JP2006514099A - 組織化前の三環系インテグラーゼインヒビター化合物 - Google Patents
組織化前の三環系インテグラーゼインヒビター化合物 Download PDFInfo
- Publication number
- JP2006514099A JP2006514099A JP2005501423A JP2005501423A JP2006514099A JP 2006514099 A JP2006514099 A JP 2006514099A JP 2005501423 A JP2005501423 A JP 2005501423A JP 2005501423 A JP2005501423 A JP 2005501423A JP 2006514099 A JP2006514099 A JP 2006514099A
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- JP
- Japan
- Prior art keywords
- compound
- substituted
- phosphonate
- alkyl
- aryl
- 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.)
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- 0 C*(C(*)=C(C)C(*)(*)C1NC(*=*=*2)=C2C(*)=C11)C1=O Chemical compound C*(C(*)=C(C)C(*)(*)C1NC(*=*=*2)=C2C(*)=C11)C1=O 0.000 description 30
- FCMLWBBLOASUSO-UHFFFAOYSA-N CC(C)(C)OC(N(CCN1)CC1=O)=O Chemical compound CC(C)(C)OC(N(CCN1)CC1=O)=O FCMLWBBLOASUSO-UHFFFAOYSA-N 0.000 description 1
- XOYDXQIVFSUKDK-UHFFFAOYSA-N CC(C)(C)OC(N(CCN1Cc(cc2)ccc2F)CC1=O)=O Chemical compound CC(C)(C)OC(N(CCN1Cc(cc2)ccc2F)CC1=O)=O XOYDXQIVFSUKDK-UHFFFAOYSA-N 0.000 description 1
- WLTLMLLLFUJCOQ-UHFFFAOYSA-N CC(C)OC(c(nccc1)c1C(N(CCN1Cc(cc2)ccc2F)CC1=O)=O)=O Chemical compound CC(C)OC(c(nccc1)c1C(N(CCN1Cc(cc2)ccc2F)CC1=O)=O)=O WLTLMLLLFUJCOQ-UHFFFAOYSA-N 0.000 description 1
- JJHMFZQIZDCYJV-UHFFFAOYSA-N CC(CC1)CN(CC2C=CC(F)=CC2)C1=O Chemical compound CC(CC1)CN(CC2C=CC(F)=CC2)C1=O JJHMFZQIZDCYJV-UHFFFAOYSA-N 0.000 description 1
- XMWINMVFKPHMJB-UHFFFAOYSA-N CC1=CCCC=C1 Chemical compound CC1=CCCC=C1 XMWINMVFKPHMJB-UHFFFAOYSA-N 0.000 description 1
- NJFLZLAEALJDFE-UHFFFAOYSA-N CCC(c(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2OC(c1ccccc1)c1ccccc1)=O Chemical compound CCC(c(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2OC(c1ccccc1)c1ccccc1)=O NJFLZLAEALJDFE-UHFFFAOYSA-N 0.000 description 1
- NWNJUOSUYIMJMN-UHFFFAOYSA-N CCCCNC(Oc(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2OC(c1ccccc1)c1ccccc1)=O Chemical compound CCCCNC(Oc(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2OC(c1ccccc1)c1ccccc1)=O NWNJUOSUYIMJMN-UHFFFAOYSA-N 0.000 description 1
- OBCBDHFCSIEZFZ-UHFFFAOYSA-N CCOC(CNC(N(CC(OCC)=O)C(Oc(c(CN1Cc(cc2)ccc2F)c2C1=O)c(cccn1)c1c2O)=O)=O)=O Chemical compound CCOC(CNC(N(CC(OCC)=O)C(Oc(c(CN1Cc(cc2)ccc2F)c2C1=O)c(cccn1)c1c2O)=O)=O)=O OBCBDHFCSIEZFZ-UHFFFAOYSA-N 0.000 description 1
- LRZPBJNCADMGPE-UHFFFAOYSA-N CCOC(CNC(N(CC(OCC)=O)C(Oc(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2OC(c1ccccc1)c1ccccc1)=O)=O)=O Chemical compound CCOC(CNC(N(CC(OCC)=O)C(Oc(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2OC(c1ccccc1)c1ccccc1)=O)=O)=O LRZPBJNCADMGPE-UHFFFAOYSA-N 0.000 description 1
