JP2010533160A5 - - Google Patents
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- Publication number
- JP2010533160A5 JP2010533160A5 JP2010515602A JP2010515602A JP2010533160A5 JP 2010533160 A5 JP2010533160 A5 JP 2010533160A5 JP 2010515602 A JP2010515602 A JP 2010515602A JP 2010515602 A JP2010515602 A JP 2010515602A JP 2010533160 A5 JP2010533160 A5 JP 2010533160A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- amino
- phenyl
- alkoxy
- methylmorpholin
- 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.)
- Granted
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- 125000000217 alkyl group Chemical group 0.000 claims 66
- 125000003545 alkoxy group Chemical group 0.000 claims 24
- -1 nitro, hydroxy Chemical group 0.000 claims 23
- 150000003839 salts Chemical class 0.000 claims 19
- 150000001875 compounds Chemical class 0.000 claims 17
- 125000001475 halogen functional group Chemical group 0.000 claims 16
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 11
- 125000004093 cyano group Chemical group *C#N 0.000 claims 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 8
- 125000000623 heterocyclic group Chemical group 0.000 claims 7
- 229910052739 hydrogen Inorganic materials 0.000 claims 7
- 239000001257 hydrogen Substances 0.000 claims 7
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 6
- 125000004452 carbocyclyl group Chemical group 0.000 claims 6
- 125000001424 substituent group Chemical group 0.000 claims 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 5
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
- 241001465754 Metazoa Species 0.000 claims 4
- 125000005236 alkanoylamino group Chemical group 0.000 claims 4
- 125000005115 alkyl carbamoyl group Chemical group 0.000 claims 4
- 125000005153 alkyl sulfamoyl group Chemical group 0.000 claims 4
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims 4
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 4
- 125000001589 carboacyl group Chemical group 0.000 claims 4
- 239000003814 drug Substances 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 claims 3
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 3
- 230000009422 growth inhibiting effect Effects 0.000 claims 3
- 150000002431 hydrogen Chemical class 0.000 claims 3
- 238000004519 manufacturing process Methods 0.000 claims 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 3
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 2
- 125000006620 amino-(C1-C6) alkyl group Chemical group 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 2
- 201000010099 disease Diseases 0.000 claims 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 2
- 230000002062 proliferating effect Effects 0.000 claims 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 125000004076 pyridyl group Chemical group 0.000 claims 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims 2
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 claims 1
- ONMGSCFILROWDA-AWEZNQCLSA-N 1-(2-hydroxyethyl)-3-[4-[4-(2-hydroxypropan-2-yl)-6-[(3s)-3-methylmorpholin-4-yl]pyrimidin-2-yl]phenyl]thiourea Chemical compound C[C@H]1COCCN1C1=CC(C(C)(C)O)=NC(C=2C=CC(NC(=S)NCCO)=CC=2)=N1 ONMGSCFILROWDA-AWEZNQCLSA-N 0.000 claims 1
