Open Access
Molecules, volume 20, issue 8, pages 13496-13517
Recent Developments and Biological Activities of N-Substituted Carbazole Derivatives: A Review
Publication type: Journal Article
Publication date: 2015-07-23
PubMed ID:
26213906
Organic Chemistry
Drug Discovery
Physical and Theoretical Chemistry
Pharmaceutical Science
Molecular Medicine
Analytical Chemistry
Chemistry (miscellaneous)
Abstract
Carbazoles represent an important class of heterocycles. These have been reported to exhibit diverse biological activities such as antimicrobial, antitumor, antiepileptic, antihistaminic, antioxidative, anti-inflammatory, antidiarrhoeal, analgesic, neuroprotective and pancreatic lipase inhibition properties. A series of carbazole derivatives such as N-substituted carbazoles, benzocarbazoles, furocarbazoles, pyrrolocarbazoles, indolocarbazoles, imidazocarbazoles, etc. have been synthesized. The N-substituted derivatives have gained the attention of researchers due to their therapeutic potential against neurological disorders and cell proliferation. Herein an attempt is made to review the medicinal importance of recently synthesized N-substituted carbazoles.
Citations by journals
|
1
2
3
4
5
6
|
|
|
Molecules
|
Molecules
6 publications, 4.26%
|
|
Russian Chemical Bulletin
|
Russian Chemical Bulletin
6 publications, 4.26%
|
|
ChemistrySelect
|
ChemistrySelect
5 publications, 3.55%
|
|
European Journal of Organic Chemistry
|
European Journal of Organic Chemistry
5 publications, 3.55%
|
|
Advanced Synthesis and Catalysis
|
Advanced Synthesis and Catalysis
5 publications, 3.55%
|
|
Organic Letters
|
Organic Letters
5 publications, 3.55%
|
|
European Journal of Medicinal Chemistry
|
European Journal of Medicinal Chemistry
4 publications, 2.84%
|
|
Tetrahedron
|
Tetrahedron
4 publications, 2.84%
|
|
Journal of Organic Chemistry
|
Journal of Organic Chemistry
4 publications, 2.84%
|
|
Bioorganic Chemistry
|
Bioorganic Chemistry
3 publications, 2.13%
|
|
Bioorganic and Medicinal Chemistry
|
Bioorganic and Medicinal Chemistry
3 publications, 2.13%
|
|
Applied Sciences (Switzerland)
|
Applied Sciences (Switzerland)
2 publications, 1.42%
|
|
European Polymer Journal
|
European Polymer Journal
2 publications, 1.42%
|
|
Tetrahedron Letters
|
Tetrahedron Letters
2 publications, 1.42%
|
|
Journal of Catalysis
|
Journal of Catalysis
2 publications, 1.42%
|
|
Journal of Molecular Structure
|
Journal of Molecular Structure
2 publications, 1.42%
|
|
Angewandte Chemie - International Edition
|
Angewandte Chemie - International Edition
2 publications, 1.42%
|
|
Angewandte Chemie
|
Angewandte Chemie
2 publications, 1.42%
|
|
Journal of Heterocyclic Chemistry
|
Journal of Heterocyclic Chemistry
2 publications, 1.42%
|
|
ACS Medicinal Chemistry Letters
|
ACS Medicinal Chemistry Letters
2 publications, 1.42%
|
|
Journal of Agricultural and Food Chemistry
|
Journal of Agricultural and Food Chemistry
2 publications, 1.42%
|
|
ACS Catalysis
|
ACS Catalysis
2 publications, 1.42%
|
|
Journal of Medicinal Chemistry
|
Journal of Medicinal Chemistry
2 publications, 1.42%
|
|
Synthetic Communications
|
Synthetic Communications
2 publications, 1.42%
|
|
Journal of Enzyme Inhibition and Medicinal Chemistry
|
Journal of Enzyme Inhibition and Medicinal Chemistry
