JP2008525502A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2008525502A5 JP2008525502A5 JP2007548611A JP2007548611A JP2008525502A5 JP 2008525502 A5 JP2008525502 A5 JP 2008525502A5 JP 2007548611 A JP2007548611 A JP 2007548611A JP 2007548611 A JP2007548611 A JP 2007548611A JP 2008525502 A5 JP2008525502 A5 JP 2008525502A5
- Authority
- JP
- Japan
- Prior art keywords
- phenyl
- pyrazol
- urea
- dichlorophenyl
- oxoethyl
- 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
- BYUVOWIJEJQFAP-UHFFFAOYSA-N 2-[3-[5-[(3-pyridin-3-yloxyphenyl)carbamoylamino]-3-thiophen-2-ylpyrazol-1-yl]phenyl]acetamide Chemical compound NC(=O)CC1=CC=CC(N2C(=CC(=N2)C=2SC=CC=2)NC(=O)NC=2C=C(OC=3C=NC=CC=3)C=CC=2)=C1 BYUVOWIJEJQFAP-UHFFFAOYSA-N 0.000 claims description 2
- -1 heterocyclylamino Chemical group 0.000 claims 51
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 23
- 150000001875 compounds Chemical class 0.000 claims 19
- 125000000217 alkyl group Chemical group 0.000 claims 15
- 125000000623 heterocyclic group Chemical group 0.000 claims 11
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 10
- 239000004202 carbamide Substances 0.000 claims 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 8
- 125000003118 aryl group Chemical group 0.000 claims 7
- 125000004076 pyridyl group Chemical group 0.000 claims 6
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 6
- 229910052736 halogen Inorganic materials 0.000 claims 5
- 150000002367 halogens Chemical class 0.000 claims 5
- 125000001072 heteroaryl group Chemical group 0.000 claims 5
- 125000002883 imidazolyl group Chemical group 0.000 claims 5
- 125000002971 oxazolyl group Chemical group 0.000 claims 5
- 125000001544 thienyl group Chemical group 0.000 claims 5
- 125000003545 alkoxy group Chemical group 0.000 claims 4
- 125000003282 alkyl amino group Chemical group 0.000 claims 4
- 125000001769 aryl amino group Chemical group 0.000 claims 4
- 125000004432 carbon atom Chemical group C* 0.000 claims 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims 4
- 125000006310 cycloalkyl amino group Chemical group 0.000 claims 4
- 125000002541 furyl group Chemical group 0.000 claims 4
- 125000001624 naphthyl group Chemical group 0.000 claims 4
- 125000001715 oxadiazolyl group Chemical group 0.000 claims 4
- 125000003226 pyrazolyl group Chemical group 0.000 claims 4
- 125000000168 pyrrolyl group Chemical group 0.000 claims 4
- 125000001113 thiadiazolyl group Chemical group 0.000 claims 4
- 125000000335 thiazolyl group Chemical group 0.000 claims 4
- 125000002947 alkylene group Chemical group 0.000 claims 3
- 125000004429 atom Chemical group 0.000 claims 3
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims 3
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims 3
- 229910052799 carbon Inorganic materials 0.000 claims 3
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 claims 3
- 125000001041 indolyl group Chemical group 0.000 claims 3
- 125000001786 isothiazolyl group Chemical group 0.000 claims 3
- 125000000842 isoxazolyl group Chemical group 0.000 claims 3
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims 3
- 125000000561 purinyl group Chemical group N1=C(N=C2N=CNC2=C1)* 0.000 claims 3
- 125000003373 pyrazinyl group Chemical group 0.000 claims 3
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 claims 2
- XRLOEXOWYIVSTJ-UHFFFAOYSA-N 2-[3-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-(3-fluorophenyl)pyrazol-1-yl]phenyl]acetamide Chemical compound NC(=O)CC1=CC=CC(N2C(=CC(=N2)C=2C=C(F)C=CC=2)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 XRLOEXOWYIVSTJ-UHFFFAOYSA-N 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 2
- 125000004414 alkyl thio group Chemical group 0.000 claims 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims 2
- 125000004104 aryloxy group Chemical group 0.000 claims 2
- 125000004604 benzisothiazolyl group Chemical group S1N=C(C2=C1C=CC=C2)* 0.000 claims 2
- 125000004603 benzisoxazolyl group Chemical group O1N=C(C2=C1C=CC=C2)* 0.000 claims 2
- 125000003310 benzodiazepinyl group Chemical group N1N=C(C=CC2=C1C=CC=C2)* 0.000 claims 2
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims 2
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 claims 2
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims 2
- 125000000259 cinnolinyl group Chemical group N1=NC(=CC2=CC=CC=C12)* 0.000 claims 2
- 125000005044 dihydroquinolinyl group Chemical group N1(CC=CC2=CC=CC=C12)* 0.000 claims 2
- 125000003709 fluoroalkyl group Chemical group 0.000 claims 2
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims 2
