JP2006505512A5 - - Google Patents
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- Publication number
- JP2006505512A5 JP2006505512A5 JP2004523674A JP2004523674A JP2006505512A5 JP 2006505512 A5 JP2006505512 A5 JP 2006505512A5 JP 2004523674 A JP2004523674 A JP 2004523674A JP 2004523674 A JP2004523674 A JP 2004523674A JP 2006505512 A5 JP2006505512 A5 JP 2006505512A5
- Authority
- JP
- Japan
- Prior art keywords
- pyrazol
- benzothiazol
- methyl
- amino
- ylamine
- 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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- -1 amino, aminosulfinyl Chemical group 0.000 claims description 35
- 125000003118 aryl group Chemical group 0.000 claims description 19
- 125000000217 alkyl group Chemical group 0.000 claims description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 5
- 125000000623 heterocyclic group Chemical group 0.000 claims description 5
- 238000006467 substitution reaction Methods 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000001188 haloalkyl group Chemical group 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims 57
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 32
- 239000001257 hydrogen Substances 0.000 claims 26
- 229910052739 hydrogen Inorganic materials 0.000 claims 26
- 125000004404 heteroalkyl group Chemical group 0.000 claims 23
- 150000002431 hydrogen Chemical class 0.000 claims 23
- 238000000034 method Methods 0.000 claims 23
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims 22
- 125000001072 heteroaryl group Chemical group 0.000 claims 21
- 150000001875 compounds Chemical class 0.000 claims 20
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 12
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 11
- 229910019142 PO4 Inorganic materials 0.000 claims 11
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 11
- 150000001540 azides Chemical class 0.000 claims 11
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims 11
- 229910052736 halogen Inorganic materials 0.000 claims 11
- 150000002367 halogens Chemical class 0.000 claims 11
- 125000000717 hydrazino group Chemical group [H]N([*])N([H])[H] 0.000 claims 11
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 11
- 125000000018 nitroso group Chemical group N(=O)* 0.000 claims 11
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims 11
- 239000010452 phosphate Substances 0.000 claims 11
