CA2338804A1 - Propenamides tenant lieu de modulateurs de ccr5 - Google Patents
Propenamides tenant lieu de modulateurs de ccr5 Download PDFInfo
- Publication number
- CA2338804A1 CA2338804A1 CA002338804A CA2338804A CA2338804A1 CA 2338804 A1 CA2338804 A1 CA 2338804A1 CA 002338804 A CA002338804 A CA 002338804A CA 2338804 A CA2338804 A CA 2338804A CA 2338804 A1 CA2338804 A1 CA 2338804A1
- Authority
- CA
- Canada
- Prior art keywords
- propenamide
- methylethyl
- amino
- methoxyphenyl
- bis
- 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
Links
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical class NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 title description 5
- 230000001404 mediated effect Effects 0.000 claims abstract description 13
- 102100035875 C-C chemokine receptor type 5 Human genes 0.000 claims abstract 3
- 101710149870 C-C chemokine receptor type 5 Proteins 0.000 claims abstract 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 236
- 239000001257 hydrogen Substances 0.000 claims description 133
- 229910052739 hydrogen Inorganic materials 0.000 claims description 133
- 150000001875 compounds Chemical class 0.000 claims description 117
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 104
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 95
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 80
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 77
- 229910052760 oxygen Inorganic materials 0.000 claims description 75
- 239000001301 oxygen Substances 0.000 claims description 75
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims description 75
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 71
- 229910052757 nitrogen Inorganic materials 0.000 claims description 67
- 229910052717 sulfur Chemical group 0.000 claims description 57
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 56
- -1 nitro, hydroxy Chemical group 0.000 claims description 52
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 49
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 45
- 239000011593 sulfur Chemical group 0.000 claims description 45
- 238000000034 method Methods 0.000 claims description 41
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 40
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 39
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 35
- 229910052736 halogen Inorganic materials 0.000 claims description 32
- 150000002367 halogens Chemical class 0.000 claims description 32
- 125000005842 heteroatom Chemical group 0.000 claims description 32
- 125000003118 aryl group Chemical group 0.000 claims description 25
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 23
- 201000010099 disease Diseases 0.000 claims description 22
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 22
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 20
- 125000003341 7 membered heterocyclic group Chemical group 0.000 claims description 18
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 18
- 125000000623 heterocyclic group Chemical group 0.000 claims description 16
- 241000124008 Mammalia Species 0.000 claims description 14
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 14
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims description 12
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 12
- 125000001424 substituent group Chemical group 0.000 claims description 12