- IKTUOUAOGSCKIL-HNNXBMFYSA-N 1-(2-hydroxyethyl)-3-[4-[4-[(3s)-3-methylmorpholin-4-yl]-6-(2-methylsulfonylpropan-2-yl)pyrimidin-2-yl]phenyl]thiourea Chemical compound C[C@H]1COCCN1C1=CC(C(C)(C)S(C)(=O)=O)=NC(C=2C=CC(NC(=S)NCCO)=CC=2)=N1 IKTUOUAOGSCKIL-HNNXBMFYSA-N 0.000 claims 1
- VNUWIQPKVVNUPA-KRWDZBQOSA-N 1-(2-hydroxyethyl)-3-[4-[4-[2-(3-hydroxypropylsulfonyl)propan-2-yl]-6-[(3s)-3-methylmorpholin-4-yl]pyrimidin-2-yl]phenyl]thiourea Chemical compound C[C@H]1COCCN1C1=CC(C(C)(C)S(=O)(=O)CCCO)=NC(C=2C=CC(NC(=S)NCCO)=CC=2)=N1 VNUWIQPKVVNUPA-KRWDZBQOSA-N 0.000 claims 1
- LKGWPTKBPOHHNP-INIZCTEOSA-N 1-(4-fluorophenyl)-3-[4-[4-[(3s)-3-methylmorpholin-4-yl]-6-(methylsulfonylmethyl)pyrimidin-2-yl]phenyl]thiourea Chemical compound C[C@H]1COCCN1C1=CC(CS(C)(=O)=O)=NC(C=2C=CC(NC(=S)NC=3C=CC(F)=CC=3)=CC=2)=N1 LKGWPTKBPOHHNP-INIZCTEOSA-N 0.000 claims 1
- MKMSWAKWCOVXBQ-KRWDZBQOSA-N 1-(4-methoxyphenyl)-3-[4-[4-[(3s)-3-methylmorpholin-4-yl]-6-(methylsulfonylmethyl)pyrimidin-2-yl]phenyl]thiourea Chemical compound C1=CC(OC)=CC=C1NC(=S)NC1=CC=C(C=2N=C(C=C(CS(C)(=O)=O)N=2)N2[C@H](COCC2)C)C=C1 MKMSWAKWCOVXBQ-KRWDZBQOSA-N 0.000 claims 1
- NOPFSYBMFRVQFJ-KRWDZBQOSA-N 1-[2-(dimethylamino)ethyl]-3-[4-[4-[(3s)-3-methylmorpholin-4-yl]-6-(2-methylsulfonylpropan-2-yl)pyrimidin-2-yl]phenyl]thiourea Chemical compound C[C@H]1COCCN1C1=CC(C(C)(C)S(C)(=O)=O)=NC(C=2C=CC(NC(=S)NCCN(C)C)=CC=2)=N1 NOPFSYBMFRVQFJ-KRWDZBQOSA-N 0.000 claims 1
- MOOWHRZFBWMOQV-ZDUSSCGKSA-N 1-[4-[4-(2-hydroxypropan-2-yl)-6-[(3s)-3-methylmorpholin-4-yl]pyrimidin-2-yl]phenyl]-3-methylthiourea Chemical compound C1=CC(NC(=S)NC)=CC=C1C1=NC(N2[C@H](COCC2)C)=CC(C(C)(C)O)=N1 MOOWHRZFBWMOQV-ZDUSSCGKSA-N 0.000 claims 1
- TYSOCOFJTDKJAJ-KRWDZBQOSA-N 1-[4-[4-[(3s)-3-methylmorpholin-4-yl]-6-(methylsulfonylmethyl)pyrimidin-2-yl]phenyl]-3-phenylthiourea Chemical compound C[C@H]1COCCN1C1=CC(CS(C)(=O)=O)=NC(C=2C=CC(NC(=S)NC=3C=CC=CC=3)=CC=2)=N1 TYSOCOFJTDKJAJ-KRWDZBQOSA-N 0.000 claims 1
- RCWJOZAZRYSSTL-INIZCTEOSA-N 1-[4-[4-[2-(3-hydroxypropylsulfonyl)propan-2-yl]-6-[(3s)-3-methylmorpholin-4-yl]pyrimidin-2-yl]phenyl]-3-methylthiourea Chemical compound C1=CC(NC(=S)NC)=CC=C1C1=NC(N2[C@H](COCC2)C)=CC(C(C)(C)S(=O)(=O)CCCO)=N1 RCWJOZAZRYSSTL-INIZCTEOSA-N 0.000 claims 1
- REUGYWKSPAKXGW-IBGZPJMESA-N 1-[4-[4-[2-(benzenesulfonyl)propan-2-yl]-6-[(3s)-3-methylmorpholin-4-yl]pyrimidin-2-yl]phenyl]-3-(2-hydroxyethyl)thiourea Chemical compound C[C@H]1COCCN1C1=CC(C(C)(C)S(=O)(=O)C=2C=CC=CC=2)=NC(C=2C=CC(NC(=S)NCCO)=CC=2)=N1 REUGYWKSPAKXGW-IBGZPJMESA-N 0.000 claims 1
- IGGDGODNOYOSNH-IBGZPJMESA-N 1-[4-[4-[2-(benzenesulfonyl)propan-2-yl]-6-[(3s)-3-methylmorpholin-4-yl]pyrimidin-2-yl]phenyl]-3-cyclopropylthiourea Chemical compound C[C@H]1COCCN1C1=CC(C(C)(C)S(=O)(=O)C=2C=CC=CC=2)=NC(C=2C=CC(NC(=S)NC3CC3)=CC=2)=N1 IGGDGODNOYOSNH-IBGZPJMESA-N 0.000 claims 1
- CYTXIRTUVUNJSO-IBGZPJMESA-N 1-[4-[4-[2-(benzenesulfonyl)propan-2-yl]-6-[(3s)-3-methylmorpholin-4-yl]pyrimidin-2-yl]phenyl]-3-ethylthiourea Chemical compound C1=CC(NC(=S)NCC)=CC=C1C1=NC(N2[C@H](COCC2)C)=CC(C(C)(C)S(=O)(=O)C=2C=CC=CC=2)=N1 CYTXIRTUVUNJSO-IBGZPJMESA-N 0.000 claims 1
