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Smiles: CN(C1C=CC(=CC=1)C(F)(F)F)C(=O)C1=C(O)C2C(=CC=CC=2N(C)C1=O)OC
Molecular Weight: 354
The Evolving Landscape in the Development of Isocitrate Dehydrogenase Mutant Inhibitors
InChiKey: HZCOFZVJMJRKIB-UHFFFAOYSA-N
PluriSIn-1 was identified by a high-throughput screening against undifferentiated human ESCs
TMP269 - Class IIa HDAC Inhibitor. CAS# 1314890-29-3 size:10mg solid Smiles: CN(C1C=CC(=CC=1)C(F)(F)F)C(=O)C1=C(O)C2C(=CC=CC=2N(C)C1=O)OCTMP269, CAS No. 1314890 29 3, is a highly potent, selective and cell permeable class IIa HDAC inhibitor with IC50 of 126 nM, 80 nM, 36 nM and 19 nM for HDAC4, HDAC5, HDAC7 and HDAC9 respectively. It has very weak or no activity targeting the other HDACs (2 40 M). TMP269 has an unprecedented metal binding group, trifluoromethyloxadiazole (TFMO), which circumvents the selectivity and pharmacologic liabilities of hydroxamates. Crystallography revealed a
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