JP2002506072A - プロテインチロシンホスファターゼ（ＰＴＰａｓｅ）のモジュレーター - Google Patents
プロテインチロシンホスファターゼ（ＰＴＰａｓｅ）のモジュレーターInfo
- Publication number
- JP2002506072A JP2002506072A JP2000535645A JP2000535645A JP2002506072A JP 2002506072 A JP2002506072 A JP 2002506072A JP 2000535645 A JP2000535645 A JP 2000535645A JP 2000535645 A JP2000535645 A JP 2000535645A JP 2002506072 A JP2002506072 A JP 2002506072A
- Authority
- JP
- Japan
- Prior art keywords
- amino
- dihydro
- thieno
- oxalyl
- carboxylic acid
- 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.)
- Withdrawn
Links
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- 108020000494 protein-tyrosine phosphatase Proteins 0.000 title claims abstract description 123
- -1 PTPα Proteins 0.000 claims abstract description 402
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- 239000000203 mixture Substances 0.000 claims abstract description 109
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 52
- 201000010099 disease Diseases 0.000 claims abstract description 45
- 238000000034 method Methods 0.000 claims abstract description 40
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 29
- 238000003786 synthesis reaction Methods 0.000 claims abstract description 27
- 108010051696 Growth Hormone Proteins 0.000 claims abstract description 25
- 102000018997 Growth Hormone Human genes 0.000 claims abstract description 25
- 239000000122 growth hormone Substances 0.000 claims abstract description 25
- 206010028980 Neoplasm Diseases 0.000 claims abstract description 24
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- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims abstract description 23
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- 229940088597 hormone Drugs 0.000 claims abstract description 14
- 239000005556 hormone Substances 0.000 claims abstract description 14
- 102000004127 Cytokines Human genes 0.000 claims abstract description 12
- 108090000695 Cytokines Proteins 0.000 claims abstract description 12
- 206010067584 Type 1 diabetes mellitus Diseases 0.000 claims abstract description 12
- 208000026935 allergic disease Diseases 0.000 claims abstract description 12
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- 208000024827 Alzheimer disease Diseases 0.000 claims abstract description 11
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- 206010022489 Insulin Resistance Diseases 0.000 claims abstract description 11
- 208000008589 Obesity Diseases 0.000 claims abstract description 11
- 201000004681 Psoriasis Diseases 0.000 claims abstract description 11
- 208000006673 asthma Diseases 0.000 claims abstract description 11
- 230000005784 autoimmunity Effects 0.000 claims abstract description 11
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- 125000003118 aryl group Chemical group 0.000 claims description 188
- LZNNMMKMGKFYLL-UHFFFAOYSA-N 2h-pyran-3-carboxylic acid Chemical compound OC(=O)C1=CC=COC1 LZNNMMKMGKFYLL-UHFFFAOYSA-N 0.000 claims description 135
- 239000007787 solid Substances 0.000 claims description 88
- 229910052739 hydrogen Inorganic materials 0.000 claims description 75
- 239000001257 hydrogen Substances 0.000 claims description 75
- 125000000217 alkyl group Chemical group 0.000 claims description 67
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 44
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 38
