86541-83-5

Upstream product

• 88192-83-0 cyclosiversioside H 
• 84687-46-7 (3β,6α,16β,20R,24S)-20,24-epoxy-16-hydroxy-3-(β-D-xylopyranosyloxy)-9,19-cyclolanostane-6,25-diyl bis[β-D-glucopyranoside] 
• 83207-58-3 astragaloside IV 
• 83207-58-3 cyclosieversioside F 
• 84687-44-5 astragaloside V 
• 84687-42-3 astragaloside III 
• 86408-19-7 Cyclosiversigenin 3-O-2)-β-D-xylopyranoside> 
• 88192-84-1 askenoside B 
• 86408-17-5 askendoside D 

Downstream Products

• 84605-18-5 cycloastragenol 
• 84687-42-3 astragaloside III 

Relevant academic research and scientific papers

Compositions and methods for skin conditioning

Methods and cosmetic compositions for conditioning the skin, utilizing as active ingredients selected compounds structurally related to astragenols, cycloastragenols, and/or protopanaxatriols, are provided. Such compounds include those of formulas (I), (II) and (III) described herein.

Triterpene glycosides of Tragacantha stipulosa and their genins. Structures of askendosides G and D and cycloglobiceposide B from one- and two-dimensional 1H and 13C NMR spectroscopy

Roots of Tragacantha stipulosa Boriss yielded three triterpene glycosides of the cycloartane series: askendoside G (1), askendoside D (2), and cycloglobiceposide B (3). Glycoside 1 is 3-O-α-L-arabinopyranosyl-(1 → 2)-β-D-xylopyranoside; 16-O-β-D-glucopyra

Cyclosieversigenin 3-O-β-D-glucopyranoside from Astragalus kuhitangi

Cyclosieversigenin, cyclosieversigenin 3-O-β-D-xylopyranoside, cyclosieversioside F, astragaloside VII, and, for the first time in native form, cyclosieversigenin 6-O-β-D-glucopyranoside have been isolated from the roots of Astragalus kubitangi (Nevski) Sirj.

TRITERPENE GLYCOSIDES OF Astragalus AND THEIR GENINS. IX. ASKENDOSIDE D FROM Astragalus taschkendicus

A new glycoside of the cycloartane series - askendoside D - has been isolated from the roots of the plants Astragalus taschkendicus Bge., and on the basis of chemical transformations and spectral characteristics its structure has been established as 20S,24R-epoxycycloartane-3β,6α,16β,25-tetraol 3-O- 2)-β-D-xylopyranoside> 6-O-β-D-xylopyranoside.

TRITERPENE GLYCOSIDES OF Astragalus AND THEIR GENINS. XIII. THE STRUCTURE OF CYCLOSIVERSIOSIDE H - A TRIGLYCERIDE FROM Astragalus sieversianus

A new triglycoside of the cycloartane series has been isolated from the roots of Astragalus sieversianus Pall.; it is cyclosieversigenin 6-O-β-D-glucopyranoside 3-O-2)-β-D-xylopyranoside>.

TRITERPENE GLYCOSIDES OF Astragalus AND THEIR GENINS. XII. ASKENDOSIDE B FROM Astragalus taschkendicus

On the basis of chemical transformations and with the aid of physicochemical characteristics it has been established that a new glycoside of the cycloartane series - askendoside B (I) - isolated from the roots of Astragalus taschkendicus Bge., is 20S,24R-epoxycycloartane-3β,6α,16β,25-tetraol 3-O-2)-(3'-O-acetyl-β-D-xylopyranoside)> 6-O-β-D-xylopyranoside, C47H76O18, mp 215-218 deg C, 20D -45.5 deg (c 1.1; pyridine).The acid hydrolysis of (I) yielded cyclosiversigenin (II) with mp 239-241 deg C, 20D +54.5 deg (c 1.2; MeOH), and cyclosiversigenin 3-O-β-D-xylopyranoside (III) with mp 262-264 deg C, 20D +41 deg (c 0.4; MeOH).The periodate oxidation of glycoside (I) followed by acid hydrolysis likewise led to (II) and to D-xylose.The alkaline hydrolysis of (I) yielded askendoside D (IV), with mp 235-236 deg C, 23D -8.5 deg (c 1.0; pyridine).The Smith degradation of (I) led to (III).The IR and PMR spectra of (I) are given.

TRITERPENE GLYCOSIDES OF Astragalus AND THEIR GENINS. V. STRUCTURE OF CYCLOSIEVERSIOSIDE F

A new glycoside of the cycloartane series has been isolated from the roots of the plant Astragalus sieversianus Pall. and it has been shown to be cyclosieversigenin 6-O-β-D-glucopyranoside 3-O-β-D-xylopyranoside.