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 claims 2
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 claims 2
- 125000003387 indolinyl group Chemical group N1(CCC2=CC=CC=C12)* 0.000 claims 2
- 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 claims 2
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 125000004043 oxo group Chemical group O=* 0.000 claims 2
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 claims 2
- 125000005545 phthalimidyl group Chemical group 0.000 claims 2
- 125000002098 pyridazinyl group Chemical group 0.000 claims 2
- 125000004943 pyrimidin-6-yl group Chemical group N1=CN=CC=C1* 0.000 claims 2
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 2
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 claims 2
- 125000003039 tetrahydroisoquinolinyl group Chemical group C1(NCCC2=CC=CC=C12)* 0.000 claims 2
- 125000000147 tetrahydroquinolinyl group Chemical group N1(CCCC2=CC=CC=C12)* 0.000 claims 2
- 125000003831 tetrazolyl group Chemical group 0.000 claims 2
- 125000004306 triazinyl group Chemical group 0.000 claims 2
- 125000001425 triazolyl group Chemical group 0.000 claims 2
- 125000006730 (C2-C5) alkynyl group Chemical group 0.000 claims 1
- XJLSEXAGTJCILF-RXMQYKEDSA-N (R)-nipecotic acid zwitterion Chemical compound OC(=O)[C@@H]1CCCNC1 XJLSEXAGTJCILF-RXMQYKEDSA-N 0.000 claims 1
- QKAONZYTSXPVLS-UHFFFAOYSA-N 1-(2,3-dichlorophenyl)-3-(5-thiophen-2-yl-1h-pyrazol-3-yl)urea Chemical compound ClC1=CC=CC(NC(=O)NC=2NN=C(C=2)C=2SC=CC=2)=C1Cl QKAONZYTSXPVLS-UHFFFAOYSA-N 0.000 claims 1
- RXKFJNZGJZMMND-UHFFFAOYSA-N 1-(2,3-dichlorophenyl)-3-[2-[3-(hydroxymethyl)phenyl]-5-phenylpyrazol-3-yl]urea Chemical compound OCC1=CC=CC(N2C(=CC(=N2)C=2C=CC=CC=2)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 RXKFJNZGJZMMND-UHFFFAOYSA-N 0.000 claims 1
- GEWPIZQTACGRHK-UHFFFAOYSA-N 1-(2,3-dichlorophenyl)-3-[2-[3-(hydroxymethyl)phenyl]-5-thiophen-2-ylpyrazol-3-yl]urea Chemical compound OCC1=CC=CC(N2C(=CC(=N2)C=2SC=CC=2)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 GEWPIZQTACGRHK-UHFFFAOYSA-N 0.000 claims 1
- MEKVKUUTWATHTN-SFHVURJKSA-N 1-(2,3-dichlorophenyl)-3-[2-[3-[2-[(3s)-3-hydroxypyrrolidin-1-yl]-2-oxoethyl]phenyl]-5-thiophen-2-ylpyrazol-3-yl]urea Chemical compound C1[C@@H](O)CCN1C(=O)CC1=CC=CC(N2C(=CC(=N2)C=2SC=CC=2)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 MEKVKUUTWATHTN-SFHVURJKSA-N 0.000 claims 1
- HKWQXYVCJUJCQD-UHFFFAOYSA-N 1-(2,3-dichlorophenyl)-3-[2-[4-[2-(4-methylpiperazin-1-yl)-2-oxoethyl]phenyl]-5-phenylpyrazol-3-yl]urea Chemical compound C1CN(C)CCN1C(=O)CC1=CC=C(N2C(=CC(=N2)C=2C=CC=CC=2)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)C=C1 HKWQXYVCJUJCQD-UHFFFAOYSA-N 0.000 claims 1
- MVMMLOUGPOQGPA-JOCHJYFZSA-N 1-(2,3-dichlorophenyl)-3-[2-[4-[2-[(2r)-2-(hydroxymethyl)pyrrolidin-1-yl]-2-oxoethyl]phenyl]-5-phenylpyrazol-3-yl]urea Chemical compound OC[C@H]1CCCN1C(=O)CC1=CC=C(N2C(=CC(=N2)C=2C=CC=CC=2)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)C=C1 MVMMLOUGPOQGPA-JOCHJYFZSA-N 0.000 claims 1
- TVYRLXMVKIOKKW-UHFFFAOYSA-N 1-(2,3-dichlorophenyl)-3-[5-(2-fluorophenyl)-2-[3-(hydroxymethyl)phenyl]pyrazol-3-yl]urea Chemical compound OCC1=CC=CC(N2C(=CC(=N2)C=2C(=CC=CC=2)F)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 TVYRLXMVKIOKKW-UHFFFAOYSA-N 0.000 claims 1
- RPXXUQOZMAJKQR-UHFFFAOYSA-N 1-[2-[3-(hydroxymethyl)phenyl]-5-thiophen-2-ylpyrazol-3-yl]-3-(2,3,4-trifluorophenyl)urea Chemical compound OCC1=CC=CC(N2C(=CC(=N2)C=2SC=CC=2)NC(=O)NC=2C(=C(F)C(F)=CC=2)F)=C1 RPXXUQOZMAJKQR-UHFFFAOYSA-N 0.000 claims 1
- NRUZWHPXNXQJRV-UHFFFAOYSA-N 1-[5-tert-butyl-2-(3-cyanophenyl)pyrazol-3-yl]-3-(2,4-difluorophenyl)urea Chemical compound C=1C=CC(C#N)=CC=1N1N=C(C(C)(C)C)C=C1NC(=O)NC1=CC=C(F)C=C1F NRUZWHPXNXQJRV-UHFFFAOYSA-N 0.000 claims 1
- DFDJLAYWXQZZIZ-HXUWFJFHSA-N 1-[5-tert-butyl-2-[3-[2-[(3r)-3-(dimethylamino)pyrrolidin-1-yl]-2-oxoethyl]phenyl]pyrazol-3-yl]-3-(2,3-dichlorophenyl)urea Chemical compound C1[C@H](N(C)C)CCN1C(=O)CC1=CC=CC(N2C(=CC(=N2)C(C)(C)C)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 DFDJLAYWXQZZIZ-HXUWFJFHSA-N 0.000 claims 1
- DFDJLAYWXQZZIZ-FQEVSTJZSA-N 1-[5-tert-butyl-2-[3-[2-[(3s)-3-(dimethylamino)pyrrolidin-1-yl]-2-oxoethyl]phenyl]pyrazol-3-yl]-3-(2,3-dichlorophenyl)urea Chemical compound C1[C@@H](N(C)C)CCN1C(=O)CC1=CC=CC(N2C(=CC(=N2)C(C)(C)C)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 DFDJLAYWXQZZIZ-FQEVSTJZSA-N 0.000 claims 1
- VNNSYZVMRNOQML-HXUWFJFHSA-N 1-[5-tert-butyl-2-[4-[2-[(3r)-3-(dimethylamino)pyrrolidin-1-yl]-2-oxoethyl]phenyl]pyrazol-3-yl]-3-(2,3-dichlorophenyl)urea Chemical compound C1[C@H](N(C)C)CCN1C(=O)CC1=CC=C(N2C(=CC(=N2)C(C)(C)C)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)C=C1 VNNSYZVMRNOQML-HXUWFJFHSA-N 0.000 claims 1
