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[(25R)-2α-Hydroxyspirosta-5-ene-3β-yl]4-O-(2-O-β-D-glucopyranosyl-3-O-β-D-xylopyranosyl-β-D-glucopyranosyl)-β-D-galactopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70880-60-3

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70880-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70880-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,8,8 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70880-60:
(7*7)+(6*0)+(5*8)+(4*8)+(3*0)+(2*6)+(1*0)=133
133 % 10 = 3
So 70880-60-3 is a valid CAS Registry Number.

70880-60-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name karatavioside A

1.2 Other means of identification

Product number -
Other names (25R)-2α-hydroxyspirost-5-en-3β-yl O-β-d-glucopyranosyl-(1 → 2)-[β-d-xylopyranosyl-(1 → 3)]-β-d-glucopyranosyl-(1 → 4)-β-d-galactopyranoside

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:70880-60-3 SDS

70880-60-3Upstream product

70880-60-3Downstream Products

70880-60-3Relevant academic research and scientific papers

Karataviosides G-K, five new bisdesmosidic steroidal glycosides from the bulbs of Allium karataviense

Kuroda, Minpei,Ori, Kazutomo,Takayama, Hiroshi,Sakagami, Hiroshi,Mimaki, Yoshihiro

, p. 96 - 104 (2015/01/16)

We have analyzed the steroidal glycosides in Allium karataviense bulbs, and isolated five new bisdesmosidic steroidal glycosides: karataviosides G-K (1-5). The structures were elucidated by extensive spectroscopic analysis, including 2D NMR and enzymatic and hydrolytic cleavage. Karatavioside G (1) is an entirely novel furostanol glycoside, which has an O-β-d-glucopyranosyl-(1 → 6)-β-d-glucopyranosyl-(1 → 6)-β-d-glucopyranosyl unit at C-26 of the aglycone. Although a variety of cholestanol glycosides have been isolated, mainly from Liliaceae and Agavaceae, karataviosides J and K (4 and 5) are also notable because they are the most polar cholestanol bisdesmosides discovered, in which a lycotetraose is attached to C-3 of the aglycone, and a glucose or O-glucosyl-(1 → 3)-glucose is attached at C-16. The isolated glycosides were also evaluated for their cytotoxic activities against cultured tumor cell lines.

STEROID SAPONINS AND SAPOGENINS OF Allium. THE STRUCTURE OF KARATAVIOSIDE B

Bollerner, Yu. S.,Abdullaev, N. D.,Gorovits, M. B.,Abubakirov, N. K.

, p. 186 - 190 (2007/10/02)

A new glycoside of the spirostan series - karatavioside B (I) - has been isolated from an ethanolic extract of the inflorescences of Allium karataviense Rgl. (family Liliaceae).On the basis of chemical transformations and spectral characteristics the structure of (I) has been established as 25(R)-spirost-5-ene-2α,3β-diol S-O--(1-3)>--O-β-D-glucopyranosyl-(1-4)-β-D-galactopyranoside>.

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