BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Xu Z, Chen Q, Zhang Y, Liang C. Coumarin-based derivatives with potential anti-HIV activity. Fitoterapia 2021;150:104863. [PMID: 33582266 DOI: 10.1016/j.fitote.2021.104863] [Cited by in Crossref: 21] [Cited by in F6Publishing: 11] [Article Influence: 10.5] [Reference Citation Analysis]
Number Citing Articles
1 Fan Y, Wu Y, Hou J, Wang P, Peng X, Ge G. Coumarin-based near-infrared fluorogenic probes: Recent advances, challenges and future perspectives. Coordination Chemistry Reviews 2023;480:215020. [DOI: 10.1016/j.ccr.2023.215020] [Reference Citation Analysis]
2 Alshaye NA, Ibrahim MA. Synthesis, characterization and biological evaluation of the novel chromenopyridothiazolopyrimidines and chromenopyridopyrimidothiazolo-pyrimidines. Synthetic Communications 2023. [DOI: 10.1080/00397911.2023.2172684] [Reference Citation Analysis]
3 A. Ibrahim M, A. Alshaye N. Synthesis and Characterization of Some Novel Heteroannulated Chromeno[4,3-b]quinolines. HETEROCYCLES 2023;106:117. [DOI: 10.3987/com-22-14770] [Reference Citation Analysis]
4 Miyata R, Shigeta T, Egi M, Kumazawa S. Selective Syntheses of Coumarin and Benzofuran Derivatives Using Phenols and α-Methoxy-β-ketoesters. SynOpen 2023;07:8-16. [DOI: 10.1055/s-0042-1751408] [Reference Citation Analysis]
5 Litasova EV, Iljin VV, Myznikov LV, Brusina MA, Piotrovskiy LB. Coumarins as a base for the drug development: yes or no? Medical academic journal 2022;22:27-36. [DOI: 10.17816/maj87582] [Reference Citation Analysis]
6 Patel DK. Therapeutic role of columbianadin in human disorders: Medicinal importance, biological properties and analytical aspects. Pharmacological Research - Modern Chinese Medicine 2022. [DOI: 10.1016/j.prmcm.2022.100212] [Reference Citation Analysis]
7 Aloia A, Casiello M, D'Accolti L, Fusco C, Nacci A, Monopoli A. Direct Synthesis of 3-Aryl Substituted Isocoumarins and Phthalides through Palladium Acetate Catalyzed C(sp(2) )-H Activation in Ionic Liquids. Chemistry 2022;28:e202202350. [PMID: 35997238 DOI: 10.1002/chem.202202350] [Reference Citation Analysis]
8 Zhou B, Yuan X, Fan L, Pan Z, Chang X, Jiang S, Wu L, Wang C, Yang G, Ji X, Shi L, Xu C. Synthesis and antifungal activities of novel trifluoroethane derivatives with coumarin, indole and thiophene. Journal of Saudi Chemical Society 2022. [DOI: 10.1016/j.jscs.2022.101572] [Reference Citation Analysis]
9 Deng C, Yan H, Wang J, Liu B, Liu K, Shi Y. The anti-HIV potential of imidazole, oxazole and thiazole hybrids: A mini-review. Arabian Journal of Chemistry 2022;15:104242. [DOI: 10.1016/j.arabjc.2022.104242] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
10 Pasuparthy SD, Maiti B. [CMMIM][BF 4 ] Ionic Liquid-Catalyzed Facile, One-Pot Synthesis of Chromeno[4,3- d ]pyrido[1,2- a ]pyrimidin-6-ones: Evaluation of Their Photophysical Properties and Theoretical Calculations. ACS Omega. [DOI: 10.1021/acsomega.2c05015] [Reference Citation Analysis]
11 Deng C, Yan H, Wang J, Liu K, Liu B, Shi Y. Current scenario on non-nucleoside reverse transcriptase inhibitors (2018-present). Arabian Journal of Chemistry 2022. [DOI: 10.1016/j.arabjc.2022.104378] [Reference Citation Analysis]
12 Luo F, Manse Y, Chaipech S, Pongpiriyadacha Y, Muraoka O, Morikawa T. Phytochemicals with Chemopreventive Activity Obtained from the Thai Medicinal Plant Mammea siamensis (Miq.) T. Anders.: Isolation and Structure Determination of New Prenylcoumarins with Inhibitory Activity against Aromatase. IJMS 2022;23:11233. [DOI: 10.3390/ijms231911233] [Reference Citation Analysis]
13 Avishi Z, Heydari R, Fatahpour M. Zirconia nanoparticle accelerated one-pot three-component synthesis of polysubstituted coumarins. J IRAN CHEM SOC 2022;19:3869-3874. [DOI: 10.1007/s13738-022-02561-4] [Reference Citation Analysis]
14 Suksawat T, Panichayupakaranant P. Herbal Medicines for HIV Infection and AIDS. Herbal Drugs for the Management of Infectious Diseases 2022. [DOI: 10.1002/9781119818779.ch11] [Reference Citation Analysis]
15 Kumar S, Saroha B, Kumar G, Lathwal E, Kumar S, Parshad B, Kumari M, Kumar N, Mphahlele-makgwane MM, Makgwane PR. Recent Developments in Nanocatalyzed Green Synthetic Protocols of Biologically Potent Diverse O-Heterocycles—A Review. Catalysts 2022;12:657. [DOI: 10.3390/catal12060657] [Reference Citation Analysis]