- IUHGVIWTEWFBQH-SFHVURJKSA-N 1-[5-tert-butyl-2-[4-[2-[(3s)-3-hydroxypyrrolidin-1-yl]-2-oxoethyl]phenyl]pyrazol-3-yl]-3-(2,3-dichlorophenyl)urea Chemical compound C=1C=C(CC(=O)N2C[C@@H](O)CC2)C=CC=1N1N=C(C(C)(C)C)C=C1NC(=O)NC1=CC=CC(Cl)=C1Cl IUHGVIWTEWFBQH-SFHVURJKSA-N 0.000 claims 1
- VNNSYZVMRNOQML-UHFFFAOYSA-N 1-[5-tert-butyl-2-[4-[2-[3-(dimethylamino)pyrrolidin-1-yl]-2-oxoethyl]phenyl]pyrazol-3-yl]-3-(2,3-dichlorophenyl)urea Chemical compound C1C(N(C)C)CCN1C(=O)CC1=CC=C(N2C(=CC(=N2)C(C)(C)C)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)C=C1 VNNSYZVMRNOQML-UHFFFAOYSA-N 0.000 claims 1
- OVPPOGWZSQYJDZ-UHFFFAOYSA-N 2-[3-[3-cyclopentyl-5-[(2,3-dichlorophenyl)carbamoylamino]pyrazol-1-yl]phenyl]-n-(2,3-dihydroxypropyl)acetamide Chemical compound OCC(O)CNC(=O)CC1=CC=CC(N2C(=CC(=N2)C2CCCC2)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 OVPPOGWZSQYJDZ-UHFFFAOYSA-N 0.000 claims 1
- CDHWPDARBORLQH-UHFFFAOYSA-N 2-[3-[3-cyclopentyl-5-[(2,3-dichlorophenyl)carbamoylamino]pyrazol-1-yl]phenyl]acetamide Chemical compound NC(=O)CC1=CC=CC(N2C(=CC(=N2)C2CCCC2)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 CDHWPDARBORLQH-UHFFFAOYSA-N 0.000 claims 1
- MRLOXPNJVSEIRZ-UHFFFAOYSA-N 2-[3-[3-cyclopentyl-5-[(2,3-dichlorophenyl)carbamoylamino]pyrazol-1-yl]phenyl]acetic acid Chemical compound OC(=O)CC1=CC=CC(N2C(=CC(=N2)C2CCCC2)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 MRLOXPNJVSEIRZ-UHFFFAOYSA-N 0.000 claims 1
- ICNXRBASKDUBJL-UHFFFAOYSA-N 2-[3-[3-tert-butyl-5-[(2,3,4-trifluorophenyl)carbamoylamino]pyrazol-1-yl]phenyl]acetamide Chemical compound C=1C=CC(CC(N)=O)=CC=1N1N=C(C(C)(C)C)C=C1NC(=O)NC1=CC=C(F)C(F)=C1F ICNXRBASKDUBJL-UHFFFAOYSA-N 0.000 claims 1
- YFCFJCIPGYKXLZ-UHFFFAOYSA-N 2-[3-[3-tert-butyl-5-[(2,4-difluorophenyl)carbamoylamino]pyrazol-1-yl]phenyl]acetamide Chemical compound C=1C=CC(CC(N)=O)=CC=1N1N=C(C(C)(C)C)C=C1NC(=O)NC1=CC=C(F)C=C1F YFCFJCIPGYKXLZ-UHFFFAOYSA-N 0.000 claims 1
- JMXPYCLGTWFRRK-UHFFFAOYSA-N 2-[3-[3-tert-butyl-5-[(3-pyrazin-2-yloxyphenyl)carbamoylamino]pyrazol-1-yl]phenyl]acetamide Chemical compound C=1C=CC(CC(N)=O)=CC=1N1N=C(C(C)(C)C)C=C1NC(=O)NC(C=1)=CC=CC=1OC1=CN=CC=N1 JMXPYCLGTWFRRK-UHFFFAOYSA-N 0.000 claims 1
- JUKPCBCERPOGMD-UHFFFAOYSA-N 2-[3-[3-tert-butyl-5-[(3-pyrazin-2-ylphenyl)carbamoylamino]pyrazol-1-yl]phenyl]acetamide Chemical compound C=1C=CC(CC(N)=O)=CC=1N1N=C(C(C)(C)C)C=C1NC(=O)NC(C=1)=CC=CC=1C1=CN=CC=N1 JUKPCBCERPOGMD-UHFFFAOYSA-N 0.000 claims 1
- MMEYNYHTUVXSCU-UHFFFAOYSA-N 2-[3-[3-tert-butyl-5-[(3-pyridin-3-yloxyphenyl)carbamoylamino]pyrazol-1-yl]phenyl]acetamide Chemical compound C=1C=CC(CC(N)=O)=CC=1N1N=C(C(C)(C)C)C=C1NC(=O)NC(C=1)=CC=CC=1OC1=CC=CN=C1 MMEYNYHTUVXSCU-UHFFFAOYSA-N 0.000 claims 1
- JCNDKKIMAKONEI-UHFFFAOYSA-N 2-[3-[3-tert-butyl-5-[(3-pyridin-3-ylphenyl)carbamoylamino]pyrazol-1-yl]phenyl]acetamide Chemical compound C=1C=CC(CC(N)=O)=CC=1N1N=C(C(C)(C)C)C=C1NC(=O)NC(C=1)=CC=CC=1C1=CC=CN=C1 JCNDKKIMAKONEI-UHFFFAOYSA-N 0.000 claims 1
- AXDMTDUAXWCVPA-UHFFFAOYSA-N 2-[3-[3-tert-butyl-5-[(4-pyridin-4-yloxyphenyl)carbamoylamino]pyrazol-1-yl]phenyl]acetamide Chemical compound C=1C=CC(CC(N)=O)=CC=1N1N=C(C(C)(C)C)C=C1NC(=O)NC(C=C1)=CC=C1OC1=CC=NC=C1 AXDMTDUAXWCVPA-UHFFFAOYSA-N 0.000 claims 1
- SIRQROHWTHZOSI-UHFFFAOYSA-N 2-[3-[3-tert-butyl-5-[[4-methyl-3-(pyrimidin-2-ylamino)phenyl]carbamoylamino]pyrazol-1-yl]phenyl]acetamide Chemical compound C1=C(NC=2N=CC=CN=2)C(C)=CC=C1NC(=O)NC1=CC(C(C)(C)C)=NN1C1=CC=CC(CC(N)=O)=C1 SIRQROHWTHZOSI-UHFFFAOYSA-N 0.000 claims 1
- KYSOKGJGZUNAFL-UHFFFAOYSA-N 2-[3-[3-tert-butyl-5-[[4-methyl-3-[(4-pyridin-3-ylpyrimidin-2-yl)amino]phenyl]carbamoylamino]pyrazol-1-yl]phenyl]acetamide Chemical compound C1=C(NC=2N=C(C=CN=2)C=2C=NC=CC=2)C(C)=CC=C1NC(=O)NC1=CC(C(C)(C)C)=NN1C1=CC=CC(CC(N)=O)=C1 KYSOKGJGZUNAFL-UHFFFAOYSA-N 0.000 claims 1
- VIMDVWLSWRBKRQ-UHFFFAOYSA-N 2-[3-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-(2-fluorophenyl)pyrazol-1-yl]phenyl]-n-(1,3-dihydroxypropan-2-yl)acetamide Chemical compound OCC(CO)NC(=O)CC1=CC=CC(N2C(=CC(=N2)C=2C(=CC=CC=2)F)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 VIMDVWLSWRBKRQ-UHFFFAOYSA-N 0.000 claims 1
- SMPOYUSWIAZPRX-UHFFFAOYSA-N 2-[3-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-(2-fluorophenyl)pyrazol-1-yl]phenyl]-n-(2-hydroxyethyl)acetamide Chemical compound OCCNC(=O)CC1=CC=CC(N2C(=CC(=N2)C=2C(=CC=CC=2)F)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 SMPOYUSWIAZPRX-UHFFFAOYSA-N 0.000 claims 1
