DE60008527T2 - Zellproliferation inhibitoren - Google Patents
Zellproliferation inhibitoren Download PDFInfo
- Publication number
- DE60008527T2 DE60008527T2 DE60008527T DE60008527T DE60008527T2 DE 60008527 T2 DE60008527 T2 DE 60008527T2 DE 60008527 T DE60008527 T DE 60008527T DE 60008527 T DE60008527 T DE 60008527T DE 60008527 T2 DE60008527 T2 DE 60008527T2
- Authority
- DE
- Germany
- Prior art keywords
- trimethoxyphenyl
- sulfonamide
- methyl
- indole
- amino
- 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
- 239000003112 inhibitor Substances 0.000 title description 3
- 150000001875 compounds Chemical class 0.000 claims description 92
- -1 pyrrolidinylcarbonyl Chemical group 0.000 claims description 58
- 239000003814 drug Substances 0.000 claims description 15
- 238000011282 treatment Methods 0.000 claims description 15
- 125000000217 alkyl group Chemical group 0.000 claims description 14
- 206010028980 Neoplasm Diseases 0.000 claims description 13
- 150000003839 salts Chemical class 0.000 claims description 12
- 229940079593 drug Drugs 0.000 claims description 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 9
- 125000001072 heteroaryl group Chemical group 0.000 claims description 9
- 239000008194 pharmaceutical composition Substances 0.000 claims description 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 9
- 241000124008 Mammalia Species 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 7
- BMVDRMMNFJEIIW-UHFFFAOYSA-N 2-(dimethylamino)-n-(1-methylindol-5-yl)sulfonyl-n-(3,4,5-trimethoxyphenyl)acetamide Chemical compound COC1=C(OC)C(OC)=CC(N(C(=O)CN(C)C)S(=O)(=O)C=2C=C3C=CN(C)C3=CC=2)=C1 BMVDRMMNFJEIIW-UHFFFAOYSA-N 0.000 claims description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 6
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 6
- 125000001424 substituent group Chemical group 0.000 claims description 6
- AUBAMWWXRXUICN-UHFFFAOYSA-N 1-methyl-5-nitro-n-(3,4,5-trimethoxyphenyl)indole-3-sulfonamide Chemical compound COC1=C(OC)C(OC)=CC(NS(=O)(=O)C=2C3=CC(=CC=C3N(C)C=2)[N+]([O-])=O)=C1 AUBAMWWXRXUICN-UHFFFAOYSA-N 0.000 claims description 5
- AURQVSQMVBPENN-UHFFFAOYSA-N 5-nitro-n-(3,4,5-trimethoxyphenyl)-1h-indole-3-sulfonamide Chemical compound COC1=C(OC)C(OC)=CC(NS(=O)(=O)C=2C3=CC(=CC=C3NC=2)[N+]([O-])=O)=C1 AURQVSQMVBPENN-UHFFFAOYSA-N 0.000 claims description 5
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims description 5
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- 125000003545 alkoxy group Chemical group 0.000 claims description 5
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- PRRBVBOKPBZAKC-IBGZPJMESA-N (2s)-2,6-diamino-n-(1-methylindol-5-yl)sulfonyl-n-(3,4,5-trimethoxyphenyl)hexanamide Chemical compound COC1=C(OC)C(OC)=CC(N(C(=O)[C@@H](N)CCCCN)S(=O)(=O)C=2C=C3C=CN(C)C3=CC=2)=C1 PRRBVBOKPBZAKC-IBGZPJMESA-N 0.000 claims description 4
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- OMBFNEPVUUXTCI-IBGZPJMESA-N (2s)-2-amino-3-(1h-imidazol-5-yl)-n-(1-methylindol-5-yl)sulfonyl-n-(3,4,5-trimethoxyphenyl)propanamide Chemical compound COC1=C(OC)C(OC)=CC(N(C(=O)[C@@H](N)CC=2NC=NC=2)S(=O)(=O)C=2C=C3C=CN(C)C3=CC=2)=C1 OMBFNEPVUUXTCI-IBGZPJMESA-N 0.000 claims description 4
- WZLMDNQJDSKQKM-NRFANRHFSA-N (2s)-2-amino-3-methyl-n-(1-methylindol-5-yl)sulfonyl-n-(3,4,5-trimethoxyphenyl)butanamide Chemical compound COC1=C(OC)C(OC)=CC(N(C(=O)[C@@H](N)C(C)C)S(=O)(=O)C=2C=C3C=CN(C)C3=CC=2)=C1 WZLMDNQJDSKQKM-NRFANRHFSA-N 0.000 claims description 4
- NKZFBALRMNWQKH-QFIPXVFZSA-N (2s)-2-amino-n-(1-methylindol-5-yl)sulfonyl-3-phenyl-n-(3,4,5-trimethoxyphenyl)propanamide Chemical compound COC1=C(OC)C(OC)=CC(N(C(=O)[C@@H](N)CC=2C=CC=CC=2)S(=O)(=O)C=2C=C3C=CN(C)C3=CC=2)=C1 NKZFBALRMNWQKH-QFIPXVFZSA-N 0.000 claims description 4
- CHUBIDOXSOIFBV-UHFFFAOYSA-N 1-methyl-n-(3,4,5-trimethoxyphenyl)indole-5-sulfonamide Chemical compound COC1=C(OC)C(OC)=CC(NS(=O)(=O)C=2C=C3C=CN(C)C3=CC=2)=C1 CHUBIDOXSOIFBV-UHFFFAOYSA-N 0.000 claims description 4
- 125000005809 3,4,5-trimethoxyphenyl group Chemical group [H]C1=C(OC([H])([H])[H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1* 0.000 claims description 4
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- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 4
- 125000001475 halogen functional group Chemical group 0.000 claims description 4
- 125000001041 indolyl group Chemical group 0.000 claims description 4
- 230000002401 inhibitory effect Effects 0.000 claims description 4
- VJSZYJNRPIOHSO-UHFFFAOYSA-N n,1-dimethyl-n-(3,4,5-trimethoxyphenyl)indole-5-sulfonamide Chemical compound COC1=C(OC)C(OC)=CC(N(C)S(=O)(=O)C=2C=C3C=CN(C)C3=CC=2)=C1 VJSZYJNRPIOHSO-UHFFFAOYSA-N 0.000 claims description 4
- KQDZSGNXKNNGLP-UHFFFAOYSA-N n-(1-methylindol-5-yl)sulfonyl-2-(4-methylpiperazin-1-yl)-n-(3,4,5-trimethoxyphenyl)acetamide Chemical compound COC1=C(OC)C(OC)=CC(N(C(=O)CN2CCN(C)CC2)S(=O)(=O)C=2C=C3C=CN(C)C3=CC=2)=C1 KQDZSGNXKNNGLP-UHFFFAOYSA-N 0.000 claims description 4
- NOUUQMYYNFKPKA-UHFFFAOYSA-N n-(1-methylindol-5-yl)sulfonyl-2-morpholin-4-yl-n-(3,4,5-trimethoxyphenyl)acetamide Chemical compound COC1=C(OC)C(OC)=CC(N(C(=O)CN2CCOCC2)S(=O)(=O)C=2C=C3C=CN(C)C3=CC=2)=C1 NOUUQMYYNFKPKA-UHFFFAOYSA-N 0.000 claims description 4
- COGFZDMHBQJXHM-UHFFFAOYSA-N n-(2-fluoroethyl)-1-methyl-n-(3,4,5-trimethoxyphenyl)indole-5-sulfonamide Chemical compound COC1=C(OC)C(OC)=CC(N(CCF)S(=O)(=O)C=2C=C3C=CN(C)C3=CC=2)=C1 COGFZDMHBQJXHM-UHFFFAOYSA-N 0.000 claims description 4
- VUBSTIDRXCFEIV-UHFFFAOYSA-N n-(2-hydroxyethyl)-1-methyl-n-(3,4,5-trimethoxyphenyl)indole-5-sulfonamide Chemical compound COC1=C(OC)C(OC)=CC(N(CCO)S(=O)(=O)C=2C=C3C=CN(C)C3=CC=2)=C1 VUBSTIDRXCFEIV-UHFFFAOYSA-N 0.000 claims description 4
- UQJPHWPYBNEUQQ-UHFFFAOYSA-N n-(3,4,5-trimethoxyphenyl)-1h-indole-5-sulfonamide Chemical compound COC1=C(OC)C(OC)=CC(NS(=O)(=O)C=2C=C3C=CNC3=CC=2)=C1 UQJPHWPYBNEUQQ-UHFFFAOYSA-N 0.000 claims description 4
- XKWWWFKMFACMCG-UHFFFAOYSA-N n-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1h-indole-5-sulfonamide Chemical compound COC1=C(OC)C(OC)=CC(NS(=O)(=O)C=2C=C3CCNC3=CC=2)=C1 XKWWWFKMFACMCG-UHFFFAOYSA-N 0.000 claims description 4
- WRNYJMBZXJYZMO-UHFFFAOYSA-N n-ethyl-1-methyl-n-(3,4,5-trimethoxyphenyl)indole-5-sulfonamide Chemical compound C=1C=C2N(C)C=CC2=CC=1S(=O)(=O)N(CC)C1=CC(OC)=C(OC)C(OC)=C1 WRNYJMBZXJYZMO-UHFFFAOYSA-N 0.000 claims description 4
