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Oleanolic acid-3-O-beta-D-xylopyranoside is a triterpenoid compound derived from various plant sources such as fruits, vegetables, and herbs. It is known for its potential pharmacological properties, including anti-inflammatory, antioxidant, anti-tumor, and hepatoprotective effects. Its ability to modulate different signaling pathways in the body makes it a promising candidate for the development of new pharmaceutical drugs and natural health products.

61617-29-6

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61617-29-6 Usage

Uses

Used in Pharmaceutical Industry:
Oleanolic acid-3-O-beta-D-xylopyranoside is used as a therapeutic agent for its potential applications in treating various health conditions, such as cancer, liver diseases, and inflammation-related disorders. Its anti-inflammatory, antioxidant, anti-tumor, and hepatoprotective properties make it a valuable compound for the development of new pharmaceutical drugs.
Used in Natural Health Products:
Oleanolic acid-3-O-beta-D-xylopyranoside is used as an active ingredient in natural health products due to its potential health benefits. Its presence in various plant sources allows for its incorporation into dietary supplements, herbal remedies, and other natural health products to support overall health and well-being.
Further research is ongoing to explore the full therapeutic potential of Oleanolic acid-3-O-beta-D-xylopyranoside and possible side effects, ensuring its safe and effective use in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 61617-29-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,1 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61617-29:
(7*6)+(6*1)+(5*6)+(4*1)+(3*7)+(2*2)+(1*9)=116
116 % 10 = 6
So 61617-29-6 is a valid CAS Registry Number.

61617-29-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Songoroside A

1.2 Other means of identification

Product number -
Other names -

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:61617-29-6 SDS

61617-29-6Relevant academic research and scientific papers

New cytotoxic oleanane saponins from the infructescences of Polyscias amplifolia from the Madagascar rainforest

Chaturvedula, V. S. Prakash,Schilling, Jennifer K.,Miller, James S.,Andriantsiferana, Rabodo,Rasamison, Vincent E.,Kingston, David G. I.

, p. 440 - 444 (2007/10/03)

Bioassay-guided fractionation of an ethanolic extract of the infructescences of Polyscias amplifolia resulted in the isolation of two new oleanolic acid saponins, polyfoliolides A (1) and B (2), in addition to the two known saponins 3-O-β-D-galactopyrano-syloleanolic acid (3) and 3-O-β-D-galactopyranosyl-(1→4)-β-D-galactopyranosyloleanolic acid (4). The structures of the two new compounds were established as 3-O-β-D-galactopyranosyl-(1→4)-β-D-xylopyranosyloleanolic acid (1) and 3-O-β-D-galactopyranosyl-(1→4)-α-L-arabinopyranosyloleanolic acid (2) on the basis of extensive 1D and 2D NMR spectroscopic data interpretation and chemical conversions. All the isolated compounds showed weak cytotoxicity against A2780 human ovarian cancer cell line, with IC50 values in the range 6.7 to 10.8 μg/mL.

TRITERPENE SAPONINS FROM Thalictrum minus. STRUCTURE OF THALICOSIDE B

Gromova, A. S.,Lutskii, V. I.,Semenov, A. A.,Valeev, R. B.,Kalabin, G. A.,El'kin, Yu. N.

, p. 629 - 635 (2007/10/02)

The epigeal part of Thalictrum minus L. has yielded a new bidesmoside - thalicoside B - which has the structure of oleanolic acid 28-O-β-D-glucopyranoside 3-O- 2)-O-β-D-glucopyranosyl-(1 -> 3)-α-L-arabinopyranoside>.

TRITERPENE GLYCOSIDES AND THEIR GENINS FROM Thalictrum foetidum. I. THE STRUCTURE OF FOETOSIDE C

Ganenko, T. V.,Isaev, M. I.,Gorovits, T. T.,Gromova, A. S.,Lutskii, V. I.,et al.

, p. 433 - 438 (2007/10/02)

A new glycoside - foetoside C - has been isolated from the epigeal part of Thalictrum foetidum L. and, on the basis of chemical transformations and spectral characteristics its structure has been established as oleanolic acid 28-6)-O-β-D-glucopyranoside> 3-O-3)-O-α-L-rhamnopyranosyl-(1->2)-α-L-arabinopyranoside>.

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