CN103097340B - 治疗活性组合物及其使用方法 - Google Patents
治疗活性组合物及其使用方法 Download PDFInfo
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- CN103097340B CN103097340B CN201180043254.6A CN201180043254A CN103097340B CN 103097340 B CN103097340 B CN 103097340B CN 201180043254 A CN201180043254 A CN 201180043254A CN 103097340 B CN103097340 B CN 103097340B
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- ylmethyl
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- 0 C*(C)(C*=CCC=CC(C)=C)CC(*(C*)(C(C(*(C1(C)C(*)(C(*2)(C22O)O)O)C1(*)C2(C(F)(F)F)O)=O)c1c(C)cccc1)c1cc(C)ccc1)=O Chemical compound C*(C)(C*=CCC=CC(C)=C)CC(*(C*)(C(C(*(C1(C)C(*)(C(*2)(C22O)O)O)C1(*)C2(C(F)(F)F)O)=O)c1c(C)cccc1)c1cc(C)ccc1)=O 0.000 description 9
- JBTRYFAMXNXGIK-QXMQTRMZSA-N C/C=C\CC(C(NC1CCCCC1)=O)N(C(CN[S](/C(/C=C\C)=C/C)(=O)#[O])=O)c1cc(F)ccc1 Chemical compound C/C=C\CC(C(NC1CCCCC1)=O)N(C(CN[S](/C(/C=C\C)=C/C)(=O)#[O])=O)c1cc(F)ccc1 JBTRYFAMXNXGIK-QXMQTRMZSA-N 0.000 description 1
- GGJSIETUFHTBFJ-UHFFFAOYSA-N C=CCC(COCC(O)O)N=C Chemical compound C=CCC(COCC(O)O)N=C GGJSIETUFHTBFJ-UHFFFAOYSA-N 0.000 description 1
- HNKPKJDHMBRJTL-WSXWNZDHSA-N CC(C)(C)OC(N1C(CC(N([C@H](C(NC2CCCCC2)=O)C2=C(C)C=CCC=C2)c2cccc(F)c2)=O)CCC1)=O Chemical compound CC(C)(C)OC(N1C(CC(N([C@H](C(NC2CCCCC2)=O)C2=C(C)C=CCC=C2)c2cccc(F)c2)=O)CCC1)=O HNKPKJDHMBRJTL-WSXWNZDHSA-N 0.000 description 1
- KPNSBXRBWXIALH-UHFFFAOYSA-N CC(C=CCC1)=C1C(C(NC1CCCC1)=O)N(C(CNS(c1ccccc1)(=O)=O)=O)c1cccc(F)c1 Chemical compound CC(C=CCC1)=C1C(C(NC1CCCC1)=O)N(C(CNS(c1ccccc1)(=O)=O)=O)c1cccc(F)c1 KPNSBXRBWXIALH-UHFFFAOYSA-N 0.000 description 1
- BNNILZHHFQJFBW-ZLIOJVPDSA-N CC/C(/C)=C(\C(C(NC1C[C@H](C)CCC1)=[Cs])N(C(Cc1c[s]cc1)=O)c1cccc(F)c1)/C=C\C Chemical compound CC/C(/C)=C(\C(C(NC1C[C@H](C)CCC1)=[Cs])N(C(Cc1c[s]cc1)=O)c1cccc(F)c1)/C=C\C BNNILZHHFQJFBW-ZLIOJVPDSA-N 0.000 description 1
- HKZANDOAYKDWAV-BFKYOTBNSA-N CC/C=C\C(\C(C(NC1CCCCC1)=O)N(C(Cc1ccc[s]1)=O)c1cccc(F)c1)=C(/C)\C(F)(F)F Chemical compound CC/C=C\C(\C(C(NC1CCCCC1)=O)N(C(Cc1ccc[s]1)=O)c1cccc(F)c1)=C(/C)\C(F)(F)F HKZANDOAYKDWAV-BFKYOTBNSA-N 0.000 description 1
- JSXUUFRWYBGXIS-ZZDWDYFCSA-N CC1C([C@@H](C(NC2CCCCC2)O)N(CC(CC(CCC2)N2C(OC(C)(C)C)=O)=O)C2=CC(F)=CCC2)=CC=CC1 Chemical compound CC1C([C@@H](C(NC2CCCCC2)O)N(CC(CC(CCC2)N2C(OC(C)(C)C)=O)=O)C2=CC(F)=CCC2)=CC=CC1 JSXUUFRWYBGXIS-ZZDWDYFCSA-N 0.000 description 1
- NYOBZRVKUVEBDT-CHPPSVKKSA-N CC1C=CC=CC1(C)[C@@H](C(NC1CCCCC1)=O)N(CC([C@H](COCC1)N1C(OC(C)(C)C)=O)=O)C(C=CC1)=CC1F Chemical compound CC1C=CC=CC1(C)[C@@H](C(NC1CCCCC1)=O)N(CC([C@H](COCC1)N1C(OC(C)(C)C)=O)=O)C(C=CC1)=CC1F NYOBZRVKUVEBDT-CHPPSVKKSA-N 0.000 description 1
- AOLUGHINKUVPOS-QELHXWDYSA-N CCC(CCCN(Cc1ccccc1)C(CN(C(C[n]1c(C)ncc1)O)/C(/C)=C/C(/F)=C\C)O)(F)F Chemical compound CCC(CCCN(Cc1ccccc1)C(CN(C(C[n]1c(C)ncc1)O)/C(/C)=C/C(/F)=C\C)O)(F)F AOLUGHINKUVPOS-QELHXWDYSA-N 0.000 description 1
- LKEXLFWSJKUTAB-UHFFFAOYSA-N Cc1ccccc1C(C(NC1CCCCC1)=O)N(C(CNC1CCC1)=O)c1cccc(F)c1 Chemical compound Cc1ccccc1C(C(NC1CCCCC1)=O)N(C(CNC1CCC1)=O)c1cccc(F)c1 LKEXLFWSJKUTAB-UHFFFAOYSA-N 0.000 description 1
