)=C1Cl NVNLTQRPMREFLU-UHFFFAOYSA-N 0.000 description 1
- FFDGPVCHZBVARC-UHFFFAOYSA-N CN(C)CC(O)=O Chemical compound CN(C)CC(O)=O FFDGPVCHZBVARC-UHFFFAOYSA-N 0.000 description 1
- SXIWDARTKZIDRY-UHFFFAOYSA-N CNC(N=C1)=[I]C=C1c1nc(N2CCOCC2)c2nc[n](CC3CC3)c2n1 Chemical compound CNC(N=C1)=[I]C=C1c1nc(N2CCOCC2)c2nc[n](CC3CC3)c2n1 SXIWDARTKZIDRY-UHFFFAOYSA-N 0.000 description 1
- NGZYRKGJWYJGRS-UHFFFAOYSA-N CNC1CNCC1 Chemical compound CNC1CNCC1 NGZYRKGJWYJGRS-UHFFFAOYSA-N 0.000 description 1
- ZARHKMRIVDUEMH-UHFFFAOYSA-N CS(N(CC1)CCN1c1nc2c(N3CCOCC3)nc(-c3cnc(N)nc3)nc2[n]1CC1CC1)(=O)=O Chemical compound CS(N(CC1)CCN1c1nc2c(N3CCOCC3)nc(-c3cnc(N)nc3)nc2[n]1CC1CC1)(=O)=O ZARHKMRIVDUEMH-UHFFFAOYSA-N 0.000 description 1
- SOJJMSYMCLIQCZ-ZDUSSCGKSA-N C[C@@H](CN(CC1)c2nc3c(N4CCOCC4)nc(-c4cnc(N)nc4)nc3[n]2CC(F)(F)F)N1C(C)=O Chemical compound C[C@@H](CN(CC1)c2nc3c(N4CCOCC4)nc(-c4cnc(N)nc4)nc3[n]2CC(F)(F)F)N1C(C)=O SOJJMSYMCLIQCZ-ZDUSSCGKSA-N 0.000 description 1
- YWGWTGPYJQLBAX-ZDUSSCGKSA-N C[C@@H](COCC1)N1c1c2nc(NCCNC(C)=O)[n](CC3CC3)c2nc(-c2cnc(N)nc2C)n1 Chemical compound C[C@@H](COCC1)N1c1c2nc(NCCNC(C)=O)[n](CC3CC3)c2nc(-c2cnc(N)nc2C)n1 YWGWTGPYJQLBAX-ZDUSSCGKSA-N 0.000 description 1
- CJDSOUWTOOHOHZ-BETUJISGSA-N C[C@H](C1)N[C@@H](C)CN1c1nc2c(N3CCOCC3)nc(-c3cnc(N)nc3)nc2[n]1CC(F)(F)F Chemical compound C[C@H](C1)N[C@@H](C)CN1c1nc2c(N3CCOCC3)nc(-c3cnc(N)nc3)nc2[n]1CC(F)(F)F CJDSOUWTOOHOHZ-BETUJISGSA-N 0.000 description 1
- SOJJMSYMCLIQCZ-CYBMUJFWSA-N C[C@H](CN(CC1)c2nc3c(N4CCOCC4)nc(-c4cnc(N)nc4)nc3[n]2CC(F)(F)F)N1C(C)=O Chemical compound C[C@H](CN(CC1)c2nc3c(N4CCOCC4)nc(-c4cnc(N)nc4)nc3[n]2CC(F)(F)F)N1C(C)=O SOJJMSYMCLIQCZ-CYBMUJFWSA-N 0.000 description 1
- ZAGIJZYMLIXIPP-HNNQXCQYSA-N C[C@H](CN(CC1)c2nc3c(N4CCOCC4)nc(C4(C)C=NC(N)=NC4)nc3[n]2CC(F)(F)F)N1C(C)=O Chemical compound C[C@H](CN(CC1)c2nc3c(N4CCOCC4)nc(C4(C)C=NC(N)=NC4)nc3[n]2CC(F)(F)F)N1C(C)=O ZAGIJZYMLIXIPP-HNNQXCQYSA-N 0.000 description 1
- NXYIHKIZZWOBJC-OKILXGFUSA-N C[C@H](CN(C[C@@H]1C)c([n]2CC(F)(F)F)nc3c2nc(-c2cnc(N)nc2)nc3N2CCOCC2)N1C(CO)=O Chemical compound C[C@H](CN(C[C@@H]1C)c([n]2CC(F)(F)F)nc3c2nc(-c2cnc(N)nc2)nc3N2CCOCC2)N1C(CO)=O NXYIHKIZZWOBJC-OKILXGFUSA-N 0.000 description 1
- IFNWESYYDINUHV-OLQVQODUSA-N C[C@H]1N[C@@H](C)CNC1 Chemical compound C[C@H]1N[C@@H](C)CNC1 IFNWESYYDINUHV-OLQVQODUSA-N 0.000 description 1
- RMFWVOLULURGJI-UHFFFAOYSA-N Clc1c2nc[nH]c2nc(Cl)n1 Chemical compound Clc1c2nc[nH]c2nc(Cl)n1 RMFWVOLULURGJI-UHFFFAOYSA-N 0.000 description 1
- CNESPYAXZDEWJM-UHFFFAOYSA-N Clc1c2nc[n](CC3COCC3)c2nc(Cl)n1 Chemical compound Clc1c2nc[n](CC3COCC3)c2nc(Cl)n1 CNESPYAXZDEWJM-UHFFFAOYSA-N 0.000 description 1
- WESLHLBTGYQEFE-UHFFFAOYSA-N Clc1nc(N2CCOCC2)c2nc[n](CC3CC3)c2n1 Chemical compound Clc1nc(N2CCOCC2)c2nc[n](CC3CC3)c2n1 WESLHLBTGYQEFE-UHFFFAOYSA-N 0.000 description 1
- RDSQFMJRHHTJMJ-UHFFFAOYSA-N Clc1nc(N2CCOCC2)c2nc[n](CC3COCC3)c2n1 Chemical compound Clc1nc(N2CCOCC2)c2nc[n](CC3COCC3)c2n1 RDSQFMJRHHTJMJ-UHFFFAOYSA-N 0.000 description 1
