CN1972932B - 治疗血脂障碍的化合物 - Google Patents
治疗血脂障碍的化合物 Download PDFInfo
- Publication number
- CN1972932B CN1972932B CN2005800206855A CN200580020685A CN1972932B CN 1972932 B CN1972932 B CN 1972932B CN 2005800206855 A CN2005800206855 A CN 2005800206855A CN 200580020685 A CN200580020685 A CN 200580020685A CN 1972932 B CN1972932 B CN 1972932B
- Authority
- CN
- China
- Prior art keywords
- methyl
- trifluoromethyl
- amino
- benzyl
- tetrazol
- 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
- 0 C*C1(C)/C=C(\*)/C(/BrC)=C\C(C)/C=C1 Chemical compound C*C1(C)/C=C(\*)/C(/BrC)=C\C(C)/C=C1 0.000 description 13
- GTMFLRLAOYVQAO-QFIPXVFZSA-N CC(C)(C)OC(N(CCC1)c2cc(C(F)(F)F)c(C)cc2[C@H]1N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](CCN)nn1)=O Chemical compound CC(C)(C)OC(N(CCC1)c2cc(C(F)(F)F)c(C)cc2[C@H]1N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](CCN)nn1)=O GTMFLRLAOYVQAO-QFIPXVFZSA-N 0.000 description 1
- FJPOLBMQNVNQJC-DEOSSOPVSA-N CC(C)(COC(N(CCC1)c2cc(CCC3)c3cc2[C@H]1N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](C)nn1)=O)C(OC)=O Chemical compound CC(C)(COC(N(CCC1)c2cc(CCC3)c3cc2[C@H]1N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](C)nn1)=O)C(OC)=O FJPOLBMQNVNQJC-DEOSSOPVSA-N 0.000 description 1
- CGMBVYQVWCBALY-QHCPKHFHSA-N CC(C)(COC(N(CCC[C@@H]1N(Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)c2n[n](C)nn2)c2c1cc(CCC1)c1c2)=O)C(O)=O Chemical compound CC(C)(COC(N(CCC[C@@H]1N(Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)c2n[n](C)nn2)c2c1cc(CCC1)c1c2)=O)C(O)=O CGMBVYQVWCBALY-QHCPKHFHSA-N 0.000 description 1
- JGYFOQYFSSXJHV-QFIPXVFZSA-N CC(C)OC(N(CCC1)c2c(C)c(C)ccc2[C@H]1N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](C)nn1)=O Chemical compound CC(C)OC(N(CCC1)c2c(C)c(C)ccc2[C@H]1N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](C)nn1)=O JGYFOQYFSSXJHV-QFIPXVFZSA-N 0.000 description 1
- VEQZWFVXCJHUEW-UHFFFAOYSA-N CC(C)OC(N(CCC1C(OC)=O)c(cc(C(F)(F)F)c(C)c2)c2C1=O)=O Chemical compound CC(C)OC(N(CCC1C(OC)=O)c(cc(C(F)(F)F)c(C)c2)c2C1=O)=O VEQZWFVXCJHUEW-UHFFFAOYSA-N 0.000 description 1
- TWZSFFPBIBKNSV-UHFFFAOYSA-N CC(C)OC(N(CCCC(OC)=O)c(cc(C(F)(F)F)c(C)c1)c1C(OC)=O)=O Chemical compound CC(C)OC(N(CCCC(OC)=O)c(cc(C(F)(F)F)c(C)c1)c1C(OC)=O)=O TWZSFFPBIBKNSV-UHFFFAOYSA-N 0.000 description 1
- ARZNWWVPDDKBOQ-UHFFFAOYSA-O CC(C)OC(N(CCCC1N(Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)C(N=N)=N[NH3+])c2c1cc(CCC1)c1c2)=O Chemical compound CC(C)OC(N(CCCC1N(Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)C(N=N)=N[NH3+])c2c1cc(CCC1)c1c2)=O ARZNWWVPDDKBOQ-UHFFFAOYSA-O 0.000 description 1
- DTQNRMJODCXFGA-UHFFFAOYSA-N CC(C)OC(N(CCCC1N(Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)c2cc(C)n[s]2)c(cc2)c1cc2Br)=O Chemical compound CC(C)OC(N(CCCC1N(Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)c2cc(C)n[s]2)c(cc2)c1cc2Br)=O DTQNRMJODCXFGA-UHFFFAOYSA-N 0.000 description 1
