TWI628165B - 具治療作用之組成物及其使用方法 - Google Patents
具治療作用之組成物及其使用方法 Download PDFInfo
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- TWI628165B TWI628165B TW101121790A TW101121790A TWI628165B TW I628165 B TWI628165 B TW I628165B TW 101121790 A TW101121790 A TW 101121790A TW 101121790 A TW101121790 A TW 101121790A TW I628165 B TWI628165 B TW I628165B
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- Prior art keywords
- alkyl
- alkenyl
- aryl
- compound
- hydroxyl
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- 238000000034 method Methods 0.000 title abstract description 157
- 239000000203 mixture Substances 0.000 title description 177
- 150000001875 compounds Chemical class 0.000 claims abstract description 414
- 206010028980 Neoplasm Diseases 0.000 claims abstract description 62
- 201000011510 cancer Diseases 0.000 claims abstract description 49
- 238000011282 treatment Methods 0.000 claims abstract description 48
- -1 C 1 -C 6 alkyl Chemical group 0.000 claims description 456
- 125000003118 aryl group Chemical group 0.000 claims description 86
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 64
- 229910052739 hydrogen Inorganic materials 0.000 claims description 62
- 239000001257 hydrogen Substances 0.000 claims description 62
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 56
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 50
- 125000000623 heterocyclic group Chemical group 0.000 claims description 47
- 125000001424 substituent group Chemical group 0.000 claims description 42
- 150000003839 salts Chemical class 0.000 claims description 41
- 238000006467 substitution reaction Methods 0.000 claims description 41
- 229910052757 nitrogen Inorganic materials 0.000 claims description 37
- 229920006395 saturated elastomer Polymers 0.000 claims description 35
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 34
- 108010075869 Isocitrate Dehydrogenase Proteins 0.000 claims description 33
- 102000012011 Isocitrate Dehydrogenase Human genes 0.000 claims description 33
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 32
- 125000005842 heteroatom Chemical group 0.000 claims description 32
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 27
- 125000000217 alkyl group Chemical group 0.000 claims description 26
- 230000035772 mutation Effects 0.000 claims description 25
- 125000001072 heteroaryl group Chemical group 0.000 claims description 24
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 22
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 22
- 229910052760 oxygen Inorganic materials 0.000 claims description 22
- 239000000126 substance Substances 0.000 claims description 22
- 239000000460 chlorine Substances 0.000 claims description 21
- 102200069690 rs121913500 Human genes 0.000 claims description 21
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 20
- 229930027945 nicotinamide-adenine dinucleotide Natural products 0.000 claims description 20
- 239000001301 oxygen Substances 0.000 claims description 20
- 239000008194 pharmaceutical composition Substances 0.000 claims description 20
- HWXBTNAVRSUOJR-UHFFFAOYSA-N 2-hydroxyglutaric acid Chemical compound OC(=O)C(O)CCC(O)=O HWXBTNAVRSUOJR-UHFFFAOYSA-N 0.000 claims description 19
- 150000004820 halides Chemical class 0.000 claims description 19
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 18
- 125000004122 cyclic group Chemical group 0.000 claims description 18
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 18
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 17
- 239000003814 drug Substances 0.000 claims description 17
- 239000011737 fluorine Substances 0.000 claims description 17
- 229910052731 fluorine Inorganic materials 0.000 claims description 17
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 17
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 17
- 229910052717 sulfur Inorganic materials 0.000 claims description 17
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 16
- 125000003342 alkenyl group Chemical group 0.000 claims description 16
- 229910052799 carbon Inorganic materials 0.000 claims description 16
- 125000004076 pyridyl group Chemical group 0.000 claims description 16
- 150000002431 hydrogen Chemical class 0.000 claims description 15
- 239000011593 sulfur Substances 0.000 claims description 14
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- 229940124597 therapeutic agent Drugs 0.000 claims description 13
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 11
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- 239000002253 acid Substances 0.000 claims description 11
- 125000002619 bicyclic group Chemical group 0.000 claims description 11
- 229910052736 halogen Inorganic materials 0.000 claims description 11
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- 125000001041 indolyl group Chemical group 0.000 claims description 11
- 125000002950 monocyclic group Chemical group 0.000 claims description 11
- 230000001419 dependent effect Effects 0.000 claims description 10
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 10
- 125000002541 furyl group Chemical group 0.000 claims description 10
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- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 7
- 125000000304 alkynyl group Chemical group 0.000 claims description 7
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 7
- 229910052794 bromium Inorganic materials 0.000 claims description 7
- 125000002837 carbocyclic group Chemical group 0.000 claims description 7
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 7
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 6
- 201000003793 Myelodysplastic syndrome Diseases 0.000 claims description 6
- 125000002947 alkylene group Chemical group 0.000 claims description 6
- 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 description 6
- 229940079593 drug Drugs 0.000 claims description 6
