ES2332135T3 - Inhibidores p-38 basados en heterociclo de 5 miembros. - Google Patents
Inhibidores p-38 basados en heterociclo de 5 miembros. Download PDFInfo
- Publication number
- ES2332135T3 ES2332135T3 ES04754233T ES04754233T ES2332135T3 ES 2332135 T3 ES2332135 T3 ES 2332135T3 ES 04754233 T ES04754233 T ES 04754233T ES 04754233 T ES04754233 T ES 04754233T ES 2332135 T3 ES2332135 T3 ES 2332135T3
- Authority
- ES
- Spain
- Prior art keywords
- methyl
- thiazol
- cyclopropyl
- phenyl
- alkyl
- 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
- 239000012826 P38 inhibitor Substances 0.000 title description 5
- 150000001875 compounds Chemical class 0.000 claims abstract description 268
- 102000002574 p38 Mitogen-Activated Protein Kinases Human genes 0.000 claims abstract description 77
- 108010068338 p38 Mitogen-Activated Protein Kinases Proteins 0.000 claims abstract description 76
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 75
- 238000011282 treatment Methods 0.000 claims abstract description 45
- 230000001404 mediated effect Effects 0.000 claims abstract description 11
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 11
- -1 -OR 4 Chemical group 0.000 claims description 323
- 125000000217 alkyl group Chemical group 0.000 claims description 150
- 239000002253 acid Substances 0.000 claims description 136
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 110
- 125000003118 aryl group Chemical group 0.000 claims description 70
- 201000010099 disease Diseases 0.000 claims description 66
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 53
- 229910052739 hydrogen Inorganic materials 0.000 claims description 52
- 125000001072 heteroaryl group Chemical group 0.000 claims description 49
- 239000001257 hydrogen Substances 0.000 claims description 43
- 239000000460 chlorine Substances 0.000 claims description 39
- 125000001424 substituent group Chemical group 0.000 claims description 37
- 150000003839 salts Chemical class 0.000 claims description 33
- 125000003545 alkoxy group Chemical group 0.000 claims description 31
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 29
- 125000000304 alkynyl group Chemical group 0.000 claims description 25
- 125000004414 alkyl thio group Chemical group 0.000 claims description 23
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 23
- 229910052757 nitrogen Inorganic materials 0.000 claims description 23
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 22
- 150000002148 esters Chemical class 0.000 claims description 22
- 125000005843 halogen group Chemical group 0.000 claims description 22
- 125000005842 heteroatom Chemical group 0.000 claims description 22
- 229910052760 oxygen Inorganic materials 0.000 claims description 22
- 125000001188 haloalkyl group Chemical group 0.000 claims description 21
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 21
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 20
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 20
- 125000003342 alkenyl group Chemical group 0.000 claims description 18
- 150000001412 amines Chemical class 0.000 claims description 18
