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125363-87-3

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125363-87-3 Usage

Uses

Cardiotonic.

Check Digit Verification of cas no

The CAS Registry Mumber 125363-87-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,3,6 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 125363-87:
(8*1)+(7*2)+(6*5)+(5*3)+(4*6)+(3*3)+(2*8)+(1*7)=123
123 % 10 = 3
So 125363-87-3 is a valid CAS Registry Number.
InChI:InChI=1/C25H26F2N6OS/c26-19-5-1-17(2-6-19)23(18-3-7-20(27)8-4-18)33-11-9-32(10-12-33)13-21(34)14-35-25-22-24(29-15-28-22)30-16-31-25/h1-8,15-16,21,23,34H,9-14H2,(H,28,29,30,31)

125363-87-3SDS

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 Carsatrin

1.2 Other means of identification

Product number -
Other names (2S)-(+)-2,3,3-trimethylbutyric 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:125363-87-3 SDS

125363-87-3Relevant academic research and scientific papers

6-substituted purinyl piperazine derivatives

-

, (2008/06/13)

6-substituted purinyl piperazine derivatives and a method of synthesis for the derivatives are described. The 6-substituted purinyl piperazine derivatives are useful as cardiotonic agents and antiarrhythmic agents.

Synthesis and SAR of 6-substituted purine derivatives as novel selective positive inotropes

Press,Falotico,Hajos,Sawyers,Kanojia,Williams,Haertlein,Kauffman,Lakas-Weiss,Salata

, p. 4509 - 4515 (2007/10/02)

A series of purine derivatives was prepared and examined for selective inotropic activity in vitro and in vivo. Thioether-linked derivatives were superior to their oxygen and nitrogen isosteres. Substitution of electron- withdrawing groups on the benzhydryl moiety of these agents increased potency. The best compound of the study, 17 (carsatrin), was examined further and demonstrated selective oral activity as a positive inotrope. These compounds are presumed to act by affecting the kinetics of the cardiac sodium channel by analogy to the prototypic agent DPI 201106 (1). Their high selectivity for increasing contractile force and dP/dt without affecting blood pressure or heart rate is consistent with this mechanism. Carsatrin (17) was selected as a potential development candidate.

6-substituted purinyl piperazine derivatives

-

, (2008/06/13)

6-Substituted purinyl piperazine derivatives and a method of synthesis for the derivatives are described. The 6-substituted purinyl piperazine derivatives are useful as cardiotonic agents and antiarrhythmic agents.

6-Substituted purinyl piperazine derivatives useful as cardiotonic and antiarrhythmic agents

-

, (2008/06/13)

6-Substituted purinyl piperazine derivatives and a method of synthesis for the derivatives are described. The 6-substituted purinyl piperazine derivatives are useful as cardiotonic agents and antiarrhythmic agents.

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