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- 230000003000 nontoxic effect Effects 0.000 claims description 4
- 238000006116 polymerization reaction Methods 0.000 claims description 4
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- HSXVJLSEYSRVMQ-DEOSSOPVSA-N (2s)-2-amino-n-(1-methylindol-5-yl)sulfonyl-2-phenyl-n-(3,4,5-trimethoxyphenyl)acetamide Chemical compound COC1=C(OC)C(OC)=CC(N(C(=O)[C@@H](N)C=2C=CC=CC=2)S(=O)(=O)C=2C=C3C=CN(C)C3=CC=2)=C1 HSXVJLSEYSRVMQ-DEOSSOPVSA-N 0.000 claims description 3
- SRSOSJJSGLWVTI-UHFFFAOYSA-N 1-ethyl-n-(3,4,5-trimethoxyphenyl)indole-5-sulfonamide Chemical compound C=1C=C2N(CC)C=CC2=CC=1S(=O)(=O)NC1=CC(OC)=C(OC)C(OC)=C1 SRSOSJJSGLWVTI-UHFFFAOYSA-N 0.000 claims description 3
- FXBDPPSSBRRFLS-UHFFFAOYSA-N 1h-indol-5-yl 3,4,5-trimethoxybenzenesulfonate Chemical compound COC1=C(OC)C(OC)=CC(S(=O)(=O)OC=2C=C3C=CNC3=CC=2)=C1 FXBDPPSSBRRFLS-UHFFFAOYSA-N 0.000 claims description 3
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- 125000003387 indolinyl group Chemical group N1(CCC2=CC=CC=C12)* 0.000 claims description 3
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- 125000005270 trialkylamine group Chemical group 0.000 description 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 1
- 125000004044 trifluoroacetyl group Chemical group FC(C(=O)*)(F)F 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
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- ZDPHROOEEOARMN-UHFFFAOYSA-N undecanoic acid Chemical compound CCCCCCCCCCC(O)=O ZDPHROOEEOARMN-UHFFFAOYSA-N 0.000 description 1
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- JXLYSJRDGCGARV-XQKSVPLYSA-N vincaleukoblastine Chemical compound C([C@@H](C[C@]1(C(=O)OC)C=2C(=CC3=C([C@]45[C@H]([C@@]([C@H](OC(C)=O)[C@]6(CC)C=CCN([C@H]56)CC4)(O)C(=O)OC)N3C)C=2)OC)C[C@@](C2)(O)CC)N2CCC2=C1NC1=CC=CC=C21 JXLYSJRDGCGARV-XQKSVPLYSA-N 0.000 description 1
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Classifications
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- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/23—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C323/24—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/29—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton containing six-membered aromatic rings
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/63—Esters of sulfonic acids
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- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/63—Esters of sulfonic acids
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- C07C309/75—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing singly-bound oxygen atoms bound to the carbon skeleton
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- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/63—Esters of sulfonic acids
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- 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
- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