- 150000002431 hydrogen Chemical class 0.000 claims description 36
- 229910052757 nitrogen Inorganic materials 0.000 claims description 35
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 33
- 239000002253 acid Substances 0.000 claims description 30
- 125000003431 oxalo group Chemical group 0.000 claims description 30
- 125000004432 carbon atom Chemical group C* 0.000 claims description 29
- 229920006395 saturated elastomer Polymers 0.000 claims description 23
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 claims description 22
- 230000003287 optical effect Effects 0.000 claims description 22
- 150000003839 salts Chemical class 0.000 claims description 20
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims description 19
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 19
- 125000004122 cyclic group Chemical group 0.000 claims description 17
- 108090000623 proteins and genes Proteins 0.000 claims description 15
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 14
- 125000000449 nitro group Chemical class [O-][N+](*)=O 0.000 claims description 14
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- 235000001968 nicotinic acid Nutrition 0.000 claims description 13
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- 125000004043 oxo group Chemical group O=* 0.000 claims description 13
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 13
- 102000004169 proteins and genes Human genes 0.000 claims description 13
- 229910052760 oxygen Inorganic materials 0.000 claims description 12
- 239000001301 oxygen Chemical group 0.000 claims description 12
- 229910052717 sulfur Chemical group 0.000 claims description 12
- 239000011593 sulfur Chemical group 0.000 claims description 12
- 102000014400 SH2 domains Human genes 0.000 claims description 11
- 108050003452 SH2 domains Proteins 0.000 claims description 11
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 11
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 10
- 125000004104 aryloxy group Chemical group 0.000 claims description 10
- 125000004076 pyridyl group Chemical group 0.000 claims description 10
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 claims description 10
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 claims description 9
- 125000005129 aryl carbonyl group Chemical group 0.000 claims description 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
- 230000001225 therapeutic effect Effects 0.000 claims description 9
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims description 8
- 125000000623 heterocyclic group Chemical group 0.000 claims description 8
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 8
- 239000008194 pharmaceutical composition Substances 0.000 claims description 8
- 238000002360 preparation method Methods 0.000 claims description 8
- 230000002265 prevention Effects 0.000 claims description 8
- 125000005110 aryl thio group Chemical group 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 125000006497 3-methoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C(OC([H])([H])[H])=C1[H])C([H])([H])* 0.000 claims description 6
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims description 6
- 125000002619 bicyclic group Chemical group 0.000 claims description 6
- 125000005842 heteroatom Chemical group 0.000 claims description 6