- 125000004434 sulfur atom Chemical group 0.000 claims description 12
- 125000000217 alkyl group Chemical group 0.000 claims description 10
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 9
- 208000006673 asthma Diseases 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 9
- 125000006569 (C5-C6) heterocyclic group Chemical group 0.000 claims description 8
- 201000001320 Atherosclerosis Diseases 0.000 claims description 8
- 208000023275 Autoimmune disease Diseases 0.000 claims description 8
- 201000006417 multiple sclerosis Diseases 0.000 claims description 8
- 206010039073 rheumatoid arthritis Diseases 0.000 claims description 8
- 125000003003 spiro group Chemical group 0.000 claims description 8
- 208000012657 Atopic disease Diseases 0.000 claims description 7
- 208000022559 Inflammatory bowel disease Diseases 0.000 claims description 7
- 201000004681 Psoriasis Diseases 0.000 claims description 7
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 7
- 230000003176 fibrotic effect Effects 0.000 claims description 7
- 201000000306 sarcoidosis Diseases 0.000 claims description 7
- 229920006395 saturated elastomer Polymers 0.000 claims description 7
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 7
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 6
- CUNZZPZFOHHRGZ-UHFFFAOYSA-N 3-(3,4-dichlorophenyl)-n-[3-[2-(4-hydroxy-2,2,6,6-tetramethylpiperidin-1-yl)ethoxy]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(OCCN2C(CC(O)CC2(C)C)(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC=C(Cl)C(Cl)=C1 CUNZZPZFOHHRGZ-UHFFFAOYSA-N 0.000 claims description 5
- 125000004043 oxo group Chemical group O=* 0.000 claims description 5
- FGNZVDRLBMFMGN-UHFFFAOYSA-N 3-(3,5-dichlorophenyl)-n-[3-[3-[di(propan-2-yl)amino]propyl]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(CCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC(Cl)=CC(Cl)=C1 FGNZVDRLBMFMGN-UHFFFAOYSA-N 0.000 claims description 4
- HRGZVUKFLZMFNF-UHFFFAOYSA-N 3-(4-chlorophenyl)-n-[3-[2-[cyclohexyl(propan-2-yl)amino]ethoxy]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(OCCN(C(C)C)C2CCCCC2)C(OC)=CC=C1NC(=O)C=CC1=CC=C(Cl)C=C1 HRGZVUKFLZMFNF-UHFFFAOYSA-N 0.000 claims description 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 4
- 125000002619 bicyclic group Chemical group 0.000 claims description 4
- BJCDHWBKBFXORB-UHFFFAOYSA-N n-[3-[2-[cyclohexyl(propan-2-yl)amino]ethoxy]-4-methoxyphenyl]-3-naphthalen-2-ylprop-2-enamide Chemical compound COC1=CC=C(NC(=O)C=CC=2C=C3C=CC=CC3=CC=2)C=C1OCCN(C(C)C)C1CCCCC1 BJCDHWBKBFXORB-UHFFFAOYSA-N 0.000 claims description 4
- ZDFITJIULSSMHI-UHFFFAOYSA-N n-[3-[2-[di(propan-2-yl)amino]ethoxy]-4-methoxyphenyl]-3-phenylprop-2-enamide Chemical compound C1=C(OCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC=CC=C1 ZDFITJIULSSMHI-UHFFFAOYSA-N 0.000 claims description 4
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 3
- JSUQONHTBZBGMJ-MLBSPLJJSA-N (e)-3-(3,5-dichlorophenyl)-n-[3-[2-[di(propan-2-yl)amino]ethoxy]-4-methoxyphenyl]prop-2-enamide;2,2,2-trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.C1=C(OCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)\C=C\C1=CC(Cl)=CC(Cl)=C1 JSUQONHTBZBGMJ-MLBSPLJJSA-N 0.000 claims description 3