- 239000002585 base Substances 0.000 claims description 18
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 18
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 17
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 17
- 229910052799 carbon Inorganic materials 0.000 claims description 16
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 16
- 229910052717 sulfur Inorganic materials 0.000 claims description 16
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 15
- 150000004702 methyl esters Chemical class 0.000 claims description 15
- 125000004076 pyridyl group Chemical group 0.000 claims description 14
- 125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 claims description 14
- 125000000335 thiazolyl group Chemical group 0.000 claims description 14
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 12
- 125000001769 aryl amino group Chemical group 0.000 claims description 12
- 125000002619 bicyclic group Chemical group 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 12
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 12
- 125000004043 oxo group Chemical group O=* 0.000 claims description 12
- 125000003282 alkyl amino group Chemical group 0.000 claims description 11
- 239000003937 drug carrier Substances 0.000 claims description 11
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 11
- 125000001544 thienyl group Chemical group 0.000 claims description 11
- 125000004423 acyloxy group Chemical group 0.000 claims description 10
- 125000004391 aryl sulfonyl group Chemical group 0.000 claims description 10
- 125000001589 carboacyl group Chemical group 0.000 claims description 10
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 10
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 9
- 125000004659 aryl alkyl thio group Chemical group 0.000 claims description 9
- 125000004429 atom Chemical group 0.000 claims description 9
- JPYQFYIEOUVJDU-UHFFFAOYSA-N beclamide Chemical compound ClCCC(=O)NCC1=CC=CC=C1 JPYQFYIEOUVJDU-UHFFFAOYSA-N 0.000 claims description 9
- 125000004494 ethyl ester group Chemical group 0.000 claims description 9
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 9
- 125000003107 substituted aryl group Chemical group 0.000 claims description 9
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical class CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 8
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 8
- 125000001691 aryl alkyl amino group Chemical group 0.000 claims description 8
- 125000004104 aryloxy group Chemical group 0.000 claims description 8
- 229910052794 bromium Inorganic materials 0.000 claims description 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 8
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- 125000002541 furyl group Chemical group 0.000 claims description 8
- 229910052736 halogen Inorganic materials 0.000 claims description 8
- 150000002367 halogens Chemical class 0.000 claims description 8
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 8
- 101100516563 Caenorhabditis elegans nhr-6 gene Proteins 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 7
- 125000003368 amide group Chemical group 0.000 claims description 7
