JP2019518770A5 - - Google Patents
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- JP2019518770A5 JP2019518770A5 JP2018567108A JP2018567108A JP2019518770A5 JP 2019518770 A5 JP2019518770 A5 JP 2019518770A5 JP 2018567108 A JP2018567108 A JP 2018567108A JP 2018567108 A JP2018567108 A JP 2018567108A JP 2019518770 A5 JP2019518770 A5 JP 2019518770A5
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- Prior art keywords
- compound
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- atropisomer
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- 150000001875 compounds Chemical class 0.000 claims 27
- 150000003839 salts Chemical class 0.000 claims 16
- 239000008194 pharmaceutical composition Substances 0.000 claims 9
- 125000001424 substituent group Chemical group 0.000 claims 5
- 230000035772 mutation Effects 0.000 claims 4
- 101001042041 Bos taurus Isocitrate dehydrogenase [NAD] subunit beta, mitochondrial Proteins 0.000 claims 3
- 101000960234 Homo sapiens Isocitrate dehydrogenase [NADP] cytoplasmic Proteins 0.000 claims 3
- 102100039905 Isocitrate dehydrogenase [NADP] cytoplasmic Human genes 0.000 claims 3
- 208000031261 Acute myeloid leukaemia Diseases 0.000 claims 2
- 208000033776 Myeloid Acute Leukemia Diseases 0.000 claims 2
- 206010028980 Neoplasm Diseases 0.000 claims 2
- 125000003277 amino group Chemical group 0.000 claims 2
- -1 and independently Inorganic materials 0.000 claims 2
- 201000011510 cancer Diseases 0.000 claims 2
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 150000002367 halogens Chemical class 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims 1
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 1
- KPGXRSRHYNQIFN-UHFFFAOYSA-N 2-oxoglutaric acid Chemical compound OC(=O)CCC(=O)C(O)=O KPGXRSRHYNQIFN-UHFFFAOYSA-N 0.000 claims 1
- 206010003571 Astrocytoma Diseases 0.000 claims 1
- 208000005243 Chondrosarcoma Diseases 0.000 claims 1
- 206010009944 Colon cancer Diseases 0.000 claims 1
- 208000000088 Enchondromatosis Diseases 0.000 claims 1
- 108090000790 Enzymes Proteins 0.000 claims 1
- 102000004190 Enzymes Human genes 0.000 claims 1
- 208000032612 Glial tumor Diseases 0.000 claims 1
- 206010018338 Glioma Diseases 0.000 claims 1
- 208000033833 Myelomonocytic Chronic Leukemia Diseases 0.000 claims 1
- 208000015914 Non-Hodgkin lymphomas Diseases 0.000 claims 1
- 208000026616 Ollier disease Diseases 0.000 claims 1
- 206010039491 Sarcoma Diseases 0.000 claims 1
- XJLXINKUBYWONI-DQQFMEOOSA-N [[(2r,3r,4r,5r)-5-(6-aminopurin-9-yl)-3-hydroxy-4-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl] [(2s,3r,4s,5s)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphate Chemical compound NC(=O)C1=CC=C[N+]([C@@H]2[C@H]([C@@H](O)[C@H](COP([O-])(=O)OP(O)(=O)OC[C@@H]3[C@H]([C@@H](OP(O)(O)=O)[C@@H](O3)N3C4=NC=NC(N)=C4N=C3)O)O2)O)=C1 XJLXINKUBYWONI-DQQFMEOOSA-N 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 208000006990 cholangiocarcinoma Diseases 0.000 claims 1
- 201000010902 chronic myelomonocytic leukemia Diseases 0.000 claims 1
- 208000029742 colonic neoplasm Diseases 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 230000001419 dependent effect Effects 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 208000005017 glioblastoma Diseases 0.000 claims 1
- 201000001441 melanoma Diseases 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 201000006462 myelodysplastic/myeloproliferative neoplasm Diseases 0.000 claims 1