- GHRWPOKXBMVDOA-UHFFFAOYSA-N CC(C)OC(N(CCCC1N(Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)c2cnccc2)c2c1cc(C)c(C(F)(F)F)c2)=O Chemical compound CC(C)OC(N(CCCC1N(Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)c2cnccc2)c2c1cc(C)c(C(F)(F)F)c2)=O GHRWPOKXBMVDOA-UHFFFAOYSA-N 0.000 description 1
- SZORBTAHPSPZCJ-UHFFFAOYSA-N CC(C)OC(N(CCCC1N(Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)c2n[n](C)nn2)c(cc2O3)c1cc2OC3(F)F)=O Chemical compound CC(C)OC(N(CCCC1N(Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)c2n[n](C)nn2)c(cc2O3)c1cc2OC3(F)F)=O SZORBTAHPSPZCJ-UHFFFAOYSA-N 0.000 description 1
- CGWUGJUZBGSIHZ-UHFFFAOYSA-N CCC(CC)OC(N(CCCC1N(Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)c2n[n](C)nn2)c2c1cc(CC)c(C(F)(F)F)c2)=O Chemical compound CCC(CC)OC(N(CCCC1N(Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)c2n[n](C)nn2)c2c1cc(CC)c(C(F)(F)F)c2)=O CGWUGJUZBGSIHZ-UHFFFAOYSA-N 0.000 description 1
- NWGDHKBYLDOBGH-QFIPXVFZSA-N CCCc(c(C)c1)cc2c1NCCC[C@@H]2N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](C)nn1 Chemical compound CCCc(c(C)c1)cc2c1NCCC[C@@H]2N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](C)nn1 NWGDHKBYLDOBGH-QFIPXVFZSA-N 0.000 description 1
- GBFATWBODAFVEU-FQEVSTJZSA-N CCOC(N(CCC1)c2cc(C(F)(F)F)c(C)cc2[C@H]1N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](C)nn1)=O Chemical compound CCOC(N(CCC1)c2cc(C(F)(F)F)c(C)cc2[C@H]1N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](C)nn1)=O GBFATWBODAFVEU-FQEVSTJZSA-N 0.000 description 1
- RDYNVFQNJQZUJZ-QFIPXVFZSA-N CCc(c(C(F)(F)F)c1)cc([C@H](CCC2)N(Cc3cc(C(F)(F)F)cc(C(F)(F)F)c3)c3n[n](C)nn3)c1N2C(OC(C)(C)C)=O Chemical compound CCc(c(C(F)(F)F)c1)cc([C@H](CCC2)N(Cc3cc(C(F)(F)F)cc(C(F)(F)F)c3)c3n[n](C)nn3)c1N2C(OC(C)(C)C)=O RDYNVFQNJQZUJZ-QFIPXVFZSA-N 0.000 description 1
- GKWYYGFMKORQEF-UHFFFAOYSA-N CCc(c(C=C)ccc1C(CCC2)N(Cc3cc(C(F)(F)F)cc(C(F)(F)F)c3)c3nnn[nH]3)c1N2C(OC(C)C)=O Chemical compound CCc(c(C=C)ccc1C(CCC2)N(Cc3cc(C(F)(F)F)cc(C(F)(F)F)c3)c3nnn[nH]3)c1N2C(OC(C)C)=O GKWYYGFMKORQEF-UHFFFAOYSA-N 0.000 description 1
- ZLTYICYLXQHWMJ-QHCPKHFHSA-N Cc(c(C(F)(F)F)c1)cc([C@H](CCC2)N(Cc3cc(C(F)(F)F)cc(C(F)(F)F)c3)c3n[n](C)nn3)c1N2C1CCOCC1 Chemical compound Cc(c(C(F)(F)F)c1)cc([C@H](CCC2)N(Cc3cc(C(F)(F)F)cc(C(F)(F)F)c3)c3n[n](C)nn3)c1N2C1CCOCC1 ZLTYICYLXQHWMJ-QHCPKHFHSA-N 0.000 description 1
- WQZRSLLOECZVHP-UHFFFAOYSA-N Cc(c(C(F)(F)F)c1)cc2c1N(CC1CCC(CC(O)=O)CC1)CCCC2N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](C)nn1 Chemical compound Cc(c(C(F)(F)F)c1)cc2c1N(CC1CCC(CC(O)=O)CC1)CCCC2N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](C)nn1 WQZRSLLOECZVHP-UHFFFAOYSA-N 0.000 description 1
- SRFXVZWSOCQNBP-DEOSSOPVSA-N Cc(c(C(F)(F)F)c1)cc2c1N(Cc(cc1)cc(C(O)=O)c1O)CCC[C@@H]2N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](C)nn1 Chemical compound Cc(c(C(F)(F)F)c1)cc2c1N(Cc(cc1)cc(C(O)=O)c1O)CCC[C@@H]2N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](C)nn1 SRFXVZWSOCQNBP-DEOSSOPVSA-N 0.000 description 1
- ACISOKYCNZUABL-SANMLTNESA-N Cc(c(C(F)(F)F)c1)cc2c1N(Cc(cc1C(OC)=O)ccc1F)CCC[C@@H]2N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](C)nn1 Chemical compound Cc(c(C(F)(F)F)c1)cc2c1N(Cc(cc1C(OC)=O)ccc1F)CCC[C@@H]2N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](C)nn1 ACISOKYCNZUABL-SANMLTNESA-N 0.000 description 1
