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Bavachin significantly inhibits melanin synthesis and TYR activity
Smiles: CC(C)(C)OC(=O)CCOCCOCCOCCOCCOCCOCCOCCOCC#C
CC(C)(C)C1C=CC(=CC=1)C(=O)NC1=CN2C=C(C=CC2=N1)N1C=NC=C1
After stimulation of bpV(phen)
mutant-selective
Alpha-Naphthoflavone xifene acetate Bavachin significantly inhibits melanin synthesisAlpha Naphthoflavone is a synthetic flavonoid, acts as a potent and competitive aromatase inhibitor with an IC50 and a Ki of 0. 5 and 0. 2 M, respectively. Product information CAS Number: 604 59 1 Molecular Weight: 272. 30 Formula: C19H12O2 Chemical Name: 2 phenyl 4H benzo[h]chromen 4 one Smiles: O=C1C=C(OC2C3=CC=CC=C3C=CC=21)C1C=CC=CC=1 InChiKey: VFMMPHCGEFXGIP UHFFFAOYSA N InChi: InChI=1S C19H12O2 c20 17 12 18(14 7 2 1 3 8 14)21 19 15 9 5 4 6
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