KR20150038363A - 지방산 아미드 가수분해효소 억제제로서 보론산 및 에스테르 - Google Patents
지방산 아미드 가수분해효소 억제제로서 보론산 및 에스테르 Download PDFInfo
- Publication number
- KR20150038363A KR20150038363A KR20157004938A KR20157004938A KR20150038363A KR 20150038363 A KR20150038363 A KR 20150038363A KR 20157004938 A KR20157004938 A KR 20157004938A KR 20157004938 A KR20157004938 A KR 20157004938A KR 20150038363 A KR20150038363 A KR 20150038363A
- Authority
- KR
- South Korea
- Prior art keywords
- compound
- pain
- disorder
- ring
- acid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
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- 0 C1*Cc2ccccc2C1 Chemical compound C1*Cc2ccccc2C1 0.000 description 7
- KZARQRVCQFAFLV-UHFFFAOYSA-N CNc1cccc(Oc2ccc(B(O)O)c(F)c2)c1 Chemical compound CNc1cccc(Oc2ccc(B(O)O)c(F)c2)c1 KZARQRVCQFAFLV-UHFFFAOYSA-N 0.000 description 2
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N C(CC1)Cc2c1cccc2 Chemical compound C(CC1)Cc2c1cccc2 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- PQNFLJBBNBOBRQ-UHFFFAOYSA-N C1Cc2ccccc2C1 Chemical compound C1Cc2ccccc2C1 PQNFLJBBNBOBRQ-UHFFFAOYSA-N 0.000 description 1
- IUPMNJLTOMOSCN-UHFFFAOYSA-N CC(C)(C)OC(Nc1cccc(Oc2ccc(B(O)O)cc2)c1)=O Chemical compound CC(C)(C)OC(Nc1cccc(Oc2ccc(B(O)O)cc2)c1)=O IUPMNJLTOMOSCN-UHFFFAOYSA-N 0.000 description 1
- BICZJRAGTCRORZ-UHFFFAOYSA-N CC1(C)OB(c(cc2)ccc2O)OC1(C)C Chemical compound CC1(C)OB(c(cc2)ccc2O)OC1(C)C BICZJRAGTCRORZ-UHFFFAOYSA-N 0.000 description 1
- GZYWXRDNPQGFDF-UHFFFAOYSA-N CC1(C)OB(c(cc2)ccc2OC(C(OC)=O)c2ccccc2)OC1(C)C Chemical compound CC1(C)OB(c(cc2)ccc2OC(C(OC)=O)c2ccccc2)OC1(C)C GZYWXRDNPQGFDF-UHFFFAOYSA-N 0.000 description 1
- KXDVXOAERXJLBN-UHFFFAOYSA-N CC1(C)OB(c(ccc(OCc2ccccn2)c2)c2F)OC1(C)C Chemical compound CC1(C)OB(c(ccc(OCc2ccccn2)c2)c2F)OC1(C)C KXDVXOAERXJLBN-UHFFFAOYSA-N 0.000 description 1
- QQCCKPKPTCJAIL-UHFFFAOYSA-N CC1(C)OB(c2ccc(COCc3ccccc3)cc2F)OC1(C)C Chemical compound CC1(C)OB(c2ccc(COCc3ccccc3)cc2F)OC1(C)C QQCCKPKPTCJAIL-UHFFFAOYSA-N 0.000 description 1
- ZXYNEWKLRDSTDE-UHFFFAOYSA-N CC1(C)OS(c(cc2)ccc2Oc(cc2OC)ccc2OC)OC1(C)C Chemical compound CC1(C)OS(c(cc2)ccc2Oc(cc2OC)ccc2OC)OC1(C)C ZXYNEWKLRDSTDE-UHFFFAOYSA-N 0.000 description 1
- RWDHLDMENYLBGI-UHFFFAOYSA-N CCCCNC(C(c1ccccc1)Oc1ccc(B(O)O)cc1)=O Chemical compound CCCCNC(C(c1ccccc1)Oc1ccc(B(O)O)cc1)=O RWDHLDMENYLBGI-UHFFFAOYSA-N 0.000 description 1
- BDEQMLVXSPXIJE-UHFFFAOYSA-N CN(C)CCNC(C(c1ccccc1)Oc1ccc(B(O)O)cc1)=O Chemical compound CN(C)CCNC(C(c1ccccc1)Oc1ccc(B(O)O)cc1)=O BDEQMLVXSPXIJE-UHFFFAOYSA-N 0.000 description 1
- XLLNWOQNGNIYKO-UHFFFAOYSA-N CNCC(C1)C=CC=C1Oc(ccc(BO)c1)c1F Chemical compound CNCC(C1)C=CC=C1Oc(ccc(BO)c1)c1F XLLNWOQNGNIYKO-UHFFFAOYSA-N 0.000 description 1
- NHFBYYMNJUMVOT-UHFFFAOYSA-N COC(C(c1ccccc1)Br)=O Chemical compound COC(C(c1ccccc1)Br)=O NHFBYYMNJUMVOT-UHFFFAOYSA-N 0.000 description 1
- NQAUERNGZXLUMH-UHFFFAOYSA-N COc(ccc(Oc1ccc(B(O)O)cc1)c1)c1OC Chemical compound COc(ccc(Oc1ccc(B(O)O)cc1)c1)c1OC NQAUERNGZXLUMH-UHFFFAOYSA-N 0.000 description 1
