JP2017530983A5 - - Google Patents

Info

Publication number

JP2017530983A5

JP2017530983A5 JP2017518541A JP2017518541A JP2017530983A5 JP 2017530983 A5 JP2017530983 A5 JP 2017530983A5 JP 2017518541 A JP2017518541 A JP 2017518541A JP 2017518541 A JP2017518541 A JP 2017518541A JP 2017530983 A5 JP2017530983 A5 JP 2017530983A5

Authority

JP

Japan

Prior art keywords

auristatin

pharmaceutically acceptable

phenyl

methyl

acceptable salt

Prior art date

2015-09-29

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.)

Granted

Links

• Espacenet
• Global Dossier
• Discuss

• DWZAEMINVBZMHQ-UHFFFAOYSA-N 1-[4-[4-(dimethylamino)piperidine-1-carbonyl]phenyl]-3-[4-(4,6-dimorpholin-4-yl-1,3,5-triazin-2-yl)phenyl]urea Chemical compound C1CC(N(C)C)CCN1C(=O)C(C=C1)=CC=C1NC(=O)NC1=CC=C(C=2N=C(N=C(N=2)N2CCOCC2)N2CCOCC2)C=C1 DWZAEMINVBZMHQ-UHFFFAOYSA-N 0.000 claims description 7
• 108010044540 auristatin Proteins 0.000 claims 14
• 150000003839 salts Chemical class 0.000 claims 13
• 229940124302 mTOR inhibitor Drugs 0.000 claims 11
• 239000003628 mammalian target of rapamycin inhibitor Substances 0.000 claims 11
• -1 1,3-thiazol-2-yl Chemical group 0.000 claims 5
• 206010028980 Neoplasm Diseases 0.000 claims 5
• 239000000611 antibody drug conjugate Substances 0.000 claims 5
• 229940049595 antibody-drug conjugate Drugs 0.000 claims 5
• 201000011510 cancer Diseases 0.000 claims 5
• 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 4
• 239000003085 diluting agent Substances 0.000 claims 4
• 239000002552 dosage form Substances 0.000 claims 4
• 239000003937 drug carrier Substances 0.000 claims 4
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 4
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 4
• 239000008194 pharmaceutical composition Substances 0.000 claims 2
• QAAFNSMAIAVCHE-BZLYQNAUSA-N (2s)-2-[(2-amino-2-methylpropanoyl)amino]-n-[(3r,4s,5s)-3-methoxy-1-[(2s)-2-[(1r,2r)-1-methoxy-2-methyl-3-oxo-3-[[(1s)-2-phenyl-1-(1,3-thiazol-2-yl)ethyl]amino]propyl]pyrrolidin-1-yl]-5-methyl-1-oxoheptan-4-yl]-n,3-dimethylbutanamide Chemical compound CC(N)(C)C(=O)N[C@@H](C(C)C)C(=O)N(C)[C@@H]([C@@H](C)CC)[C@H](OC)CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)N[C@H](C=1SC=CN=1)CC1=CC=CC=C1 QAAFNSMAIAVCHE-BZLYQNAUSA-N 0.000 claims 1
• 206010006187 Breast cancer Diseases 0.000 claims 1
• 208000026310 Breast neoplasm Diseases 0.000 claims 1
• 206010058467 Lung neoplasm malignant Diseases 0.000 claims 1
• XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 1
• 239000004202 carbamide Substances 0.000 claims 1
• 239000003814 drug Substances 0.000 claims 1
• 201000005202 lung cancer Diseases 0.000 claims 1
• 208000020816 lung neoplasm Diseases 0.000 claims 1
• 238000004519 manufacturing process Methods 0.000 claims 1
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
• 230000001225 therapeutic effect Effects 0.000 claims 1
• NRMQEWBZFDNUHD-VKRRFRHLSA-N CC[C@H](C)[C@@H]([C@@H](CC(N(CCC1)[C@@H]1[C@@H]([C@@H](C)C(N[C@H](C)[C@H](c1ccccc1)O)=O)OC)=O)OC)N(C)C([C@@H](C(C)C)NC(C(C)(C)N)=O)=O Chemical compound CC[C@H](C)[C@@H]([C@@H](CC(N(CCC1)[C@@H]1[C@@H]([C@@H](C)C(N[C@H](C)[C@H](c1ccccc1)O)=O)OC)=O)OC)N(C)C([C@@H](C(C)C)NC(C(C)(C)N)=O)=O NRMQEWBZFDNUHD-VKRRFRHLSA-N 0.000 description 3
• BYZVPLCBAAEVLB-JQWMWWJASA-N CC[C@H](C)C(C(CC(N(CCC1)[C@@H]1/C(/C(C)C(NC(C)C(C)(c1ccccc1)O)=O)=[O]/C)=O)OC)N(C)C(/C(/C(C)C)=N/C(C(C)(C)N)=O)=O Chemical compound CC[C@H](C)C(C(CC(N(CCC1)[C@@H]1/C(/C(C)C(NC(C)C(C)(c1ccccc1)O)=O)=[O]/C)=O)OC)N(C)C(/C(/C(C)C)=N/C(C(C)(C)N)=O)=O BYZVPLCBAAEVLB-JQWMWWJASA-N 0.000 description 1
• MUJOCDBVNQNVSF-YIBJTWMJSA-N CC[C@H](C)[C@@H]([C@@H](CC(N(CCC1)[C@@H]1[C@@H]([C@@H](C)C(N[C@H](C)[C@H](c1ccccc1)O)=O)OC)=O)OC)N(C)C(CC(C)C/[O]=C(/C(C)(C)N)\N)=O Chemical compound CC[C@H](C)[C@@H]([C@@H](CC(N(CCC1)[C@@H]1[C@@H]([C@@H](C)C(N[C@H](C)[C@H](c1ccccc1)O)=O)OC)=O)OC)N(C)C(CC(C)C/[O]=C(/C(C)(C)N)\N)=O MUJOCDBVNQNVSF-YIBJTWMJSA-N 0.000 description 1
• 0 CN(C)C(CC1)CCN1C(C(C=C1)=CCC1NC(Nc(cc1)ccc1-c1nc(N2CCOCC2)nc(N2CCOCC2)n1)=O)=* Chemical compound CN(C)C(CC1)CCN1C(C(C=C1)=CCC1NC(Nc(cc1)ccc1-c1nc(N2CCOCC2)nc(N2CCOCC2)n1)=O)=* 0.000 description 1