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For: Bai M, Chen J, Xu W, Dong S, Liu Q, Lin B, Huang X, Yao G, Song S. Elephantopinolide A-P, germacrane-type sesquiterpene lactones from Elephantopus scaber induce apoptosis, autophagy and G2/M phase arrest in hepatocellular carcinoma cells. European Journal of Medicinal Chemistry 2020;198:112362. [DOI: 10.1016/j.ejmech.2020.112362] [Cited by in Crossref: 24] [Cited by in F6Publishing: 25] [Article Influence: 12.0] [Reference Citation Analysis]
Number Citing Articles
1 Chen J, Yan Q, Bai M, Liu Q, Song S, Yao G. Deoxyelephantopin, a germacrane‐type sesquiterpene lactone from Elephantopus scaber , induces mitochondrial apoptosis of hepatocarcinoma cells by targeting Hsp90 α in vitro and in vivo. Phytotherapy Research 2022. [DOI: 10.1002/ptr.7654] [Reference Citation Analysis]
2 Bai M, Xu W, Li Q, Liu DF, Lv TM, Du NN, Yao GD, Lin B, Song SJ, Huang XX. Highly Oxidized Germacranolides from Elephantopus tomentosus and the Configurational Revision of Some Previously Reported Analogues. J Nat Prod 2022. [PMID: 36223633 DOI: 10.1021/acs.jnatprod.2c00630] [Reference Citation Analysis]
3 Zhou WY, Hou JY, Li Q, Wang YJ, Wang JY, Jiang MH, Yao GD, Huang XX, Song SJ. Targeted isolation of diterpenoids and sesquiterpenoids from Daphne gemmata E. Pritz. ex Diels using molecular networking together with network annotation propagation and MS2LDA. Phytochemistry 2022;:113468. [PMID: 36191659 DOI: 10.1016/j.phytochem.2022.113468] [Reference Citation Analysis]
4 Gao ZH, Duan ZK, Ma ZT, Ye L, Yao GD, Huang XX, Song SJ. Chouchunsteride A-D, four new steroids from the leaves of Ailanthus altissima (Mill.) Swingle. Steroids 2022;188:109117. [PMID: 36181833 DOI: 10.1016/j.steroids.2022.109117] [Reference Citation Analysis]
5 Yan Q, Wang X, Bai M, Zhang X, Song S, Yao G. Sesquiterpene lactones from Elephantopus scaber exhibit cytotoxic effects on glioma cells by targeting GSTP1. Bioorganic Chemistry 2022. [DOI: 10.1016/j.bioorg.2022.106183] [Reference Citation Analysis]
6 Zhang Y, Bai M, Li J, Qin S, Liu Y, Huang X, Zheng J, Song S. Diverse sesquiterpenoids from Litsea lancilimba Merr. with potential neuroprotective effects against H2O2-induced SH-SY5Y cell injury. Chinese Journal of Natural Medicines 2022;20:701-11. [DOI: 10.1016/s1875-5364(22)60199-7] [Reference Citation Analysis]
7 Ai Y, Dong S, Lin B, Huang X, Song S. Acylated sucroses and butenolide analog from the leaves of Tripterygium wilfordii Hook. f. and their potential anti-tyrosinase effects. Fitoterapia 2022;161:105250. [DOI: 10.1016/j.fitote.2022.105250] [Reference Citation Analysis]
8 Guo R, Li Q, Mi SH, Jia SH, Yao GD, Lin B, Huang XX, Liu YY, Song SJ. Target isolation of cytotoxic diterpenoid esters and orthoesters from Daphne tangutica maxim based on molecular networking. Phytochemistry 2022;203:113358. [PMID: 35977604 DOI: 10.1016/j.phytochem.2022.113358] [Reference Citation Analysis]
9 Xu W, Bai M, Du NN, Song SJ, Lin B, Huang XX. Chemical structures and anti-tyrosinase activity of the constituents from Elephantopus scaber L. Fitoterapia 2022;162:105259. [PMID: 35931288 DOI: 10.1016/j.fitote.2022.105259] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
10 Xue GM, Zhao CG, Xue JF, Du K, Duan JJ, Pan H, Li M, Chen H, Sun YJ, Feng WS, Ma T, Zhang WD. Germacranolide- and guaianolide-type sesquiterpenoids from Achillea alpina L. reduce insulin resistance in palmitic acid-treated HepG2 cells via inhibition of the NLRP3 inflammasome pathway. Phytochemistry 2022;202:113297. [PMID: 35803306 DOI: 10.1016/j.phytochem.2022.113297] [Reference Citation Analysis]
11 Xu W, Bai M, Liu D, Qin S, Lv T, Li Q, Lin B, Song S, Huang X. MS/MS-based molecular networking accelerated discovery of germacrane-type sesquiterpene lactones from Elephantopus scaber L. Phytochemistry 2022;198:113136. [DOI: 10.1016/j.phytochem.2022.113136] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 5.0] [Reference Citation Analysis]
