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For: Shen Y, Liang WJ, Shi YN, Kennelly EJ, Zhao DK. Structural diversity, bioactivities, and biosynthesis of natural diterpenoid alkaloids. Nat Prod Rep 2020;37:763-96. [PMID: 32129397 DOI: 10.1039/d0np00002g] [Cited by in Crossref: 45] [Cited by in F6Publishing: 47] [Article Influence: 22.5] [Reference Citation Analysis]
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14 Chen L, Tian M, Jin B, Yin B, Chen T, Guo J, Tang J, Cui G, Huang L. Integrating Metabolomics and Transcriptomics to Unveil Atisine Biosynthesis in Aconitum gymnandrum Maxim. IJMS 2022;23:13463. [DOI: 10.3390/ijms232113463] [Reference Citation Analysis]
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18 Yan Y, Jiang H, Yang X, Ding Z, Yin T. Grandiflolines A–F, new anti-inflammatory diterpenoid alkaloids isolated from Delphinium grandiflorum. Front Chem 2022;10:1012874. [DOI: 10.3389/fchem.2022.1012874] [Reference Citation Analysis]
19 Li Y, Shang Y, Li X, Zhang Y, Xie J, Chen L, Gao F, Zhou XL. Design, synthesis, and biological evaluation of low-toxic lappaconitine derivatives as potential analgesics. Eur J Med Chem 2022;243:114776. [PMID: 36162215 DOI: 10.1016/j.ejmech.2022.114776] [Reference Citation Analysis]
20 Tao H, Liu X, Tian R, Liu Y, Zeng Y, Meng X, Zhang Y. A review: Pharmacokinetics and pharmacology of aminoalcohol-diterpenoid alkaloids from Aconitum species. Journal of Ethnopharmacology 2022. [DOI: 10.1016/j.jep.2022.115726] [Reference Citation Analysis]
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23 Jin S, Zhao X, Ma D. Divergent Total Syntheses of Napelline-Type C20-Diterpenoid Alkaloids: (-)-Napelline, (+)-Dehydronapelline, (-)-Songorine, (-)-Songoramine, (-)-Acoapetaldine D, and (-)-Liangshanone. J Am Chem Soc 2022. [PMID: 35948501 DOI: 10.1021/jacs.2c06738] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
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25 Gong C, Zhou G, Jing D, Song H, Xu J, Meng D. Three New Compounds from Delphinium kamaonense Hunth and Their in Vitro Cytotoxic and Potential Antioxidant Activities. Chem Biodivers 2022;:e202200463. [PMID: 35785443 DOI: 10.1002/cbdv.202200463] [Reference Citation Analysis]
26 Verma C, Quraishi MA, Rhee K. Natural ligands: Promising ecofriendly alternatives for corrosion protection and plethora of many prospects. Process Safety and Environmental Protection 2022;162:253-90. [DOI: 10.1016/j.psep.2022.04.014] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
27 Jin Y, Wang M, Yan Y, Zhang X, Li X, Gao H. Bridged cassane derivatives from the seeds of Caesalpinia sappan L. and their cytotoxic activities. Phytochemistry 2022;197:113111. [DOI: 10.1016/j.phytochem.2022.113111] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
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29 Zhang J, Lei X, Wei Y, Liu H, Guo Q, Zhang T, Shi J. Two unique C21-diterpenoid alkaloids from Aconitum carmichaelii. Chinese Chemical Letters 2022. [DOI: 10.1016/j.cclet.2022.03.104] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
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31 Mohammed A, Tajuddeen N, Ibrahim MA, Isah MB, Aliyu AB, Islam MS. Potential of Diterpenes as Antidiabetic Agents: Evidence from Clinical and Pre-Clinical Studies. Pharmacol Res 2022;:106158. [PMID: 35272043 DOI: 10.1016/j.phrs.2022.106158] [Reference Citation Analysis]
32 Anmol, Kumari S, Kumar R, Singh R, Aggarwal G, Agrawal P, Sahal D, Sharma U. Antiplasmodial diterpenoid alkaloid from Aconitum heterophyllum Wall. ex Royle: Isolation, characterization, and UHPLC-DAD based quantification. J Ethnopharmacol 2021;287:114931. [PMID: 34942322 DOI: 10.1016/j.jep.2021.114931] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
33 Yan Y, Li X, Wang Z, Yang X, Yin T. C18-diterpenoid alkaloids in tribe Delphineae (Ranunculaceae): phytochemistry, chemotaxonomy, and bioactivities. RSC Adv 2021;12:395-405. [PMID: 35424499 DOI: 10.1039/d1ra08132b] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
34 Umekubo N, Taniguchi T, Monde K, Hayashi Y. Synthesis of Bicyclo[2.2.2]octanes with a Quaternary Bridgehead Carbon by Diphenylprolinol Silyl Ether‐mediated Domino Reaction. Asian J Org Chem 2021;10:3261-3265. [DOI: 10.1002/ajoc.202100573] [Reference Citation Analysis]
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37 Song Z, Gao C, Jiang Q, Xu J, Xiong L, Liu K, Sun D, Li H, Chen L. Diterpenoid alkaloids from Delphinium forrestii var. viride and their anti-inflammation activity. Phytochemistry 2021;192:112971. [PMID: 34628107 DOI: 10.1016/j.phytochem.2021.112971] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
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39 Li Y, Zhuo L, Li X, Zhu Y, Wu S, Shen T, Hu W, Li Y, Wu C. Myxadazoles, Myxobacterium‐Derived Isoxazole–Benzimidazole Hybrids with Cardiovascular Activities. Angewandte Chemie 2021;133:21847-21852. [DOI: 10.1002/ange.202106275] [Reference Citation Analysis]
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41 Yu K, Yao F, Zeng Q, Xie H, Ding H. Asymmetric Total Syntheses of (+)-Davisinol and (+)-18-Benzoyldavisinol: A HAT-Initiated Transannular Redox Radical Approach. J Am Chem Soc 2021;143:10576-81. [PMID: 34240855 DOI: 10.1021/jacs.1c05703] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 3.5] [Reference Citation Analysis]
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