BG106850A - ПИРИДО [2,3-d] ПИРИМИДИН - 2,7 - ДИАМИН КИНАЗА ИНХИБИТОРИ - Google Patents

ПИРИДО [2,3-d] ПИРИМИДИН - 2,7 - ДИАМИН КИНАЗА ИНХИБИТОРИ Download PDF

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Publication number: BG106850A
Authority: BG; Bulgaria
Prior art keywords: pyrimidin; pyrido; urea; piperazin; phenylamino
Prior art date: 2000-01-25

Application number

BG106850A

Other languages

Bulgarian (bg)

English (en)

Inventor

Richard Booth

Ellen Dobrusin

Vara Josyula

Dennis McNAMARA

Peter Toogood

Original Assignee

Warner-Lambert Company Llc

Priority date (The priority date 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 date listed.)

2000-01-25

Filing date

2002-06-20

Publication date

2003-02-28

2002-06-20 Application filed by Warner-Lambert Company Llc filed Critical Warner-Lambert Company Llc

2003-02-28 Publication of BG106850A publication Critical patent/BG106850A/bg

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QRRCMVPZJCHBLQ-UHFFFAOYSA-N pyrido[2,3-d]pyrimidine-2,7-diamine Chemical compound C1=NC(N)=NC2=NC(N)=CC=C21 QRRCMVPZJCHBLQ-UHFFFAOYSA-N 0.000 title description 2
229940043355 kinase inhibitor Drugs 0.000 title 1
239000003757 phosphotransferase inhibitor Substances 0.000 title 1
150000001875 compounds Chemical class 0.000 claims abstract description 147
125000000217 alkyl group Chemical group 0.000 claims abstract description 69
229910052736 halogen Inorganic materials 0.000 claims abstract description 56
239000001257 hydrogen Substances 0.000 claims abstract description 40
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 40
125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 37
125000001072 heteroaryl group Chemical group 0.000 claims abstract description 29
125000000623 heterocyclic group Chemical group 0.000 claims abstract description 28
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 28
125000003118 aryl group Chemical group 0.000 claims abstract description 27
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 23
125000003342 alkenyl group Chemical group 0.000 claims abstract description 21
125000000304 alkynyl group Chemical group 0.000 claims abstract description 21
206010028980 Neoplasm Diseases 0.000 claims abstract description 19
125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 18
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 16
201000011510 cancer Diseases 0.000 claims abstract description 13
239000003102 growth factor Substances 0.000 claims abstract description 12
230000002062 proliferating effect Effects 0.000 claims abstract description 11
230000001404 mediated effect Effects 0.000 claims abstract description 8
239000008194 pharmaceutical composition Substances 0.000 claims abstract description 8
208000037803 restenosis Diseases 0.000 claims abstract description 8
-1 nitro, carboxy Chemical group 0.000 claims description 179
239000004202 carbamide Substances 0.000 claims description 61
150000002367 halogens Chemical class 0.000 claims description 54
238000000034 method Methods 0.000 claims description 39
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 31
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 26
125000003545 alkoxy group Chemical group 0.000 claims description 25
125000004663 dialkyl amino group Chemical group 0.000 claims description 23
102000004190 Enzymes Human genes 0.000 claims description 21
108090000790 Enzymes Proteins 0.000 claims description 21
101150073031 cdk2 gene Proteins 0.000 claims description 21
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 21
150000003839 salts Chemical class 0.000 claims description 21
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 19
150000002148 esters Chemical class 0.000 claims description 17
229910052757 nitrogen Inorganic materials 0.000 claims description 17
150000002431 hydrogen Chemical class 0.000 claims description 16
150000001408 amides Chemical class 0.000 claims description 15
229910052760 oxygen Inorganic materials 0.000 claims description 15
239000000651 prodrug Substances 0.000 claims description 15
