1 |
Malla BA, Rafiq S, Hadi A, Ali A, Kaloo ZA, Wagay NA, Dar NA. Downregulation of pro-inflammatory markers NF-κB1, RelA and COX-2 using Aconitum chasmanthum Stapf ex Holmes -in vitro and in-silico study. Industrial Crops and Products 2023;197:116564. [DOI: 10.1016/j.indcrop.2023.116564] [Reference Citation Analysis]
|
2 |
Qasem AMA, Rowan MG, Blagbrough IS. Poisonous Piperidine Plants and the Biodiversity of Norditerpenoid Alkaloids for Leads in Drug Discovery: Experimental Aspects. IJMS 2022;23:12128. [DOI: 10.3390/ijms232012128] [Reference Citation Analysis]
|
3 |
Li L, Zhang L, Liao T, Zhang C, Chen K, Huang Q. Advances on pharmacology and toxicology of aconitine. Fundam Clin Pharmacol 2022;36:601-11. [PMID: 35060168 DOI: 10.1111/fcp.12761] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
|
4 |
Rafiq S, Wagay NA, Elansary HO, Malik MA, Bhat IA, Kaloo ZA, Hadi A, Alataway A, Dewidar AZ, El-sabrout AM, Yessoufou K, Mahmoud EA. Phytochemical Screening, Antioxidant and Antifungal Activities of Aconitum chasmanthum Stapf ex Holmes Wild Rhizome Extracts. Antioxidants 2022;11:1052. [DOI: 10.3390/antiox11061052] [Reference Citation Analysis]
|
5 |
Wong AR, Fastuca NJ, Mak VW, Kerkovius JK, Stevenson SM, Reisman SE. Total Syntheses of the C19 Diterpenoid Alkaloids (-)-Talatisamine, (-)-Liljestrandisine, and (-)-Liljestrandinine by a Fragment Coupling Approach. ACS Cent Sci 2021;7:1311-6. [PMID: 34471676 DOI: 10.1021/acscentsci.1c00540] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
|
6 |
Zhou X, Song Z, Xu K, Li J, Xie Y, Li X, Huang S, Gao F, Chen L. Semi-Synthetic Chasmanthinine Analogues with Antifeedant Effects against Spodoptera exigua. HETEROCYCLES 2021;102:2341. [DOI: 10.3987/com-21-14544] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
|
7 |
Yin T, Cai L, Ding Z. A systematic review on the chemical constituents of the genus Consolida (Ranunculaceae) and their biological activities. RSC Adv 2020;10:35072-89. [PMID: 35515663 DOI: 10.1039/d0ra06811j] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
|
8 |
Heravi MM, Momeni T, Mirzaei M, Zadsirjan V, Tahmasebi M. An amino acid@isopolyoxometalate nanoparticles catalyst containing aspartic acid and octamolybdate for the synthesis of functionalized spirochromenes. Inorganic and Nano-Metal Chemistry 2021;51:896-909. [DOI: 10.1080/24701556.2020.1813172] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.7] [Reference Citation Analysis]
|
9 |
Pang L, Liu CY, Gong GH, Quan ZS. Synthesis, in vitro and in vivo biological evaluation of novel lappaconitine derivatives as potential anti-inflammatory agents. Acta Pharm Sin B 2020;10:628-45. [PMID: 32322467 DOI: 10.1016/j.apsb.2019.09.002] [Cited by in Crossref: 21] [Cited by in F6Publishing: 25] [Article Influence: 7.0] [Reference Citation Analysis]
|
10 |
Wada K, Yamashita H. Cytotoxic Effects of Diterpenoid Alkaloids Against Human Cancer Cells. Molecules 2019;24:E2317. [PMID: 31234546 DOI: 10.3390/molecules24122317] [Cited by in Crossref: 18] [Cited by in F6Publishing: 19] [Article Influence: 4.5] [Reference Citation Analysis]
|
11 |
