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Entinostat (MS-275, SNDX-275) strongly inhibited HDAC1 and HDAC3, with IC50 of 0.51 μM and 1.7 μM, respectively, in cell-free tests, which was stronger than HDACs 4, 6, 8, and 10. Entinostat can induce autophagy and apoptosis. Phase 3.
Brand: BCM
Target: Apoptosis; Autophagy; HDAC
Signaling Pathways: Apoptosis; Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair
Melting Point: 159-160 ºC
Boiling Point: 566.7±50.0 °C(Predicted)
pKa: 11.32±0.46(Predicted)
Solubility: Soluble in DMSO. Insoluble in Water; insoluble in Ethanol.
GHS: GHS06, GHS08
Isomeric SMILES: C1=CC=C(C(=C1)N)NC(=O)C2=CC=C(C=C2)CNC(=O)OCC3=CN=CC=C3
InChIKey: INVTYAOGFAGBOE-UHFFFAOYSA-N
InChI: InChI=1S/C21H20N4O3/c22-18-5-1-2-6-19(18)25-20(26)17-9-7-15(8-10-17)13-24-21(27)28-14-16-4-3-11-23-12-16/h1-12H,13-14,22H2,(H,24,27)(H,25,26)
Attribute [Chem Name] pyridin-3-ylmethyl N-[[4-[(2-aminophenyl)carbamoyl]phenyl]methyl]carbamate [Synonym] Entinostat; SNDX-275; MS-275 [CAS No.] 209783-80-2 [MDL No.] MFCD08272435 [Formula] C21H20N4O3 [Molecular] 376.41 [Form] Pale yellow solid [Storage] Keep in dark place. Sealed in dry. Store in freezer, under -20°C
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