- RGGDCCFIVJIXBD-SFHVURJKSA-N 1-[4-[4-[2-(benzenesulfonyl)propan-2-yl]-6-[(3s)-3-methylmorpholin-4-yl]pyrimidin-2-yl]phenyl]-3-methylthiourea Chemical compound C1=CC(NC(=S)NC)=CC=C1C1=NC(N2[C@H](COCC2)C)=CC(C(C)(C)S(=O)(=O)C=2C=CC=CC=2)=N1 RGGDCCFIVJIXBD-SFHVURJKSA-N 0.000 claims 1
- WICIPQUDAGHUEP-AWEZNQCLSA-N 1-cyclopropyl-3-[4-[4-(2-hydroxypropan-2-yl)-6-[(3s)-3-methylmorpholin-4-yl]pyrimidin-2-yl]phenyl]thiourea Chemical compound C[C@H]1COCCN1C1=CC(C(C)(C)O)=NC(C=2C=CC(NC(=S)NC3CC3)=CC=2)=N1 WICIPQUDAGHUEP-AWEZNQCLSA-N 0.000 claims 1
- SEHCYWVKUYGYLL-HNNXBMFYSA-N 1-cyclopropyl-3-[4-[4-[(3s)-3-methylmorpholin-4-yl]-6-(2-methylsulfonylpropan-2-yl)pyrimidin-2-yl]phenyl]thiourea Chemical compound C[C@H]1COCCN1C1=CC(C(C)(C)S(C)(=O)=O)=NC(C=2C=CC(NC(=S)NC3CC3)=CC=2)=N1 SEHCYWVKUYGYLL-HNNXBMFYSA-N 0.000 claims 1
- OCIFAFLXUOYULU-AWEZNQCLSA-N 1-cyclopropyl-3-[4-[4-[(3s)-3-methylmorpholin-4-yl]-6-(methylsulfonylmethyl)pyrimidin-2-yl]phenyl]thiourea Chemical compound C[C@H]1COCCN1C1=CC(CS(C)(=O)=O)=NC(C=2C=CC(NC(=S)NC3CC3)=CC=2)=N1 OCIFAFLXUOYULU-AWEZNQCLSA-N 0.000 claims 1
- FYQQFHSCAQTNDC-KRWDZBQOSA-N 1-cyclopropyl-3-[4-[4-[2-(3-hydroxypropylsulfonyl)propan-2-yl]-6-[(3s)-3-methylmorpholin-4-yl]pyrimidin-2-yl]phenyl]thiourea Chemical compound C[C@H]1COCCN1C1=CC(C(C)(C)S(=O)(=O)CCCO)=NC(C=2C=CC(NC(=S)NC3CC3)=CC=2)=N1 FYQQFHSCAQTNDC-KRWDZBQOSA-N 0.000 claims 1
- GASFVWYGHNKDQU-AWEZNQCLSA-N 1-ethyl-3-[4-[4-(2-hydroxypropan-2-yl)-6-[(3s)-3-methylmorpholin-4-yl]pyrimidin-2-yl]phenyl]thiourea Chemical compound C1=CC(NC(=S)NCC)=CC=C1C1=NC(N2[C@H](COCC2)C)=CC(C(C)(C)O)=N1 GASFVWYGHNKDQU-AWEZNQCLSA-N 0.000 claims 1
- DUTPGWMWELBIPF-HNNXBMFYSA-N 1-ethyl-3-[4-[4-[(3s)-3-methylmorpholin-4-yl]-6-(2-methylsulfonylpropan-2-yl)pyrimidin-2-yl]phenyl]thiourea Chemical compound C1=CC(NC(=S)NCC)=CC=C1C1=NC(N2[C@H](COCC2)C)=CC(C(C)(C)S(C)(=O)=O)=N1 DUTPGWMWELBIPF-HNNXBMFYSA-N 0.000 claims 1
- UPODFXWDGFKDKN-AWEZNQCLSA-N 1-ethyl-3-[4-[4-[(3s)-3-methylmorpholin-4-yl]-6-(methylsulfonylmethyl)pyrimidin-2-yl]phenyl]thiourea Chemical compound C1=CC(NC(=S)NCC)=CC=C1C1=NC(CS(C)(=O)=O)=CC(N2[C@H](COCC2)C)=N1 UPODFXWDGFKDKN-AWEZNQCLSA-N 0.000 claims 1
- ALGLLMWKQYVQDC-KRWDZBQOSA-N 1-ethyl-3-[4-[4-[2-(3-hydroxypropylsulfonyl)propan-2-yl]-6-[(3s)-3-methylmorpholin-4-yl]pyrimidin-2-yl]phenyl]thiourea Chemical compound C1=CC(NC(=S)NCC)=CC=C1C1=NC(N2[C@H](COCC2)C)=CC(C(C)(C)S(=O)(=O)CCCO)=N1 ALGLLMWKQYVQDC-KRWDZBQOSA-N 0.000 claims 1
- JDWWSSNJYPSCJU-AWEZNQCLSA-N 1-methyl-3-[4-[4-[(3s)-3-methylmorpholin-4-yl]-6-(2-methylsulfonylpropan-2-yl)pyrimidin-2-yl]phenyl]thiourea Chemical compound C1=CC(NC(=S)NC)=CC=C1C1=NC(N2[C@H](COCC2)C)=CC(C(C)(C)S(C)(=O)=O)=N1 JDWWSSNJYPSCJU-AWEZNQCLSA-N 0.000 claims 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims 1
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 1
- 208000024172 Cardiovascular disease Diseases 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 201000011510 cancer Diseases 0.000 claims 1
- 125000002837 carbocyclic group Chemical group 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 208000026278 immune system disease Diseases 0.000 claims 1