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 claims description 6
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 5
- 208000032612 Glial tumor Diseases 0.000 claims description 5
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- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 5
- 125000005054 dihydropyrrolyl group Chemical group [H]C1=C([H])C([H])([H])C([H])([H])N1* 0.000 claims description 5
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- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
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- ODBLHEXUDAPZAU-UHFFFAOYSA-N isocitric acid Chemical compound OC(=O)C(O)C(C(O)=O)CC(O)=O ODBLHEXUDAPZAU-UHFFFAOYSA-N 0.000 claims description 4
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 claims description 4
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- 238000004519 manufacturing process Methods 0.000 claims description 4
- 201000001441 melanoma Diseases 0.000 claims description 4
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 4
- 125000004593 naphthyridinyl group Chemical group N1=C(C=CC2=CC=CN=C12)* 0.000 claims description 4
- 208000002154 non-small cell lung carcinoma Diseases 0.000 claims description 4
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 claims description 4
- 230000009467 reduction Effects 0.000 claims description 4
- 125000004853 tetrahydropyridinyl group Chemical group N1(CCCC=C1)* 0.000 claims description 4
- 208000029729 tumor suppressor gene on chromosome 11 Diseases 0.000 claims description 4
- YJRMHIKEMDTYDR-UHFFFAOYSA-N 2-methylisoquinolin-1-one Chemical compound C1=CC=C2C(=O)N(C)C=CC2=C1 YJRMHIKEMDTYDR-UHFFFAOYSA-N 0.000 claims description 3
- 239000004215 Carbon black (E152) Substances 0.000 claims description 3
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- 201000007224 Myeloproliferative neoplasm Diseases 0.000 claims description 3
- OOXWYYGXTJLWHA-UHFFFAOYSA-N cyclopropene Chemical compound C1C=C1 OOXWYYGXTJLWHA-UHFFFAOYSA-N 0.000 claims description 3
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- 230000036961 partial effect Effects 0.000 claims description 3
- 125000006085 pyrrolopyridyl group Chemical group 0.000 claims description 3
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- RSQUAQMIGSMNNE-UHFFFAOYSA-N 1-methyl-3h-indol-2-one Chemical compound C1=CC=C2N(C)C(=O)CC2=C1 RSQUAQMIGSMNNE-UHFFFAOYSA-N 0.000 claims description 2
- AAILEWXSEQLMNI-UHFFFAOYSA-N 1h-pyridazin-6-one Chemical group OC1=CC=CN=N1 AAILEWXSEQLMNI-UHFFFAOYSA-N 0.000 claims description 2
- FECNVDHIIJYRIA-UHFFFAOYSA-N 2-oxopentanedioic acid Chemical compound OC(=O)CCC(=O)C(O)=O.OC(=O)CCC(=O)C(O)=O FECNVDHIIJYRIA-UHFFFAOYSA-N 0.000 claims description 2
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- JYGFTBXVXVMTGB-UHFFFAOYSA-N indolin-2-one Chemical group C1=CC=C2NC(=O)CC2=C1 JYGFTBXVXVMTGB-UHFFFAOYSA-N 0.000 claims description 2
- FGFUBBNNYLNVLJ-UHFFFAOYSA-N indolone Natural products C1=CC=C2C(=O)C=NC2=C1 FGFUBBNNYLNVLJ-UHFFFAOYSA-N 0.000 claims description 2
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- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 7
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 4
- XJLXINKUBYWONI-NNYOXOHSSA-N NADP zwitterion 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-NNYOXOHSSA-N 0.000 claims 2
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 claims 2
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| WO2015003360A2 (en) | 2013-07-11 | 2015-01-15 | Agios Pharmaceuticals, Inc. | Therapeutically active compounds and their methods of use |
| US9579324B2 (en) | 2013-07-11 | 2017-02-28 | Agios Pharmaceuticals, Inc | Therapeutically active compounds and their methods of use |
| US20150031627A1 (en) | 2013-07-25 | 2015-01-29 | Agios Pharmaceuticals, Inc | Therapeutically active compounds and their methods of use |
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2011
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2012
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- 2012-06-18 JP JP2014515041A patent/JP6152098B2/ja not_active Expired - Fee Related
- 2012-06-18 EP EP12800001.5A patent/EP2721019B1/en active Active
- 2012-06-18 AR ARP120102167A patent/AR086977A1/es unknown
- 2012-06-18 AU AU2012269648A patent/AU2012269648B2/en not_active Ceased
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- 2012-06-18 TW TW101121790A patent/TWI628165B/zh not_active IP Right Cessation
- 2012-06-18 CA CA2839675A patent/CA2839675C/en not_active Expired - Fee Related
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| US20050261268A1 (en) * | 2003-08-06 | 2005-11-24 | Arnost Michael J | Aminotriazole compounds useful as inhibitors of protein kinases |
| US20080132490A1 (en) * | 2006-12-01 | 2008-06-05 | Bergman Jeffrey M | Substituted diazepan orexin receptor antagonists |
| US20090281089A1 (en) * | 2008-04-11 | 2009-11-12 | Genentech, Inc. | Pyridyl inhibitors of hedgehog signalling |
| TW201028381A (en) * | 2008-07-14 | 2010-08-01 | Shionogi & Co | Pyridine derivative having ttk inhibition activity |
| WO2011027249A2 (en) * | 2009-09-01 | 2011-03-10 | Pfizer Inc. | Benzimidazole derivatives |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2012171337A1 (en) | 2012-12-20 |
| US9856279B2 (en) | 2018-01-02 |
| AU2012269648A1 (en) | 2014-01-16 |
| AR086977A1 (es) | 2014-02-05 |
| CN102827073A (zh) | 2012-12-19 |
| EP2721019B1 (en) | 2018-08-08 |
| JP2014519518A (ja) | 2014-08-14 |
| EP2721019A1 (en) | 2014-04-23 |
| CA2839675A1 (en) | 2012-12-20 |
| ES2694160T3 (es) | 2018-12-18 |
| EP2721019A4 (en) | 2014-11-19 |
| CA2839675C (en) | 2019-06-11 |
| MX2013014922A (es) | 2014-02-11 |
| US20160229876A1 (en) | 2016-08-11 |
| JP6152098B2 (ja) | 2017-06-21 |
| AU2012269648B2 (en) | 2017-04-20 |
| US20140213580A1 (en) | 2014-07-31 |
| TW201317215A (zh) | 2013-05-01 |
| MX345928B (es) | 2017-02-23 |
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