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For: Hubert J, Nuzillard J, Renault J. Dereplication strategies in natural product research: How many tools and methodologies behind the same concept? Phytochem Rev 2017;16:55-95. [DOI: 10.1007/s11101-015-9448-7] [Cited by in Crossref: 129] [Cited by in F6Publishing: 67] [Article Influence: 18.4] [Reference Citation Analysis]
Number Citing Articles
1 Yin T, Yu Y, Liu Q, Zhu G, Bai L, Zhang W, Jiang Z. 13C-NMR-based MixONat strategy coupled with 2D NMR for rapid dereplication and identification of new secondary metabolites from Aloe vera. Journal of Food Composition and Analysis 2023;115:104975. [DOI: 10.1016/j.jfca.2022.104975] [Reference Citation Analysis]
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3 Anh CV, Kwon J, Kang JS, Lee H, Heo C, Shin HJ. New Angucycline Glycosides from a Marine-Derived Bacterium Streptomyces ardesiacus. IJMS 2022;23:13779. [DOI: 10.3390/ijms232213779] [Reference Citation Analysis]
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6 Kuhn S, Nuzillard J. Easy Structural Dereplication of Natural Products by Means of Predicted Carbon‐13 Nuclear Magnetic Resonance Spectroscopy Data**. Chemistry Methods 2022. [DOI: 10.1002/cmtd.202200054] [Reference Citation Analysis]
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8 McCord JP, Kohanov ZA, Lowell AN. Thermorubin Biosynthesis Initiated by a Salicylate Synthase Suggests an Unusual Conversion of Phenols to Pyrones. ACS Chem Biol 2022. [PMID: 36255735 DOI: 10.1021/acschembio.2c00606] [Reference Citation Analysis]
9 Herbert LA, Bruguière A, Derbré S, Richomme P, Peña-Rodríguez LM. 13C NMR dereplication-assisted isolation of bioactive polyphenolic metabolites from Clusia flava Jacq. Nat Prod Res 2022;:1-10. [PMID: 36214555 DOI: 10.1080/14786419.2022.2130917] [Reference Citation Analysis]
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12 E Silva JPR, Pereira LCO, Abreu LS, Lins FSV, de Souza TA, do Espírito-Santo RF, Barros RPC, Villarreal CF, de Melo JIM, Scotti MT, Costa VCO, Martorano LH, Dos Santos FM Jr, Filho RB, da Silva MS, Tavares JF. Targeted Isolation of Anti-inflammatory Lignans from Justicia aequilabris by Molecular Networking Approach. J Nat Prod 2022. [PMID: 35998343 DOI: 10.1021/acs.jnatprod.2c00478] [Reference Citation Analysis]
13 Das P, Ashraf GJ, Baishya T, Dua TK, Paul P, Nandi G, Sahu R. High-performance thin-layer chromatography coupled attenuated total reflectance-Fourier-transform infrared and NMR spectroscopy-based identification of α-amylase inhibitor from the aerial part of Asparagus racemosus Willd. Phytochem Anal 2022. [PMID: 35730071 DOI: 10.1002/pca.3155] [Reference Citation Analysis]
14 Rivera-Chávez J, Ceapă CD, Figueroa M. Biological Dark Matter Exploration using Data Mining for the Discovery of Antimicrobial Natural Products. Planta Med 2022. [PMID: 35697058 DOI: 10.1055/a-1795-0562] [Reference Citation Analysis]
15 Milman BL, Zhurkovich IK. Present-Day Practice of Non-Target Chemical Analysis. J Anal Chem 2022;77:537-49. [DOI: 10.1134/s1061934822050070] [Reference Citation Analysis]
16 Freire VF, Gubiani JR, Spencer TM, Hajdu E, Ferreira AG, Ferreira DAS, de Castro Levatti EV, Burdette JE, Camargo CH, Tempone AG, Berlinck RGS. Feature-Based Molecular Networking Discovery of Bromopyrrole Alkaloids from the Marine Sponge Agelas dispar. J Nat Prod . [DOI: 10.1021/acs.jnatprod.2c00094] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
17 Hadacek F. Secondary or Specialized Metabolites, or Natural Products: A Case Study of Untargeted LC–QTOF Auto-MS/MS Analysis. Cells 2022;11:1025. [DOI: 10.3390/cells11061025] [Reference Citation Analysis]
18 Lardos A, Aghaebrahimian A, Koroleva A, Sidorova J, Wolfram E, Anisimova M, Gil M. Computational Literature-based Discovery for Natural Products Research: Current State and Future Prospects. Front Bioinform 2022;2:827207. [DOI: 10.3389/fbinf.2022.827207] [Reference Citation Analysis]
19 Wainwright CL, Teixeira MM, Adelson DL, Buenz EJ, David B, Glaser KB, Harata-Lee Y, Howes MJ, Izzo AA, Maffia P, Mayer A, Mazars C, Newman DJ, Nic Lughadha E, Pimenta A, Parra J, Qu Z, Shen H, Spedding M, Wolfender JL. Future Directions for the Discovery of Natural Product-Derived Immunomodulating Drugs. Pharmacol Res 2022;:106076. [PMID: 35074524 DOI: 10.1016/j.phrs.2022.106076] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
20 Reveglia P, Raimondo ML, Masi M, Cimmino A, Nuzzo G, Corso G, Fontana A, Carlucci A, Evidente A. Untargeted and Targeted LC-MS/MS Based Metabolomics Study on In Vitro Culture of Phaeoacremonium Species. JoF 2022;8:55. [DOI: 10.3390/jof8010055] [Reference Citation Analysis]