- FSNCRSIVDAWNRJ-UHFFFAOYSA-N CCOC(c1ccccc1-c(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2OC(c1ccccc1)c1ccccc1)=O Chemical compound CCOC(c1ccccc1-c(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2OC(c1ccccc1)c1ccccc1)=O FSNCRSIVDAWNRJ-UHFFFAOYSA-N 0.000 description 1
- QZKVVOXAEBCLPZ-UHFFFAOYSA-N CCOC(c1ccccc1B(O)O)=O Chemical compound CCOC(c1ccccc1B(O)O)=O QZKVVOXAEBCLPZ-UHFFFAOYSA-N 0.000 description 1
- YOWPRXGSHUETEH-UHFFFAOYSA-N CCOP(CN(CC1)CCN1C(Oc(c(CN1Cc(cc2)ccc2F)c2C1=O)c(cccn1)c1c2O)=O)(OCC)=O Chemical compound CCOP(CN(CC1)CCN1C(Oc(c(CN1Cc(cc2)ccc2F)c2C1=O)c(cccn1)c1c2O)=O)(OCC)=O YOWPRXGSHUETEH-UHFFFAOYSA-N 0.000 description 1
- HULJRNLUJZHSAT-UHFFFAOYSA-N CCOP(CN(CC1)CCN1C(Oc(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2OC(c1ccccc1)c1ccccc1)=O)(OCC)=O Chemical compound CCOP(CN(CC1)CCN1C(Oc(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2OC(c1ccccc1)c1ccccc1)=O)(OCC)=O HULJRNLUJZHSAT-UHFFFAOYSA-N 0.000 description 1
- BJLCQRNXUYMQGX-UHFFFAOYSA-N CCOP(COc(c(C(N1Cc(cc2)ccc2F)=O)c2C1=O)c(cccn1)c1c2OCOC)(OCC)=O Chemical compound CCOP(COc(c(C(N1Cc(cc2)ccc2F)=O)c2C1=O)c(cccn1)c1c2OCOC)(OCC)=O BJLCQRNXUYMQGX-UHFFFAOYSA-N 0.000 description 1
- WRIZLDGIENMLKJ-UHFFFAOYSA-N CN(C)C(Oc(c1c(c(OC(c2ccccc2)c2ccccc2)c2C(N3Cc(cc4)ccc4F)=O)nccc1)c2C3=O)=O Chemical compound CN(C)C(Oc(c1c(c(OC(c2ccccc2)c2ccccc2)c2C(N3Cc(cc4)ccc4F)=O)nccc1)c2C3=O)=O WRIZLDGIENMLKJ-UHFFFAOYSA-N 0.000 description 1
- XMVLPQQBYBKRSC-UHFFFAOYSA-N CN(CC1)CCN1C(c(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2O)=O Chemical compound CN(CC1)CCN1C(c(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2O)=O XMVLPQQBYBKRSC-UHFFFAOYSA-N 0.000 description 1
- LZLCRLFICGGDOL-UHFFFAOYSA-N CN(CC1)CCN1C(c(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2OC(c1ccccc1)c1ccccc1)=O Chemical compound CN(CC1)CCN1C(c(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2OC(c1ccccc1)c1ccccc1)=O LZLCRLFICGGDOL-UHFFFAOYSA-N 0.000 description 1
- CDRSBPYJKRZQAY-UHFFFAOYSA-N COC(N1CCOCC1)=O Chemical compound COC(N1CCOCC1)=O CDRSBPYJKRZQAY-UHFFFAOYSA-N 0.000 description 1
- NBHQVSARENATMP-UHFFFAOYSA-N COC(c(c1c(c2c3cccn2)O)c3OC)N(Cc(cc2)ccc2F)C1=O Chemical compound COC(c(c1c(c2c3cccn2)O)c3OC)N(Cc(cc2)ccc2F)C1=O NBHQVSARENATMP-UHFFFAOYSA-N 0.000 description 1
- YLGIBCYHQZTFQL-UHFFFAOYSA-N COC(c1c(C(OC)=O)nccc1)=O Chemical compound COC(c1c(C(OC)=O)nccc1)=O YLGIBCYHQZTFQL-UHFFFAOYSA-N 0.000 description 1
- GNPAJMHWDXTGEU-UHFFFAOYSA-N COCc(c(CN1Cc(cc2)ccc2F)c2C1=O)c(cccn1)c1c2O Chemical compound COCc(c(CN1Cc(cc2)ccc2F)c2C1=O)c(cccn1)c1c2O GNPAJMHWDXTGEU-UHFFFAOYSA-N 0.000 description 1
- BVCPOBBMOIJWQM-UHFFFAOYSA-N COS(N1CCOCC1)(=O)=O Chemical compound COS(N1CCOCC1)(=O)=O BVCPOBBMOIJWQM-UHFFFAOYSA-N 0.000 description 1