- 208000027866 inflammatory disease Diseases 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000000842 isoxazolyl group Chemical group 0.000 claims 1
- 125000005647 linker group Chemical group 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 230000000414 obstructive effect Effects 0.000 claims 1
- 125000004043 oxo group Chemical group O=* 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 125000003226 pyrazolyl group Chemical group 0.000 claims 1
- 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 claims 1
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 1
- 208000023504 respiratory system disease Diseases 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 125000005302 thiazolylmethyl group Chemical group [H]C1=C([H])N=C(S1)C([H])([H])* 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- 125000005301 thienylmethyl group Chemical group [H]C1=C([H])C([H])=C(S1)C([H])([H])* 0.000 claims 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US94853907P | 2007-07-09 | 2007-07-09 | |
| US60/948,539 | 2007-07-09 | ||
| PCT/GB2008/050548 WO2009007750A1 (en) | 2007-07-09 | 2008-07-08 | Morpholino pyrimidine derivatives used in diseases linked to mtor kinase and/or pi3k |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010533160A JP2010533160A (ja) | 2010-10-21 |
| JP2010533160A5 true JP2010533160A5 (enExample) | 2012-08-16 |
| JP5508260B2 JP5508260B2 (ja) | 2014-05-28 |
Family
ID=39791229
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010515602A Expired - Fee Related JP5508260B2 (ja) | 2007-07-09 | 2008-07-08 | ｍＴＯＲキナーゼおよび／またはＰ１３Ｋに関連する病気に用いられるモルホリノピリミジン誘導体 |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US8138183B2 (enExample) |
| EP (1) | EP2176238B1 (enExample) |
| JP (1) | JP5508260B2 (enExample) |
| KR (1) | KR20100042280A (enExample) |
| CN (1) | CN101809002B (enExample) |
| AR (1) | AR070079A1 (enExample) |
| AT (1) | ATE554075T1 (enExample) |
| AU (1) | AU2008273891B2 (enExample) |
| BR (1) | BRPI0814688A2 (enExample) |
| CA (1) | CA2692720A1 (enExample) |
| CL (1) | CL2008003940A1 (enExample) |
| CO (1) | CO6251364A2 (enExample) |
| CR (1) | CR11200A (enExample) |
| DO (1) | DOP2010000012A (enExample) |
| EA (1) | EA018708B1 (enExample) |
| EC (1) | ECSP109935A (enExample) |
| ES (1) | ES2385692T3 (enExample) |
| NI (1) | NI201000002A (enExample) |
| PE (1) | PE20100138A1 (enExample) |
| WO (1) | WO2009007750A1 (enExample) |
| ZA (1) | ZA200909224B (enExample) |
Families Citing this family (53)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20100031639A (ko) * | 2007-07-09 | 2010-03-23 | 아스트라제네카 아베 | 증식성 질환의 치료용 삼중 치환된 피리미딘 유도체 |
| EP2307400B1 (en) | 2008-05-30 | 2014-04-23 | Amgen, Inc | Inhibitors of pi3 kinase |
| WO2010103094A1 (en) | 2009-03-13 | 2010-09-16 | Cellzome Limited | PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS |
| UY32582A (es) | 2009-04-28 | 2010-11-30 | Amgen Inc | Inhibidores de fosfoinositida 3 cinasa y/u objetivo mamífero |
| WO2011001115A1 (fr) | 2009-07-02 | 2011-01-06 | Sanofi-Aventis | Nouveaux derives de 6-morpholin-4-yl-pyrimidin-4- ( 3h ) -one, leur preparation pharmaceutique comme inhibiteurs de phos phorylat i on d ' akt ( pkb ) |
