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6-Amino-2,3-dihydro-1,3-dimethyl-2-thioxopyrimidin-4(1H)-one is a heterocyclic organic compound characterized by a pyrimidine core structure and the molecular formula C6H8N2OS. It is known for its biological and pharmacological properties, particularly its potential as an antiviral agent. 6-aMino-2,3-dihydro-1,3-diMethyl-2-thioxopyriMidin-4(1H)-one's structure and properties have garnered interest in the field of medicinal chemistry for its inhibitory effects on viral replication and its promise in treating certain viral infections.

3120-52-3

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3120-52-3 Usage

Uses

Used in Antiviral Applications:
6-Amino-2,3-dihydro-1,3-dimethyl-2-thioxopyrimidin-4(1H)-one is utilized as an antiviral agent for its inhibitory effects on viral replication. It has shown promise in the treatment of specific viral infections, making it a valuable compound in the development of new antiviral drugs.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 6-Amino-2,3-dihydro-1,3-dimethyl-2-thioxopyrimidin-4(1H)-one is used as a key component in the development of new drugs for various medical applications. Its unique structure and properties contribute to the creation of innovative therapeutic agents that address unmet medical needs.
Used in Medicinal Chemistry Research:
6-Amino-2,3-dihydro-1,3-dimethyl-2-thioxopyrimidin-4(1H)-one serves as a subject of interest in medicinal chemistry research. Scientists and researchers explore its potential applications, mechanisms of action, and interactions with biological targets to enhance understanding and facilitate the development of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 3120-52-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,2 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3120-52:
(6*3)+(5*1)+(4*2)+(3*0)+(2*5)+(1*2)=43
43 % 10 = 3
So 3120-52-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H9N3OS/c1-8-4(7)3-5(10)9(2)6(8)11/h3H,7H2,1-2H3

3120-52-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-amino-1,3-dimethyl-2-sulfanylidenepyrimidin-4-one

1.2 Other means of identification

Product number -
Other names 6-amino-1,3-dimethyl-2-thioxo-2,3-dihydro-1H-pyrimidin-4-one

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:3120-52-3 SDS

3120-52-3Relevant academic research and scientific papers

Synthesis and Pharmacological Screening of Pyridopyrimidines as Effective Anti-Diarrheal Agents through the Suppression of Cyclic Nucleotide Accumulation

Zaminelli, Tiago,Magli, Elisa,Frecentese, Francesco,Lescano, Caroline H.,Campos, Rafael,Saccone, Irene,Corvino, Angela,Di Vaio, Paola,Giordano, Flavia,Luciano, Paolo,Fiorino, Ferdinando,Perissutti, Elisa,Santagada, Vincenzo,Severino, Beatrice,Caliendo, Giuseppe,De Nucci, Gilberto

, p. 464 - 475 (2019)

The increased levels of cyclic nucleotides (cGMP and cAMP) in enterocytes trigger intracellular mechanisms of ion and fluid secretion into the lumen, causing secretory diarrhea. Twelve novel pyridopyrimidines derived from 5-(3,5-bistrifluoromethylphenyl)-

NEW PYRIDOPYRIMIDINES DERIVATIVES COMPOUNDS

-

Paragraph 0067-0070, (2016/04/09)

The present invention describes new pyridopyrimidine derivatives compounds with structure represented by General Formula (I): or pharmaceutically acceptable salts thereof, or their mixtures (in any ratio), a pharmaceutical composition containing them, a method for using the new pyridopyrimidine derivatives compounds as inhibitor of the cyclic nucleotide synthesis or as inhibitor of the cAMP and cGMP synthesis, and their uses in the prophylactic and/or curative treatment of diarrhea, colitis and irritable bowel syndrome.

Structure-Activity Relationships of 1,3-Dialkylxanthine Derivatives at Rat A3 Adenosine Receptors

Kim, Hea Ok,Ji, Xiao-duo,Melman, Neli,Olah, Mark E.,Stiles, Gary L.,Jacobson, Kenneth A.

, p. 3373 - 3382 (2007/10/02)

1,3-Dialkylxanthine analogues containing carboxylic acid and other charged groups on 8-position substituents were synthesized.These derivatives were examined for affinity in radioligand binding assays at rat brain A3 adenosine receptors stably

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