HDAC1 and HDAC3 inhibitor (ID50 = 0.01 and 0.07 μM

CBHA – 5 mg

Brand:
Cayman
CAS:
174664-65-4
Storage:
-20
UN-No:
Non-Hazardous - /

Histone deacetylase (HDAC) inhibitors hyperacetylate histones and increase transcriptional activity in selected genes. Importantly, HDAC inhibitors induce apoptosis in some cancer cells and show promise in the treatment of certain forms of cancer. CBHA is a potent HDAC inhibitor, exhibiting ID50 values of 0.01 and 0.07 μM in vitro for HDAC1 and HDAC3, respectively.{17174} CBHA also induces apoptosis in nine different neuroblastoma cell lines in culture (0.5-4.0 μM){17175} and completely suppresses neuroblastoma tumor growth in SCID mice at 200 mg/kg.{17176} The efficacy of CBHA for suppressing tumor growth in mice is enhanced by the addition of retinoic acid.{17176}  

 

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Description

HDAC1 and HDAC3 inhibitor (ID50 = 0.01 and 0.07 μM, respectively, in vitro); induces apoptosis in nine different neuroblastoma cell lines in culture (0.5-4.0 μM) and completely suppresses neuroblastoma tumor growth in SCID mice at 200 mg/kg

Formal name: N-hydroxy-3-[3-(hydroxyamino)-3-oxo-1-propen-1-yl]-benzamide

Synonyms:  Histone Deacetylase Inhibitor II|m-Carboxycinnamic Acid bis-Hydroxamide

Molecular weight: 222.2

CAS: 174664-65-4

Purity: ≥98%

Formulation: A crystalline solid

Product Type|Biochemicals|Small Molecule Inhibitors|Deacetylases||Research Area|Cancer|Cell Death|Apoptosis||Research Area|Epigenetics, Transcription, & Translation|Erasers|Histone Deacetylation

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