CN102395567A - 在治疗糖尿病和肥胖症中用作的tgr5激动剂的三唑和咪唑衍生物 - Google Patents
在治疗糖尿病和肥胖症中用作的tgr5激动剂的三唑和咪唑衍生物 Download PDFInfo
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- CN102395567A CN102395567A CN2010800163259A CN201080016325A CN102395567A CN 102395567 A CN102395567 A CN 102395567A CN 2010800163259 A CN2010800163259 A CN 2010800163259A CN 201080016325 A CN201080016325 A CN 201080016325A CN 102395567 A CN102395567 A CN 102395567A
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- Prior art keywords
- fluorophenyl
- methyl
- alkyl
- imidazoles
- methylethyl
- Prior art date
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- 239000000556 agonist Substances 0.000 title claims abstract description 30
- 208000008589 Obesity Diseases 0.000 title claims description 10
- 235000020824 obesity Nutrition 0.000 title claims description 10
- 150000002460 imidazoles Chemical class 0.000 title description 8
- 150000003852 triazoles Chemical class 0.000 title description 5
- 206010012601 diabetes mellitus Diseases 0.000 title description 2
- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 title 1
- 229940042055 systemic antimycotics triazole derivative Drugs 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 415
- 150000003839 salts Chemical class 0.000 claims abstract description 112
- 239000003814 drug Substances 0.000 claims abstract description 32
- 201000010099 disease Diseases 0.000 claims abstract description 23
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 23
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 386
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 386
- -1 methoxyl group Chemical group 0.000 claims description 369
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims description 330
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 328
- 125000004646 sulfenyl group Chemical group S(*)* 0.000 claims description 325
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 323
- 229910052736 halogen Inorganic materials 0.000 claims description 242
- 150000002367 halogens Chemical class 0.000 claims description 224
- 229910052739 hydrogen Inorganic materials 0.000 claims description 192
- 239000001257 hydrogen Substances 0.000 claims description 192
- 229910052757 nitrogen Inorganic materials 0.000 claims description 168
- 125000000217 alkyl group Chemical group 0.000 claims description 166
- 229910052799 carbon Inorganic materials 0.000 claims description 161
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 155
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 128
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 127
- 125000001072 heteroaryl group Chemical group 0.000 claims description 121
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 113
- 229910052760 oxygen Inorganic materials 0.000 claims description 78
- 239000001301 oxygen Substances 0.000 claims description 69
- XLJMAIOERFSOGZ-UHFFFAOYSA-N cyanic acid Chemical compound OC#N XLJMAIOERFSOGZ-UHFFFAOYSA-N 0.000 claims description 63
- 238000000034 method Methods 0.000 claims description 62
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 58
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 56
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 48
- 125000003118 aryl group Chemical group 0.000 claims description 47
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims description 41
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 38
- 125000004122 cyclic group Chemical group 0.000 claims description 38
- 229910052731 fluorine Inorganic materials 0.000 claims description 38
- 239000011737 fluorine Substances 0.000 claims description 37
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 36
- ZRALSGWEFCBTJO-UHFFFAOYSA-N anhydrous guanidine Natural products NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims description 35
