CN102731499B - 内酰胺化合物及其作为药物的应用 - Google Patents
内酰胺化合物及其作为药物的应用 Download PDFInfo
- Publication number
- CN102731499B CN102731499B CN201210167780.XA CN201210167780A CN102731499B CN 102731499 B CN102731499 B CN 102731499B CN 201210167780 A CN201210167780 A CN 201210167780A CN 102731499 B CN102731499 B CN 102731499B
- Authority
- CN
- China
- Prior art keywords
- compound
- alkyl
- diazaspiro
- prepared
- synthesis
- 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 - Lifetime
Links
- 0 **(CCC1(CCC2)C*2N)C1=O Chemical compound **(CCC1(CCC2)C*2N)C1=O 0.000 description 15
- WJMMJXPWOYFGTH-XMMPIXPASA-N C#CCOC(Nc(cc1C(F)(F)F)ccc1N(CCC1)C[C@@]1(CCN1C2CCCCC2)C1=O)=O Chemical compound C#CCOC(Nc(cc1C(F)(F)F)ccc1N(CCC1)C[C@@]1(CCN1C2CCCCC2)C1=O)=O WJMMJXPWOYFGTH-XMMPIXPASA-N 0.000 description 1
- WKEUOCSIOMUSPX-HSZRJFAPSA-N CC(C)OC(Nc(cc1)ccc1N(CCC1)C[C@@]1(CCN1C2CCOCC2)C1=O)=O Chemical compound CC(C)OC(Nc(cc1)ccc1N(CCC1)C[C@@]1(CCN1C2CCOCC2)C1=O)=O WKEUOCSIOMUSPX-HSZRJFAPSA-N 0.000 description 1
- KGEBZMPOLLKDKT-JOCHJYFZSA-N CC(C)OC(Nc1cc(Cl)c(N(CCC2)C[C@@]2(CCN2C3CCOCC3)C2=O)nc1)=O Chemical compound CC(C)OC(Nc1cc(Cl)c(N(CCC2)C[C@@]2(CCN2C3CCOCC3)C2=O)nc1)=O KGEBZMPOLLKDKT-JOCHJYFZSA-N 0.000 description 1
- KWCGQUPSRQPASV-PUUKEUDRSA-N CC(Nc1cccc(-c(cc2)cnc2N(CCC2)C[C@@]2(CCN2C(CC3)CCC3O)C2=O)c1)=O Chemical compound CC(Nc1cccc(-c(cc2)cnc2N(CCC2)C[C@@]2(CCN2C(CC3)CCC3O)C2=O)c1)=O KWCGQUPSRQPASV-PUUKEUDRSA-N 0.000 description 1
- CZFQFZALKPXYKO-UHFFFAOYSA-N CCC(CC)N(CCC1(CCC2)CN2C2C=CC(C(F)(F)F)=CC2)C1=O Chemical compound CCC(CC)N(CCC1(CCC2)CN2C2C=CC(C(F)(F)F)=CC2)C1=O CZFQFZALKPXYKO-UHFFFAOYSA-N 0.000 description 1
- QSRGBXAPQKWFKM-BZIHDHQJSA-N CCCOC(Nc(cc1F)ccc1N(CCC1)C[C@@]1(CCN1C2(CC3CC(C4)C2)CC4C3O)C1=O)=O Chemical compound CCCOC(Nc(cc1F)ccc1N(CCC1)C[C@@]1(CCN1C2(CC3CC(C4)C2)CC4C3O)C1=O)=O QSRGBXAPQKWFKM-BZIHDHQJSA-N 0.000 description 1
- FGHYKWWTDVDNAI-JOCHJYFZSA-N CCCOC(Nc1cc(Cl)c(N(CCC2)C[C@@]2(CCN2C3CCOCC3)C2=O)nc1)=O Chemical compound CCCOC(Nc1cc(Cl)c(N(CCC2)C[C@@]2(CCN2C3CCOCC3)C2=O)nc1)=O FGHYKWWTDVDNAI-JOCHJYFZSA-N 0.000 description 1
- XGBCCRJTOBFMGE-IEGUWTFLSA-N CCCOC(Nc1cc(Cl)c(N(CCC2)C[C@@]2(CCN2[C@H](CC3)CC[C@H]3O)C2=O)nc1)=O Chemical compound CCCOC(Nc1cc(Cl)c(N(CCC2)C[C@@]2(CCN2[C@H](CC3)CC[C@H]3O)C2=O)nc1)=O XGBCCRJTOBFMGE-IEGUWTFLSA-N 0.000 description 1
- UYBZNYZVUXGFLV-PMAPCBKXSA-N CCOC(Nc(cc1C(F)(F)F)ccc1N(CCC1)C[C@@]1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O)=O Chemical compound CCOC(Nc(cc1C(F)(F)F)ccc1N(CCC1)C[C@@]1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O)=O UYBZNYZVUXGFLV-PMAPCBKXSA-N 0.000 description 1
- LRWWNOUFNXCPAR-OAQYLSRUSA-N CCOC(Nc1cc(Cl)c(N(CCC2)C[C@@]2(CCN2C3CCOCC3)C2=O)nc1)=O Chemical compound CCOC(Nc1cc(Cl)c(N(CCC2)C[C@@]2(CCN2C3CCOCC3)C2=O)nc1)=O LRWWNOUFNXCPAR-OAQYLSRUSA-N 0.000 description 1
- VKVUWKQHBRXTIK-VHPWLNBFSA-N CCc(c(C(F)(F)F)ccc1)c1N(CCC1)CC1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O Chemical compound CCc(c(C(F)(F)F)ccc1)c1N(CCC1)CC1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O VKVUWKQHBRXTIK-VHPWLNBFSA-N 0.000 description 1
- HRAQWVWFMFGVOI-AJRIBIQBSA-N CCc1cnc(N(CCC2)C[C@@]2(CCC(C/C=C(/CC2CCC3)\C3C2O)C2)C2=O)nc1 Chemical compound CCc1cnc(N(CCC2)C[C@@]2(CCC(C/C=C(/CC2CCC3)\C3C2O)C2)C2=O)nc1 HRAQWVWFMFGVOI-AJRIBIQBSA-N 0.000 description 1
- KWNXVZWLJGIMQJ-FIQHHBPZSA-N CCc1cnc(N(CCC2)C[C@@]2(CCNC(C2)(C3)C4=CC3(C)C2C4O)C=O)nc1 Chemical compound CCc1cnc(N(CCC2)C[C@@]2(CCNC(C2)(C3)C4=CC3(C)C2C4O)C=O)nc1 KWNXVZWLJGIMQJ-FIQHHBPZSA-N 0.000 description 1
- NXZQZARXCRPFRE-GOSISDBHSA-N CN(CC1)CCC1N(CC[C@]1(CCC2)CN2c(nccn2)c2Cl)C1=O Chemical compound CN(CC1)CCC1N(CC[C@]1(CCC2)CN2c(nccn2)c2Cl)C1=O NXZQZARXCRPFRE-GOSISDBHSA-N 0.000 description 1
- JMXCNUODTOFRFP-JXXFODFXSA-N CO[C@H](CC1)CC[C@@H]1N(CC[C@]1(CCC2)CN2c(ncc(F)c2)c2F)C1=O Chemical compound CO[C@H](CC1)CC[C@@H]1N(CC[C@]1(CCC2)CN2c(ncc(F)c2)c2F)C1=O JMXCNUODTOFRFP-JXXFODFXSA-N 0.000 description 1
- KBKAYJKEHHMKMX-YDIMBITNSA-N COc1c(N(CCC2)C[C@@]2(CCN2[C@H](CC3)CC[C@H]3O)C2=O)ncc(NC(OCC#C)=O)c1 Chemical compound COc1c(N(CCC2)C[C@@]2(CCN2[C@H](CC3)CC[C@H]3O)C2=O)ncc(NC(OCC#C)=O)c1 KBKAYJKEHHMKMX-YDIMBITNSA-N 0.000 description 1
- SVBXSSUHGNULIT-RQNQAMLKSA-N COc1cccc(N(CC2)CCN2C(N(CCC2)C[C@@]2(CCN2[C@H](CC3)CC[C@@H]3O)C2=O)=O)c1 Chemical compound COc1cccc(N(CC2)CCN2C(N(CCC2)C[C@@]2(CCN2[C@H](CC3)CC[C@@H]3O)C2=O)=O)c1 SVBXSSUHGNULIT-RQNQAMLKSA-N 0.000 description 1
