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10335-62-3

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10335-62-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10335-62-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,3 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10335-62:
(7*1)+(6*0)+(5*3)+(4*3)+(3*5)+(2*6)+(1*2)=63
63 % 10 = 3
So 10335-62-3 is a valid CAS Registry Number.

10335-62-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name salicylaldehyde-pyrimidin-2-ylhydrazone

1.2 Other means of identification

Product number -
Other names Salicylaldehyd-pyrimidin-2-ylhydrazon

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:10335-62-3 SDS

10335-62-3Downstream Products

10335-62-3Relevant articles and documents

Synthesis, biological activity, and mechanism of action of new 2-pyrimidinyl hydrazone and N-acylhydrazone derivatives, a potent and new classes of antileishmanial agents

Coimbra, Elaine Soares,Nora de Souza, Marcus Vinícius,Terror, Mariana Sequetto,Pinheiro, Alessandra Campbell,da Trindade Granato, Juliana

, (2019)

In this work, we report the antileishmanial activity of 15 compounds based on 2-pyrimidinyl hydrazone and N-acylhydrazone derivatives, being 13 new compounds. All compounds were tested against promastigotes and Leishmania amazonensis-GFP amastigotes, as well as murine macrophages. Besides, studies about the mechanism of action of the best antileishmanial compounds and in silico physicochemical and pharmacokinetic properties were performed. Studies about the mechanism of action of representative compounds of each class showed slight differences in mode of action and both are able to cause mitochondrial depolarization and increase of intracellular ROS levels. Through computational tool and further analysis of the physicochemical and pharmacokinetic parameters, the results indicating good oral bioavailability. These results confirm the potential of 2-pyrimidinyl derivatives as lead compounds in antileishmanial drug discovery.

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