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Details

Stereochemistry ACHIRAL
Molecular Formula C19H18O7
Molecular Weight 358.342
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RETUSIN

SMILES

COC1=CC2=C(C(=O)C(OC)=C(O2)C3=CC(OC)=C(OC)C=C3)C(O)=C1

InChI

InChIKey=HHGPYJLEJGNWJA-UHFFFAOYSA-N
InChI=1S/C19H18O7/c1-22-11-8-12(20)16-15(9-11)26-18(19(25-4)17(16)21)10-5-6-13(23-2)14(7-10)24-3/h5-9,20H,1-4H3

HIDE SMILES / InChI

Description

Retusin is an O-methylated isoflavone, a type of flavonoid. It can be found in Fabaceae species like Dipteryx odorata, in Dalbergia retusa and in Millettia nitida. Retusin exhibited potent free-radical-scavenging capacity as well as efficient inhibition of cellular melanogenesis, suggesting that it is a valuable hit compound with potential for advanced cosmeceutical development. Retusin showed efficient inhibition both of cellular melanin formation and anti-tyrosinase activity in B16F10 melanocytes. Retusin exhibited an anti-emetic effect in chick model.

Approval Year

Targets

Primary TargetPharmacologyConditionPotency
50.9 µM [IC50]
390.0 nM [IC50]

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

PubMed

Patents

Sample Use Guides

In Vivo Use Guide
Retusin inhibited emetic action of copper sulfate at two doses of 20 mg/kg and 50 mg/kg.
Route of Administration: Oral
In Vitro Use Guide
Retusin inhibited mushroom tyrosinase activity with the IC50 value of 50.9 uM at 30 min.