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For: Issa S, Prandina A, Bedel N, Rongved P, Yous S, Le Borgne M, Bouaziz Z. Carbazole scaffolds in cancer therapy: a review from 2012 to 2018. J Enzyme Inhib Med Chem 2019;34:1321-46. [PMID: 31328585 DOI: 10.1080/14756366.2019.1640692] [Cited by in Crossref: 58] [Cited by in F6Publishing: 44] [Article Influence: 19.3] [Reference Citation Analysis]
Number Citing Articles
1 Kumar N, Gupta P, Bansal S. Progress and Development of Carbazole Scaffold Based as Potential Anti- Alzheimer Agents Using MTDL Approach. LDDD 2022;19:1049-1067. [DOI: 10.2174/1570180819666220314144219] [Reference Citation Analysis]
2 Alam S, Karim R, Khan A, Mallick AR, Sepay N, Ghosh S. Microwave-assisted synthesis of functionalized carbazoles via palladium-catalyzed aryl C–H activation and study of their interactions with calf-thymus DNA. Synthetic Communications. [DOI: 10.1080/00397911.2022.2116344] [Reference Citation Analysis]
3 Roy D, Tharra P, Baire B. An approach to functionalized carbazoles from Z-enoate propargylic alcohols. A unified total synthesis of N-Me-carazostatin, N-Me-carbazoquinocin C and N-Me-lipocarbazole A4. Chem Commun (Camb) 2022. [PMID: 36000534 DOI: 10.1039/d2cc03526j] [Reference Citation Analysis]
4 Jyoti, Dmitrieva E, Żołek T, Maciejewska D, Rybakiewicz-sekita R, Kutner W, Noworyta KR. An Insight into the Polymerization Process of the Selected Carbazole Derivatives - Why does It not always Lead to a Polymer Formation? Electrochimica Acta 2022. [DOI: 10.1016/j.electacta.2022.140948] [Reference Citation Analysis]
5 Kiseleva MP, Borisova LM, Smirnova GB, Borisova YA, Lantsova AV, Sanarova EV, Nikolaeva LL, Ektova LV, Komarova MV. Antiproliferative activity of a new derivative from the class of N-glycoside of indolo[2,3-a]pyrrolo[3,4-c]carbazoles. RRP 2022;8:49-57. [DOI: 10.3897/rrpharmacology.8.79424] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
6 Celik S, Akyuz S, Ozel AE. Molecular modeling, DFT quantum chemical analysis, and molecular docking on edotecarin, an indolocarbazole anticancer agent. Molecular Crystals and Liquid Crystals. [DOI: 10.1080/15421406.2022.2084240] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Ngoc Binh V, Adorisio S, Delfino DV, Ngo QA. New 1,4-Dihydropyrazolo[4,3- b ]indoles Induce Antiproliferation of Acute Myeloid Leukemia Cells and Inhibition of Selective Inflammatory Cytokines. Natural Product Communications 2022;17:1934578X2211056. [DOI: 10.1177/1934578x221105692] [Reference Citation Analysis]
8 Kaur R, Banga S, Babu SA. Construction of carbazole-based unnatural amino acid scaffolds via Pd(II)-catalyzed C(sp3)-H functionalization. Org Biomol Chem 2022;20:4391-414. [PMID: 35583129 DOI: 10.1039/d2ob00658h] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
9 Tang L, Jiang S, Huang X, Song Z, Wang JB, Ma M, Chen B, Ma Y. Cascade of C(sp2)-H Addition to Carbonyl and C(sp2)-CN/C(sp2)-H Coupling Enabled by Brønsted Acid: Construction of Benzo[a]carbazole Frameworks. Org Lett 2022;24:3232-7. [PMID: 35475641 DOI: 10.1021/acs.orglett.2c01027] [Reference Citation Analysis]
10 Jahan H, Siddiqui NN, Iqbal S, Basha FZ, Shaikh S, Pizzi M, Choudhary MI. Suppression of COX-2/PGE2 levels by carbazole-linked triazoles via modulating methylglyoxal-AGEs and glucose-AGEs – Induced ROS/NF-κB signaling in monocytes. Cellular Signalling 2022. [DOI: 10.1016/j.cellsig.2022.110372] [Reference Citation Analysis]
11 Venkata Suseela Y, Sengupta P, Roychowdhury T, Panda S, Talukdar S, Chattopadhyay S, Chatterjee S, Govindaraju T. Targeting Oncogene Promoters and Ribosomal RNA Biogenesis by G-Quadruplex Binding Ligands Translate to Anticancer Activity. ACS Bio Med Chem Au 2022;2:125-39. [DOI: 10.1021/acsbiomedchemau.1c00039] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Campbell E, Taladriz-Sender A, Paisley OI, Kennedy AR, Bush JT, Burley GA. A Chemo- and Regioselective Tandem [3 + 2]Heteroannulation Strategy for Carbazole Synthesis: Combining Two Mechanistically Distinct Bond-Forming Processes. J Org Chem 2022;87:4603-16. [PMID: 35302774 DOI: 10.1021/acs.joc.1c02943] [Reference Citation Analysis]