229940002612 prodrug Drugs 0.000 claims description 15
102000004022 Protein-Tyrosine Kinases Human genes 0.000 claims description 14
108090000412 Protein-Tyrosine Kinases Proteins 0.000 claims description 14
125000002837 carbocyclic group Chemical group 0.000 claims description 12
230000002401 inhibitory effect Effects 0.000 claims description 12
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 12
125000004448 alkyl carbonyl group Chemical group 0.000 claims description 11
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 11
125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims description 11
101100005789 Caenorhabditis elegans cdk-4 gene Proteins 0.000 claims description 10
125000003710 aryl alkyl group Chemical group 0.000 claims description 10
125000004181 carboxyalkyl group Chemical group 0.000 claims description 10
101150012716 CDK1 gene Proteins 0.000 claims description 9
101100059559 Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) nimX gene Proteins 0.000 claims description 9
125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 9
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 9
239000001301 oxygen Substances 0.000 claims description 9
229910052717 sulfur Inorganic materials 0.000 claims description 9
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 8
208000035475 disorder Diseases 0.000 claims description 8
125000005842 heteroatom Chemical group 0.000 claims description 8
201000010099 disease Diseases 0.000 claims description 7
125000004446 heteroarylalkyl group Chemical group 0.000 claims description 7
125000004433 nitrogen atom Chemical group N* 0.000 claims description 6
230000035755 proliferation Effects 0.000 claims description 6
201000001320 Atherosclerosis Diseases 0.000 claims description 5
201000004681 Psoriasis Diseases 0.000 claims description 5
239000003085 diluting agent Substances 0.000 claims description 5
210000002464 muscle smooth vascular Anatomy 0.000 claims description 5
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 5
VFDPUSVWSHRPRA-UHFFFAOYSA-N 1-cyclohexyl-3-[2-[4-(piperazine-1-carbonyl)anilino]pyrido[2,3-d]pyrimidin-7-yl]urea Chemical compound C=1C=C2C=NC(NC=3C=CC(=CC=3)C(=O)N3CCNCC3)=NC2=NC=1NC(=O)NC1CCCCC1 VFDPUSVWSHRPRA-UHFFFAOYSA-N 0.000 claims description 4
206010006187 Breast cancer Diseases 0.000 claims description 4
208000026310 Breast neoplasm Diseases 0.000 claims description 4
230000004663 cell proliferation Effects 0.000 claims description 4
210000001072 colon Anatomy 0.000 claims description 4
239000003937 drug carrier Substances 0.000 claims description 4
DWRWSNAREGLUHZ-UHFFFAOYSA-N ethyl pyrimidine-4-carboxylate Chemical compound CCOC(=O)C1=CC=NC=N1 DWRWSNAREGLUHZ-UHFFFAOYSA-N 0.000 claims description 4
239000000546 pharmaceutical excipient Substances 0.000 claims description 4
206010058467 Lung neoplasm malignant Diseases 0.000 claims description 3
125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 3
125000004415 heterocyclylalkyl group Chemical group 0.000 claims description 3
208000032839 leukemia Diseases 0.000 claims description 3
201000005202 lung cancer Diseases 0.000 claims description 3
208000020816 lung neoplasm Diseases 0.000 claims description 3
201000001441 melanoma Diseases 0.000 claims description 3
206010041823 squamous cell carcinoma Diseases 0.000 claims description 3
XMINZZZOTRYZGB-UHFFFAOYSA-N 1-(2-hydroxyethyl)-3-[2-(4-piperazin-1-ylanilino)pyrido[2,3-d]pyrimidin-7-yl]urea Chemical compound N=1C2=NC(NC(=O)NCCO)=CC=C2C=NC=1NC(C=C1)=CC=C1N1CCNCC1 XMINZZZOTRYZGB-UHFFFAOYSA-N 0.000 claims description 2
XFILUMCRLWWGHF-UHFFFAOYSA-N 1-(2-hydroxyethyl)-3-[5-methyl-2-(4-piperazin-1-ylanilino)pyrido[2,3-d]pyrimidin-7-yl]urea Chemical compound N=1C=C2C(C)=CC(NC(=O)NCCO)=NC2=NC=1NC(C=C1)=CC=C1N1CCNCC1 XFILUMCRLWWGHF-UHFFFAOYSA-N 0.000 claims description 2
OJAWTIFCYCKDIF-UHFFFAOYSA-N 1-(2-hydroxyethyl)-3-[5-methyl-2-(pyridin-4-ylamino)pyrido[2,3-d]pyrimidin-7-yl]urea Chemical compound N=1C=C2C(C)=CC(NC(=O)NCCO)=NC2=NC=1NC1=CC=NC=C1 OJAWTIFCYCKDIF-UHFFFAOYSA-N 0.000 claims description 2
