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For: Li K, Gustafson KR. Sesterterpenoids: chemistry, biology, and biosynthesis. Nat Prod Rep 2021;38:1251-81. [PMID: 33350420 DOI: 10.1039/d0np00070a] [Cited by in Crossref: 15] [Cited by in F6Publishing: 18] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Jiang L, Lv K, Zhu G, Lin Z, Zhang X, Xing C, Yang H, Zhang W, Wang Z, Liu C, Qu X, Hsiang T, Zhang L, Liu X. Norditerpenoids biosynthesized by variediene synthase-associated P450 machinery along with modifications by the host cell Aspergillus oryzae. Synthetic and Systems Biotechnology 2022;7:1142-7. [DOI: 10.1016/j.synbio.2022.08.002] [Reference Citation Analysis]
2 Zhang P, Qi J, Duan Y, Gao JM, Liu C. Research Progress on Fungal Sesterterpenoids Biosynthesis. J Fungi (Basel) 2022;8:1080. [PMID: 36294645 DOI: 10.3390/jof8101080] [Reference Citation Analysis]
3 Jiang L, Yang H, Zhang X, Li X, Lv K, Zhang W, Zhu G, Liu C, Wang Y, Hsiang T, Zhang L, Liu X. Schultriene and nigtetraene: two sesterterpenes characterized from pathogenetic fungi via genome mining approach. Appl Microbiol Biotechnol 2022. [PMID: 36040489 DOI: 10.1007/s00253-022-12125-4] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Majer T, Bhattarai K, Straetener J, Pohlmann J, Cahill P, Zimmermann MO, Hübner MP, Kaiser M, Svenson J, Schindler M, Brötz-Oesterhelt H, Boeckler FM, Gross H. Discovery of Ircinianin Lactones B and C-Two New Cyclic Sesterterpenes from the Marine Sponge Ircinia wistarii. Mar Drugs 2022;20:532. [PMID: 36005535 DOI: 10.3390/md20080532] [Reference Citation Analysis]
5 Ge J, Liu Z, Zhong Z, Wang L, Zhuo X, Li J, Jiang X, Ye X, Xie T, Bai R. Natural terpenoids with anti-inflammatory activities: Potential leads for anti-inflammatory drug discovery. Bioorganic Chemistry 2022;124:105817. [DOI: 10.1016/j.bioorg.2022.105817] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
6 Chen Z, Chen X, Tang Y, Zhou Y, Deng H, He J, Liu Y, Zhao Z, Cui H. Linderasesterterpenoids A and B: Two 7-Cyclohexyldecahydroazulene Carbon Skeleton Sesterterpenoids Isolated from the Root of Lindera glauca. Org Lett 2022. [PMID: 35559688 DOI: 10.1021/acs.orglett.2c01364] [Reference Citation Analysis]
7 Kuang Q, Lei L, Li Q, Peng W, Wang Y, Dai Y, Wang D, Gu Y, Deng Y, Guo D. Investigation of the Anti-Inflammatory Activity of Fusaproliferin Analogues Guided by Transcriptome Analysis. Front Pharmacol 2022;13:881182. [DOI: 10.3389/fphar.2022.881182] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
8 Jiang T, Dai X, Gao T, Wang L, Yang F, Zhang Y, Wang N, Huang G, Cao J. Ancepsone A, a New Cheilanthane Sesterterpene from Aleuritopteris anceps. Tetrahedron Letters 2022. [DOI: 10.1016/j.tetlet.2022.153869] [Reference Citation Analysis]
9 Chen Q, Yuan G, Yuan T, Zeng H, Zou ZR, Tu ZC, Gao J, Zou Y. Set of Cytochrome P450s Cooperatively Catalyzes the Synthesis of a Highly Oxidized and Rearranged Diterpene-Class Sordarinane Architecture. J Am Chem Soc 2022. [PMID: 35170947 DOI: 10.1021/jacs.1c12427] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
10 Chen Y, Li D, Ling Y, Liu Y, Zuo Z, Gan L, Luo S, Hua J, Chen D, Xu F, Li M, Guo K, Liu Y, Gershenzon J, Li S. A Cryptic Plant Terpene Cyclase Producing Unconventional 18‐ and 14‐Membered Macrocyclic C 25 and C 20 Terpenoids with Immunosuppressive Activity. Angewandte Chemie 2021;133:25672-80. [DOI: 10.1002/ange.202110842] [Reference Citation Analysis]
11 Morarescu O, Grinco M, Kulciţki V, Shova S, Ungur N. An Alternative Approach towards C-12 Functionalized Scalaranic Sesterterpenoids Synthesis of 17-Oxo-20-norscalaran-12α,19-O-lactone. Mar Drugs 2021;19:636. [PMID: 34822507 DOI: 10.3390/md19110636] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
12 Li DS, Hua J, Luo SH, Liu YC, Chen YG, Ling Y, Guo K, Liu Y, Li SH. An extremely promiscuous terpenoid synthase from the Lamiaceae plant Colquhounia coccinea var. mollis catalyzes the formation of sester-/di-/sesqui-/mono-terpenoids. Plant Commun 2021;2:100233. [PMID: 34746763 DOI: 10.1016/j.xplc.2021.100233] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
13 Chen Q, Li J, Ma Y, Yuan W, Zhang P, Wang G. Occurrence and biosynthesis of plant sesterterpenes (C25), a new addition to terpene diversity. Plant Commun 2021;2:100184. [PMID: 34746758 DOI: 10.1016/j.xplc.2021.100184] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
14 Kim MC, Winter JM, Asolkar RN, Boonlarppradab C, Cullum R, Fenical W. Marinoterpins A-C: Rare Linear Merosesterterpenoids from Marine-Derived Actinomycete Bacteria of the Family Streptomycetaceae. J Org Chem 2021;86:11140-8. [PMID: 33844925 DOI: 10.1021/acs.joc.1c00262] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
15 Huang Z, Ye R, Yu H, Li A, Xu J. Mining methods and typical structural mechanisms of terpene cyclases. Bioresour Bioprocess 2021;8. [DOI: 10.1186/s40643-021-00421-2] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]