- 125000001041 indolyl group Chemical group 0.000 claims description 6
- DCWXELXMIBXGTH-QMMMGPOBSA-N phosphonotyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(OP(O)(O)=O)C=C1 DCWXELXMIBXGTH-QMMMGPOBSA-N 0.000 claims description 6
- 230000002829 reductive effect Effects 0.000 claims description 6
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims description 6
- YNVOMSDITJMNET-UHFFFAOYSA-N thiophene-3-carboxylic acid Chemical compound OC(=O)C=1C=CSC=1 YNVOMSDITJMNET-UHFFFAOYSA-N 0.000 claims description 6
- 125000004953 trihalomethyl group Chemical group 0.000 claims description 6
- 150000001299 aldehydes Chemical class 0.000 claims description 5
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 5
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims description 5
- 239000003085 diluting agent Substances 0.000 claims description 5
- 239000002552 dosage form Substances 0.000 claims description 5
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 claims description 5
- 125000000842 isoxazolyl group Chemical group 0.000 claims description 5
- 150000003951 lactams Chemical class 0.000 claims description 5
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims description 4
- 125000005605 benzo group Chemical group 0.000 claims description 4
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims description 4
- 210000004556 brain Anatomy 0.000 claims description 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 4
- 229940079593 drug Drugs 0.000 claims description 4
- 239000003937 drug carrier Substances 0.000 claims description 4
- SOWBFZRMHSNYGE-UHFFFAOYSA-N oxamic acid Chemical compound NC(=O)C(O)=O SOWBFZRMHSNYGE-UHFFFAOYSA-N 0.000 claims description 4
- 150000003141 primary amines Chemical class 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 4
- DWLHTIPCWYOEMT-UHFFFAOYSA-N 2h-thiopyran-3-carboxylic acid Chemical compound OC(=O)C1=CC=CSC1 DWLHTIPCWYOEMT-UHFFFAOYSA-N 0.000 claims description 3
- DNUOCYUTEIKZFI-UHFFFAOYSA-N 6-benzyl-2-(oxaloamino)-5,7-dihydro-4h-thieno[2,3-c]pyridine-3-carboxylic acid Chemical compound C1CC=2C(C(O)=O)=C(NC(=O)C(=O)O)SC=2CN1CC1=CC=CC=C1 DNUOCYUTEIKZFI-UHFFFAOYSA-N 0.000 claims description 3
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims description 3
- 208000015181 infectious disease Diseases 0.000 claims description 3
- 239000003446 ligand Substances 0.000 claims description 3
- XUGANLGVQLASCQ-UHFFFAOYSA-N 2-(oxaloamino)-6-(pyridin-4-ylmethyl)-5,7-dihydro-4h-thieno[2,3-c]pyridine-3-carboxylic acid Chemical compound C1CC=2C(C(O)=O)=C(NC(=O)C(=O)O)SC=2CN1CC1=CC=NC=C1 XUGANLGVQLASCQ-UHFFFAOYSA-N 0.000 claims description 2
- SNNOZMNTPOIDSI-UHFFFAOYSA-N 2-(oxalyl-amino)-4,7-dihydro-5h-thieno[2,3-c]pyran-3-carboxylic acid Chemical compound C1OCCC2=C1SC(NC(=O)C(=O)O)=C2C(O)=O SNNOZMNTPOIDSI-UHFFFAOYSA-N 0.000 claims description 2
- JUARYADRYQXCBJ-UHFFFAOYSA-N 2-[[4-(carboxymethyl)-4,5,6,7-tetrahydro-1-benzothiophen-2-yl]amino]-2-oxoacetic acid Chemical compound OC(=O)CC1CCCC2=C1C=C(NC(=O)C(O)=O)S2 JUARYADRYQXCBJ-UHFFFAOYSA-N 0.000 claims description 2
- WQTYHFAJPLKIJR-UHFFFAOYSA-N 2-[[4-(carboxymethyl)-5,7-dihydro-4h-thieno[2,3-c]pyran-2-yl]amino]-2-oxoacetic acid Chemical compound OC(=O)CC1COCC2=C1C=C(NC(=O)C(O)=O)S2 WQTYHFAJPLKIJR-UHFFFAOYSA-N 0.000 claims description 2
