D-ring modified novel isosteviol derivatives: design, synthesis and cytotoxic activity evaluation.
Zhang, Tao; Lu, Li-Hui; Liu, Hao; Wang, Jun-Wei; Wang, Rui-Xue; Zhang, Yun-Xiao; Tao, Jing-Chao.
Bioorg Med Chem Lett
; 22(18): 5827-32, 2012 Sep 15.
Artigo em Inglês | MEDLINE | ID: mdl-22901386
Syntheses, cytotoxic activity evaluation and HQSAR study of 1,2,3-triazole-linked isosteviol derivatives as potential anticancer agents.
Synthesis and cytotoxic activity of nitric oxide-releasing isosteviol derivatives.
Convergent Route to ent-Kaurane Diterpenoids: Total Synthesis of Lungshengenin D and 1α,6α-Diacetoxy-ent-kaura-9(11),16-dien-12,15-dione.
Design and Synthesis of C-19 Isosteviol Derivatives as Potent and Highly Selective Antiproliferative Agents.
Design and synthesis of novel oridonin analogues as potent anticancer agents.
Triphenylphosphonium Cations of the Diterpenoid Isosteviol: Synthesis and Antimitotic Activity in a Sea Urchin Embryo Model.
Novel anticancer oridonin derivatives possessing a diazen-1-ium-1,2-diolate nitric oxide donor moiety: Design, synthesis, biological evaluation and nitric oxide release studies.
Synthesis and cytotoxic activity of MOM-ether analogs of isosteviol.
Design and synthesis of isosteviol triazole conjugates for cancer therapy.
Oridonin, a Promising ent-Kaurane Diterpenoid Lead Compound.