LWWHQXYBJDKMHB-UHFFFAOYSA-N 1-(4-hydroxycyclohexyl)-3-[2-(4-piperazin-1-ylanilino)pyrido[2,3-d]pyrimidin-7-yl]urea Chemical compound C1CC(O)CCC1NC(=O)NC1=CC=C(C=NC(NC=2C=CC(=CC=2)N2CCNCC2)=N2)C2=N1 LWWHQXYBJDKMHB-UHFFFAOYSA-N 0.000 claims description 2
OAZKKGFIMGBLNP-UHFFFAOYSA-N 1-[2-(4-fluoroanilino)pyrido[2,3-d]pyrimidin-7-yl]-3-(2-hydroxyethyl)urea Chemical compound N=1C2=NC(NC(=O)NCCO)=CC=C2C=NC=1NC1=CC=C(F)C=C1 OAZKKGFIMGBLNP-UHFFFAOYSA-N 0.000 claims description 2
XNJIKCCLIKXVKC-UHFFFAOYSA-N 1-[2-(dimethylamino)ethyl]-3-[2-(4-piperazin-1-ylanilino)pyrido[2,3-d]pyrimidin-7-yl]urea Chemical compound N=1C2=NC(NC(=O)NCCN(C)C)=CC=C2C=NC=1NC(C=C1)=CC=C1N1CCNCC1 XNJIKCCLIKXVKC-UHFFFAOYSA-N 0.000 claims description 2
HIDCSIGTHYPMDE-UHFFFAOYSA-N 1-[2-[4-(4-acetylpiperazin-1-yl)-3-chloroanilino]pyrido[2,3-d]pyrimidin-7-yl]-3-cyclohexylurea Chemical compound C1CN(C(=O)C)CCN1C(C(=C1)Cl)=CC=C1NC1=NC=C(C=CC(NC(=O)NC2CCCCC2)=N2)C2=N1 HIDCSIGTHYPMDE-UHFFFAOYSA-N 0.000 claims description 2
DWKOQXAXRXLTRO-UHFFFAOYSA-N 1-[2-[4-(4-acetylpiperazin-1-yl)anilino]-5-methylpyrido[2,3-d]pyrimidin-7-yl]-3-(2-hydroxyethyl)urea Chemical compound C1CN(C(=O)C)CCN1C(C=C1)=CC=C1NC1=NC=C(C(C)=CC(NC(=O)NCCO)=N2)C2=N1 DWKOQXAXRXLTRO-UHFFFAOYSA-N 0.000 claims description 2
NSELCHMQELGYCQ-UHFFFAOYSA-N 1-[2-[4-(4-acetylpiperazin-1-yl)anilino]-5-methylpyrido[2,3-d]pyrimidin-7-yl]-3-cyclohexylurea Chemical compound C1CN(C(=O)C)CCN1C(C=C1)=CC=C1NC1=NC=C(C(C)=CC(NC(=O)NC2CCCCC2)=N2)C2=N1 NSELCHMQELGYCQ-UHFFFAOYSA-N 0.000 claims description 2
BPMKMCMJBBHAMO-UHFFFAOYSA-N 1-[2-[4-(4-acetylpiperazin-1-yl)anilino]-5-methylpyrido[2,3-d]pyrimidin-7-yl]-3-ethylurea Chemical compound N=1C2=NC(NC(=O)NCC)=CC(C)=C2C=NC=1NC(C=C1)=CC=C1N1CCN(C(C)=O)CC1 BPMKMCMJBBHAMO-UHFFFAOYSA-N 0.000 claims description 2
QSYGBWVAZZCIDX-UHFFFAOYSA-N 1-[2-[4-(4-acetylpiperazin-1-yl)anilino]pyrido[2,3-d]pyrimidin-7-yl]-3-cyclohexylurea Chemical compound C1CN(C(=O)C)CCN1C(C=C1)=CC=C1NC1=NC=C(C=CC(NC(=O)NC2CCCCC2)=N2)C2=N1 QSYGBWVAZZCIDX-UHFFFAOYSA-N 0.000 claims description 2
YWQNBCXNLXJJFZ-UHFFFAOYSA-N 1-[2-[4-[4-(2-amino-4-methylpentanoyl)piperazin-1-yl]anilino]pyrido[2,3-d]pyrimidin-7-yl]-3-cyclohexylurea Chemical compound C1CN(C(=O)C(N)CC(C)C)CCN1C(C=C1)=CC=C1NC1=NC=C(C=CC(NC(=O)NC2CCCCC2)=N2)C2=N1 YWQNBCXNLXJJFZ-UHFFFAOYSA-N 0.000 claims description 2
MQLDVUKGKUIAAL-UHFFFAOYSA-N 1-[5-methyl-2-(4-piperazin-1-ylanilino)pyrido[2,3-d]pyrimidin-7-yl]-3-propan-2-ylurea Chemical compound N=1C2=NC(NC(=O)NC(C)C)=CC(C)=C2C=NC=1NC(C=C1)=CC=C1N1CCNCC1 MQLDVUKGKUIAAL-UHFFFAOYSA-N 0.000 claims description 2
MGJUUZSZYQUWRL-UHFFFAOYSA-N 1-[6-bromo-2-(4-piperazin-1-ylanilino)pyrido[2,3-d]pyrimidin-7-yl]-3-cyclohexylurea Chemical compound N1=C2N=C(NC(=O)NC3CCCCC3)C(Br)=CC2=CN=C1NC(C=C1)=CC=C1N1CCNCC1 MGJUUZSZYQUWRL-UHFFFAOYSA-N 0.000 claims description 2
BWORXTLBVMGUGI-UHFFFAOYSA-N 1-[6-bromo-5-methyl-2-(4-piperazin-1-ylanilino)pyrido[2,3-d]pyrimidin-7-yl]-3-cyclohexylurea Chemical compound N=1C2=NC(NC=3C=CC(=CC=3)N3CCNCC3)=NC=C2C(C)=C(Br)C=1NC(=O)NC1CCCCC1 BWORXTLBVMGUGI-UHFFFAOYSA-N 0.000 claims description 2
ITGHYDKCLQIJEO-UHFFFAOYSA-N 1-[6-chloro-2-(4-piperazin-1-ylanilino)pyrido[2,3-d]pyrimidin-7-yl]-3-cyclohexylurea Chemical compound N1=C2N=C(NC(=O)NC3CCCCC3)C(Cl)=CC2=CN=C1NC(C=C1)=CC=C1N1CCNCC1 ITGHYDKCLQIJEO-UHFFFAOYSA-N 0.000 claims description 2
UXBCLFZSEPAATK-UHFFFAOYSA-N 1-[6-chloro-5-methyl-2-(4-piperazin-1-ylanilino)pyrido[2,3-d]pyrimidin-7-yl]-3-cyclohexylurea Chemical compound N=1C2=NC(NC=3C=CC(=CC=3)N3CCNCC3)=NC=C2C(C)=C(Cl)C=1NC(=O)NC1CCCCC1 UXBCLFZSEPAATK-UHFFFAOYSA-N 0.000 claims description 2
FCZSXTNTJURAMC-CALCHBBNSA-N 1-cyclohexyl-3-[2-[4-[(3r,5s)-3,5-dimethylpiperazin-1-yl]anilino]-6-fluoropyrido[2,3-d]pyrimidin-7-yl]urea Chemical compound C1[C@@H](C)N[C@@H](C)CN1C(C=C1)=CC=C1NC1=NC=C(C=C(F)C(NC(=O)NC2CCCCC2)=N2)C2=N1 FCZSXTNTJURAMC-CALCHBBNSA-N 0.000 claims description 2
