Carbazoles

"Carbazoles" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

Benzo-indoles similar to CARBOLINES which are pyrido-indoles. In plants, carbazoles are derived from indole and form some of the INDOLE ALKALOIDS.

Descriptor ID	D002227
MeSH Number(s)	D03.633.100.473.144 D03.633.300.148
Concept/Terms	Carbazoles Carbazoles

Below are MeSH descriptors whose meaning is more general than "Carbazoles".

Chemicals and Drugs [D]
Heterocyclic Compounds [D03]
Heterocyclic Compounds, Fused-Ring [D03.633]
Heterocyclic Compounds, 2-Ring [D03.633.100]
Indoles [D03.633.100.473]
Carbazoles [D03.633.100.473.144]
Heterocyclic Compounds, 3-Ring [D03.633.300]
Carbazoles [D03.633.300.148]

Below are MeSH descriptors whose meaning is more specific than "Carbazoles".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Carbazoles" by people in this website by year, and whether "Carbazoles" was a major or minor topic of these publications.

Bar chart showing 39 publications over 19 distinct years, with a maximum of 4 publications in 2014 and 2018

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
1993	0	1	1
1996	0	1	1
2000	1	1	2
2001	0	1	1
2003	0	2	2
2004	0	3	3
2006	2	0	2
2007	2	0	2
2008	2	0	2
2009	1	0	1
2010	2	0	2
2011	1	1	2
2014	2	2	4
2015	1	1	2
2017	1	2	3
2018	0	4	4
2019	0	1	1
2020	1	0	1
2021	2	1	3

Below are the most recent publications written about "Carbazoles" by people in Profiles.

Mayer AMS, Hall ML, Lach J, Clifford J, Chandrasena K, Canton C, Kontoyianni M, Choo YM, Karan D, Hamann MT. RSK1 vs. RSK2 Inhibitory Activity of the Marine ß-Carboline Alkaloid Manzamine A: A Biochemical, Cervical Cancer Protein Expression, and Computational Study. Mar Drugs. 2021 Sep 07; 19(9).

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Abdulla OA, Neamah W, Sultan M, Alghetaa HK, Singh N, Busbee PB, Nagarkatti M, Nagarkatti P. The Ability of AhR Ligands to Attenuate Delayed Type Hypersensitivity Reaction Is Associated With Alterations in the Gut Microbiota. Front Immunol. 2021; 12:684727.

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Abdulla OA, Neamah W, Sultan M, Chatterjee S, Singh N, Nagarkatti M, Nagarkatti P. AhR Ligands Differentially Regulate miRNA-132 Which Targets HMGB1 and to Control the Differentiation of Tregs and Th-17 Cells During Delayed-Type Hypersensitivity Response. Front Immunol. 2021; 12:635903.

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Karan D, Dubey S, Pirisi L, Nagel A, Pina I, Choo YM, Hamann MT. The Marine Natural Product Manzamine A Inhibits Cervical Cancer by Targeting the SIX1 Protein. J Nat Prod. 2020 02 28; 83(2):286-295.

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Dupre TV, Jenkins DP, Muise-Helmericks RC, Schnellmann RG. The 5-hydroxytryptamine receptor 1F stimulates mitochondrial biogenesis and angiogenesis in endothelial cells. Biochem Pharmacol. 2019 11; 169:113644.

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Chitrala KN, Yang X, Nagarkatti P, Nagarkatti M. Comparative analysis of interactions between aryl hydrocarbon receptor ligand binding domain with its ligands: a computational study. BMC Struct Biol. 2018 12 06; 18(1):15.

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Daenthanasanmak A, Iamsawat S, Chakraborty P, Nguyen HD, Bastian D, Liu C, Mehrotra S, Yu XZ. Targeting Sirt-1 controls GVHD by inhibiting T-cell allo-response and promoting Treg stability in mice. Blood. 2019 01 17; 133(3):266-279.

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Ma XL, Li J, Zheng J, Gu XP, Ferreira D, Zjawiony JK, Zhao MB, Guo XY, Tu PF, Jiang Y. LC-MS-Guided Isolation of Insulin-Secretion-Promoting Monoterpenoid Carbazole Alkaloids from Murraya microphylla. J Nat Prod. 2018 11 26; 81(11):2371-2380.

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Simithy J, Fuanta NR, Alturki M, Hobrath JV, Wahba AE, Pina I, Rath J, Hamann MT, DeRuiter J, Goodwin DC, Calderón AI. Slow-Binding Inhibition of Mycobacterium tuberculosis Shikimate Kinase by Manzamine Alkaloids. Biochemistry. 2018 08 14; 57(32):4923-4933.

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Scholpa NE, Lynn MK, Corum D, Boger HA, Schnellmann RG. 5-HT1F receptor-mediated mitochondrial biogenesis for the treatment of Parkinson's disease. Br J Pharmacol. 2018 01; 175(2):348-358.

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