Leachianone G

Modify Date: 2025-08-25 15:22:41

Leachianone G Structure
Leachianone G structure
Common Name Leachianone G
CAS Number 152464-78-3 Molecular Weight 356.369
Density 1.4±0.1 g/cm3 Boiling Point 639.6±55.0 °C at 760 mmHg
Molecular Formula C20H20O6 Melting Point N/A
MSDS N/A Flash Point 231.4±25.0 °C

 Use of Leachianone G


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].

 Names

Name Leachianone G
Synonym More Synonyms

 Leachianone G Biological Activity

Description 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].
Related Catalog
Target

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.  

 Chemical & Physical Properties

Density 1.4±0.1 g/cm3
Boiling Point 639.6±55.0 °C at 760 mmHg
Molecular Formula C20H20O6
Molecular Weight 356.369
Flash Point 231.4±25.0 °C
Exact Mass 356.125977
PSA 107.22000
LogP 4.56
Vapour Pressure 0.0±2.0 mmHg at 25°C
Index of Refraction 1.664

 Safety Information

Hazard Codes Xi

 Synonyms

4H-1-Benzopyran-4-one, 2-(2,4-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-8-(3-methyl-2-butenyl)-, (2S)-
(2S)-2-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-8-(3-methyl-2-buten-1-yl)-2,3-dihydro-4H-chromen-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)-
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.
Top Suppliers:I want be here


Get all suppliers and price by the below link:

Leachianone G suppliers

Leachianone G price

Related Compounds: More...
Leachianone A
97938-31-3
Gancaonin G
126716-34-5
luffariolide G
147663-79-4
Palavit G
130661-21-1
Saikosaponin G
99365-19-2
Benzo[g]pyridazino[1,2-b]phthalazine-6,13-dione, 1,4-dihydro-
65417-03-0
benzo[g]quinoline-2,4-dicarboxylic acid
2770-31-2
Benzo[g]chrysene-9-carboxaldehyde
159692-75-8
Benzenebutanenitrile, g-(1-methylethoxy)-
70289-00-8
2-[(2R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-(4-hydroxyphenyl)-N-methylpropanamido]acetic acid
2171218-76-9
3-{4-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]phenyl}butanoic acid
2171619-27-3
(2S)-2-{3-[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)phenyl]butanamido}propanoic acid
2648911-34-4
2-ethyl-1-[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2,2-dimethylbutanoyl]pyrrolidine-2-carboxylic acid
2172281-36-4
2-[3-cyclopropyl-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]cyclohexane-1-carboxylic acid
2171661-27-9
1-{[3-cyclopropyl-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]methyl}cyclopentane-1-carboxylic acid
2171624-86-3
3-cyclopropyl-2-({5-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]oxolan-2-yl}formamido)propanoic acid
2171696-34-5
3-cyclopropyl-2-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2-(thiophen-2-yl)acetamido]propanoic acid
2171496-52-7
1-[(2S)-3-cyclopropyl-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanoyl]-4-methylpiperidine-4-carboxylic acid
2171147-68-3
1-[(2S)-3-cyclopropyl-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanoyl]-3-methylpiperidine-3-carboxylic acid
2171426-52-9