- NWOGJAKKLLVTRV-UHFFFAOYSA-N 2-[3-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-(2-fluorophenyl)pyrazol-1-yl]phenyl]acetic acid Chemical compound OC(=O)CC1=CC=CC(N2C(=CC(=N2)C=2C(=CC=CC=2)F)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 NWOGJAKKLLVTRV-UHFFFAOYSA-N 0.000 claims 1
- LWBOLOZIWJSQTJ-UHFFFAOYSA-N 2-[3-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-(3-fluorophenyl)pyrazol-1-yl]phenyl]-n-(2-hydroxyethyl)acetamide Chemical compound OCCNC(=O)CC1=CC=CC(N2C(=CC(=N2)C=2C=C(F)C=CC=2)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 LWBOLOZIWJSQTJ-UHFFFAOYSA-N 0.000 claims 1
- AOWMMTGVBWWQNT-UHFFFAOYSA-N 2-[3-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-(3-fluorophenyl)pyrazol-1-yl]phenyl]acetic acid Chemical compound OC(=O)CC1=CC=CC(N2C(=CC(=N2)C=2C=C(F)C=CC=2)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 AOWMMTGVBWWQNT-UHFFFAOYSA-N 0.000 claims 1
- SKTLEEMTNMTIAX-UHFFFAOYSA-N 2-[3-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-(4-fluorophenyl)pyrazol-1-yl]phenyl]acetic acid Chemical compound OC(=O)CC1=CC=CC(N2C(=CC(=N2)C=2C=CC(F)=CC=2)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 SKTLEEMTNMTIAX-UHFFFAOYSA-N 0.000 claims 1
- VDMNSWVUAZIWIY-UHFFFAOYSA-N 2-[3-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-phenylpyrazol-1-yl]phenyl]acetamide Chemical compound NC(=O)CC1=CC=CC(N2C(=CC(=N2)C=2C=CC=CC=2)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 VDMNSWVUAZIWIY-UHFFFAOYSA-N 0.000 claims 1
- FMQSUBFLPYIYFS-UHFFFAOYSA-N 2-[3-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-phenylpyrazol-1-yl]phenyl]acetic acid Chemical compound OC(=O)CC1=CC=CC(N2C(=CC(=N2)C=2C=CC=CC=2)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 FMQSUBFLPYIYFS-UHFFFAOYSA-N 0.000 claims 1
- KFBIHMGBKKHVPX-UHFFFAOYSA-N 2-[3-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-thiophen-2-ylpyrazol-1-yl]phenyl]-n-(1,3-dihydroxypropan-2-yl)acetamide Chemical compound OCC(CO)NC(=O)CC1=CC=CC(N2C(=CC(=N2)C=2SC=CC=2)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 KFBIHMGBKKHVPX-UHFFFAOYSA-N 0.000 claims 1
- QEXVFLQQPGOUMH-UHFFFAOYSA-N 2-[3-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-thiophen-2-ylpyrazol-1-yl]phenyl]-n-(2,3-dihydroxypropyl)acetamide Chemical compound OCC(O)CNC(=O)CC1=CC=CC(N2C(=CC(=N2)C=2SC=CC=2)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 QEXVFLQQPGOUMH-UHFFFAOYSA-N 0.000 claims 1
- KYXUHXFIPBMLNL-UHFFFAOYSA-N 2-[3-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-thiophen-2-ylpyrazol-1-yl]phenyl]acetic acid Chemical compound OC(=O)CC1=CC=CC(N2C(=CC(=N2)C=2SC=CC=2)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 KYXUHXFIPBMLNL-UHFFFAOYSA-N 0.000 claims 1
- NIWSVPPNERAVRN-UHFFFAOYSA-N 2-[3-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-thiophen-3-ylpyrazol-1-yl]phenyl]-n-(2-hydroxyethyl)acetamide Chemical compound OCCNC(=O)CC1=CC=CC(N2C(=CC(=N2)C2=CSC=C2)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 NIWSVPPNERAVRN-UHFFFAOYSA-N 0.000 claims 1
- FQLTVXWHQWGJRK-UHFFFAOYSA-N 2-[3-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-thiophen-3-ylpyrazol-1-yl]phenyl]acetamide Chemical compound NC(=O)CC1=CC=CC(N2C(=CC(=N2)C2=CSC=C2)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 FQLTVXWHQWGJRK-UHFFFAOYSA-N 0.000 claims 1
- JMAQBCQLEORUHM-UHFFFAOYSA-N 2-[3-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-thiophen-3-ylpyrazol-1-yl]phenyl]acetic acid Chemical compound OC(=O)CC1=CC=CC(N2C(=CC(=N2)C2=CSC=C2)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 JMAQBCQLEORUHM-UHFFFAOYSA-N 0.000 claims 1
- NKJAGUXMPRICDB-UHFFFAOYSA-N 2-[3-[5-[(3-pyridin-3-yloxyphenyl)carbamoylamino]-3-(trifluoromethyl)pyrazol-1-yl]phenyl]acetamide Chemical compound NC(=O)CC1=CC=CC(N2C(=CC(=N2)C(F)(F)F)NC(=O)NC=2C=C(OC=3C=NC=CC=3)C=CC=2)=C1 NKJAGUXMPRICDB-UHFFFAOYSA-N 0.000 claims 1
- SMGVJYJXZIVZLY-UHFFFAOYSA-N 2-[3-[5-[[3-(6-aminopyridin-3-yl)phenyl]carbamoylamino]-3-tert-butylpyrazol-1-yl]phenyl]acetamide Chemical compound C=1C=CC(CC(N)=O)=CC=1N1N=C(C(C)(C)C)C=C1NC(=O)NC(C=1)=CC=CC=1C1=CC=C(N)N=C1 SMGVJYJXZIVZLY-UHFFFAOYSA-N 0.000 claims 1
- IWHATZMYBFVKBT-UHFFFAOYSA-N 2-[4-[3-cyclopentyl-5-[(2,3-dichlorophenyl)carbamoylamino]pyrazol-1-yl]phenyl]acetic acid Chemical compound C1=CC(CC(=O)O)=CC=C1N1C(NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=CC(C2CCCC2)=N1 IWHATZMYBFVKBT-UHFFFAOYSA-N 0.000 claims 1
- OQBIDSRETIPIJV-UHFFFAOYSA-N 2-[4-[3-tert-butyl-5-[(2,3,4-trifluorophenyl)carbamoylamino]pyrazol-1-yl]phenyl]acetic acid Chemical compound C=1C=C(CC(O)=O)C=CC=1N1N=C(C(C)(C)C)C=C1NC(=O)NC1=CC=C(F)C(F)=C1F OQBIDSRETIPIJV-UHFFFAOYSA-N 0.000 claims 1