- ORECMWXWQUTRKQ-KRWCAOSLSA-N (e)-n-[3-[2-[di(propan-2-yl)amino]ethoxy]-4-methoxyphenyl]-3-(5,6,7,8-tetrahydronaphthalen-2-yl)prop-2-enamide;2,2,2-trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.C1=C(OCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)\C=C\C1=CC=C(CCCC2)C2=C1 ORECMWXWQUTRKQ-KRWCAOSLSA-N 0.000 claims description 3
- CZQKMCWEXUCYMU-UHFFFAOYSA-N 3-(1,3-benzodioxol-5-yl)-n-[3-[2-[di(propan-2-yl)amino]ethoxy]-4-methylphenyl]prop-2-enamide Chemical compound C1=C(C)C(OCCN(C(C)C)C(C)C)=CC(NC(=O)C=CC=2C=C3OCOC3=CC=2)=C1 CZQKMCWEXUCYMU-UHFFFAOYSA-N 0.000 claims description 3
- FBBJNEXZORSTLE-UHFFFAOYSA-N 3-(2,5-difluorophenyl)-n-[3-[3-[di(propan-2-yl)amino]propyl]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(CCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC(F)=CC=C1F FBBJNEXZORSTLE-UHFFFAOYSA-N 0.000 claims description 3
- SNDCNLDGQGHRBB-UHFFFAOYSA-N 3-(2,6-dichlorophenyl)-n-[3-[2-[di(propan-2-yl)amino]ethoxy]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(OCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=C(Cl)C=CC=C1Cl SNDCNLDGQGHRBB-UHFFFAOYSA-N 0.000 claims description 3
- NJBOCQKSCAGYEH-UHFFFAOYSA-N 3-(3,4-dichlorophenyl)-n-[3-[2-[di(propan-2-yl)amino]ethoxy]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(OCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC=C(Cl)C(Cl)=C1 NJBOCQKSCAGYEH-UHFFFAOYSA-N 0.000 claims description 3
- WJQHVTYRZXZVJO-UHFFFAOYSA-N 3-(3,4-dichlorophenyl)-n-[4-[2-[di(propan-2-yl)amino]ethyl]-3-oxo-1,4-benzoxazin-6-yl]prop-2-enamide Chemical compound C1=C2N(CCN(C(C)C)C(C)C)C(=O)COC2=CC=C1NC(=O)C=CC1=CC=C(Cl)C(Cl)=C1 WJQHVTYRZXZVJO-UHFFFAOYSA-N 0.000 claims description 3
- VZBOMBKITKYXET-HDICACEKSA-N 3-(3,4-difluorophenyl)-N-[3-[2-[(2R,6S)-2,6-dimethylpiperidin-1-yl]ethoxy]-4-methoxyphenyl]prop-2-enamide Chemical compound COc1ccc(NC(=O)C=Cc2ccc(F)c(F)c2)cc1OCCN1[C@@H](C)CCC[C@H]1C VZBOMBKITKYXET-HDICACEKSA-N 0.000 claims description 3
- JAWLWSSBGMYFDT-KDURUIRLSA-N 3-(3-chlorophenyl)-N-[3-[2-[(2R,6S)-2,6-dimethylpiperidin-1-yl]ethoxy]-4-methoxyphenyl]prop-2-enamide Chemical compound COc1ccc(NC(=O)C=Cc2cccc(Cl)c2)cc1OCCN1[C@@H](C)CCC[C@H]1C JAWLWSSBGMYFDT-KDURUIRLSA-N 0.000 claims description 3
- TUPCTOSSDCQKLZ-UHFFFAOYSA-N 3-(3-chlorophenyl)-n-[3-[2-[cyclohexyl(propan-2-yl)amino]ethoxy]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(OCCN(C(C)C)C2CCCCC2)C(OC)=CC=C1NC(=O)C=CC1=CC=CC(Cl)=C1 TUPCTOSSDCQKLZ-UHFFFAOYSA-N 0.000 claims description 3
- KOZDAMYTKYBGML-UHFFFAOYSA-N 3-(4-bromo-2-fluorophenyl)-n-[3-[3-[di(propan-2-yl)amino]propyl]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(CCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC=C(Br)C=C1F KOZDAMYTKYBGML-UHFFFAOYSA-N 0.000 claims description 3
- PINCXZLCYFBLPX-UHFFFAOYSA-N 3-(4-bromophenyl)-n-[3-[3-[di(propan-2-yl)amino]propyl]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(CCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC=C(Br)C=C1 PINCXZLCYFBLPX-UHFFFAOYSA-N 0.000 claims description 3
- GFECRZGWNDOJQD-KDURUIRLSA-N 3-(4-chlorophenyl)-N-[3-[2-[(2R,6S)-2,6-dimethylpiperidin-1-yl]ethoxy]-4-methoxyphenyl]prop-2-enamide Chemical compound COc1ccc(NC(=O)C=Cc2ccc(Cl)cc2)cc1OCCN1[C@@H](C)CCC[C@H]1C GFECRZGWNDOJQD-KDURUIRLSA-N 0.000 claims description 3
- DHWFVFMBOGQDKN-UHFFFAOYSA-N 3-(4-chlorophenyl)-n-[3-[2-[di(propan-2-yl)amino]ethoxy]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(OCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC=C(Cl)C=C1 DHWFVFMBOGQDKN-UHFFFAOYSA-N 0.000 claims description 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 3