- HMOMWLAUCLSOHI-UYJZDEDHSA-N Cc(c(Cl)ccc1)c1S(N(CCC1)CC1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O)(=O)=O Chemical compound Cc(c(Cl)ccc1)c1S(N(CCC1)CC1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O)(=O)=O HMOMWLAUCLSOHI-UYJZDEDHSA-N 0.000 description 1
- VJVIQCDOWSKYIZ-CPLAMXDQSA-N Cc(c(S(N(CCC1)CC1(CCN1[C@H](CC2)CC[C@H]2Oc2ccncc2)C1=O)(=O)=O)ccc1)c1Cl Chemical compound Cc(c(S(N(CCC1)CC1(CCN1[C@H](CC2)CC[C@H]2Oc2ccncc2)C1=O)(=O)=O)ccc1)c1Cl VJVIQCDOWSKYIZ-CPLAMXDQSA-N 0.000 description 1
- NMMIUBYFYGYYCI-CBGDNZLLSA-N Cc(cc(nc1)OC)c1N(CCC1)C[C@@]1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O Chemical compound Cc(cc(nc1)OC)c1N(CCC1)C[C@@]1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O NMMIUBYFYGYYCI-CBGDNZLLSA-N 0.000 description 1
- YLGNEVUGWLPQFN-CBGDNZLLSA-N Cc(cc1)cc(F)c1N(CCC1)C[C@@]1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O Chemical compound Cc(cc1)cc(F)c1N(CCC1)C[C@@]1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O YLGNEVUGWLPQFN-CBGDNZLLSA-N 0.000 description 1
- MREHNJOTTWYXPO-FOIQADDNSA-O Cc1cc[nH+]c(N(CCC2)C[C@@]2(CCN2[C@@H](CC3)CC=C3O)C2=O)c1F Chemical compound Cc1cc[nH+]c(N(CCC2)C[C@@]2(CCN2[C@@H](CC3)CC=C3O)C2=O)c1F MREHNJOTTWYXPO-FOIQADDNSA-O 0.000 description 1
- UTZPXKXTYUWJKH-HXUWFJFHSA-N Cc1ccc(N(CCC2)C[C@@]2(CCN2C3CCCCC3)C2=O)nc1 Chemical compound Cc1ccc(N(CCC2)C[C@@]2(CCN2C3CCCCC3)C2=O)nc1 UTZPXKXTYUWJKH-HXUWFJFHSA-N 0.000 description 1
- YPRGYYBHIYWKHG-VFIGECHUSA-N N#CC(CC1)CCC1N(CC[C@]1(CCC2)CN2c2ccc(C(F)(F)F)cc2)C1=O Chemical compound N#CC(CC1)CCC1N(CC[C@]1(CCC2)CN2c2ccc(C(F)(F)F)cc2)C1=O YPRGYYBHIYWKHG-VFIGECHUSA-N 0.000 description 1
- UWVPABGFYKFOFW-AZSVPQILSA-N N#Cc(cc(cc1)NC(C2CCCC2)=O)c1N(CCC1)C[C@@]1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O Chemical compound N#Cc(cc(cc1)NC(C2CCCC2)=O)c1N(CCC1)C[C@@]1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O UWVPABGFYKFOFW-AZSVPQILSA-N 0.000 description 1
- LODJORHWQNBLMF-UHFFFAOYSA-N N#Cc(cc1)ccc1N(CCC1)CC1(CCN1C2CCCCC2)C1=O Chemical compound N#Cc(cc1)ccc1N(CCC1)CC1(CCN1C2CCCCC2)C1=O LODJORHWQNBLMF-UHFFFAOYSA-N 0.000 description 1
- XGOAHGVGSJSUMC-UHFFFAOYSA-N O=C(C(CC1)(CCC2)CN2C2=CCC(C(F)(F)F)C=N2)N1C1CCCCC1 Chemical compound O=C(C(CC1)(CCC2)CN2C2=CCC(C(F)(F)F)C=N2)N1C1CCCCC1 XGOAHGVGSJSUMC-UHFFFAOYSA-N 0.000 description 1
- TXFLSSHYNRCHKI-UHFFFAOYSA-N O=C(C(CCC1)(CN1c(nccc1)c1F)N1)N(C2CCCCC2)C1=O Chemical compound O=C(C(CCC1)(CN1c(nccc1)c1F)N1)N(C2CCCCC2)C1=O TXFLSSHYNRCHKI-UHFFFAOYSA-N 0.000 description 1
- XHOYBOYJHZVVQT-UHFFFAOYSA-N O=C(N(CC1)CCN1c1c(C(F)(F)F)cccc1)N(CCC1)CC1(C=CN1C2CCCCC2)C1=O Chemical compound O=C(N(CC1)CCN1c1c(C(F)(F)F)cccc1)N(CCC1)CC1(C=CN1C2CCCCC2)C1=O XHOYBOYJHZVVQT-UHFFFAOYSA-N 0.000 description 1
- PZLXJCCGKZAZQQ-UHFFFAOYSA-N O=C(N1CCCCC1)N(CCC1)CC1(CCN1C2CCCCC2)C1=O Chemical compound O=C(N1CCCCC1)N(CCC1)CC1(CCN1C2CCCCC2)C1=O PZLXJCCGKZAZQQ-UHFFFAOYSA-N 0.000 description 1
- BGVDOJPSTYWOOC-KBGWVZEBSA-N OC(C(CC(C1)C2)C3)C1CC23N(CC[C@]1(CCC2)CN2c(nc2)ccc2Cl)C1=O Chemical compound OC(C(CC(C1)C2)C3)C1CC23N(CC[C@]1(CCC2)CN2c(nc2)ccc2Cl)C1=O BGVDOJPSTYWOOC-KBGWVZEBSA-N 0.000 description 1
- SYBXMTGLHVEVHK-HAPLJMJGSA-N OC(CC1)CCC1N(CC[C@]1(CCC2)CN2c(c(Cl)c2)ccc2NC(C2CCCCC2)=O)C1=O Chemical compound OC(CC1)CCC1N(CC[C@]1(CCC2)CN2c(c(Cl)c2)ccc2NC(C2CCCCC2)=O)C1=O SYBXMTGLHVEVHK-HAPLJMJGSA-N 0.000 description 1
- SMRITTXZFMSZKL-JFIBYHEFSA-N OC(CC1)CCC1N(CC[C@]1(CCC2)CN2c(c(F)c2)ncc2Br)C1=O Chemical compound OC(CC1)CCC1N(CC[C@]1(CCC2)CN2c(c(F)c2)ncc2Br)C1=O SMRITTXZFMSZKL-JFIBYHEFSA-N 0.000 description 1
- ILGQXKCPTJBTIO-POYIXZFFSA-N OC([C@@](CC1)(CCC2)CN2C(CC2)C(F)=CC2N(CCCO2)C2=O)N1[C@H](CC1)CC[C@@H]1O Chemical compound OC([C@@](CC1)(CCC2)CN2C(CC2)C(F)=CC2N(CCCO2)C2=O)N1[C@H](CC1)CC[C@@H]1O ILGQXKCPTJBTIO-POYIXZFFSA-N 0.000 description 1
- RKFQHVCDFDJBPW-YYSPQECZSA-N O[C@H](CC1)CC[C@@H]1N(CCC1(CCC2)CN2C(N(CC2)CCN2c2ccccc2F)=O)C1=O Chemical compound O[C@H](CC1)CC[C@@H]1N(CCC1(CCC2)CN2C(N(CC2)CCN2c2ccccc2F)=O)C1=O RKFQHVCDFDJBPW-YYSPQECZSA-N 0.000 description 1
- NFQBCPXHAMDPNX-UILFTOMESA-N O[C@H](CC1)CC[C@@H]1N(CCC1(CCC2)CN2C(N(CCC2)CCC2c2ccccc2)=O)C1=[U] Chemical compound O[C@H](CC1)CC[C@@H]1N(CCC1(CCC2)CN2C(N(CCC2)CCC2c2ccccc2)=O)C1=[U] NFQBCPXHAMDPNX-UILFTOMESA-N 0.000 description 1
- XFJLEDNJFVNKFZ-YFVAEKQCSA-N O[C@H](CC1)CC[C@@H]1N(CCC[C@]1(CCC2)CN2c2cc(C(F)(F)F)cc(F)c2)C1=O Chemical compound O[C@H](CC1)CC[C@@H]1N(CCC[C@]1(CCC2)CN2c2cc(C(F)(F)F)cc(F)c2)C1=O XFJLEDNJFVNKFZ-YFVAEKQCSA-N 0.000 description 1