- 125000004193 piperazinyl group Chemical group 0.000 claims description 35
- 125000004076 pyridyl group Chemical group 0.000 claims description 30
- 150000002431 hydrogen Chemical group 0.000 claims description 29
- 125000002757 morpholinyl group Chemical group 0.000 claims description 27
- 125000005936 piperidyl group Chemical group 0.000 claims description 27
- 239000000460 chlorine Substances 0.000 claims description 25
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 23
- 150000003053 piperidines Chemical class 0.000 claims description 23
- 125000005037 alkyl phenyl group Chemical group 0.000 claims description 22
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 21
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 claims description 20
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 20
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 claims description 20
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 19
- 229910052801 chlorine Inorganic materials 0.000 claims description 17
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 16
- 239000000126 substance Substances 0.000 claims description 15
- MXNBDFWNYRNIBH-UHFFFAOYSA-N 3-fluorobenzoic acid Chemical compound OC(=O)C1=CC=CC(F)=C1 MXNBDFWNYRNIBH-UHFFFAOYSA-N 0.000 claims description 14
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 14
- 125000005493 quinolyl group Chemical group 0.000 claims description 13
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 12
- 125000004366 heterocycloalkenyl group Chemical group 0.000 claims description 12
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 10
- 125000003545 alkoxy group Chemical group 0.000 claims description 10
- CCIVGXIOQKPBKL-UHFFFAOYSA-N ethanesulfonic acid Chemical compound CCS(O)(=O)=O CCIVGXIOQKPBKL-UHFFFAOYSA-N 0.000 claims description 10
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 9
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 9
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 8
- DTHNMHAUYICORS-KTKZVXAJSA-N Glucagon-like peptide 1 Chemical compound C([C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](CCCNC(N)=N)C(N)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC=1N=CNC=1)[C@@H](C)O)[C@@H](C)O)C(C)C)C1=CC=CC=C1 DTHNMHAUYICORS-KTKZVXAJSA-N 0.000 claims description 8
- 239000000843 powder Substances 0.000 claims description 8
- 102220065736 rs543286136 Human genes 0.000 claims description 8
- 229940124530 sulfonamide Drugs 0.000 claims description 8
- VEUMBMHMMCOFAG-UHFFFAOYSA-N 2,3-dihydrooxadiazole Chemical compound N1NC=CO1 VEUMBMHMMCOFAG-UHFFFAOYSA-N 0.000 claims description 7
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 7
- AHLPHDHHMVZTML-BYPYZUCNSA-N L-Ornithine Chemical compound NCCC[C@H](N)C(O)=O AHLPHDHHMVZTML-BYPYZUCNSA-N 0.000 claims description 7
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 7
- 230000003178 anti-diabetic effect Effects 0.000 claims description 7
- 239000003472 antidiabetic agent Substances 0.000 claims description 7
- 239000008103 glucose Substances 0.000 claims description 7
- 125000005843 halogen group Chemical group 0.000 claims description 7
- 125000002883 imidazolyl group Chemical group 0.000 claims description 7
- 125000002971 oxazolyl group Chemical group 0.000 claims description 7
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 7
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 7
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 claims description 7
- 230000028327 secretion Effects 0.000 claims description 7
- 125000000335 thiazolyl group Chemical group 0.000 claims description 7
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims description 7
- LYLMVTXRPNLJMI-UHFFFAOYSA-N 2,3,4a,8a-tetrahydro-1,4-benzodioxine Chemical compound C1=CC=CC2OCCOC21 LYLMVTXRPNLJMI-UHFFFAOYSA-N 0.000 claims description 6