12 Zhang YY, Ren H, Yan QL, Li YL, Liu Q, Yao GD, Song SJ. SCP-7, a germacrane-type sesquiterpene lactone derivative, induces ROS-mediated apoptosis in NSCLC cells in vitro and in vivo. Eur J Pharmacol 2022;925:174989. [PMID: 35490722 DOI: 10.1016/j.ejphar.2022.174989] [Reference Citation Analysis]
13 Huang Q, Wang X, Cheng A, Zhang H, Yu Q, Shen C, Awadasseid A, Zhao X, Xiong X, Wu Y, Zhang W. Design, synthesis and anti-tumor activity of novel benzothiophenonaphthalimide derivatives targeting mitochondrial DNA (mtDNA) G-quadruplex. Biochemical Pharmacology 2022. [DOI: 10.1016/j.bcp.2022.115062] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
14 Mi S, Zhao P, Li Q, Zhang H, Guo R, Liu Y, Lin B, Yao G, Song S, Huang X. Guided isolation of daphnane-type diterpenes from Daphne genkwa by molecular network strategies. Phytochemistry 2022. [DOI: 10.1016/j.phytochem.2022.113144] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 7.0] [Reference Citation Analysis]
15 Chao J, Chen T, Pao L, Deng J, Cheng Y, Su S, Huang S. Ethnobotanical Survey on Bitter Tea in Taiwan. Front Pharmacol 2022;13:816029. [DOI: 10.3389/fphar.2022.816029] [Reference Citation Analysis]
16 Zhou L, Bai M, He Q, Hou Z, Lu L, Wang J, Huang X, Lin B, Song S. Nine new dihydro-β-agarofuran sesquiterpene polyesters from the leaves of Tripterygium wilfordii. New J Chem 2022;46:2423-30. [DOI: 10.1039/d1nj03800a] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
17 Li S, Lv T, Li Y, Yu X, Yao G, Lin B, Huang X, Song S. Vibsanoids A–D, four new subtypes of vibsane diterpenoids with a distinctive tricyclo[8.2.1.0 2,9 ]tridecane core from Viburnum odoratissimum. Org Chem Front . [DOI: 10.1039/d2qo00674j] [Reference Citation Analysis]
18 Liu YF, Yu SS. Survey of natural products reported by Asian research groups in 2020. J Asian Nat Prod Res 2021;23:1115-34. [PMID: 34825847 DOI: 10.1080/10286020.2021.2004131] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
19 Ho WY, Liew SS, Yeap SK, Alitheen NB. Synergistic Cytotoxicity between Elephantopus scaber and Tamoxifen on MCF-7-Derived Multicellular Tumor Spheroid. Evid Based Complement Alternat Med 2021;2021:6355236. [PMID: 34712346 DOI: 10.1155/2021/6355236] [Reference Citation Analysis]
20 Al-Bari MAA, Ito Y, Ahmed S, Radwan N, Ahmed HS, Eid N. Targeting Autophagy with Natural Products as a Potential Therapeutic Approach for Cancer. Int J Mol Sci 2021;22:9807. [PMID: 34575981 DOI: 10.3390/ijms22189807] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 8.0] [Reference Citation Analysis]
21 Su LH, Ma YB, Geng CA, Li TZ, Huang XY, Hu J, Xin Zhang, Tang S, Shen C, Gao Z, Zhang XM, Chen JJ. Artematrovirenins A-P, guaiane-type sesquiterpenoids with cytotoxicities against two hepatoma cell lines from Artemisia atrovirens. Bioorg Chem 2021;114:105072. [PMID: 34144276 DOI: 10.1016/j.bioorg.2021.105072] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
22 Du Y, Bai M, Yu X, Lv T, Lin B, Huang X, Song S. Quassinoids from the Root Barks of Ailanthus altissima : Isolation, Configurational Assignment, and Cytotoxic Activities. Chin J Chem 2021;39:879-86. [DOI: 10.1002/cjoc.202000558] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 6.0] [Reference Citation Analysis]
23 Bai M, Zhang Y, Dong S, Ren H, Chen J, Yao G, Liu Q, Lin B, Huang X, Song S. Targeted isolation of cytotoxic germacranolide sesquiterpenes from Elephantopus scaber L. using small molecule accurate recognition technology. Bioorganic Chemistry 2020;104:104314. [DOI: 10.1016/j.bioorg.2020.104314] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 6.0] [Reference Citation Analysis]
24 Elhady SS, Eltamany EE, Shaaban AE, Bagalagel AA, Muhammad YA, El-Sayed NM, Ayyad SN, Ahmed AAM, Elgawish MS, Ahmed SA. Jaceidin Flavonoid Isolated from Chiliadenus montanus Attenuates Tumor Progression in Mice via VEGF Inhibition: In Vivo and In Silico Studies. Plants (Basel) 2020;9:E1031. [PMID: 32823927 DOI: 10.3390/plants9081031] [Cited by in Crossref: 14] [Cited by in F6Publishing: 14] [Article Influence: 7.0] [Reference Citation Analysis]