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 3
- 150000001204 N-oxides Chemical class 0.000 claims description 3
- 125000004423 acyloxy group Chemical group 0.000 claims description 3
- 125000002837 carbocyclic group Chemical group 0.000 claims description 3
- ICPMFUCRIGRMLZ-UHFFFAOYSA-N n-[3-[2-[cyclohexyl(propan-2-yl)amino]ethoxy]-4-methoxyphenyl]-3-thiophen-3-ylprop-2-enamide Chemical compound C1=C(OCCN(C(C)C)C2CCCCC2)C(OC)=CC=C1NC(=O)C=CC=1C=CSC=1 ICPMFUCRIGRMLZ-UHFFFAOYSA-N 0.000 claims description 3
- GSLUTUWKTUXCJR-UHFFFAOYSA-N n-[3-[2-[di(propan-2-yl)amino]ethoxy]-4-methoxyphenyl]-3-(4-propan-2-ylphenyl)prop-2-enamide Chemical compound C1=C(OCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC=C(C(C)C)C=C1 GSLUTUWKTUXCJR-UHFFFAOYSA-N 0.000 claims description 3
- UIYQBQOAXIXLEU-UHFFFAOYSA-N n-[3-[2-[di(propan-2-yl)amino]ethoxy]-4-methoxyphenyl]-3-naphthalen-2-ylprop-2-enamide;hydrochloride Chemical compound Cl.C1=C(OCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC=C(C=CC=C2)C2=C1 UIYQBQOAXIXLEU-UHFFFAOYSA-N 0.000 claims description 3
- 229910052700 potassium Inorganic materials 0.000 claims description 3
- DMSULQZMZCVLNU-FMIVXFBMSA-N (e)-3-(3-chlorophenyl)-n-[3-[2-[di(propan-2-yl)amino]ethoxy]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(OCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)\C=C\C1=CC=CC(Cl)=C1 DMSULQZMZCVLNU-FMIVXFBMSA-N 0.000 claims description 2
- FHVXLYWHSUGMHK-XYOKQWHBSA-N (e)-3-(4-chloro-3-methylphenyl)-n-[3-[2-[di(propan-2-yl)amino]ethoxy]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(OCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)\C=C\C1=CC=C(Cl)C(C)=C1 FHVXLYWHSUGMHK-XYOKQWHBSA-N 0.000 claims description 2
- SUCOGJAGYUKETD-YRNVUSSQSA-N (e)-n-[3-[2-[di(propan-2-yl)amino]ethoxy]-4-methoxyphenyl]-3-(1h-indol-5-yl)prop-2-enamide Chemical compound C1=C(OCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)\C=C\C1=CC=C(NC=C2)C2=C1 SUCOGJAGYUKETD-YRNVUSSQSA-N 0.000 claims description 2
- NCUMGBLUFZNWAE-MDWZMJQESA-N (e)-n-[3-[2-[di(propan-2-yl)amino]ethoxy]-4-methoxyphenyl]-3-[4-(trifluoromethyl)phenyl]prop-2-enamide Chemical compound C1=C(OCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)\C=C\C1=CC=C(C(F)(F)F)C=C1 NCUMGBLUFZNWAE-MDWZMJQESA-N 0.000 claims description 2
- HPIYRAVKJPKVQA-UHFFFAOYSA-N 3-(1,3-benzodioxol-5-yl)-n-[3-[2-[cyclohexyl(propan-2-yl)amino]ethoxy]-4-methoxyphenyl]prop-2-enamide Chemical compound COC1=CC=C(NC(=O)C=CC=2C=C3OCOC3=CC=2)C=C1OCCN(C(C)C)C1CCCCC1 HPIYRAVKJPKVQA-UHFFFAOYSA-N 0.000 claims description 2
- NMWWCYLSVIQBND-UHFFFAOYSA-N 3-(1-benzofuran-2-yl)-n-[3-[2-[di(propan-2-yl)amino]ethoxy]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(OCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC2=CC=CC=C2O1 NMWWCYLSVIQBND-UHFFFAOYSA-N 0.000 claims description 2
- MHLZPFWUYKDFER-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-n-[3-[3-[di(propan-2-yl)amino]propyl]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(CCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC=C(Cl)C=C1Cl MHLZPFWUYKDFER-UHFFFAOYSA-N 0.000 claims description 2
- ZQOJJLAZWBMPQI-UHFFFAOYSA-N 3-(2-chloro-6-fluorophenyl)-n-[3-[3-[di(propan-2-yl)amino]propyl]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(CCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=C(F)C=CC=C1Cl ZQOJJLAZWBMPQI-UHFFFAOYSA-N 0.000 claims description 2
