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72504-58-6

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72504-58-6 Usage

Description

(3a,5b,12a)-23-carboxy-12-hydroxy-24-norcholan-3-yl b-D-glucopyranosiduronic acid is a complex steroidal compound featuring a glucopyranosiduronic acid moiety. It is characterized by the presence of a carboxy group, a hydroxy group, and a norcholan-3-yl moiety, which contribute to its multifunctional nature. This molecule is part of the steroid class, known for its crucial biological roles and diverse physiological functions.

Uses

Used in Biochemical Research:
(3a,5b,12a)-23-carboxy-12-hydroxy-24-norcholan-3-yl b-D-glucopyranosiduronic acid is utilized as a subject of biochemical research to explore its interactions with biological systems and potential roles in carbohydrate metabolism or other sugar derivative-related processes.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (3a,5b,12a)-23-carboxy-12-hydroxy-24-norcholan-3-yl b-D-glucopyranosiduronic acid is considered for its potential as a therapeutic agent. Its complex structure and multifunctional groups may offer novel avenues for drug design and development, particularly in targeting specific biological pathways or receptors.
Used in Medical Applications:
(3a,5b,12a)-23-carboxy-12-hydroxy-24-norcholan-3-yl b-D-glucopyranosiduronic acid may be employed in medical applications once its biological significance is fully understood. Its potential roles in physiological functions could lead to its use in treating various medical conditions or as a diagnostic tool.
Further research is necessary to uncover the full spectrum of applications and properties of (3a,5b,12a)-23-carboxy-12-hydroxy-24-norcholan-3-yl b-D-glucopyranosiduronic acid, as its complex nature and belonging to the steroid class suggest a wide range of possibilities in biochemistry, pharmacology, and medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 72504-58-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,5,0 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 72504-58:
(7*7)+(6*2)+(5*5)+(4*0)+(3*4)+(2*5)+(1*8)=116
116 % 10 = 6
So 72504-58-6 is a valid CAS Registry Number.
InChI:InChI=1/C30H48O10/c1-14(4-9-22(32)33)18-7-8-19-17-6-5-15-12-16(10-11-29(15,2)20(17)13-21(31)30(18,19)3)39-28-25(36)23(34)24(35)26(40-28)27(37)38/h14-21,23-26,28,31,34-36H,4-13H2,1-3H3,(H,32,33)(H,37,38)/t14-,15-,16-,17+,18-,19+,20+,21+,23+,24+,25-,26+,28?,29+,30-/m1/s1

72504-58-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-α-O-(β-D-glucopyranuronosyl)desoxylcholsaeure

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:72504-58-6 SDS

72504-58-6Upstream product

72504-58-6Downstream Products

72504-58-6Relevant articles and documents

Synthesis of desoxycholic acid glucuronides. Part 4: CMT-selectin syntheses

Oehlke

, p. 383 - 386,384,385 (2007/10/11)

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