13 Berndsen R, Cunningham T, Kaelin L, Callender M, Boldog WD, Viering B, King A, Labban N, Pollock JA, Miller HB, Blackledge MS. Identification and Evaluation of Brominated Carbazoles as a Novel Antibiotic Adjuvant Scaffold in MRSA. ACS Med Chem Lett 2022;13:483-91. [PMID: 35295086 DOI: 10.1021/acsmedchemlett.1c00680] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
14 Yu Y, Liu A, He J, Wang C, Mei H, Han J. Visible-light-irradiated tandem sulfonylation/cyclization of indole tethered alkenes for the synthesis of tetrahydrocarbazoles. Chinese Chemical Letters 2022. [DOI: 10.1016/j.cclet.2022.03.038] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
15 Su X, Chen Y, Wu J, Wu X, Li K, Wang X, Sun J, Wang H, Ou T. Design, synthesis, and evaluation of 9-(pyrimidin-2-yl)-9H-carbazole derivatives disrupting mitochondrial homeostasis in human lung adenocarcinoma. European Journal of Medicinal Chemistry 2022. [DOI: 10.1016/j.ejmech.2022.114200] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
16 Niu Y, Qiao Y, Wang K, Sha B, Li G. Cu( i )-catalyzed cross-coupling of primary amines with 2,2′-dibromo-1,1′-biphenyl for the synthesis of polysubstituted carbazole. RSC Adv 2022;12:24232-6. [DOI: 10.1039/d2ra03323b] [Reference Citation Analysis]
17 Tamilthendral V, Ramesh R, Malecki JG. New ruthenium(ii) catalysts enable the synthesis of 2-amino-4H-chromenes using primary alcohols via acceptorless dehydrogenative coupling. New J Chem 2022;46:21568-21578. [DOI: 10.1039/d2nj03268f] [Reference Citation Analysis]
18 Nadeem Q, Battistin F, Blacque O, Alberto R. Naphthalene Exchange in [Re(η6 -napht)2 ]+ with Pharmaceuticals Leads to Highly Functionalized Sandwich Complexes [M(η6 -pharm)2 ]+ (M=Re/99m Tc). Chemistry 2021. [PMID: 34817903 DOI: 10.1002/chem.202103566] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
19 Wang G, Sun S, Guo H. Current status of carbazole hybrids as anticancer agents. Eur J Med Chem 2021;:113999. [PMID: 34838335 DOI: 10.1016/j.ejmech.2021.113999] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 8.0] [Reference Citation Analysis]
20 Nandan S, Singh SK, Singh P, Bajpai V, Mishra AK, Joshi T, Mahar R, Shukla SK, Mishra DK, Kanojiya S. Quantitative Analysis of Bioactive Carbazole Alkaloids in Murraya koenigii (L.) from Six Different Climatic Zones of India Using UPLC/MS/MS and Their Principal Component Analysis. Chem Biodivers 2021;:e2100557. [PMID: 34643999 DOI: 10.1002/cbdv.202100557] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
21 Sirin S, Duyar H, Aslım B, Seferoğlu Z. Synthesis and biological activity of pyrrolidine/piperidine substituted 3-amido-9-ethylcarbazole derivatives. Journal of Molecular Structure 2021;1242:130687. [DOI: 10.1016/j.molstruc.2021.130687] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
22 Tremlett WD, Goodman DM, Steel TR, Kumar S, Wieczorek-błauż A, Walsh FP, Sullivan MP, Hanif M, Hartinger CG. Design concepts of half-sandwich organoruthenium anticancer agents based on bidentate bioactive ligands. Coordination Chemistry Reviews 2021;445:213950. [DOI: 10.1016/j.ccr.2021.213950] [Cited by in Crossref: 17] [Cited by in F6Publishing: 16] [Article Influence: 17.0] [Reference Citation Analysis]
23 Sinicropi MS, Tavani C, Rosano C, Ceramella J, Iacopetta D, Barbarossa A, Bianchi L, Benzi A, Maccagno M, Ponassi M, Spinelli D, Petrillo G. A Nitrocarbazole as a New Microtubule-Targeting Agent in Breast Cancer Treatment. Applied Sciences 2021;11:9139. [DOI: 10.3390/app11199139] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
24 Song F, Liu D, Huo X, Qiu D. The anticancer activity of carbazole alkaloids. Arch Pharm (Weinheim) 2021;:e2100277. [PMID: 34486161 DOI: 10.1002/ardp.202100277] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
25 Müller D, Saha P, Panda D, Dash J, Schwalbe H. Insights from Binding on Quadruplex Selective Carbazole Ligands. Chemistry 2021;27:12726-36. [PMID: 34138492 DOI: 10.1002/chem.202101866] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