- YLAWGBLMYWOYKP-UHFFFAOYSA-N 2-[[4-(carboxymethylidene)-6,7-dihydro-5h-1-benzothiophen-2-yl]amino]-2-oxoacetic acid Chemical compound OC(=O)C=C1CCCC2=C1C=C(NC(=O)C(O)=O)S2 YLAWGBLMYWOYKP-UHFFFAOYSA-N 0.000 claims description 2
- CGMRTGKHKUUCRH-UHFFFAOYSA-N 2-[[4-(carboxymethylidene)-7h-thieno[2,3-c]pyran-2-yl]amino]-2-oxoacetic acid Chemical compound OC(=O)C=C1COCC2=C1C=C(NC(=O)C(O)=O)S2 CGMRTGKHKUUCRH-UHFFFAOYSA-N 0.000 claims description 2
- NKHDPHJFMYZNMI-UHFFFAOYSA-N 6-(oxaloamino)-1h-indole-7-carboxylic acid Chemical compound OC(=O)C(=O)NC1=CC=C2C=CNC2=C1C(O)=O NKHDPHJFMYZNMI-UHFFFAOYSA-N 0.000 claims description 2
- AHWMERGBWWROMM-UHFFFAOYSA-N 6-(oxalyl-amino)-1h-indole-5-carboxylic acid Chemical compound C1=C(C(O)=O)C(NC(=O)C(=O)O)=CC2=C1C=CN2 AHWMERGBWWROMM-UHFFFAOYSA-N 0.000 claims description 2
- CLPLHASNHDFGBI-UHFFFAOYSA-N 6-methyl-2-(oxaloamino)-5,7-dihydro-4h-thieno[2,3-c]pyridine-3-carboxylic acid Chemical compound C1N(C)CCC2=C1SC(NC(=O)C(O)=O)=C2C(O)=O CLPLHASNHDFGBI-UHFFFAOYSA-N 0.000 claims description 2
- VUIGGTBOFZGZHK-UHFFFAOYSA-N 6-phenylmethoxycarbonylpyridine-3-carboxylic acid Chemical compound N1=CC(C(=O)O)=CC=C1C(=O)OCC1=CC=CC=C1 VUIGGTBOFZGZHK-UHFFFAOYSA-N 0.000 claims description 2
- 238000006058 Ugi-reaction Methods 0.000 claims description 2
- 230000008569 process Effects 0.000 claims description 2
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- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims 7
- 239000004327 boric acid Substances 0.000 claims 7
- JWHOQZUREKYPBY-UHFFFAOYSA-N rubonic acid Natural products CC1(C)CCC2(CCC3(C)C(=CCC4C5(C)CCC(=O)C(C)(C)C5CC(=O)C34C)C2C1)C(=O)O JWHOQZUREKYPBY-UHFFFAOYSA-N 0.000 claims 5
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- YKPQGAUZNXNNEK-UHFFFAOYSA-N 2-(2h-tetrazole-5-carbonylamino)-5,7-dihydro-4h-thieno[2,3-c]pyran-3-carboxylic acid Chemical compound S1C=2COCCC=2C(C(=O)O)=C1NC(=O)C=1N=NNN=1 YKPQGAUZNXNNEK-UHFFFAOYSA-N 0.000 claims 1
- ISZAWTJNJSOJQB-UHFFFAOYSA-N 2-(oxaloamino)-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylic acid Chemical compound C1CCCC2=C1SC(NC(=O)C(=O)O)=C2C(O)=O ISZAWTJNJSOJQB-UHFFFAOYSA-N 0.000 claims 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims 1
- JAQHXLFNIRKZDT-UHFFFAOYSA-N 2-oxo-2-[[4-(2h-tetrazol-5-ylmethyl)-5,7-dihydro-4h-thieno[2,3-c]pyran-2-yl]amino]acetic acid Chemical compound C1OCC=2SC(NC(=O)C(=O)O)=CC=2C1CC=1N=NNN=1 JAQHXLFNIRKZDT-UHFFFAOYSA-N 0.000 claims 1
- 125000003762 3,4-dimethoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1* 0.000 claims 1
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- VBEQCZHXXJYVRD-GACYYNSASA-N uroanthelone Chemical compound C([C@@H](C(=O)N[C@H](C(=O)N[C@@H](CS)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CS)C(=O)N[C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)NCC(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)C(C)C)[C@@H](C)O)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](NC(=O)[C@H](CC=1NC=NC=1)NC(=O)[C@H](CCSC)NC(=O)[C@H](CS)NC(=O)[C@@H](NC(=O)CNC(=O)CNC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CS)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)CNC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](CS)NC(=O)CNC(=O)[C@H]1N(CCC1)C(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CC(N)=O)C(C)C)[C@@H](C)CC)C1=CC=C(O)C=C1 VBEQCZHXXJYVRD-GACYYNSASA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