- VYEJOIMOSZRZSM-UHFFFAOYSA-N Cc1ccccc1C(C(NC1CCCCC1)=O)N(C(CNCc1cnccc1)=O)c1cccc(F)c1 Chemical compound Cc1ccccc1C(C(NC1CCCCC1)=O)N(C(CNCc1cnccc1)=O)c1cccc(F)c1 VYEJOIMOSZRZSM-UHFFFAOYSA-N 0.000 description 1
- RWPKVXZWLYSAKD-UHFFFAOYSA-N Cc1ccccc1C(C(NC1CCCCC1)=O)N(C(CNc(cc1)ccc1F)=O)c1cccc(F)c1 Chemical compound Cc1ccccc1C(C(NC1CCCCC1)=O)N(C(CNc(cc1)ccc1F)=O)c1cccc(F)c1 RWPKVXZWLYSAKD-UHFFFAOYSA-N 0.000 description 1
- PQAFEOISXXEZFN-UHFFFAOYSA-N Cc1ccccc1C(C(NC1CCCCC1)=O)N(C(C[n]1nccc1)=O)c1cccc(F)c1 Chemical compound Cc1ccccc1C(C(NC1CCCCC1)=O)N(C(C[n]1nccc1)=O)c1cccc(F)c1 PQAFEOISXXEZFN-UHFFFAOYSA-N 0.000 description 1
- OBJPRNXSWPRFMF-UHFFFAOYSA-N Cc1ccccc1C(C(NC1CCCCC1)=O)N(CC(Cc1ccc[s]1)=O)c1cc(Cl)c(C)cc1 Chemical compound Cc1ccccc1C(C(NC1CCCCC1)=O)N(CC(Cc1ccc[s]1)=O)c1cc(Cl)c(C)cc1 OBJPRNXSWPRFMF-UHFFFAOYSA-N 0.000 description 1
- OIFLJXRCLBIJJG-BBTNWVSFSA-N Cc1ccccc1C(C(NC1CCCCC1)O)N(C(CNc(cc1)ccc1/C(/N=C)=N/O)O)c1cccc(F)c1 Chemical compound Cc1ccccc1C(C(NC1CCCCC1)O)N(C(CNc(cc1)ccc1/C(/N=C)=N/O)O)c1cccc(F)c1 OIFLJXRCLBIJJG-BBTNWVSFSA-N 0.000 description 1
- AUXUDAWWLWCWBM-UHFFFAOYSA-N Cc1ccccc1C(CNC1CCCCC1)N(C(Cc1ccc[s]1)=O)c(cccc1)c1F Chemical compound Cc1ccccc1C(CNC1CCCCC1)N(C(Cc1ccc[s]1)=O)c(cccc1)c1F AUXUDAWWLWCWBM-UHFFFAOYSA-N 0.000 description 1
- ASQKJJKIJIZAEA-RPBOFIJWSA-N Cc1ccccc1[C@@H](C(NC1CCCCC1)=[O-])N(C([C@@H](CCC1)N1C(OC)=O)=O)c1cccc(F)c1 Chemical compound Cc1ccccc1[C@@H](C(NC1CCCCC1)=[O-])N(C([C@@H](CCC1)N1C(OC)=O)=O)c1cccc(F)c1 ASQKJJKIJIZAEA-RPBOFIJWSA-N 0.000 description 1
- FNYGWXSATBUBER-UHFFFAOYSA-N Cc1ncc[n]1CC(N(C(C(NC1CCCCC1)=O)c1ccccc1C)c1cccc(F)c1)=O Chemical compound Cc1ncc[n]1CC(N(C(C(NC1CCCCC1)=O)c1ccccc1C)c1cccc(F)c1)=O FNYGWXSATBUBER-UHFFFAOYSA-N 0.000 description 1
- RJRBEHKQETZKLX-VQQFLKOLSA-N Cc1ncc[n]1CC(N([C@@H](C(NC1CCCCC1)O)c1ccccc1C)C(CC/C=C/c1c[n](C)nc1)=C)O Chemical compound Cc1ncc[n]1CC(N([C@@H](C(NC1CCCCC1)O)c1ccccc1C)C(CC/C=C/c1c[n](C)nc1)=C)O RJRBEHKQETZKLX-VQQFLKOLSA-N 0.000 description 1
- SWGXDLRCJNEEGZ-UHFFFAOYSA-N O=CNC1CCCCC1 Chemical compound O=CNC1CCCCC1 SWGXDLRCJNEEGZ-UHFFFAOYSA-N 0.000 description 1
- VWSWWWOLLQGVGN-UHFFFAOYSA-N OC(CNc1ncccc1)=O Chemical compound OC(CNc1ncccc1)=O VWSWWWOLLQGVGN-UHFFFAOYSA-N 0.000 description 1
- PYLFZGBAIQDVIT-LURJTMIESA-N OC(CO[C@@H]1COCCC1)=O Chemical compound OC(CO[C@@H]1COCCC1)=O PYLFZGBAIQDVIT-LURJTMIESA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06008—Dipeptides with the first amino acid being neutral
- C07K5/06078—Dipeptides with the first amino acid being neutral and aromatic or cycloaliphatic
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- 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
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- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/22—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/22—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by carboxyl groups
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- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/40—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings
- C07C271/42—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/44—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