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical compound [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 claims 11
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims 11
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 claims 11
- LFGREXWGYUGZLY-UHFFFAOYSA-N phosphoryl Chemical group [P]=O LFGREXWGYUGZLY-UHFFFAOYSA-N 0.000 claims 11
- BUUPQKDIAURBJP-UHFFFAOYSA-N sulfinic acid Chemical compound OS=O BUUPQKDIAURBJP-UHFFFAOYSA-N 0.000 claims 11
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims 11
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 11
- 150000003462 sulfoxides Chemical class 0.000 claims 11
- 150000003573 thiols Chemical class 0.000 claims 11
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 claims 11
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 10
- 150000003839 salts Chemical class 0.000 claims 10
- 229940124530 sulfonamide Drugs 0.000 claims 10
- 150000003456 sulfonamides Chemical class 0.000 claims 10
- 239000012453 solvate Substances 0.000 claims 9
- 125000002993 cycloalkylene group Chemical group 0.000 claims 8
- 206010061218 Inflammation Diseases 0.000 claims 7
- 125000000753 cycloalkyl group Chemical group 0.000 claims 7
- 201000010099 disease Diseases 0.000 claims 7
- 230000004054 inflammatory process Effects 0.000 claims 7
- 125000003342 alkenyl group Chemical group 0.000 claims 6
- 125000000304 alkynyl group Chemical group 0.000 claims 6
- 230000003463 hyperproliferative effect Effects 0.000 claims 6
- 206010029113 Neovascularisation Diseases 0.000 claims 5
- DXZQRFSKAGSMFH-UHFFFAOYSA-N 2-(3-amino-5-methyl-1h-pyrazol-4-yl)-1,3-benzothiazol-5-ol Chemical compound CC1=NNC(N)=C1C1=NC2=CC(O)=CC=C2S1 DXZQRFSKAGSMFH-UHFFFAOYSA-N 0.000 claims 4
- LDAKZUPMVFBRML-UHFFFAOYSA-N 2-(3-amino-5-methyl-1h-pyrazol-4-yl)-1,3-benzothiazole-6-carboxamide Chemical compound CC1=NNC(N)=C1C1=NC2=CC=C(C(N)=O)C=C2S1 LDAKZUPMVFBRML-UHFFFAOYSA-N 0.000 claims 4
- RVGKCCVUQDDNPV-UHFFFAOYSA-N 2-(3-amino-5-methyl-1h-pyrazol-4-yl)-1,3-benzothiazole-6-carboxylic acid Chemical compound N1N=C(N)C(C=2SC3=CC(=CC=C3N=2)C(O)=O)=C1C RVGKCCVUQDDNPV-UHFFFAOYSA-N 0.000 claims 4
- NIINYWZQSXMXEO-UHFFFAOYSA-N 2-(3-amino-5-methyl-1h-pyrazol-4-yl)-1,3-benzothiazole-6-sulfonamide Chemical compound N1N=C(N)C(C=2SC3=CC(=CC=C3N=2)S(N)(=O)=O)=C1C NIINYWZQSXMXEO-UHFFFAOYSA-N 0.000 claims 4
