V-9302 ido-PEG3-C1-PFP ester InChi: InChI=1S/C24H31N5O2/c30-20-10-12-28(16-20)22-13-21(23(31)25-14-17-8-9-17)26-24(27-22)29-11-4-7-19(15-29)18-5-2-1-3-6-18/h1-3

InChi: InChI=1S/C24H31N5O2/c30-20-10-12-28(16-20)22-13-21(23(31)25-14-17-8-9-17)26-24(27-22)29-11-4-7-19(15-29)18-5-2-1-3-6-18/h1-3

for 28 days

Flufenamic acid binds to the central pocket of TEAD2 YBD and inhibits both TEAD function and TEAD-YAP-dependent processes

is activated by thromboxane A2 (TXA2)

Heimbrecht J

V-9302 ido-PEG3-C1-PFP ester InChi: InChI=1S/C24H31N5O2/c30-20-10-12-28(16-20)22-13-21(23(31)25-14-17-8-9-17)26-24(27-22)29-11-4-7-19(15-29)18-5-2-1-3-6-18/h1-3V 9302 is a competitive antagonist of transmembrane glutamine flux. V 9302 selectively and potently targets the amino acid transporter ASCT2 (SLC1A5) not ASCT1. V 9302 inhibits ASCT2 mediated glutamine uptake (IC50=9. 6 M) in HEK 293 cells. Product information CAS Number: 1855871 76 9 Molecular Weight: 538. 68 Formula: C34H38N2O4 Chemical Name: (2S) 2 amino 4 [bis({2 [(3 methylphenyl)methoxy]phenyl}methyl)amino]butanoic acid Smiles: