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Cabozantinib Malate CAS 1140909-48-3
Cabozantinib Malate CAS 1140909-48-3
PaymentL/C,T/T,D/P,Paypal,Money Gram,Western Union
IncotermFOB,CFR,CIF,EXW,FCA,CPT,CIP
Min. Order10 Gram
TransportationOcean,Land,Air,DHL,TNT
PortShanghai port,Qingdao port
Product Attributes
BrandTianfu
Model No.TF-4271
minOrder10 Gram
Supply Ability & Additional Information
Productivity100Ton
Payment TypeL/C,T/T,D/P,Paypal,Money Gram,Western Union
Place of OriginChina
TransportationOcean,Land,Air,DHL,TNT
PortShanghai port,Qingdao port
IncotermFOB,CFR,CIF,EXW,FCA,CPT,CIP
PackagingAs Buyer's Request
Supply Ability50Ton
CertificateISO
Packaging & Delivery
Selling Units:Gram
Package Type:As Buyer's Request
Description
Product Name: Cabozantinib Malate
Synonyms: (2S)-2-Hydroxybutanedioic acid compd. with N-[4-[(6,7-dimethoxy-4-quinolinyl)oxy]phenyl]-N'-(4-fluorophenyl)-1,1-cyclopropanedicarboxamide (1:1);Cabozantinib (S)-malate;Cabozantinib L-Malate Salt;N-[4-[(6,7-DiMethoxy-4-quinolinyl)oxy]phenyl]-N'-(4-fluorophenyl)-1,1-cyclopropanedicarboxaMide (2S)-;Cabozantinib (S)-Malate(XL-184);Cabozantinib L-Malate;XL184(S)-malate;1-N-[4-(6,7-dimethoxyquinolin-4-yl)oxyphenyl]-1-N'-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide,( 57364218, 57185885,2S)-2-hydroxybutanedioic acid
CAS: 1140909-48-3
MF: C32H30FN3O10
MW: 635.5931032
EINECS: 691-711-0
Product Categories: -;Inhibitors;API
Uses Cabozantinib is a small molecule C-Met modulator. Cabozantinib acts as a potent multitargeted VEGFR2, Met, FLT3, Tie2, Kit and Ret inhibitor with IC50 of 0.035, 1.8, 14.4, 14.3 and 4.6 nM for VEGFR2, Met, FLT3, Tie2 and Kit, respectively. Cabozantinib shows dose-dependent inhibition of tumor growth and tumor regression, associated with disruption of the tumor vasculature and extensive tumor cell a poptosis.
Uses XL184 (Cabozantinib, BMS-907351) is a potent multitargeted VEGFR2, Met, FLT3, Tie2, Kit and Ret inhibitor with IC50 of 0.035, 1.8, 14.4, 14.3 and 4.6 nM for VEGFR2, Met, FLT3, Tie2 and Kit, respectively.
Uses Cabozantinib malate is the malate of Cabozantinib, a potent VEGFR2 inhibitor with IC50 of 0.035 nM and also inhibits c-Met, Ret, Kit, Flt-1/3/4, Tie2, and AXL with IC50 of 1.3 nM, 4 nM, 4.6 nM, 12 nM/11.3 nM/6 nM, 14.3 nM and 7 nM, respectively.