- BSMKCSHOGNJYOA-UHFFFAOYSA-N 3-(3,4-dichlorophenyl)-n-[3-[2-[di(propan-2-yl)amino]ethyl]-2-oxo-1,3-benzoxazol-5-yl]prop-2-enamide Chemical compound C=1C=C2OC(=O)N(CCN(C(C)C)C(C)C)C2=CC=1NC(=O)C=CC1=CC=C(Cl)C(Cl)=C1 BSMKCSHOGNJYOA-UHFFFAOYSA-N 0.000 claims description 2
- GINRIGAKBVVGLV-UHFFFAOYSA-N 3-(3,4-dichlorophenyl)-n-[4-methoxy-3-[2-(2,2,6,6-tetramethylpiperidin-1-yl)ethoxy]phenyl]prop-2-enamide Chemical compound C1=C(OCCN2C(CCCC2(C)C)(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC=C(Cl)C(Cl)=C1 GINRIGAKBVVGLV-UHFFFAOYSA-N 0.000 claims description 2
- BAVDRDDWMKYVPK-UHFFFAOYSA-N 3-(3,4-difluorophenyl)-n-[3-[2-[di(propan-2-yl)amino]ethoxy]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(OCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC=C(F)C(F)=C1 BAVDRDDWMKYVPK-UHFFFAOYSA-N 0.000 claims description 2
- SIDYMZZFBDHGBR-UHFFFAOYSA-N 3-(3,4-difluorophenyl)-n-[3-[3-[di(propan-2-yl)amino]propoxy]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(OCCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC=C(F)C(F)=C1 SIDYMZZFBDHGBR-UHFFFAOYSA-N 0.000 claims description 2
- QKQFUQHCTKIHTE-UHFFFAOYSA-N 3-(3,5-difluorophenyl)-n-[3-[2-[di(propan-2-yl)amino]ethoxy]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(OCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC(F)=CC(F)=C1 QKQFUQHCTKIHTE-UHFFFAOYSA-N 0.000 claims description 2
- CSGOBAWPGAVHSZ-UHFFFAOYSA-N 3-(3-chlorophenyl)-n-[3-[3-[di(propan-2-yl)amino]propoxy]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(OCCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC=CC(Cl)=C1 CSGOBAWPGAVHSZ-UHFFFAOYSA-N 0.000 claims description 2
- IKUPROKQDWOUEP-UHFFFAOYSA-N 3-(3-chlorophenyl)-n-[3-[3-[di(propan-2-yl)amino]propyl]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(CCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC=CC(Cl)=C1 IKUPROKQDWOUEP-UHFFFAOYSA-N 0.000 claims description 2
- NIQOATOLKAEVMS-UHFFFAOYSA-N 3-(4-chloro-2-fluorophenyl)-n-[3-[3-[di(propan-2-yl)amino]propyl]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(CCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC=C(Cl)C=C1F NIQOATOLKAEVMS-UHFFFAOYSA-N 0.000 claims description 2
- OFXITBCILYAHTL-UHFFFAOYSA-N 3-(4-chloro-3-nitrophenyl)-n-[3-[2-[di(propan-2-yl)amino]ethoxy]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(OCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC=C(Cl)C([N+]([O-])=O)=C1 OFXITBCILYAHTL-UHFFFAOYSA-N 0.000 claims description 2
- AVMQUFFPBOBMID-UHFFFAOYSA-N 3-(4-chloro-3-nitrophenyl)-n-[3-[3-[di(propan-2-yl)amino]propyl]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(CCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC=C(Cl)C([N+]([O-])=O)=C1 AVMQUFFPBOBMID-UHFFFAOYSA-N 0.000 claims description 2
- STZMMNALJSTEDN-UHFFFAOYSA-N 3-(4-chlorophenyl)-n-[3-[3-[di(propan-2-yl)amino]propyl]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(CCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC=C(Cl)C=C1 STZMMNALJSTEDN-UHFFFAOYSA-N 0.000 claims description 2
- JPDJWLJEJZUYEM-UHFFFAOYSA-N 3-(4-cyanophenyl)-n-[3-[3-[di(propan-2-yl)amino]propyl]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(CCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC=C(C#N)C=C1 JPDJWLJEJZUYEM-UHFFFAOYSA-N 0.000 claims description 2