- 229910052731 fluorine Inorganic materials 0.000 claims description 7
- 125000002795 guanidino group Chemical group C(N)(=N)N* 0.000 claims description 7
- 125000002883 imidazolyl group Chemical group 0.000 claims description 7
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 7
- 239000012453 solvate Substances 0.000 claims description 7
- RGICCULPCWNRAB-UHFFFAOYSA-N 2-[2-(2-hexoxyethoxy)ethoxy]ethanol Chemical compound CCCCCCOCCOCCOCCO RGICCULPCWNRAB-UHFFFAOYSA-N 0.000 claims description 6
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 6
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 6
- 125000005143 heteroarylsulfonyl group Chemical group 0.000 claims description 6
- 125000001041 indolyl group Chemical group 0.000 claims description 6
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 6
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims description 6
- 125000002971 oxazolyl group Chemical group 0.000 claims description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 5
- 125000005140 aralkylsulfonyl group Chemical group 0.000 claims description 5
- 125000005239 aroylamino group Chemical group 0.000 claims description 5
- 125000005110 aryl thio group Chemical group 0.000 claims description 5
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical group O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 claims description 5
- 125000001715 oxadiazolyl group Chemical group 0.000 claims description 5
- 125000001113 thiadiazolyl group Chemical group 0.000 claims description 5
- 125000004306 triazinyl group Chemical group 0.000 claims description 5
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 4
- 101100294115 Caenorhabditis elegans nhr-4 gene Proteins 0.000 claims description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 4
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 claims description 4
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims description 4
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims description 4
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims description 4
- 125000004966 cyanoalkyl group Chemical group 0.000 claims description 4
- 150000002085 enols Chemical class 0.000 claims description 4
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims description 4
- 239000011737 fluorine Substances 0.000 claims description 4
- 125000001984 thiazolidinyl group Chemical group 0.000 claims description 4
- 125000004568 thiomorpholinyl group Chemical group 0.000 claims description 4
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 3
- SMQUKEWWJWEHIJ-UHFFFAOYSA-N 4-methyl-3-[(4-phenyl-1,3-thiazol-2-yl)amino]-n-propan-2-ylbenzamide Chemical compound CC(C)NC(=O)C1=CC=C(C)C(NC=2SC=C(N=2)C=2C=CC=CC=2)=C1 SMQUKEWWJWEHIJ-UHFFFAOYSA-N 0.000 claims description 3
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 3
- 125000005213 alkyl heteroaryl group Chemical group 0.000 claims description 3
- 125000005189 alkyl hydroxy group Chemical group 0.000 claims description 3
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 claims description 3
