CA2552090A1 - Disubstituted chalcone oximes as selective agonists of rar.gamma. retinoid receptors - Google Patents
Disubstituted chalcone oximes as selective agonists of rar.gamma. retinoid receptors Download PDFInfo
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- CA2552090A1 CA2552090A1 CA002552090A CA2552090A CA2552090A1 CA 2552090 A1 CA2552090 A1 CA 2552090A1 CA 002552090 A CA002552090 A CA 002552090A CA 2552090 A CA2552090 A CA 2552090A CA 2552090 A1 CA2552090 A1 CA 2552090A1
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- carbons
- compound
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- 239000000556 agonist Substances 0.000 title claims abstract description 17
- -1 Disubstituted chalcone oximes Chemical class 0.000 title claims description 37
- 102000027483 retinoid hormone receptors Human genes 0.000 title description 14
- 108091008679 retinoid hormone receptors Proteins 0.000 title description 14
- 150000001875 compounds Chemical class 0.000 claims abstract description 273
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 34
- 201000010099 disease Diseases 0.000 claims abstract description 33
- 241000124008 Mammalia Species 0.000 claims abstract description 21
- 206010014561 Emphysema Diseases 0.000 claims abstract description 15
- 230000002685 pulmonary effect Effects 0.000 claims abstract description 12
- 208000002874 Acne Vulgaris Diseases 0.000 claims abstract description 6
- 201000004681 Psoriasis Diseases 0.000 claims abstract description 6
- 206010000496 acne Diseases 0.000 claims abstract description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 96
- 238000000034 method Methods 0.000 claims description 66
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims description 54
- 150000003839 salts Chemical class 0.000 claims description 33
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 32
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 32
- 229910052731 fluorine Inorganic materials 0.000 claims description 22
- 229910052740 iodine Inorganic materials 0.000 claims description 17
- 125000003342 alkenyl group Chemical group 0.000 claims description 16
- 125000003545 alkoxy group Chemical group 0.000 claims description 16
- 125000004414 alkyl thio group Chemical group 0.000 claims description 16
- 229910052794 bromium Inorganic materials 0.000 claims description 16
- 229910052801 chlorine Inorganic materials 0.000 claims description 16
- 229910052739 hydrogen Inorganic materials 0.000 claims description 16
- 239000001257 hydrogen Substances 0.000 claims description 16
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 10
- 229910052799 carbon Inorganic materials 0.000 claims description 10
- 229910052736 halogen Inorganic materials 0.000 claims description 10
- 125000005843 halogen group Chemical group 0.000 claims description 10
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims description 8
- 125000005037 alkyl phenyl group Chemical group 0.000 claims description 8
- 125000005103 alkyl silyl group Chemical group 0.000 claims description 8
- 125000000304 alkynyl group Chemical group 0.000 claims description 8
- 150000002431 hydrogen Chemical class 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 229910052717 sulfur Inorganic materials 0.000 claims description 8
- 125000001072 heteroaryl group Chemical group 0.000 claims description 6
- 125000002541 furyl group Chemical group 0.000 claims description 5