26 Points GL 3rd, Beaudry CM. Regioselective Synthesis of Substituted Carbazoles, Bicarbazoles, and Clausine C. Org Lett 2021;23:6882-5. [PMID: 34424701 DOI: 10.1021/acs.orglett.1c02449] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
27 Lupidi G, Bassetti B, Ballini R, Petrini M, Palmieri A. A New and Effective One‐Pot Synthesis of Polysubstituted Carbazoles Starting from β‐Nitro‐β,γ‐Unsaturated‐Ketones and Indoles. Asian J of Organic Chemis 2021;10:2334-2337. [DOI: 10.1002/ajoc.202100342] [Reference Citation Analysis]
28 Ignateva EV, Yartseva IV, Shprakh ZS, Bud'ko AP, Ektova LV, Kozin DA, Reshetnyak VY, Nesterova OV, Pankratova EA. Standardization of the Pharmaceutical Substance of the Drug LCS-1208. Razrabotka i registraciâ lekarstvennyh sredstv 2021;10:88-94. [DOI: 10.33380/2305-2066-2021-10-3-88-94] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
29 Patel M, Pandey N, Timaniya J, Parikh P, Chauhan A, Jain N, Patel K. Coumarin-carbazole based functionalized pyrazolines: synthesis, characterization, anticancer investigation and molecular docking. RSC Adv 2021;11:27627-44. [PMID: 35480680 DOI: 10.1039/d1ra03970a] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 9.0] [Reference Citation Analysis]
30 Pocock IA, Alotaibi AM, Jagdev K, Prior C, Burgess GR, Male L, Grainger RS. Direct formation of 4,5-disubstituted carbazoles via regioselective dilithiation. Chem Commun (Camb) 2021;57:7252-5. [PMID: 34190745 DOI: 10.1039/d1cc02892h] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
31 Caruso A, Barbarossa A, Carocci A, Salzano G, Sinicropi MS, Saturnino C. Carbazole Derivatives as STAT Inhibitors: An Overview. Applied Sciences 2021;11:6192. [DOI: 10.3390/app11136192] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
32 Kaur M, Mehta V, Abdullah Wani A, Arora S, Bharatam PV, Sharon A, Singh S, Kumar R. Synthesis of 1,4-dihydropyrazolo[4,3-b]indoles via intramolecular C(sp2)-N bond formation involving nitrene insertion, DFT study and their anticancer assessment. Bioorg Chem 2021;114:105114. [PMID: 34243073 DOI: 10.1016/j.bioorg.2021.105114] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
33 Ma XL, Zhu SS, Liu Y, Chen HW, Shi YT, Zeng KW, Tu PF, Jiang Y. Carbazole alkaloids with potential cytotoxic activities targeted on PCK2 protein from Murraya microphylla. Bioorg Chem 2021;114:105113. [PMID: 34175718 DOI: 10.1016/j.bioorg.2021.105113] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
34 Wen J, Chen W, Zhao B, Xu Q, Liu C, Zhang Q, Xie Z, Yan Y, Guo J, Huang J, Miao J, Wu X. A carbazole compound, 9-ethyl-9H-carbazole-3-carbaldehyde, plays an antitumor function through reactivation of the p53 pathway in human melanoma cells. Cell Death Dis 2021;12:591. [PMID: 34103468 DOI: 10.1038/s41419-021-03867-6] [Reference Citation Analysis]
35 Sathiya Kamatchi T, Mohamed Subarkhan MK, Ramesh R, Wang H, Małecki JG. Investigation into antiproliferative activity and apoptosis mechanism of new arene Ru(ii) carbazole-based hydrazone complexes. Dalton Trans 2020;49:11385-95. [PMID: 32776042 DOI: 10.1039/d0dt01476a] [Cited by in Crossref: 80] [Cited by in F6Publishing: 82] [Article Influence: 80.0] [Reference Citation Analysis]
36 Zhang Z, Zhang H, Yang H, Xu Z. Heptaphylline inhibits the proliferation and epithelial to mesenchymal transition of human pancreatic cancer cells via induction of apoptosis and autophagy. All Life 2021;14:484-91. [DOI: 10.1080/26895293.2021.1925357] [Reference Citation Analysis]
37 Polley A, Varalaxmi K, Nandi A, Jana R. Divergent Total Synthesis of (±)‐Mahanine and Other Carbazole Alkaloids. Asian J of Organic Chemis 2021;10:1207-15. [DOI: 10.1002/ajoc.202100176] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
38 Luparello C, Cruciata I, Joerger AC, Ocasio CA, Jones R, Tareque RK, Bagley MC, Spencer J, Walker M, Austin C, Ferrara T, D Oca P, Bellina R, Branni R, Caradonna F. Genotoxicity and Epigenotoxicity of Carbazole-Derived Molecules on MCF-7 Breast Cancer Cells. Int J Mol Sci 2021;22:3410. [PMID: 33810274 DOI: 10.3390/ijms22073410] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
