CAS 16285-74-8
:thieno[3,2-d]pyrimidin-4-amine
Description:
Thieno[3,2-d]pyrimidin-4-amine is a heterocyclic organic compound characterized by a fused ring system that includes both a thiophene and a pyrimidine moiety. This compound features an amine functional group at the 4-position of the pyrimidine ring, which contributes to its reactivity and potential biological activity. It is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the amine group. Thieno[3,2-d]pyrimidin-4-amine is of interest in medicinal chemistry, particularly for its potential as a scaffold in drug development, as it may interact with various biological targets. The compound's structure allows for diverse substitution patterns, which can influence its pharmacological properties. Additionally, it may exhibit properties such as fluorescence or photostability, depending on its specific substituents. Overall, thieno[3,2-d]pyrimidin-4-amine is a versatile compound with applications in research and development within the fields of pharmaceuticals and agrochemicals.
Formula:C6H5N3S
InChI:InChI=1/C6H5N3S/c7-6-5-4(1-2-10-5)8-3-9-6/h1-3H,(H2,7,8,9)
SMILES:c1csc2c1nc[nH]c2=N
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Found 5 products.
thieno[3,2-d]pyrimidin-4-amine
CAS:Formula:C6H5N3SPurity:97%Color and Shape:SolidMolecular weight:151.1890Thieno[3,2-d]pyrimidin-4-amine
CAS:Thieno[3,2-d]pyrimidin-4-aminePurity:97%Molecular weight:151.19g/mol4-Aminothieno[3,2-d]pyrimidine
CAS:Controlled Product<p>Applications 4-Aminothieno[3,2-d]pyrimidine is a useful research intermediate<br>References Robba, M., et al.: Tetrahedron, 27, 487 (1971); Park, J. H., et al.: Heterocycles, 91, 835 (2015)<br></p>Formula:C6H5N3SColor and Shape:NeatMolecular weight:151.19Thieno[3,2-d]pyrimidin-4-amine
CAS:<p>Thieno[3,2-d]pyrimidin-4-amine is an inhibitor of the enzyme dihydrofolate reductase. This drug is being studied for the treatment of tuberculosis and other bacterial infections. It is a potent inhibitor of the uptake of thiocyanate by erythrocytes. The metabolic pathway for this drug has been shown to involve oxidation by cytochrome p450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid. Thieno[3,2-d]pyrimidin-4-amine inhibits the synthesis of purine nucleotides in the mitochondria by inhibiting oxidative phosphorylation at complex III and IV. It also inhibits protein synthesis in bacteria. Thieno[3,2-d]pyrimidin-4-amine has been shown to have antiplasmodial activity against Plasmodium falciparum (</p>Formula:C6H5N3SPurity:Min. 95%Molecular weight:151.19 g/mol