- OMYDADTZOQJGJY-UHFFFAOYSA-N COc(c1c2nccc1)c(C(N(Cc(cc1)ccc1F)C1=O)O)c1c2O Chemical compound COc(c1c2nccc1)c(C(N(Cc(cc1)ccc1F)C1=O)O)c1c2O OMYDADTZOQJGJY-UHFFFAOYSA-N 0.000 description 1
- MOFOVVZFIXSIBO-UHFFFAOYSA-N COc(c1c2nccc1)c(CNCc1ccc(C(F)(F)F)cc1)c(C=O)c2O Chemical compound COc(c1c2nccc1)c(CNCc1ccc(C(F)(F)F)cc1)c(C=O)c2O MOFOVVZFIXSIBO-UHFFFAOYSA-N 0.000 description 1
- ALCKIYMYIPZUSA-UHFFFAOYSA-N COc1ccc(COc(c(nccc2)c2c(OC)c2CCC3Cc4ccc(C(C5)C5F)cc4)c2C3=O)cc1 Chemical compound COc1ccc(COc(c(nccc2)c2c(OC)c2CCC3Cc4ccc(C(C5)C5F)cc4)c2C3=O)cc1 ALCKIYMYIPZUSA-UHFFFAOYSA-N 0.000 description 1
- UHGMNYPRMIAFOS-UHFFFAOYSA-N C[BrH]Cc(cc1)ccc1[FH+] Chemical compound C[BrH]Cc(cc1)ccc1[FH+] UHGMNYPRMIAFOS-UHFFFAOYSA-N 0.000 description 1
- FLRUNCJXOVYWDH-UHFFFAOYSA-N Fc1ccc(CCBr)cc1 Chemical compound Fc1ccc(CCBr)cc1 FLRUNCJXOVYWDH-UHFFFAOYSA-N 0.000 description 1
- CEEWLJFUTGENPZ-UHFFFAOYSA-N O=C(N1CCOCC1)Oc(c1c(c(OC(c2ccccc2)c2ccccc2)c2C(N3Cc(cc4)ccc4F)=O)nccc1)c2C3=O Chemical compound O=C(N1CCOCC1)Oc(c1c(c(OC(c2ccccc2)c2ccccc2)c2C(N3Cc(cc4)ccc4F)=O)nccc1)c2C3=O CEEWLJFUTGENPZ-UHFFFAOYSA-N 0.000 description 1
- NEJCULBWOMKEQW-UHFFFAOYSA-N O=C(c(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2OC(c1ccccc1)c1ccccc1)N1CCOCC1 Chemical compound O=C(c(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2OC(c1ccccc1)c1ccccc1)N1CCOCC1 NEJCULBWOMKEQW-UHFFFAOYSA-N 0.000 description 1
- YGRYIEXQGCBECY-UHFFFAOYSA-N O=C(c(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2OC(c1ccccc1)c1ccccc1)NCc1ncccc1 Chemical compound O=C(c(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2OC(c1ccccc1)c1ccccc1)NCc1ncccc1 YGRYIEXQGCBECY-UHFFFAOYSA-N 0.000 description 1
- JXUZFCKBLOLVNA-UHFFFAOYSA-N O=C(c1c(c2c3cccn2)OC(c2ccccc2)c2ccccc2)N(Cc(cc2)ccc2F)Cc1c3-c1cccnc1F Chemical compound O=C(c1c(c2c3cccn2)OC(c2ccccc2)c2ccccc2)N(Cc(cc2)ccc2F)Cc1c3-c1cccnc1F JXUZFCKBLOLVNA-UHFFFAOYSA-N 0.000 description 1
- RCWYUURMVCVMDC-UHFFFAOYSA-N O=C(c1c2OC(c3ccccc3)c3ccccc3)N(Cc(cc3)ccc3F)Cc1c(C[Tl])c1c2nccc1 Chemical compound O=C(c1c2OC(c3ccccc3)c3ccccc3)N(Cc(cc3)ccc3F)Cc1c(C[Tl])c1c2nccc1 RCWYUURMVCVMDC-UHFFFAOYSA-N 0.000 description 1
- YUHZIUAREWNXJT-UHFFFAOYSA-N OB(c1cccnc1F)O Chemical compound OB(c1cccnc1F)O YUHZIUAREWNXJT-UHFFFAOYSA-N 0.000 description 1
- SXKNKZFUVSCCQQ-UHFFFAOYSA-N OC(c(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2OC(c1ccccc1)c1ccccc1)=O Chemical compound OC(c(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2OC(c1ccccc1)c1ccccc1)=O SXKNKZFUVSCCQQ-UHFFFAOYSA-N 0.000 description 1
- HWDKPMIPFNVPRN-UHFFFAOYSA-N OC(c1c2cccn1)=C(C(N(Cc(cc1)ccc1F)CC1)=O)N1C2=O Chemical compound OC(c1c2cccn1)=C(C(N(Cc(cc1)ccc1F)CC1)=O)N1C2=O HWDKPMIPFNVPRN-UHFFFAOYSA-N 0.000 description 1
