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At 2 mM of ATP concentrations
it is selectively and irreversibly converted to its active phosphoramidate-based
may be a useful agent for the study of AhR-mediated signal transduction and the prevention of TCDD-associated pathology
unless is specified otherwise
The ability of LY-303511 to increase gap junctional intercellular communication (GJIC) does not occur concomitant with inhibition of phosphorylation of AKT as measured by immunoblotting
SU-5402 - FGFR inhibitor. CAS# 215543-92-3 size:2mg solid At 2 mM of ATPSU 5402, CAS No. 215543 92 3, is a potent inhibitor of FGFR, VEGFR, and PDGFR. SU 5402 has been used in many studies to inhibit cancer cell growth, or modulate stem cell phenotypes, including maintenance of mouse ESCs, or inducing generation of functional human nociceptors from human ESCs iPSCs when combined with LDN193189 BMP inhibitor, SB431542 TGF inhibitor, CHIR99021 GSK3 inhibitor, and DAPT Notch inhibitor. Product information CAS Number: 215543
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