- SJZFSDRSUJHBEQ-UHFFFAOYSA-N 2-(3-amino-5-methyl-1h-pyrazol-4-yl)-4,5,6-trifluoro-1,3-benzothiazole-7-sulfonamide Chemical compound N1N=C(N)C(C=2SC3=C(C(F)=C(F)C(F)=C3N=2)S(N)(=O)=O)=C1C SJZFSDRSUJHBEQ-UHFFFAOYSA-N 0.000 claims 4
- FUDLGGGXXSVQGI-UHFFFAOYSA-N 2-(3-amino-5-methyl-1h-pyrazol-4-yl)-4-fluoro-1,3-benzothiazole-6-sulfonamide Chemical compound CC1=NNC(N)=C1C1=NC2=C(F)C=C(S(N)(=O)=O)C=C2S1 FUDLGGGXXSVQGI-UHFFFAOYSA-N 0.000 claims 4
- VBUGCZILHWRGPF-UHFFFAOYSA-N 2-(3-amino-5-methyl-1h-pyrazol-4-yl)-5-fluoro-1,3-benzothiazole-6-sulfonamide Chemical compound CC1=NNC(N)=C1C1=NC2=CC(F)=C(S(N)(=O)=O)C=C2S1 VBUGCZILHWRGPF-UHFFFAOYSA-N 0.000 claims 4
- FIJKJYNYFHYOLF-UHFFFAOYSA-N 4-(1,3-benzothiazol-2-yl)-3-piperazin-1-yl-1h-pyrazol-5-amine Chemical compound N=1C2=CC=CC=C2SC=1C1=C(N)NN=C1N1CCNCC1 FIJKJYNYFHYOLF-UHFFFAOYSA-N 0.000 claims 4
- ALALFTRMHTVSLL-UHFFFAOYSA-N 4-(4-fluoro-1,3-benzothiazol-2-yl)-5-methyl-1h-pyrazol-3-amine Chemical compound CC1=NNC(N)=C1C1=NC2=C(F)C=CC=C2S1 ALALFTRMHTVSLL-UHFFFAOYSA-N 0.000 claims 4
- UPFLHWHGWALIPT-UHFFFAOYSA-N 4-(5-fluoro-1,3-benzothiazol-2-yl)-5-methyl-1h-pyrazol-3-amine Chemical compound CC1=NNC(N)=C1C1=NC2=CC(F)=CC=C2S1 UPFLHWHGWALIPT-UHFFFAOYSA-N 0.000 claims 4
- NOWPDVBJSWLRTD-UHFFFAOYSA-N 4-(5-fluoro-6-methoxy-1,3-benzothiazol-2-yl)-5-(2-phenylcyclopropyl)-1h-pyrazol-3-amine Chemical compound N=1C=2C=C(F)C(OC)=CC=2SC=1C1=C(N)NN=C1C1CC1C1=CC=CC=C1 NOWPDVBJSWLRTD-UHFFFAOYSA-N 0.000 claims 4
- TYGJLYAMPYVJEC-UHFFFAOYSA-N 4-(5-fluoro-6-methoxy-1,3-benzothiazol-2-yl)-5-methyl-1h-pyrazol-3-amine Chemical compound N=1C=2C=C(F)C(OC)=CC=2SC=1C1=C(C)NN=C1N TYGJLYAMPYVJEC-UHFFFAOYSA-N 0.000 claims 4
- SWYXGMQXRBABPD-UHFFFAOYSA-N 4-(5-fluoro-6-methoxy-1,3-benzothiazol-2-yl)-5-phenyl-1h-pyrazol-3-amine Chemical compound N=1C=2C=C(F)C(OC)=CC=2SC=1C1=C(N)NN=C1C1=CC=CC=C1 SWYXGMQXRBABPD-UHFFFAOYSA-N 0.000 claims 4
- SVURQPBGWDIMSF-UHFFFAOYSA-N 4-(5-fluoro-6-methyl-1,3-benzothiazol-2-yl)-5-methyl-1h-pyrazol-3-amine Chemical compound CC1=NNC(N)=C1C1=NC2=CC(F)=C(C)C=C2S1 SVURQPBGWDIMSF-UHFFFAOYSA-N 0.000 claims 4
- PNNINDSPAQWMTR-UHFFFAOYSA-N 4-(5-methoxy-1,3-benzothiazol-2-yl)-5-methyl-1h-pyrazol-3-amine Chemical compound N=1C2=CC(OC)=CC=C2SC=1C=1C(C)=NNC=1N PNNINDSPAQWMTR-UHFFFAOYSA-N 0.000 claims 4
- KAMNFXYPIHJODD-UHFFFAOYSA-N 4-(6-bromo-1,3-benzothiazol-2-yl)-5-methyl-1h-pyrazol-3-amine Chemical compound N1N=C(N)C(C=2SC3=CC(Br)=CC=C3N=2)=C1C KAMNFXYPIHJODD-UHFFFAOYSA-N 0.000 claims 4