- IXQYPXRYRSEMAA-UHFFFAOYSA-N n-(1,3-diphenylprop-2-enylidene)hydroxylamine Chemical group C=1C=CC=CC=1C(=NO)C=CC1=CC=CC=C1 IXQYPXRYRSEMAA-UHFFFAOYSA-N 0.000 claims description 5
- 125000004076 pyridyl group Chemical group 0.000 claims description 5
- 208000017520 skin disease Diseases 0.000 claims description 5
- 125000001544 thienyl group Chemical group 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 150000003254 radicals Chemical class 0.000 claims description 4
- 125000002883 imidazolyl group Chemical group 0.000 claims description 2
- 125000001624 naphthyl group Chemical group 0.000 claims description 2
- 125000002971 oxazolyl group Chemical group 0.000 claims description 2
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 2
- 125000002098 pyridazinyl group Chemical group 0.000 claims description 2
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 2
- 125000000335 thiazolyl group Chemical group 0.000 claims description 2
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 claims 7
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 claims 7
- 229910052796 boron Chemical group 0.000 claims 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 93
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 79
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 75
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 64
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- 238000005160 1H NMR spectroscopy Methods 0.000 description 57
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- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 48
- 239000000203 mixture Substances 0.000 description 48
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- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 42
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 38
- 239000007787 solid Substances 0.000 description 38
- 239000007858 starting material Substances 0.000 description 36
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 33
- 239000005711 Benzoic acid Substances 0.000 description 32
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 30
- 239000000243 solution Substances 0.000 description 28
- 239000012267 brine Substances 0.000 description 26
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 26
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 23
- 101150041968 CDC13 gene Proteins 0.000 description 18
- 238000003820 Medium-pressure liquid chromatography Methods 0.000 description 18
- 150000002148 esters Chemical class 0.000 description 16
- LVEYOSJUKRVCCF-UHFFFAOYSA-N 1,3-Bis(diphenylphosphino)propane Substances C=1C=CC=CC=1P(C=1C=CC=CC=1)CCCP(C=1C=CC=CC=1)C1=CC=CC=C1 LVEYOSJUKRVCCF-UHFFFAOYSA-N 0.000 description 15
- CSCPPACGZOOCGX-WFGJKAKNSA-N acetone d6 Chemical compound [2H]C([2H])([2H])C(=O)C([2H])([2H])[2H] CSCPPACGZOOCGX-WFGJKAKNSA-N 0.000 description 15
- 230000000694 effects Effects 0.000 description 15
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- 238000005481 NMR spectroscopy Methods 0.000 description 13
- 238000001953 recrystallisation Methods 0.000 description 13
- 238000003756 stirring Methods 0.000 description 13
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
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- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 12
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 12
- 239000003921 oil Substances 0.000 description 12