- SMYXZMOISBUNSW-UHFFFAOYSA-N 2-[4-[3-tert-butyl-5-[(2,4-difluorophenyl)carbamoylamino]pyrazol-1-yl]phenyl]acetamide Chemical compound C=1C=C(CC(N)=O)C=CC=1N1N=C(C(C)(C)C)C=C1NC(=O)NC1=CC=C(F)C=C1F SMYXZMOISBUNSW-UHFFFAOYSA-N 0.000 claims 1
- UFHBILWPPXDONX-UHFFFAOYSA-N 2-[4-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-(2-fluorophenyl)pyrazol-1-yl]phenyl]-n-(1,3-dihydroxypropan-2-yl)acetamide Chemical compound C1=CC(CC(=O)NC(CO)CO)=CC=C1N1C(NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=CC(C=2C(=CC=CC=2)F)=N1 UFHBILWPPXDONX-UHFFFAOYSA-N 0.000 claims 1
- YVNFQHCMFYVWLK-UHFFFAOYSA-N 2-[4-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-(2-fluorophenyl)pyrazol-1-yl]phenyl]-n-(2,3-dihydroxypropyl)acetamide Chemical compound C1=CC(CC(=O)NCC(O)CO)=CC=C1N1C(NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=CC(C=2C(=CC=CC=2)F)=N1 YVNFQHCMFYVWLK-UHFFFAOYSA-N 0.000 claims 1
- QLQPMARGOADRMP-UHFFFAOYSA-N 2-[4-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-(2-fluorophenyl)pyrazol-1-yl]phenyl]acetic acid Chemical compound C1=CC(CC(=O)O)=CC=C1N1C(NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=CC(C=2C(=CC=CC=2)F)=N1 QLQPMARGOADRMP-UHFFFAOYSA-N 0.000 claims 1
- BIBIWIBQLSTDFJ-UHFFFAOYSA-N 2-[4-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-(3-fluorophenyl)pyrazol-1-yl]phenyl]acetic acid Chemical compound C1=CC(CC(=O)O)=CC=C1N1C(NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=CC(C=2C=C(F)C=CC=2)=N1 BIBIWIBQLSTDFJ-UHFFFAOYSA-N 0.000 claims 1
- PSMACVOCFOSMPX-UHFFFAOYSA-N 2-[4-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-phenylpyrazol-1-yl]phenyl]-n-(2-hydroxyethyl)acetamide Chemical compound C1=CC(CC(=O)NCCO)=CC=C1N1C(NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=CC(C=2C=CC=CC=2)=N1 PSMACVOCFOSMPX-UHFFFAOYSA-N 0.000 claims 1
- QOZXGJHWUHPFLH-UHFFFAOYSA-N 2-[4-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-phenylpyrazol-1-yl]phenyl]acetic acid Chemical compound C1=CC(CC(=O)O)=CC=C1N1C(NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=CC(C=2C=CC=CC=2)=N1 QOZXGJHWUHPFLH-UHFFFAOYSA-N 0.000 claims 1
- KLHVRBBSCMAUPR-UHFFFAOYSA-N 2-[4-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-thiophen-2-ylpyrazol-1-yl]phenyl]-n-(2,3-dihydroxypropyl)acetamide Chemical compound C1=CC(CC(=O)NCC(O)CO)=CC=C1N1C(NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=CC(C=2SC=CC=2)=N1 KLHVRBBSCMAUPR-UHFFFAOYSA-N 0.000 claims 1
- GSTIQIULHFGCEE-UHFFFAOYSA-N 2-[4-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-thiophen-3-ylpyrazol-1-yl]phenyl]acetamide Chemical compound C1=CC(CC(=O)N)=CC=C1N1C(NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=CC(C2=CSC=C2)=N1 GSTIQIULHFGCEE-UHFFFAOYSA-N 0.000 claims 1
- YHZGFVUWAVGFQU-UHFFFAOYSA-N 2-[4-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-thiophen-3-ylpyrazol-1-yl]phenyl]acetic acid Chemical compound C1=CC(CC(=O)O)=CC=C1N1C(NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=CC(C2=CSC=C2)=N1 YHZGFVUWAVGFQU-UHFFFAOYSA-N 0.000 claims 1
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 1
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims 1
- HWYBOIVSMQCPAC-UHFFFAOYSA-N 3-[3-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-(2-fluorophenyl)pyrazol-1-yl]phenyl]-2-methylpropanamide Chemical compound NC(=O)C(C)CC1=CC=CC(N2C(=CC(=N2)C=2C(=CC=CC=2)F)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 HWYBOIVSMQCPAC-UHFFFAOYSA-N 0.000 claims 1
- ZDIOOCKIWNQUDW-UHFFFAOYSA-N 3-[3-[5-[(2,3-dichlorophenyl)carbamoylamino]-3-thiophen-2-ylpyrazol-1-yl]phenyl]-2-methylpropanoic acid Chemical compound OC(=O)C(C)CC1=CC=CC(N2C(=CC(=N2)C=2SC=CC=2)NC(=O)NC=2C(=C(Cl)C=CC=2)Cl)=C1 ZDIOOCKIWNQUDW-UHFFFAOYSA-N 0.000 claims 1
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims 1
- 125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 claims 1
- FSMRZOMHPBBBAX-UHFFFAOYSA-N 4-[4-[[2-[3-(2-amino-2-oxoethyl)phenyl]-5-tert-butylpyrazol-3-yl]carbamoylamino]phenoxy]-n-methylpyridine-2-carboxamide Chemical compound C1=NC(C(=O)NC)=CC(OC=2C=CC(NC(=O)NC=3N(N=C(C=3)C(C)(C)C)C=3C=C(CC(N)=O)C=CC=3)=CC=2)=C1 FSMRZOMHPBBBAX-UHFFFAOYSA-N 0.000 claims 1
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims 1
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims 1
- JRLTTZUODKEYDH-UHFFFAOYSA-N 8-methylquinoline Chemical group C1=CN=C2C(C)=CC=CC2=C1 JRLTTZUODKEYDH-UHFFFAOYSA-N 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- BFPYWIDHMRZLRN-SLHNCBLASA-N Ethinyl estradiol Chemical group OC1=CC=C2[C@H]3CC[C@](C)([C@](CC4)(O)C#C)[C@@H]4[C@@H]3CCC2=C1 BFPYWIDHMRZLRN-SLHNCBLASA-N 0.000 claims 1
- AVRWEULSKHQETA-UHFFFAOYSA-N Thiophene-2 Chemical compound S1C=2CCCCCC=2C(C(=O)OC)=C1NC(=O)C1=C(F)C(F)=C(F)C(F)=C1F AVRWEULSKHQETA-UHFFFAOYSA-N 0.000 claims 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims 1
