CAS 108906-13-4
:1H-Indole-2-carboxamide,2,3-dihydro-(9CI)
Description:
1H-Indole-2-carboxamide, 2,3-dihydro- (9CI) is a chemical compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. This compound features a carboxamide functional group at the 2-position of the indole ring, contributing to its potential biological activity. The dihydro designation indicates that the compound has two additional hydrogen atoms, suggesting it is a saturated derivative of indole. This modification can influence its solubility, reactivity, and interaction with biological targets. The compound is often studied for its pharmacological properties, including potential roles in medicinal chemistry and drug development. Its CAS number, 108906-13-4, serves as a unique identifier for regulatory and research purposes. Overall, 1H-Indole-2-carboxamide, 2,3-dihydro- is of interest in various fields, including organic synthesis and pharmaceutical research, due to its structural features and potential applications.
Formula:C9H10N2O
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Found 4 products.
1H-Indole-2-carboxamide,2,3-dihydro-(9CI)
CAS:Formula:C9H10N2OPurity:98%Color and Shape:SolidMolecular weight:162.18852,3-Dihydro-1H-indole-2-carboxylic acid amide
CAS:<p>2,3-Dihydro-1H-indole-2-carboxylic acid amide</p>Purity:98%2,3-Dihydro-1H-indole-2-carboxamide
CAS:<p>2,3-Dihydro-1H-indole-2-carboxamide is a synthetic peptidomimetic that inhibits NS3 protease, which is involved in the viral life cycle. 2,3-Dihydro-1H-indole-2-carboxamide has been shown to have potent inhibitory activity against the hepatitis C virus (HCV) and HIV. It also inhibits the replication of HCV in mammalian cells. This drug has pharmacokinetic properties that are similar to glibenclamide and penetrates the blood brain barrier. Clinical studies have been conducted on patients with chronic hepatitis B and C infection.</p>Formula:C9H10N2OPurity:Min. 95%Molecular weight:162.19 g/mol