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- C07C271/06—Esters of carbamic acids
- C07C271/40—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings
- C07C271/58—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring
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- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/03—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C311/06—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms to acyclic carbon atoms of hydrocarbon radicals substituted by carboxyl groups
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- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/12—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing rings
- C07C311/13—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing rings the carbon skeleton containing six-membered aromatic rings
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- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
- C07C311/16—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
- C07C311/19—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom to an acyclic carbon atom of a hydrocarbon radical substituted by carboxyl groups
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- C07C317/00—Sulfones; Sulfoxides
- C07C317/26—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C317/32—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C317/34—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having sulfone or sulfoxide groups and amino groups bound to carbon atoms of six-membered aromatic rings being part of the same non-condensed ring or of a condensed ring system containing that ring
- C07C317/36—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having sulfone or sulfoxide groups and amino groups bound to carbon atoms of six-membered aromatic rings being part of the same non-condensed ring or of a condensed ring system containing that ring with the nitrogen atoms of the amino groups bound to hydrogen atoms or to carbon atoms
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- C07C335/00—Thioureas, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C335/30—Isothioureas
- C07C335/32—Isothioureas having sulfur atoms of isothiourea groups bound to acyclic carbon atoms
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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 to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
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- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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 to ring carbon atoms
- C07D207/16—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
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- C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
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- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
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- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/14—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