CKDGTPVNAKRPFN-UHFFFAOYSA-N 1-cyclohexyl-3-[5-methyl-2-(4-piperazin-1-ylanilino)pyrido[2,3-d]pyrimidin-7-yl]thiourea Chemical compound N=1C2=NC(NC=3C=CC(=CC=3)N3CCNCC3)=NC=C2C(C)=CC=1NC(=S)NC1CCCCC1 CKDGTPVNAKRPFN-UHFFFAOYSA-N 0.000 claims description 2
MPBWULVFTHBBOK-UHFFFAOYSA-N 1-cyclohexyl-3-[5-methyl-2-(4-piperazin-1-ylanilino)pyrido[2,3-d]pyrimidin-7-yl]urea Chemical compound N=1C2=NC(NC=3C=CC(=CC=3)N3CCNCC3)=NC=C2C(C)=CC=1NC(=O)NC1CCCCC1 MPBWULVFTHBBOK-UHFFFAOYSA-N 0.000 claims description 2
URTRAPGHHQONHL-UHFFFAOYSA-N 1-cyclohexyl-3-[5-methyl-2-(pyridin-4-ylamino)pyrido[2,3-d]pyrimidin-7-yl]urea Chemical compound N=1C2=NC(NC=3C=CN=CC=3)=NC=C2C(C)=CC=1NC(=O)NC1CCCCC1 URTRAPGHHQONHL-UHFFFAOYSA-N 0.000 claims description 2
ZMWBWZXAOFKNCZ-UHFFFAOYSA-N 1-cyclohexyl-3-[6-fluoro-5-methyl-2-(4-piperazin-1-ylanilino)pyrido[2,3-d]pyrimidin-7-yl]urea Chemical compound N=1C2=NC(NC=3C=CC(=CC=3)N3CCNCC3)=NC=C2C(C)=C(F)C=1NC(=O)NC1CCCCC1 ZMWBWZXAOFKNCZ-UHFFFAOYSA-N 0.000 claims description 2
OIFYXWOZMWGIJQ-UHFFFAOYSA-N 1-ethyl-3-[6-fluoro-2-(4-piperazin-1-ylanilino)pyrido[2,3-d]pyrimidin-7-yl]urea Chemical compound N=1C=C2C=C(F)C(NC(=O)NCC)=NC2=NC=1NC(C=C1)=CC=C1N1CCNCC1 OIFYXWOZMWGIJQ-UHFFFAOYSA-N 0.000 claims description 2
JMQKXBRWLIMTIU-IYBDPMFKSA-N 1-tert-butyl-3-[2-[4-[(3r,5s)-3,5-dimethylpiperazin-1-yl]anilino]pyrido[2,3-d]pyrimidin-7-yl]urea Chemical compound C1[C@@H](C)N[C@@H](C)CN1C(C=C1)=CC=C1NC1=NC=C(C=CC(NC(=O)NC(C)(C)C)=N2)C2=N1 JMQKXBRWLIMTIU-IYBDPMFKSA-N 0.000 claims description 2
125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 claims description 2
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims description 2
241000124008 Mammalia Species 0.000 claims description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
VVARBBDVASONRD-UHFFFAOYSA-N n-[2-(4-piperazin-1-ylanilino)pyrido[2,3-d]pyrimidin-7-yl]piperazine-1-carboxamide Chemical compound C1CNCCN1C(=O)NC(N=C1N=2)=CC=C1C=NC=2NC(C=C1)=CC=C1N1CCNCC1 VVARBBDVASONRD-UHFFFAOYSA-N 0.000 claims description 2
125000005143 heteroarylsulfonyl group Chemical group 0.000 claims 4
IZPRSDVSVWVZOM-UHFFFAOYSA-N 1,1-bis(2-hydroxyethyl)-3-[2-(4-piperazin-1-ylanilino)pyrido[2,3-d]pyrimidin-7-yl]urea Chemical compound N=1C2=NC(NC(=O)N(CCO)CCO)=CC=C2C=NC=1NC(C=C1)=CC=C1N1CCNCC1 IZPRSDVSVWVZOM-UHFFFAOYSA-N 0.000 claims 1
YACCIEHTQKOSOZ-UHFFFAOYSA-N 1-(3-hydroxypropyl)-3-[2-(4-piperazin-1-ylanilino)pyrido[2,3-d]pyrimidin-7-yl]urea Chemical compound N=1C2=NC(NC(=O)NCCCO)=CC=C2C=NC=1NC(C=C1)=CC=C1N1CCNCC1 YACCIEHTQKOSOZ-UHFFFAOYSA-N 0.000 claims 1
OHOPJOZAUWXPDP-UHFFFAOYSA-N 1-(4-chlorophenyl)-3-[2-(4-fluoro-3-methylanilino)pyrido[2,3-d]pyrimidin-7-yl]urea Chemical compound C1=C(F)C(C)=CC(NC=2N=C3N=C(NC(=O)NC=4C=CC(Cl)=CC=4)C=CC3=CN=2)=C1 OHOPJOZAUWXPDP-UHFFFAOYSA-N 0.000 claims 1
YFNIERFVGYMMPV-IBGZPJMESA-N 1-[(2r)-1-hydroxy-3-methylbutan-2-yl]-3-[2-(4-piperazin-1-ylanilino)pyrido[2,3-d]pyrimidin-7-yl]urea Chemical compound N=1C2=NC(NC(=O)N[C@@H](CO)C(C)C)=CC=C2C=NC=1NC(C=C1)=CC=C1N1CCNCC1 YFNIERFVGYMMPV-IBGZPJMESA-N 0.000 claims 1
YIGPZBASWQSHAE-IBGZPJMESA-N 1-[(2s)-1-hydroxy-4-methylpentan-2-yl]-3-[2-(4-piperazin-1-ylanilino)pyrido[2,3-d]pyrimidin-7-yl]urea Chemical compound N=1C2=NC(NC(=O)N[C@H](CO)CC(C)C)=CC=C2C=NC=1NC(C=C1)=CC=C1N1CCNCC1 YIGPZBASWQSHAE-IBGZPJMESA-N 0.000 claims 1
IWNKWJVEAVWLNF-UHFFFAOYSA-N 1-[2-(4-fluoroanilino)pyrido[2,3-d]pyrimidin-7-yl]-3-(3-morpholin-4-ylpropyl)urea Chemical compound C1=CC(F)=CC=C1NC1=NC=C(C=CC(NC(=O)NCCCN2CCOCC2)=N2)C2=N1 IWNKWJVEAVWLNF-UHFFFAOYSA-N 0.000 claims 1
KEDVKYIYPFUXJF-UHFFFAOYSA-N 1-[2-(4-piperazin-1-ylanilino)pyrido[2,3-d]pyrimidin-7-yl]-3-propan-2-ylurea Chemical compound N=1C2=NC(NC(=O)NC(C)C)=CC=C2C=NC=1NC(C=C1)=CC=C1N1CCNCC1 KEDVKYIYPFUXJF-UHFFFAOYSA-N 0.000 claims 1
CSHJWZUPBIECMW-UHFFFAOYSA-N 1-[2-(dimethylamino)ethyl]-3-[2-(4-fluoroanilino)pyrido[2,3-d]pyrimidin-7-yl]urea Chemical compound N=1C2=NC(NC(=O)NCCN(C)C)=CC=C2C=NC=1NC1=CC=C(F)C=C1 CSHJWZUPBIECMW-UHFFFAOYSA-N 0.000 claims 1
ZOUYYHCVTKXASL-UHFFFAOYSA-N 1-[2-[4-(4-acetylpiperazin-1-yl)-3-chloroanilino]pyrido[2,3-d]pyrimidin-7-yl]-3-(2-hydroxyethyl)urea Chemical compound C1CN(C(=O)C)CCN1C(C(=C1)Cl)=CC=C1NC1=NC=C(C=CC(NC(=O)NCCO)=N2)C2=N1 ZOUYYHCVTKXASL-UHFFFAOYSA-N 0.000 claims 1