- 125000002723 alicyclic group Chemical group 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 1
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims 1
- 125000004471 alkyl aminosulfonyl group Chemical group 0.000 claims 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 125000004103 aminoalkyl group Chemical group 0.000 claims 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims 1
- 125000005110 aryl thio group Chemical group 0.000 claims 1
- 125000002785 azepinyl group Chemical group 0.000 claims 1
- HNYOPLTXPVRDBG-UHFFFAOYSA-N barbituric acid Chemical compound O=C1CC(=O)NC(=O)N1 HNYOPLTXPVRDBG-UHFFFAOYSA-N 0.000 claims 1
- 125000003354 benzotriazolyl group Chemical group N1N=NC2=C1C=CC=C2* 0.000 claims 1
- 125000002618 bicyclic heterocycle group Chemical group 0.000 claims 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 1
- 150000001721 carbon Chemical group 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims 1
- 125000004472 dialkylaminosulfonyl group Chemical group 0.000 claims 1
- 125000005045 dihydroisoquinolinyl group Chemical group C1(NC=CC2=CC=CC=C12)* 0.000 claims 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 1
- 150000002148 esters Chemical group 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- FATAVLOOLIRUNA-UHFFFAOYSA-N formylmethyl Chemical group [CH2]C=O FATAVLOOLIRUNA-UHFFFAOYSA-N 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 125000004857 imidazopyridinyl group Chemical group N1C(=NC2=C1C=CC=N2)* 0.000 claims 1
- 125000005956 isoquinolyl group Chemical group 0.000 claims 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 1
- 125000002911 monocyclic heterocycle group Chemical group 0.000 claims 1
- 125000002757 morpholinyl group Chemical group 0.000 claims 1
- DUWWHGPELOTTOE-UHFFFAOYSA-N n-(5-chloro-2,4-dimethoxyphenyl)-3-oxobutanamide Chemical compound COC1=CC(OC)=C(NC(=O)CC(C)=O)C=C1Cl DUWWHGPELOTTOE-UHFFFAOYSA-N 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000003566 oxetanyl group Chemical group 0.000 claims 1
- 125000004193 piperazinyl group Chemical group 0.000 claims 1
- 125000003386 piperidinyl group Chemical group 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 235000019260 propionic acid Nutrition 0.000 claims 1
- 125000004309 pyranyl group Chemical group O1C(C=CC=C1)* 0.000 claims 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims 1
- 125000005493 quinolyl group Chemical group 0.000 claims 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 claims 1
- 125000004568 thiomorpholinyl group Chemical group 0.000 claims 1
- 0 C*C(NS(N(*)*)(=O)=O)=O Chemical compound C*C(NS(N(*)*)(=O)=O)=O 0.000 description 8
- BRAKGANXHZKVQP-UHFFFAOYSA-N NC(Cc1cccc(-[n](c(NC(Nc2cccc(Oc3cccnc3)c2)=O)c2)nc2-c2ccccc2)c1)=O Chemical compound NC(Cc1cccc(-[n](c(NC(Nc2cccc(Oc3cccnc3)c2)=O)c2)nc2-c2ccccc2)c1)=O BRAKGANXHZKVQP-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US63898704P | 2004-12-23 | 2004-12-23 | |
| PCT/US2005/047597 WO2006081034A2 (en) | 2004-12-23 | 2005-12-23 | Anti-inflammatory medicaments |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2008525502A JP2008525502A (ja) | 2008-07-17 |
| JP2008525502A5 true JP2008525502A5 (enExample) | 2009-01-29 |
Family
ID=36740941
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007548611A Abandoned JP2008525502A (ja) | 2004-12-23 | 2005-12-23 | 抗炎症薬 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20090312349A1 (enExample) |
| EP (1) | EP1836173A4 (enExample) |
| JP (1) | JP2008525502A (enExample) |
| AU (1) | AU2005325676A1 (enExample) |
| CA (1) | CA2592116A1 (enExample) |
| WO (1) | WO2006081034A2 (enExample) |
Families Citing this family (51)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1835934A4 (en) | 2004-12-23 | 2010-07-28 | Deciphera Pharmaceuticals Llc | ENZYME MODULATORS AND TREATMENTS |
| DE102006029795A1 (de) * | 2006-06-27 | 2008-01-03 | Schebo Biotech Ag | Neue Harnstoff-Derivate und deren Verwendungen |
| WO2008026704A1 (en) * | 2006-08-31 | 2008-03-06 | Kyowa Hakko Kogyo Co., Ltd. | Isoquinoline derivative |
| US8188113B2 (en) * | 2006-09-14 | 2012-05-29 | Deciphera Pharmaceuticals, Inc. | Dihydropyridopyrimidinyl, dihydronaphthyidinyl and related compounds useful as kinase inhibitors for the treatment of proliferative diseases |
| US7897762B2 (en) * | 2006-09-14 | 2011-03-01 | Deciphera Pharmaceuticals, Llc | Kinase inhibitors useful for the treatment of proliferative diseases |
