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For: Khatri HR, Bhattarai B, Kaplan W, Li Z, Curtis Long MJ, Aye Y, Nagorny P. Modular Total Synthesis and Cell-Based Anticancer Activity Evaluation of Ouabagenin and Other Cardiotonic Steroids with Varying Degrees of Oxygenation. J Am Chem Soc 2019;141:4849-60. [PMID: 30802047 DOI: 10.1021/jacs.8b12870] [Cited by in Crossref: 37] [Cited by in F6Publishing: 36] [Article Influence: 12.3] [Reference Citation Analysis]
Number Citing Articles
1 Zhou Z, Xu D, Jiang W, Chen J, Zhen Y, Huo J, Yan J, Gao J, Xie W. Convergent Synthesis of Enantioenriched ortho-Fused Tricyclic Diketones via Catalytic Asymmetric Intramolecular Vinylogous Aldol Condensation. Org Lett 2022. [DOI: 10.1021/acs.orglett.2c03645] [Reference Citation Analysis]
2 Eid S, Zerbes T, Williams D, Wang X, Sackmann C, Meier S, Dulin NO, Nagorny P, Schmitt-ulms G. Identification of a Cardiac Glycoside Exhibiting Favorable Brain Bioavailability and Potency for Reducing Levels of the Cellular Prion Protein. IJMS 2022;23:14823. [DOI: 10.3390/ijms232314823] [Reference Citation Analysis]
3 Abouzied AS, Abd-Rabo MM, Huwaimel B, Almahmoud SA, Almarshdi AA, Alharbi FM, Alenzi SS, Albsher BN, Alafnan A. In Silico Pharmacokinetic Profiling of the Identified Bioactive Metabolites of Pergularia tomentosa L. Latex Extract and In Vitro Cytotoxic Activity via the Induction of Caspase-Dependent Apoptosis with S-Phase Arrest. Pharmaceuticals (Basel) 2022;15:1132. [PMID: 36145353 DOI: 10.3390/ph15091132] [Reference Citation Analysis]
4 Eid S, Zerbes T, Williams D, Wang X, Sackmann C, Meier S, Dulin NO, Nagorny P, Schmitt-ulms G. Identification of a cardiac glycoside exhibiting favorable brain bioavailability and potency for reducing levels of the cellular prion protein.. [DOI: 10.1101/2022.08.22.504810] [Reference Citation Analysis]
5 Huang Z, Pan X, Guo L, Tang W. A Concise Total Synthesis of Steroid Scaffolds via a Palladium-Catalyzed Dearomatization Cyclization. Synlett. [DOI: 10.1055/s-0042-1751356] [Reference Citation Analysis]
6 Zhao Y, Zhang B, Sun ZQ, Zhang H, Wang W, Wang ZR, Guo ZK, Yu S, Tan RX, Ge HM. Biocatalytic C14-Hydroxylation on Androstenedione Enabled Modular Synthesis of Cardiotonic Steroids. ACS Catal . [DOI: 10.1021/acscatal.2c02185] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
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8 Huang W, He Y, Jiang R, Deng Z, Long F. Functional and Structural Dissection of a Plant Steroid 3- O -Glycosyltransferase Facilitated the Engineering Enhancement of Sugar Donor Promiscuity. ACS Catal 2022;12:2927-37. [DOI: 10.1021/acscatal.1c05729] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
9 Chen W, Chen C, Chang T, Hsieh F, Chen W, Li W. Design, synthesis, and characterization of oxadiazolopyrazine analogs with application as anticancer agents. J Chinese Chemical Soc. [DOI: 10.1002/jccs.202100438] [Reference Citation Analysis]
10 Husain A, Bedi S, Parveen S, Khan SA, Ahmad A, Iqbal MA, Farooq A, Ahmed A. Furanone-functionalized benzothiazole derivatives: synthesis, in vitro cytotoxicity, ADME, and molecular docking studies. Zeitschrift für Naturforschung B 2022;77:41-53. [DOI: 10.1515/znb-2021-0146] [Reference Citation Analysis]
11 Fejedelem Z, Carney N, Nagorny P. Synthesis of Cardiotonic Steroids Oleandrigenin and Rhodexin B. J Org Chem 2021;86:10249-62. [PMID: 34255963 DOI: 10.1021/acs.joc.1c00985] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
12 Long MJC, Aye Y. Science's Response to CoVID-19. ChemMedChem 2021;16:2288-314. [PMID: 33811458 DOI: 10.1002/cmdc.202100079] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