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- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/18—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D209/26—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with an acyl radical attached to the ring nitrogen atom
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/42—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/10—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with radicals containing only carbon and hydrogen atoms attached to ring carbon atoms
- C07D211/14—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with radicals containing only carbon and hydrogen atoms attached to ring carbon atoms with hydrocarbon or substituted hydrocarbon radicals attached to the ring nitrogen atom
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- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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| US20120121515A1 (en) | 2009-03-13 | 2012-05-17 | Lenny Dang | Methods and compositions for cell-proliferation-related disorders |
| TWI598337B (zh) | 2009-06-29 | 2017-09-11 | 阿吉歐斯製藥公司 | 治療化合物及組成物 |
| WO2011050210A1 (en) | 2009-10-21 | 2011-04-28 | Agios Pharmaceuticals, Inc. | Methods and compositions for cell-proliferation-related disorders |
| EP2525790B1 (en) | 2009-10-21 | 2020-05-27 | Agios Pharmaceuticals, Inc. | Methods and compositions for cell-proliferation-related disorders |
| SMT202400081T1 (it) | 2011-05-03 | 2024-03-13 | Agios Pharmaceuticals Inc | Attivatori della piruvato chinasi per uso in terapia |
| CN102827073A (zh) | 2011-06-17 | 2012-12-19 | 安吉奥斯医药品有限公司 | 治疗活性组合物和它们的使用方法 |
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| BR112014007310A2 (pt) | 2011-09-27 | 2017-04-04 | Novartis Ag | 3-pirimidin-4-il-oxazolidin-2-onas como inibidores de idh mutante |
| MX2014006072A (es) * | 2011-11-25 | 2014-08-08 | Bayer Ip Gmbh | Derivados de 2-yodo-imidazol. |
| US9877962B2 (en) | 2011-12-30 | 2018-01-30 | Marc Henry Pitty | Piperazinyl derivatives for the treatment of cancer |
| FR2985256B1 (fr) * | 2011-12-30 | 2016-03-04 | Pitty Marc Henry | Derives piperazinyles pour le traitement de cancers |
| PE20142098A1 (es) | 2012-01-06 | 2015-01-08 | Agios Pharmaceuticals Inc | Compuestos terapeuticamente activos y sus metodos de uso |
| US9474779B2 (en) | 2012-01-19 | 2016-10-25 | Agios Pharmaceuticals, Inc. | Therapeutically active compositions and their methods of use |
| US20150087600A1 (en) * | 2012-01-19 | 2015-03-26 | Agios Pharmaceuticals, Inc | Therapeutically active compounds and their methods of use |
| UY34632A (es) | 2012-02-24 | 2013-05-31 | Novartis Ag | Compuestos de oxazolidin- 2- ona y usos de los mismos |
| US20150038541A1 (en) * | 2012-03-19 | 2015-02-05 | Aposignal Bioscience Llc | Composition and methods for cell modulation |
| EP2906212A4 (en) | 2012-10-15 | 2016-06-08 | Agios Pharmaceuticals Inc | THERAPEUTIC COMPOUNDS AND COMPOSITIONS |
| US9296733B2 (en) | 2012-11-12 | 2016-03-29 | Novartis Ag | Oxazolidin-2-one-pyrimidine derivative and use thereof for the treatment of conditions, diseases and disorders dependent upon PI3 kinases |
| TWI637951B (zh) | 2013-02-15 | 2018-10-11 | 英商葛蘭素史克智慧財產發展有限公司 | 作為激酶抑制劑之雜環醯胺類 |
