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3-ALPHA-HYDROXY-6-KETOCHOLANIC ACID, also known as 5-β-Cholanic Acid-3α-ol-6-one, is a naturally occurring compound derived from α-Hyodeoxycholic Acid, which is isolated from pig bile. It is a steroidal molecule with a unique structure that has been identified for its potential biological activities.

2393-61-5

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2393-61-5 Usage

Uses

Used in Pharmaceutical Industry:
3-ALPHA-HYDROXY-6-KETOCHOLANIC ACID is used as an antitumor agent for its potential role in combating cancer. It is believed to exert its effects by interfering with the cellular processes that contribute to tumor growth and progression, making it a promising candidate for further research and development in cancer therapeutics.
Used in Anticancer Applications:
3-ALPHA-HYDROXY-6-KETOCHOLANIC ACID is used as a therapeutic agent for its potential to target and inhibit the growth of cancer cells. It may modulate various signaling pathways and cellular processes that are dysregulated in cancer, thereby exhibiting inhibitory effects on tumor growth and progression.

Check Digit Verification of cas no

The CAS Registry Mumber 2393-61-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,9 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2393-61:
(6*2)+(5*3)+(4*9)+(3*3)+(2*6)+(1*1)=85
85 % 10 = 5
So 2393-61-5 is a valid CAS Registry Number.
InChI:InChI=1/C24H38O4/c1-14(4-7-22(27)28)17-5-6-18-16-13-21(26)20-12-15(25)8-10-24(20,3)19(16)9-11-23(17,18)2/h14-20,25H,4-13H2,1-3H3,(H,27,28)/t14-,15-,16+,17-,18+,19+,20+,23-,24-/m1/s1

2393-61-5SDS

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 (4R)-4-[(3R,5R,8S,9S,10R,13R,14S,17R)-3-hydroxy-10,13-dimethyl-6-oxo-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]pentanoic acid

1.2 Other means of identification

Product number -
Other names 3alpha-Hydroxy-6-oxo-5beta-cholan-24-oic Acid

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:2393-61-5 SDS

2393-61-5Relevant academic research and scientific papers

Preparation method of 3-hydroxy-6-ketocholanic acid with low cost and high yield

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Paragraph 0036-0041, (2020/06/20)

The invention discloses a preparation method of 3 alpha-hydroxy-6-keto-5 beta-cholestane-24-acid with low cost and high yield, which is characterized by comprising the following steps: adding hyodeoxycholic acid into a mixed solution of an organic solvent and water, and stirring to dissolve; adding bromide and acid, stirring and dissolving; bromate is added for reaction; adding a terminating agent, and stirring to terminate the reaction; adding water to crystallize the product; and carrying out solid-liquid separation, washing a solid product with water for multiple times, and drying to obtainthe 3 alpha-hydroxy-6-keto-5 beta-cholestane-24-acid. According to the method, a common and safe reagent is adopted, the hyodeoxycholic acid is selectively oxidized into the 3 alpha-hydroxy-6-keto-5beta-cholestane-24-acid under a relatively mild condition, the product purity is greater than 98.0%, and the yield is greater than 85%. The method has the advantages of cheap reagents, simple operation, high process reproducibility, simple post-treatment, high product purity and high yield, and can easily implement industrial production.

Synthetic method for 6-carbonyl lithocholic acid

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, (2019/02/19)

The invention discloses a synthetic method for 6-carbonyl lithocholic acid. The synthetic method comprises the following steps of by adopting hyodeoxycholic acid as a starting material, sequentially performing 4-step reaction of 24-carboxyl esterification, oxidization of 3 alpha-OH and 6 alpha-OH into carbonyl groups, selective reduction and hydrolyzation to obtain a target product. The synthetictechnology is simple in flow, liable to control, wide in raw material source and available in raw material and can realize mass production.

Method for synthesizing lithocholic acid from hyodesoxycholic acid

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Paragraph 0036; 0037; 0038; 0039, (2017/08/29)

The invention discloses a method for synthesizing lithocholic acid, comprising: using hyodesoxycholic acid as a start material, and performing two-step reaction of 6Alpha-OH selective oxidation and Huang Minglon reduction to synthesize the lithocholic acid. The start material herein is low in price and easy to obtain, the synthetic steps are short, posttreatment is simple, few side reactions are employed, and the method is applicable to industrial production.

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