Wada K, Goto M, Shimizu T, Kusanagi N, Mizukami M, Suzuki Y, Li KP, Lee KH, Yamashita H. Structure-activity relationships and evaluation of esterified diterpenoid alkaloid derivatives as antiproliferative agents. J Nat Med 2019;73:789-99. [PMID: 31222559 DOI: 10.1007/s11418-019-01331-6] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
|
12 |
Doering NA, Kou KGM, Norseeda K, Lee JC, Marth CJ, Gallego GM, Sarpong R. A Copper-Mediated Conjugate Addition Approach to Analogues of Aconitine-Type Diterpenoid Alkaloids. J Org Chem 2018;83:12911-20. [PMID: 30216070 DOI: 10.1021/acs.joc.8b01967] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 1.8] [Reference Citation Analysis]
|
13 |
Guo Q, Xia H, Meng X, Shi G, Xu C, Zhu C, Zhang T, Shi J. C19-Diterpenoid alkaloid arabinosides from an aqueous extract of the lateral root of Aconitum carmichaelii and their analgesic activities. Acta Pharm Sin B 2018;8:409-19. [PMID: 29881680 DOI: 10.1016/j.apsb.2018.03.009] [Cited by in Crossref: 28] [Cited by in F6Publishing: 32] [Article Influence: 5.6] [Reference Citation Analysis]
|
14 |
Yamashita H, Katoh M, Kokubun A, Uchimura A, Mikami S, Takeuchi A, Kaneda K, Suzuki Y, Mizukami M, Goto M, Lee KH, Wada K. Four new C19-diterpenoid alkaloids from Delphinium elatum. Phytochem Lett 2018;24:6-9. [PMID: 29375725 DOI: 10.1016/j.phytol.2017.12.013] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 1.8] [Reference Citation Analysis]
|
15 |
Yamashita H, Takeda K, Haraguchi M, Abe Y, Kuwahara N, Suzuki S, Terui A, Masaka T, Munakata N, Uchida M, Nunokawa M, Kaneda K, Goto M, Lee KH, Wada K. Four new diterpenoid alkaloids from Aconitum japonicum subsp. subcuneatum. J Nat Med 2018;72:230-7. [PMID: 29052027 DOI: 10.1007/s11418-017-1139-9] [Cited by in Crossref: 13] [Cited by in F6Publishing: 15] [Article Influence: 2.2] [Reference Citation Analysis]
|
16 |
Kou KGM, Kulyk S, Marth CJ, Lee JC, Doering NA, Li BX, Gallego GM, Lebold TP, Sarpong R. A Unifying Synthesis Approach to the C18-, C19-, and C20-Diterpenoid Alkaloids. J Am Chem Soc 2017;139:13882-96. [PMID: 28858498 DOI: 10.1021/jacs.7b07706] [Cited by in Crossref: 52] [Cited by in F6Publishing: 54] [Article Influence: 8.7] [Reference Citation Analysis]
|
17 |
Ren MY, Yu QT, Shi CY, Luo JB. Anticancer Activities of C18-, C19-, C20-, and Bis-Diterpenoid Alkaloids Derived from Genus Aconitum. Molecules 2017;22:E267. [PMID: 28208826 DOI: 10.3390/molecules22020267] [Cited by in Crossref: 20] [Cited by in F6Publishing: 21] [Article Influence: 3.3] [Reference Citation Analysis]
|
18 |
Kou KG, Li BX, Lee JC, Gallego GM, Lebold TP, DiPasquale AG, Sarpong R. Syntheses of Denudatine Diterpenoid Alkaloids: Cochlearenine, N-Ethyl-1α-hydroxy-17-veratroyldictyzine, and Paniculamine. J Am Chem Soc 2016;138:10830-3. [PMID: 27525345 DOI: 10.1021/jacs.6b07268] [Cited by in Crossref: 42] [Cited by in F6Publishing: 42] [Article Influence: 6.0] [Reference Citation Analysis]
|
19 |
Liang Y, Wu JL, Leung EL, Zhou H, Liu Z, Yan G, Liu Y, Liu L, Li N. Identification of Oxygenated Fatty Acid as a Side Chain of Lipo-Alkaloids in Aconitum carmichaelii by UHPLC-Q-TOF-MS and a Database. Molecules 2016;21:437. [PMID: 27043515 DOI: 10.3390/molecules21040437] [Cited by in Crossref: 13] [Cited by in F6Publishing: 15] [Article Influence: 1.9] [Reference Citation Analysis]
|
20 |