BRJVIFGBXXBAAR-UHFFFAOYSA-N 1-[2-[4-(4-acetylpiperazin-1-yl)anilino]-6-fluoropyrido[2,3-d]pyrimidin-7-yl]-3-ethylurea Chemical compound N=1C=C2C=C(F)C(NC(=O)NCC)=NC2=NC=1NC(C=C1)=CC=C1N1CCN(C(C)=O)CC1 BRJVIFGBXXBAAR-UHFFFAOYSA-N 0.000 claims 1
FZPOQOBRNOTAOD-UHFFFAOYSA-N 1-[2-[4-(4-acetylpiperazin-1-yl)anilino]pyrido[2,3-d]pyrimidin-7-yl]-3-(3-morpholin-4-ylpropyl)urea Chemical compound C1CN(C(=O)C)CCN1C(C=C1)=CC=C1NC1=NC=C(C=CC(NC(=O)NCCCN2CCOCC2)=N2)C2=N1 FZPOQOBRNOTAOD-UHFFFAOYSA-N 0.000 claims 1
SFPLIUUSRNIYCV-CALCHBBNSA-N 1-[2-[4-[(3r,5s)-3,5-dimethylpiperazin-1-yl]anilino]-6-methylpyrido[2,3-d]pyrimidin-7-yl]-3-propan-2-ylurea Chemical compound N=1C=C2C=C(C)C(NC(=O)NC(C)C)=NC2=NC=1NC(C=C1)=CC=C1N1C[C@H](C)N[C@H](C)C1 SFPLIUUSRNIYCV-CALCHBBNSA-N 0.000 claims 1
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CBNUMRNHDJPEFG-UHFFFAOYSA-N tert-butyl 4-[4-[7-[cyclohexylcarbamoyl(methyl)amino]pyrido[2,3-d]pyrimidin-2-yl]phenyl]piperazine-1-carboxylate Chemical compound C=1C=C2C=NC(C=3C=CC(=CC=3)N3CCN(CC3)C(=O)OC(C)(C)C)=NC2=NC=1N(C)C(=O)NC1CCCCC1 CBNUMRNHDJPEFG-UHFFFAOYSA-N 0.000 description 1
YYQUQHCUSHLDGL-UHFFFAOYSA-N tert-butyl 4-[4-[[6-bromo-7-(methylcarbamoylamino)pyrido[2,3-d]pyrimidin-2-yl]amino]phenyl]piperazine-1-carboxylate Chemical compound N=1C=C2C=C(Br)C(NC(=O)NC)=NC2=NC=1NC(C=C1)=CC=C1N1CCN(C(=O)OC(C)(C)C)CC1 YYQUQHCUSHLDGL-UHFFFAOYSA-N 0.000 description 1
TXQNFPMJJVZLHW-UHFFFAOYSA-N tert-butyl 4-[4-[[7-(propan-2-ylcarbamoylamino)pyrido[2,3-d]pyrimidin-2-yl]amino]phenyl]piperazine-1-carboxylate Chemical compound N=1C2=NC(NC(=O)NC(C)C)=CC=C2C=NC=1NC(C=C1)=CC=C1N1CCN(C(=O)OC(C)(C)C)CC1 TXQNFPMJJVZLHW-UHFFFAOYSA-N 0.000 description 1
210000001550 testis Anatomy 0.000 description 1
125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Substances C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 1
125000005958 tetrahydrothienyl group Chemical group 0.000 description 1
QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
125000003831 tetrazolyl group Chemical group 0.000 description 1
229940124597 therapeutic agent Drugs 0.000 description 1
238000011287 therapeutic dose Methods 0.000 description 1
125000000335 thiazolyl group Chemical group 0.000 description 1
125000001544 thienyl group Chemical group 0.000 description 1
210000001685 thyroid gland Anatomy 0.000 description 1
208000030901 thyroid gland follicular carcinoma Diseases 0.000 description 1
210000001519 tissue Anatomy 0.000 description 1
XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
210000002105 tongue Anatomy 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
239000000196 tragacanth Substances 0.000 description 1
235000010487 tragacanth Nutrition 0.000 description 1
229940116362 tragacanth Drugs 0.000 description 1
125000004665 trialkylsilyl group Chemical group 0.000 description 1
IIHPVYJPDKJYOU-UHFFFAOYSA-N triphenylcarbethoxymethylenephosphorane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=CC(=O)OCC)C1=CC=CC=C1 IIHPVYJPDKJYOU-UHFFFAOYSA-N 0.000 description 1
125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
208000010576 undifferentiated carcinoma Diseases 0.000 description 1
241001529453 unidentified herpesvirus Species 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
229940070710 valerate Drugs 0.000 description 1
NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
125000003774 valeryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
LSGOVYNHVSXFFJ-UHFFFAOYSA-N vanadate(3-) Chemical compound [O-][V]([O-])([O-])=O LSGOVYNHVSXFFJ-UHFFFAOYSA-N 0.000 description 1
210000004509 vascular smooth muscle cell Anatomy 0.000 description 1
239000011345 viscous material Substances 0.000 description 1
239000003871 white petrolatum Substances 0.000 description 1
229910000166 zirconium phosphate Inorganic materials 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic 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
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings

