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1404-23-5

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1404-23-5 Usage

General Description

Pleurotin is a chemical compound derived from Pleurotus, a genus of gilled mushrooms, commonly known as oyster mushrooms. It is known for its biological properties, including antimicrobial, antiviral, and antitumor activities. It also plays a significant role in the biological defense mechanisms of the organism. Pleurotin is categorized under cyclic peptides, which are important due to their potential therapeutic uses. However, the exact mechanism of its action and physiological activities are not yet completely understood, requiring further research.

Check Digit Verification of cas no

The CAS Registry Mumber 1404-23-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,0 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1404-23:
(6*1)+(5*4)+(4*0)+(3*4)+(2*2)+(1*3)=45
45 % 10 = 5
So 1404-23-5 is a valid CAS Registry Number.

1404-23-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Pleurotine

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:1404-23-5 SDS

1404-23-5Downstream Products

1404-23-5Relevant articles and documents

Free-Radical Cyclizations: Application to the Total Synthesis of dl-Pleurotin and dl-Dihydropleurotin Acid

Hart, David J.,Huang, Horng-Chih,Krishnamurthy, Ram,Schwartz, Theresa

, p. 7507 - 7519 (2007/10/02)

Total syntheses of the antitumor antibiotic pleurotin (1) and dihydropleurotin acid (2) are described.Early stages of the synthesis feature the construction of a trans perhydroindan substructure using a stereoselective free-radical cyclization, and the final stage of the synthesis involves the biomimetic conversion of dihydropleurotin acid (2) to pleurotin (1).

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