CAS 943602-97-9
:4(3H)-Quinazolinone, 8-iodo-7-methyl-
Description:
4(3H)-Quinazolinone, 8-iodo-7-methyl- is a chemical compound characterized by its quinazolinone core structure, which consists of a fused benzene and pyrimidine ring. The presence of an iodine atom at the 8-position and a methyl group at the 7-position contributes to its unique reactivity and potential biological activity. This compound is typically classified as a heterocyclic organic compound, and its structure suggests it may exhibit properties relevant to medicinal chemistry, particularly in the development of pharmaceuticals. The iodine substituent can enhance lipophilicity and may influence the compound's interaction with biological targets. Additionally, quinazolinones are known for their diverse pharmacological activities, including anti-inflammatory, antimicrobial, and anticancer properties. The specific characteristics of 4(3H)-Quinazolinone, 8-iodo-7-methyl- can be further explored through its synthesis, reactivity, and potential applications in drug discovery and development. As with many chemical substances, safety and handling precautions should be observed due to the presence of iodine and the potential for biological activity.
Formula:C9H7IN2O
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 2 products.
8-Iodo-7-methylquinazolin-4(3H)-one
CAS:<p>8-Iodo-7-methylquinazolin-4(3H)-one (8-IMQ) is a research tool that can be used to activate ion channels. It is also known as Ligand, Receptor, Cell Biology, Antibody, Ion channels, High purity, Protein interactions, Pharmacology and Peptides. 8-IMQ has been shown to inhibit the activity of ligand binding to G protein coupled receptors and ion channels in vitro. 8-IMQ binds to the receptor site on these proteins and inhibits the opening of ion channels. This inhibition leads to an increase in the membrane potential.</p>Formula:C9H7IN2OPurity:Min. 95%Molecular weight:286.07 g/mol