- 229930027945 nicotinamide-adenine dinucleotide Natural products 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 208000002154 non-small cell lung carcinoma Diseases 0.000 claims 1
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical compound OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 claims 1
- 102200069708 rs121913499 Human genes 0.000 claims 1
- 102200069690 rs121913500 Human genes 0.000 claims 1
- 208000011580 syndromic disease Diseases 0.000 claims 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1
- 229940124597 therapeutic agent Drugs 0.000 claims 1
- 208000029729 tumor suppressor gene on chromosome 11 Diseases 0.000 claims 1
- 0 CC(C)=CC(N(C(C(c1nc(C2=CCC(*)=C*=C2)c[s]1)=C1)=O)C2=CC=C*(*)C=C2)=C1C(*)=O Chemical compound CC(C)=CC(N(C(C(c1nc(C2=CCC(*)=C*=C2)c[s]1)=C1)=O)C2=CC=C*(*)C=C2)=C1C(*)=O 0.000 description 1
- MYZVYKPBACOLTA-UHFFFAOYSA-N CCOc(c(N(C(C=C(C)C)=C(C=C1c2nc(-c(cc3)ccc3C#N)c[s]2)C(N2CC(CC3)NC3C2)=O)C1=O)c1)ccc1Cl Chemical compound CCOc(c(N(C(C=C(C)C)=C(C=C1c2nc(-c(cc3)ccc3C#N)c[s]2)C(N2CC(CC3)NC3C2)=O)C1=O)c1)ccc1Cl MYZVYKPBACOLTA-UHFFFAOYSA-N 0.000 description 1
- DVEMFVYDDZQXDK-UHFFFAOYSA-N CCOc(cc1N(C(C=C(C)C)=C(C(N2CC(CC3)NC3C2)O)C=C2c3nc(-c(cc4)ccc4Cl)c[s]3)C2=O)ccc1Cl Chemical compound CCOc(cc1N(C(C=C(C)C)=C(C(N2CC(CC3)NC3C2)O)C=C2c3nc(-c(cc4)ccc4Cl)c[s]3)C2=O)ccc1Cl DVEMFVYDDZQXDK-UHFFFAOYSA-N 0.000 description 1
- ZADFWCZFXVOCTO-UHFFFAOYSA-N CCc(c(N(C(CC(C)C)=C(C=C1c2nc(-c3ccc(C(F)(F)F)nc3)c[s]2)C(N2CCNCC2)=O)C1=O)c1)ccc1Cl Chemical compound CCc(c(N(C(CC(C)C)=C(C=C1c2nc(-c3ccc(C(F)(F)F)nc3)c[s]2)C(N2CCNCC2)=O)C1=O)c1)ccc1Cl ZADFWCZFXVOCTO-UHFFFAOYSA-N 0.000 description 1
Claims (19)
- 式IIの化合物、
又はその薬学的に許容される塩
(式中、CyNは、窒素原子を介して結合される環式のアミン基であり、独立して、ハロゲン、C1−C2アルキル及びC1−C2アルコキシから選択される1つ以上の置換基によって、任意に置換されてもよく、
Xは、C又はNであり、
R1及びR2は、各々独立して、ハロゲン、CN、CF3、CHF2、CH2F、C1−C10アルキル基、C1−C10アルコキシ基、ジ(C1−C5アルキル)アミノ基であり、
M及びnは、各々独立して、1、2又は3であり、及び
は、単結合又は二重結合を表し、
但し、3−(4−(4−クロロフェニル)チアゾール−2−イル)−1−(2−エチル−5−メトキシフェニル)−6−(2−メチルプロプ−1−エン−1−イル)−5−(ピペラジン−1−カルボニル)ピリジン−2(1H)−オンアトロプ異性体のラセミ混合物は除く)。 - 前記アトロプ異性体が、実質的に対応するエナンチオマを含まない、請求項2から5のいずれか一項に記載のアトロプ異性体化合物又は塩。
- mが1であり、R2が4−置換基である、または、
R 2 が4−Cl、4−CF 3 、4−CHF 2 、4−CH 3 Oもしくは4−CNである、または、
XがCであり、R 2 が4−Cl、4−CF 3 、4−CHF 2 もしくは4−NCである、または、
XがNであり、R 2 が4−CF 3 、4−CHF 2 もしくは4−CH 3 Oである、請求項1から6のいずれか一項に記載の化合物又は塩。 - nが2であり、R1が2,2−C2H5であるか、又は2−C2H5、5−CH3Oであるか、又は2−C2H5、5−Clであるか、又は2−Cl、5−(CH3)2Nであるか、又は2−C2H5O、5−C2H5Oであるか、又は2−C2H5O、5−Clであるか、又は3−C2H5O、5−NCであるか、又はジ−2,6−C2H5である、請求項1から7のいずれか一項に記載の化合物又は塩。
- 請求項1〜13のいずれか1つの化合物又は塩を、薬学的に許容される担体と共に含む、医薬組成物。
- IDH1変異の存在を特徴とする癌の治療のための医薬組成物であって、該IDH1変異が、患者においてNADPH依存的なα−ケトグルタレートのR(−)−2−ヒドロキシグルタレートへの還元を触媒する酵素の新規な能力をもたらし、前記医薬組成物が請求項1から13のいずれか一項に記載の化合物又は塩を含む、医薬組成物。
- 前記IDH1変異が、IDH1 R132H又はIDH1 R132C変異である、請求項15に記載の医薬組成物。
- 前記癌が、膠腫(グリア芽細胞腫)、急性骨髄性白血病、急性骨髄性白血病、脊髄形成異常/骨髄増殖性の新生物、肉腫、慢性骨髄単球性白血病、非ホジキンリンパ腫、星細胞腫、黒色腫、非小細胞性肺癌、胆管癌、軟骨肉腫又は大腸癌から選択される、請求項15に記載の医薬組成物。
- Ollier病またはMafucci症候群の治療のための医薬組成物であって、前記医薬組成物が請求項1から13のいずれか一項に記載の化合物又はその塩を含む、医薬組成物。
- 1つ以上の更なる治療剤を更に含む、請求項15から18のいずれか一項に記載の医薬組成物。
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662353298P | 2016-06-22 | 2016-06-22 | |
| US62/353,298 | 2016-06-22 | ||
| PCT/US2017/038549 WO2017223202A1 (en) | 2016-06-22 | 2017-06-21 | Thiazole derivatives useful as mutant idh1 inhibitors for treating cancer |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2019518770A JP2019518770A (ja) | 2019-07-04 |
| JP2019518770A5 true JP2019518770A5 (ja) | 2020-07-30 |
