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Details

Stereochemistry ABSOLUTE
Molecular Formula C25H22O10
Molecular Weight 482.4362
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ISOSILYBIN A

SMILES

COC1=C(O)C=CC(=C1)[C@H]2OC3=CC=C(C=C3O[C@@H]2CO)[C@H]4OC5=CC(O)=CC(O)=C5C(=O)[C@@H]4O

InChI

InChIKey=FDQAOULAVFHKBX-HKTJVKLFSA-N
InChI=1S/C25H22O10/c1-32-17-6-11(2-4-14(17)28)24-20(10-26)33-18-7-12(3-5-16(18)34-24)25-23(31)22(30)21-15(29)8-13(27)9-19(21)35-25/h2-9,20,23-29,31H,10H2,1H3/t20-,23+,24-,25-/m1/s1

HIDE SMILES / InChI

Description

Milk thistle (Silybum marianum) has been used for centuries for the treatment of liver disorders and as a hepatoprotectant. The primary extract of milk thistle is termed silymarin, a complex mixture that contains a number of structurally-related flavonolignans, the flavonoid, taxifolin, and a number of other constituents. The major flavonolignans present in most extracts are silybin A, silybin B, isosilybin A and isosilybin B, silydianin, silychristin and isosilychristin. Isosilybin A has been identified as the first flavonolignan PPAR-gamma agonist. Isosilybin A, elicited the strongest anti-NF-kappaB and anti-HCV actions. The data suggest that silymarin-derived compounds may influence HCV disease course in some patients. Isosilybin A activates apoptotic machinery in prostate cancer cells via targeting Akt-NF-κB-AR axis; thereby, indicating a promising role for this phytochemical in the management of clinical prostate cancer.

Approval Year

Targets

Primary TargetPharmacologyConditionPotency
100.0 µM [IC50]

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown
Primary
Unknown

PubMed

Sample Use Guides

In Vivo Use Guide
Mice: 50 and 100 mg/kg body weight
Route of Administration: Oral
In Vitro Use Guide
Isosilybin A (1, 3, 10 and 30 uM) concentration-dependently induced cholesterol efflux from 1 to 30 uM (EC50 =4.1 uM), mimicking the effect of pioglitazone (10 uM), a well-established PPAR-gamma agonist.