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2-METHYLTHIOADENOSINE 5-MONOPHOSPHATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22140-20-1

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22140-20-1 Usage

Biochem/physiol Actions

The only known preferential antagonist for P2Y(AC) receptor; this is the platelet ADP receptor that is coupled to adenyl cyclase and is also referred to as the P2Y ADP receptor.

Check Digit Verification of cas no

The CAS Registry Mumber 22140-20-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,1,4 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22140-20:
(7*2)+(6*2)+(5*1)+(4*4)+(3*0)+(2*2)+(1*0)=51
51 % 10 = 1
So 22140-20-1 is a valid CAS Registry Number.

22140-20-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-METHYLTHIOADENOSINE 5-MONOPHOSPHATE

1.2 Other means of identification

Product number -
Other names 2-methylthioadenosine 5'-monophosphate triethylammonium salt hydrate

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:22140-20-1 SDS

22140-20-1Downstream Products

22140-20-1Relevant academic research and scientific papers

NOVEL ANTITHROMBOTIC DIADENOSINE TETRAPHOSPHATES AND RELATED ANALOGS

-

Page/Page column 17-19, (2010/07/10)

The invention features compounds of formula I and methods of their use as antiplatelet and antithrombotic compounds: H /N=Qχ2 O O O O Λ Q2 — N, H R6/ N I f ) ( ^ XM O-Mγτ OM°τ X1MQ' ) r ( ^rf HO OH HO OQHi Nχi R2 Formula (I).

Identification of hydrolytically stable and selective P2Y1 receptor agonists

Eliahu, Shay E.,Camden, Jean,Lecka, Joanna,Weisman, Gary A.,Sevigny, Jean,Gelinas, Sylvie,Fischer, Bilha

experimental part, p. 1525 - 1536 (2009/08/15)

P2Y nucleotide receptors (P2YRs) are attractive pharmaceutical targets. Most P2YR agonists proposed as drugs consist of a nucleotide scaffold, but their use is limited due to their chemical and enzymatic instabilities. To identify drug candidates, we deve

Adenine nucleotide analogues locked in a Northern methanocarba conformation: Enhanced stability and potency as P2Y1 receptor agonists

Ravi, R. Gnana,Kim, Hak Sung,Servos, J?rg,Zimmermann, Herbert,Lee, Kyeong,Maddileti, Savitri,Boyer, José L.,Harden, T. Kendall,Jacobson, Kenneth A.

, p. 2090 - 2100 (2007/10/03)

Preference for the Northern (N) ring conformation of the ribose moiety of nucleotide 5′-triphosphate agonists at P2Y1, P2Y2, P2Y4, and P2Y11 receptors, but not P2Y6 receptors, was established using a

The preparation of 32P-labeled 2-methylthioadenosine di- and triphosphates

Skoblov,Yas'ko,Skoblov

, p. 623 - 627 (2007/10/03)

2-Methylthioadenosine 5′-mono- and diphosphates were prepared by chemical synthesis, and enzymatically phosphorylated to 5′-[β-32P]-diphosphate and 5′-[γ-32P]-triphosphate, respectively. They were isolated by HPLC and had activity exceeding 1000 Ci/mmol and radiochemical purity higher than 95%.

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