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims description 6
- 125000005605 benzo group Chemical group 0.000 claims description 6
- 125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 claims description 6
- 230000001965 increasing effect Effects 0.000 claims description 6
- 125000004043 oxo group Chemical group O=* 0.000 claims description 6
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 6
- BBVIDBNAYOIXOE-UHFFFAOYSA-N 1,2,4-oxadiazole Chemical compound C=1N=CON=1 BBVIDBNAYOIXOE-UHFFFAOYSA-N 0.000 claims description 5
- RZQQXRVPPOOCQR-UHFFFAOYSA-N 2,3-dihydro-1,3,4-oxadiazole Chemical compound C1NN=CO1 RZQQXRVPPOOCQR-UHFFFAOYSA-N 0.000 claims description 5
- 230000015572 biosynthetic process Effects 0.000 claims description 5
- 210000004369 blood Anatomy 0.000 claims description 5
- 239000008280 blood Substances 0.000 claims description 5
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 5
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims description 5
- 108010067722 Dipeptidyl Peptidase 4 Proteins 0.000 claims description 4
- 102100025012 Dipeptidyl peptidase 4 Human genes 0.000 claims description 4
- 108010088406 Glucagon-Like Peptides Proteins 0.000 claims description 4
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 4
- AHLPHDHHMVZTML-UHFFFAOYSA-N Orn-delta-NH2 Natural products NCCCC(N)C(O)=O AHLPHDHHMVZTML-UHFFFAOYSA-N 0.000 claims description 4
- 230000003914 insulin secretion Effects 0.000 claims description 4
- 229960003104 ornithine Drugs 0.000 claims description 4
- HSINOMROUCMIEA-FGVHQWLLSA-N (2s,4r)-4-[(3r,5s,6r,7r,8s,9s,10s,13r,14s,17r)-6-ethyl-3,7-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl]-2-methylpentanoic acid Chemical compound C([C@@]12C)C[C@@H](O)C[C@H]1[C@@H](CC)[C@@H](O)[C@@H]1[C@@H]2CC[C@]2(C)[C@@H]([C@H](C)C[C@H](C)C(O)=O)CC[C@H]21 HSINOMROUCMIEA-FGVHQWLLSA-N 0.000 claims description 3
- QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 claims description 3
- 208000031226 Hyperlipidaemia Diseases 0.000 claims description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 3
- 229940100389 Sulfonylurea Drugs 0.000 claims description 3
- 230000003143 atherosclerotic effect Effects 0.000 claims description 3
- 239000003613 bile acid Substances 0.000 claims description 3
- FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 claims description 3
- YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 claims description 3
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 2
- SWLAMJPTOQZTAE-UHFFFAOYSA-N 4-[2-[(5-chloro-2-methoxybenzoyl)amino]ethyl]benzoic acid Chemical compound COC1=CC=C(Cl)C=C1C(=O)NCCC1=CC=C(C(O)=O)C=C1 SWLAMJPTOQZTAE-UHFFFAOYSA-N 0.000 claims description 2
- 229940077274 Alpha glucosidase inhibitor Drugs 0.000 claims description 2
- 229940123208 Biguanide Drugs 0.000 claims description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 2
- 239000003888 alpha glucosidase inhibitor Substances 0.000 claims description 2
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 claims description 2
- 150000004283 biguanides Chemical class 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- QDPMLKBAQOZXEF-UHFFFAOYSA-N ethanesulfonic acid;sodium Chemical compound [Na].CCS(O)(=O)=O QDPMLKBAQOZXEF-UHFFFAOYSA-N 0.000 claims description 2
- 230000000763 evoking effect Effects 0.000 claims description 2
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 claims description 2
- 229950004994 meglitinide Drugs 0.000 claims description 2
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 239000002512 suppressor factor Substances 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 claims 43
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 35
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 33