21 Goryashchenko AS, Uvarova VI, Osolodkin DI, Ishmukhametov AA. Discovery of small molecule antivirals targeting tick-borne encephalitis virus. Annual Reports in Medicinal Chemistry 2022. [DOI: 10.1016/bs.armc.2022.08.007] [Reference Citation Analysis]
22 Puri S, Sahal D, Sharma U. A conversation between hyphenated spectroscopic techniques and phytometabolites from medicinal plants. Analytical Science Advances 2021;2:579-593. [DOI: 10.1002/ansa.202100021] [Reference Citation Analysis]
23 Jarmusch SA, van der Hooft JJJ, Dorrestein PC, Jarmusch AK. Advancements in capturing and mining mass spectrometry data are transforming natural products research. Nat Prod Rep 2021;38:2066-82. [PMID: 34612288 DOI: 10.1039/d1np00040c] [Cited by in Crossref: 15] [Cited by in F6Publishing: 16] [Article Influence: 15.0] [Reference Citation Analysis]
24 Li G, Lin P, Wang K, Gu CC, Kusari S. Artificial intelligence-guided discovery of anticancer lead compounds from plants and associated microorganisms. Trends Cancer 2022;8:65-80. [PMID: 34750090 DOI: 10.1016/j.trecan.2021.10.002] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
25 Pollastro F, Minassi A. Exploring the Universe of Natural Products: Recent Advances in Synthesis, Isolation and Structural Elucidation. Plants 2021;10:2368. [DOI: 10.3390/plants10112368] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
26 Caldas LA, Soares DM, Menolli N, Stevani CV, Sartorelli P. Metabolomics of the wild mushroom Gymnopilus imperialis (Agaricomycetes, Basidiomycota) by UHPLC-HRMS/MS analysis and molecular network. Fungal Biology 2021. [DOI: 10.1016/j.funbio.2021.11.005] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
27 Bracegirdle J, Hou P, Nowak VV, Ackerley DF, Keyzers RA, Owen JG. Skyllamycins D and E, Non-Ribosomal Cyclic Depsipeptides from Lichen-Sourced Streptomyces anulatus. J Nat Prod 2021;84:2536-43. [PMID: 34490774 DOI: 10.1021/acs.jnatprod.1c00547] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
28 de Mello RFA, de Souza Pinheiro WB, Benjamim JKF, de Siqueira FC, Chisté RC, Santos AS. A fast and efficient preparative method for separation and purification of main bioactive xanthones from the waste of Garcinia mangostana L. by high-speed countercurrent chromatography. Arabian Journal of Chemistry 2021;14:103252. [DOI: 10.1016/j.arabjc.2021.103252] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
29 Tomou E, Lytra K, Chrysargyris A, Tzortzakis N, Skaltsa H. NMR Fingerprint Comparison of Cultivated Sideritis spp. from Cyprus. Agronomy 2021;11:1503. [DOI: 10.3390/agronomy11081503] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
30 Nuzillard J. Taxonomy-Focused Natural Product Databases for Carbon-13 NMR-Based Dereplication. Analytica 2021;2:50-6. [DOI: 10.3390/analytica2030006] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
31 Sarkar A, Kim EY, Jang T, Hongdusit A, Kim H, Choi JM, Fox JM. Microbially Guided Discovery and Biosynthesis of Biologically Active Natural Products. ACS Synth Biol 2021;10:1505-19. [PMID: 33988973 DOI: 10.1021/acssynbio.1c00074] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
32 de Carvalho Martins V, França LP, da Silva Ferreira Y, Pires DC, de Souza Cardoso B, Pessanha de Araújo Santiago MC, Pacheco S, da Costa Souza M, Riger CJ, de Oliveira Godoy RL, Geraldo de Carvalho M. Determination of the Phytochemical Composition and Antioxidant Potential of Eugenia copacabanensis and Myrciaria tenella Leaves (Myrtaceae) Using a Saccharomyces cerevisiae Model. Chem Biodivers 2021;18:e2100054. [PMID: 33915032 DOI: 10.1002/cbdv.202100054] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
33 Silva-Castro LF, Derbré S, Le Ray AM, Richomme P, García-Sosa K, Peña-Rodriguez LM. Using 13 C-NMR dereplication to aid in the identification of xanthones present in the stem bark extract of Calophyllum brasiliense. Phytochem Anal 2021. [PMID: 33938065 DOI: 10.1002/pca.3051] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
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35 Dantas CAG, Abreu LS, da Cunha HN, Veloso CAG, Souto AL, de Fátima Agra M, de Oliveira Costa VC, da Silva MS, Tavares JF. Dereplication of phenolic derivatives of three Erythroxylum species using liquid chromatography coupled with ESI-MSn and HRESIMS. Phytochem Anal 2021. [PMID: 33738879 DOI: 10.1002/pca.3043] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
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42 Abbas-Mohammadi M, Moridi Farimani M, Salehi P, Ebrahimi SN, Sonboli A, Kelso C, Skropeta D. Molecular networking based dereplication of AChE inhibitory compounds from the medicinal plant Vincetoxicum funebre (Boiss. & Kotschy). J Biomol Struct Dyn 2020;:1-10. [PMID: 33054569 DOI: 10.1080/07391102.2020.1834455] [Reference Citation Analysis]
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