WARNING: This product is for research use only, not for human or veterinary use.
MedKoo CAT#: 522465
Description: BRD73954 is a small molecule inhibitor that potently inhibits HDAC6 and HDAC8. It inhibits HDAC6, a class IIb histone that deacetylates cytoplasmic proteins, including tubulin, heat shock protein 90, and cortactin, and has roles in cell adhesion and motility. It is also an inhibitor of HDAC8, a class I histone that primarily targets nuclear proteins, including histones and cohesins, and regulates gene expression.
MedKoo Cat#: 522465
Chemical Formula: C16H16N2O3
Exact Mass: 284.11609
Molecular Weight: 284.32
Elemental Analysis: C, 67.59; H, 5.67; N, 9.85; O, 16.88
BRD73954, purity > 98%, is in stock. Current shipping out time is about 2 weeks after order is received. CoA, QC data and MSDS documents are available in one week after order is received.
Synonym: BRD73954; BRD-73954; BRD 73954.
IUPAC/Chemical Name: N1-hydroxy-N3-(2-phenylethyl)-1,3-benzenedicarboxamide
InChi Key: FIHKWEQJEDRIFS-UHFFFAOYSA-N
InChi Code: InChI=1S/C16H16N2O3/c19-15(17-10-9-12-5-2-1-3-6-12)13-7-4-8-14(11-13)16(20)18-21/h1-8,11,21H,9-10H2,(H,17,19)(H,18,20)
SMILES Code: O=C(C1=CC=CC(C(NO)=O)=C1)NCCC2=CC=CC=C2
The following data is based on the product molecular weight 284.32 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
|Concentration / Solvent Volume / Mass||1 mg||5 mg||10 mg|
|1 mM||1.15 mL||5.76 mL||11.51 mL|
|5 mM||0.23 mL||1.15 mL||2.3 mL|
|10 mM||0.12 mL||0.58 mL||1.15 mL|
|50 mM||0.02 mL||0.12 mL||0.23 mL|
1: Olson DE, Wagner FF, Kaya T, Gale JP, Aidoud N, Davoine EL, Lazzaro F, Weïwer M, Zhang YL, Holson EB. Discovery of the first histone deacetylase 6/8 dual inhibitors. J Med Chem. 2013 Jun 13;56(11):4816-20. doi: 10.1021/jm400390r. Epub 2013 May 29. PubMed PMID: 23672185.
(Last update: 4/20/2016).