- 125000005098 aryl alkoxy carbonyl group Chemical group 0.000 claims description 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 3
- HWDVTQAXQJQROO-UHFFFAOYSA-N cyclopropylazanide Chemical compound [NH-]C1CC1 HWDVTQAXQJQROO-UHFFFAOYSA-N 0.000 claims description 3
- 125000005303 dithiazolyl group Chemical group S1SNC(=C1)* 0.000 claims description 3
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 3
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 3
- 125000004674 methylcarbonyl group Chemical group CC(=O)* 0.000 claims description 3
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 3
- 125000005322 morpholin-1-yl group Chemical group 0.000 claims description 3
- QWNXYSNYDKBHKX-UHFFFAOYSA-N n-cyclopropyl-4-methyl-3-[(3-phenyl-1,2,4-thiadiazol-5-yl)amino]benzamide Chemical compound CC1=CC=C(C(=O)NC2CC2)C=C1NC(SN=1)=NC=1C1=CC=CC=C1 QWNXYSNYDKBHKX-UHFFFAOYSA-N 0.000 claims description 3
- QNQQSWPDHZLEEZ-UHFFFAOYSA-N n-cyclopropyl-4-methyl-3-[(4-phenyl-1,3-thiazol-2-yl)amino]benzamide Chemical compound CC1=CC=C(C(=O)NC2CC2)C=C1NC(SC=1)=NC=1C1=CC=CC=C1 QNQQSWPDHZLEEZ-UHFFFAOYSA-N 0.000 claims description 3
- NUFPZYCKOZSPTH-UHFFFAOYSA-N n-cyclopropyl-4-methyl-3-[(5-phenyl-1,3,4-thiadiazol-2-yl)amino]benzamide Chemical compound CC1=CC=C(C(=O)NC2CC2)C=C1NC(S1)=NN=C1C1=CC=CC=C1 NUFPZYCKOZSPTH-UHFFFAOYSA-N 0.000 claims description 3
- CKPWPYNTFBAPMP-UHFFFAOYSA-N n-cyclopropyl-4-methyl-3-[(5-phenyl-1,3-oxazol-2-yl)amino]benzamide Chemical compound CC1=CC=C(C(=O)NC2CC2)C=C1NC(O1)=NC=C1C1=CC=CC=C1 CKPWPYNTFBAPMP-UHFFFAOYSA-N 0.000 claims description 3
- VIQABIAQWAZJLM-UHFFFAOYSA-N n-cyclopropyl-4-methyl-3-[(5-phenyl-1h-1,2,4-triazol-3-yl)amino]benzamide Chemical compound CC1=CC=C(C(=O)NC2CC2)C=C1NC(N1)=NN=C1C1=CC=CC=C1 VIQABIAQWAZJLM-UHFFFAOYSA-N 0.000 claims description 3
- WPTHXTIVDNEWDS-UHFFFAOYSA-N n-methoxy-4-methyl-3-[(5-phenyl-1h-1,2,4-triazol-3-yl)amino]benzamide Chemical compound CONC(=O)C1=CC=C(C)C(NC=2NC(=NN=2)C=2C=CC=CC=2)=C1 WPTHXTIVDNEWDS-UHFFFAOYSA-N 0.000 claims description 3
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 3
- BBVIDBNAYOIXOE-UHFFFAOYSA-N 1,2,4-oxadiazole Chemical group C=1N=CON=1 BBVIDBNAYOIXOE-UHFFFAOYSA-N 0.000 claims description 2
- YGTAZGSLCXNBQL-UHFFFAOYSA-N 1,2,4-thiadiazole Chemical group C=1N=CSN=1 YGTAZGSLCXNBQL-UHFFFAOYSA-N 0.000 claims description 2
- 125000001376 1,2,4-triazolyl group Chemical group N1N=C(N=C1)* 0.000 claims description 2
- MBIZXFATKUQOOA-UHFFFAOYSA-N 1,3,4-thiadiazole Chemical group C1=NN=CS1 MBIZXFATKUQOOA-UHFFFAOYSA-N 0.000 claims description 2
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 claims description 2
- CNSPTSKZQDDULZ-UHFFFAOYSA-N 3-[[4-(4-cyanophenyl)-1,3-thiazol-2-yl]amino]-n-cyclopropyl-4-methylbenzamide Chemical compound CC1=CC=C(C(=O)NC2CC2)C=C1NC(SC=1)=NC=1C1=CC=C(C#N)C=C1 CNSPTSKZQDDULZ-UHFFFAOYSA-N 0.000 claims description 2
- XAFXTWJDDHQNPQ-UHFFFAOYSA-N 3-[[5-bromo-4-(4-nitrophenyl)-1,3-thiazol-2-yl]amino]-n-cyclopropyl-4-methylbenzamide Chemical compound CC1=CC=C(C(=O)NC2CC2)C=C1NC(SC=1Br)=NC=1C1=CC=C([N+]([O-])=O)C=C1 XAFXTWJDDHQNPQ-UHFFFAOYSA-N 0.000 claims description 2
- 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims description 2
- 125000004801 4-cyanophenyl group Chemical group [H]C1=C([H])C(C#N)=C([H])C([H])=C1* 0.000 claims description 2
- PIFMFKSWUQYDJF-UHFFFAOYSA-N 4-methyl-3-[(4-phenyl-1,3-thiazol-2-yl)amino]-n-(1,2,4-triazol-4-yl)benzamide Chemical compound CC1=CC=C(C(=O)NN2C=NN=C2)C=C1NC(SC=1)=NC=1C1=CC=CC=C1 PIFMFKSWUQYDJF-UHFFFAOYSA-N 0.000 claims description 2
- LHWHNRWSVMZQKC-UHFFFAOYSA-N 4-methyl-5-[(4-phenyl-1,3-thiazol-2-yl)amino]-1-(1,3-thiazol-2-yl)cyclohexa-2,4-diene-1-carboxamide Chemical compound C1=CC(C)=C(NC=2SC=C(N=2)C=2C=CC=CC=2)CC1(C(N)=O)C1=NC=CS1 LHWHNRWSVMZQKC-UHFFFAOYSA-N 0.000 claims description 2
- OTAXXNTXLPMBGI-UHFFFAOYSA-N 4-methyl-n-(5-methyl-1,3,4-thiadiazol-2-yl)-3-[(4-phenyl-1,3-thiazol-2-yl)amino]benzamide Chemical compound S1C(C)=NN=C1NC(=O)C1=CC=C(C)C(NC=2SC=C(N=2)C=2C=CC=CC=2)=C1 OTAXXNTXLPMBGI-UHFFFAOYSA-N 0.000 claims description 2
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical group C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 claims description 2
- 229910006069 SO3H Inorganic materials 0.000 claims description 2
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical group C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims description 2
- RRHCEJCTEIGQNA-UHFFFAOYSA-N [4-methyl-3-[(4-phenyl-1,3-thiazol-2-yl)amino]phenyl]-morpholin-4-ylmethanone Chemical compound CC1=CC=C(C(=O)N2CCOCC2)C=C1NC(SC=1)=NC=1C1=CC=CC=C1 RRHCEJCTEIGQNA-UHFFFAOYSA-N 0.000 claims description 2
- 150000002373 hemiacetals Chemical class 0.000 claims description 2
- 125000005343 heterocyclic alkyl group Chemical group 0.000 claims description 2
- UDGWQRMNULDRJR-UHFFFAOYSA-N n-(2-methoxyethyl)-4-methyl-3-[(4-phenyl-1,3-thiazol-2-yl)amino]benzamide Chemical compound COCCNC(=O)C1=CC=C(C)C(NC=2SC=C(N=2)C=2C=CC=CC=2)=C1 UDGWQRMNULDRJR-UHFFFAOYSA-N 0.000 claims description 2
- DUKISKBCIROUAU-UHFFFAOYSA-N n-cyclopropyl-3-[[4-(2-methoxyphenyl)-1,3-thiazol-2-yl]amino]-4-methylbenzamide Chemical compound COC1=CC=CC=C1C1=CSC(NC=2C(=CC=C(C=2)C(=O)NC2CC2)C)=N1 DUKISKBCIROUAU-UHFFFAOYSA-N 0.000 claims description 2
- BVMJHLWOIQRDDZ-UHFFFAOYSA-N n-cyclopropyl-3-[[4-(4-fluorophenyl)-1,3-thiazol-2-yl]amino]-4-methylbenzamide Chemical compound CC1=CC=C(C(=O)NC2CC2)C=C1NC(SC=1)=NC=1C1=CC=C(F)C=C1 BVMJHLWOIQRDDZ-UHFFFAOYSA-N 0.000 claims description 2
- SMLHKPSWOLMYRM-UHFFFAOYSA-N n-cyclopropyl-3-[[4-(4-methoxyphenyl)-1,3-thiazol-2-yl]amino]-4-methylbenzamide Chemical compound C1=CC(OC)=CC=C1C1=CSC(NC=2C(=CC=C(C=2)C(=O)NC2CC2)C)=N1 SMLHKPSWOLMYRM-UHFFFAOYSA-N 0.000 claims description 2
- BOGVGVABAWLPGV-UHFFFAOYSA-N n-cyclopropyl-4-methyl-3-[(5-methyl-4-phenyl-1,3-thiazol-2-yl)amino]benzamide Chemical compound N=1C(C=2C=CC=CC=2)=C(C)SC=1NC(C(=CC=1)C)=CC=1C(=O)NC1CC1 BOGVGVABAWLPGV-UHFFFAOYSA-N 0.000 claims description 2
- XRHBQUYAZDHOPT-UHFFFAOYSA-N n-cyclopropyl-4-methyl-3-[[4-(4-nitrophenyl)-1,3-thiazol-2-yl]amino]benzamide Chemical compound CC1=CC=C(C(=O)NC2CC2)C=C1NC(SC=1)=NC=1C1=CC=C([N+]([O-])=O)C=C1 XRHBQUYAZDHOPT-UHFFFAOYSA-N 0.000 claims description 2
- DTSHHFQPWUBYJW-UHFFFAOYSA-N n-ethyl-4-methyl-3-[(4-phenyl-1,3-thiazol-2-yl)amino]benzamide Chemical compound CCNC(=O)C1=CC=C(C)C(NC=2SC=C(N=2)C=2C=CC=CC=2)=C1 DTSHHFQPWUBYJW-UHFFFAOYSA-N 0.000 claims description 2
