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16-HYDROXYVERRUCARINA is a chemical compound that belongs to the verrucarin family of trichothecene mycotoxins, which are produced by various species of fungi. It is structurally related to verrucarin A, a potent inhibitor of protein synthesis. 16-HYDROXYVERRUCARINA has been identified as a metabolite of certain fungi and has been shown to have cytotoxic and antiproliferative effects in biological systems.
Used in Food Safety Industry:
16-HYDROXYVERRUCARINA is used as a biomarker for monitoring mycotoxin contamination in agricultural products for the purpose of ensuring food safety and protecting human health.
Used in Research and Development:
16-HYDROXYVERRUCARINA is used as a subject of research for understanding its potential role in food safety and its implications for human health, particularly in the context of mycotoxin contamination in agricultural products. Studies have indicated that 16-HYDROXYVERRUCARINA may be a significant contributor to the toxic effects associated with other trichothecene mycotoxins.

74516-64-6

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74516-64-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74516-64-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,5,1 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 74516-64:
(7*7)+(6*4)+(5*5)+(4*1)+(3*6)+(2*6)+(1*4)=136
136 % 10 = 6
So 74516-64-6 is a valid CAS Registry Number.

74516-64-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name VERRUCARIN A, PRIMARY ALLYLIC ALCOHOL OF

1.2 Other means of identification

Product number -
Other names 16-hydroxyverrucarin A

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:74516-64-6 SDS

74516-64-6Upstream product

74516-64-6Relevant academic research and scientific papers

Antileukemic Compounds Derived from the Chemical Modification of Macrocyclic Trichothecenes. 1. Derivatives of Verrucarin A

Jarvis, Bruce B.,Stahly, G. Patrick,Pavanasasivam, Gowsala,Mazzola, Eugene P.

, p. 1054 - 1058 (2007/10/02)

Verrucarin A (2) was epoxidized to give the β-9,10-epoxide 7 (major product) and α-9,10-epoxide 9 (minor product).The β-epoxide 7 and its acetate 8 exhibit high in vivo antileukemic activity against P-388 mouse leukemia, whereas 2 and 9 are inactive.Epoxidation of verrucarin B (3) and roridin A (1) to their respective β-9,10-epoxides (11 and 12, respectively) also yields compounds with substantially increased activity.Allylic alcohols derived from 2, α-C8 (20), β-C8 (14), and C16 (15), were synthesized and tested; only 15 exhibited substantial in vivo activity.

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