- 125000005287 vanadyl group Chemical group 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000002424 x-ray crystallography Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- 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
- C07D209/10—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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D333/52—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes
- C07D333/62—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes 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 carbon atoms of the hetero ring
- C07D333/66—Nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D495/18—Bridged systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Electrodes Of Semiconductors (AREA)
- Enzymes And Modification Thereof (AREA)
- Bipolar Transistors (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Control Of El Displays (AREA)
- Indole Compounds (AREA)
Applications Claiming Priority (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DK0344/98 | 1998-03-12 | ||
| DK34498 | 1998-03-12 | ||
| DK0480/98 | 1998-04-03 | ||
| DK48098 | 1998-04-03 | ||
| DKPA199800938 | 1998-07-15 | ||
| DKPA199801385 | 1998-10-28 | ||
| DK199801612 | 1998-12-07 | ||
| DK199801385 | 1998-12-07 | ||
| DK199800938 | 1998-12-07 | ||
| DKPA199801612 | 1998-12-07 | ||
| PCT/DK1999/000121 WO1999046267A1 (en) | 1998-03-12 | 1999-03-11 | Modulators of protein tyrosine phosphatases (ptpases) |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2002506072A true JP2002506072A (ja) | 2002-02-26 |
| JP2002506072A5 JP2002506072A5 (enExample) | 2006-04-27 |
Family
ID=27512769
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000535645A Withdrawn JP2002506072A (ja) | 1998-03-12 | 1999-03-11 | プロテインチロシンホスファターゼ（ＰＴＰａｓｅ）のモジュレーター |
Country Status (13)
| Country | Link |
|---|---|
| EP (1) | EP1080095B1 (enExample) |
| JP (1) | JP2002506072A (enExample) |
| KR (1) | KR20010041814A (enExample) |
| CN (1) | CN1300291A (enExample) |
| AT (1) | ATE308546T1 (enExample) |
| AU (1) | AU2713599A (enExample) |
| BR (1) | BR9908726A (enExample) |
| CA (1) | CA2323493A1 (enExample) |
| DE (1) | DE69928100D1 (enExample) |
| HU (1) | HUP0104984A3 (enExample) |
| IL (1) | IL138319A0 (enExample) |
| NO (1) | NO20004527L (enExample) |
| PL (1) | PL342816A1 (enExample) |
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003103648A1 (ja) * | 2002-06-05 | 2003-12-18 | 株式会社医薬分子設計研究所 | 糖尿病治療薬 |
| WO2003103647A1 (ja) * | 2002-06-05 | 2003-12-18 | 株式会社医薬分子設計研究所 | Ａｐ−１及びｎｆａｔ活性化阻害剤 |
| JP2008500993A (ja) * | 2004-05-28 | 2008-01-17 | ニコメッド ゲゼルシャフト ミット ベシュレンクテル ハフツング | 新規のテトラヒドロピリドチオフェン |
| JP2008501768A (ja) * | 2004-06-11 | 2008-01-24 | ニコメッド ゲゼルシャフト ミット ベシュレンクテル ハフツング | 新規の化合物及びテトラヒドロピリドチオフェンの使用 |
| JP2008501668A (ja) * | 2004-06-04 | 2008-01-24 | ニコメッド ゲゼルシャフト ミット ベシュレンクテル ハフツング | 癌の治療に使用するためのテトラヒドロピリドチオフェン |
| JP2008529989A (ja) * | 2005-02-09 | 2008-08-07 | ニコメッド ゲゼルシャフト ミット ベシュレンクテル ハフツング | 癌のような増殖性の疾病の治療用のテトラヒドロピリドチオフェン |
| JP2008530053A (ja) * | 2005-02-11 | 2008-08-07 | ニコメッド ゲゼルシャフト ミット ベシュレンクテル ハフツング | 癌の治療のための抗増殖性剤としてのテトラヒドロピリドチオフェン |
| US7626042B2 (en) | 2002-06-06 | 2009-12-01 | Institute Of Medicinal Molecular Design, Inc. | O-substituted hydroxyaryl derivatives |
| US7700655B2 (en) | 2002-06-06 | 2010-04-20 | Institute Of Medicinal Molecular Design, Inc. | Antiallergic agents |