Landscapes

Health & Medical Sciences (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
General Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Bioinformatics & Cheminformatics (AREA)
Engineering & Computer Science (AREA)
Veterinary Medicine (AREA)
Pharmacology & Pharmacy (AREA)
Medicinal Chemistry (AREA)
Animal Behavior & Ethology (AREA)
General Chemical & Material Sciences (AREA)
Public Health (AREA)
Chemical Kinetics & Catalysis (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Neurology (AREA)
Molecular Biology (AREA)
Biochemistry (AREA)
Neurosurgery (AREA)
Biomedical Technology (AREA)
Heart & Thoracic Surgery (AREA)
Hospice & Palliative Care (AREA)
Cardiology (AREA)
Psychiatry (AREA)
Dermatology (AREA)
Vascular Medicine (AREA)
Urology & Nephrology (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Enzymes And Modification Thereof (AREA)

BG106850A 2000-01-25 2002-06-20 ПИРИДО [2,3-d] ПИРИМИДИН - 2,7 - ДИАМИН КИНАЗА ИНХИБИТОРИ BG106850A (bg)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US17826100P	2000-01-25	2000-01-25
PCT/IB2001/000069 WO2001055147A1 (en)	2000-01-25	2001-01-23	PYRIDO[2,3-d]PYRIMIDINE-2,7-DIAMINE KINASE INHIBITORS

Publications (1)

Publication Number	Publication Date
BG106850A true BG106850A (bg)	2003-02-28

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ID=22651853

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BG106850A BG106850A (bg)	2000-01-25	2002-06-20	ПИРИДО [2,3-d] ПИРИМИДИН - 2,7 - ДИАМИН КИНАЗА ИНХИБИТОРИ

Country Status (34)

Country	Link
EP (1)	EP1254137A1 (is)
JP (1)	JP4047010B2 (is)
KR (1)	KR20020065939A (is)
CN (1)	CN1395578A (is)
AP (1)	AP2002002586A0 (is)
AR (1)	AR030044A1 (is)
AU (1)	AU2542501A (is)
BG (1)	BG106850A (is)
BR (1)	BR0107751A (is)
CA (1)	CA2397961C (is)
CO (1)	CO5261549A1 (is)
CR (1)	CR6706A (is)
CZ (1)	CZ20022475A3 (is)
DZ (1)	DZ3266A1 (is)
EA (1)	EA200200643A1 (is)
EE (1)	EE200200405A (is)
GT (1)	GT200100016A (is)
HN (1)	HN2001000013A (is)
HU (1)	HUP0204141A3 (is)
IL (1)	IL150545A0 (is)
IS (1)	IS6443A (is)
MA (1)	MA26868A1 (is)
MX (1)	MXPA02007221A (is)
NO (1)	NO20023527L (is)
OA (1)	OA12161A (is)
PA (1)	PA8510701A1 (is)
PE (1)	PE20011066A1 (is)
PL (1)	PL356802A1 (is)
SK (1)	SK10632002A3 (is)
SV (1)	SV2002000294A (is)
TN (1)	TNSN01014A1 (is)
WO (1)	WO2001055147A1 (is)
YU (1)	YU50402A (is)
ZA (1)	ZA200205879B (is)