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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
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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
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- C07C311/44—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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- C07C311/45—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups at least one of the singly-bound nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom, e.g. N-acylaminosulfonamides
- C07C311/46—Y being a hydrogen or a carbon atom
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- C07C317/16—Sulfones; Sulfoxides having sulfone or sulfoxide groups and singly-bound oxygen atoms bound to the same carbon skeleton
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- C07C317/44—Sulfones; Sulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton
- C07C317/46—Sulfones; Sulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton the carbon skeleton being further substituted by singly-bound oxygen atoms
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
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- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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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- Chemical & Material Sciences (AREA)
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Indole Compounds (AREA)
- Quinoline Compounds (AREA)
- Pyridine Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
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| US32233999A | 1999-05-28 | 1999-05-28 | |
| US322339 | 1999-05-28 | ||
| PCT/US2000/014742 WO2000073264A1 (en) | 1999-05-28 | 2000-05-26 | Cell proliferation inhibitors |
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| DE60008527D1 DE60008527D1 (de) | 2004-04-01 |
| DE60008527T2 true DE60008527T2 (de) | 2004-12-23 |
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| DE60008527T Expired - Fee Related DE60008527T2 (de) | 1999-05-28 | 2000-05-26 | Zellproliferation inhibitoren |
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| EP1343782B1 (en) * | 2000-12-21 | 2009-05-06 | SmithKline Beecham Corporation | Pyrimidineamines as angiogenesis modulators |
| JP2005516927A (ja) * | 2001-12-13 | 2005-06-09 | アボット・ラボラトリーズ | 癌治療用のキナーゼ阻害剤としての3−(フェニル−アルコキシ)−5−(フェニル)−ピリジン誘導体および関連化合物 |
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| FR2836914B1 (fr) * | 2002-03-11 | 2008-03-14 | Aventis Pharma Sa | Indazoles substitues, compositions les contenant, procede de fabrication et utilisation |
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| US8017781B2 (en) * | 2005-11-15 | 2011-09-13 | Vertex Pharmaceuticals Incorporated | Azaindazoles useful as inhibitors of kinases |
| WO2008061247A2 (en) * | 2006-11-16 | 2008-05-22 | The Regent Of The University Of California | Benzenesulfonanilide compound inhibitors of urea transporters |
| WO2008114831A1 (ja) * | 2007-03-20 | 2008-09-25 | National University Corporation Okayama University | スルホンアミド基を有する抗菌剤 |