- CTGCYEJPFDKLMG-UHFFFAOYSA-N COc1cc(CCOc2ccc(B(O)O)c(F)c2)ccc1 Chemical compound COc1cc(CCOc2ccc(B(O)O)c(F)c2)ccc1 CTGCYEJPFDKLMG-UHFFFAOYSA-N 0.000 description 1
- NIFMWOZJWQMYHR-UHFFFAOYSA-N COc1ccc(CCOc2cc(F)c(B(O)O)cc2)cc1 Chemical compound COc1ccc(CCOc2cc(F)c(B(O)O)cc2)cc1 NIFMWOZJWQMYHR-UHFFFAOYSA-N 0.000 description 1
- PLTJTMQTLUYGRI-UHFFFAOYSA-N Cc(c(Cl)c1)ccc1Oc1cc(F)c(B(O)O)cc1 Chemical compound Cc(c(Cl)c1)ccc1Oc1cc(F)c(B(O)O)cc1 PLTJTMQTLUYGRI-UHFFFAOYSA-N 0.000 description 1
- ISYGGWCHIABPJM-UHFFFAOYSA-N Cc(c(Cl)c1)ccc1Oc1ccc(B(O)O)cc1 Chemical compound Cc(c(Cl)c1)ccc1Oc1ccc(B(O)O)cc1 ISYGGWCHIABPJM-UHFFFAOYSA-N 0.000 description 1
- BFJKLSUHKODVAZ-UHFFFAOYSA-N Cc(cc(COc1ccc(B(O)O)cc1)cc1)c1F Chemical compound Cc(cc(COc1ccc(B(O)O)cc1)cc1)c1F BFJKLSUHKODVAZ-UHFFFAOYSA-N 0.000 description 1
- VKIIQKMQOFDPTG-UHFFFAOYSA-N Nc1cccc(Oc2ccc(B(O)O)cc2)c1 Chemical compound Nc1cccc(Oc2ccc(B(O)O)cc2)c1 VKIIQKMQOFDPTG-UHFFFAOYSA-N 0.000 description 1
- XHLHPRDBBAGVEG-UHFFFAOYSA-N O=C1c2ccccc2CCC1 Chemical compound O=C1c2ccccc2CCC1 XHLHPRDBBAGVEG-UHFFFAOYSA-N 0.000 description 1
- PUXUKRSBJVVKMD-UHFFFAOYSA-N OB(c(cc1)ccc1C(N1CCCCC1)=O)O Chemical compound OB(c(cc1)ccc1C(N1CCCCC1)=O)O PUXUKRSBJVVKMD-UHFFFAOYSA-N 0.000 description 1
- BXLDWIUCAAJXIZ-UHFFFAOYSA-N OB(c(cc1)ccc1Oc(cc1)ccc1F)O Chemical compound OB(c(cc1)ccc1Oc(cc1)ccc1F)O BXLDWIUCAAJXIZ-UHFFFAOYSA-N 0.000 description 1
- ZAAIGKIEQCTAJN-UHFFFAOYSA-N OB(c1cccc(OCCc2ccccc2)c1)O Chemical compound OB(c1cccc(OCCc2ccccc2)c1)O ZAAIGKIEQCTAJN-UHFFFAOYSA-N 0.000 description 1
- AGKUZEDHOYVCTA-UHFFFAOYSA-N OS(c1ccc(COCc2ccccc2)cc1F)O Chemical compound OS(c1ccc(COCc2ccccc2)cc1F)O AGKUZEDHOYVCTA-UHFFFAOYSA-N 0.000 description 1
- TXCDCPKCNAJMEE-UHFFFAOYSA-N c(cc1)cc2c1[o]c1ccccc21 Chemical compound c(cc1)cc2c1[o]c1ccccc21 TXCDCPKCNAJMEE-UHFFFAOYSA-N 0.000 description 1
- MFYPSDMVCKGABG-UHFFFAOYSA-N c(cc1)cc2c1[s]c1c2C=CC=C=C1 Chemical compound c(cc1)cc2c1[s]c1c2C=CC=C=C1 MFYPSDMVCKGABG-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/025—Boronic and borinic acid compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/04—Esters of boric acids
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- C07F5/05—Cyclic compounds having at least one ring containing boron but no carbon in the ring
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Diabetes (AREA)
- Pain & Pain Management (AREA)
- Ophthalmology & Optometry (AREA)
- Hematology (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Oncology (AREA)
- Cardiology (AREA)
- Immunology (AREA)
- Psychiatry (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Dermatology (AREA)
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US85052006P | 2006-10-10 | 2006-10-10 | |
| US60/850,520 | 2006-10-10 | ||
| PCT/US2007/021626 WO2008063300A2 (en) | 2006-10-10 | 2007-10-10 | Boronic acids and esters as inhibitors of fatty acid amide hydrolase |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020097009547A Division KR20090085623A (ko) | 2006-10-10 | 2007-10-10 | 지방산 아미드 가수분해효소 억제제로서 보론산 및 에스테르 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
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