Pyrroloindoles
Pyrroloindoles are a class of organic compounds derived from the fusion of pyrrole and indole rings, showcasing unique structural features that have attracted significant attention in medicinal chemistry. These molecules exhibit diverse biological activities, making them promising candidates for drug discovery processes. Pyrroloindoles can be synthesized through various methodologies including condensation reactions between corresponding amine and acid derivatives. Notably, their potential applications span across various fields such as anti-inflammatory, antimicrobial, and antitumor effects due to the presence of functional groups that facilitate molecular recognition with biological targets. The structural diversity afforded by the pyrrole-indole core allows for extensive chemical modification, thereby offering a wide range of possibilities in designing new therapeutic agents.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Carbamic acid,[10-(1-piperidinyl)decyl]-,1,2,3,3a,8,8a-hexahydro-1,3a,8-trimethylpyrrolo[2,3-b]indol-5-yl ester,(3aS-cis)- (9CI) | 154619-91-7 | C29H48N4O2 |
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Okaramine D | 162413-54-9 | C33H34N4O6 |
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Ethanone,1-(3,3a,8,8a-tetrahydro-8a-hydroxy-5-methoxypyrrolo[2,3-b]indol-1(2H)-yl)- | 109210-52-8 | C13H16N2O3 |
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(+)-Physostigmine | 29347-10-2 | C15H21N3O2 |
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Drimentine D | 204398-93-6 | C32H45N3O2 |
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Fructigenine A; N-De-Ac | 192183-17-8 | C25H27N3O2 |
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158060-73-2 | 158060-73-2 | C21H30N2 |
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Leptosin N1 | 406213-90-9 | C33H36N6O8S3 |
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Leptosin Q | 721960-18-5 | C33H36N6O7S |
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Flustramine J | 1187956-24-6 | C21H28Br2N2O |
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