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| US20130109672A1 (en) | 2010-04-29 | 2013-05-02 | The United States Of America,As Represented By The Secretary, Department Of Health And Human Service | Activators of human pyruvate kinase |
| WO2014089177A2 (en) | 2012-12-04 | 2014-06-12 | Massachusetts Institute Of Technology | Compounds, conjugates and compositions of epipolythiodiketopiperazines and polythiodiketopiperazines |
| US10201623B2 (en) | 2013-03-15 | 2019-02-12 | Memorial Sloan Kettering Cancer Center | HSP90-targeted cardiac imaging and therapy |
| FR3030516B1 (fr) * | 2014-12-19 | 2019-12-27 | Galderma Research & Development | Derives sulfonamides bicycles en tant qu'agonistes inverses du recepteur gamma orphelin associe aux retinoides ror gamma (t) |
| EP3337495A4 (en) | 2015-08-18 | 2019-04-10 | Mateon Therapeutics, Inc. | USE OF VDA TO ENHANCE IMMUNOMODULATION THERAPIES AGAINST TUMORS |
| US10918627B2 (en) | 2016-05-11 | 2021-02-16 | Massachusetts Institute Of Technology | Convergent and enantioselective total synthesis of Communesin analogs |
| WO2018209239A1 (en) | 2017-05-11 | 2018-11-15 | Massachusetts Institute Of Technology | Potent agelastatin derivatives as modulators for cancer invasion and metastasis |
| US10640508B2 (en) | 2017-10-13 | 2020-05-05 | Massachusetts Institute Of Technology | Diazene directed modular synthesis of compounds with quaternary carbon centers |
| US11535634B2 (en) | 2019-06-05 | 2022-12-27 | Massachusetts Institute Of Technology | Compounds, conjugates, and compositions of epipolythiodiketopiperazines and polythiodiketopiperazines and uses thereof |
| CN112375027B (zh) * | 2020-12-07 | 2023-03-31 | 中国药科大学 | 吲哚磺酰胺类衍生物及其医药用途 |
| WO2022182415A1 (en) | 2021-02-24 | 2022-09-01 | Massachusetts Institute Of Technology | Himastatin derivatives, and processes of preparation thereof, and uses thereof |
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| US4013621A (en) * | 1975-04-29 | 1977-03-22 | Ciba-Geigy Corporation | Substituted sulfonamide derivatives of hindered phenols and stabilized compositions |
| IT1050750B (it) * | 1975-12-05 | 1981-03-20 | Erba Carlo Spa | Derivati della 3.4 di idro chinazolina |
| JPS52125170A (en) * | 1976-04-12 | 1977-10-20 | Yoshitomi Pharmaceut Ind Ltd | Pyridine derivatives |
| GB8804457D0 (en) * | 1988-02-25 | 1988-03-23 | Ciba Geigy Ag | Compositions |
| US5238652A (en) * | 1990-06-20 | 1993-08-24 | Drug Screening Systems, Inc. | Analytical test devices for competition assay for drugs of non-protein antigens using immunochromatographic techniques |
| JPH04202173A (ja) * | 1990-11-30 | 1992-07-22 | Zeria Pharmaceut Co Ltd | スルホンアミド誘導体及びそれを含有する5―リポキシゲナーゼ阻害剤 |
| GB9200415D0 (en) * | 1992-01-09 | 1992-02-26 | Bagshawe Kenneth D | Inactivation of cytotoxic drugs |
| JPH06206805A (ja) * | 1992-02-17 | 1994-07-26 | Hisamitsu Pharmaceut Co Inc | チロシナーゼ阻害剤及びそれを用いた皮膚外用剤 |
| JPH06199047A (ja) * | 1993-01-08 | 1994-07-19 | New Oji Paper Co Ltd | 感熱記録体 |
| JPH08176113A (ja) * | 1993-11-12 | 1996-07-09 | Dainippon Pharmaceut Co Ltd | 2−スルフィニルニコチンアミド誘導体及びその中間体並びにそれを有効成分とする消化性潰瘍治療薬 |
| JPH09179257A (ja) * | 1995-12-22 | 1997-07-11 | Konica Corp | ハロゲン化銀カラー写真感光材料 |
