Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C15H22O2 |
| Molecular Weight | 234.334 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@H]1[C@H](O)CCC2=CC(=O)C(C[C@]12C)=C(C)C
InChI
InChIKey=TVDMUSYVWJLIDK-PSOPSSQASA-N
InChI=1S/C15H22O2/c1-9(2)12-8-15(4)10(3)13(16)6-5-11(15)7-14(12)17/h7,10,13,16H,5-6,8H2,1-4H3/t10-,13+,15+/m0/s1
DescriptionSources: doi:10.1016/0031-9422(83)80099-5Curator's Comment: description was created based on several sources, including:
doi:10.1016/S0040-4020(01)96317-3
http://www.acgpubs.org/RNP/2014/Volume8/Issue%201/21-RNP-1211-204.pdf
Sources: doi:10.1016/0031-9422(83)80099-5
Curator's Comment: description was created based on several sources, including:
doi:10.1016/S0040-4020(01)96317-3
http://www.acgpubs.org/RNP/2014/Volume8/Issue%201/21-RNP-1211-204.pdf
The components of several Petasites species have been investigated and shown to include petasin furanopetasin derivatives belonging to the eremophilane type of sesquiterpene, and bakkenolide derivatives. It has been reported that the petasin derivatives have spasmolytic properties and bakkenolide-A has cytotoxic activity. Natural is (+)-isopetasol. It was also isolated from the rhizomes of Ligularia fischeri grown in Henan province of China. Isopetasol derivatives with an unsaturated acid ester moiety will selectively inhibit RNA synthesis in the ascites tumor of mouse.
Originator
Approval Year
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469-67-0
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11746594
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3612JYH60G
Created by
admin on Mon Mar 31 23:41:04 GMT 2025 , Edited by admin on Mon Mar 31 23:41:04 GMT 2025
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SUBSTANCE RECORD