- ZEYHGPUSGRMNKV-DEOSSOPVSA-N Cc(c(C(F)(F)F)c1)cc2c1N(Cc1ccncc1)CCC[C@@H]2N(Cc1cc(F)cc(C(F)(F)F)c1)c1n[n](C)nn1 Chemical compound Cc(c(C(F)(F)F)c1)cc2c1N(Cc1ccncc1)CCC[C@@H]2N(Cc1cc(F)cc(C(F)(F)F)c1)c1n[n](C)nn1 ZEYHGPUSGRMNKV-DEOSSOPVSA-N 0.000 description 1
- RQSXYGCBBWGSBC-UHFFFAOYSA-N Cc(c(C(F)(F)F)c1)cc2c1NCCCC2=O Chemical compound Cc(c(C(F)(F)F)c1)cc2c1NCCCC2=O RQSXYGCBBWGSBC-UHFFFAOYSA-N 0.000 description 1
- UXCIROVQYOROEA-UHFFFAOYSA-N Cc(c(C(F)(F)F)c1)cc2c1NCCCC2N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1nnn[nH]1 Chemical compound Cc(c(C(F)(F)F)c1)cc2c1NCCCC2N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1nnn[nH]1 UXCIROVQYOROEA-UHFFFAOYSA-N 0.000 description 1
- IWCOOKGAHXZJEU-SANMLTNESA-N Cc(c(C)c1)cc2c1N(Cc1cc(C(OC)=O)cnc1)CCC[C@@H]2N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](C)nn1 Chemical compound Cc(c(C)c1)cc2c1N(Cc1cc(C(OC)=O)cnc1)CCC[C@@H]2N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](C)nn1 IWCOOKGAHXZJEU-SANMLTNESA-N 0.000 description 1
- USRZCBARXDVXGB-DEOSSOPVSA-N Cc(c(COC1)c1cc12)c1N(CC1CC1)CCC[C@@H]2N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](C)nn1 Chemical compound Cc(c(COC1)c1cc12)c1N(CC1CC1)CCC[C@@H]2N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](C)nn1 USRZCBARXDVXGB-DEOSSOPVSA-N 0.000 description 1
- KKVPMMLGMOAIIX-DEOSSOPVSA-N Cc(c(COC1)c1cc12)c1N(Cc1ccc(C(O)=O)[s]1)CCC[C@@H]2N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](C)nn1 Chemical compound Cc(c(COC1)c1cc12)c1N(Cc1ccc(C(O)=O)[s]1)CCC[C@@H]2N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](C)nn1 KKVPMMLGMOAIIX-DEOSSOPVSA-N 0.000 description 1
- LPPKALAMFHYYAT-DEOSSOPVSA-N Cc(cc12)c(C(F)(F)F)c(C)c1N(CC1CCCC1)CCC[C@@H]2N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](C)nn1 Chemical compound Cc(cc12)c(C(F)(F)F)c(C)c1N(CC1CCCC1)CCC[C@@H]2N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](C)nn1 LPPKALAMFHYYAT-DEOSSOPVSA-N 0.000 description 1
- HKMWSJOWJARKII-DEOSSOPVSA-N Cc(cc12)c(C(F)(F)F)c(C)c1N(Cc1ccncc1)CCC[C@@H]2N(Cc1cc(C(F)(F)F)cc(Cl)c1)c1n[n](C)nn1 Chemical compound Cc(cc12)c(C(F)(F)F)c(C)c1N(Cc1ccncc1)CCC[C@@H]2N(Cc1cc(C(F)(F)F)cc(Cl)c1)c1n[n](C)nn1 HKMWSJOWJARKII-DEOSSOPVSA-N 0.000 description 1
- LLJTWUUUVZUQEP-LJAQVGFWSA-N Cc(cc12)c(C(F)(F)F)cc1N(CC1CC1)CCC[C@@H]2N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](CCN(C(c2ccccc22)=O)C2=O)nn1 Chemical compound Cc(cc12)c(C(F)(F)F)cc1N(CC1CC1)CCC[C@@H]2N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](CCN(C(c2ccccc22)=O)C2=O)nn1 LLJTWUUUVZUQEP-LJAQVGFWSA-N 0.000 description 1
- JVHSSSVASVBZGF-QHCPKHFHSA-N Cc(cc12)c(C(F)(F)F)cc1N(CC1CC1)CCC[C@@H]2N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](CCN)nn1 Chemical compound Cc(cc12)c(C(F)(F)F)cc1N(CC1CC1)CCC[C@@H]2N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1n[n](CCN)nn1 JVHSSSVASVBZGF-QHCPKHFHSA-N 0.000 description 1