| PT939627E (pt) * | 1996-07-19 | 2004-02-27 | Tularik Inc | Pentafluorobenzenossulfonamidas e analogos |
| BR9714087A (pt) * | 1996-12-27 | 2000-05-09 | Daiichi Seiyaku Co | Derivados de propionil substituìdo. |
| JPH10316650A (ja) * | 1997-05-13 | 1998-12-02 | Dev Center For Biotechnol | 新規な抗アテローム性動脈硬化薬 |
| IL164568A0 (en) * | 1997-05-14 | 2005-12-18 | Atherogenics Inc | Compounds and methods for the inhibition of the expression of vcam-1 |
| US6191170B1 (en) * | 1998-01-13 | 2001-02-20 | Tularik Inc. | Benzenesulfonamides and benzamides as therapeutic agents |
| ATE248845T1 (de) * | 1998-06-25 | 2003-09-15 | Tularik Inc | Arylsulfonanilid-phosphate |
| CN1332849A (zh) * | 1998-11-09 | 2002-01-23 | 埃瑟若詹尼克斯公司 | 降低血浆胆固醇水平的方法和组合物 |
-
2000
- 2000-05-24 CO CO00038242A patent/CO5170498A1/es not_active Application Discontinuation
- 2000-05-26 AU AU51709/00A patent/AU5170900A/en not_active Abandoned
- 2000-05-26 EP EP00936388A patent/EP1181269B1/en not_active Expired - Lifetime
- 2000-05-26 MX MXPA01012226A patent/MXPA01012226A/es active IP Right Grant
- 2000-05-26 WO PCT/US2000/014742 patent/WO2000073264A1/en not_active Ceased
- 2000-05-26 AR ARP000102634A patent/AR024138A1/es not_active Application Discontinuation
- 2000-05-26 AT AT00936388T patent/ATE260248T1/de not_active IP Right Cessation
- 2000-05-26 DE DE60008527T patent/DE60008527T2/de not_active Expired - Fee Related
- 2000-05-26 CA CA002371092A patent/CA2371092A1/en not_active Abandoned
- 2000-05-26 PT PT00936388T patent/PT1181269E/pt unknown
- 2000-05-26 JP JP2000621331A patent/JP3702183B2/ja not_active Expired - Fee Related
- 2000-05-26 HK HK02105330.6A patent/HK1045299B/en not_active IP Right Cessation
- 2000-05-26 ES ES00936388T patent/ES2215668T3/es not_active Expired - Lifetime
- 2000-05-26 DK DK00936388T patent/DK1181269T3/da active
- 2000-05-26 BR BR0007589-2A patent/BR0007589A/pt not_active Application Discontinuation
- 2000-05-30 TW TW089110268A patent/TWI221837B/zh not_active IP Right Cessation
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2005
- 2005-06-14 JP JP2005174115A patent/JP3869847B2/ja not_active Expired - Fee Related
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2006
- 2006-01-25 JP JP2006016490A patent/JP2006188525A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| BR0007589A (pt) | 2002-10-15 |
| JP3869847B2 (ja) | 2007-01-17 |
| EP1181269B1 (en) | 2004-02-25 |
| CO5170498A1 (es) | 2002-06-27 |
| JP2003500470A (ja) | 2003-01-07 |
| HK1045299B (en) | 2004-12-03 |
| CA2371092A1 (en) | 2000-12-07 |
| ATE260248T1 (de) | 2004-03-15 |
| JP3702183B2 (ja) | 2005-10-05 |
| PT1181269E (pt) | 2004-07-30 |
| AU5170900A (en) | 2000-12-18 |
| TWI221837B (en) | 2004-10-11 |
| EP1181269A1 (en) | 2002-02-27 |
| DE60008527D1 (de) | 2004-04-01 |
| ES2215668T3 (es) | 2004-10-16 |
| JP2005336195A (ja) | 2005-12-08 |
| JP2006188525A (ja) | 2006-07-20 |
| DK1181269T3 (da) | 2004-07-05 |
| MXPA01012226A (es) | 2002-08-12 |
| AR024138A1 (es) | 2002-09-04 |
| WO2000073264A1 (en) | 2000-12-07 |
| HK1045299A1 (en) | 2002-11-22 |
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