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Vorinostat

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Category Human papillomavirus (HPV)
CAS 149647-78-9
Description Vorinostat (suberoylanilide hydroxamic acid, SAHA) is an HDAC inhibitor with IC50 of ~10 nM.
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Product Information

Synonyms MK-0683, MK 0683, MK0683, SAHA, M344, CCRIS 8456, HSDB 7930, Vorinostat, suberoylanilide hydroxamic acid, Zolinza
IUPAC Name N'-hydroxy-N-phenyloctanediamide
Molecular Weight 264.3
Molecular Formula C14H20N2O3
Canonical SMILES C1=CC=C(C=C1)NC(=O)CCCCCCC(=O)NO
InChI InChI=1S/C14H20N2O3/c17-13(15-12-8-4-3-5-9-12)10-6-1-2-7-11-14(18)16-19/h3-5,8-9,19H,1-2,6-7,10-11H2,(H,15,17)(H,16,18)
InChIKey WAEXFXRVDQXREF-UHFFFAOYSA-N
Melting Point 161-164 °C
Purity >98%
Density 1.174 g/cm³
Solubility In Vitro:
10 mM in DMSO
Appearance White Solid
Application Antineoplastic agents; histone deacetylase inhibitors
Storage Powder:
-20°C: 3 years
4°C: 2 years
In solvent:
-80°C: 6 months
-20°C: 1 month
Complexity 276
Exact Mass 264.14739250
Index Of Refraction 1.567
In Vitro Vorinostat efficiently suppresses MES-SA cell growth at a low dosage (3 μM) already after 24 hours treatment. HDACs class I (HDAC2 and 3) as well as class II (HDAC7) are preferentially affected by this treatment. Vorinostat significantly increases p21WAF1 expression and Apoptosis in MES-SA cells.
Vorinostat inhibits SK-N-SH and SK-N-Be(2)C with the IC25 values of 1 µM and 0.5 µM, respectively.
Vorinostat is an effective inhibitor of HPV-18 DNA amplification, reduces oncoproteins E6 and E7 activities and triggers Apoptosis in HPV-infected, differentiated cells.
In Vivo Vorinostat (50 mg/kg/day) reduces tumor growth by more than 50% in nude mice injected with 5×106 MES-SA cells.
PSA 78.43
Target HDAC; Autophagy; Mitophagy; Filovirus; Apoptosis; HPV
XLogP3-AA 1.9

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