ChemicalBook--->CAS DataBase List--->152464-78-3

152464-78-3

152464-78-3 Structure

152464-78-3 Structure
IdentificationBack Directory
[Name]

Leachianone G
[CAS]

152464-78-3
[Synonyms]

Leachianone G
(2S)-2-(2,4-Dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one
4H-1-Benzopyran-4-one, 2-(2,4-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-8-(3-methyl-2-buten-1-yl)-, (2S)-
[Molecular Formula]

C20H20O6
[MOL File]

152464-78-3.mol
[Molecular Weight]

356.37
Chemical PropertiesBack Directory
[Boiling point ]

639.6±55.0 °C(Predicted)
[density ]

1.384±0.06 g/cm3(Predicted)
[solubility ]

Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
[form ]

Powder
[pka]

7.65±0.40(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Uses]

Leachianone G is an antiviral flavonoid from the root bark of Morus alba L. Leachianone G shows potent antiviral activity against herpes simplex type 1 virus (HSV-1) with an IC50 value of 1.6 μg/mL[1].
[Definition]

ChEBI: Leachianone G is a tetrahydroxyflavanone having the hydroxy groups at the 2'-, 4'-, 5- and 7-positions and a prenyl group at 8-position. It is a tetrahydroxyflavanone, a member of 4'-hydroxyflavanones and a (2S)-flavan-4-one. It is functionally related to a (S)-naringenin. It is a conjugate acid of a leachianone G(1-).
[IC 50]

HSV-1: 1.6 μg/mL (IC50)
[References]

[1] Du J, et al. Antiviral flavonoids from the root bark of Morus alba L. Phytochemistry. 2003 Apr;62(8):1235-8. DOI:10.1016/s0031-9422(02)00753-7
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