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SU11652 

Cat. No. M29909
SU11652  Structure
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Biological Activity

SU11652 is a potent receptor tyrosine kinase (RTK) inhibitor. SU11652 also inhibits several members of the split kinase family of RTKs, including VEGFR, FGFR, PDGFR, and Kit. SU11652 can be uesd for spontaneous cancers expressing Kit mutations research.

Chemical Information
Molecular Weight 414.93
Formula C22H27ClN4O2
CAS Number 326914-10-7
Storage Please store the product under the recommended conditions in the Certificate of Analysis.
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Jinle Tang, et al. Biochem J. Sunitinib inhibits RNase L by destabilizing its active dimer conformation

[2] Plínio Salmazo Vieira, et al. Biochem Biophys Res Commun. Pyrrole-indolinone SU11652 targets the nucleoside diphosphate kinase from Leishmania parasites

[3] Anne-Marie Ellegaard, et al. Mol Cancer Ther. Sunitinib and SU11652 inhibit acid sphingomyelinase, destabilize lysosomes, and inhibit multidrug resistance

[4] Yao Guo, et al. J Hematol Oncol. SU11652 Inhibits tyrosine kinase activity of FLT3 and growth of MV-4-11 cells

[5] B Heryanto, et al. Reproduction. Effect of angiogenesis inhibitors on oestrogen-mediated endometrial endothelial cell proliferation in the ovariectomized mouse

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  Catalog
Abmole Inhibitor Catalog




Keywords: SU11652  supplier, VEGFR/PDGFR, inhibitors, activators


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