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87425-34-1

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87425-34-1 Usage

Uses

Liriopesides B is the main saponin content in Hubei liriope (Liriope spicata var. prolifera). Liriopesides B exhibites potential anticancer activity against human ovarian cancer A2780 cells.

Check Digit Verification of cas no

The CAS Registry Mumber 87425-34-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,4,2 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 87425-34:
(7*8)+(6*7)+(5*4)+(4*2)+(3*5)+(2*3)+(1*4)=151
151 % 10 = 1
So 87425-34-1 is a valid CAS Registry Number.

87425-34-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name β-D-Galactopyranoside, (1β,3β,25S)-3-[(6-deoxy-α-L-mannopyranosyl)oxy]spirost-5-en-1-yl 6-deoxy-

1.2 Other means of identification

Product number -
Other names Nolinospiroside F

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:87425-34-1 SDS

87425-34-1Upstream product

87425-34-1Relevant articles and documents

Steroidal glycosides from the subterranean parts of Liriope spicata var. prolifera

Yu, Bo-Yang,Qiu, Sheng-Xiang,Zaw, Kyaw,Xu, Guo-Jun,Hirai, Yusuaki,Shoji, Junzo,Fong, Harry H. S.,Kinghorn, A. Douglas

, p. 201 - 206 (1996)

In a continuation of phytochemical studies on the underground organs of Liriope spicata var. prolifera, four new steroidal glycosides, lirioproliosides A-D, along with two known compounds, 25(S)-ruscogenin 1- O[a-L-rhamnopyranosyl(1 → 2)]β-D-xylopyranosyl(1 → 3)-β-D-fucopyranoside and ophiopogonin A, were identified. The structures of lirioproliosides A-D were established by a combination of spectroscopic and chemical methods as 25(S)-ruscogenin 1-O-[α-L-rhamnopyranosyl(1 → 2)][β-D-xylopyranosyl(1 → 3)]-β-D-fucopyranoside-3-O-α-L-rhamnopyranoside, 25(S)-ruscogenin 1-O-[3- O-acetyl-α-L-rhamnopyranosyl(1 → 2)]-β-D-fucopyranoside, 25(S)-ruscogenin (1-O-[2-O-acetyl-α-L-rhamnopyranosyl(1 → 2)]-β-D-fucopyranoside and ruscogenin (1-O-[2-O-acetyl-α-L-rhamnopyranosyl(I → 2)]-β-D- fucopyranoside, respectively. Among these steroidal glycosides, ophiopogonm A and lirioprolioside B, and lirioproliosides C and D, were isolated as epimeric pairs.

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