- WDCSMQJHCMCCMO-MRNPHLECSA-N Cc(cc12)c(C(F)(F)F)cc1N(CCO)CCC[C@@H]2N(CC(CC(C(F)(F)F)=C1)C=C1[N](F)(F)F)c1n[n](CCN)nn1 Chemical compound Cc(cc12)c(C(F)(F)F)cc1N(CCO)CCC[C@@H]2N(CC(CC(C(F)(F)F)=C1)C=C1[N](F)(F)F)c1n[n](CCN)nn1 WDCSMQJHCMCCMO-MRNPHLECSA-N 0.000 description 1
- RISSTXRFPZVNIW-UHFFFAOYSA-N Cc1c(CCC2)c2cc(C(OC)=O)c1N Chemical compound Cc1c(CCC2)c2cc(C(OC)=O)c1N RISSTXRFPZVNIW-UHFFFAOYSA-N 0.000 description 1
- QBPJNYAKHMOPHZ-UHFFFAOYSA-N Cc1n[o]c(N(Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)C2c(cc(C)c(C(F)(F)F)c3)c3NCCC2)c1 Chemical compound Cc1n[o]c(N(Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)C2c(cc(C)c(C(F)(F)F)c3)c3NCCC2)c1 QBPJNYAKHMOPHZ-UHFFFAOYSA-N 0.000 description 1
- BRPWZGZBDZUXCA-TUNMPCEVSA-N Cc1n[o]c(N(Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)C2c3cc(C)c(C(F)(F)F)cc3N(C[C@H]3CC[C@H](CC(O)=O)CC3)CCC2)c1 Chemical compound Cc1n[o]c(N(Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)C2c3cc(C)c(C(F)(F)F)cc3N(C[C@H]3CC[C@H](CC(O)=O)CC3)CCC2)c1 BRPWZGZBDZUXCA-TUNMPCEVSA-N 0.000 description 1
- JWRYZTSUCVVUOS-QFIPXVFZSA-N NCC[n]1nnc(N(Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)[C@@H]2c3cc(COC4)c4cc3N(CCC(F)(F)F)CCC2)n1 Chemical compound NCC[n]1nnc(N(Cc2cc(C(F)(F)F)cc(C(F)(F)F)c2)[C@@H]2c3cc(COC4)c4cc3N(CCC(F)(F)F)CCC2)n1 JWRYZTSUCVVUOS-QFIPXVFZSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D403/02—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 two hetero rings
- C07D403/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen 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
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Cardiology (AREA)
- Diabetes (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US58270804P | 2004-06-24 | 2004-06-24 | |
| US60/582,708 | 2004-06-24 | ||
| US62724104P | 2004-11-12 | 2004-11-12 | |
| US60/627,241 | 2004-11-12 | ||
| US66486205P | 2005-03-24 | 2005-03-24 | |
| US60/664,862 | 2005-03-24 | ||
| PCT/US2005/022389 WO2006002342A1 (en) | 2004-06-24 | 2005-06-23 | Compounds and methods for treating dyslipidemia |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1972932A CN1972932A (zh) | 2007-05-30 |
| CN1972932B true CN1972932B (zh) | 2011-06-29 |
Family
ID=35056992
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2005800206855A Expired - Fee Related CN1972932B (zh) | 2004-06-24 | 2005-06-23 | 治疗血脂障碍的化合物 |
Country Status (26)
| Country | Link |
|---|---|
| US (3) | US20080269284A1 (enExample) |
| EP (3) | EP1761521A1 (enExample) |
| JP (2) | JP2008504266A (enExample) |
| KR (1) | KR20070041452A (enExample) |
| CN (1) | CN1972932B (enExample) |
| AT (1) | ATE528304T1 (enExample) |
| AU (2) | AU2005267436A1 (enExample) |
| BR (2) | BRPI0512523A (enExample) |
| CA (2) | CA2570688A1 (enExample) |
| CR (1) | CR8831A (enExample) |
| CY (1) | CY1112124T1 (enExample) |
| DK (1) | DK1761522T3 (enExample) |
| EA (2) | EA200700119A1 (enExample) |
| EC (2) | ECSP067095A (enExample) |
| ES (1) | ES2372291T3 (enExample) |
| HR (1) | HRP20110761T1 (enExample) |
| IL (2) | IL180276A0 (enExample) |
| MA (2) | MA28729B1 (enExample) |