- LVVKTROMUCSVFM-UHFFFAOYSA-N 4-(6-bromo-5-fluoro-1,3-benzothiazol-2-yl)-5-methyl-1h-pyrazol-3-amine Chemical compound N1N=C(N)C(C=2SC3=CC(Br)=C(F)C=C3N=2)=C1C LVVKTROMUCSVFM-UHFFFAOYSA-N 0.000 claims 4
- WRIQXYKFINZWKB-UHFFFAOYSA-N 4-(6-chloro-1,3-benzothiazol-2-yl)-5-methyl-1h-pyrazol-3-amine Chemical compound CC1=NNC(N)=C1C1=NC2=CC=C(Cl)C=C2S1 WRIQXYKFINZWKB-UHFFFAOYSA-N 0.000 claims 4
- FJMJCOZSZTXBLP-UHFFFAOYSA-N 4-(6-fluoro-1,3-benzothiazol-2-yl)-5-methyl-1h-pyrazol-3-amine Chemical compound N1N=C(N)C(C=2SC3=CC(F)=CC=C3N=2)=C1C FJMJCOZSZTXBLP-UHFFFAOYSA-N 0.000 claims 4
- LPXKPTBYKQEWNS-UHFFFAOYSA-N 4-(7-chloro-4-methoxy-1,3-benzothiazol-2-yl)-5-methyl-1h-pyrazol-3-amine Chemical compound N=1C=2C(OC)=CC=C(Cl)C=2SC=1C=1C(C)=NNC=1N LPXKPTBYKQEWNS-UHFFFAOYSA-N 0.000 claims 4
- WCDAXJVVWPUBRH-UHFFFAOYSA-N 4-(7-chloro-5-fluoro-6-methoxy-1,3-benzothiazol-2-yl)-5-methyl-1h-pyrazol-3-amine Chemical compound S1C2=C(Cl)C(OC)=C(F)C=C2N=C1C1=C(C)NN=C1N WCDAXJVVWPUBRH-UHFFFAOYSA-N 0.000 claims 4
- IUINLGIEEUGQST-UHFFFAOYSA-N 4-[6-[(dimethylamino)methyl]-1,3-benzothiazol-2-yl]-5-methyl-1h-pyrazol-3-amine Chemical compound S1C2=CC(CN(C)C)=CC=C2N=C1C=1C(C)=NNC=1N IUINLGIEEUGQST-UHFFFAOYSA-N 0.000 claims 4
- SEUQVSLHPQREFI-UHFFFAOYSA-N 4-[6-[(dimethylamino)methyl]-5-fluoro-1,3-benzothiazol-2-yl]-5-methyl-1h-pyrazol-3-amine Chemical compound N=1C=2C=C(F)C(CN(C)C)=CC=2SC=1C1=C(C)NN=C1N SEUQVSLHPQREFI-UHFFFAOYSA-N 0.000 claims 4
- LJOGSXNDUUPYSU-UHFFFAOYSA-N 5-cyclopropyl-4-(5-fluoro-6-methoxy-1,3-benzothiazol-2-yl)-1h-pyrazol-3-amine Chemical compound N=1C=2C=C(F)C(OC)=CC=2SC=1C1=C(N)NN=C1C1CC1 LJOGSXNDUUPYSU-UHFFFAOYSA-N 0.000 claims 4
- YBGBUAAMXHCKKT-UHFFFAOYSA-N 5-methyl-4-(4,5,6-trifluoro-1,3-benzothiazol-2-yl)-1h-pyrazol-3-amine Chemical compound N1N=C(N)C(C=2SC3=CC(F)=C(F)C(F)=C3N=2)=C1C YBGBUAAMXHCKKT-UHFFFAOYSA-N 0.000 claims 4
- MOTWNZWIXFFOBR-UHFFFAOYSA-N 5-methyl-4-[5-(trifluoromethyl)-1,3-benzothiazol-2-yl]-1h-pyrazol-3-amine Chemical compound CC1=NNC(N)=C1C1=NC2=CC(C(F)(F)F)=CC=C2S1 MOTWNZWIXFFOBR-UHFFFAOYSA-N 0.000 claims 4
- NQWZDRDBSYKWHS-UHFFFAOYSA-N 5-methyl-4-[6-(methylaminomethyl)-1,3-benzothiazol-2-yl]-1h-pyrazol-3-amine Chemical compound S1C2=CC(CNC)=CC=C2N=C1C=1C(C)=NNC=1N NQWZDRDBSYKWHS-UHFFFAOYSA-N 0.000 claims 4
- XTFSZJMZNLOHCZ-UHFFFAOYSA-N [2-(3-amino-5-methyl-1h-pyrazol-4-yl)-1,3-benzothiazol-5-yl]methanol Chemical compound CC1=NNC(N)=C1C1=NC2=CC(CO)=CC=C2S1 XTFSZJMZNLOHCZ-UHFFFAOYSA-N 0.000 claims 4
