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Product
Cardanol Cardanol. Group: Biochemicals. CAS No. 37330-39-5. Pack Sizes: 10g, 25g, 50g, 100g, 250g. US Biological Life Sciences. USBiological 6
Worldwide
Cardanolide,3-[(6-deoxy-a-L-mannopyranosyl)oxy]-1,5,11,14,19-pentahydroxy-,(1b,3b,5b,11a,20x)- Heterocyclic Organic Compound. Alternative Names: DIHYDROOUABAIN, 1183-35-3. CAS No. 1183-35-3. Molecular formula: C29H46O12. Mole weight: 586.67. Purity: 0.96. IUPACName: 4-[(1R,3S,5S,10S,13R,14S)-1,5,11,14-tetrahydroxy-10-(hydroxymethyl)-13-methyl-3-[(2S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]oxolan-2-one. Canonical SMILES: CC1C (C (C (C (O1)OC2CC (C3 (C4C (CCC3 (C2)O)C5 (CCC (C5 (CC4O)C)C6CC (=O)OC6)O)CO)O)O)O)O. Density: 1.49 g/cm³. ECNumber: 214-663-0. Catalog: ACM1183353. Alfa Chemistry. 2
Cardanol monoene Cardanol monoene is also known as anacardic acid (C15:1). It inhibits the linoleic acid peroxidation catalyzed by soybean lipoxygenase-1 with an IC50 of 6.8 mM. Cardanol monoene is also a phenol found in cashew nut shell liquid that reversibly inhibits tyrosinase with an IC50 value of 56 μM in vitro. It halts the cell cycle at the S phase and inhibits proliferation dose- and time-dependently in M14 melanoma cells (IC50s = 23.15 and 12.30 μM after 24 and 48 hours of treatment, respectively). A mixture of cardanol mono-, di-, and triene is used to synthesize cardanol-metal complexes that inhibit uropathogenic E. coli biofilm formation. Synonyms: Cardanol C15:1; 6[8'(Z)-pentadecenyl]salicylic acid. Grades: ≥98%. CAS No. 501-26-8. Molecular formula: C21H34O. Mole weight: 302.5. BOC Sciences 9

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