Rhodiolosides A-E, monoterpene glycosides from Rhodiola rosea.

Five new monoterpene glycosides, rhodiolosides A-E (1-5), were isolated from the roots of Rhodiola rosea (Crassulaceae). Their structures were elucidated as (2E,6E,4R)-4,8-dihydroxy-3,7-dimethyl-2,6-octadienyl beta-D-glucopyranoside (1), (2E,4R)-4-hydroxy-3,7-dimethyl-2,6-octadienyl alpha-D-glucopyranosyl(1-->6)-beta-D-glucopyranoside (2), (2E,4R)-4-hydroxy-3,7-dimethyl-2,6-octadienyl beta-D-glucopyranosyl(1-->3)-beta-D-glucopyranoside (3), (2E,4R)-4,7-dihydroxy-3,7-dimethyl-2-octenyl beta-D-glucopyranoside (4), and (2E)-7-hydroxy-3,7-dimethyl-2-octenyl alpha-L-arabinopyranosyl(1-->6)-beta-D-glucopyranoside (5), on the basis of various spectroscopic analyses and chemical degradation.

[1]  Farhath Khanum,et al.  Rhodiola rosea: A Versatile Adaptogen. , 2005, Comprehensive reviews in food science and food safety.

[2]  Wei Li,et al.  Cynanosides A–J, ten novel pregnane glycosides from Cynanchum atratum , 2005 .

[3]  Wei Li,et al.  Silenorubicosides A-D, triterpenoid saponins from Silene rubicunda. , 2005, Journal of natural products.

[4]  Wei Li,et al.  New phenolic glycosides from the seeds of Cucurbita moschata. , 2005, Chemical & pharmaceutical bulletin.

[5]  Wei Li,et al.  Nigramides A-S, dimeric amide alkaloids from the roots of Piper nigrum. , 2005, The Journal of organic chemistry.

[6]  D. Ferreira,et al.  Lotaustralin from Rhodiola rosea roots. , 2004, Fitoterapia.

[7]  J. Rohloff Volatiles from rhizomes of Rhodiola rosea L. , 2002, Phytochemistry.

[8]  S. Kadota,et al.  Prolyl endopeptidase inhibitors from the underground part of Rhodiola sachalinensis. , 2001, Chemical & pharmaceutical bulletin.

[9]  I. Khan,et al.  Analysis of the marker compounds of Rhodiola rosea L. (golden root) by reversed phase high performance liquid chromatography. , 2001, Chemical & pharmaceutical bulletin.

[10]  H. Shimoda,et al.  Bioactive constituents of Chinese natural medicines. IV. Rhodiolae radix. (2).: On the histamine release inhibitors from the underground part of Rhodiola sacra (Prain ex Hamet) S. H. Fu (Crassulaceae): chemical structures of rhodiocyanoside D and sacranosides A and B. , 1997, Chemical & pharmaceutical bulletin.

[11]  T. Kusumi,et al.  High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids , 1991 .

[12]  H. Okabe,et al.  Gas-liquid chromatographic separation of aldose enantiomers as trimethylsilyl ethers of methyl 2-(polyhydroxyalkyl)thiazolidine-4(R)-carboxylates , 1987 .