| ES2464125T3 (es) | 2009-07-02 | 2014-05-30 | Sanofi | Nuevos derivados de (6-oxo-1,6-dihidro-pirimidin-2-il)-amida, su preparación y su utilización farmacéutica como inhibidores de fosforilación de AKT |
| EP2493460A4 (en) | 2009-10-30 | 2013-04-24 | Ariad Pharma Inc | METHOD AND COMPOSITIONS FOR THE TREATMENT OF CANCER |
| EP2531194B1 (en) | 2010-02-03 | 2018-04-18 | Signal Pharmaceuticals, LLC | Identification of lkb1 mutation as a predictive biomarker for sensitivity to tor kinase inhibitors |
| WO2011107585A1 (en) | 2010-03-04 | 2011-09-09 | Cellzome Limited | Morpholino substituted urea derivatives as mtor inhibitors |
| JO2998B1 (ar) | 2010-06-04 | 2016-09-05 | Amgen Inc | مشتقات بيبيريدينون كمثبطات mdm2 لعلاج السرطان |
| HRP20170119T1 (hr) | 2010-12-28 | 2017-03-24 | Sanofi | Novi derivati pirimidina, njihovo pripremanje, te njihova farmaceutska uporaba kao inhibitora akt (pkb) fosforilacije |
| WO2012136622A1 (en) | 2011-04-04 | 2012-10-11 | Cellzome Limited | Dihydropyrrolo pyrimidine derivatives as mtor inhibitors |
| JP6491879B2 (ja) | 2011-04-29 | 2019-03-27 | セレクタ バイオサイエンシーズ インコーポレーテッドＳｅｌｅｃｔａ Ｂｉｏｓｃｉｅｎｃｅｓ，Ｉｎｃ． | 制御性ｂ細胞を誘導するための寛容原性合成ナノキャリア |
| CN105039520A (zh) | 2011-08-03 | 2015-11-11 | 西格诺药品有限公司 | 作为lkb1状态的预测性生物标志物的基因表达谱的鉴定 |
| ES2609606T3 (es) | 2011-09-21 | 2017-04-21 | Cellzome Limited | Derivados de urea y carbamato de 2-morfolino-1,3,5-triazina como inhibidores de mTOR para el tratamiento de enfermedades inmunológicas o proliferativas |
| MX352672B (es) | 2011-09-27 | 2017-12-04 | Amgen Inc | Compuestos heterocíclicos como inhibidores de mdm2 para el tratamiento del cáncer. |
| ES2592219T3 (es) | 2011-10-07 | 2016-11-28 | Cellzome Limited | Derivados de {(4-(4-morfolino-dihidrotieno[3,4-d]pirimidin-2-il)aril}urea o carbamato como inhibidores de mTOR |
| JP6148729B2 (ja) | 2012-07-04 | 2017-06-14 | エフ．ホフマン−ラ ロシュ アーゲーＦ． Ｈｏｆｆｍａｎｎ−Ｌａ Ｒｏｃｈｅ Ａｋｔｉｅｎｇｅｓｅｌｌｓｃｈａｆｔ | 共有結合している抗原−抗体結合体 |
| FR2994572B1 (fr) * | 2012-08-17 | 2015-04-17 | Centre Nat Rech Scient | Pyrido[3,2-d]pyrimidines trisubstituees, leurs procedes de preparation et leurs utilisation en therapeutique |
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2008
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- 2008-07-08 US US12/668,056 patent/US8138183B2/en not_active Expired - Fee Related
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- 2008-07-08 JP JP2010515602A patent/JP5508260B2/ja not_active Expired - Fee Related
- 2008-07-08 CA CA 2692720 patent/CA2692720A1/en not_active Abandoned
- 2008-07-08 ES ES08776183T patent/ES2385692T3/es active Active
- 2008-07-08 KR KR1020107002942A patent/KR20100042280A/ko not_active Ceased
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- 2008-07-08 AT AT08776183T patent/ATE554075T1/de active
- 2008-07-08 WO PCT/GB2008/050548 patent/WO2009007750A1/en not_active Ceased
- 2008-12-19 PE PE2008002157A patent/PE20100138A1/es not_active Application Discontinuation
- 2008-12-30 CL CL2008003940A patent/CL2008003940A1/es unknown
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