- ULALTYCGJZSKAB-UHFFFAOYSA-N [2-(3-amino-5-methyl-1h-pyrazol-4-yl)-1,3-benzothiazol-6-yl]methanol Chemical compound CC1=NNC(N)=C1C1=NC2=CC=C(CO)C=C2S1 ULALTYCGJZSKAB-UHFFFAOYSA-N 0.000 claims 4
- IIKBSVJXNRIRLB-UHFFFAOYSA-N [2-(3-amino-5-methyl-1h-pyrazol-4-yl)-5-fluoro-1,3-benzothiazol-6-yl]methanol Chemical compound N1N=C(N)C(C=2SC3=CC(CO)=C(F)C=C3N=2)=C1C IIKBSVJXNRIRLB-UHFFFAOYSA-N 0.000 claims 4
- 210000004027 cell Anatomy 0.000 claims 4
- 230000012292 cell migration Effects 0.000 claims 4
- BWAHGXAUIRPIHE-UHFFFAOYSA-N ethyl 2-(3-amino-5-methyl-1h-pyrazol-4-yl)-1,3-benzothiazole-5-carboxylate Chemical compound N=1C2=CC(C(=O)OCC)=CC=C2SC=1C=1C(C)=NNC=1N BWAHGXAUIRPIHE-UHFFFAOYSA-N 0.000 claims 4
- 208000017169 kidney disease Diseases 0.000 claims 4
- ZFENCOLQOBJLNZ-UHFFFAOYSA-N methyl 2-(3-amino-5-methyl-1h-pyrazol-4-yl)-1,3-benzothiazole-6-carboxylate Chemical compound S1C2=CC(C(=O)OC)=CC=C2N=C1C1=C(C)NN=C1N ZFENCOLQOBJLNZ-UHFFFAOYSA-N 0.000 claims 4
- IKOJEQSDJHXFQW-UHFFFAOYSA-N methyl 2-(3-amino-5-methyl-1h-pyrazol-4-yl)-1,3-benzothiazole-7-carboxylate Chemical compound S1C=2C(C(=O)OC)=CC=CC=2N=C1C1=C(C)NN=C1N IKOJEQSDJHXFQW-UHFFFAOYSA-N 0.000 claims 4
- UKMWNGBPFOCSTQ-UHFFFAOYSA-N methyl 2-(3-amino-5-methyl-1h-pyrazol-4-yl)-5-fluoro-1,3-benzothiazole-6-carboxylate Chemical compound N=1C=2C=C(F)C(C(=O)OC)=CC=2SC=1C1=C(C)NN=C1N UKMWNGBPFOCSTQ-UHFFFAOYSA-N 0.000 claims 4
- NNIZGWWKOQEOAW-UHFFFAOYSA-N n-[2-(3-amino-5-methyl-1h-pyrazol-4-yl)-1,3-benzothiazol-6-yl]acetamide Chemical compound S1C2=CC(NC(=O)C)=CC=C2N=C1C=1C(C)=NNC=1N NNIZGWWKOQEOAW-UHFFFAOYSA-N 0.000 claims 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 4
- PMLPUDHASUGHLR-UHFFFAOYSA-N 2-(1h-pyrazol-4-yl)-1,3-benzothiazole-6-sulfonamide Chemical compound S1C2=CC(S(=O)(=O)N)=CC=C2N=C1C=1C=NNC=1 PMLPUDHASUGHLR-UHFFFAOYSA-N 0.000 claims 3
- ZGXDTMKHHQRSEX-UHFFFAOYSA-N 2-(3-amino-5-pyridin-4-yl-1h-pyrazol-4-yl)-1,3-benzothiazole-6-sulfonamide Chemical compound N=1C2=CC=C(S(N)(=O)=O)C=C2SC=1C1=C(N)NN=C1C1=CC=NC=C1 ZGXDTMKHHQRSEX-UHFFFAOYSA-N 0.000 claims 3
- HGNBEIZSJKIPRI-UHFFFAOYSA-N 2-(5-amino-1h-pyrazol-4-yl)-1,3-benzothiazol-6-amine Chemical compound N1N=CC(C=2SC3=CC(N)=CC=C3N=2)=C1N HGNBEIZSJKIPRI-UHFFFAOYSA-N 0.000 claims 3
- MJSWBRWBMZMVTH-UHFFFAOYSA-N 2-(5-amino-1h-pyrazol-4-yl)-5-fluoro-1,3-benzothiazole-6-sulfonamide Chemical compound NC1=NNC=C1C1=NC2=CC(F)=C(S(N)(=O)=O)C=C2S1 MJSWBRWBMZMVTH-UHFFFAOYSA-N 0.000 claims 3
