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Cited by in F6Publishing
For: Yu W, Tong L, Hu B, Zhong B, Hao J, Ji T, Zan S, Coburn CA, Selyutin O, Chen L, Rokosz L, Agrawal S, Liu R, Curry S, McMonagle P, Ingravallo P, Asante-Appiah E, Chen S, Kozlowski JA. Discovery of Chromane Containing Hepatitis C Virus (HCV) NS5A Inhibitors with Improved Potency against Resistance-Associated Variants. J Med Chem 2016;59:10228-43. [PMID: 27792320 DOI: 10.1021/acs.jmedchem.6b01234] [Cited by in Crossref: 20] [Cited by in F6Publishing: 15] [Article Influence: 3.3] [Reference Citation Analysis]
Number Citing Articles
1 Grande F, Occhiuzzi MA, Ioele G, Ragno G, Garofalo A. Benzopyrroloxazines containing a bridgehead nitrogen atom as promising scaffolds for the achievement of biologically active agents. European Journal of Medicinal Chemistry 2018;151:121-44. [DOI: 10.1016/j.ejmech.2018.03.061] [Cited by in Crossref: 10] [Cited by in F6Publishing: 4] [Article Influence: 2.5] [Reference Citation Analysis]
2 Zhu R, Zhang Y, Yang J, Yang Y, Xue Y. Computational insight into the mechanism and origin of high regioselectivity in the ring-opening cyclization of spirocyclopropanes with stabilized sulfonium ylides by the DFT. J Mol Model 2020;26:255. [PMID: 32876902 DOI: 10.1007/s00894-020-04522-1] [Reference Citation Analysis]
3 Yuan Y, Pan G, Zhang X, Huang Q. One pot synthesis of pyrrolo[3,2,1- de ]phenanthridines from 7-phenylindoles via tandem C–H olefination/aza-Michael addition. Org Chem Front 2020;7:53-63. [DOI: 10.1039/c9qo01135h] [Cited by in Crossref: 6] [Article Influence: 3.0] [Reference Citation Analysis]
4 Pan G, Lu L, Zhuang W, Huang Q. Synthesis of Indole-Fused Six-, Seven-, or Eight-Membered N,O-Heterocycles via Rhodium-Catalyzed NH-Indole-Directed C-H Acetoxylation/Hydrolysis/Annulation. J Org Chem 2021;86:16753-63. [PMID: 34756052 DOI: 10.1021/acs.joc.1c01982] [Reference Citation Analysis]
5 Meng L, Wang Q, Tang T, Xiao S, Zhang L, Zhou D, Yu F. Design, Synthesis and Biological Evaluation of Pentacyclic Triterpene Dimers as HCV Entry Inhibitors: Design, Synthesis and Biological Evaluation of Pentacyclic Triterpene Dimers as HCV Entry Inhibitors. Chin J Chem 2017;35:1322-8. [DOI: 10.1002/cjoc.201700272] [Cited by in Crossref: 2] [Article Influence: 0.4] [Reference Citation Analysis]
6 Asante-Appiah E, Liu R, Curry S, McMonagle P, Agrawal S, Carr D, Rokosz L, Lahser F, Bystol K, Chase R, Black S, Ferrari E, Ingravallo P, Tong L, Yu W, Kozlowski J. In Vitro Antiviral Profile of Ruzasvir, a Potent and Pangenotype Inhibitor of Hepatitis C Virus NS5A. Antimicrob Agents Chemother 2018;62:e01280-18. [PMID: 30150466 DOI: 10.1128/AAC.01280-18] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
7 Tong L, Yu W, Coburn CA, Chen L, Selyutin O, Zeng Q, Dwyer MP, Nair AG, Shankar BB, Kim SH, Yang DY, Rosenblum SB, Ruck RT, Davies IW, Hu B, Zhong B, Hao J, Ji T, Zan S, Liu R, Agrawal S, Carr D, Curry S, McMonagle P, Bystol K, Lahser F, Ingravallo P, Chen S, Asante-Appiah E, Kozlowski JA. Structure-activity relationships of proline modifications around the tetracyclic-indole class of NS5A inhibitors. Bioorg Med Chem Lett 2016;26:5354-60. [PMID: 27680588 DOI: 10.1016/j.bmcl.2016.08.097] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 1.5] [Reference Citation Analysis]
8 Boureghda C, Macé A, Berrée F, Roisnel T, Debache A, Carboni B. Ene reactions of 2-borylated α-methylstyrenes: a practical route to 4-methylenechromanes and derivatives. Org Biomol Chem 2019;17:5789-800. [PMID: 31135020 DOI: 10.1039/c9ob00963a] [Cited by in Crossref: 2] [Article Influence: 0.7] [Reference Citation Analysis]
9 Zheng Y, Qiu L, Hong K, Dong S, Xu X. Copper- or Thermally Induced Divergent Outcomes: Synthesis of 4-Methyl 2 H -Chromenes and Spiro-4 H -Pyrazoles. Chem Eur J 2018;24:6705-11. [DOI: 10.1002/chem.201704759] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 2.2] [Reference Citation Analysis]
10 Wu YJ, Meanwell NA. Geminal Diheteroatomic Motifs: Some Applications of Acetals, Ketals, and Their Sulfur and Nitrogen Homologues in Medicinal Chemistry and Drug Design. J Med Chem 2021;64:9786-874. [PMID: 34213340 DOI: 10.1021/acs.jmedchem.1c00790] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
11 Zhang C, Dong S, Zheng Y, He C, Chen J, Zhen J, Qiu L, Xu X. Synthesis of spiro-4H-pyrazole-oxindoles and fused 1H-pyrazoles via divergent, thermally induced tandem cyclization/migration of alkyne-tethered diazo compounds. Org Biomol Chem 2018;16:688-92. [PMID: 29239450 DOI: 10.1039/c7ob02802d] [Cited by in Crossref: 10] [Cited by in F6Publishing: 1] [Article Influence: 3.3] [Reference Citation Analysis]
12 Tong L, Yu W, Chen L, Selyutin O, Dwyer MP, Nair AG, Mazzola R, Kim JH, Sha D, Yin J. Discovery of Ruzasvir (MK-8408): A Potent, Pan-Genotype HCV NS5A Inhibitor with Optimized Activity against Common Resistance-Associated Polymorphisms. J Med Chem. 2017;60:290-306. [PMID: 27808515 DOI: 10.1021/acs.jmedchem.6b01310] [Cited by in Crossref: 33] [Cited by in F6Publishing: 29] [Article Influence: 5.5] [Reference Citation Analysis]
13 Yu W, Tong L, Selyutin O, Chen L, Hu B, Zhong B, Hao J, Ji T, Zan S, Yin J, Ruck RT, Curry S, McMonagle P, Agrawal S, Rokosz L, Carr D, Ingravallo P, Bystol K, Lahser F, Liu R, Chen S, Feng KI, Cartwright M, Asante-Appiah E, Kozlowski JA. Discovery of MK-6169, a Potent Pan-Genotype Hepatitis C Virus NS5A Inhibitor with Optimized Activity against Common Resistance-Associated Substitutions. J Med Chem 2018;61:3984-4003. [PMID: 29681153 DOI: 10.1021/acs.jmedchem.7b01927] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
14 Ilya E, Kulikova L, Van der Eycken EV, Voskressensky L. Recent Advances in Phthalan and Coumaran Chemistry. ChemistryOpen 2018;7:914-29. [PMID: 30498677 DOI: 10.1002/open.201800184] [Cited by in Crossref: 7] [Cited by in F6Publishing: 2] [Article Influence: 1.8] [Reference Citation Analysis]
15 Ma Y, Yin D, Ye J, Wei X, Pei Y, Li X, Si G, Chen XY, Chen ZS, Dong Y, Zou F, Shi W, Qiu Q, Qian H, Liu G. Discovery of Potent Inhibitors against P-Glycoprotein-Mediated Multidrug Resistance Aided by Late-Stage Functionalization of a 2-(4-(Pyridin-2-yl)phenoxy)pyridine Analogue. J Med Chem 2020;63:5458-76. [PMID: 32329342 DOI: 10.1021/acs.jmedchem.0c00337] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 3.5] [Reference Citation Analysis]
16 Ramdas V, Talwar R, Banerjee M, Joshi AA, Das AK, Walke DS, Borhade P, Dhayagude U, Loriya R, Gote G, Bommakanti A, Sivaram A, Agarwal G, Goswami A, Nigade P, Mehta M, Patil V, Modi D, Kumar H, Mallurwar S, Dash A, Modi F, Kuldharan S, Srivastava P, Singh M, Narasimham L, Gundu J, Sharma S, Kamboj RK, Palle VP. Discovery and Characterization of Potent Pan-Genotypic HCV NS5A Inhibitors Containing Novel Tricyclic Central Core Leading to Clinical Candidate. J Med Chem 2019;62:10563-82. [PMID: 31710479 DOI: 10.1021/acs.jmedchem.9b01562] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
17 Qin Z, Yan A. QSAR studies on hepatitis C virus NS5A protein tetracyclic inhibitors in wild type and mutants by CoMFA and CoMSIA. SAR QSAR Environ Res 2020;31:281-311. [PMID: 32208783 DOI: 10.1080/1062936X.2020.1740889] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
18 Peng F, Tan L, Chen L, Dalby SM, Dirocco DA, Duan J, Feng M, Gong G, Guo H, Hethcox JC, Jin L, Johnson HC, Kim J, Le D, Lin Y, Liu W, Shen J, Wan Y, Xiao C, Xiang B, Xiang Q, Xu J, Yan L, Yang W, Ye H, Yu Y, Zhang J. Manufacturing Process Development for Belzutifan, Part 1: A Concise Synthesis of the Indanone Starting Material. Org Process Res Dev . [DOI: 10.1021/acs.oprd.1c00236] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 5.0] [Reference Citation Analysis]
19 Borowiecki P, Justyniak I, Ochal Z. Lipase-catalyzed kinetic resolution approach toward enantiomerically enriched 1-(β-hydroxypropyl)indoles. Tetrahedron: Asymmetry 2017;28:1717-32. [DOI: 10.1016/j.tetasy.2017.10.010] [Cited by in Crossref: 11] [Cited by in F6Publishing: 8] [Article Influence: 2.2] [Reference Citation Analysis]