| GEP201606600B (en) | 2013-02-22 | 2017-01-10 | Pfizer | Pyrrolo [2, 3 -d]pyrimidine derivatives as inhibitors of janus- related kinases (jak) |
| JP6387360B2 (ja) | 2013-03-14 | 2018-09-05 | ノバルティス アーゲー | 変異idhの阻害薬としての3−ピリミジン−4−イル−オキサゾリジン−2−オン |
| WO2014184272A2 (en) * | 2013-05-14 | 2014-11-20 | Medizinische Hochschule Hannover | Means and methods for treating cancer |
| AU2014287122B9 (en) | 2013-07-11 | 2018-11-01 | Les Laboratoires Servier | N,6-bis(aryl or heteroaryl)-1,3,5-triazine-2,4-diamine compounds as IDH2 mutants inhibitors for the treatment of cancer |
| CN105593215B (zh) | 2013-07-11 | 2019-01-15 | 安吉奥斯医药品有限公司 | 用于治疗癌症的作为idh2突变体抑制剂的2,4-或4,6-二氨基嘧啶化合物 |
| WO2015003360A2 (en) | 2013-07-11 | 2015-01-15 | Agios Pharmaceuticals, Inc. | Therapeutically active compounds and their methods of use |
| WO2015003355A2 (en) | 2013-07-11 | 2015-01-15 | Agios Pharmaceuticals, Inc. | Therapeutically active compounds and their methods of use |
| WO2015010297A1 (en) * | 2013-07-25 | 2015-01-29 | Agios Pharmaceuticals, Inc. | Therapeutically active compounds and their methods of use |
| KR101861869B1 (ko) * | 2013-09-10 | 2018-05-28 | 경희대학교 산학협력단 | 신규한 비스-아미드 유도체 및 이의 용도 |
| NZ723859A (en) | 2014-03-14 | 2023-01-27 | Servier Lab | Pharmaceutical compositions of therapeutically active compounds and their uses |
| WO2016024185A1 (en) | 2014-08-12 | 2016-02-18 | Pfizer Inc. | Pyrrolo[2,3-d]pyrimidine derivatives useful for inhibiting janus kinase |
| BR112017006425B8 (pt) * | 2014-10-01 | 2023-05-16 | Daiichi Sankyo Co Ltd | Compostos derivados de isoxazol, seus usos, inibidores de isocitrato desidrogenase 1 mutante e da produção de d-2 hidroxiglutamato, agente antitumoral e composição farmacêutica compreendendo os mesmos |
| JP6672288B2 (ja) * | 2014-10-23 | 2020-03-25 | バイエル・ファルマ・アクティエンゲゼルシャフト | 腫瘍の治療のためのmidh1阻害剤としての1−シクロヘキシル−2−フェニルアミノベンゾイミダゾール |
| AU2015369712B2 (en) | 2014-12-22 | 2020-05-07 | The United States Of America As Represented By The Secretary, Department Of Health And Human Services | Mutant IDH1 inhibitors useful for treating cancer |
| CA2989111C (en) | 2015-06-11 | 2023-10-03 | Agios Pharmaceuticals, Inc. | Methods of using pyruvate kinase activators |
| JP6824954B2 (ja) * | 2015-07-16 | 2021-02-03 | ドイチェス クレープスフォルシュングスツェントルム シュティフトゥング デス エッフェントリッヒェン レヒツ | mIDH1阻害剤としての5−ヒドロキシアルキルベンズイミダゾール |
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| CA2805669A1 (en) | 2012-01-19 |
| EP2593425B1 (en) | 2018-10-17 |
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| BR112013001122A2 (pt) | 2017-07-11 |
| WO2012009678A8 (en) | 2012-03-29 |
| US20160264621A1 (en) | 2016-09-15 |
| AU2011278998B2 (en) | 2016-06-09 |
| BR112013001122B1 (pt) | 2021-06-08 |
| CN103097340A (zh) | 2013-05-08 |
| JP2013536168A (ja) | 2013-09-19 |
| US20130184222A1 (en) | 2013-07-18 |
| ES2704862T3 (es) | 2019-03-20 |
| WO2012009678A1 (en) | 2012-01-19 |
| JP6081354B2 (ja) | 2017-02-15 |
| EP2593425A1 (en) | 2013-05-22 |
| JP2017039725A (ja) | 2017-02-23 |
| CA2805669C (en) | 2018-08-21 |
| AU2011278998A1 (en) | 2013-01-31 |
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