Pyrido[4,3-b]indole is a heterocyclic organic compound characterized by its fused pyridine and indole structures. This compound features a bicyclic framework that contributes to its unique chemical properties. It typically exhibits a planar structure, which can facilitate interactions with biological targets, making it of interest in medicinal chemistry. Pyrido[4,3-b]indole is known for its potential biological activities, including antitumor and antimicrobial properties, which have been explored in various studies. The compound is generally soluble in organic solvents, and its reactivity can be influenced by the presence of functional groups on the indole or pyridine moieties. Additionally, it may undergo various chemical transformations, such as oxidation or substitution reactions, depending on the reaction conditions. Its distinct structure and properties make pyrido[4,3-b]indole a subject of interest in both synthetic organic chemistry and pharmacological research.

pyrido[4,3-b]indole

244-69-9: Gamma-Carboline, 5H-pyrido[4,3-b]indole, 3-Azacarbazole

5H-Pyrido[4,3-b]indole

Dimebon is a heterocyclic drug that is used in the treatment of psychotic disorders. It has been shown to have neuroprotective effects and its pharmacokinetic properties are similar to those of fluoxetine. Dimebon has been shown to have antipsychotic effects in vivo, and it also binds with high affinity to 5-HT2A receptors, but not to 5-HT2C receptors. Dimebon can be synthesized from trifluoroacetic acid and hydroxyl group. Hydrogenated dimebon analogues are also possible synthesis methods for this drug.

CAS 244-69-9: pyrido[4,3-b]indole

5H-Pyrido[4,3-b]indole

Ref: 3B-P2362

5H-Pyrido[4,3-b]indole

Ref: 10-F301540

5H-Pyrido[4,3-b]indole

Ref: IN-DA007N3G

5H-Pyrido[4,3-b]indole

Ref: 54-OR951880

5H-Pyrido[4,3-b]indole

Ref: 3D-AAA24469