- XVPZNONNSIDKTQ-RQBNJVACSA-N O[C@H](CC1)CC[C@@H]1N(CC[C@]1(CCC2)CN2C(N(CC2)CCN2c(cc2)cc(Cl)c2Cl)=O)C1=O Chemical compound O[C@H](CC1)CC[C@@H]1N(CC[C@]1(CCC2)CN2C(N(CC2)CCN2c(cc2)cc(Cl)c2Cl)=O)C1=O XVPZNONNSIDKTQ-RQBNJVACSA-N 0.000 description 1
- HGSMANHDPUPKJV-YOSAUDMPSA-N O[C@H](CC1)CC[C@@H]1N(CC[C@]1(CCC2)CN2C(N(CC2)CCN2c2ccc(C(F)(F)F)cn2)=O)C1=O Chemical compound O[C@H](CC1)CC[C@@H]1N(CC[C@]1(CCC2)CN2C(N(CC2)CCN2c2ccc(C(F)(F)F)cn2)=O)C1=O HGSMANHDPUPKJV-YOSAUDMPSA-N 0.000 description 1
- UUVXMZXKVLNHHQ-STXHMFSFSA-N O[C@H](CC1)CC[C@@H]1N(CC[C@]1(CCC2)CN2c(c(Cl)ccc2)c2Cl)C1=O Chemical compound O[C@H](CC1)CC[C@@H]1N(CC[C@]1(CCC2)CN2c(c(Cl)ccc2)c2Cl)C1=O UUVXMZXKVLNHHQ-STXHMFSFSA-N 0.000 description 1
- UEHGWRVNJSMWMP-YVWKXTFCSA-N O[C@H](CC1)CC[C@@H]1N(CC[C@]1(CCC2)CN2c2cc(F)ccc2)C1=O Chemical compound O[C@H](CC1)CC[C@@H]1N(CC[C@]1(CCC2)CN2c2cc(F)ccc2)C1=O UEHGWRVNJSMWMP-YVWKXTFCSA-N 0.000 description 1
- BPMJDQPBWFVVJC-YDHSSHFGSA-N O[C@H](CC1)CC[C@@H]1NC([C@@](CS)(CCC1)CN1c(c(Cl)c1)ncc1-c1ccncc1)=O Chemical compound O[C@H](CC1)CC[C@@H]1NC([C@@](CS)(CCC1)CN1c(c(Cl)c1)ncc1-c1ccncc1)=O BPMJDQPBWFVVJC-YDHSSHFGSA-N 0.000 description 1
- OBCJNYAILSUGDF-AKCHCHLHSA-N [O-][N+](c(cc1F)ccc1N(CCC1)C[C@@]1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O)=O Chemical compound [O-][N+](c(cc1F)ccc1N(CCC1)C[C@@]1(CCN1[C@H](CC2)CC[C@@H]2O)C1=O)=O OBCJNYAILSUGDF-AKCHCHLHSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
- C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
- C07D221/20—Spiro-condensed ring systems
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/438—The ring being spiro-condensed with carbocyclic or heterocyclic ring systems
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4747—Quinolines; Isoquinolines spiro-condensed
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61P3/04—Anorexiants; Antiobesity agents
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
-
- 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
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- 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
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- 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
-
- 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
- A61P9/12—Antihypertensives
-
- 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
- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Epidemiology (AREA)
- Biomedical Technology (AREA)
- Physical Education & Sports Medicine (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Rheumatology (AREA)
- Urology & Nephrology (AREA)
- Pain & Pain Management (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Ophthalmology & Optometry (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Emergency Medicine (AREA)
- Vascular Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US62661704P | 2004-11-10 | 2004-11-10 | |
| US60/626,617 | 2004-11-10 | ||
| US71502005P | 2005-09-08 | 2005-09-08 | |
| US60/715,020 | 2005-09-08 | ||
| CNA2005800459986A CN101098856A (zh) | 2004-11-10 | 2005-11-09 | 内酰胺化合物及其作为药物的应用 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNA2005800459986A Division CN101098856A (zh) | 2004-11-10 | 2005-11-09 | 内酰胺化合物及其作为药物的应用 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN102731499A CN102731499A (zh) | 2012-10-17 |
| CN102731499B true CN102731499B (zh) | 2016-01-13 |
Family
ID=36337171
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201210167780.XA Expired - Lifetime CN102731499B (zh) | 2004-11-10 | 2005-11-09 | 内酰胺化合物及其作为药物的应用 |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US20060116382A1 (enExample) |
| EP (2) | EP2450351A1 (enExample) |
| JP (1) | JP5202954B2 (enExample) |
| KR (1) | KR101368228B1 (enExample) |
| CN (1) | CN102731499B (enExample) |
| AU (1) | AU2005304560C1 (enExample) |
| BR (1) | BRPI0518022A (enExample) |
| CA (1) | CA2585797C (enExample) |
| EA (1) | EA019747B1 (enExample) |
| ES (1) | ES2547724T3 (enExample) |
| GE (1) | GEP20125565B (enExample) |
| IL (1) | IL182876A (enExample) |
| MX (1) | MX2007005527A (enExample) |
| NO (1) | NO340365B1 (enExample) |
| NZ (1) | NZ554906A (enExample) |
| SG (1) | SG161261A1 (enExample) |
| TW (1) | TWI400239B (enExample) |
| WO (1) | WO2006053024A2 (enExample) |
| ZA (1) | ZA200703754B (enExample) |
Families Citing this family (92)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7880001B2 (en) | 2004-04-29 | 2011-02-01 | Abbott Laboratories | Inhibitors of the 11-beta-hydroxysteroid dehydrogenase Type 1 enzyme |