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US7235551B2 (en)	2000-03-02	2007-06-26	Smithkline Beecham Corporation	1,5-disubstituted-3,4-dihydro-1h-pyrimido[4,5-d]pyrimidin-2-one compounds and their use in treating csbp/p38 kinase mediated diseases
CN1847229B (zh)	2000-10-23	2011-05-04	史密丝克莱恩比彻姆公司	2，4，8-三取代-8H-吡啶并[2，3-d]嘧啶-7-酮化合物
PE20030008A1 (es) *	2001-06-19	2003-01-22	Bristol Myers Squibb Co	Inhibidores duales de pde 7 y pde 4
EP1499320B1 (en)	2002-04-19	2007-08-22	Smithkline Beecham Corporation	Novel compounds
US7504410B2 (en) *	2002-11-28	2009-03-17	Schering Aktiengesellschaft	Chk-, Pdk- and Akt-inhibitory pyrimidines, their production and use as pharmaceutical agents
US7157455B2 (en) *	2003-02-10	2007-01-02	Hoffmann-La Roche Inc.	4-Aminopyrimidine-5-one derivatives
TW200502236A (en) *	2003-03-28	2005-01-16	Hoffmann La Roche	Novel pyrido[2,3-d]pyrimidin-7-carboxylic acid derivatives, their manufacture and use as pharmaceutical agents
FR2873118B1 (fr)	2004-07-15	2007-11-23	Sanofi Synthelabo	Derives de pyrido-pyrimidine, leur application en therapeutique
EP1794160A1 (en) *	2004-09-21	2007-06-13	F.Hoffmann-La Roche Ag	6-(2-alkyl-phenyl) - pyrido[2,3-d] pyrimidines useful as proteine kinase inhibitors
EP1868612A4 (en)	2005-03-25	2010-03-24	Glaxo Group Ltd	NOVEL CONNECTIONS
PE20061193A1 (es)	2005-03-25	2006-12-02	Glaxo Group Ltd	DERIVADOS DE 3,4-DIHIDROPIRIMIDO[4,5-d]PIRIMIDIN-2-[1H]-0NA COMO INHIBIDORES DE QUINASA p38
UY29440A1 (es)	2005-03-25	2006-10-02	Glaxo Group Ltd	Nuevos compuestos
CN101495475A (zh)	2005-03-25	2009-07-29	葛兰素集团有限公司	制备吡啶并[2,3-d]嘧啶-7-酮和3,4-二氢嘧啶并[4,5-d]嘧啶-2(1H)-酮衍生物的方法
FR2887882B1 (fr)	2005-07-01	2007-09-07	Sanofi Aventis Sa	Derives de pyrido[2,3-d] pyrimidine, leur preparation, leur application en therapeutique
CN101243081A (zh) *	2005-07-21	2008-08-13	霍夫曼-拉罗奇有限公司	作为PTP1B抑制剂的吡啶并[2,3-d]嘧啶-2,4-二胺化合物
BRPI0614804A2 (pt) *	2005-08-09	2011-04-12	Irm Llc	compostos e composições como inibidores de proteìna cinase
FR2896246B1 (fr)	2006-01-13	2008-08-15	Sanofi Aventis Sa	Derives de pyrido-pyrimidone, leur preparation, leur application en therapeutique.
EP1914234A1 (en)	2006-10-16	2008-04-23	GPC Biotech Inc.	Pyrido[2,3-d]pyrimidines and their use as kinase inhibitors
JO2985B1 (ar)	2006-12-20	2016-09-05	Takeda Pharmaceuticals Co	مثبطات كينازmapk/erk
FR2910813B1 (fr) *	2006-12-28	2009-02-06	Sanofi Aventis Sa	Nouvelle utilisation therapeutique pour le traitement des leucemies
EP2112150B1 (en)	2008-04-22	2013-10-16	Forma Therapeutics, Inc.	Improved raf inhibitors
EP2352732B1 (en) *	2008-12-01	2013-02-20	Merck Patent GmbH	2,5-DIAMINO-SUBSTITUTED PYRIDO[4, 3-d]PYRIMIDINES AS AUTOTAXIN INHIBITORS AGAINST CANCER
GB201104267D0 (en)	2011-03-14	2011-04-27	Cancer Rec Tech Ltd	Pyrrolopyridineamino derivatives
GB201216018D0 (en)	2012-09-07	2012-10-24	Cancer Rec Tech Ltd	Pharmacologically active compounds
GB201216017D0 (en)	2012-09-07	2012-10-24	Cancer Rec Tech Ltd	Inhibitor compounds
ES2817448T3 (es)	2013-03-14	2021-04-07	Icahn School Med Mount Sinai	Compuestos de pirimidina como inhibidores de quinasas
GB201403536D0 (en)	2014-02-28	2014-04-16	Cancer Rec Tech Ltd	Inhibitor compounds
KR101671404B1 (ko) *	2014-09-02	2016-11-02	한국원자력의학원	항암 효과, 방사선 병용치료 효과 및 당뇨병 치료 효과를 갖는 피리미딘 유도체 및 이의 의학적 용도
CN107286180B (zh) *	2016-04-11	2019-07-02	上海勋和医药科技有限公司	杂代吡啶并嘧啶酮衍生物作为cdk抑制剂及其应用
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IL115256A0 (en) *	1994-11-14	1995-12-31	Warner Lambert Co	6-Aryl pyrido (2,3-d) pyrimidines and naphthyridines and their use
US5620981A (en) *	1995-05-03	1997-04-15	Warner-Lambert Company	Pyrido [2,3-D]pyrimidines for inhibiting protein tyrosine kinase mediated cellular proliferation
KR20010043829A (ko) *	1998-05-26	2001-05-25	로즈 암스트롱, 크리스틴 에이. 트러트웨인	세포 증식 억제제로서의 비시클릭 피리미딘 및 비시클릭3,4-디히드로피리미딘

