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(3α,5α,16α)is a triterpene molecule, characterized by the presence of three oxygen atoms at positions 3, 5, and 16 on its carbon backbone. Triterpenes are natural compounds found in a variety of plants and have been studied for their potential therapeutic properties, including anti-inflammatory, anticancer, and antioxidant effects. The specific structure of (3α,5α,16α)may confer unique biological activities that make it of interest for further research and potential pharmaceutical development.

545-27-7

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545-27-7 Usage

Uses

Used in Pharmaceutical Industry:
(3α,5α,16α)is used as a potential therapeutic agent for its anti-inflammatory, anticancer, and antioxidant properties. Its unique structure may provide novel biological activities that can be further explored for the development of new drugs.
Used in Cosmetic Industry:
(3α,5α,16α)can be used as an active ingredient in cosmetic products for its potential anti-inflammatory and antioxidant effects, which may help in reducing skin inflammation and promoting skin health.
Used in Nutraceutical Industry:
(3α,5α,16α)can be incorporated into dietary supplements or functional foods for its potential health benefits, such as reducing inflammation and promoting overall well-being.
Used in Agricultural Industry:
(3α,5α,16α)can be used as a natural pesticide or growth promoter in agriculture, due to its potential anti-inflammatory and antioxidant properties, which may help in improving crop health and yield.

Check Digit Verification of cas no

The CAS Registry Mumber 545-27-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,4 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 545-27:
(5*5)+(4*4)+(3*5)+(2*2)+(1*7)=67
67 % 10 = 7
So 545-27-7 is a valid CAS Registry Number.

545-27-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name gitoxigenin 3β-digitoxoside

1.2 Other means of identification

Product number -
Other names 4-[(3S,5R,8R,9S,10S,13R,14S,16S,17R)-3-((2R,4S,5S,6R)-4,5-Dihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-14,16-dihydroxy-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-17-yl]-5H-furan-2-one

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:545-27-7 SDS

545-27-7Relevant academic research and scientific papers

Cardiac Glycosides. 6. Gitoxigenin C16 Acetates, Formates, Methoxycarbonates, and Digitoxosides. Synthesis and Na+, K+ -ATPase Inhibitory Activities

Hashimoto, Toshihiro,Rathore, Hargovind,Satoh, Daisuke,Hong, George,Griffin, Jane F.,et al.

, p. 997 - 1003 (2007/10/02)

A series of 17 gitoxigenin 16β-formates, acetates, and methoxycarbonates was synthesized, including their 3β-acetates, formates, and digitoxosides.A 16β-formate group was generally found to increase activity 30 times, a 16β-acetate group 9-12 times, while a 16β-methoxycarbonate decreased activity by two-thirds. 3β-Formates and acetates had little effect on activity by themselves, but sometimes reduced the activity-increasing properties of 16β-formates and acetates.A 3β-digitoxoside increases the activity of ditoxigenin by 15 times, but the effect is less ifthe 16β-group is esterified.And finally, a 16-one decreases activity dramatically.These data suggest an important role for C16 esters and possibly the presence of a separate binding site on Na+, K+ -ATPase corresponding to the cardenolide C16 position.

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