| JP6987798B2 JP6987798B2 (ja) | 2022-01-05 |
Family
ID=59276859
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018567108A Active JP6987798B2 (ja) | 2016-06-22 | 2017-06-21 | 癌の治療に変異体idh1阻害剤として有用なチアゾール誘導体 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US10836759B2 (ja) |
| EP (1) | EP3475276B1 (ja) |
| JP (1) | JP6987798B2 (ja) |
| CN (1) | CN109641887B (ja) |
| AU (1) | AU2017281088B2 (ja) |
| CA (1) | CA3028999A1 (ja) |
| ES (1) | ES2880347T3 (ja) |
| WO (1) | WO2017223202A1 (ja) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2961793C (en) | 2014-09-19 | 2021-03-16 | Forma Therapeutics, Inc. | Quinolinone pyrimidines compositions as mutant-isocitrate dehydrogenase inhibitors |
| PT3194376T (pt) | 2014-09-19 | 2019-02-04 | Forma Therapeutics Inc | Derivados da piridin-2(1h)-ona-quinolinona como inibidores da isocitrato-desidrogenase mutante |
| EP3194375B1 (en) | 2014-09-19 | 2018-11-21 | Forma Therapeutics, Inc. | Phenyl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors |
| ES2706525T3 (es) | 2014-09-19 | 2019-03-29 | Forma Therapeutics Inc | Derivados de piridinilquinolinona como inhibidores de isocitrato deshidrogenasa mutante |
| US10294206B2 (en) | 2015-04-21 | 2019-05-21 | Forma Tm2, Inc. | Fused-bicyclic aryl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors |
| US10407419B2 (en) | 2015-04-21 | 2019-09-10 | Forma Therapeutics, Inc. | Quinolinone five-membered heterocyclic compounds as mutant-isocitrate dehydrogenase inhibitors |
| WO2019222551A1 (en) | 2018-05-16 | 2019-11-21 | Forma Therapeutics, Inc. | Solid forms of ((s)-5-((1-(6-chloro-2-oxo-1,2-dihydroquinolin-3-yl)ethyl)amino)-1-methyl-6-oxo-1,6-dihydropyridine-2-carbonitrile |
| WO2019222553A1 (en) | 2018-05-16 | 2019-11-21 | Forma Therapeutics, Inc. | Inhibiting mutant idh-1 |
| US11311527B2 (en) | 2018-05-16 | 2022-04-26 | Forma Therapeutics, Inc. | Inhibiting mutant isocitrate dehydrogenase 1 (mIDH-1) |
| US11013733B2 (en) | 2018-05-16 | 2021-05-25 | Forma Therapeutics, Inc. | Inhibiting mutant isocitrate dehydrogenase 1 (mlDH-1) |
| US11013734B2 (en) | 2018-05-16 | 2021-05-25 | Forma Therapeutics, Inc. | Treating patients harboring an isocitrate dehydrogenase-1 (IDH-1) mutation |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108524505A (zh) * | 2009-03-13 | 2018-09-14 | 安吉奥斯医药品有限公司 | 用于细胞增殖相关病症的方法和组合物 |
| WO2010111432A1 (en) | 2009-03-24 | 2010-09-30 | Calistoga Pharmaceuticals Inc. | Atropisomers of2-purinyl-3-tolyl-quinazolinone derivatives and methods of use |
| WO2014141153A1 (en) * | 2013-03-14 | 2014-09-18 | Novartis Ag | 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh |
| CA2971872C (en) * | 2014-12-22 | 2023-10-10 | The United States Of America As Represented By The Secretary, Department Of Health And Human Services | Mutant idh1 inhibitors useful for treating cancer |
-
2017
- 2017-06-21 US US16/312,206 patent/US10836759B2/en active Active
- 2017-06-21 JP JP2018567108A patent/JP6987798B2/ja active Active
- 2017-06-21 CN CN201780051410.0A patent/CN109641887B/zh active Active
- 2017-06-21 CA CA3028999A patent/CA3028999A1/en active Pending
- 2017-06-21 AU AU2017281088A patent/AU2017281088B2/en active Active
- 2017-06-21 EP EP17735296.0A patent/EP3475276B1/en active Active
- 2017-06-21 ES ES17735296T patent/ES2880347T3/es active Active
- 2017-06-21 WO PCT/US2017/038549 patent/WO2017223202A1/en not_active Ceased
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