Isobavachin

Modify Date: 2024-01-02 19:23:42

Isobavachin Structure
Isobavachin structure
 Common Name Isobavachin
CAS Number 31524-62-6 Molecular Weight 324.370
Density 1.2±0.1 g/cm3 Boiling Point 558.3±50.0 °C at 760 mmHg
Molecular Formula C20H20O4 Melting Point 187-188℃
MSDS N/A Flash Point 202.1±23.6 °C

 Use of Isobavachin


Isobavachin, an antioxidant isaolated from Psoralea morisiana with a prenyl group at position 8 of ring A, promotes neuronal differentiation and the potential role of its protein prenylation[1][2].

 Names

Name Isobavachin
Synonym More Synonyms

 Isobavachin Biological Activity

Description Isobavachin, an antioxidant isaolated from Psoralea morisiana with a prenyl group at position 8 of ring A, promotes neuronal differentiation and the potential role of its protein prenylation[1][2].
Related Catalog
References

[1]. Wang DY, et al. Promoting effects of isobavachin on neurogenesis of mouse embryonic stem cells were associated with protein prenylation. Acta Pharmacol Sin. 2011 Apr;32(4):425-32.

[2]. Antonella Rosa, et al. Antioxidant properties of extracts and compounds from Psoralea morisiana. European Journal of Lipid Science and Technology. 2005.

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 558.3±50.0 °C at 760 mmHg
Melting Point 187-188℃
Molecular Formula C20H20O4
Molecular Weight 324.370
Flash Point 202.1±23.6 °C
Exact Mass 324.136169
PSA 66.76000
LogP 4.85
Vapour Pressure 0.0±1.6 mmHg at 25°C
Index of Refraction 1.622
Storage condition 2-8C

 Safety Information

HS Code 2932999099

 Precursor & DownStream

Precursor  2

DownStream  0

 Customs

HS Code 2932999099
Summary 2932999099. other heterocyclic compounds with oxygen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Synonyms

4',7-dihydroxy-8-prenylflavanone
(+-)-6-chloro-7
4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-, (2S)-
C16H16ClNO2
SK&6-Chlor-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepin
(2S)-7-Hydroxy-2-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-2,3-dihydro-4H-chromen-4-one
6-chloro-1-phenyl-2,3,4,5-tetrahydro-1h-3-benzazepine-7,8-diol
6-Chloro-2,3,4,5-tetrahydro-1-phenyl-1H-3-benzazepine-7,8-diol
8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine
1H-3-Benzazepine-7,8-diol,6-chloro-2,3,4,5-tetrahydro-1-phenyl
8-prenylliquiritigenin
8-dimethylallylliquiritigenin
6-chloro-7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine
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