- 238000003786 synthesis reaction Methods 0.000 description 12
- 239000012230 colorless oil Substances 0.000 description 11
- 239000012044 organic layer Substances 0.000 description 11
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 10
- 239000002253 acid Substances 0.000 description 10
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- 125000003118 aryl group Chemical group 0.000 description 9
- YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 9
- 238000003556 assay Methods 0.000 description 8
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- 238000000926 separation method Methods 0.000 description 8
- AISXBZVAYNUAKB-UHFFFAOYSA-N 1,1,4,4,6-pentamethyl-2,3-dihydronaphthalene Chemical compound CC1(C)CCC(C)(C)C=2C1=CC(C)=CC=2 AISXBZVAYNUAKB-UHFFFAOYSA-N 0.000 description 7
- 125000001246 bromo group Chemical group Br* 0.000 description 7
- 235000019441 ethanol Nutrition 0.000 description 7
- 210000004072 lung Anatomy 0.000 description 7
- ZRYZBQLXDKPBDU-UHFFFAOYSA-N 4-bromobenzaldehyde Chemical compound BrC1=CC=C(C=O)C=C1 ZRYZBQLXDKPBDU-UHFFFAOYSA-N 0.000 description 6
- WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 6
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- NXPHGHWWQRMDIA-UHFFFAOYSA-M magnesium;carbanide;bromide Chemical compound [CH3-].[Mg+2].[Br-] NXPHGHWWQRMDIA-UHFFFAOYSA-M 0.000 description 6
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 6
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical compound C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 description 6
- 102000003702 retinoic acid receptors Human genes 0.000 description 6
- 108090000064 retinoic acid receptors Proteins 0.000 description 6
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 6
- GLGNXYJARSMNGJ-VKTIVEEGSA-N (1s,2s,3r,4r)-3-[[5-chloro-2-[(1-ethyl-6-methoxy-2-oxo-4,5-dihydro-3h-1-benzazepin-7-yl)amino]pyrimidin-4-yl]amino]bicyclo[2.2.1]hept-5-ene-2-carboxamide Chemical compound CCN1C(=O)CCCC2=C(OC)C(NC=3N=C(C(=CN=3)Cl)N[C@H]3[C@H]([C@@]4([H])C[C@@]3(C=C4)[H])C(N)=O)=CC=C21 GLGNXYJARSMNGJ-VKTIVEEGSA-N 0.000 description 5
- YNHIGQDRGKUECZ-UHFFFAOYSA-L PdCl2(PPh3)2 Substances [Cl-].[Cl-].[Pd+2].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 YNHIGQDRGKUECZ-UHFFFAOYSA-L 0.000 description 5
- 102000034527 Retinoid X Receptors Human genes 0.000 description 5
- 108010038912 Retinoid X Receptors Proteins 0.000 description 5
- 229940125758 compound 15 Drugs 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 229940079593 drug Drugs 0.000 description 5
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
- 150000002923 oximes Chemical group 0.000 description 5
- 102000005962 receptors Human genes 0.000 description 5
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- 229910000104 sodium hydride Inorganic materials 0.000 description 5
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- 125000001424 substituent group Chemical group 0.000 description 5
- LAJAFFLJAJMYLK-CVOKMOJFSA-N (1s,2s,3r,4r)-3-[[5-chloro-2-[[(7s)-4-methoxy-7-morpholin-4-yl-6,7,8,9-tetrahydro-5h-benzo[7]annulen-3-yl]amino]pyrimidin-4-yl]amino]bicyclo[2.2.1]hept-5-ene-2-carboxamide Chemical compound N1([C@H]2CCC3=CC=C(C(=C3CC2)OC)NC=2N=C(C(=CN=2)Cl)N[C@H]2[C@H]([C@@]3([H])C[C@@]2(C=C3)[H])C(N)=O)CCOCC1 LAJAFFLJAJMYLK-CVOKMOJFSA-N 0.000 description 4
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- IDWNVLSIPQWRAX-UHFFFAOYSA-N ethyl 3-fluoro-4-[3-oxo-3-(5,5,8,8-tetramethyl-6,7-dihydronaphthalen-2-yl)prop-1-enyl]benzoate Chemical compound FC1=CC(C(=O)OCC)=CC=C1C=CC(=O)C1=CC=C2C(C)(C)CCC(C)(C)C2=C1 IDWNVLSIPQWRAX-UHFFFAOYSA-N 0.000 description 1
- YFOKVHDAWQZCLC-UHFFFAOYSA-N ethyl 4-[3-(3-methoxy-5,5,8,8-tetramethyl-6,7-dihydronaphthalen-2-yl)-3-oxoprop-1-enyl]benzoate Chemical compound C1=CC(C(=O)OCC)=CC=C1C=CC(=O)C1=CC(C(CCC2(C)C)(C)C)=C2C=C1OC YFOKVHDAWQZCLC-UHFFFAOYSA-N 0.000 description 1
- OGSIVRRGRDDMCY-UHFFFAOYSA-N ethyl 4-[3-(4,4-dimethyl-2,3-dihydrothiochromen-6-yl)-3-oxoprop-1-enyl]-3-fluorobenzoate Chemical compound FC1=CC(C(=O)OCC)=CC=C1C=CC(=O)C1=CC=C(SCCC2(C)C)C2=C1 OGSIVRRGRDDMCY-UHFFFAOYSA-N 0.000 description 1
- DIZFLSMMVMPBOV-UHFFFAOYSA-N ethyl 4-[3-(4,4-dimethyl-2,3-dihydrothiochromen-6-yl)-3-oxoprop-1-enyl]benzoate Chemical compound C1=CC(C(=O)OCC)=CC=C1C=CC(=O)C1=CC=C(SCCC2(C)C)C2=C1 DIZFLSMMVMPBOV-UHFFFAOYSA-N 0.000 description 1
- OBDGHGCVJLFIBI-UHFFFAOYSA-N ethyl 4-[3-(5,5-dimethyl-7,8-dihydro-6h-naphthalen-2-yl)-3-oxoprop-1-enyl]benzoate Chemical compound C1=CC(C(=O)OCC)=CC=C1C=CC(=O)C1=CC=C2C(C)(C)CCCC2=C1 OBDGHGCVJLFIBI-UHFFFAOYSA-N 0.000 description 1
- ZOVHLDBRUVYFQT-UHFFFAOYSA-N ethyl 4-[3-(8,8-dimethyl-6,7-dihydro-5h-naphthalen-2-yl)-3-oxoprop-1-enyl]-3-fluorobenzoate Chemical compound FC1=CC(C(=O)OCC)=CC=C1C=CC(=O)C1=CC=C(CCCC2(C)C)C2=C1 ZOVHLDBRUVYFQT-UHFFFAOYSA-N 0.000 description 1
- AWQRMUYSBYTJCE-UHFFFAOYSA-N ethyl 4-[3-(8,8-dimethyl-6,7-dihydro-5h-naphthalen-2-yl)-3-oxoprop-1-enyl]benzoate Chemical compound C1=CC(C(=O)OCC)=CC=C1C=CC(=O)C1=CC=C(CCCC2(C)C)C2=C1 AWQRMUYSBYTJCE-UHFFFAOYSA-N 0.000 description 1
- DCSSHXSOWDVJCO-UHFFFAOYSA-N ethyl 4-[3-oxo-3-(3,5,5,8,8-pentamethyl-6,7-dihydronaphthalen-2-yl)prop-1-enyl]benzoate Chemical compound C1=CC(C(=O)OCC)=CC=C1C=CC(=O)C1=CC(C(CCC2(C)C)(C)C)=C2C=C1C DCSSHXSOWDVJCO-UHFFFAOYSA-N 0.000 description 1
- ADZGEFNBWMJVPA-UHFFFAOYSA-N ethyl 4-[3-oxo-3-(5,5,8,8-tetramethyl-6,7-dihydroquinoxalin-2-yl)prop-1-enyl]benzoate Chemical compound C1=CC(C(=O)OCC)=CC=C1C=CC(=O)C1=CN=C2C(C)(C)CCC(C)(C)C2=N1 ADZGEFNBWMJVPA-UHFFFAOYSA-N 0.000 description 1
- 238000013265 extended release Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000003862 glucocorticoid Substances 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 230000003463 hyperproliferative effect Effects 0.000 description 1
- 206010021198 ichthyosis Diseases 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 229910001410 inorganic ion Inorganic materials 0.000 description 1
- 238000010255 intramuscular injection Methods 0.000 description 1
- 239000007927 intramuscular injection Substances 0.000 description 1
- 238000007912 intraperitoneal administration Methods 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 230000003780 keratinization Effects 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 201000011486 lichen planus Diseases 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- 238000002483 medication Methods 0.000 description 1
- SHOJXDKTYKFBRD-UHFFFAOYSA-N mesityl oxide Natural products CC(C)=CC(C)=O SHOJXDKTYKFBRD-UHFFFAOYSA-N 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
- NIMOWSMVLXMDSE-UHFFFAOYSA-N methyl 2-fluoro-3-formylbenzoate Chemical compound COC(=O)C1=CC=CC(C=O)=C1F NIMOWSMVLXMDSE-UHFFFAOYSA-N 0.000 description 1
- CFMGPKZYEUOERS-UHFFFAOYSA-N methyl 2-fluoro-4-formylbenzoate Chemical compound COC(=O)C1=CC=C(C=O)C=C1F CFMGPKZYEUOERS-UHFFFAOYSA-N 0.000 description 1