16 Korkmaz A. Synthesis, Characterization, ADMET prediction, and Molecular Docking Studies of Novel Coumarin Sulfonate Derivatives. Journal of the Institute of Science and Technology. [DOI: 10.21597/jist.1089701] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
17 Hasanpour Galehban M, Zeynizadeh B, Mousavi H. Diverse and efficient catalytic applications of new cockscomb flower-like Fe3O4@SiO2@KCC-1@MPTMS@CuII mesoporous nanocomposite in the environmentally benign reduction and reductive acetylation of nitroarenes and one-pot synthesis of some coumarin compounds. RSC Adv 2022;12:11164-89. [PMID: 35479105 DOI: 10.1039/d1ra08763k] [Cited by in Crossref: 2] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
18 Adimule VM, Nandi SS, Kerur SS, Khadapure SA, Chinnam S. Recent Advances in the One-Pot Synthesis of Coumarin Derivatives from Different Starting Materials Using Nanoparticles: A Review. Top Catal. [DOI: 10.1007/s11244-022-01571-z] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 6.0] [Reference Citation Analysis]
19 Görmez Ö, Akay S, Gözmen B, Kayan B, Kalderis D. Degradation of emerging contaminant coumarin based on anodic oxidation, electro-Fenton and subcritical water oxidation processes. Environ Res 2022;:112736. [PMID: 35041815 DOI: 10.1016/j.envres.2022.112736] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
20 E. Ali T, A. Assiri M, Y. Alzahrani A, A. Salem M. Ultrasound Assisted One Pot, Three-Component Reaction for Facile Design of Novel 1,2,3-Diazaphosphole, 1,5,2-Diazaphosphinine and 1,5,2-Diazaphosphepine Compounds Containing Coumarin Ring. HETEROCYCLES 2022;104. [DOI: 10.3987/com-22-14666] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
21 El-mahalawy AM, Abdou MM, Wassel AR. Physical and optoelectronic characteristics of novel low-cost synthesized coumarin dye-based metal-free thin films for light sensing applications. Materials Science in Semiconductor Processing 2022;137:106225. [DOI: 10.1016/j.mssp.2021.106225] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 10.0] [Reference Citation Analysis]
22 A. Ibrahim M, A. Alshaye N. 4-Amino-3-formylcoumarin as Building Block for Construction of Novel Heteroannulated Coumarins: Synthesis, Characterization and Antimicrobial Evaluation. HETEROCYCLES 2022;104. [DOI: 10.3987/com-22-14748] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
23 Li Z, Wang F, Liu Y, Zhai D, Zhang X, Ying Q, Jia M, Xue X, Meng J, Li J, Wu X, Li M. Coumarin Derivative N6 as a Novel anti-hantavirus Infection Agent Targeting AKT. Front Pharmacol 2021;12:745646. [PMID: 34938178 DOI: 10.3389/fphar.2021.745646] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
24 Xu L, Yang H, Hu R, Liang Y, Li Y, Xu W, Fan X, Liu Y. Comparing the interaction of four structurally similar coumarins from Fraxinus Chinensis Roxb. with HSA through multi-spectroscopic and docking studies. Journal of Molecular Liquids 2021;340:117234. [DOI: 10.1016/j.molliq.2021.117234] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
25 Kang D, Urhan Ç, Wei F, Frutos-Beltrán E, Sun L, Álvarez M, Feng D, Tao Y, Pannecouque C, De Clercq E, Menéndez-Arias L, Liu X, Zhan P. Discovery, optimization, and target identification of novel coumarin derivatives as HIV-1 reverse transcriptase-associated ribonuclease H inhibitors. Eur J Med Chem 2021;225:113769. [PMID: 34403976 DOI: 10.1016/j.ejmech.2021.113769] [Cited by in Crossref: 3] [Cited by in F6Publishing: 5] [Article Influence: 1.5] [Reference Citation Analysis]
26 Simic M, Petkovic M, Jovanovic P, Jovanovic M, Tasic G, Besu I, Zizak Z, Aleksic I, Nikodinovic-Runic J, Savic V. Fragment-type 4-azolylcoumarin derivatives with anticancer properties. Arch Pharm (Weinheim) 2021;:e2100238. [PMID: 34374111 DOI: 10.1002/ardp.202100238] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
27 Carvalho RL, de Miranda AS, Nunes MP, Gomes RS, Jardim GAM, Júnior ENDS. On the application of 3d metals for C-H activation toward bioactive compounds: The key step for the synthesis of silver bullets. Beilstein J Org Chem 2021;17:1849-938. [PMID: 34386103 DOI: 10.3762/bjoc.17.126] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 3.5] [Reference Citation Analysis]
28 Xu X, Yan Y, Huang W, Mo T, Wang X, Wang J, Li J, Shi S, Liu X, Tu P. Molecular cloning and biochemical characterization of a new coumarin glycosyltransferase CtUGT1 from Cistanche tubulosa. Fitoterapia 2021;153:104995. [PMID: 34293438 DOI: 10.1016/j.fitote.2021.104995] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]