CAS 149647-78-9
:Vorinostat
Description:
Vorinostat, also known by its chemical name suberoylanilide hydroxamic acid (SAHA), is a histone deacetylase (HDAC) inhibitor used primarily in cancer therapy. It is classified as an antineoplastic agent and is particularly effective in treating cutaneous T-cell lymphoma (CTCL). Vorinostat works by altering the expression of genes involved in cell cycle regulation and apoptosis, leading to the induction of cell differentiation and death in cancer cells. The compound is characterized by its hydroxamic acid functional group, which is crucial for its HDAC inhibitory activity. Vorinostat is typically administered orally and is known for its side effects, which may include fatigue, gastrointestinal disturbances, and hematological changes. Its pharmacokinetics involve extensive metabolism, primarily in the liver, and it has a relatively short half-life. Vorinostat's development marked a significant advancement in epigenetic therapy, highlighting the potential of targeting histone modifications in cancer treatment.
Formula:C14H20N2O3
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)
InChI key:InChIKey=WAEXFXRVDQXREF-UHFFFAOYSA-N
SMILES:N(C(CCCCCCC(NO)=O)=O)C1=CC=CC=C1
Synonyms:- Ccris 8456
- M344
- N-Hydroxy-N'-phenyloctanediamide
- N-Hyrdroxy-N'-phenyloctanediamide
- N<sup>1</sup>-Hydroxy-N<sup>8</sup>-phenyloctanediamide
- Octanediamide, N-hydroxy-N'-phenyl-
- Octanediamide, N<sup>1</sup>-hydroxy-N<sup>8</sup>-phenyl-
- SAHA cpd
- Suberanilohydroxamic acid
- Suberoyl anilide bishydroxamide
- Suberoylanilide Hydroxamic Acid
- Unii-58Ifb293Ji
- Vorinostat [USAN]
- Wt 171
- Zolinza
- Octanediamide, N1-hydroxy-N8-phenyl-
- SAHA
- See more synonyms
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Found 15 products.
N-Hydroxy-N'-phenyloctanediamide
CAS:Formula:C14H20N2O3Purity:>98.0%(HPLC)(N)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:264.33N-Hydroxy-N'-phenyloctanediamide
CAS:Formula:C14H20N2O3Purity:98%Color and Shape:SolidMolecular weight:264.3202Ref: IN-DA00382H
1g28.00€5g68.00€10g108.00€1kgTo inquire25g213.00€5kgTo inquire500gTo inquire250mg24.00€Vorinostat
CAS:<p>Vorinostat (SAHA) is a pan-histone deacetylase (HDAC) inhibitor (IC50=10 nM) with inhibitory activity against HDAC1/2/3/6/7/11.</p>Formula:C14H20N2O3Purity:99.47% - 99.65%Color and Shape:White Crystalline SolidMolecular weight:264.32N-Hydroxy-N'-Phenyloctanediamide
CAS:N-Hydroxy-N'-PhenyloctanediamidePurity:99%Molecular weight:264.32g/molVorinostat
CAS:Formula:C14H20N2O3Purity:≥ 98.0%Color and Shape:White to off-white powderMolecular weight:264.32Suberoylanilide Hydroxamic Acid
CAS:Controlled ProductFormula:C14H20N2O3Color and Shape:White SolidMolecular weight:264.32Vorinostat
CAS:<p>M06303 - Vorinostat</p>Formula:C14H20N2O3Purity:97%Color and Shape:SolidMolecular weight:264.325Vorinostat
CAS:<p>Vorinostat is a histone deacetylase inhibitor which interferes with gene transcription regulatory mechanisms. It targets histones and non-histone proteins within transcription factor complexes involved in regulation of cell proliferation (p53), protein stability (Hsp90), apoptosis (Bcl-2 family), cell motility (α-tublin), and angiogenesis (HIF-1α). Vorinostat affects epigenetic regulation in various cancers and has been used in clinical trials as anticancer drug.</p>Formula:C14H20N2O3Purity:Min. 98 Area-%Color and Shape:White PowderMolecular weight:264.32 g/molVorinostat - Bio-X ™
CAS:<p>Vorinostat is a histone deacetylase inhibitor which interferes with gene transcription regulatory mechanisms. It is used to treat cutaneous manifestations in patients with progressive, persistent, or recurrent cutaneous T- cell lymphoma (CTCL) following prior systemic therapies. This drug inhibits the enzymatic activity of histone deacetylases HDAC1, HDAC2 and HDAC3 (Class I) and HDAC6 (Class II).</p>Formula:C14H20N2O3Purity:Min. 99 Area-%Color and Shape:PowderMolecular weight:264.32 g/molSuberoylanilide Hydroxamic Acid-13C6
CAS:Controlled Product<p>Applications is the labeled form of Suberoylanilide Hydroxamic Acid (S688700), which is a potent, selective, cell permeable histone deacetylase inhibitor (HDAC), displays anti-angiogenic activity by interfering with VEGF signaling in human umbilical vein endothelial cells (HUVECs) and induces differentiation in human breast cancer cells. Also it is a potent histone deacetylase inhibitor.<br>References Richon, V.M., et al.: Proc. Natl. Acad.Sci. USA, 95, 3003 (1988), Munster, P.N., et al.: Cancer Res., 61, 8492 (2001), Deroanne, C.F., et al.: Oncogene, 21, 247 (2002)<br></p>Formula:C6C8H20N2O3Color and Shape:NeatMolecular weight:270.276