| MX (2) | MXPA06014716A (enExample) |
| NO (2) | NO20070470L (enExample) |
| NZ (1) | NZ550978A (enExample) |
| PL (1) | PL1761522T3 (enExample) |
| PT (1) | PT1761522E (enExample) |
| RS (1) | RS52064B (enExample) |
| SI (1) | SI1761522T1 (enExample) |
| WO (2) | WO2006012093A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103833637A (zh) * | 2014-03-31 | 2014-06-04 | 武汉武药制药有限公司 | 一种制备依塞曲匹(Evacetrapib)中间体的方法 |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE602004023100D1 (de) * | 2003-10-08 | 2009-10-22 | Lilly Co Eli | Verbindungen und verfahren zur behandlung von dyslipidemie |
| JP2007530550A (ja) * | 2004-03-26 | 2007-11-01 | イーライ リリー アンド カンパニー | 異脂肪血症を治療するための化合物および方法 |
| UA90269C2 (ru) | 2004-04-02 | 2010-04-26 | Мицубиси Танабе Фарма Корпорейшн | Тетрагидрохинолиновые производные и способ их получения |
| EA200700119A1 (ru) | 2004-06-24 | 2007-10-26 | Эли Лилли Энд Компани | Соединения и способы лечения дислипидемии |
| WO2007107843A1 (en) * | 2006-03-22 | 2007-09-27 | Pfizer Products Inc. | Methods of treatment with cetp inhibitors |
| UY30244A1 (es) | 2006-03-30 | 2007-11-30 | Tanabe Seiyaku Co | Un proceso para preparar derivados de tetrahidroquinolina |
| EP2061767B1 (de) | 2006-08-08 | 2014-12-17 | Sanofi | Arylaminoaryl-alkyl-substituierte Imidazolidin-2,4-dione, Verfahren zu ihrer Herstellung, diese Verbindungen enthaltende Arzneimittel und ihre Verwendung |
| DE102007005045B4 (de) | 2007-01-26 | 2008-12-18 | Sanofi-Aventis | Phenothiazin Derivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| EP2157190B1 (en) * | 2007-05-17 | 2017-05-03 | EA Pharma Co., Ltd. | Method of measuring the activity of lipid-modified enzyme |
| EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| DE102007054497B3 (de) | 2007-11-13 | 2009-07-23 | Sanofi-Aventis Deutschland Gmbh | Neue kristalline Diphenylazetidinonhydrate und Verfahren zu deren Herstellung |
| UY31968A (es) | 2008-07-09 | 2010-01-29 | Sanofi Aventis | Nuevos derivados heterocíclicos, sus procesos para su preparación, y sus usos terapéuticos |
| WO2010068601A1 (en) | 2008-12-08 | 2010-06-17 | Sanofi-Aventis | A crystalline heteroaromatic fluoroglycoside hydrate, processes for making, methods of use and pharmaceutical compositions thereof |
| TWI450896B (zh) * | 2009-06-30 | 2014-09-01 | Lilly Co Eli | 反式-4-〔〔(5s)-5-〔〔〔3,5-雙(三氟甲基)苯基〕甲基〕(2-甲基-2h-四唑-5-基)胺基〕-2,3,4,5-四氫-7,9-二甲基-1h-1-苯并氮呯-1-基〕甲基〕-環己基羧酸 |
| KR20120060207A (ko) | 2009-08-26 | 2012-06-11 | 사노피 | 신규한 결정성 헤테로방향족 플루오로글리코시드 수화물, 이들 화합물을 포함하는 약제 및 이들의 용도 |
| EP2582709B1 (de) | 2010-06-18 | 2018-01-24 | Sanofi | Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen |
| EP2683699B1 (de) | 2011-03-08 | 2015-06-24 | Sanofi | Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| WO2012120056A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Tetrasubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| WO2012120058A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Mit benzyl- oder heteromethylengruppen substituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| EP2766349B1 (de) | 2011-03-08 | 2016-06-01 | Sanofi | Mit carbozyklen oder heterozyklen substituierte oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