39 Kasama K, Kanomata K, Hinami Y, Mizuno K, Uetake Y, Amaya T, Sako M, Takizawa S, Sasai H, Akai S. Chemo- and regioselective cross-dehydrogenative coupling reaction of 3-hydroxycarbazoles with arenols catalyzed by a mesoporous silica-supported oxovanadium. RSC Adv 2021;11:35342-35350. [DOI: 10.1039/d1ra07723f] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
40 Shalini, Kumar V. Have molecular hybrids delivered effective anti-cancer treatments and what should future drug discovery focus on? Expert Opin Drug Discov 2021;16:335-63. [PMID: 33305635 DOI: 10.1080/17460441.2021.1850686] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
41 Lang DK, Kaur R, Arora R, Saini B, Arora S. Nitrogen-Containing Heterocycles as Anticancer Agents: An Overview. ACAMC 2020;20:2150-68. [DOI: 10.2174/1871520620666200705214917] [Cited by in Crossref: 42] [Cited by in F6Publishing: 49] [Article Influence: 21.0] [Reference Citation Analysis]
42 Dierks A, Fliegel L, Schmidtmann M, Christoffers J. Preparation of Hexahydrocarbazole Derivatives by Reductive Indolization. Eur J Org Chem 2020;2020:7164-75. [DOI: 10.1002/ejoc.202001226] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
43 Pandey V, Raza MK, Sonowal M, Gupta I. BODIPY based red emitters: Synthesis, computational and biological studies. Bioorg Chem 2021;106:104467. [PMID: 33223201 DOI: 10.1016/j.bioorg.2020.104467] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
44 Bondock S, Nasr T, Alqahtanti S. Synthesis and In Vitro Antitumor Evaluation of Some Carbazole‐Based Thiazole, Thiophene, and 1,3,4‐Thiadiazole Derivatives. ChemistrySelect 2020;5:12087-97. [DOI: 10.1002/slct.202002912] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
45 Debnath S, Das T, Pati TK, Majumdar S, Maiti DK. Metal-Free Indole-Phenacyl Bromide Cyclization: A Regioselective Synthesis of 3,5-Diarylcarbazoles. J Org Chem 2020;85:13272-9. [PMID: 33006280 DOI: 10.1021/acs.joc.0c01670] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
46 Bondock S, Alqahtani S, Fouda AM. Synthesis and anticancer evaluation of some new pyrazolo[3,4‐ d ][1,2,3]triazin‐4‐ones, pyrazolo[1,5‐ a ]pyrimidines, and imidazo[1,2‐ b ]pyrazoles clubbed with carbazole. J Heterocyclic Chem 2021;58:56-73. [DOI: 10.1002/jhet.4148] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 4.5] [Reference Citation Analysis]
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48 Chylewska A, Dąbrowska AM, Ramotowska S, Maciejewska N, Olszewski M, Bagiński M, Makowski M. Photosensitive and pH-dependent activity of pyrazine-functionalized carbazole derivative as promising antifungal and imaging agent. Sci Rep 2020;10:11767. [PMID: 32678219 DOI: 10.1038/s41598-020-68758-w] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
49 Choi S, Park J, Yu E, Sim J, Park CM. Electrosynthesis of Dihydropyrano[4,3-b]indoles Based on a Double Oxidative [3+3] Cycloaddition. Angew Chem Int Ed Engl 2020;59:11886-91. [PMID: 32329937 DOI: 10.1002/anie.202003364] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 7.5] [Reference Citation Analysis]
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52 Saha S, Maji MS. One-pot access to tetrahydrobenzo[ c ]carbazoles from simple ketones by using O 2 as an oxidant. Org Biomol Chem 2020;18:1765-8. [DOI: 10.1039/c9ob02751c] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
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54 Yaragorla S, Dada R, Bag D. An Expeditious Benzannulation Reaction of Indol-3-yl-but-3-yn-2-ols to Substituted 2-Iodocarbazoles via Domino 5- endo Spirocyclization/Selective Vinyl Shift and Aromatization: An Expeditious Benzannulation Reaction of Indol-3-yl-but-3-yn-2-ols to Substituted 2-Iodocarbazoles via Domino 5-endo Spirocyclization/Selective Vinyl. Eur J Org Chem 2019;2019:6983-8. [DOI: 10.1002/ejoc.201901393] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 3.3] [Reference Citation Analysis]