13 Mowery P, Filkorn MM, Hurysz B, Kwansare DO, Lafferty MM, McFadden MA, Neerukonda ND, Patel RR, Pierce K, Sockett KA, Truax NJ, Webster NR, Pelkey ET. Discovery of an indole-substituted furanone with tubulin polymerization inhibition activity. Bioorg Med Chem Lett 2021;41:127991. [PMID: 33775833 DOI: 10.1016/j.bmcl.2021.127991] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
14 Marahatha R, Gyawali K, Sharma K, Gyawali N, Tandan P, Adhikari A, Timilsina G, Bhattarai S, Lamichhane G, Acharya A, Pathak I, Devkota HP, Parajuli N. Pharmacologic activities of phytosteroids in inflammatory diseases: Mechanism of action and therapeutic potentials. Phytother Res 2021. [PMID: 33957012 DOI: 10.1002/ptr.7138] [Cited by in Crossref: 14] [Cited by in F6Publishing: 17] [Article Influence: 14.0] [Reference Citation Analysis]
15 Wang Z, Hui C. Contemporary advancements in the semi-synthesis of bioactive terpenoids and steroids. Org Biomol Chem 2021;19:3791-812. [PMID: 33949606 DOI: 10.1039/d1ob00448d] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
16 Shalit ZA, Valdes LC, Kim WS, Micalizio GC. From an ent-Estrane, through a nat-Androstane, to the Total Synthesis of the Marine-Derived Δ8,9-Pregnene (+)-03219A. Org Lett 2021;23:2248-52. [PMID: 33635666 DOI: 10.1021/acs.orglett.1c00382] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
17 Watanabe S, Nishikawa T, Nakazaki A. Total Synthesis of the Cardiotonic Steroid (+)-Cannogenol. J Org Chem 2021;86:3605-14. [PMID: 33538172 DOI: 10.1021/acs.joc.0c02966] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
18 Wei MX, Yu JY, Liu XX, Li XQ, Zhang MW, Yang PW, Yang JH. Synthesis of artemisinin-piperazine-furan ether hybrids and evaluation of in vitro cytotoxic activity. Eur J Med Chem 2021;215:113295. [PMID: 33636536 DOI: 10.1016/j.ejmech.2021.113295] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 10.0] [Reference Citation Analysis]
19 Jiang Y, Mcnamee RE, Smith PJ, Sozanschi A, Tong Z, Anderson EA. Advances in polycyclization cascades in natural product synthesis. Chem Soc Rev 2021;50:58-71. [DOI: 10.1039/d0cs00768d] [Cited by in Crossref: 20] [Cited by in F6Publishing: 22] [Article Influence: 20.0] [Reference Citation Analysis]
20 Yang K, Yang JQ, Luo SH, Mei WJ, Lin JY, Zhan JQ, Wang ZY. Synthesis of N-2(5H)-furanonyl sulfonyl hydrazone derivatives and their biological evaluation in vitro and in vivo activity against MCF-7 breast cancer cells. Bioorg Chem 2021;107:104518. [PMID: 33303210 DOI: 10.1016/j.bioorg.2020.104518] [Cited by in Crossref: 13] [Cited by in F6Publishing: 14] [Article Influence: 6.5] [Reference Citation Analysis]
21 Ayogu JI, Odoh AS. Prospects and Therapeutic Applications of Cardiac Glycosides in Cancer Remediation. ACS Comb Sci 2020;22:543-53. [PMID: 32786321 DOI: 10.1021/acscombsci.0c00082] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 4.0] [Reference Citation Analysis]
22 Shimizu S, Hagiwara K, Itoh H, Inoue M. Unified Total Synthesis of Five Bufadienolides. Org Lett 2020;22:8652-7. [PMID: 33104363 DOI: 10.1021/acs.orglett.0c03251] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
23 Juang YP, Liang PH. Biological and Pharmacological Effects of Synthetic Saponins. Molecules 2020;25:E4974. [PMID: 33121124 DOI: 10.3390/molecules25214974] [Cited by in Crossref: 21] [Cited by in F6Publishing: 21] [Article Influence: 10.5] [Reference Citation Analysis]
24 Fedoseev SV, Belikov MY, Ershov OV, Tafeenko VA. Synthesis of 4-Halofuro[3,4-c]pyridin-3(1H)-ones from 2-Halopyridine-3,4-dicarbonitriles. Russ J Org Chem 2020;56:1540-4. [DOI: 10.1134/s1070428020090067] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
25 Husain A, Bhutani M, Parveen S, Khan SA, Ahmad A, Iqbal MA. Synthesis, in vitro cytotoxicity, ADME, and molecular docking studies of benzimidazole‐bearing furanone derivatives. J Chin Chem Soc 2021;68:362-73. [DOI: 10.1002/jccs.202000130] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
