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34209-85-3

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34209-85-3 Usage

Description

(2beta,3beta,5beta,14xi,17xi)-2,3,14,25-tetrahydroxycholest-7-en-6-one is a steroidal compound with a tetracyclic structure, featuring a hydroxy group at the 2nd, 3rd, 14th, and 25th carbon positions and a ketone group at the 6th carbon position. As a derivative of cholesterol, it serves as a precursor for the synthesis of various steroid hormones and bile acids, playing a vital role in the regulation of lipid metabolism and the development and function of the reproductive system. The unique arrangement of hydroxy and ketone groups endows this compound with distinct biological properties, making it a significant molecule in the endocrine system.

Uses

Used in Pharmaceutical Industry:
(2beta,3beta,5beta,14xi,17xi)-2,3,14,25-tetrahydroxycholest-7-en-6-one is used as a precursor in the synthesis of steroid hormones and bile acids for the treatment of various hormonal imbalances and liver-related conditions. Its unique structure allows for the development of pharmaceuticals targeting specific physiological processes.
Used in Research and Development:
(2beta,3beta,5beta,14xi,17xi)-2,3,14,25-tetrahydroxycholest-7-en-6-one is utilized in research settings to study the role of steroid hormones and bile acids in physiological processes, as well as their potential therapeutic applications. It aids in understanding the molecular mechanisms underlying lipid metabolism and reproductive system function.
Used in Diagnostic Applications:
(2beta,3beta,5beta,14xi,17xi)-2,3,14,25-tetrahydroxycholest-7-en-6-one can be employed as a biomarker in diagnostic tests to assess the levels of steroid hormones and bile acids in the body, helping in the identification of hormonal imbalances and liver dysfunctions.

Check Digit Verification of cas no

The CAS Registry Mumber 34209-85-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,2,0 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 34209-85:
(7*3)+(6*4)+(5*2)+(4*0)+(3*9)+(2*8)+(1*5)=103
103 % 10 = 3
So 34209-85-3 is a valid CAS Registry Number.

34209-85-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 22-Deoxyecdysone

1.2 Other means of identification

Product number -
Other names 22-deoxyecdysone

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:34209-85-3 SDS

34209-85-3Upstream product

34209-85-3Downstream Products

34209-85-3Relevant articles and documents

STUDY ON THE BIOSYNTHESIS OF ECDYSONE PART IV: Synthesis of high specific activity -2,22-dideoxyecdysone Tissue distribution of the C-22 hydroxylase in Locusta migratoria

Haag, Thierry,Hetru, Charles,Kappler, Christine,Moustier, Anne Marie,Hoffmann, Jules A.,Luu, Bang

, p. 1397 - 1408 (1988)

We have synthesized a tritiated form of 2,22-dideoxyecdysone -3β,14α,25-trihydroxy-5β-cholest-7-en-6-one> of high specific activity (2.2 TBq/mmol).We have examined the capacity of various endocrine (prothoracic glands, follicle cells) and peripheral (fat body, Malpighian tubules) tissues of Locusta migratoria to use this molecule as a precursor of ecdysone biosynthesis.Efficient conversion of 2,22-dideoxyecdysone to 2-deoxyecdysone and to ecdysone could principally be monitored in the prothoracic glands and follicle cells.

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