2001
- 2001-01-23 PE PE2001000072A patent/PE20011066A1/es not_active Application Discontinuation
- 2001-01-23 PA PA20018510701A patent/PA8510701A1/es unknown
- 2001-01-23 DZ DZ013266A patent/DZ3266A1/fr active
- 2001-01-23 AR ARP010100285A patent/AR030044A1/es not_active Application Discontinuation
- 2001-01-23 HU HU0204141A patent/HUP0204141A3/hu unknown
- 2001-01-23 EA EA200200643A patent/EA200200643A1/ru unknown
- 2001-01-23 YU YU50402A patent/YU50402A/sh unknown
- 2001-01-23 EP EP01900591A patent/EP1254137A1/en not_active Withdrawn
- 2001-01-23 JP JP2001561006A patent/JP4047010B2/ja not_active Expired - Fee Related
- 2001-01-23 AU AU25425/01A patent/AU2542501A/en not_active Abandoned
- 2001-01-23 WO PCT/IB2001/000069 patent/WO2001055147A1/en not_active Ceased
- 2001-01-23 EE EEP200200405A patent/EE200200405A/xx unknown
- 2001-01-23 CA CA002397961A patent/CA2397961C/en not_active Expired - Fee Related
- 2001-01-23 PL PL01356802A patent/PL356802A1/xx not_active Application Discontinuation
- 2001-01-23 CZ CZ20022475A patent/CZ20022475A3/cs unknown
- 2001-01-23 IL IL15054501A patent/IL150545A0/xx unknown
- 2001-01-23 AP APAP/P/2002/002586A patent/AP2002002586A0/en unknown
- 2001-01-23 GT GT200100016A patent/GT200100016A/es unknown
- 2001-01-23 MX MXPA02007221A patent/MXPA02007221A/es not_active Application Discontinuation
- 2001-01-23 SK SK1063-2002A patent/SK10632002A3/sk not_active Application Discontinuation
- 2001-01-23 KR KR1020027009516A patent/KR20020065939A/ko not_active Ceased
- 2001-01-23 BR BR0107751-1A patent/BR0107751A/pt not_active IP Right Cessation
- 2001-01-23 OA OA1200200213A patent/OA12161A/en unknown
- 2001-01-23 CN CN01804048A patent/CN1395578A/zh active Pending
- 2001-01-24 HN HN2001000013A patent/HN2001000013A/es unknown
- 2001-01-24 SV SV2001000294A patent/SV2002000294A/es not_active Application Discontinuation
- 2001-01-24 TN TNTNSN01014A patent/TNSN01014A1/fr unknown
- 2001-01-24 CO CO01005268A patent/CO5261549A1/es not_active Application Discontinuation
2002
- 2002-06-20 BG BG106850A patent/BG106850A/bg unknown
- 2002-06-25 IS IS6443A patent/IS6443A/is unknown
- 2002-07-17 CR CR6706A patent/CR6706A/es not_active Application Discontinuation
- 2002-07-22 MA MA26736A patent/MA26868A1/fr unknown
- 2002-07-23 ZA ZA200205879A patent/ZA200205879B/en unknown
- 2002-07-24 NO NO20023527A patent/NO20023527L/no not_active Application Discontinuation

Also Published As

Publication number	Publication date
EA200200643A1 (ru)	2002-12-26
OA12161A (en)	2006-05-08
PE20011066A1 (es)	2001-10-22
AP2002002586A0 (en)	2002-09-30
ZA200205879B (en)	2003-09-29
WO2001055147A1 (en)	2001-08-02
SV2002000294A (es)	2002-07-16
EP1254137A1 (en)	2002-11-06
YU50402A (sh)	2005-11-28
IS6443A (is)	2002-06-25
GT200100016A (es)	2001-10-19
IL150545A0 (en)	2003-02-12
PL356802A1 (en)	2004-07-12
CN1395578A (zh)	2003-02-05
CA2397961C (en)	2008-08-26
NO20023527L (no)	2002-09-10
CA2397961A1 (en)	2001-08-02
CO5261549A1 (es)	2003-03-31
EE200200405A (et)	2003-12-15
MA26868A1 (fr)	2004-12-20
AU2542501A (en)	2001-08-07
DZ3266A1 (fr)	2001-08-02
AR030044A1 (es)	2003-08-13
JP2003523357A (ja)	2003-08-05
CR6706A (es)	2005-04-04
HN2001000013A (es)	2001-06-18
PA8510701A1 (es)	2002-12-11
NO20023527D0 (no)	2002-07-24
HUP0204141A2 (hu)	2003-04-28
JP4047010B2 (ja)	2008-02-13
HUP0204141A3 (en)	2005-03-29
SK10632002A3 (sk)	2003-06-03
KR20020065939A (ko)	2002-08-14
CZ20022475A3 (cs)	2003-03-12
BR0107751A (pt)	2002-11-12
TNSN01014A1 (fr)	2005-11-10
MXPA02007221A (es)	2002-11-29

Publication	Publication Date	Title
BG106850A (bg)	2003-02-28	ПИРИДО [2,3-d] ПИРИМИДИН - 2,7 - ДИАМИН КИНАЗА ИНХИБИТОРИ
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AU2004260689B8 (en)	2008-05-15	Compounds and compositions as protein kinase inhibitors
AU2004279427B2 (en)	2008-07-03	Compounds and compositions as protein kinase inhibitors
JP5134548B2 (ja)	2013-01-30	過剰増殖性疾患の処置のためのＥｒｂＢＩ型受容体チロシンキナーゼ阻害剤としてのＮ４−フェニルキナゾリン−４−アミン誘導体および関連化合物
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