| US20100222316A1 (en) | 2004-04-29 | 2010-09-02 | Abbott Laboratories | Inhibitors of the 11-beta-hydroxysteroid dehydrogenase type 1 enzyme |
| US8415354B2 (en) | 2004-04-29 | 2013-04-09 | Abbott Laboratories | Methods of use of inhibitors of the 11-beta-hydroxysteroid dehydrogenase type 1 enzyme |
| TWI350168B (en) * | 2004-05-07 | 2011-10-11 | Incyte Corp | Amido compounds and their use as pharmaceuticals |
| US20050288338A1 (en) * | 2004-06-24 | 2005-12-29 | Wenqing Yao | Amido compounds and their use as pharmaceuticals |
| CA2589565A1 (en) * | 2004-06-24 | 2006-01-05 | Incyte Corporation | Amido compounds and their use as pharmaceuticals |
| JP2008504278A (ja) * | 2004-06-24 | 2008-02-14 | インサイト・コーポレイション | アミド化合物およびその医薬としての使用 |
| JP2008504280A (ja) * | 2004-06-24 | 2008-02-14 | インサイト・コーポレイション | 2−メチルプロパンアミドおよびその医薬としての使用 |
| US20050288317A1 (en) * | 2004-06-24 | 2005-12-29 | Wenqing Yao | Amido compounds and their use as pharmaceuticals |
| US8071624B2 (en) * | 2004-06-24 | 2011-12-06 | Incyte Corporation | N-substituted piperidines and their use as pharmaceuticals |
| WO2006020598A2 (en) * | 2004-08-10 | 2006-02-23 | Incyte Corporation | Amido compounds and their use as pharmaceuticals |
| US8110581B2 (en) | 2004-11-10 | 2012-02-07 | Incyte Corporation | Lactam compounds and their use as pharmaceuticals |
| CN101103016A (zh) * | 2004-11-18 | 2008-01-09 | 因塞特公司 | 11-β羟基类固醇脱氢酶1型抑制剂及其使用方法 |
| CA2594098C (en) | 2005-01-05 | 2014-04-01 | Abbott Laboratories | Inhibitors of the 11-beta-hydroxysteroid dehydrogenase type 1 enzyme |
| US20090192198A1 (en) | 2005-01-05 | 2009-07-30 | Abbott Laboratories | Inhibitors of the 11-beta-hydroxysteroid dehydrogenase type 1 enzyme |
| AU2006203918B2 (en) | 2005-01-05 | 2011-05-19 | Abbvie Inc. | Inhibitors of the 11-beta-hydroxysteroid dehydrogenase Type 1 enzyme |
| US8198331B2 (en) | 2005-01-05 | 2012-06-12 | Abbott Laboratories | Inhibitors of the 11-beta-hydroxysteroid dehydrogenase type 1 enzyme |
| WO2006126654A1 (ja) * | 2005-05-26 | 2006-11-30 | Daiichi Sankyo Company, Limited | 新規化合物 コレト酸 |
| CA2621255A1 (en) * | 2005-09-21 | 2007-04-05 | Incyte Corporation | Amido compounds and their use as pharmaceuticals |
| WO2007067504A2 (en) * | 2005-12-05 | 2007-06-14 | Incyte Corporation | Lactam compounds and methods of using the same |
| WO2007084314A2 (en) * | 2006-01-12 | 2007-07-26 | Incyte Corporation | MODULATORS OF 11-ß HYDROXYL STEROID DEHYDROGENASE TYPE 1, PHARMACEUTICAL COMPOSITIONS THEREOF, AND METHODS OF USING THE SAME |
| TW200804341A (en) * | 2006-01-31 | 2008-01-16 | Incyte Corp | Amido compounds and their use as pharmaceuticals |
| US20070213311A1 (en) * | 2006-03-02 | 2007-09-13 | Yun-Long Li | Modulators of 11-beta hydroxyl steroid dehydrogenase type 1, pharmaceutical compositions thereof, and methods of using the same |
| WO2007103719A2 (en) * | 2006-03-03 | 2007-09-13 | Incyte Corporation | MODULATORS OF 11-β HYDROXYL STEROID DEHYDROGENASE TYPE 1, PHARMACEUTICAL COMPOSITIONS THEREOF, AND METHODS OF USING THE SAME |
| NZ571175A (en) | 2006-04-21 | 2011-10-28 | Lilly Co Eli | Cyclohexylpyrazole-lactam derivatives as inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
| MX2008013485A (es) | 2006-04-21 | 2008-10-30 | Lilly Co Eli | Derivados de lactamas de bifenilamida como inhibidores de 11-beta-hidroxiesteroide deshidrogenasa 1. |
| EP2029576B1 (en) | 2006-04-21 | 2013-06-19 | Eli Lilly & Company | Cyclohexylimidazole lactam derivatives as inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
| ES2378574T3 (es) | 2006-04-24 | 2012-04-16 | Eli Lilly & Company | Pirrolidinonas ciclohexilo substituidas como inhibidores de 11-beta-hidroxiesteroide deshidrogenasa 1 |
| MX2008013644A (es) | 2006-04-24 | 2009-03-06 | Lilly Co Eli | Pirrolidinonas sustituidas como inhibidores de 11-beta-hidroxiesteroide deshidrogenasa 1. |
| NZ571176A (en) | 2006-04-24 | 2011-10-28 | Lilly Co Eli | Inhibitors of 11-beta-hydroxysteriod dehydrogenase 1 |
| AU2007244904B2 (en) | 2006-04-25 | 2012-05-31 | Eli Lilly And Company | Inhibitors of 11-Beta-hydroxysteroid dehydrogenase 1 |
| AU2007244863B2 (en) | 2006-04-25 | 2012-01-19 | Eli Lilly And Company | Inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
| AU2007244861B2 (en) | 2006-04-25 | 2012-03-15 | Eli Lilly And Company | Inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 |
