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InChiKey: JLSVDPQAIKFBTO-CFEYTUSBSA-N
Smiles: CC1(C)C[C@H]2C3=CC[C@@H]4[C@@]5(C)CC[C@H](O)[C@@](C)(CO)[C@@H]5CC[C@@]4(C)[C@]3(C)C[C@H](O)[C@]2(C[C@@H]1O)CO
Flufenamic acid binds to the central pocket of TEAD2 YBD and inhibits both TEAD function and TEAD-YAP-dependent processes
the affinity of M-II for MT2 receptors is approximately 5- and 1
Smiles: COC1=CC=C2N=CC=C([C@@H](O)[C@H]3C[C@@H]4CC[N@]3C[C@@H]4C=C)C2=C1
V-9302 ido-PEG3-C1-PFP ester InChiKey: JLSVDPQAIKFBTO-CFEYTUSBSA-NV 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:
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