- UVSBCUAQEZINCQ-UHFFFAOYSA-N methyl 3-formylbenzoate Chemical compound COC(=O)C1=CC=CC(C=O)=C1 UVSBCUAQEZINCQ-UHFFFAOYSA-N 0.000 description 1
- KDPOOUQFAUOHHX-UHFFFAOYSA-N methyl 5-formylfuran-2-carboxylate Chemical compound COC(=O)C1=CC=C(C=O)O1 KDPOOUQFAUOHHX-UHFFFAOYSA-N 0.000 description 1
- RKSNUGDDGDFSRP-UHFFFAOYSA-N methyl 5-formylfuran-3-carboxylate Chemical compound COC(=O)C1=COC(C=O)=C1 RKSNUGDDGDFSRP-UHFFFAOYSA-N 0.000 description 1
- PZNFNYWSXSIWRS-UHFFFAOYSA-N methyl 5-formylnaphthalene-1-carboxylate Chemical compound C1=CC=C2C(C(=O)OC)=CC=CC2=C1C=O PZNFNYWSXSIWRS-UHFFFAOYSA-N 0.000 description 1
- GNXNZRYWBFMVHK-UHFFFAOYSA-N methyl 5-formylthiophene-3-carboxylate Chemical compound COC(=O)C1=CSC(C=O)=C1 GNXNZRYWBFMVHK-UHFFFAOYSA-N 0.000 description 1
- BXSPIMHRXGJUDS-UHFFFAOYSA-N methyl 6-formylnaphthalene-1-carboxylate Chemical compound O=CC1=CC=C2C(C(=O)OC)=CC=CC2=C1 BXSPIMHRXGJUDS-UHFFFAOYSA-N 0.000 description 1
- CERBENZCBVYKEF-UHFFFAOYSA-N methyl 6-formylpyridine-2-carboxylate Chemical compound COC(=O)C1=CC=CC(C=O)=N1 CERBENZCBVYKEF-UHFFFAOYSA-N 0.000 description 1
- BZOWIADSJYMJJJ-UHFFFAOYSA-N methyl 6-formylpyridine-3-carboxylate Chemical compound COC(=O)C1=CC=C(C=O)N=C1 BZOWIADSJYMJJJ-UHFFFAOYSA-N 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 230000008832 photodamage Effects 0.000 description 1
- 230000019612 pigmentation Effects 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000000159 protein binding assay Methods 0.000 description 1
- 230000000241 respiratory effect Effects 0.000 description 1
- 102000027478 retinoid receptor subtypes Human genes 0.000 description 1
- 108091008678 retinoid receptor subtypes Proteins 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000036620 skin dryness Effects 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 150000003431 steroids Chemical class 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 229960000281 trometamol Drugs 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/87—Benzo [c] furans; Hydrogenated benzo [c] furans
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/10—Anti-acne agents
-
- 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
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
- C07D215/20—Oxygen atoms
- C07D215/22—Oxygen atoms attached in position 2 or 4
- C07D215/227—Oxygen atoms attached in position 2 or 4 only one oxygen atom which is attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D335/00—Heterocyclic compounds containing six-membered rings having one sulfur atom as the only ring hetero atom
- C07D335/04—Heterocyclic compounds containing six-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D335/06—Benzothiopyrans; Hydrogenated benzothiopyrans
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Dermatology (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Quinoline Compounds (AREA)
- Pyrane Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US53373303P | 2003-12-30 | 2003-12-30 | |
| US60/533,733 | 2003-12-30 | ||
| PCT/US2004/043148 WO2005066116A1 (en) | 2003-12-30 | 2004-12-21 | Disubstituted chalcone oximes as selective agonists of rarϝ retinoid receptors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2552090A1 true CA2552090A1 (en) | 2005-07-21 |
Family
ID=34748950
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002552090A Abandoned CA2552090A1 (en) | 2003-12-30 | 2004-12-21 | Disubstituted chalcone oximes as selective agonists of rar.gamma. retinoid receptors |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US7476673B2 (enExample) |