| DK2049513T3 (da) | 2006-04-28 | 2012-02-27 | Lilly Co Eli | Piperidinylsubstituerede pyrrolidinoner som inhibitorer af 11-beta-hydroxysteroiddehydrogenase 1 |
| EP2013163A1 (en) * | 2006-05-01 | 2009-01-14 | Incyte Corporation | Tetrasubstituted ureas as modulators of 11-beta hydroxyl steroid dehydrogenase type 1 |
| PE20110235A1 (es) | 2006-05-04 | 2011-04-14 | Boehringer Ingelheim Int | Combinaciones farmaceuticas que comprenden linagliptina y metmorfina |
| EP2018378A2 (en) * | 2006-05-17 | 2009-01-28 | Incyte Corporation | Heterocyclic inhibitors of 11-b hydroxyl steroid dehydrogenase type i and methods of using the same |
| PE20080344A1 (es) | 2006-06-27 | 2008-06-09 | Sanofi Aventis | Compuestos 8-azabiciclo[3.2.1]oct-8-il-1,2,3,4-tetrahidroquinolina sustituidos como inhibidores 11b-hsd1 |
| PE20080212A1 (es) * | 2006-06-27 | 2008-04-25 | Sanofi Aventis | Derivados de ureas de piperidina o pirrolidina como moduladores de la 11b-hidroxiesteroide deshidrogenasa tipo 1 (11bhsd1) |
| WO2008079945A2 (en) * | 2006-12-20 | 2008-07-03 | University Of South Florida | Rock inhibitors and uses thereof |
| JPWO2008090944A1 (ja) | 2007-01-25 | 2010-05-20 | 武田薬品工業株式会社 | スピロ環化合物 |
| US8575167B2 (en) | 2007-02-06 | 2013-11-05 | Takeda Pharmaceutical Company Limited | Spiro compounds having stearoyl-CoA desaturase action |
| WO2008102749A1 (ja) | 2007-02-20 | 2008-08-28 | Takeda Pharmaceutical Company Limited | 複素環化合物 |
| JP5486928B2 (ja) * | 2007-02-26 | 2014-05-07 | ヴァイティー ファーマシューティカルズ,インコーポレイテッド | 11β−ヒドロキシステロイドデヒドロゲナーゼ1のサイクリックウレアおよびカルバメートインヒビター |
| US20080306102A1 (en) * | 2007-05-18 | 2008-12-11 | Kowa Co., Ltd. | Novel spirooxyindole compounds and drugs containing same |
| AU2014218443B2 (en) * | 2007-06-21 | 2016-05-19 | Incyte Holdings Corporation | Spirocycles as inhibitors of 11-beta hydroxyl steroid dehydrogenase type 1 |
| CL2008001839A1 (es) | 2007-06-21 | 2009-01-16 | Incyte Holdings Corp | Compuestos derivados de 2,7-diazaespirociclos, inhibidores de 11-beta hidroxil esteroide deshidrogenasa tipo 1; composicion farmaceutica que comprende a dichos compuestos; utiles para tratar la obesidad, diabetes, intolerancia a la glucosa, diabetes tipo ii, entre otras enfermedades. |
| JP5470557B2 (ja) * | 2007-07-26 | 2014-04-16 | ヴァイティー ファーマシューティカルズ,インコーポレイテッド | 11β−ヒドロキシステロイドデヒドロゲナーゼ1型の阻害剤の合成 |
| JP5736098B2 (ja) | 2007-08-21 | 2015-06-17 | アッヴィ・インコーポレイテッド | 中枢神経系障害を治療するための医薬組成物 |
| AR069207A1 (es) * | 2007-11-07 | 2010-01-06 | Vitae Pharmaceuticals Inc | Ureas ciclicas como inhibidores de la 11 beta - hidroxi-esteroide deshidrogenasa 1 |
| JP5490014B2 (ja) | 2007-12-11 | 2014-05-14 | ヴァイティー ファーマシューティカルズ,インコーポレイテッド | 11β−ヒドロキシステロイドデヒドロゲナーゼ1型の環状尿素阻害剤 |
| PE20091057A1 (es) | 2007-12-19 | 2009-07-20 | Lilly Co Eli | Antagonistas del receptor mineralcorticoide y metodos de uso |
| TW200934490A (en) * | 2008-01-07 | 2009-08-16 | Vitae Pharmaceuticals Inc | Lactam inhibitors of 11 &abgr;-hydroxysteroid dehydrogenase 1 |
| US8592409B2 (en) * | 2008-01-24 | 2013-11-26 | Vitae Pharmaceuticals, Inc. | Cyclic carbazate and semicarbazide inhibitors of 11β-hydroxysteroid dehydrogenase 1 |
| EP2252598A2 (en) * | 2008-02-11 | 2010-11-24 | Vitae Pharmaceuticals, Inc. | 1,3-oxazepan-2-one and 1,3-diazepan-2-one inhibitors of 11beta-hydroxysteroid dehydrogenase 1 |
| CA2715290A1 (en) * | 2008-02-15 | 2009-08-20 | Vitae Pharmaceuticals, Inc. | Inhibitors of 11beta-hydroxysteroid dehydrogenase 1 |
| WO2009117109A1 (en) * | 2008-03-18 | 2009-09-24 | Vitae Pharmaceuticals, Inc. | Inhibitors of 11beta-hydroxysteroid dehydrogenase type 1 |
| US8242111B2 (en) * | 2008-05-01 | 2012-08-14 | Vitae Pharmaceuticals, Inc. | Cyclic inhibitors of 11β-hydroxysteroid dehydrogenase 1 |
| CA2723034A1 (en) | 2008-05-01 | 2009-11-05 | Vitae Pharmaceuticals, Inc. | Cyclic inhibitors of 11beta-hydroxysteroid dehydrogenase 1 |
| WO2009134392A1 (en) | 2008-05-01 | 2009-11-05 | Vitae Pharmaceuticals, Inc. | Cyclic inhibitors of 11beta-hydroxysteroid dehydrogenase 1 |
| US8138178B2 (en) * | 2008-05-01 | 2012-03-20 | Vitae Pharmaceuticals, Inc. | Cyclic inhibitors of 11beta-hydroxysteroid dehydrogenase 1 |
| US20100022572A1 (en) | 2008-07-18 | 2010-01-28 | Kowa Company, Ltd. | Novel spiro compound and medicine comprising the same |
| TW201016691A (en) | 2008-07-25 | 2010-05-01 | Boehringer Ingelheim Int | Inhibitors of 11beta-hydroxysteroid dehydrogenase 1 |
| KR20110050459A (ko) | 2008-07-25 | 2011-05-13 | 비타이 파마슈티컬즈, 인코포레이티드 | 11베타-하이드록시스테로이드 탈수소효소 1의 고리형 억제제 |