- 150000002905 orthoesters Chemical class 0.000 claims description 2
- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 claims description 2
- FQFILJKFZCVHNH-UHFFFAOYSA-N tert-butyl n-[3-[(5-bromo-2-chloropyrimidin-4-yl)amino]propyl]carbamate Chemical compound CC(C)(C)OC(=O)NCCCNC1=NC(Cl)=NC=C1Br FQFILJKFZCVHNH-UHFFFAOYSA-N 0.000 claims 4
- DYCIDOIWBQYMEP-UHFFFAOYSA-N 2-(n-carbamoyl-5-cyclopropyl-2-methylanilino)-1,3-thiazole-5-carboxylic acid Chemical compound CC1=CC=C(C2CC2)C=C1N(C(N)=O)C1=NC=C(C(O)=O)S1 DYCIDOIWBQYMEP-UHFFFAOYSA-N 0.000 claims 3
- 125000003396 thiol group Chemical class [H]S* 0.000 claims 3
- 125000006555 (C3-C5) cycloalkyl group Chemical group 0.000 claims 2
- QIHDJYRBEZXINB-UHFFFAOYSA-N 4-(3-aminophenyl)-n-benzyl-2-(n-carbamoyl-5-cyclopropyl-2-methylanilino)-1,3-thiazole-5-carboxamide Chemical compound CC1=CC=C(C2CC2)C=C1N(C(N)=O)C(S1)=NC(C=2C=C(N)C=CC=2)=C1C(=O)NCC1=CC=CC=C1 QIHDJYRBEZXINB-UHFFFAOYSA-N 0.000 claims 1
- IXYZLXGJXNBJRH-UHFFFAOYSA-N 4-[5-(benzylcarbamoyl)-2-(n-carbamoyl-5-cyclopropyl-2-methylanilino)-1,3-thiazol-4-yl]benzoic acid Chemical compound CC1=CC=C(C2CC2)C=C1N(C(N)=O)C(S1)=NC(C=2C=CC(=CC=2)C(O)=O)=C1C(=O)NCC1=CC=CC=C1 IXYZLXGJXNBJRH-UHFFFAOYSA-N 0.000 claims 1
- HBZVNWNSRNTWPS-UHFFFAOYSA-N 6-amino-4-hydroxynaphthalene-2-sulfonic acid Chemical compound C1=C(S(O)(=O)=O)C=C(O)C2=CC(N)=CC=C21 HBZVNWNSRNTWPS-UHFFFAOYSA-N 0.000 claims 1
- DTQVDTLACAAQTR-UHFFFAOYSA-M Trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-M 0.000 claims 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 claims 1
- 125000004981 cycloalkylmethyl group Chemical group 0.000 claims 1
- VLFLDFQFKLSHMB-UHFFFAOYSA-N n-benzyl-2-(n-carbamoyl-5-cyclopropyl-2-methylanilino)-4-methyl-1,3-thiazole-5-carboxamide Chemical compound CC=1N=C(N(C(N)=O)C=2C(=CC=C(C=2)C2CC2)C)SC=1C(=O)NCC1=CC=CC=C1 VLFLDFQFKLSHMB-UHFFFAOYSA-N 0.000 claims 1
- GZBCKDMCPDQECD-UHFFFAOYSA-N n-cyclopropyl-3-[[4-(3-methoxyphenyl)-1,3-thiazol-2-yl]amino]-4-methylbenzamide Chemical compound COC1=CC=CC(C=2N=C(NC=3C(=CC=C(C=3)C(=O)NC3CC3)C)SC=2)=C1 GZBCKDMCPDQECD-UHFFFAOYSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 151
- 238000000034 method Methods 0.000 abstract description 119
- 208000024891 symptom Diseases 0.000 abstract description 22
- 208000027866 inflammatory disease Diseases 0.000 abstract description 17
- 239000003112 inhibitor Substances 0.000 abstract description 11
- 230000002265 prevention Effects 0.000 abstract description 9
- 102000001253 Protein Kinase Human genes 0.000 abstract description 3
- 108060006633 protein kinase Proteins 0.000 abstract description 3
- 208000037765 diseases and disorders Diseases 0.000 abstract 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 117
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- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
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| GB0104050D0 (en) * | 2001-02-19 | 2001-04-04 | Astrazeneca Ab | Chemical compounds |