- VEGVHNGSVSGVMG-UHFFFAOYSA-N 4-(1,3-benzothiazol-2-yl)-5-cyclopropyl-1h-pyrazol-3-amine Chemical compound N=1C2=CC=CC=C2SC=1C=1C(N)=NNC=1C1CC1 VEGVHNGSVSGVMG-UHFFFAOYSA-N 0.000 claims 3
- IXSYRRSIOMPVHT-UHFFFAOYSA-N 4-(1,3-benzothiazol-2-yl)-5-ethyl-1h-pyrazol-3-amine Chemical compound N1N=C(N)C(C=2SC3=CC=CC=C3N=2)=C1CC IXSYRRSIOMPVHT-UHFFFAOYSA-N 0.000 claims 3
- CSQQPNHSMIACDK-UHFFFAOYSA-N 4-(1,3-benzothiazol-2-yl)-5-methyl-1h-pyrazol-3-amine Chemical compound CC1=NNC(N)=C1C1=NC2=CC=CC=C2S1 CSQQPNHSMIACDK-UHFFFAOYSA-N 0.000 claims 3
- ZBRUXVVKRSVWTF-UHFFFAOYSA-N 4-(1,3-benzothiazol-2-yl)-5-phenyl-1h-pyrazol-3-amine Chemical compound N=1C2=CC=CC=C2SC=1C=1C(N)=NNC=1C1=CC=CC=C1 ZBRUXVVKRSVWTF-UHFFFAOYSA-N 0.000 claims 3
- DZSCNAWRDWGVKH-UHFFFAOYSA-N 4-(5-fluoro-6-methoxy-1,3-benzothiazol-2-yl)-3-piperazin-1-yl-1h-pyrazol-5-amine Chemical compound N=1C=2C=C(F)C(OC)=CC=2SC=1C1=C(N)NN=C1N1CCNCC1 DZSCNAWRDWGVKH-UHFFFAOYSA-N 0.000 claims 3
- YMZGLBIKIDCVFV-UHFFFAOYSA-N 4-(5-fluoro-6-methoxy-1,3-benzothiazol-2-yl)-5-(2-fluorophenyl)-1h-pyrazol-3-amine Chemical compound N=1C=2C=C(F)C(OC)=CC=2SC=1C1=C(N)NN=C1C1=CC=CC=C1F YMZGLBIKIDCVFV-UHFFFAOYSA-N 0.000 claims 3
- PYBQETIYZPINDU-UHFFFAOYSA-N 4-(5-fluoro-6-methoxy-1,3-benzothiazol-2-yl)-5-(3-fluorophenyl)-1h-pyrazol-3-amine Chemical compound N=1C=2C=C(F)C(OC)=CC=2SC=1C1=C(N)NN=C1C1=CC=CC(F)=C1 PYBQETIYZPINDU-UHFFFAOYSA-N 0.000 claims 3
- JDRWZPMNLJGQAX-UHFFFAOYSA-N 4-(5-fluoro-6-methoxy-1,3-benzothiazol-2-yl)-5-(4-fluorophenyl)-1h-pyrazol-3-amine Chemical compound N=1C=2C=C(F)C(OC)=CC=2SC=1C1=C(N)NN=C1C1=CC=C(F)C=C1 JDRWZPMNLJGQAX-UHFFFAOYSA-N 0.000 claims 3
- JZJCYCNGEXYTSB-UHFFFAOYSA-N 4-(5-fluoro-6-methoxy-1,3-benzothiazol-2-yl)-5-pyridin-4-yl-1h-pyrazol-3-amine Chemical compound N=1C=2C=C(F)C(OC)=CC=2SC=1C1=C(N)NN=C1C1=CC=NC=C1 JZJCYCNGEXYTSB-UHFFFAOYSA-N 0.000 claims 3
- ZNQDQBQRNRBYST-UHFFFAOYSA-N 4-(5-fluoro-6-methyl-1,3-benzothiazol-2-yl)-1h-pyrazol-5-amine Chemical compound N=1C=2C=C(F)C(C)=CC=2SC=1C=1C=NNC=1N ZNQDQBQRNRBYST-UHFFFAOYSA-N 0.000 claims 3
- UPUVYZJKZGVBSN-UHFFFAOYSA-N 4-(6-fluoro-1,3-benzothiazol-2-yl)-1h-pyrazol-5-amine Chemical compound NC1=NNC=C1C1=NC2=CC=C(F)C=C2S1 UPUVYZJKZGVBSN-UHFFFAOYSA-N 0.000 claims 3
- AASMCUUUEHKZKE-UHFFFAOYSA-N 4-(6-methoxy-1,3-benzothiazol-2-yl)-3-piperazin-1-yl-1h-pyrazol-5-amine Chemical compound S1C2=CC(OC)=CC=C2N=C1C1=C(N)NN=C1N1CCNCC1 AASMCUUUEHKZKE-UHFFFAOYSA-N 0.000 claims 3
