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BRD3308

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Category Human immunodeficiency Virus (HIV)
CAS 1550053-02-5
Description BRD3308 is a highly selective HDAC3 inhibitor with IC50 of 54 nM. BRD3308 inhibits pancreatic β-cell apoptosis induced by inflammatory cytokines or glycolipid toxic stress, and increases the release of functional insulin. BRD3308 activates HIV-1 transcription and destroys the HIV-1 incubation period.
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Product Information

Synonyms 4-Acetylamino-N-(2-Amino-4-Fluorophenyl)-Benzamide; CHEMBL4293858; SCHEMBL15551809; BDBM178100
IUPAC Name 4-acetamido-N-(2-amino-4-fluorophenyl)benzamide
Molecular Weight 287.29
Molecular Formula C15H14FN3O2
Canonical SMILES CC(=O)NC1=CC=C(C=C1)C(=O)NC2=C(C=C(C=C2)F)N
InChI InChI=1S/C15H14FN3O2/c1-9(20)18-12-5-2-10(3-6-12)15(21)19-14-7-4-11(16)8-13(14)17/h2-8H,17H2,1H3,(H,18,20)(H,19,21)
InChIKey RRJDFENBXIEAPD-UHFFFAOYSA-N
Boiling Point 449.9±45.0 °C(Predicted)
Flash Point 225.9±28.7 °C
Purity 98%
Density 1.382±0.06 g/cm3(Predicted)
Solubility Soluble in DMF (30 mg/ml), DMSO (30 mg/ml), Ethanol (30 mg/ml)
Appearance Off-white to light yellow (Solid)
Storage Store at -20°C
Complexity 383
Exact Mass 287.10700486
Index Of Refraction 1.689
In Vitro BRD3308 (5-30 µM; 6-24 hours) treatment increases HIV-1 expression in the 2D10 cell line.
BRD3308 (15 µM; overnight) is able to induce outgrowth of HIV-1 from latently infected cells ex vivo in resting CD4+ T cells.
BRD3308 inhibits HDAC1, HDAC2 and HDAC3 with Ki values of 5.1 μM, 6.3 μM and 29 nM, respectively.
In Vivo BRD3308 reduced hyperglycaemia and increased insulin secretion in a rat model of type 2 diabetes.
Target HDAC; HIV; Apoptosis
Vapor Pressure 0.0±1.1 mmHg at 25°C
XLogP3-AA 1.4

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