| EP2683702B1 (de) | 2011-03-08 | 2014-12-24 | Sanofi | Neue substituierte phenyl-oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
| US8828994B2 (en) | 2011-03-08 | 2014-09-09 | Sanofi | Di- and tri-substituted oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
| WO2012120051A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Mit adamantan- oder noradamantan substituierte benzyl-oxathiazinderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
| US8895547B2 (en) | 2011-03-08 | 2014-11-25 | Sanofi | Substituted phenyl-oxathiazine derivatives, method for producing them, drugs containing said compounds and the use thereof |
| EP2683704B1 (de) | 2011-03-08 | 2014-12-17 | Sanofi | Verzweigte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| SG10201605304VA (en) * | 2011-07-08 | 2016-08-30 | Novartis Ag | Method of treating atherosclerosis in high triglyceride subjects |
| EP2567959B1 (en) | 2011-09-12 | 2014-04-16 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| DK2860175T3 (da) * | 2012-06-11 | 2018-01-29 | Tacurion | Fremgangsmåde til fremstilling af 4,4,7-trifluor-1,2,3,4-tetrahydro-5h-1-benzazepin-forbindelse og intermediat til syntese deraf |
| WO2014012401A1 (zh) * | 2012-07-16 | 2014-01-23 | 上海恒瑞医药有限公司 | 苯并七元杂环类衍生物、其制备方法及其在医药上的应用 |
| MX369471B (es) * | 2014-02-05 | 2019-11-08 | Dezima Pharma B V | Inhibidor de proteina de transferencia del ester de colesterilo (cetp) y composiciones farmaceuticas que comprenden el inhibidor para uso en el tratamiento o prevencion de enfermedades cardiovasculares. |
| JP6549735B2 (ja) | 2015-06-09 | 2019-07-24 | アッヴィ・インコーポレイテッド | 核内受容体調節剤 |
| WO2016198908A1 (en) | 2015-06-09 | 2016-12-15 | Abbvie Inc. | Ror nuclear receptor modulators |
| AU2019318209B2 (en) | 2018-08-10 | 2025-09-25 | Diapin Therapeutics, Llc | Tri-peptides and treatment of metabolic, cardiovascular and inflammatory disorders |
| WO2024249901A2 (en) * | 2023-06-01 | 2024-12-05 | Nico Therapeutics, Inc. | Compounds, compositions, and methods |
| CN117263810B (zh) * | 2023-09-19 | 2026-01-27 | 上海凌凯科技股份有限公司 | 还原硝基苯制备苯胺类化合物以及选择性碘代苯胺类化合物的方法 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1318057A (zh) * | 1998-09-17 | 2001-10-17 | 辉瑞产品公司 | 用作cetp抑制剂的4-氨基取代的-2-取代的-1,2,3,4-四氢喹啉 |
| CN1402711A (zh) * | 1999-11-30 | 2003-03-12 | 辉瑞产品公司 | 作为cetp抑制剂的4-羧基氨基-2-乙基-1,2,3,4-四氢喹啉结晶 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2402506A1 (fr) * | 1977-09-09 | 1979-04-06 | Guelennec Emile Le | Cisaille pour la decoupe de ferrailles de grandes dimensions |
| US6147089A (en) * | 1998-09-17 | 2000-11-14 | Pfizer Inc. | Annulated 4-carboxyamino-2-methyl-1,2,3,4,-tetrahydroquinolines |
| US6197786B1 (en) * | 1998-09-17 | 2001-03-06 | Pfizer Inc | 4-Carboxyamino-2-substituted-1,2,3,4-tetrahydroquinolines |
| HN2000000203A (es) * | 1999-11-30 | 2001-06-13 | Pfizer Prod Inc | Procedimiento para la obtencion de 1,2,3,4-tetrahidroquinolinas 4-carboxiamino-2- sustituidas. |