- RJBVTSUHMNAPCQ-UHFFFAOYSA-N 3-(5-bromo-2-methoxyphenyl)-n-[3-[2-[di(propan-2-yl)amino]ethoxy]-4-methoxyphenyl]prop-2-enamide Chemical compound C1=C(OCCN(C(C)C)C(C)C)C(OC)=CC=C1NC(=O)C=CC1=CC(Br)=CC=C1OC RJBVTSUHMNAPCQ-UHFFFAOYSA-N 0.000 claims description 2
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Classifications
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- 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
- C07D207/04—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 no double bonds between ring members or between ring members and non-ring members
- C07D207/08—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 no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
-
- 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
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
- A61K31/167—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
-
- 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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
- A61K31/341—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide not condensed with another ring, e.g. ranitidine, furosemide, bufetolol, muscarine
-
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Abstract
L'invention concerne des anilides substitués qui tiennent lieu de modulateurs, d'agonistes ou d'antagonistes vis-à-vis du récepteur CCR5. L'invention concerne également le traitement et la prévention d'affections dont la médiation est assurée par ledit récepteur.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9440598P | 1998-07-28 | 1998-07-28 | |
| US60/094,405 | 1998-07-28 | ||
| PCT/US1999/017117 WO2000006153A1 (fr) | 1998-07-28 | 1999-07-28 | Propenamides tenant lieu de modulateurs de ccr5 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2338804A1 true CA2338804A1 (fr) | 2000-02-10 |
Family
ID=22244982
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002338804A Abandoned CA2338804A1 (fr) | 1998-07-28 | 1999-07-28 | Propenamides tenant lieu de modulateurs de ccr5 |
Country Status (4)
| Country | Link |
|---|---|
| EP (1) | EP1100495A4 (fr) |
| JP (1) | JP2002521441A (fr) |
| CA (1) | CA2338804A1 (fr) |
| WO (1) | WO2000006153A1 (fr) |
Families Citing this family (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6025154A (en) | 1995-06-06 | 2000-02-15 | Human Genome Sciences, Inc. | Polynucleotides encoding human G-protein chemokine receptor HDGNR10 |
| DE19935219A1 (de) | 1999-07-27 | 2001-02-01 | Boehringer Ingelheim Pharma | Carbonsäureamide, diese Verbindungen enthaltende Arzneimittel, deren Verwendung und Herstellung |
| AU2001241128A1 (en) * | 2000-03-14 | 2001-09-24 | Fujisawa Pharmaceutical Co. Ltd. | Novel amide compounds |
| US7175988B2 (en) | 2001-02-09 | 2007-02-13 | Human Genome Sciences, Inc. | Human G-protein Chemokine Receptor (CCR5) HDGNR10 |
| JP2005518371A (ja) | 2001-12-10 | 2005-06-23 | アムジエン・インコーポレーテツド | バニロイド受容体リガンド及び治療に於けるこれらの使用 |
| US7393934B2 (en) | 2001-12-21 | 2008-07-01 | Human Genome Sciences, Inc. | Human G-protein chemokine receptor (CCR5) HDGNR10 |
| US7482488B2 (en) * | 2002-08-29 | 2009-01-27 | Temple University - Of The Commonwealth System Of Higher Education | Aryl and heteroaryl propene amides, derivatives thereof and therapeutic uses thereof |
| US7504508B2 (en) | 2002-10-04 | 2009-03-17 | Millennium Pharmaceuticals, Inc. | PGD2 receptor antagonists for the treatment of inflammatory diseases |