| WO2010023931A1 (ja) | 2008-08-29 | 2010-03-04 | 興和株式会社 | 1-アダマンチルアゼチジン-2-オン誘導体及びこれを含有する医薬 |
| GB0818241D0 (en) | 2008-10-06 | 2008-11-12 | Cancer Res Technology | Compounds and their use |
| TW201022210A (en) | 2008-10-29 | 2010-06-16 | Kowa Co | 1,2-diazetidin-3-one derivatives and drugs containing same |
| JP5679997B2 (ja) | 2009-02-04 | 2015-03-04 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 11β−ヒドロキシステロイドデヒドロゲナーゼ1の環状阻害剤 |
| JP2012136439A (ja) * | 2009-04-24 | 2012-07-19 | Nippon Chemiphar Co Ltd | ジアザスピロアルカン誘導体 |
| TW201039034A (en) * | 2009-04-27 | 2010-11-01 | Chunghwa Picture Tubes Ltd | Pixel structure and the method of forming the same |
| US20100331320A1 (en) * | 2009-04-30 | 2010-12-30 | Vitae Pharmaceuticals, Inc. | Cyclic inhibitors of 11beta-hydroxysteroid dehydrogenase 1 |
| US8680093B2 (en) | 2009-04-30 | 2014-03-25 | Vitae Pharmaceuticals, Inc. | Cyclic inhibitors of 11beta-hydroxysteroid dehydrogenase 1 |
| US8329904B2 (en) * | 2009-05-12 | 2012-12-11 | Hoffmann-La Roche Inc. | Azacyclic derivatives |
| EP2440537A1 (en) | 2009-06-11 | 2012-04-18 | Vitae Pharmaceuticals, Inc. | Cyclic inhibitors of 11beta-hydroxysteroid dehydrogenase 1 based on the 1,3 -oxazinan- 2 -one structure |
| US8883778B2 (en) | 2009-07-01 | 2014-11-11 | Vitae Pharmaceuticals, Inc. | Cyclic inhibitors of 11 beta-hydroxysteroid dehydrogenase 1 |
| US8389539B2 (en) * | 2009-12-01 | 2013-03-05 | Hoffman-La Roche Inc. | Azacyclic derivatives |
| CN102267995A (zh) * | 2010-06-04 | 2011-12-07 | 艾琪康医药科技(上海)有限公司 | 一种制备二氮杂螺环化合物的方法 |
| EP2582698B1 (en) | 2010-06-16 | 2016-09-14 | Vitae Pharmaceuticals, Inc. | Substituted 5-,6- and 7-membered heterocycles, medicaments containing such compounds, and their use |
| JP5813106B2 (ja) | 2010-06-25 | 2015-11-17 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 代謝障害の処置のための11−β−HSD1のインヒビターとしてのアザスピロヘキサノン |
| BR112013000249A2 (pt) * | 2010-07-13 | 2016-05-24 | Hoffmann La Roche | novos compostos azacíclicos |
| US8552024B2 (en) * | 2010-08-13 | 2013-10-08 | Hoffman-La Roche Inc. | Azacyclic compounds |
| EA201300522A1 (ru) | 2010-11-02 | 2013-11-29 | Бёрингер Ингельхайм Интернациональ Гмбх | Фармацевтические комбинации для лечения метаболических нарушений |
| JPWO2013115294A1 (ja) * | 2012-01-31 | 2015-05-11 | 東レ株式会社 | ジアザスピロウレア誘導体及びその医薬用途 |
| EP3235813A1 (en) | 2016-04-19 | 2017-10-25 | Cidqo 2012, S.L. | Aza-tetra-cyclo derivatives |
| WO2018034917A1 (en) * | 2016-08-15 | 2018-02-22 | Merck Sharp & Dohme Corp. | Compounds useful for altering the levels of bile acids for the treatment of diabetes and cardiometabolic disease |
| WO2018034918A1 (en) * | 2016-08-15 | 2018-02-22 | Merck Sharp & Dohme Corp. | Compounds useful for altering the levels of bile acids for the treatment of diabetes and cardiometabolic disease |
| CN117777121A (zh) | 2016-10-24 | 2024-03-29 | 詹森药业有限公司 | 化合物及其用途 |
| EA201991650A1 (ru) | 2017-01-06 | 2020-01-20 | Юманити Терапьютикс, Инк. | Способы лечения неврологических расстройств |
| WO2019084157A1 (en) | 2017-10-24 | 2019-05-02 | Yumanity Therapeutics, Inc. | COMPOUNDS AND USES THEREOF |
| AU2019238326B2 (en) | 2018-03-23 | 2025-03-06 | Janssen Pharmaceutica Nv | Compounds and uses thereof |
| JP7742775B2 (ja) | 2019-01-24 | 2025-09-22 | ヤンセン ファーマシューティカ エヌ.ベー. | 化合物及びその使用 |
| EA202192047A1 (ru) | 2019-11-13 | 2021-12-08 | Юманити Терапьютикс, Инк. | Соединения и их применение |
Family Cites Families (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4439606A (en) * | 1982-05-06 | 1984-03-27 | American Cyanamid Company | Antiatherosclerotic 1-piperazinecarbonyl compounds |
| JPH05213957A (ja) * | 1992-02-07 | 1993-08-24 | Tsumura & Co | 新規なスピロピロリジンイミダゾリン誘導体および新規なアミノピロリジンカルボン酸誘導体並びに該化合物を有効成分とする鎮けい剤 |
| DE4234295A1 (de) * | 1992-10-12 | 1994-04-14 | Thomae Gmbh Dr K | Carbonsäurederivate, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung |
| FR2705343B1 (fr) * | 1993-05-17 | 1995-07-21 | Fournier Ind & Sante | Dérivés de beta,beta-diméthyl-4-pipéridineéthanamine, leur procédé de préparation et leur utilisation en thérapeutique. |
| FR2724656B1 (fr) * | 1994-09-15 | 1996-12-13 | Adir | Nouveaux derives du benzopyranne, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| FR2734265B1 (fr) * | 1995-05-17 | 1997-06-13 | Adir | Nouveaux composes spiro heterocycliques, leur procede de preparation et les compositions pharmaceutiques les contenant |