2 publications, 1.42%
|
|
Journal of Biomolecular Structure and Dynamics
|
Journal of Biomolecular Structure and Dynamics
2 publications, 1.42%
|
|
Advances in Heterocyclic Chemistry
|
Advances in Heterocyclic Chemistry
2 publications, 1.42%
|
|
Anti-Infective Agents
|
Anti-Infective Agents
1 publication, 0.71%
|
|
Beilstein Journal of Organic Chemistry
|
Beilstein Journal of Organic Chemistry
1 publication, 0.71%
|
|
1
2
3
4
5
6
|
Citations by publishers
|
5
10
15
20
25
30
35
|
|
|
Elsevier
|
Elsevier
35 publications, 24.82%
|
|
Wiley
|
Wiley
30 publications, 21.28%
|
|
American Chemical Society (ACS)
|
American Chemical Society (ACS)
20 publications, 14.18%
|
|
Multidisciplinary Digital Publishing Institute (MDPI)
|
Multidisciplinary Digital Publishing Institute (MDPI)
13 publications, 9.22%
|
|
Springer Nature
|
Springer Nature
12 publications, 8.51%
|
|
Royal Society of Chemistry (RSC)
|
Royal Society of Chemistry (RSC)
6 publications, 4.26%
|
|
Taylor & Francis
|
Taylor & Francis
6 publications, 4.26%
|
|
Bentham Science
|
Bentham Science
3 publications, 2.13%
|
|
King Saud University
|
King Saud University
2 publications, 1.42%
|
|
IOP Publishing
|
IOP Publishing
2 publications, 1.42%
|
|
Thieme
|
Thieme
2 publications, 1.42%
|
|
Beilstein-Institut
|
Beilstein-Institut
1 publication, 0.71%
|
|
International Union of Crystallography (IUCr)
|
International Union of Crystallography (IUCr)
1 publication, 0.71%
|
|
SAGE
|
SAGE
1 publication, 0.71%
|
|
Frontiers Media S.A.
|
Frontiers Media S.A.
1 publication, 0.71%
|
|
Polymer Society of Korea
|
Polymer Society of Korea, 1, 0.71%
Polymer Society of Korea
1 publication, 0.71%
|
|
American Association for the Advancement of Science (AAAS)
|
American Association for the Advancement of Science (AAAS)
1 publication, 0.71%
|
|
Publishing House ABV Press
|
Publishing House ABV Press
1 publication, 0.71%
|
|
Volgograd State Medical University
|
Volgograd State Medical University
1 publication, 0.71%
|
|
5
10
15
20
25
30
35
|
- We do not take into account publications that without a DOI.
- Statistics recalculated only for publications connected to researchers, organizations and labs registered on the platform.
- Statistics recalculated weekly.
{"yearsCitations":{"type":"bar","data":{"show":true,"labels":[2015,2016,2017,2018,2019,2020,2021,2022,2023,2024],"ids":[0,0,0,0,0,0,0,0,0,0],"codes":[0,0,0,0,0,0,0,0,0,0],"imageUrls":["","","","","","","","","",""],"datasets":[{"label":"Citations number","data":[1,10,9,18,20,22,17,18,23,3],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":["0.71","7.09","6.38","12.77","14.18","15.6","12.06","12.77","16.31","2.13"],"barThickness":null}]},"options":{"indexAxis":"x","maintainAspectRatio":true,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"}},"x":{"ticks":{"stepSize":1,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"}}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Citations per year","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}},"journals":{"type":"bar","data":{"show":true,"labels":["Molecules","Russian Chemical Bulletin","ChemistrySelect","European Journal of Organic Chemistry","Advanced Synthesis and Catalysis","Organic Letters","European Journal of Medicinal Chemistry","Tetrahedron","Journal