- XTPMFKUKVFNGHE-UHFFFAOYSA-N OCc(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2O Chemical compound OCc(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2O XTPMFKUKVFNGHE-UHFFFAOYSA-N 0.000 description 1
- OUVKQCAXDVOIIT-UHFFFAOYSA-N Oc(c(nccc1)c1c(C(NCc1ncccc1)=O)c1CN2Cc(cc3)ccc3F)c1C2=O Chemical compound Oc(c(nccc1)c1c(C(NCc1ncccc1)=O)c1CN2Cc(cc3)ccc3F)c1C2=O OUVKQCAXDVOIIT-UHFFFAOYSA-N 0.000 description 1
- BKQRDTTVKLDXEW-UHFFFAOYSA-N Oc(c1c(c(OC(c2ccccc2)c2ccccc2)c2C(N3Cc(cc4)ccc4F)=O)nccc1)c2C3=O Chemical compound Oc(c1c(c(OC(c2ccccc2)c2ccccc2)c2C(N3Cc(cc4)ccc4F)=O)nccc1)c2C3=O BKQRDTTVKLDXEW-UHFFFAOYSA-N 0.000 description 1
- CXEDAXOASGQHFN-UHFFFAOYSA-N Oc(c1c2CN(Cc(cc3)ccc3F)C1=O)c1ncccc1c2-c1cccnc1F Chemical compound Oc(c1c2CN(Cc(cc3)ccc3F)C1=O)c1ncccc1c2-c1cccnc1F CXEDAXOASGQHFN-UHFFFAOYSA-N 0.000 description 1
- VLNUQIHFXPXQNT-UHFFFAOYSA-N [O-][N+](CCc(cc1)ccc1F)(Cc1c2c(O)c3ncccc3c1O)C2=O Chemical compound [O-][N+](CCc(cc1)ccc1F)(Cc1c2c(O)c3ncccc3c1O)C2=O VLNUQIHFXPXQNT-UHFFFAOYSA-N 0.000 description 1
- VSFMEENYJBQXBL-UHFFFAOYSA-N [O-][N+](c(cc1)ccc1OC(Oc(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2OC(c1ccccc1)c1ccccc1)=O)=O Chemical compound [O-][N+](c(cc1)ccc1OC(Oc(c1c2nccc1)c(CN(Cc(cc1)ccc1F)C1=O)c1c2OC(c1ccccc1)c1ccccc1)=O)=O VSFMEENYJBQXBL-UHFFFAOYSA-N 0.000 description 1
- KRCDZVCKWRELBZ-UHFFFAOYSA-N [O-][NH+](CCC=O)NCCc(cc1)ccc1F Chemical compound [O-][NH+](CCC=O)NCCc(cc1)ccc1F KRCDZVCKWRELBZ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D207/36—Oxygen or sulfur atoms
- C07D207/40—2,5-Pyrrolidine-diones
- C07D207/404—2,5-Pyrrolidine-diones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms, e.g. succinimide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
-
- 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
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/20—Spiro-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Virology (AREA)
- Public Health (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US41896302P | 2002-10-16 | 2002-10-16 | |
| US47878303P | 2003-06-16 | 2003-06-16 | |
| PCT/US2003/032666 WO2004035576A2 (en) | 2002-10-16 | 2003-10-16 | Pre-organized tricyclic integrase inhibitor compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006514099A true JP2006514099A (ja) | 2006-04-27 |
| JP2006514099A5 JP2006514099A5 (https=) | 2007-01-25 |
Family
ID=32110203
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2005501423A Pending JP2006514099A (ja) | 2002-10-16 | 2003-10-16 | 組織化前の三環系インテグラーゼインヒビター化合物 |
Country Status (19)
| Country | Link |
|---|---|
| US (3) | US20040157804A1 (https=) |
| EP (1) | EP1558613A2 (https=) |
| JP (1) | JP2006514099A (https=) |
| KR (1) | KR20050087787A (https=) |
| CN (1) | CN100374438C (https=) |
| AP (1) | AP1858A (https=) |