| FR2736053B1 (fr) * | 1995-06-28 | 1997-09-19 | Sanofi Sa | Nouvelles 1-phenylalkyl-1,2,3,6-tetrahydropyridines |
| ES2227612T3 (es) * | 1995-09-29 | 2005-04-01 | Eli Lilly And Company | Compuestos espiro como inhibidores de agregacion plaquetaria dependiente del fibrinogeno. |
| RU2265021C2 (ru) * | 1999-12-03 | 2005-11-27 | Оно Фармасьютикал Ко., Лтд. | Производные триазаспиро[5,5]ундекана (варианты), фармацевтическая композиция и способ регулирования хемокина/рецептора хемокина |
| US7294637B2 (en) * | 2000-09-11 | 2007-11-13 | Sepracor, Inc. | Method of treating addiction or dependence using a ligand for a monamine receptor or transporter |
| US6547958B1 (en) * | 2001-07-13 | 2003-04-15 | Chevron U.S.A. Inc. | Hydrocarbon conversion using zeolite SSZ-59 |
| CN1596253A (zh) * | 2001-10-01 | 2005-03-16 | 布里斯托尔-迈尔斯斯奎布公司 | 用作抗炎药的螺-乙内酰脲化合物 |
| RU2315051C2 (ru) * | 2001-12-28 | 2008-01-20 | Акадиа Фармасьютикалз, Инк. | Спироазациклические соединения, способ ингибирования активности или активации серотонинового 5-нт2а рецептора, способ лечения болезненного состояния, связанного с серотониновым 5-нт2а рецептором, и их применение |
| US6818772B2 (en) * | 2002-02-22 | 2004-11-16 | Abbott Laboratories | Antagonists of melanin concentrating hormone effects on the melanin concentrating hormone receptor |
| GB0213715D0 (en) * | 2002-06-14 | 2002-07-24 | Syngenta Ltd | Chemical compounds |
| US20060019977A1 (en) * | 2002-10-18 | 2006-01-26 | Ono Pharmaceutical Co., Ltd. | Spiroheterocyclic derivative compounds and drugs comprising the compound as the active ingredient |
| DE602004027171D1 (de) * | 2003-04-11 | 2010-06-24 | High Point Pharmaceuticals Llc | Verbindungen mit Aktivität an der 11Beta-Hydroxasteroiddehydrogenase |
| EP1683797A1 (en) * | 2003-11-13 | 2006-07-26 | Ono Pharmaceutical Co., Ltd. | Heterocyclic spiro compound |
| TWI350168B (en) * | 2004-05-07 | 2011-10-11 | Incyte Corp | Amido compounds and their use as pharmaceuticals |
| US20050288338A1 (en) * | 2004-06-24 | 2005-12-29 | Wenqing Yao | Amido compounds and their use as pharmaceuticals |
| JP2008504278A (ja) * | 2004-06-24 | 2008-02-14 | インサイト・コーポレイション | アミド化合物およびその医薬としての使用 |
| US20050288317A1 (en) * | 2004-06-24 | 2005-12-29 | Wenqing Yao | Amido compounds and their use as pharmaceuticals |
| CA2589565A1 (en) * | 2004-06-24 | 2006-01-05 | Incyte Corporation | Amido compounds and their use as pharmaceuticals |
| JP2008504280A (ja) * | 2004-06-24 | 2008-02-14 | インサイト・コーポレイション | 2−メチルプロパンアミドおよびその医薬としての使用 |
| US8071624B2 (en) * | 2004-06-24 | 2011-12-06 | Incyte Corporation | N-substituted piperidines and their use as pharmaceuticals |
| WO2006020598A2 (en) * | 2004-08-10 | 2006-02-23 | Incyte Corporation | Amido compounds and their use as pharmaceuticals |
| TW200616634A (en) * | 2004-10-01 | 2006-06-01 | Bristol Myers Squibb Co | Crystalline forms and process for preparing spiro-hydantoin compounds |
| CN101103016A (zh) * | 2004-11-18 | 2008-01-09 | 因塞特公司 | 11-β羟基类固醇脱氢酶1型抑制剂及其使用方法 |
| US20060142319A1 (en) * | 2004-12-14 | 2006-06-29 | Bang-Chi Chen | Pyridyl-substituted spiro-hydantoin crystalline forms and process |
| AU2006203918B2 (en) * | 2005-01-05 | 2011-05-19 | Abbvie Inc. | Inhibitors of the 11-beta-hydroxysteroid dehydrogenase Type 1 enzyme |
| BRPI0609062A2 (pt) * | 2005-03-03 | 2010-02-17 | F. Hofmann-La Roche Ag | composição farmacêutica, compostos, método para o tratamento terapêutico e/ou profilático de enfermidades que são moduladas por inibidores de deidrogenase de hidroxiesteróide-11ß e utilização dos compostos |
| CA2621255A1 (en) * | 2005-09-21 | 2007-04-05 | Incyte Corporation | Amido compounds and their use as pharmaceuticals |
| WO2007067504A2 (en) * | 2005-12-05 | 2007-06-14 | Incyte Corporation | Lactam compounds and methods of using the same |
| WO2007084314A2 (en) * | 2006-01-12 | 2007-07-26 | Incyte Corporation | MODULATORS OF 11-ß HYDROXYL STEROID DEHYDROGENASE TYPE 1, PHARMACEUTICAL COMPOSITIONS THEREOF, AND METHODS OF USING THE SAME |
| TW200804341A (en) * | 2006-01-31 | 2008-01-16 | Incyte Corp | Amido compounds and their use as pharmaceuticals |
| US20070213311A1 (en) * | 2006-03-02 | 2007-09-13 | Yun-Long Li | Modulators of 11-beta hydroxyl steroid dehydrogenase type 1, pharmaceutical compositions thereof, and methods of using the same |
| WO2007103719A2 (en) * | 2006-03-03 | 2007-09-13 | Incyte Corporation | MODULATORS OF 11-β HYDROXYL STEROID DEHYDROGENASE TYPE 1, PHARMACEUTICAL COMPOSITIONS THEREOF, AND METHODS OF USING THE SAME |
