Secondary metabolites from the roots of Phlomis umbrosa.J Asian Nat Prod Res. 2011 Mar; 13(3):230-7.JA
Abstract
The phytochemical study of the roots of Phlomis umbrosa Turcz afforded a new phenylethanoid glycoside, 3-hydroxy-4-methoxy-β-phenylethoxy-O-[2,3-diacetyl-α-l-rhamnopyranosyl-(1 → 3)]-4-O-cis-feruloyl-[β-d-apiofuranosyl-(1 → 6)]-β-d-glucopyranoside (1), and two new 28-noroleanane-derived spirocyclic triterpenoids, phlomishexaol C (2) and phlomishexaol D (3). Their structures were elucidated on the basis of 1D and 2D NMR analyses, in combination with high-resolution MS experiment.
Links
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
21409684
Citation
Deng, Rui-Xue, et al. "Secondary Metabolites From the Roots of Phlomis Umbrosa." Journal of Asian Natural Products Research, vol. 13, no. 3, 2011, pp. 230-7.
Deng RX, Duan WL, Liu P, et al. Secondary metabolites from the roots of Phlomis umbrosa. J Asian Nat Prod Res. 2011;13(3):230-7.
Deng, R. X., Duan, W. L., Liu, P., Yang, Y. L., & Yin, W. P. (2011). Secondary metabolites from the roots of Phlomis umbrosa. Journal of Asian Natural Products Research, 13(3), 230-7. https://doi.org/10.1080/10286020.2010.550886
Deng RX, et al. Secondary Metabolites From the Roots of Phlomis Umbrosa. J Asian Nat Prod Res. 2011;13(3):230-7. PubMed PMID: 21409684.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Secondary metabolites from the roots of Phlomis umbrosa.
AU - Deng,Rui-Xue,
AU - Duan,Wen-Lu,
AU - Liu,Pu,
AU - Yang,You-Liang,
AU - Yin,Wei-Ping,
PY - 2011/3/17/entrez
PY - 2011/3/17/pubmed
PY - 2011/5/19/medline
SP - 230
EP - 7
JF - Journal of Asian natural products research
JO - J Asian Nat Prod Res
VL - 13
IS - 3
N2 - The phytochemical study of the roots of Phlomis umbrosa Turcz afforded a new phenylethanoid glycoside, 3-hydroxy-4-methoxy-β-phenylethoxy-O-[2,3-diacetyl-α-l-rhamnopyranosyl-(1 → 3)]-4-O-cis-feruloyl-[β-d-apiofuranosyl-(1 → 6)]-β-d-glucopyranoside (1), and two new 28-noroleanane-derived spirocyclic triterpenoids, phlomishexaol C (2) and phlomishexaol D (3). Their structures were elucidated on the basis of 1D and 2D NMR analyses, in combination with high-resolution MS experiment.
SN - 1477-2213
UR - https://www.unboundmedicine.com/medline/citation/21409684/Secondary_metabolites_from_the_roots_of_Phlomis_umbrosa_
L2 - https://www.tandfonline.com/doi/full/10.1080/10286020.2010.550886
DB - PRIME
DP - Unbound Medicine
ER -