| EP (1) | EP1704139A1 (enExample) |
| JP (1) | JP2007517037A (enExample) |
| CA (1) | CA2552090A1 (enExample) |
| MX (1) | MXPA06007560A (enExample) |
| WO (1) | WO2005066116A1 (enExample) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2881137B1 (fr) * | 2005-01-27 | 2007-03-02 | Servier Lab | Nouveaux derives d'oximes heterocycliques, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| SG179453A1 (en) * | 2007-03-09 | 2012-04-27 | Sanofi Aventis | Substituted dihydro and tetrahydro oxazolopyrimidinones, preparation and use thereof |
| CA2751820A1 (en) * | 2009-02-10 | 2010-08-19 | Nippon Soda Co., Ltd. | Nitrogen-containing compounds and harmful organism control agents |
| CN101941919B (zh) * | 2009-07-07 | 2014-07-02 | 天津药物研究院 | 一种制备顺式肟及肟醚衍生物的方法 |
| GB0915523D0 (en) | 2009-09-07 | 2009-10-07 | Genome Res Ltd | Cells and methods for obtaining them |
| AR078171A1 (es) | 2009-09-15 | 2011-10-19 | Sanofi Aventis | Dihidrobenzocicloalquiloximetil-oxazolopirimidinonas sustituidas, preparacion y uso de las mismas |
| MX2012006776A (es) | 2009-12-14 | 2012-10-05 | Merck Patent Gmbh | Inhibidores de la esfingosina quinasa. |
| AU2010341229A1 (en) | 2009-12-17 | 2012-08-02 | Merck Patent Gmbh | Sphingosine kinase inhibitors |
| US11026932B2 (en) | 2015-09-10 | 2021-06-08 | National University Corporation Okayama University | Medicinal composition for preventing or treating inflammatory respiratory disease |
| PL3380086T3 (pl) | 2015-11-25 | 2022-02-21 | Io Therapeutics, Inc. | Oporne na cyp26 agonisty selektywne względem rar-alfa w leczeniu nowotworu |
| CN109952298B (zh) | 2017-07-06 | 2021-09-03 | 江苏恒瑞医药股份有限公司 | 吲哚甲酰胺类衍生物、其制备方法及其在医药上的应用 |
| EP3651757A4 (en) * | 2017-07-13 | 2021-08-25 | IO Therapeutics, Inc. | RECEPTOR SUB-TYPE AND SELECTIVE RETINOID AND REXINOID COMPOUNDS FOR A FUNCTION IN COMBINATION WITH IMMUNE MODULATORS FOR ANTI-CANCER IMMUNOTHERAPY |
| AU2018326617B2 (en) | 2017-08-31 | 2022-12-01 | Io Therapeutics, Inc. | Rar selective agonists in combination with immune modulators for cancer immunotherapy |
| BR112020004611A2 (pt) | 2017-09-12 | 2020-09-24 | Jiangsu Hengrui Medicine Co., Ltd. | derivado de indol formamida substituído por átomo de deutério, método de preparação do mesmo e aplicações médicas do mesmo |
| AU2018341099B2 (en) | 2017-09-28 | 2023-11-02 | Kenvue Brands Llc | Cosmetic compositions and method of treating the skin |
| AU2020307631B9 (en) * | 2019-06-27 | 2024-07-04 | Hangzhou Healzen Therapeutics Co., Ltd. | Casein kinase 1ε inhibitor, pharmaceutical composition and application thereof |
| IL313052A (en) * | 2021-11-23 | 2024-07-01 | Io Therapeutics Inc | Methods of using rarγ agonists for cancer treatment |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU679171B2 (en) | 1991-12-18 | 1997-06-26 | Baylor College Of Medicine | Means for the modulation of processes mediated by retinoid receptors and compounds useful therefor |
| US5455265A (en) * | 1993-02-11 | 1995-10-03 | Allergan, Inc. | Method of treatment with compounds having selective agonist-like activity on RXR retinoid receptors |
| WO1996011210A1 (en) * | 1994-10-07 | 1996-04-18 | Fujisawa Pharmaceutical Co., Ltd. | Cyclic hexapeptides having antibiotic activity |
| US5599967A (en) * | 1994-12-29 | 1997-02-04 | Allergan | Acetylenes disubstituted with a 5 substituted tetrahydronaphthyl group and with an aryl of heteroaryl group having retinoid-like biological activity |