of Organic Chemistry","Bioorganic Chemistry","Bioorganic and Medicinal Chemistry","Applied Sciences (Switzerland)","European Polymer Journal","Tetrahedron Letters","Journal of Catalysis","Journal of Molecular Structure","Angewandte Chemie - International Edition","Angewandte Chemie","Journal of Heterocyclic Chemistry","ACS Medicinal Chemistry Letters","Journal of Agricultural and Food Chemistry","ACS Catalysis","Journal of Medicinal Chemistry","Synthetic Communications","Journal of Enzyme Inhibition and Medicinal Chemistry","Journal of Biomolecular Structure and Dynamics","Advances in Heterocyclic Chemistry","Anti-Infective Agents","Beilstein Journal of Organic Chemistry"],"ids":[1770,10918,8021,19472,3906,3315,8171,3439,8697,4196,1162,16650,17319,6133,20883,9347,19215,25450,3189,360,22576,4873,3673,1646,864,3040,7227,20038,21928],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/5YZtvLvkPZuc2JHOaZsjCvGSHFCuC3drUwN3YAc5_medium.webp","\/storage\/images\/resized\/5YZtvLvkPZuc2JHOaZsjCvGSHFCuC3drUwN3YAc5_medium.webp","\/storage\/images\/resized\/5YZtvLvkPZuc2JHOaZsjCvGSHFCuC3drUwN3YAc5_medium.webp","\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/doUaFUZdxUEQjLi1TwZjGHi8HXYNWWSk04dSC6Xh_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp"],"datasets":[{"label":"","data":[6,6,5,5,5,5,4,4,4,3,3,2,2,2,2,2,2,2,2,2,2,2,2,2,2,2,2,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[4.26,4.26,3.55,3.55,3.55,3.55,2.84,2.84,2.84,2.13,2.13,1.42,1.42,1.42,1.42,1.42,1.42,1.42,1.42,1.42,1.42,1.42,1.42,1.42,1.42,1.42,1.42,0.71,0.71],"barThickness":13}]},"options":{"indexAxis":"y","maintainAspectRatio":false,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"}},"x":{"ticks":{"stepSize":null,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"}}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Journals","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}},"publishers":{"type":"bar","data":{"show":true,"labels":["Elsevier","Wiley","American Chemical Society (ACS)","Multidisciplinary Digital Publishing Institute (MDPI)","Springer Nature","Royal Society of Chemistry (RSC)","Taylor & Francis","Bentham Science","King Saud University","IOP Publishing","Thieme","Beilstein-Institut","International Union of Crystallography (IUCr)","SAGE","Frontiers Media S.A.","Polymer Society of Korea","American Association for the Advancement of Science (AAAS)","Publishing House ABV Press","Volgograd State Medical University"],"ids":[17,11,40,202,8,123,18,39,171,2075,135,6139,730,31,208,4849,189,7001,7257],"codes":[0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],"imageUrls":["\/storage\/images\/resized\/GDnYOu1UpMMfMMRV6Aqle4H0YLLsraeD9IP9qScG_medium.webp","\/storage\/images\/resized\/bRyGpdm98BkAUYiK1YFNpl5Z7hPu6Gd87gbIeuG3_medium.webp","\/storage\/images\/resized\/iLiQsFqFaSEx6chlGQ5fbAwF6VYU3WWa08hkss0g_medium.webp","\/storage\/images\/resized\/MjH1ITP7lMYGxeqUZfkt2BnVLgjkk413jwBV97XX_medium.webp","\/storage\/images\/resized\/voXLqlsvTwv5p3iMQ8Dhs95nqB4AXOG7Taj7G4ra_medium.webp","\/storage\/images\/resized\/leiAYcRDGTSl5B1eCnwpSGqmDEUEfDPPoYisFGhT_medium.webp","\/storage\/images\/resized\/5YZtvLvkPZuc2JHOaZsjCvGSHFCuC3drUwN3YAc5_medium.webp","\/storage\/images\/resized\/doUaFUZdxUEQjLi1TwZjGHi8HXYNWWSk04dSC6Xh_