- JOXALYLEIHVMFX-UHFFFAOYSA-N FC(C[n]1c2nc(Cl)nc(N3CCOCC3)c2nc1)(F)F Chemical compound FC(C[n]1c2nc(Cl)nc(N3CCOCC3)c2nc1)(F)F JOXALYLEIHVMFX-UHFFFAOYSA-N 0.000 description 1
- QUFRNCFCTULNFP-UHFFFAOYSA-N Nc(nc1)ncc1-c(nc1[n]2CC(F)(F)F)nc(N3CCOCC3)c1nc2N(CC1)CCN1S=O Chemical compound Nc(nc1)ncc1-c(nc1[n]2CC(F)(F)F)nc(N3CCOCC3)c1nc2N(CC1)CCN1S=O QUFRNCFCTULNFP-UHFFFAOYSA-N 0.000 description 1
- UWFQDZIBAQLYIZ-UHFFFAOYSA-N O=C(CN1Cc2ccccc2)NC2(CC2)C1=O Chemical compound O=C(CN1Cc2ccccc2)NC2(CC2)C1=O UWFQDZIBAQLYIZ-UHFFFAOYSA-N 0.000 description 1
- UQMBQFLVIMSAGV-UHFFFAOYSA-N OC(C(F)(F)F)N(CCNC1)C11C=C1 Chemical compound OC(C(F)(F)F)N(CCNC1)C11C=C1 UQMBQFLVIMSAGV-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
- C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
-
- 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
- A61P35/00—Antineoplastic agents
-
- 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
-
- 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
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2008-264797 | 2008-10-14 | ||
| JP2008264797 | 2008-10-14 | ||
| JP2009121690 | 2009-05-20 | ||
| JP2009-121690 | 2009-05-20 | ||
| PCT/JP2009/067738 WO2010044401A1 (ja) | 2008-10-14 | 2009-10-13 | モルホリノプリン誘導体 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN102245607A CN102245607A (zh) | 2011-11-16 |
| CN102245607B true CN102245607B (zh) | 2014-07-02 |
Family
ID=42106564
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN200980151585.4A Expired - Fee Related CN102245607B (zh) | 2008-10-14 | 2009-10-13 | 吗啉代嘌呤衍生物 |
Country Status (21)
| Country | Link |
|---|---|
| US (2) | US8097622B2 (enExample) |
| EP (1) | EP2336132B1 (enExample) |
| JP (1) | JP5090423B2 (enExample) |
| KR (1) | KR101614976B1 (enExample) |
| CN (1) | CN102245607B (enExample) |
| AU (1) | AU2009304789B2 (enExample) |
| BR (1) | BRPI0920199A2 (enExample) |
| CA (1) | CA2740471C (enExample) |
| CO (1) | CO6362009A2 (enExample) |
| DK (1) | DK2336132T3 (enExample) |
| ES (1) | ES2452541T3 (enExample) |
| IL (1) | IL212278A (enExample) |
| MX (1) | MX2011003490A (enExample) |
| MY (1) | MY156456A (enExample) |
| NZ (1) | NZ592761A (enExample) |
| PL (1) | PL2336132T3 (enExample) |
| PT (1) | PT2336132E (enExample) |
| RU (1) | RU2490269C2 (enExample) |
| TW (1) | TWI378933B (enExample) |
| WO (1) | WO2010044401A1 (enExample) |
| ZA (1) | ZA201102449B (enExample) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011521968A (ja) * | 2008-05-30 | 2011-07-28 | ジェネンテック, インコーポレイテッド | プリンpi3k阻害剤化合物および使用方法 |
| TWI378933B (en) * | 2008-10-14 | 2012-12-11 | Daiichi Sankyo Co Ltd | Morpholinopurine derivatives |
| BR112012011188A2 (pt) * | 2009-11-12 | 2021-06-29 | F.Hoffmann - La Roche Ag | ''composto,composição farmacêutica e uso de um composto" |
| CN102260263A (zh) * | 2010-05-26 | 2011-11-30 | 四川大学 | 一类二苯胺基嘌呤衍生物及制备方法和医药用途 |
