Pracinostat (SB939)

Catalog #

27771-1

$275 *

Size: 10 mg

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Description

Potent and oral inhibitor of histone deacetylase (HDAC), selective for class I, II and IV HDACs. SB939 shows significant antiproliferative activity against a wide variety of tumor cell lines, with high tumor exposure and efficacy in mouse models of colorectal cancer.

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Synonyms

SB-939; SB 939; (E)-3-[2-butyl-1-[2-(diethylamino)ethyl]benzimidazol-5-yl]-N-hydroxyprop-2-enamide

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Product Data Gallery

Product Info

Storage and Usage

Citations

Target(s)

HDAC

Formula

C₂₀H₃₀N₄O₂

358.48 Da

Solubility

Soluble in DMSO

Biological Activity

SB 939 is an HDAC inhibitor that inhibits HDAC1 (IC50 = 49 nM), HDAC3 (IC50 = 43 nM), HDAC4 (IC50 = 56nM), HDAC5 (IC50 = 47 nM), HDAC9 (IC50 = 70 nM), HDAC10 (IC50 = 40 nM). Only poorly inhibits HDACs 6 or 7 (Kis = 247 and 104 nM, respectively). Prevents proliferation of ovarian (A2780), colon (COLO 205 and HCT-116), and prostate cancer (PC-3) cell lines at IC50 values of 0.48, 0.56, 0.48, and 0.34 µM, respectively.

CAS Registry #

929016-96-6

Background

Pracinostat (SB939) is an orally bioavailable, small-molecule histone deacetylase (HDAC) inhibitor with potential antineoplastic activity. Pracinostat inhibits HDACs, which may result in the accumulation of highly acetylated histones. It is a pan-HDAC inhibitor, inhibiting all HDAC isozymes except HDAC6 and HDAC7.

References

1. Novotny-Diermayr V, et al. Mol Cancer Ther. 2010 Mar;9(3):642-52.
2. Wang, H., et al. 2011. J. Med. Chem. 54(17): 4694-4720.
3. Novotny-Diermayr V, et al. Blood Cancer J. 2012 May;2(5):e69.

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Pracinostat (SB939)

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