Ji H, Wang F, Chen Q. Epoxide Opening of a 7,17- Seco –7,8-Epoxy-C 19 -Diterpenoid Alkaloid. Natural Product Communications 2015;10:1934578X1501001. [DOI: 10.1177/1934578x1501001215] [Reference Citation Analysis]
|
21 |
Zhao Q, Gou X, Liu W, He G, Liang L, Chen F. Majusine D: A New C 19 -diterpenoid Alkaloid from Delphinium majus. Natural Product Communications 2015;10:1934578X1501001. [DOI: 10.1177/1934578x1501001214] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
|
22 |
Weber M, Owens K, Sarpong R. Atropurpuran - Missing Biosynthetic Link Leading to the Hetidine and Arcutine C20-Diterpenoid Alkaloids or an Oxidative Degradation Product? Tetrahedron Lett 2015;56:3600-3. [PMID: 26028789 DOI: 10.1016/j.tetlet.2015.01.111] [Cited by in Crossref: 20] [Cited by in F6Publishing: 20] [Article Influence: 2.5] [Reference Citation Analysis]
|
23 |
Wada K, Ohkoshi E, Zhao Y, Goto M, Morris-Natschke SL, Lee KH. Evaluation of Aconitum diterpenoid alkaloids as antiproliferative agents. Bioorg Med Chem Lett 2015;25:1525-31. [PMID: 25770782 DOI: 10.1016/j.bmcl.2015.02.018] [Cited by in Crossref: 28] [Cited by in F6Publishing: 23] [Article Influence: 3.5] [Reference Citation Analysis]
|
24 |
Zheng LL, Wang D, Li YY, Peng HY, Yuan MY, Gao F. Ultrasound-assisted extraction of total flavonoids from Aconitum gymnandrum. Pharmacogn Mag 2014;10:S141-6. [PMID: 24914295 DOI: 10.4103/0973-1296.127364] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 0.2] [Reference Citation Analysis]
|
25 |
Shi Y, Wilmot JT, Nordstrøm LU, Tan DS, Gin DY. Total synthesis, relay synthesis, and structural confirmation of the C18-norditerpenoid alkaloid neofinaconitine. J Am Chem Soc 2013;135:14313-20. [PMID: 24040959 DOI: 10.1021/ja4064958] [Cited by in Crossref: 66] [Cited by in F6Publishing: 67] [Article Influence: 6.6] [Reference Citation Analysis]
|
26 |
Wang L, Chen Q, Wang F. Unusual Reactions of a 7,17- seco -type C 19 -Diterpenoid Alkaloid Derived from Deltaline. Natural Product Communications 2012;7:1934578X1200700. [DOI: 10.1177/1934578x1200700607] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.2] [Reference Citation Analysis]
|
27 |
Chen Q, Jian X, Chen Q, Wang F. AnO-to-Nintramolecular acyl migration in C19-diterpenoid alkaloids. Journal of Asian Natural Products Research 2012;14:586-591. [DOI: 10.1080/10286020.2012.680444] [Cited by in Crossref: 1] [Article Influence: 0.1] [Reference Citation Analysis]
|
28 |
Wada K, Ohkoshi E, Morris-Natschke SL, Bastow KF, Lee KH. Cytotoxic esterified diterpenoid alkaloid derivatives with increased selectivity against a drug-resistant cancer cell line. Bioorg Med Chem Lett 2012;22:249-52. [PMID: 22142543 DOI: 10.1016/j.bmcl.2011.11.026] [Cited by in Crossref: 22] [Cited by in F6Publishing: 24] [Article Influence: 1.8] [Reference Citation Analysis]
|
29 |
Ji H, Chen QH, Zhu M, Wang FP. Conversional studies towards taxoids from C(19)-diterpenoid alkaloids by the BAC sequence. J Asian Nat Prod Res 2010;12:968-77. [PMID: 21061219 DOI: 10.1080/10286020.2010.510796] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
|
30 |
Liu X, Song L, Chen Q, Wang F. Two New C 20 -Diterpenoid Alkaloids from Delphinium anthriscifolium var. savatieri. Natural Product Communications 2010;5:1934578X1000500. [DOI: 10.1177/1934578x1000500703] [Reference Citation Analysis]
|