Anacardic Acid

SKU: orb1300811

Description

Anacardic Acid

Research Area

Cardiovascular Research, Epigenetics & Chromatin, Immunology & Inflammation, Stem Cell & Developmental Biology

Key Properties

• CAS Number: 16611-84-0
• MW: 348.5
• Purity: >98%
• Formula: C₂₂H₃₆O₃
• SMILES: CCCCCCCCCCCCCCCc1cccc(O)c1C(O)=O
• Target: Acetyltransferase
• Solubility: Soluble in DMSO (up to at least 25 mg/ml) or in Ethanol (15 mg/ml)

Bioactivity

• Target IC50:
  PCAF(p300/CREB-binding protein-associated factor):5 μM|p300 HAT:8.5 μM
• In Vivo:
  Anacardic acid decreases over-expression of Gata4, α-MHC, and cTnT in fetal mouse hearts exposed to ethanol. Anacardic acid inhibits binding of PCAF, P300 to the promoter of Gata4.
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• In Vitro:
  Anacardic acid is an inhibitor of several Clinicalally targeted enzymes such as HATs, NF-kB, LOX-1, xanthine oxidase, tyrosinase, and ureases. Anacardic acid is also an effective inhibitor of Tip60 in vitro. It inhibits the Tip60-dependent acetylation and activation of the ATM protein kinase in HeLa cells and sensitizes the cells to the cytotoxic effects of radiation.
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• Cell Research:
  HeLa and 293T cells are grown in Dulbecco's modified Eagle's medium/10% fetal calf serum. SQ20B and SCC35 squamous cell carcinoma cell lines are cultured in modified eagles medium/10% fetal calf serum. For anacardic acid (EMD Biosciences, CA) exposure, cells are preincubated with anacardic acid (0-100 μM) for 40 min, irradiated, then allowed to recover for 4 h. Cells are then switched to fresh media and allowed to grow for 10 days.
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• Animal Research:
  Animal Models: 9 to 11 week old Kunming mice. Formulation: Dissolved in DMSO,co-injected with ethanol. Dosages: 0,1.25,2.5,5,10 mg/kg. Administration: i.p.
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Storage & Handling

• Storage: -20°C
• Expiration Date: 12 months from date of receipt.
• Disclaimer: For research use only

Alternative Names

6-Pentadecylsalicylic acid; 6-PDSA

Compound Identifiers

PubChem CID

167551