- KJUGUADJHNHALS-UHFFFAOYSA-N 1H-tetrazole Chemical compound C=1N=NNN=1 KJUGUADJHNHALS-UHFFFAOYSA-N 0.000 claims 25
- 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims 6
- RAXXELZNTBOGNW-UHFFFAOYSA-N 1H-imidazole Chemical class C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims 5
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims 5
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 5
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 claims 4
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims 4
- PVOAHINGSUIXLS-UHFFFAOYSA-N 1-Methylpiperazine Chemical compound CN1CCNCC1 PVOAHINGSUIXLS-UHFFFAOYSA-N 0.000 claims 3
- XIGPZJPFILCQSC-UHFFFAOYSA-N 2-fluoro-n-hydroxybenzamide Chemical class ONC(=O)C1=CC=CC=C1F XIGPZJPFILCQSC-UHFFFAOYSA-N 0.000 claims 3
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 claims 3
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims 3
- 235000013905 glycine and its sodium salt Nutrition 0.000 claims 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 2
- ZPQOPVIELGIULI-UHFFFAOYSA-N 1,3-dichlorobenzene Chemical compound ClC1=CC=CC(Cl)=C1 ZPQOPVIELGIULI-UHFFFAOYSA-N 0.000 claims 2
- KGGHWIKBOIQEAJ-UHFFFAOYSA-N 2-fluorobenzamide Chemical compound NC(=O)C1=CC=CC=C1F KGGHWIKBOIQEAJ-UHFFFAOYSA-N 0.000 claims 2
- NSTREUWFTAOOKS-UHFFFAOYSA-N 2-fluorobenzoic acid Chemical compound OC(=O)C1=CC=CC=C1F NSTREUWFTAOOKS-UHFFFAOYSA-N 0.000 claims 2
- YPIGHNIIXYSPKF-UHFFFAOYSA-N 3-fluorobenzamide Chemical compound NC(=O)C1=CC=CC(F)=C1 YPIGHNIIXYSPKF-UHFFFAOYSA-N 0.000 claims 2
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims 2
- AGYPSGLKNHWXBF-UHFFFAOYSA-N CCN(CC)CC[O] Chemical compound CCN(CC)CC[O] AGYPSGLKNHWXBF-UHFFFAOYSA-N 0.000 claims 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims 2
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- SVDVKEBISAOWJT-UHFFFAOYSA-N n-methylbenzenesulfonamide Chemical compound CNS(=O)(=O)C1=CC=CC=C1 SVDVKEBISAOWJT-UHFFFAOYSA-N 0.000 claims 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N perisophthalic acid Natural products OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims 2
- KKKSMWMXKUAZHK-UHFFFAOYSA-N 1-(4-fluorophenyl)imidazole Chemical class C1=CC(F)=CC=C1N1C=NC=C1 KKKSMWMXKUAZHK-UHFFFAOYSA-N 0.000 claims 1
- PTHLPYKPCQLAOF-UHFFFAOYSA-N 2,4-difluorobenzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=C(F)C=C1F PTHLPYKPCQLAOF-UHFFFAOYSA-N 0.000 claims 1
- BWGBFGHHNMRFRM-UHFFFAOYSA-N 2-[(2-chloro-6-fluorophenyl)methylsulfanyl]-1-(4-fluorophenyl)-5-[2-(4-fluorophenyl)propan-2-yl]imidazole Chemical class C=1C=C(F)C=CC=1C(C)(C)C(N1C=2C=CC(F)=CC=2)=CN=C1SCC1=C(F)C=CC=C1Cl BWGBFGHHNMRFRM-UHFFFAOYSA-N 0.000 claims 1
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- XFCSOLIKYAGPSP-UHFFFAOYSA-N 2-[(2-chloro-6-fluorophenyl)methylsulfanyl]-5-[2-(4-chloro-2-fluorophenyl)propan-2-yl]-1-(4-fluorophenyl)imidazole Chemical class C=1C=C(Cl)C=C(F)C=1C(C)(C)C(N1C=2C=CC(F)=CC=2)=CN=C1SCC1=C(F)C=CC=C1Cl XFCSOLIKYAGPSP-UHFFFAOYSA-N 0.000 claims 1
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- QZVQQUVWFIZUBQ-UHFFFAOYSA-N 3-fluoroaniline Chemical compound NC1=CC=CC(F)=C1 QZVQQUVWFIZUBQ-UHFFFAOYSA-N 0.000 claims 1
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- RNOVGJWJVRESAA-UHFFFAOYSA-N 4-fluoro-2-(trifluoromethyl)phenol Chemical group OC1=CC=C(F)C=C1C(F)(F)F RNOVGJWJVRESAA-UHFFFAOYSA-N 0.000 claims 1
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims 1
- 102100025101 GATA-type zinc finger protein 1 Human genes 0.000 claims 1
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- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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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- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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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Applications Claiming Priority (5)