- VRTQVPLLTFUHCM-UHFFFAOYSA-N 4-(6-methoxy-1,3-benzothiazol-2-yl)-5-methyl-1h-pyrazol-3-amine Chemical compound S1C2=CC(OC)=CC=C2N=C1C1=C(C)NN=C1N VRTQVPLLTFUHCM-UHFFFAOYSA-N 0.000 claims 3
- PIMULLTXNIWAMA-UHFFFAOYSA-N 4-(6-nitro-1,3-benzothiazol-2-yl)-1h-pyrazol-5-amine Chemical compound N1N=CC(C=2SC3=CC(=CC=C3N=2)[N+]([O-])=O)=C1N PIMULLTXNIWAMA-UHFFFAOYSA-N 0.000 claims 3
- LXMBHKHXRGNWDB-UHFFFAOYSA-N 5-(2-chloropyridin-3-yl)-4-(5-fluoro-6-methoxy-1,3-benzothiazol-2-yl)-1h-pyrazol-3-amine Chemical compound N=1C=2C=C(F)C(OC)=CC=2SC=1C1=C(N)NN=C1C1=CC=CN=C1Cl LXMBHKHXRGNWDB-UHFFFAOYSA-N 0.000 claims 3
- 150000001408 amides Chemical class 0.000 claims 3
- 230000004709 cell invasion Effects 0.000 claims 3
- 208000035475 disorder Diseases 0.000 claims 3
- 230000002401 inhibitory effect Effects 0.000 claims 3
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| US7608635B2 (en) * | 2005-08-12 | 2009-10-27 | Synta Pharmaceuticals Corp. | Pyrazole compounds that modulate HSP90 activity |
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| RU2553225C2 (ru) | 2008-05-23 | 2015-06-10 | Сива Корпорейшн | Способ облегчения регенерации |
| US8731655B2 (en) | 2009-05-12 | 2014-05-20 | Mallinckrodt Llc | Compounds containing acyclic N-N bonds for phototherapy |
| WO2010132554A2 (en) | 2009-05-12 | 2010-11-18 | Mallinckrodt Inc. | Diaza heterocyclic compounds for phototherapy |
| AU2010270797B2 (en) | 2009-07-08 | 2015-03-19 | Dermira (Canada), Inc. | TOFA analogs useful in treating dermatological disorders or conditions |
| ES2725852T3 (es) | 2010-09-27 | 2019-09-27 | Siwa Corp | Eliminación selectiva de células modificadas por AGE para el tratamiento de la aterosclerosis |
| US8721571B2 (en) | 2010-11-22 | 2014-05-13 | Siwa Corporation | Selective removal of cells having accumulated agents |
| KR101902973B1 (ko) | 2010-11-24 | 2018-10-04 | 오하이오 스테이트 이노베이션 파운데이션 | 인테그린 결합 키나아제 억제제 |
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| LT6064B (lt) | 2012-10-15 | 2014-08-25 | Vilniaus Universitetas | Fluorinti benzensulfonamidai kaip karboanhidrazės inhibitoriai |
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| WO2015127548A1 (en) * | 2014-02-28 | 2015-09-03 | The Royal Institution For The Advancement Of Learning / Mcgill University | Tc-ptp inhibitors as apc activators for immunotherapy |
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