Diastereoisomeric ent-Labdane Diterpenoids from Andrographis paniculata
โ Scribed by Yong-Mei Hu; Guo-Cai Wang; Ying Wang; Herman H.-Y. Sung; Ian D. Williams; Wen-Cai Ye
- Publisher
- John Wiley and Sons
- Year
- 2012
- Tongue
- German
- Weight
- 374 KB
- Volume
- 95
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
โฆ Synopsis
Four C(8),C(12)-diastereoisomers, (8S,12S)-isoandrographolide (1), (8S,12R)-isoandrographolide (2), (8R,12R)-isoandrographolide (3), and (8R,12S)-isoandrographolide (4) were isolated from the aerial parts of Andrographis paniculata. The structures of the new compounds 1 -3 were established on the basis of the spectroscopic data including UV, IR, NMR, HR-ESI-MS, and X-ray diffraction analysis.
๐ SIMILAR VOLUMES
Nine new ent-labdane-type diterpenoids (1 -9), mostly in the form of the corresponding 16,15-lactones, were isolated from the 85%-EtOH extract of the aerial parts of Andrographis paniculata NEES., together with nine known compounds (10 -18). Their structures were deduced by in-depth NMR spectroscopy
A rapid and simple high-performance thin-layer chromatographic (HPTLC) method has been developed for the simultaneous quantitative estimation of the biologically active diterpenoids, 14-deoxy-11,12didehydroandrographolide, andrographolide, neoandrographolide and andrographiside in Andrographis panic
## Abstract An extensive study of metabolites present in __Excoecaria agallocha__ Linn. led to the isolation of three new __ent__โlabdaneโtype diterpenoids, named agallochaexcoerins AโC (**1**โ**3**), besides three known compounds. The skeleton present in compound **1** is rather unusual, containin