2002
DOI: 10.1021/cr020059j
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Isolation and Synthesis of Biologically Active Carbazole Alkaloids

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Cited by 1,332 publications
(579 citation statements)
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References 882 publications
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“…The flavonoids found in ME were as abundant as the phenolic compounds. The absence of alkaloid, steroid, and saponin secondary metabolites from the stem extract can be explained by their typically limited presence in leaves (Knölker and Reddy 2002). On the other hand, flavonoid and phenolic compounds are abundant in the stems as they (particularly the phenolic compounds) are the precursors for the biosynthesis of primary wood components such as lignin and cellulose (Harborne 1984;Obst 1998;Umezawa 2001).…”
Section: Physico-chemical Characteristicsmentioning
confidence: 99%
“…The flavonoids found in ME were as abundant as the phenolic compounds. The absence of alkaloid, steroid, and saponin secondary metabolites from the stem extract can be explained by their typically limited presence in leaves (Knölker and Reddy 2002). On the other hand, flavonoid and phenolic compounds are abundant in the stems as they (particularly the phenolic compounds) are the precursors for the biosynthesis of primary wood components such as lignin and cellulose (Harborne 1984;Obst 1998;Umezawa 2001).…”
Section: Physico-chemical Characteristicsmentioning
confidence: 99%
“…Like pyrimidines, carbazole compounds also exhibits diverse biological properties. Carbazole and its derivatives are the important class of heterocyclic compounds endowed with various pharmacological activities such as anticancer, antimicrobial, antiviral, anti-inflammatory and antioxidant activity 29 . Carbazole scaffold is present in many drugs such as carvedilol and carprofen ( Figure 1).…”
Section: Research Articlementioning
confidence: 99%
“…The interest in topoisomerase I as a therapeutic target promoted various efforts to identify other chemotypes effective as topoisomerase inhibitors and chemical/modelling efforts to rationally design specific analogs among known inhibitors [8,9,10,11] . During the last years several tetra-and pentacyclic structures containing the indoline fragment has received much attention due to the structural correlation with natural compounds belonging to the alkaloids class endowed with biological activity as cyclooxygenase/5-lipooxygenase inhibitors, characterized by the presence of the pyrrolo[3,2-de]acridine subunit [12] , indolocarbazoles non-CPT topo I inhibitors [13,14,15,16] and analogues of physostigmine alkaloids [17,18,19,20] .…”
Section: Introductionmentioning
confidence: 99%