INTEGRISTERONE A,22-DEOXY
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Drawn and modelled with RDKit, 3D viewer 3Dmol.js. PubChem CID 70691108
Name
INTEGRISTERONE A,22-DEOXY
IUPAC name
(1S,2R,3R,5R,9R,10R,13R,14S,17S)-17-((S)-2,6-dihydroxy-6-methylheptan-2-yl)-1,2,3,14-tetrahydroxy-10,13-dimethyl-1,2,3,4,5,9,10,11,12,13,14,15,16,17-tetradecahydro-6H-cyclopenta[a]phenanthren-6-one
SMILES
C[C@]34CC[C@H]1C(=CC(=O)[C@H]2[C@@]1([C@@H]([C@@H]([C@@H](C2)O)O)O)C)[C@@]3(CC[C@@H]4[C@](C)(C([H])CCC(C)(C)O)O)O
Molecular formula
C27H44O7
Molecular weight
480.64 g/mol
Monoisotopic mass
480.3087 Da
Chemical classification: NPClassifier (Kim et al., 2021)
| Plant | Plant part | Amount | Reference |
|---|---|---|---|
| Silene italica (L.) Pers. subsp. italica | aerial parts | - |
Simon, A., Pongracz, Z., Toth, G., Mak, M., Mathe, I., Banthori, M. (2004). A new ecdysteroid with unique 9 beta-oh and four other ecdysteroids from Silene italica ssp. nemoralis. Steroids, 69(6), 389-394 doi:10.1016/j.steroids.2004.03.009
|
| Silene nutans L. subsp. nutans | - | - |
Girault, J.P., Bathori, M., Varga, E., Szendrei, K., Lafont, R. (1990). Isolation and identification of new ecdysteroids from the Caryophyllaceae. J Nat Prod, 53(2), 279-293 doi:10.1021/np50068a002
|