| WO2004032848A2 (fr) | 2002-10-04 | 2004-04-22 | Millennium Pharmaceuticals, Inc. | Antagonistes vis-a-vis du recepteur pgd2 pour le traitement de maladies inflammatoires |
| DE10250743A1 (de) * | 2002-10-31 | 2004-05-19 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue Amid-Verbindungen mit MCH-antagonistischer Wirkung und diese Verbindungen enthaltende Arzneimittel |
| US7351719B2 (en) | 2002-10-31 | 2008-04-01 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Amide compounds having MCH-antagonistic activity and medicaments comprising these compounds |
| RU2366655C2 (ru) | 2003-03-14 | 2009-09-10 | Оно Фармасьютикал Ко., Лтд. | Азотсодержащие гетероциклические производные и лекарственные средства, содержащие их в качестве активного ингредиента |
| WO2004092169A1 (fr) | 2003-04-18 | 2004-10-28 | Ono Pharmaceutical Co., Ltd. | Compose de spiropiperidine et son utilisation medicinale |
| US7592373B2 (en) | 2003-12-23 | 2009-09-22 | Boehringer Ingelheim International Gmbh | Amide compounds with MCH antagonistic activity and medicaments comprising these compounds |
| EP1723178A4 (fr) | 2004-03-12 | 2007-12-12 | Human Genome Sciences Inc | Recepteur humain (ccr5) hdgnr10 de chimiokine de la proteine g |
| US7524862B2 (en) | 2004-04-14 | 2009-04-28 | Boehringer Ingelheim International Gmbh | Alkyne compounds with MCH antagonistic activity and medicaments comprising these compounds |
| DE102004017934A1 (de) | 2004-04-14 | 2005-11-03 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue Alkin-Verbindungen mit MCH-antagonistischer Wirkung und diese Verbindungen enthaltende Arzneimittel |
| KR20070034524A (ko) | 2004-05-28 | 2007-03-28 | 버텍스 파마슈티칼스 인코포레이티드 | 무스카린 수용체 조정자 |
| EP2374455A3 (fr) | 2004-08-19 | 2012-03-28 | Vertex Pharmaceuticals Incorporated | Modulateurs des recepteurs muscariniques |
| US7786141B2 (en) | 2004-08-19 | 2010-08-31 | Vertex Pharmaceuticals Incorporated | Dihydrospiroindene modulators of muscarinic receptors |
| US8143404B2 (en) | 2004-09-13 | 2012-03-27 | Ono Pharmaceutical Co., Ltd | Nitrogenous heterocylic derivative and medicine containing the same as an active ingredient |
| JPWO2006054793A1 (ja) * | 2004-11-19 | 2008-06-05 | 財団法人新産業創造研究機構 | ベンゾフラン化合物、およびそれを含有してなる医薬組成物 |
| RU2007124373A (ru) | 2004-11-29 | 2009-01-10 | Вертекс Фармасьютикалз Инкорпорейтед (Us) | Модуляторы мускариновых рецептеров |
| WO2006091674A1 (fr) | 2005-02-24 | 2006-08-31 | Millennium Pharmaceuticals, Inc. | Antagonistes de recepteur de pgd2 pour le traitement des maladies inflammatoires |
| EP1889622A4 (fr) | 2005-05-31 | 2009-12-23 | Ono Pharmaceutical Co | Compose de spiropiperidine et son utilisation medicinale |
| CN100519524C (zh) * | 2005-09-29 | 2009-07-29 | 中国人民解放军军事医学科学院毒物药物研究所 | 吲哚丙烯酸衍生物及其用于制备免疫抑制剂的用途 |
| EP2657235A1 (fr) | 2005-10-28 | 2013-10-30 | Ono Pharmaceutical Co., Ltd. | Composé contenant un groupe basique et son utilisation |
| WO2007058322A1 (fr) | 2005-11-18 | 2007-05-24 | Ono Pharmaceutical Co., Ltd. | Composé contenant un groupe basique et son utilisation |
| AU2006330866A1 (en) | 2005-12-22 | 2007-07-05 | Vertex Pharmaceuticals Incorporated | Modulators of muscarinic receptors |
| KR20080098070A (ko) | 2006-02-22 | 2008-11-06 | 버텍스 파마슈티칼스 인코포레이티드 | 무스카린성 수용체의 조절제로서의 스피로 축합된 피페리딘 |
| AU2007221214A1 (en) | 2006-02-22 | 2007-09-07 | Vertex Pharmaceuticals Incorporated | Modulators of muscarinic receptors |