| EP2013163A1 (en) * | 2006-05-01 | 2009-01-14 | Incyte Corporation | Tetrasubstituted ureas as modulators of 11-beta hydroxyl steroid dehydrogenase type 1 |
| EP2018378A2 (en) * | 2006-05-17 | 2009-01-28 | Incyte Corporation | Heterocyclic inhibitors of 11-b hydroxyl steroid dehydrogenase type i and methods of using the same |
-
2005
- 2005-11-09 CA CA2585797A patent/CA2585797C/en not_active Expired - Lifetime
- 2005-11-09 EA EA200701036A patent/EA019747B1/ru unknown
- 2005-11-09 NZ NZ554906A patent/NZ554906A/en not_active IP Right Cessation
- 2005-11-09 CN CN201210167780.XA patent/CN102731499B/zh not_active Expired - Lifetime
- 2005-11-09 TW TW094139285A patent/TWI400239B/zh active
- 2005-11-09 WO PCT/US2005/040550 patent/WO2006053024A2/en not_active Ceased
- 2005-11-09 BR BRPI0518022-8A patent/BRPI0518022A/pt not_active Application Discontinuation
- 2005-11-09 SG SG201002512-0A patent/SG161261A1/en unknown
- 2005-11-09 US US11/269,984 patent/US20060116382A1/en not_active Abandoned
- 2005-11-09 JP JP2007540189A patent/JP5202954B2/ja not_active Expired - Fee Related
- 2005-11-09 KR KR1020077012990A patent/KR101368228B1/ko not_active Expired - Fee Related
- 2005-11-09 GE GEAP200510125A patent/GEP20125565B/en unknown
- 2005-11-09 MX MX2007005527A patent/MX2007005527A/es active IP Right Grant
- 2005-11-09 EP EP12153931A patent/EP2450351A1/en not_active Withdrawn
- 2005-11-09 EP EP05818772.5A patent/EP1812005B1/en not_active Expired - Lifetime
- 2005-11-09 AU AU2005304560A patent/AU2005304560C1/en not_active Expired
- 2005-11-09 ES ES05818772.5T patent/ES2547724T3/es not_active Expired - Lifetime
-
2007
- 2007-04-30 IL IL182876A patent/IL182876A/en active IP Right Grant
- 2007-05-03 NO NO20072322A patent/NO340365B1/no unknown
- 2007-05-09 ZA ZA2007/03754A patent/ZA200703754B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| MX2007005527A (es) | 2007-07-09 |
| NZ554906A (en) | 2011-01-28 |
| EP1812005A4 (en) | 2009-09-30 |
| TWI400239B (zh) | 2013-07-01 |
| JP2008519765A (ja) | 2008-06-12 |
| BRPI0518022A (pt) | 2008-10-21 |
| WO2006053024A2 (en) | 2006-05-18 |
| AU2005304560C1 (en) | 2013-05-09 |
| EA200701036A1 (ru) | 2007-12-28 |
| EP1812005B1 (en) | 2015-09-16 |
| ZA200703754B (en) | 2008-01-08 |
| AU2005304560B2 (en) | 2012-05-03 |
| EA019747B1 (ru) | 2014-06-30 |
| KR20070085944A (ko) | 2007-08-27 |
| SG161261A1 (en) | 2010-05-27 |
| AU2005304560A1 (en) | 2006-05-18 |
| CA2585797A1 (en) | 2006-05-18 |
| TW200621763A (en) | 2006-07-01 |
| JP5202954B2 (ja) | 2013-06-05 |
| NO20072322L (no) | 2007-07-19 |
| EP1812005A2 (en) | 2007-08-01 |
| CA2585797C (en) | 2015-01-06 |
| WO2006053024A3 (en) | 2007-07-05 |
| CN102731499A (zh) | 2012-10-17 |
| EP2450351A1 (en) | 2012-05-09 |
| GEP20125565B (en) | 2012-07-10 |
| IL182876A (en) | 2015-10-29 |
| ES2547724T3 (es) | 2015-10-08 |
| IL182876A0 (en) | 2007-08-19 |
| HK1113305A1 (zh) | 2008-10-03 |
| KR101368228B1 (ko) | 2014-02-27 |
| US20060116382A1 (en) | 2006-06-01 |
| NO340365B1 (no) | 2017-04-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN102731499B (zh) | 内酰胺化合物及其作为药物的应用 | |
| US8193207B2 (en) | Lactam compounds and methods of using the same | |
| KR101252227B1 (ko) | 아미도 화합물 및 약제로서의 이의 용도 | |
| US20070208001A1 (en) | Modulators of 11- beta hydroxyl steroid dehydrogenase type 1, pharmaceutical compositions thereof, and methods of using the same | |
| US20070197530A1 (en) | Amido compounds and their use as pharmaceuticals | |
| CN101103016A (zh) | 11-β羟基类固醇脱氢酶1型抑制剂及其使用方法 | |
| US8563570B2 (en) | Lactam compounds and their use as pharmaceuticals | |
| CN101098856A (zh) | 内酰胺化合物及其作为药物的应用 | |
| CN101336243A (zh) | 内酰胺化合物和其使用方法 | |
| AU2012211350A1 (en) | Lactam compounds and their use as pharmaceuticals | |
| CN101405265A (zh) | 酰氨基化合物及其作为药物的应用 | |
| HK1173138A (en) | Lactam compounds and their use as pharmaceuticals |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C41 | Transfer of patent application or patent right or utility model | ||
| TA01 | Transfer of patent application right |
Effective date of registration: 20151111 Address after: The United States Delaware Applicant after: Incyte Holdings Corp. Address before: The United States Delaware Applicant before: Incyte Corp. |
|
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CX01 | Expiry of patent term |
Granted publication date: 20160113 |
|
| CX01 | Expiry of patent term |