| AU (2) | AU2003301439A1 (https=) |
| BR (1) | BR0315405A (https=) |
| CA (1) | CA2501881A1 (https=) |
| EA (1) | EA011399B1 (https=) |
| HR (1) | HRP20050431A2 (https=) |
| IS (1) | IS7845A (https=) |
| MX (1) | MXPA05003950A (https=) |
| NO (1) | NO20052378L (https=) |
| NZ (1) | NZ539264A (https=) |
| OA (1) | OA13079A (https=) |
| PL (1) | PL377966A1 (https=) |
| UA (1) | UA79830C2 (https=) |
| WO (2) | WO2004035577A2 (https=) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007532665A (ja) * | 2004-04-14 | 2007-11-15 | ギリアード サイエンシーズ, インコーポレイテッド | Hivインテグラーゼ阻害剤化合物のホスホネート類似物 |
| JP2009537546A (ja) * | 2006-05-16 | 2009-10-29 | ギリアード サイエンシーズ, インコーポレイテッド | インテグラーゼ阻害剤 |
| JP2015510927A (ja) * | 2012-03-28 | 2015-04-13 | キュン ドン ファーマ. カンパニー. リミテッド. | ソリフェナシン又はその塩の製造方法及びここに用いられる新規な中間体 |
Families Citing this family (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
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- 2003-10-16 EA EA200500660A patent/EA011399B1/ru not_active IP Right Cessation
- 2003-10-16 OA OA1200500108A patent/OA13079A/en unknown
- 2003-10-16 BR BR0315405-0A patent/BR0315405A/pt not_active IP Right Cessation
- 2003-10-16 NZ NZ539264A patent/NZ539264A/en not_active IP Right Cessation
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| JP2007532665A (ja) * | 2004-04-14 | 2007-11-15 | ギリアード サイエンシーズ, インコーポレイテッド | Hivインテグラーゼ阻害剤化合物のホスホネート類似物 |
| JP2009537546A (ja) * | 2006-05-16 | 2009-10-29 | ギリアード サイエンシーズ, インコーポレイテッド | インテグラーゼ阻害剤 |
| JP2015510927A (ja) * | 2012-03-28 | 2015-04-13 | キュン ドン ファーマ. カンパニー. リミテッド. | ソリフェナシン又はその塩の製造方法及びここに用いられる新規な中間体 |
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| IS7845A (is) | 2005-05-13 |
| KR20050087787A (ko) | 2005-08-31 |
| WO2004035577A2 (en) | 2004-04-29 |
| NO20052378D0 (no) | 2005-05-13 |
| EA011399B1 (ru) | 2009-02-27 |
| NZ539264A (en) | 2007-08-31 |
| PL377966A1 (pl) | 2006-02-20 |
| WO2004035577A3 (en) | 2004-07-29 |
| CA2501881A1 (en) | 2004-04-29 |
| AP2005003279A0 (en) | 2005-06-30 |
| CN1726212A (zh) | 2006-01-25 |
| BR0315405A (pt) | 2005-08-09 |
| CN100374438C (zh) | 2008-03-12 |
| AP1858A (en) | 2008-06-30 |
| US20090029939A1 (en) | 2009-01-29 |
| AU2003301306A1 (en) | 2004-05-04 |
| NO20052378L (no) | 2005-07-18 |
| EA200500660A1 (ru) | 2005-10-27 |
| WO2004035576A2 (en) | 2004-04-29 |
| HRP20050431A2 (en) | 2005-10-31 |
| AU2003301439A8 (en) | 2004-05-04 |
| US7253180B2 (en) | 2007-08-07 |
| AU2003301439A1 (en) | 2004-05-04 |
| OA13079A (en) | 2006-11-10 |
| UA79830C2 (en) | 2007-07-25 |
| MXPA05003950A (es) | 2005-06-17 |
| US20040157804A1 (en) | 2004-08-12 |
| US20040167124A1 (en) | 2004-08-26 |
| EP1558613A2 (en) | 2005-08-03 |
| WO2004035576A3 (en) | 2004-06-24 |
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