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| US61/284,139 | 2009-12-11 | ||
| PCT/US2010/023981 WO2010093845A1 (en) | 2009-02-12 | 2010-02-12 | Triazole and imidazole derivatives for use as tgr5 agonists in the treatment of diabetes and obesity |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN102781922A (zh) * | 2009-12-11 | 2012-11-14 | 埃克塞利希斯股份有限公司 | Tgr5激动剂 |
| CN103755652A (zh) * | 2013-12-20 | 2014-04-30 | 陕西理工学院 | 一种磺酰胺类化合物及其应用 |
| CN103864754A (zh) * | 2012-12-10 | 2014-06-18 | 中国科学院上海药物研究所 | 五元唑类杂环化合物及其制备方法、药物组合物和用途 |
| CN104987312A (zh) * | 2015-07-13 | 2015-10-21 | 佛山市赛维斯医药科技有限公司 | 一类胺基苯三氮唑亚砜类11β-HSD1抑制剂及其用途 |
| CN104987313A (zh) * | 2015-07-13 | 2015-10-21 | 佛山市赛维斯医药科技有限公司 | 一类末端取代的三氮唑亚砜类化合物、其制备方法及其用途 |
| CN105001171A (zh) * | 2015-07-13 | 2015-10-28 | 佛山市赛维斯医药科技有限公司 | 一类硝基苯三氮唑亚砜类11β-HSD1抑制剂及其用途 |
| CN105017170A (zh) * | 2015-07-13 | 2015-11-04 | 佛山市赛维斯医药科技有限公司 | 一类腈基苯三氮唑亚砜类11β-HSD1抑制剂及其用途 |
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| WO2025162114A1 (zh) * | 2024-02-04 | 2025-08-07 | 成都麻沸散医药科技有限公司 | 一种杂环化合物及其用途 |
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| US11236055B2 (en) | 2016-07-01 | 2022-02-01 | Venenum Biodesign, LLC | Non-systemic TGR5 agonists |
| KR20220150270A (ko) | 2019-10-07 | 2022-11-10 | 칼리오페, 인크. | Gpr119 효능제 |
| JP7745559B2 (ja) | 2020-02-28 | 2025-09-29 | キャリーオペ,インク. | Gpr40アゴニスト |
| BR112022023359A2 (pt) | 2020-05-19 | 2023-04-18 | Kallyope Inc | Ativadores de ampk |
| JP2023531726A (ja) | 2020-06-26 | 2023-07-25 | キャリーオペ,インク. | Ampkアクチベーター |
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- 2010-02-12 KR KR1020117021128A patent/KR20110119790A/ko not_active Withdrawn
- 2010-02-12 US US13/148,811 patent/US8785488B2/en active Active
- 2010-02-12 CN CN2010800163259A patent/CN102395567A/zh active Pending
- 2010-02-12 EP EP10704701A patent/EP2396304A1/en not_active Withdrawn
- 2010-02-12 WO PCT/US2010/023981 patent/WO2010093845A1/en not_active Ceased
- 2010-02-12 TW TW099104908A patent/TW201040168A/zh unknown
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Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102781922A (zh) * | 2009-12-11 | 2012-11-14 | 埃克塞利希斯股份有限公司 | Tgr5激动剂 |
| CN103864754A (zh) * | 2012-12-10 | 2014-06-18 | 中国科学院上海药物研究所 | 五元唑类杂环化合物及其制备方法、药物组合物和用途 |
| CN103864754B (zh) * | 2012-12-10 | 2016-12-21 | 中国科学院上海药物研究所 | 五元唑类杂环化合物及其制备方法、药物组合物和用途 |
| CN103755652A (zh) * | 2013-12-20 | 2014-04-30 | 陕西理工学院 | 一种磺酰胺类化合物及其应用 |
| CN105017170A (zh) * | 2015-07-13 | 2015-11-04 | 佛山市赛维斯医药科技有限公司 | 一类腈基苯三氮唑亚砜类11β-HSD1抑制剂及其用途 |
| CN105001171A (zh) * | 2015-07-13 | 2015-10-28 | 佛山市赛维斯医药科技有限公司 | 一类硝基苯三氮唑亚砜类11β-HSD1抑制剂及其用途 |
| CN104987313A (zh) * | 2015-07-13 | 2015-10-21 | 佛山市赛维斯医药科技有限公司 | 一类末端取代的三氮唑亚砜类化合物、其制备方法及其用途 |
| CN104987312A (zh) * | 2015-07-13 | 2015-10-21 | 佛山市赛维斯医药科技有限公司 | 一类胺基苯三氮唑亚砜类11β-HSD1抑制剂及其用途 |
| CN106432222A (zh) * | 2016-09-19 | 2017-02-22 | 丹诺医药(苏州)有限公司 | 8‑氯‑1‑环丙基‑7‑氟‑9‑甲基‑4‑氧‑4‑氢‑喹嗪‑3‑羧酸酯及其制备方法 |
| CN111039880A (zh) * | 2019-12-10 | 2020-04-21 | 河南大学 | 咪康唑及其衍生物作为tgr5激动剂的应用 |
| CN111039880B (zh) * | 2019-12-10 | 2022-06-21 | 河南大学 | 咪康唑及其衍生物作为tgr5激动剂的应用 |
| CN111763173A (zh) * | 2020-07-14 | 2020-10-13 | 河南大学 | 苯乙基咪唑类衍生物及其用途 |
| CN111763173B (zh) * | 2020-07-14 | 2022-11-01 | 河南大学 | 苯乙基咪唑类衍生物及其用途 |
| WO2025162114A1 (zh) * | 2024-02-04 | 2025-08-07 | 成都麻沸散医药科技有限公司 | 一种杂环化合物及其用途 |
Also Published As
| Publication number | Publication date |
|---|---|
| US20120040985A1 (en) | 2012-02-16 |
| EP2396304A1 (en) | 2011-12-21 |
| JP2012517479A (ja) | 2012-08-02 |
| KR20110119790A (ko) | 2011-11-02 |
| WO2010093845A1 (en) | 2010-08-19 |
| JP2014240421A (ja) | 2014-12-25 |
| AR075255A1 (es) | 2011-03-16 |
| US8785488B2 (en) | 2014-07-22 |
| TW201040168A (en) | 2010-11-16 |
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