medium.webp","\/storage\/images\/resized\/9z7b0TQJNgUxZHYXLrTmbnjJn9y5iq56Wxtqb1Lv_medium.webp","\/storage\/images\/resized\/LsKy6OnmmmRGcAU6CZgWQvNiP1polbaSLNrN7zqj_medium.webp","\/storage\/images\/resized\/xqixcltwJYe6H8Uco2JbAFfIOzt7UNKH0OcPOPzO_medium.webp","\/storage\/images\/resized\/ex6KJoZujZOZFZh7jGfeHauiftuB3CI7iwJVFRDg_medium.webp","\/storage\/images\/resized\/xG3oC19920mmFVqkoVEGKGaMCeoalzyvWxPkVox5_medium.webp","\/storage\/images\/resized\/ruydfaB80LDjlkYqsfOeUAZohOIODyq7bQzis5O7_medium.webp","\/storage\/images\/resized\/4QWA67eqfcfyOiA8Wk7YnqroHFqQbTsmDJUYTCTg_medium.webp","","\/storage\/images\/resized\/s10mcsCV4OAUg9O2KrqOquQC0PhyLMI8hUUkuflM_medium.webp","\/storage\/images\/resized\/h7VqwIS9SIdw1p0X0HgUDKwed9MCAt9vlf7wMp3w_medium.webp","\/storage\/images\/resized\/XUWwztG6EZHfgHDCpqlKF9AxcFr5Om1iuEK0587D_medium.webp"],"datasets":[{"label":"","data":[35,30,20,13,12,6,6,3,2,2,2,1,1,1,1,1,1,1,1],"backgroundColor":["#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6","#3B82F6"],"percentage":[24.82,21.28,14.18,9.22,8.51,4.26,4.26,2.13,1.42,1.42,1.42,0.71,0.71,0.71,0.71,0.71,0.71,0.71,0.71],"barThickness":13}]},"options":{"indexAxis":"y","maintainAspectRatio":false,"scales":{"y":{"ticks":{"precision":0,"autoSkip":false,"font":{"family":"Montserrat"},"color":"#000000"}},"x":{"ticks":{"stepSize":null,"precision":0,"font":{"family":"Montserrat"},"color":"#000000"}}},"plugins":{"legend":{"position":"top","labels":{"font":{"family":"Montserrat"},"color":"#000000"}},"title":{"display":true,"text":"Publishers","font":{"size":24,"family":"Montserrat","weight":600},"color":"#000000"}}}}}
Metrics
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
Bashir M. et al. Recent Developments and Biological Activities of N-Substituted Carbazole Derivatives: A Review // Molecules. 2015. Vol. 20. No. 8. pp. 13496-13517.
GOST all authors (up to 50)
Copy
Bashir M., Bano A., Ijaz A., Chaudhary B. Recent Developments and Biological Activities of N-Substituted Carbazole Derivatives: A Review // Molecules. 2015. Vol. 20. No. 8. pp. 13496-13517.
Cite this
RIS
Copy
TY - JOUR
DO - 10.3390/molecules200813496
UR - https://doi.org/10.3390%2Fmolecules200813496
TI - Recent Developments and Biological Activities of N-Substituted Carbazole Derivatives: A Review
T2 - Molecules
AU - Bashir, Maryam
AU - Bano, Afifa
AU - Ijaz, Abdul
AU - Chaudhary, Bashir
PY - 2015
DA - 2015/07/23 00:00:00
PB - Multidisciplinary Digital Publishing Institute (MDPI)
SP - 13496-13517
IS - 8
VL - 20
PMID - 26213906
SN - 1420-3049
ER -
Cite this
BibTex
Copy
@article{2015_Bashir,
author = {Maryam Bashir and Afifa Bano and Abdul Ijaz and Bashir Chaudhary},
title = {Recent Developments and Biological Activities of N-Substituted Carbazole Derivatives: A Review},
journal = {Molecules},
year = {2015},
volume = {20},
publisher = {Multidisciplinary Digital Publishing Institute (MDPI)},
month = {jul},
url = {https://doi.org/10.3390%2Fmolecules200813496},
number = {8},
pages = {13496--13517},
doi = {10.3390/molecules200813496}
}
Cite this
MLA
Copy
Bashir, Maryam, et al. “Recent Developments and Biological Activities of N-Substituted Carbazole Derivatives: A Review.” Molecules, vol. 20, no. 8, Jul. 2015, pp. 13496-13517. https://doi.org/10.3390%2Fmolecules200813496.