| MXPA03009935A (es) * | 2001-04-30 | 2004-01-29 | Pfizer Prod Inc | Metodos e intermedios para preparar inhibidores 4-aminoquinolina de cetp. |
| US7332514B2 (en) | 2002-08-30 | 2008-02-19 | Japan Tobacco Inc. | Dibenzylamine compound and medicinal use thereof |
| WO2004032848A2 (en) | 2002-10-04 | 2004-04-22 | Millennium Pharmaceuticals, Inc. | Pgd2 receptor antagonists for the treatment of inflammatory diseases |
| EP1601655A2 (en) | 2003-03-04 | 2005-12-07 | Takasago International Corporation | Method for producing optically active amines |
| US20040204450A1 (en) * | 2003-03-28 | 2004-10-14 | Pfizer Inc | Quinoline and quinoxaline compounds |
| DE602004023100D1 (de) | 2003-10-08 | 2009-10-22 | Lilly Co Eli | Verbindungen und verfahren zur behandlung von dyslipidemie |
| JP2007530550A (ja) | 2004-03-26 | 2007-11-01 | イーライ リリー アンド カンパニー | 異脂肪血症を治療するための化合物および方法 |
| UA90269C2 (ru) * | 2004-04-02 | 2010-04-26 | Мицубиси Танабе Фарма Корпорейшн | Тетрагидрохинолиновые производные и способ их получения |
| EA200700119A1 (ru) | 2004-06-24 | 2007-10-26 | Эли Лилли Энд Компани | Соединения и способы лечения дислипидемии |
| US7700774B2 (en) | 2004-12-20 | 2010-04-20 | Dr. Reddy's Laboratories Ltd. | Heterocyclic compounds and their pharmaceutical compositions |
| TWI450896B (zh) * | 2009-06-30 | 2014-09-01 | Lilly Co Eli | 反式-4-〔〔(5s)-5-〔〔〔3,5-雙(三氟甲基)苯基〕甲基〕(2-甲基-2h-四唑-5-基)胺基〕-2,3,4,5-四氫-7,9-二甲基-1h-1-苯并氮呯-1-基〕甲基〕-環己基羧酸 |
-
2005
- 2005-06-22 EA EA200700119A patent/EA200700119A1/ru unknown
- 2005-06-22 WO PCT/US2005/021789 patent/WO2006012093A1/en not_active Ceased
- 2005-06-22 BR BRPI0512523-5A patent/BRPI0512523A/pt not_active Application Discontinuation
- 2005-06-22 US US11/570,540 patent/US20080269284A1/en not_active Abandoned
- 2005-06-22 CA CA002570688A patent/CA2570688A1/en not_active Abandoned
- 2005-06-22 AU AU2005267436A patent/AU2005267436A1/en not_active Abandoned
- 2005-06-22 EP EP05768995A patent/EP1761521A1/en not_active Withdrawn
- 2005-06-22 JP JP2007518182A patent/JP2008504266A/ja active Pending
- 2005-06-22 KR KR1020067027038A patent/KR20070041452A/ko not_active Ceased
- 2005-06-22 MX MXPA06014716A patent/MXPA06014716A/es not_active Application Discontinuation
- 2005-06-23 MX MXPA06014706A patent/MXPA06014706A/es active IP Right Grant
- 2005-06-23 CN CN2005800206855A patent/CN1972932B/zh not_active Expired - Fee Related
- 2005-06-23 AU AU2005258241A patent/AU2005258241B2/en not_active Ceased
- 2005-06-23 JP JP2007518296A patent/JP4836945B2/ja not_active Expired - Fee Related
- 2005-06-23 PL PL05763328T patent/PL1761522T3/pl unknown
- 2005-06-23 RS RS20110559A patent/RS52064B/sr unknown
- 2005-06-23 SI SI200531438T patent/SI1761522T1/sl unknown
- 2005-06-23 NZ NZ550978A patent/NZ550978A/en not_active IP Right Cessation
- 2005-06-23 AT AT05763328T patent/ATE528304T1/de active
- 2005-06-23 HR HR20110761T patent/HRP20110761T1/hr unknown
- 2005-06-23 ES ES05763328T patent/ES2372291T3/es not_active Expired - Lifetime