| EP1406875B1 (en) * | 2001-06-26 | 2013-07-31 | Bristol-Myers Squibb Company | N-heterocyclic inhibitors of tnf-alpha expression |
| HN2002000156A (es) | 2001-07-06 | 2003-11-27 | Inc Agouron Pharmaceuticals | Derivados de benzamida tiazol y composiciones farmaceuticas para inhibir la proliferacion de celulas y metodos para su utilización. |
| GB0124928D0 (en) | 2001-10-17 | 2001-12-05 | Glaxo Group Ltd | Chemical compounds |
| GB0124932D0 (en) | 2001-10-17 | 2001-12-05 | Glaxo Group Ltd | Chemical compounds |
| GB0124939D0 (en) | 2001-10-17 | 2001-12-05 | Glaxo Group Ltd | Chemical compounds |
| GB0124934D0 (en) | 2001-10-17 | 2001-12-05 | Glaxo Group Ltd | Chemical compounds |
| GB0124936D0 (en) | 2001-10-17 | 2001-12-05 | Glaxo Group Ltd | Chemical compounds |
| GB0124941D0 (en) | 2001-10-17 | 2001-12-05 | Glaxo Group Ltd | Chemical compounds |
| GB0124933D0 (en) | 2001-10-17 | 2001-12-05 | Glaxo Group Ltd | Chemical compounds |
| GB0124931D0 (en) | 2001-10-17 | 2001-12-05 | Glaxo Group Ltd | Chemical compounds |
| GB0124938D0 (en) | 2001-10-17 | 2001-12-05 | Glaxo Group Ltd | Chemical compounds |
| GB0217757D0 (en) | 2002-07-31 | 2002-09-11 | Glaxo Group Ltd | Novel compounds |
| JP2006517234A (ja) * | 2003-02-10 | 2006-07-20 | 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および治療におけるこれらのリガンドの使用 |
| US7718676B2 (en) * | 2003-10-23 | 2010-05-18 | Ab Science | 2-aminoaryloxazole compounds as tyrosine kinase inhibitors |
-
2004
- 2004-06-02 WO PCT/US2004/017580 patent/WO2005000298A2/en not_active Ceased
- 2004-06-02 DE DE602004022668T patent/DE602004022668D1/de not_active Expired - Lifetime
- 2004-06-02 PL PL04754233T patent/PL1635824T3/pl unknown
- 2004-06-02 EP EP04754233A patent/EP1635824B1/en not_active Expired - Lifetime
- 2004-06-02 PT PT04754233T patent/PT1635824E/pt unknown
- 2004-06-02 JP JP2006515154A patent/JP2006526656A/ja active Pending
- 2004-06-02 MX MXPA05013075A patent/MXPA05013075A/es active IP Right Grant
- 2004-06-02 AT AT04754233T patent/ATE439837T1/de not_active IP Right Cessation
- 2004-06-02 US US10/860,768 patent/US7652044B2/en not_active Expired - Fee Related
- 2004-06-02 BR BRPI0410905-8A patent/BRPI0410905A/pt not_active IP Right Cessation
- 2004-06-02 ES ES04754233T patent/ES2332135T3/es not_active Expired - Lifetime
- 2004-06-02 AU AU2004251668A patent/AU2004251668B2/en not_active Ceased
- 2004-06-02 CA CA002528438A patent/CA2528438A1/en not_active Abandoned
-
2009
- 2009-09-11 US US12/557,835 patent/US20100004298A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US7652044B2 (en) | 2010-01-26 |
| PT1635824E (pt) | 2009-11-24 |
| US20100004298A1 (en) | 2010-01-07 |
| WO2005000298A2 (en) | 2005-01-06 |
| PL1635824T3 (pl) | 2010-01-29 |
| EP1635824B1 (en) | 2009-08-19 |
| AU2004251668A1 (en) | 2005-01-06 |
| CA2528438A1 (en) | 2005-01-06 |
| ATE439837T1 (de) | 2009-09-15 |
| WO2005000298A3 (en) | 2005-03-03 |
| AU2004251668B2 (en) | 2008-03-20 |
| EP1635824A2 (en) | 2006-03-22 |
| MXPA05013075A (es) | 2006-03-17 |
| US20040254236A1 (en) | 2004-12-16 |
| JP2006526656A (ja) | 2006-11-24 |
| BRPI0410905A (pt) | 2006-06-27 |
| DE602004022668D1 (de) | 2009-10-01 |
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