NatID | 592 |
Common Name | grindelic acid |
Molecular Formula | C20H32O3 |
Chemical Class | Prenol lipids > Diterpenoids |
Molecular Weight | 320.235 g/mol |
Other names |
Smiles | CC1=CC[C@H]2C(C)(C)CCC[C@]2(C)[C@@]12CC[C@@](C)(CC(=O)O)O2 |
Inchi | InChI=1S/C20H32O3/c1-14-7-8-15-17(2,3)9-6-10-19(15,5)20(14)12-11-18(4,23-20)13-16(21)22/h7,15H,6,8-13H2,1-5H3,(H,21,22)/t15-,18-,19-,20+/m0/s1 |
Inchi Key | XLWWERNKTLITEF-MVJPYGJCSA-N |
3D Structure |
clogP | 4.95 |
TPSA | 46.53 |
HBD | 1 |
HBA | 2 |
Rotatable Bonds | 2 |
Aromatic Rings | 0 |
Heavy Atoms | 23 |
Aromatic Carbocycles | 0 |
Aromatic Heterocycles | 0 |
Number of NO | 3 |
EID | Source | Semisynthetic? | Confidence level | References |
---|---|---|---|---|
9447 | Grindelia pulchella | No | Very High | Reta, G. F., Chiaramello, A. I., García, C., León, L. G., Martín, V. S., Padrón, J. M., Tonn, C. E., & Donadel, O. J. (2013). Derivatives of grindelic acid: From a non-active natural diterpene to synthetic antitumor derivatives. European Journal of Medicinal Chemistry, 67, 28–38. https://doi.org/10.1016/j.ejmech.2013.06.013 |
9916 | Grindelia chiloensis | No | High |
Bioassay ID | NPASS ID | Target | Activity type | Activity |
---|---|---|---|---|
Loading... |