| US7790756B2 (en) | 2006-10-11 | 2010-09-07 | Deciphera Pharmaceuticals, Llc | Kinase inhibitors useful for the treatment of myleoproliferative diseases and other proliferative diseases |
| JP2010506948A (ja) * | 2006-10-20 | 2010-03-04 | アイアールエム・リミテッド・ライアビリティ・カンパニー | Ｃ−ｋｉｔおよびｐｄｇｆｒ受容体を調節するための組成物および方法 |
| CN101622244A (zh) * | 2006-11-03 | 2010-01-06 | Irm责任有限公司 | 作为蛋白激酶抑制剂的化合物和组合物 |
| US20110189167A1 (en) * | 2007-04-20 | 2011-08-04 | Flynn Daniel L | Methods and Compositions for the Treatment of Myeloproliferative Diseases and other Proliferative Diseases |
| US20080269267A1 (en) * | 2007-04-20 | 2008-10-30 | Deciphera Pharmaceuticals, Llc | Kinase inhibitors useful for the treatment of myleoprolific diseases and other proliferative diseases |
| JP5160637B2 (ja) | 2007-05-04 | 2013-03-13 | アイアールエム・リミテッド・ライアビリティ・カンパニー | ｃ−ｋｉｔおよびＰＤＧＦＲキナーゼインヒビターとしての化合物および組成物 |
| PL2190825T3 (pl) | 2007-08-22 | 2014-09-30 | Novartis Ag | Związki 5-(4-(chlorowcoalkoksy)-fenylo)-pirymidyno-2-aminowe i kompozycje jako inhibitory kinazy |
| EA017392B1 (ru) | 2007-08-22 | 2012-12-28 | Айрм Ллк | Производные 2-гетероариламинопиримидина в качестве ингибиторов киназ |
| PE20091492A1 (es) * | 2008-02-22 | 2009-10-22 | Irm Llc | Compuestos y composiciones como inhibidores de c-kit y de la cinasa pdgfr |
| WO2010017902A1 (de) | 2008-08-14 | 2010-02-18 | Bayer Cropscience Aktiengesellschaft | Insektizide 4-phenyl-1h-pyrazole |
| GB0818033D0 (en) | 2008-10-02 | 2008-11-05 | Respivert Ltd | Novel compound |
| BRPI0920707A2 (pt) | 2008-10-02 | 2015-12-29 | Respivert Ltd | compostos |
| CN102256493A (zh) * | 2008-10-29 | 2011-11-23 | 迪赛孚尔制药有限公司 | 表现出抗癌活性和抗增殖活性的环丙烷酰胺及其类似物 |
| US8299074B2 (en) | 2008-12-11 | 2012-10-30 | Respivert Ltd. | P38 MAP kinase inhibitors |
| GB0905955D0 (en) | 2009-04-06 | 2009-05-20 | Respivert Ltd | Novel compounds |
| WO2012125981A2 (en) * | 2011-03-17 | 2012-09-20 | Selexagen Therapeutics, Inc. | Raf kinase inhibitors |
| HRP20161786T1 (hr) | 2011-05-13 | 2017-03-10 | Array Biopharma, Inc. | Pirolidinil urea, pirolidinil tiourea i pirolidinil gvanidin spojevi kao inhibitori trka kinaze |
| BR112014001714A2 (pt) | 2011-07-26 | 2017-02-14 | Gruenenthal Gmbh | derivados de carboxamida e ureia aromáticos bicíclicos substituídos como ligantes de receptor vaniloide |
| GB201113538D0 (en) | 2011-08-04 | 2011-09-21 | Karobio Ab | Novel estrogen receptor ligands |
| US8461179B1 (en) | 2012-06-07 | 2013-06-11 | Deciphera Pharmaceuticals, Llc | Dihydronaphthyridines and related compounds useful as kinase inhibitors for the treatment of proliferative diseases |
| WO2014078328A1 (en) | 2012-11-13 | 2014-05-22 | Array Biopharma Inc. | N-bicyclic aryl,n'-pyrazolyl urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors |
| WO2014078331A1 (en) | 2012-11-13 | 2014-05-22 | Array Biopharma Inc. | N-(arylalkyl)-n'-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors |
| UA117573C2 (uk) | 2012-11-13 | 2018-08-27 | Ерей Біофарма Інк. | Біциклічні сполуки сечовини, тіосечовини, гуанідину й ціаногуанідину, придатні для лікування болю |
| WO2014078372A1 (en) | 2012-11-13 | 2014-05-22 | Array Biopharma Inc. | Pyrrolidinyl urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors |
| UA116455C2 (uk) | 2012-11-13 | 2018-03-26 | Еррей Біофарма Інк. | Сполуки n-піролідинілсечовини, n'-піразолілсечовини, тіосечовини, гуанідину та ціаногуанідину як інгібітори кінази trka |
| WO2014078325A1 (en) | 2012-11-13 | 2014-05-22 | Array Biopharma Inc. | N-(monocyclic aryl),n'-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors |
| US9828360B2 (en) | 2012-11-13 | 2017-11-28 | Array Biopharma Inc. | Pyrrolidinyl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors |
| US9809578B2 (en) | 2012-11-13 | 2017-11-07 | Array Biopharma Inc. | Pyrazolyl urea, thiourea, guanidine and cyanoguanidine compounds as trkA kinase inhibitors |
| US9822118B2 (en) | 2012-11-13 | 2017-11-21 | Array Biopharma Inc. | Bicyclic heteroaryl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors |
| US9981959B2 (en) | 2012-11-13 | 2018-05-29 | Array Biopharma Inc. | Thiazolyl and oxazolyl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors |
| CN109970614B (zh) | 2014-05-15 | 2023-01-13 | 阵列生物制药公司 | 作为trka激酶抑制剂的化合物及其用途 |
| GB201721185D0 (en) | 2017-12-18 | 2018-01-31 | Nodthera Ltd | Sulphonyl urea derivatives |
| JP2021512105A (ja) | 2018-01-31 | 2021-05-13 | デシフェラ・ファーマシューティカルズ，エルエルシー | 消化管間質腫瘍の治療のための併用療法 |
| CN118903436A (zh) | 2018-01-31 | 2024-11-08 | 德西费拉制药有限责任公司 | 治疗肥大细胞增多症的组合疗法 |
| US11952370B2 (en) | 2018-06-11 | 2024-04-09 | Northeastern University | Selective ligands for modulation of GIRK channels |
| CN109134451A (zh) * | 2018-09-10 | 2019-01-04 | 遵义医学院 | 1,3-二取代脲类与硫脲类衍生物及其应用 |