| US8097759B2 (en) | 2000-12-18 | 2012-01-17 | Institute Of Medicinal Molecular Design, Inc. | Inflammatory cytokine release inhibitor |
| JP2016505063A (ja) * | 2013-01-28 | 2016-02-18 | ハー・ルンドベック・アクチエゼルスカベット | ソルチリン阻害剤としてのｎ置換された５置換フタルアミド酸 |
| JP2016196497A (ja) * | 2009-12-04 | 2016-11-24 | スノビオン プハルマセウトイカルス インコーポレイテッド | 多環式化合物及びその使用方法 |
| JP2023522647A (ja) * | 2020-04-14 | 2023-05-31 | パーデュー・リサーチ・ファウンデーション | 新規なリンパ特異的チロシンホスファターゼ（ｌｙｐ）インヒビター |
| JP2023134749A (ja) * | 2019-05-21 | 2023-09-27 | 浙江海正薬業股▲ふん▼有限公司 | マクロライド誘導体、その製造方法および用途 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PT1773816E (pt) * | 2004-06-24 | 2015-04-29 | Vertex Pharma | Moduladores de transportadores de cassete de ligação de atp |
| AU2006290802B2 (en) * | 2005-09-15 | 2012-06-07 | F. Hoffmann-La Roche Ag | 4-amino-thieno[3,2-c]pyridine-7-carboxylic acid derivatives |
| CN1939922B (zh) * | 2005-09-27 | 2010-10-13 | 天津和美生物技术有限公司 | 可抑制细胞释放肿瘤坏死因子的5H-噻吩[3，4-c]吡咯-4，6-二酮衍生物 |
| CN102382076B (zh) * | 2010-09-03 | 2016-08-17 | 中国医学科学院药物研究所 | 芳酮和芳酰胺类化合物及其制法和药物用途 |
| CN102838625B (zh) * | 2011-06-22 | 2015-04-15 | 中国科学院上海药物研究所 | 四氢吡啶并噻唑类化合物、其制备方法、包含该化合物的药物组合物及其用途 |
| CN104788425A (zh) * | 2015-03-12 | 2015-07-22 | 佛山市赛维斯医药科技有限公司 | 一类含烟酸酰胺和哌啶结构ptp1b抑制剂、制备方法及其用途 |
| CN106748999A (zh) * | 2015-03-12 | 2017-05-31 | 佛山市赛维斯医药科技有限公司 | 一类含烟酸酰胺结构的ptp1b抑制剂、制备方法及其用途 |
| CN104788424A (zh) * | 2015-03-12 | 2015-07-22 | 佛山市赛维斯医药科技有限公司 | 含烟酸酰胺和哌啶结构的ptp1b抑制剂、制备方法及其用途 |
| CN106866523A (zh) * | 2015-03-12 | 2017-06-20 | 佛山市赛维斯医药科技有限公司 | 含烟酸酰胺结构的ptp1b抑制剂、制备方法及其用途 |
| CN104829629B (zh) * | 2015-03-26 | 2017-03-15 | 天津药物研究院有限公司 | 含磺酰胺基的四氢噻吩并[2,3‑c]吡啶衍生物、其制备方法和用途 |
| CA3032302A1 (en) | 2016-07-29 | 2018-02-01 | Taleen G. Hanania | Compounds and compositions and uses thereof |
| CN110087687A (zh) | 2016-07-29 | 2019-08-02 | 赛诺维信制药公司 | 化合物、组合物及其用途 |
| JP7146782B2 (ja) | 2017-02-16 | 2022-10-04 | サノビオン ファーマシューティカルズ インク | 統合失調症を処置する方法 |
| CN111183138A (zh) | 2017-08-02 | 2020-05-19 | 赛诺维信制药公司 | 异色满化合物以及用途 |
| KR102746817B1 (ko) | 2018-02-16 | 2024-12-24 | 스미토모 파마 아메리카, 인크. | 염, 결정 형태 및 이들의 제조 방법 |
| MX2021010880A (es) | 2019-03-14 | 2022-01-18 | Sunovion Pharmaceuticals Inc | Sales de un compuesto de isocromanilo y formas cristalinas, procesos de preparacion, usos terapeuticos y composiciones farmaceuticas de las mismas. |
| AU2021257786A1 (en) | 2020-04-14 | 2022-11-03 | Sunovion Pharmaceuticals Inc. | (S)-(4,5-dihydro-7H-thieno[2,3-c]pyran-7-yl)-N-methylmethanamine for treating neurological and psychiatric disorders |
-
1999
- 1999-03-11 JP JP2000535645A patent/JP2002506072A/ja not_active Withdrawn
- 1999-03-11 KR KR1020007010093A patent/KR20010041814A/ko not_active Withdrawn
- 1999-03-11 DE DE69928100T patent/DE69928100D1/de not_active Expired - Lifetime
- 1999-03-11 CN CN99806016A patent/CN1300291A/zh active Pending
- 1999-03-11 AT AT99907332T patent/ATE308546T1/de not_active IP Right Cessation
- 1999-03-11 PL PL99342816A patent/PL342816A1/xx not_active Application Discontinuation
- 1999-03-11 HU HU0104984A patent/HUP0104984A3/hu unknown
- 1999-03-11 IL IL13831999A patent/IL138319A0/xx unknown
- 1999-03-11 AU AU27135/99A patent/AU2713599A/en not_active Abandoned
- 1999-03-11 EP EP99907332A patent/EP1080095B1/en not_active Expired - Lifetime
- 1999-03-11 BR BR9908726-0A patent/BR9908726A/pt not_active IP Right Cessation
- 1999-03-11 CA CA002323493A patent/CA2323493A1/en not_active Abandoned