| US6008204A (en) * | 1995-09-01 | 1999-12-28 | Allergan Sales, Inc. | Synthesis and use of retinoid compounds having negative hormone and/or antagonist activities |
| US5723666A (en) * | 1996-06-21 | 1998-03-03 | Allergan | Oxime substituted tetrahydronaphthalene derivatives having retinoid and/or retinoid antagonist-like biological activity |
| US5739338A (en) * | 1996-11-05 | 1998-04-14 | Allergan | N-aryl substituted tetrahydroquinolines having retinoid agonist, retinoid antagonist or retinoid inverse agonist type biological activity |
| US5760276A (en) * | 1997-03-06 | 1998-06-02 | Allergan | Aryl-and heteroarylcyclohexenyl substituted alkenes having retinoid agonist, antagonist or inverse agonist type biological activity |
| US6037488A (en) * | 1997-04-19 | 2000-03-14 | Allergan Sales, Inc. | Trisubstituted phenyl derivatives having retinoid agonist, antagonist or inverse agonist type biological activity |
| US5919970A (en) * | 1997-04-24 | 1999-07-06 | Allergan Sales, Inc. | Substituted diaryl or diheteroaryl methanes, ethers and amines having retinoid agonist, antagonist or inverse agonist type biological activity |
| US6048873A (en) * | 1998-10-01 | 2000-04-11 | Allergan Sales, Inc. | Tetrahdroquinolin-2-one 6 or 7-yl, tetrahdroquinilin-2-thione 6 or 7-yl pentadienoic acid and related derivatives having retinoid-like biological activity |
| WO2000061233A2 (en) * | 1999-04-14 | 2000-10-19 | Allergan Sales, Inc. | Methods and compositions for the treatment and prevention of lung disease involving a specific rar-gamma agonist |
| US6313168B1 (en) * | 1999-12-15 | 2001-11-06 | Allergan Sales, Inc. | Use of retinoid receptor antagonists in the treatment of cartilage and bone pathologies |
| US6403810B2 (en) * | 2000-07-10 | 2002-06-11 | Hoffmann-La Roche Inc. | Thiophene derivatives |
| US6303785B1 (en) * | 2000-08-29 | 2001-10-16 | Allergan Sales, Inc. | Compounds having activity as inhibitors of cytochrome P450RAI |
| JP4118675B2 (ja) | 2000-10-02 | 2008-07-16 | エフ．ホフマン−ラ ロシュ アーゲー | 気腫治療用新規レチノイド |
| US20030003517A1 (en) | 2001-03-22 | 2003-01-02 | Klein Elliott S. | Methods of detecting dissociated nuclear hormone receptor ligands |
| US20020193403A1 (en) * | 2001-05-03 | 2002-12-19 | Allergan Sales, Inc. | Methods of treating hyperlipidemia |
| DE602004019685D1 (de) * | 2003-12-26 | 2009-04-09 | Allergan Inc | DISUBSTITUIERTE CHALCOGENOXIME MIT ANTAGONISTISCHER WIRKUNG AM RAR(Gamma)-RETINOIDREZEPTOR |
-
2004
- 2004-12-17 US US11/015,994 patent/US7476673B2/en not_active Expired - Fee Related
- 2004-12-21 JP JP2006547316A patent/JP2007517037A/ja active Pending
- 2004-12-21 EP EP04815251A patent/EP1704139A1/en not_active Withdrawn
- 2004-12-21 WO PCT/US2004/043148 patent/WO2005066116A1/en not_active Ceased
- 2004-12-21 CA CA002552090A patent/CA2552090A1/en not_active Abandoned
- 2004-12-21 MX MXPA06007560A patent/MXPA06007560A/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| WO2005066116A8 (en) | 2005-10-20 |
| MXPA06007560A (es) | 2006-08-31 |
| JP2007517037A (ja) | 2007-06-28 |
| WO2005066116A1 (en) | 2005-07-21 |
| US20050148590A1 (en) | 2005-07-07 |
| US7476673B2 (en) | 2009-01-13 |
| EP1704139A1 (en) | 2006-09-27 |
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| Date | Code | Title | Description |
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