- 2005-06-23 EP EP05763328A patent/EP1761522B1/en not_active Expired - Lifetime
- 2005-06-23 EA EA200700120A patent/EA012585B1/ru not_active IP Right Cessation
- 2005-06-23 DK DK05763328.1T patent/DK1761522T3/da active
- 2005-06-23 PT PT05763328T patent/PT1761522E/pt unknown
- 2005-06-23 EP EP11184746A patent/EP2479175A1/en not_active Withdrawn
- 2005-06-23 WO PCT/US2005/022389 patent/WO2006002342A1/en not_active Ceased
- 2005-06-23 BR BRPI0512516-2A patent/BRPI0512516A/pt active Search and Examination
- 2005-06-23 US US11/570,542 patent/US7786108B2/en not_active Expired - Fee Related
- 2005-06-23 CA CA2570673A patent/CA2570673C/en not_active Expired - Fee Related
-
2006
- 2006-12-19 EC EC2006007095A patent/ECSP067095A/es unknown
- 2006-12-19 EC EC2006007098A patent/ECSP067098A/es unknown
- 2006-12-22 CR CR8831A patent/CR8831A/es unknown
- 2006-12-24 IL IL180276A patent/IL180276A0/en unknown
- 2006-12-24 IL IL180277A patent/IL180277A/en not_active IP Right Cessation
- 2006-12-29 MA MA29595A patent/MA28729B1/fr unknown
- 2006-12-29 MA MA29596A patent/MA28730B1/fr unknown
-
2007
- 2007-01-24 NO NO20070470A patent/NO20070470L/no not_active Application Discontinuation
- 2007-01-24 NO NO20070468A patent/NO20070468L/no not_active Application Discontinuation
-
2010
- 2010-04-20 US US12/763,344 patent/US20100204207A1/en not_active Abandoned
-
2011
- 2011-11-25 CY CY20111101160T patent/CY1112124T1/el unknown
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1318057A (zh) * | 1998-09-17 | 2001-10-17 | 辉瑞产品公司 | 用作cetp抑制剂的4-氨基取代的-2-取代的-1,2,3,4-四氢喹啉 |
| CN1402711A (zh) * | 1999-11-30 | 2003-03-12 | 辉瑞产品公司 | 作为cetp抑制剂的4-羧基氨基-2-乙基-1,2,3,4-四氢喹啉结晶 |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103833637A (zh) * | 2014-03-31 | 2014-06-04 | 武汉武药制药有限公司 | 一种制备依塞曲匹(Evacetrapib)中间体的方法 |
| CN103833637B (zh) * | 2014-03-31 | 2016-01-06 | 武汉武药制药有限公司 | 一种制备依塞曲匹(Evacetrapib)中间体的方法 |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN1972932B (zh) | 治疗血脂障碍的化合物 | |
| JP7811578B2 (ja) | 中環状または大環状ベンジル置換複素環誘導体およびオレキシン-2受容体アゴニストとしてのそれらの使用 | |
| CN103012259B (zh) | 1,4-二取代的3-氰基-吡啶酮衍生物及其作为mglur2受体正性变构调节剂的用途 | |
| TW202229285A (zh) | Kras g12d抑制劑 | |
| CN101094848A (zh) | 有机化合物 | |
| CN105073741A (zh) | 作为rock抑制剂的酞嗪酮及异喹啉酮 | |
| CN108884070B (zh) | 作为溴结构域抑制剂的吡啶基衍生物 | |
| CN115380036A (zh) | Sstr5拮抗剂 | |
| CN106536491A (zh) | 作为盐皮质激素受体调节剂的苯并噁嗪酮酰胺 | |
| TW201348213A (zh) | 喹唑啉二酮衍生物 | |
| CN1449386B (zh) | 作为血管升压素拮抗剂的非肽取代的螺苯并氮杂* | |
| JP2007517868A (ja) | 治療薬i | |
| CN110582485A (zh) | 作为溴结构域抑制剂的吡唑衍生物 | |
| JP4773969B2 (ja) | 脂質代謝異常の治療ための化合物及び方法 | |
| WO2022174796A1 (zh) | 作为Wee-1抑制剂的嘧啶化合物 | |
| KR100859223B1 (ko) | 이상지혈증 치료를 위한 화합물 및 방법 | |
| HK1166981A (en) | Compounds and methods for treating dyslipidemia | |
| HK1104528B (en) | Compounds and methods for treating dyslipidemia | |
| HK40029587B (zh) | 化合物、组合物及方法 | |
| CN1972927A (zh) | 用于治疗血脂障碍的化合物和方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20110629 Termination date: 20160623 |
|
| CF01 | Termination of patent right due to non-payment of annual fee |