-
2000
- 2000-09-11 NO NO20004527A patent/NO20004527L/no unknown
Cited By (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8263657B2 (en) | 2000-12-18 | 2012-09-11 | Institute Of Medicinal Molecular Design, Inc. | Inhibitors against the production and release of inflammatory cytokines |
| US8097759B2 (en) | 2000-12-18 | 2012-01-17 | Institute Of Medicinal Molecular Design, Inc. | Inflammatory cytokine release inhibitor |
| WO2003103647A1 (ja) * | 2002-06-05 | 2003-12-18 | 株式会社医薬分子設計研究所 | Ａｐ−１及びｎｆａｔ活性化阻害剤 |
| EA008769B1 (ru) * | 2002-06-05 | 2007-08-31 | Инститьют Оф Медисинал Молекьюлар Дизайн. Инк. | Лекарственное средство для лечения диабета |
| WO2003103648A1 (ja) * | 2002-06-05 | 2003-12-18 | 株式会社医薬分子設計研究所 | 糖尿病治療薬 |
| EA009523B1 (ru) * | 2002-06-05 | 2008-02-28 | Инститьют Оф Медисинал Молекьюлар Дизайн. Инк. | Ингибиторы в отношении активации ар-1 и nfat |
| US7700655B2 (en) | 2002-06-06 | 2010-04-20 | Institute Of Medicinal Molecular Design, Inc. | Antiallergic agents |
| US7626042B2 (en) | 2002-06-06 | 2009-12-01 | Institute Of Medicinal Molecular Design, Inc. | O-substituted hydroxyaryl derivatives |
| JP2008500993A (ja) * | 2004-05-28 | 2008-01-17 | ニコメッド ゲゼルシャフト ミット ベシュレンクテル ハフツング | 新規のテトラヒドロピリドチオフェン |
| JP4881297B2 (ja) * | 2004-05-28 | 2012-02-22 | フォーエスシー アクチエンゲゼルシャフト | 新規のテトラヒドロピリドチオフェン |
| JP2008501668A (ja) * | 2004-06-04 | 2008-01-24 | ニコメッド ゲゼルシャフト ミット ベシュレンクテル ハフツング | 癌の治療に使用するためのテトラヒドロピリドチオフェン |
| JP2008501768A (ja) * | 2004-06-11 | 2008-01-24 | ニコメッド ゲゼルシャフト ミット ベシュレンクテル ハフツング | 新規の化合物及びテトラヒドロピリドチオフェンの使用 |
| JP2008529989A (ja) * | 2005-02-09 | 2008-08-07 | ニコメッド ゲゼルシャフト ミット ベシュレンクテル ハフツング | 癌のような増殖性の疾病の治療用のテトラヒドロピリドチオフェン |
| JP2008530053A (ja) * | 2005-02-11 | 2008-08-07 | ニコメッド ゲゼルシャフト ミット ベシュレンクテル ハフツング | 癌の治療のための抗増殖性剤としてのテトラヒドロピリドチオフェン |
| JP2016196497A (ja) * | 2009-12-04 | 2016-11-24 | スノビオン プハルマセウトイカルス インコーポレイテッド | 多環式化合物及びその使用方法 |
| JP2017031198A (ja) * | 2009-12-04 | 2017-02-09 | スノビオン プハルマセウトイカルス インコーポレイテッド | 多環式化合物及びその使用方法 |
| JP2016505063A (ja) * | 2013-01-28 | 2016-02-18 | ハー・ルンドベック・アクチエゼルスカベット | ソルチリン阻害剤としてのｎ置換された５置換フタルアミド酸 |
| US10195186B2 (en) | 2013-01-28 | 2019-02-05 | H. Lundbeck A/S | N-substituted-5-substituted phthalamic acids as sortilin inhibitors |
| JP2023134749A (ja) * | 2019-05-21 | 2023-09-27 | 浙江海正薬業股▲ふん▼有限公司 | マクロライド誘導体、その製造方法および用途 |
| JP7675136B2 (ja) | 2019-05-21 | 2025-05-12 | 浙江海正薬業股▲ふん▼有限公司 | マクロライド誘導体、その製造方法および用途 |
| US12410191B2 (en) | 2019-05-21 | 2025-09-09 | Zhejiang Hisun Pharmaceutical Co., Ltd. | Macrolide derivatives, preparation method and application thereof |
| JP2023522647A (ja) * | 2020-04-14 | 2023-05-31 | パーデュー・リサーチ・ファウンデーション | 新規なリンパ特異的チロシンホスファターゼ（ｌｙｐ）インヒビター |
Also Published As
| Publication number | Publication date |
|---|---|
| IL138319A0 (en) | 2001-10-31 |
| EP1080095A1 (en) | 2001-03-07 |
| HUP0104984A2 (hu) | 2002-04-29 |
| EP1080095B1 (en) | 2005-11-02 |
| KR20010041814A (ko) | 2001-05-25 |
| AU2713599A (en) | 1999-09-27 |
| HUP0104984A3 (en) | 2003-07-28 |
| ATE308546T1 (de) | 2005-11-15 |
| CA2323493A1 (en) | 1999-09-16 |
| NO20004527D0 (no) | 2000-09-11 |
| DE69928100D1 (de) | 2005-12-08 |
| PL342816A1 (en) | 2001-07-02 |
| NO20004527L (no) | 2000-11-07 |
| BR9908726A (pt) | 2000-11-21 |
| CN1300291A (zh) | 2001-06-20 |
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