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1790-74-5

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1790-74-5 Usage

Functionality

Central nervous system stimulant

Consumption

Most widely consumed psychoactive substance in the world

Sources

Found in coffee, tea, energy drinks, and some medications

Mechanism of Action

Blocks the action of adenosine, a neurotransmitter causing relaxation and drowsiness

Effects

Increases alertness and improves cognitive function

Additional Properties

Diuretic, stimulates urine release, helps prevent and treat fluid retention

Potential Side Effects

Jitteriness, insomnia, increased heart rate (with excessive consumption)

Consumption Recommendation

Moderate intake to avoid negative side effects

Check Digit Verification of cas no

The CAS Registry Mumber 1790-74-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,9 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1790-74:
(6*1)+(5*7)+(4*9)+(3*0)+(2*7)+(1*4)=95
95 % 10 = 5
So 1790-74-5 is a valid CAS Registry Number.

1790-74-5SDS

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 1,3,7-trimethyl-8-sulfanylidene-9H-purine-2,6-dione

1.2 Other means of identification

Product number -
Other names 1,3,7-Trimethyl-8-thio-harnsaeure

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:1790-74-5 SDS

1790-74-5Relevant articles and documents

Discovery of a new class of highly potent necroptosis inhibitors targeting the mixed lineage kinase domain-like protein

Yan, Bo,Liu, Lei,Huang, Shaoqiang,Ren, Yan,Wang, Huayi,Yao, Zhenglin,Li, Lin,Chen, She,Wang, Xiaodong,Zhang, Zhiyuan

, p. 3637 - 3640 (2017)

We report the development of novel Mixed Lineage Kinase Domain-Like protein (MLKL) inhibitors with single nanomolar potency (compound 15 is also named as TC13172). Using the converting biochemistry to chemistry activity-based protein profiling (BTC-ABPP) method, we were able to determine that the inhibitors covalently bind to Cysteine86 (Cys-86) of MLKL. This is the first example of the use of LC-MS/MS to identify the binding site of an MLKL inhibitor. The novel MLKL inhibitors provide powerful tools to study the biological function of MLKL and demonstrate that MLKL should be viewed as a druggable target.

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