| WO2007132846A1 (fr) | 2006-05-16 | 2007-11-22 | Ono Pharmaceutical Co., Ltd. | Composé ayant un groupe acide qui peut être protégé et utilisation dudit composé |
| CN101500565A (zh) | 2006-06-29 | 2009-08-05 | 弗特克斯药品有限公司 | 毒蕈碱性受体的调节剂 |
| JP5245827B2 (ja) | 2006-07-31 | 2013-07-24 | 小野薬品工業株式会社 | スピロ結合した環状基を含有する化合物およびその用途 |
| AU2007284548A1 (en) | 2006-08-15 | 2008-02-21 | Vertex Pharmaceuticals Incorporated | Modulators of muscarinic receptors |
| CA2660974A1 (fr) | 2006-08-18 | 2008-02-21 | Vertex Pharmaceuticals Incorporated | Modulateurs des recepteurs muscariniques |
| JP2010540640A (ja) | 2007-10-03 | 2010-12-24 | バーテックス ファーマシューティカルズ インコーポレイテッド | ムスカリン作用性レセプターのモジュレーター |
| JP2011504499A (ja) | 2007-11-21 | 2011-02-10 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | トリプターゼ阻害剤として使用するためのスピロピペリジン |
| JP2012006837A (ja) * | 2008-09-30 | 2012-01-12 | Mochida Pharmaceut Co Ltd | 2−インドールアクリルアミド類縁体 |
| WO2010129351A1 (fr) | 2009-04-28 | 2010-11-11 | Schepens Eye Research Institute | Procédé pour identifier et pour traiter une dégénérescence maculaire liée à l'âge |
| WO2013024022A1 (fr) | 2011-08-12 | 2013-02-21 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Méthodes et compositions pharmaceutiques pour traiter l'hypertension pulmonaire |
| US11629196B2 (en) | 2020-04-27 | 2023-04-18 | Incelldx, Inc. | Method of treating SARS-CoV-2-associated hypercytokinemia by administering a human monoclonal antibody (PRO-140) that inhibits CCR5/CCL5 binding interactions |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3167556A (en) * | 1963-11-19 | 1965-01-26 | Olin Mathieson | Basic derivatives of anilides |
| US3201401A (en) * | 1964-09-17 | 1965-08-17 | Olin Mathieson | Aminoalkoxy and aminoalkylthioanilide compounds |
| GB1099829A (en) * | 1965-02-09 | 1968-01-17 | Squibb & Sons Inc | Derivatives of aromatic amines |
| ES464943A1 (es) * | 1977-12-10 | 1978-09-01 | Cuatrecasas Labor M | Procedimiento para la obtencion de amidas de interes farma- cologico. |
| US4343813A (en) * | 1980-08-28 | 1982-08-10 | Pfizer Inc. | Carboxamide compounds as SRS-A antagonists |
| US4296129A (en) * | 1980-10-29 | 1981-10-20 | Pfizer, Inc. | (Carboxyacylamino)phenylalkenamides and esters thereof as SRS-A antagonists |
| DE3803775A1 (de) * | 1988-02-09 | 1989-08-17 | Boehringer Mannheim Gmbh | Neue substituierte lactame, verfahren zu ihrer herstellung und arzneimittel, die diese verbindungen enthalten |
| WO1992008474A2 (fr) * | 1990-11-20 | 1992-05-29 | The National Heart & Lung Institute | Traitement des maladies pulmonaires |
| GB9300083D0 (en) * | 1993-01-05 | 1993-03-03 | Roussel Lab Ltd | Chemical compounds |
| AU751139B2 (en) * | 1997-10-13 | 2002-08-08 | Astellas Pharma Inc. | Amide derivative |
| EP1039899A2 (fr) * | 1997-12-19 | 2000-10-04 | Takeda Chemical Industries, Ltd. | Composition pharmaceutique antagoniste de ccr5 et contenant un derive d'anilide |
-
1999
- 1999-07-28 CA CA002338804A patent/CA2338804A1/fr not_active Abandoned
- 1999-07-28 EP EP99937585A patent/EP1100495A4/fr not_active Withdrawn
- 1999-07-28 JP JP2000562008A patent/JP2002521441A/ja not_active Withdrawn
- 1999-07-28 WO PCT/US1999/017117 patent/WO2000006153A1/fr not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| WO2000006153A1 (fr) | 2000-02-10 |
| EP1100495A1 (fr) | 2001-05-23 |
| JP2002521441A (ja) | 2002-07-16 |
| EP1100495A4 (fr) | 2002-09-25 |
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