Name |
Theviridoside Theveside methyl ester |
Formula |
C17H24O11 |
Mw |
404.13186161 |
CAS RN |
23407-76-3 |
C_ID |
C00010720
,
|
InChIKey |
LDBMLOLBWUOZGG-IKEKUCNSNA-N |
InChICode |
InChI=1S/C17H24O11/c1-25-14(23)8-6-26-15(10-7(4-18)2-3-17(8,10)24)28-16-13(22)12(21)11(20)9(5-19)27-16/h2,6,9-13,15-16,18-22,24H,3-5H2,1H3/t9-,10+,11-,12+,13+,15+,16-,17+/m1/s1 |
SMILES |
[C@@]12([C@H]([C@@H](OC=C1C(=O)OC)O[C@H]1O[C@@H]([C@H]([C@@H]([C@@H]1O)O)O)CO)C(=CC2)CO)O |
Start Substs in Alk. Biosynthesis (Prediction) |
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Organism |
Kingdom |
Family |
Species |
Reference |
Plantae | Apocynaceae | Thevetia neriifolia | Ref. |
Plantae | Apocynaceae | Thevetia peruviana | Ref. |
Plantae | Verbenaceae | Lantana camara | Ref. |
Plantae | Verbenaceae | Lantana camera L. | Ref. |
Plantae | Verbenaceae | Verbenoxylum reitzii | Ref. |
- | - | Pithecotenium crucigerum (L.) A.H Gentry | Ref. |
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Organism | Lantana camara | Reference | Edited by Jiangsu New Medicinal College, Chinese Medicine Dictionary, Shanghai Science and technology Press, Shanghai, (1979).
Pan, et al., APS, 27, (1992), 515.
TEWTRAKUL, et al., Chem Pharm Bull, 50, (2002), 630 |
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