| EP3886854A4 (en) | 2018-11-30 | 2022-07-06 | Nuvation Bio Inc. | Pyrrole and pyrazole compounds and methods of use thereof |
| CN109456280B (zh) * | 2018-12-24 | 2020-11-10 | 锦州医科大学 | 含有脲结构的4-苯基噻唑-2-胺类衍生物及其制备方法与应用 |
| LT3983387T (lt) | 2019-06-12 | 2024-07-25 | NodThera Limited | Sulfonilkarbamido dariniai ir jų naudojimas |
| CA3140017A1 (en) | 2019-07-19 | 2021-01-28 | Aurore HICK | Polyaromatic urea derivatives and their use in the treatment of muscle diseases |
| TWI878335B (zh) | 2019-08-12 | 2025-04-01 | 美商迪賽孚爾製藥有限公司 | 治療胃腸道基質瘤方法 |
| NZ784949A (en) | 2019-08-12 | 2025-09-26 | Deciphera Pharmaceuticals Llc | Ripretinib for treating gastrointestinal stromal tumors |
| SMT202400484T1 (it) | 2019-12-30 | 2025-01-14 | Deciphera Pharmaceuticals Llc | Composizioni di 1-(4-bromo-5-(1-etil-7-(metilammino)-2-osso-1,2-diidro-1,6-naftiridin-3-il)-2-fluorofenil)-3-fenilurea |
| FI4084778T3 (fi) | 2019-12-30 | 2023-12-18 | Deciphera Pharmaceuticals Llc | Amorfisia kinaasi-inhibiittoriformulaatioita ja menetelmiä niiden käyttämiseksi |
| EP4029501A1 (en) | 2021-01-19 | 2022-07-20 | Anagenesis Biotechnologies | Combination of polyaromatic urea derivatives and glucocorticoid or hdac inhibitor for the treatment of diseases or conditions associated with muscle cells and/or satellite cells |
| US11779572B1 (en) | 2022-09-02 | 2023-10-10 | Deciphera Pharmaceuticals, Llc | Methods of treating gastrointestinal stromal tumors |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3818024A (en) * | 1972-02-16 | 1974-06-18 | Velsicol Chemical Corp | Benzothiazol substituted thiadiazolidines |
| US4093624A (en) * | 1977-01-31 | 1978-06-06 | Icn Pharmaceuticals, Inc. | 1,2,4-Thiadiazolidine-3,5-dione |
| US4296237A (en) * | 1979-09-11 | 1981-10-20 | Merck & Co., Inc. | 4-(Pyridyl, piperazinyl and thiazolyl substituted thiazolyl)-3-hydroxy-3-pyrroline-2,5-diones |
| US6235786B1 (en) * | 1997-08-06 | 2001-05-22 | Abbott Laboratories | Reverse hydroxamate inhibitors of matrix metalloproteinases |
| UA73492C2 (en) * | 1999-01-19 | 2005-08-15 | Aromatic heterocyclic compounds as antiinflammatory agents | |
| US6525046B1 (en) * | 2000-01-18 | 2003-02-25 | Boehringer Ingelheim Pharmaceuticals, Inc. | Aromatic heterocyclic compounds as antiinflammatory agents |
| US6645990B2 (en) * | 2000-08-15 | 2003-11-11 | Amgen Inc. | Thiazolyl urea compounds and methods of uses |
| CA2435446A1 (en) * | 2001-02-15 | 2002-08-29 | Boehringer Ingelheim Pharmaceuticals, Inc. | Process for synthesis of heteroaryl-substituted urea compounds useful as antiinflammatory agents |
| JP4343534B2 (ja) * | 2001-03-02 | 2009-10-14 | ゲーペーツェー バイオテック アクチェンゲゼルシャフト | ３ハイブリッド・アッセイ・システム |
| US7202257B2 (en) * | 2003-12-24 | 2007-04-10 | Deciphera Pharmaceuticals, Llc | Anti-inflammatory medicaments |
| US7144911B2 (en) * | 2002-12-31 | 2006-12-05 | Deciphera Pharmaceuticals Llc | Anti-inflammatory medicaments |
| US20070191336A1 (en) * | 2003-12-24 | 2007-08-16 | Flynn Daniel L | Anti-inflammatory medicaments |
-
2005
- 2005-12-23 US US11/721,026 patent/US20090312349A1/en not_active Abandoned
- 2005-12-23 AU AU2005325676A patent/AU2005325676A1/en not_active Abandoned
- 2005-12-23 EP EP05857260A patent/EP1836173A4/en not_active Withdrawn
- 2005-12-23 WO PCT/US2005/047597 patent/WO2006081034A2/en not_active Ceased
- 2005-12-23 JP JP2007548611A patent/JP2008525502A/ja not_active Abandoned
- 2005-12-23 CA CA002592116A patent/CA2592116A1/en not_active Abandoned
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2008525502A5 (enExample) | ||
| JP2008525498A5 (enExample) | ||
| JP2018515555A5 (enExample) | ||
| JP2006500348A5 (enExample) | ||
| JP2016519096A5 (enExample) | ||
| CA2587642A1 (en) | Substituted heterocycles and methods of use | |
| RU2001122111A (ru) | Ароматические гетероциклические соединения в качестве противовоспалительных агентов | |
| JP2006502112A5 (enExample) | ||
| JP2021500345A5 (enExample) | ||
| JP2008521900A5 (enExample) | ||
| JP2007504148A5 (enExample) | ||
| JP2008525502A (ja) | 抗炎症薬 | |
| RU2019132212A (ru) | Селективные ингибиторы hdac6 | |
| JP2020516671A5 (enExample) | ||
| JP2010529991A5 (enExample) | ||
| JP2012510989A5 (enExample) | ||
| JP2002523502A5 (enExample) | ||
| JP2020512343A5 (enExample) | ||
| JP2007501189A5 (enExample) | ||
| RU2006112046A (ru) | Производные пиррола с антибактериальным действием | |
| JP2016523911A5 (enExample) | ||
| JP2010513304A5 (enExample) | ||
| KR910009705A (ko) | 수용성이 개선된 이미다조[4,5-b] 퀴놀리닐 옥시알칸산 아미드 | |
| JP2009542721A5 (enExample) | ||
| HRP20192323T1 (hr) | Novi derivati dihidrokinolin-2-ona |