| EP2593455B1 (en) | 2010-07-14 | 2015-03-18 | F.Hoffmann-La Roche Ag | Purine compounds selective for i3 p110 delta, and methods of use |
| SG10201510347QA (en) | 2010-12-16 | 2016-01-28 | Hoffmann La Roche | Tricyclic pi3k inhibitor compounds and methods of use |
| US9334271B2 (en) | 2011-10-28 | 2016-05-10 | Novarits Ag | Purine derivatives and their use in the treatment of disease |
| CN103012284A (zh) * | 2012-12-26 | 2013-04-03 | 无锡捷化医药科技有限公司 | 一种2-氨基-5-溴嘧啶类化合物的制备方法 |
| WO2014185368A1 (ja) * | 2013-05-13 | 2014-11-20 | 第一三共株式会社 | 5-{8-[(3r)-4-アセチル-3-メチルピペラジン-1-イル]-6-モルホリン-4-イル-9-(2,2,2-トリフルオロエチル)-9h-プリン-2-イル}ピリミジン-2-アミン、およびその薬理上許容される塩の新規な結晶、およびその製造方法 |
| WO2014185367A1 (ja) * | 2013-05-13 | 2014-11-20 | 第一三共株式会社 | モルホリノプリン誘導体の製造方法 |
| US9993460B2 (en) | 2013-07-26 | 2018-06-12 | Race Oncology Ltd. | Compositions to improve the therapeutic benefit of bisantrene and analogs and derivatives thereof |
| KR102369925B1 (ko) * | 2013-10-04 | 2022-03-03 | 우니베르시태트 바젤 | 구조적으로 제한된 PI3K 및 mTOR 억제제 |
| MY185268A (en) | 2015-03-30 | 2021-04-30 | Daiichi Sankyo Co Ltd | Pyrazole derivative useful as pi3k inhibitor |
| US10765681B2 (en) | 2016-02-05 | 2020-09-08 | Academia Sinica | Purine compounds possessing anticancer activity |
| WO2017156350A1 (en) | 2016-03-09 | 2017-09-14 | K-Gen, Inc. | Methods of cancer treatment |
| US11208442B2 (en) | 2016-12-02 | 2021-12-28 | Daiichi Sankyo Company, Limited | Endo-beta-N-acetylglucosaminidase |
| EP3360865A1 (en) | 2017-02-13 | 2018-08-15 | F.I.S.- Fabbrica Italiana Sintetici S.p.A. | Process for the preparation of cyclopropyldiketopiperazines, and of a key intermediate of ds-5272 |
| TWI837231B (zh) | 2018-11-29 | 2024-04-01 | 日商第一三共股份有限公司 | 含有ezh1/2雙重抑制劑之醫藥組合及其用途 |
| CN113368114B (zh) * | 2020-03-10 | 2022-04-22 | 四川大学 | 一种吗啉嘧啶类化合物的抗肿瘤应用 |
| JP2024511996A (ja) * | 2021-03-17 | 2024-03-18 | タンゴ セラピューティクス, インコーポレイテッド | 抗がん剤としてのプリン誘導体 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005117909A2 (en) * | 2004-04-23 | 2005-12-15 | Exelixis, Inc. | Kinase modulators and methods of use |
Family Cites Families (76)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB864145A (en) * | 1959-06-02 | 1961-03-29 | Thomae Gmbh Dr K | Novel purines and a process for their manufacture |
| US6608053B2 (en) | 2000-04-27 | 2003-08-19 | Yamanouchi Pharmaceutical Co., Ltd. | Fused heteroaryl derivatives |
| JP3810017B2 (ja) | 2000-04-27 | 2006-08-16 | アステラス製薬株式会社 | 縮合ヘテロアリール誘導体 |
| ATE503743T1 (de) | 2000-04-27 | 2011-04-15 | Astellas Pharma Inc | Kondensierte heteroarylderivate |
| WO2002088112A1 (en) | 2001-04-27 | 2002-11-07 | Zenyaku Kogyo Kabushiki Kaisha | Heterocyclic compound and antitumor agent containing the same as active ingredient |
| AU2003284142A1 (en) | 2002-10-15 | 2004-05-04 | Synta Pharmaceuticals Corp | Aromatic bicyclic heterocyles to modulate 1L-12 production |
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