Vorinostat (SAHA, MK0683)

Vorinostat (SAHA, MK0683)

Catalog Number:
L002369001APE
Mfr. No.:
APE-A4084
Price:
$188
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      • Overview
        • Please contact us at for specific academic pricing.

          Background

          Vorinostat (suberoylanilide hydroxamic acid, SAHA) is a histone deacetylase inhibitor (HDACi), that plays key roles in epigenetic or non-epigenetic regulation, inducing growth arrest, differentiation and apoptosis of tumor cells.[1] Vorinostat is a small molecular with the formular of C14H20N2O3 and molecular weight of 264.3. The major mechanism of HDACi-induced apoptosis is the activation of the intrinsic apoptotic pathway. HDACi can activate the intrinsic apoptotic pathway by releasing of cytochrome c from mitochondria and regulating of Bcl-2 family expression.[2]

          [1] Hui-ming Z, Qian-hai D, Wei-ping C, Ru-bin L. Vorinostat, a HDAC inhibitor, showed anti-osteoarthritic activities through inhibition of iNOS and MMP expression, p38 and ERK phosphorylation and blocking NF-kB nuclear translocation. International Immunopharmacology. 2013, 17. 329-335.
          [2] Norihisa U, Sayaka K, Hisanori M, Katsuhiko Y, Airo T. Requirement of p38 MAPK for a cell-death pathway triggered by vorinostat in MDA-MB-231 human breast cancer cells. Cancer Letters. 2012, 315. 112-121.

      • Properties
        • Alternative Name
          SAHA, suberoylanilide hydroxamic acid, Suberanilohydroxamic acid, SAHA cpd; N'-hydroxy-N-phenyloctanediamide
          CAS Number
          149647-78-9
          Molecular Formula
          C14H20N2O3
          Molecular Weight
          264.3
          Appearance
          A solid
          Purity
          98.36%
          Solubility
          insoluble in EtOH; insoluble in H2O; ≥4.41 mg/mL in DMSO
          Storage
          Store at -20°C

          * For Research Use Only

      • Reference
        • 1. Yanhong Xu, Shiqiao Peng, et al. "High doses of butyrate induce a reversible body temperature drop through transient proton leak in mitochondria of brain neurons." Life Sci. 2021 Aug 1;278:119614. PMID:34022200
          2. Maojun Zhou, Hao Zheng, et al. "Discovery of a novel AR/HDAC6 dual inhibitor for prostate cancer treatment." Aging (Albany NY). 2021 Feb 17;13(5):6982-6998. PMID:33621955
          3. Haiyang Yu, Shan Lu, et al. "TDP-43 and HSP70 phase separate into anisotropic, intranuclear liquid spherical annuli." bioRxiv. March 29, 2020.
          4. Liu W, Song YY, et al. "Dysregulation of FOXO transcription factors in Epstein-Barr virus-associated gastric carcinoma." Virus Res. 2020;276:197808. PMID:31712122
          5. Emily L Morton, Christian V Forst, et al. "Transcriptional Circuit Fragility Influences HIV Proviral Fate." bioRxiv. 2018 December 23.
          6. Feng XL, Deng HB, et al. "Suberoylanilide Hydroxamic Acid Triggers Autophagy by Influencing the mTOR Pathway in the Spinal Dorsal Horn in a Rat Neuropathic Pain Model." Neurochem Res. 2018 Dec 17. PMID:30560396
          7. Deng R, Zhang P, et al. "HDAC is indispensable for IFN-γ-induced B7-H1 expression in gastric cancer." Clin Epigenetics. 2018 Dec 11;10(1):153. PMID:30537988
          8. Kim SR, Lewis JM, et al. "BET inhibition in advanced cutaneous T cell lymphoma is synergistically potentiated by BCL2 inhibition or HDAC inhibition." Oncotarget. 2018 Jun 26;9(49):29193-29207. PMID:30018745
          9. Hari Prasad, Rajini Rao. "The Amyloid Clearance Defect in ApoE4 Astrocytes is Corrected by Epigenetic Restoration of NHE6." bioRxiv. 2018.January. 4 PMID:29498802
          10. Mirza AN, Fry MA, et al. "Combined inhibition of atypical PKC and histone deacetylase 1 is cooperative in basal cell carcinoma treatment." JCI Insight. 2017 Nov 2;2(21). pii: 97071. PMID:29093271
          11. Hai Y, Shinsky SA, et al. "Histone deacetylase 10 structure and molecular function as a polyamine deacetylase." Nat Commun. 2017 May 18;8:15368. PMID:28516954
          12. Bagnall NH, Hines BM, et al. "Insecticidal activities of histone deacetylase inhibitors against a dipteran parasite of sheep, Lucilia cuprina." Int J Parasitol Drugs Drug Resist. 2017 Apr;7(1):51-60. PMID:28110187
          13. Sun, Yuefeng, et al. "Fe65 Suppresses Breast Cancer Cell Migration and Invasion through Tip60 Mediated Cortactin Acetylation." Scientific reports 5 (2015). PMID:26166158

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