Angustific acid
Appearance
Names | |
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IUPAC names
A:(2Z)-6-[(1R,3S,6S,10S,11S,12R,17R)-17-Isopropenyl-6,10-dimethyl-14-oxo-13-oxapentacyclo[10.4.2.01,3.03,11.06,10]octadec-7-en-7-yl]-2-methyl-2,6-heptadienoic acid
B: (2Z,6S)-6-[(3S,3aS,3bR,4S,6S,6aR,7aS,9aS)-6a-(2-Carboxyethyl)-3,4-dihydroxy-6-isopropenyl-3a,9a-dimethyl-3a,3b,4,5,6,6a,7,8,9,9a-decahydro-3H-cyclopenta[a]cyclopropa[e]naphthalen-1-yl]-6-hydroxy-2-methyl-2-heptenoic acid | |
Identifiers | |
3D model (JSmol)
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ChEMBL | |
ChemSpider | |
PubChem CID
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Properties | |
A: C30H40O4 B:C30H44O7 | |
Molar mass | A: 464.64 g/mol B: 516.67 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Angustific acid A and angustific acid B are antiviral compounds isolated from Kadsura angustifolia.[1] They are triterpenoids.[2]
See also
[edit]References
[edit]- ^ Sun, R.; Song, HC.; Wang, CR.; Shen, KZ.; Xu, YB.; Gao, YX.; Chen, YG.; Dong, JY. (Feb 2011). "Compounds from Kadsura angustifolia with anti-HIV activity". Bioorg Med Chem Lett. 21 (3): 961–5. doi:10.1016/j.bmcl.2010.12.055. PMID 21232955.
- ^ Xia, Yong-Gang; Yang, Bing-You; Kuang, Hai-Xue (April 2015). "Schisandraceae triterpenoids: a review". Phytochemistry Reviews. 14 (2): 155–187. Bibcode:2015PChRv..14..155X. doi:10.1007/s11101-014-9343-7. ISSN 1568-7767. S2CID 6920531.