26 Schuppe AW, Liu Y, Newhouse TR. An invocation for computational evaluation of isomerization transforms: cationic skeletal reorganizations as a case study. Nat Prod Rep 2021;38:510-27. [PMID: 32931541 DOI: 10.1039/d0np00005a] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
27 Cheng MJ, Zhong LP, Gu CC, Zhu XJ, Chen B, Liu JS, Wang L, Ye WC, Li CC. Asymmetric Total Synthesis of Bufospirostenin A. J Am Chem Soc 2020;142:12602-7. [PMID: 32658467 DOI: 10.1021/jacs.0c05479] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 8.5] [Reference Citation Analysis]
28 Shostko DY, Liubina A, Kozyrkov Y, Beliaev S. The synthesis of 4-chloro-17β-hydroxymethyl-17α-methyl-18-norandrosta-4,13-diene-3α-ol – Proposed long term metabolite (M4) of oralturinabol. Steroids 2020;158:108601. [DOI: 10.1016/j.steroids.2020.108601] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
29 Townsend D, Shankland K, Weymouth‐wilson A, Komsta Z, Evans T, Cobb AJA. Highly Enantioselective, Organocatalytic, and Scalable Synthesis of a Rare cis,cis ‐Tricyclic Diterpenoid. Chem Eur J 2020;26:3504-8. [DOI: 10.1002/chem.202000164] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
30 Ren Y, Ribas HT, Heath K, Wu S, Ren J, Shriwas P, Chen X, Johnson ME, Cheng X, Burdette JE, Kinghorn AD. Na+/K+-ATPase-Targeted Cytotoxicity of (+)-Digoxin and Several Semisynthetic Derivatives. J Nat Prod 2020;83:638-48. [PMID: 32096998 DOI: 10.1021/acs.jnatprod.9b01060] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 8.5] [Reference Citation Analysis]
31 Khatri HR, Carney N, Rutkoski R, Bhattarai B, Nagorny P. Recent Progress in Steroid Synthesis Triggered by the Emergence of New Catalytic Methods: Recent Progress in Steroid Synthesis Triggered by the Emergence of New Catalytic Methods. Eur J Org Chem 2020;2020:755-76. [DOI: 10.1002/ejoc.201901466] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 6.5] [Reference Citation Analysis]
32 Fu S, Liu B. Recent progress in the synthesis of limonoids and limonoid-like natural products. Org Chem Front 2020;7:1903-47. [DOI: 10.1039/d0qo00203h] [Cited by in Crossref: 12] [Cited by in F6Publishing: 14] [Article Influence: 6.0] [Reference Citation Analysis]
33 Sun AW, Lackner S, Stoltz BM. Modularity: Adding New Dimensions to Total Synthesis. Trends in Chemistry 2019;1:630-43. [DOI: 10.1016/j.trechm.2019.05.008] [Cited by in Crossref: 23] [Cited by in F6Publishing: 24] [Article Influence: 7.7] [Reference Citation Analysis]
34 Watanabe S, Nishikawa T, Nakazaki A. Synthesis of Oxy-Functionalized Steroidal Skeletons via Mizoroki-Heck and Intramolecular Diels-Alder Reactions. Org Lett 2019;21:7410-4. [PMID: 31498649 DOI: 10.1021/acs.orglett.9b02716] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 2.7] [Reference Citation Analysis]
35 Wu H, Yang K, Luo S, Wu X, Wang N, Chen S, Wang Z. C4-Selective Synthesis of Vinyl Thiocyanates and Selenocyanates Through 3,4-Dihalo-2(5 H )-furanones: C4-Selective Synthesis of Vinyl Thiocyanates and Selenocyanates Through 3,4-Dihalo-2(5 H )-furanones. Eur J Org Chem 2019;2019:4572-80. [DOI: 10.1002/ejoc.201900749] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 3.3] [Reference Citation Analysis]
36 Luo SH, Yang K, Lin JY, Gao JJ, Wu XY, Wang ZY. Synthesis of amino acid derivatives of 5-alkoxy-3,4-dihalo-2(5H)-furanones and their preliminary bioactivity investigation as linkers. Org Biomol Chem 2019;17:5138-47. [PMID: 31073571 DOI: 10.1039/c9ob00736a] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 3.3] [Reference Citation Analysis]
37 Wu H, Yang K, Chen X, Arulkumar M, Wang N, Chen S, Wang Z. A 3,4-dihalo-2(5 H )-furanone initiated ring-opening reaction of DABCO in the absence of a metal catalyst and additive and its application in a one-pot two-step reaction. Green Chem 2019;21:3782-8. [DOI: 10.1039/c9gc01740b] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 4.0] [Reference Citation Analysis]