NatID | 962 |
Common Name | NatID_962 |
Molecular Formula | C20H34O3 |
Chemical Class | Prenol lipids > Diterpenoids |
Molecular Weight | 322.251 g/mol |
Other names |
Smiles | CC1=CC[C@H]2C(C)(C)[C@@H](O)CC[C@]2(C)[C@H]1CC[C@H](C)CC(=O)O |
Inchi | InChI=1S/C20H34O3/c1-13(12-18(22)23)6-8-15-14(2)7-9-16-19(3,4)17(21)10-11-20(15,16)5/h7,13,15-17,21H,6,8-12H2,1-5H3,(H,22,23)/t13-,15-,16-,17-,20+/m0/s1 |
Inchi Key | LAGHKRLLDKVJHS-GINSCSNVSA-N |
3D Structure |
clogP | 4.65 |
TPSA | 57.53 |
HBD | 2 |
HBA | 2 |
Rotatable Bonds | 5 |
Aromatic Rings | 0 |
Heavy Atoms | 23 |
Aromatic Carbocycles | 0 |
Aromatic Heterocycles | 0 |
Number of NO | 3 |
EID | Source | Semisynthetic? | Confidence level | References |
---|---|---|---|---|
9049 | Baccharis scandens | No | Very High | Gianello, J. C., Pestchanker, M. J., Tonn, C. E., Guo, M., & Giordano, O. S. (1990). 2α,3α-Dihydroxycativic acid, a diterpenoid from Baccharis petiolata. Phytochemistry, 29(2), 656–659. https://doi.org/10.1016/0031-9422(90)85138-6 |
Bioassay ID | NPASS ID | Target | Activity type | Activity |
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