Modular assembly of cytotoxic acetogenin mimetics by click linkage with nitrogen functionalities
暂无分享,去创建一个
Z. Yao | B. Han | Li‐Shun Wang | Shaozhong Wang | Chan Mao
[1] Z. Yao,et al. Potent antitumor mimetics of annonaceous acetogenins embedded with an aromatic moiety in the left hydrocarbon chain part. , 2011, Journal of medicinal chemistry.
[2] S. Horvath,et al. Monoclonal antibody targeting of N-cadherin inhibits prostate cancer growth, metastasis and castration resistance , 2010, Nature Medicine.
[3] Z. Yao,et al. Synthesis of a Mimicking Hybrid of Annonaceous Acetogenin with Steroid for Antitumoral Activity Investigation , 2010 .
[4] C. Liaw,et al. Historic Perspectives on Annonaceous Acetogenins from the Chemical Bench to Preclinical Trials , 2010, Planta medica.
[5] G. Marazzi,et al. Novel analogues of Istaroxime, a potent inhibitor of Na(+),K(+)-ATPase: Synthesis, structure-activity relationship and 3D-quantitative structure-activity relationship of derivatives at position 6 on the androstane scaffold. , 2010, Bioorganic & medicinal chemistry.
[6] Guoqiang Chen,et al. Synergistic mitosis-arresting effects of arsenic trioxide and paclitaxel on human malignant lymphocytes. , 2010, Chemico-biological interactions.
[7] Richard C. D. Brown,et al. Total Synthesis of Annonaceous Acetogenins Belonging to the Non-Adjacent Bis-THF and Non-Adjacent THF-THP Sub-Classes , 2010, Molecules.
[8] M. Ruberg,et al. Natural lipophilic inhibitors of mitochondrial complex I are candidate toxins for sporadic neurodegenerative tau pathologies , 2009, Experimental Neurology.
[9] Tetsuaki Tanaka,et al. Medicinal Chemistry of Annonaceous Acetogenins: Design, Synthesis, and Biological Evaluation of Novel Analogues , 2009, Molecules.
[10] O. Pàmies,et al. Modular Furanoside Phosphite‐Phosphoroamidites, a Readily Available Ligand Library for Asymmetric Palladium‐Catalyzed Allylic Substitution Reactions. Origin of Enantioselectivity , 2009 .
[11] Bolan Yu,et al. Comparative methods for analysis of protein covalent modification by electrophilic quinoids formed from xenobiotics. , 2009, Bioconjugate chemistry.
[12] V. Nicolas,et al. Highly cytotoxic and neurotoxic acetogenins of the Annonaceae: new putative biological targets of squamocin detected by activity-based protein profiling. , 2008, Bioorganic & medicinal chemistry letters.
[13] Z. Yao,et al. Tuning the acyclic ether moiety of anticancer agent AA005 with conformationally constrained fragments. , 2008, Chemistry.
[14] J. McLaughlin. Paw paw and cancer: annonaceous acetogenins from discovery to commercial products. , 2008, Journal of natural products.
[15] Z. Yao,et al. Annonaceous acetogenin mimics bearing a terminal lactam and their cytotoxicity against cancer cells. , 2007, Bioorganic & medicinal chemistry letters.
[16] Z. Yao,et al. A Structure–Activity Guided Strategy for Fluorescent Labeling of Annonaceous Acetogenin Mimetics and their Application in Cell Biology , 2007, Chembiochem : a European journal of chemical biology.
[17] Bradley D. Smith,et al. Phosphatidylcholine-derived bolaamphiphiles via click chemistry. , 2007, Organic letters.
[18] G. Roué,et al. Annonaceous Acetogenins: The Hydroxyl Groups and THF Rings Are Crucial Structural Elements for Targeting the Mitochondria, Demonstration with the Synthesis of Fluorescent Squamocin Analogues , 2005, Chembiochem : a European journal of chemical biology.
[19] A. Bermejo,et al. Acetogenins from Annonaceae: recent progress in isolation, synthesis and mechanisms of action. , 2005, Natural product reports.
[20] M. Toda,et al. Highly potent PDE4 inhibitors with therapeutic potential. , 2004, Bioorganic & medicinal chemistry.
[21] W. Kitching,et al. Synthesis and Enantioselective Gas Chromatography of Stereoisomers of 7,11‐Dimethylheptadecane − A Pheromone Component of Lambdina Species , 2004 .
[22] Z. Yao,et al. Parallel fragment assembly strategy towards multiple-ether mimicry of anticancer annonaceous acetogenins. , 2004, Angewandte Chemie.
[23] Z. Yao,et al. Induction of Cell Death of Gastric Cancer Cells by a Modified Compound of the Annonaceous Acetogenin Family , 2003, Chembiochem : a European journal of chemical biology.
[24] Z. Yao,et al. Studies on mimicry of naturally occurring annonaceous acetogenins: non-THF analogues leading to remarkable selective cytotoxicity against human tumor cells. , 2003, Chemistry.
[25] T. Katoh,et al. Synthetic studies of himbacine, a potent antagonist of the muscarinic M2 subtype receptor 1. Stereoselective total synthesis and antagonistic activity of enantiomeric pairs of himbacine and (2′S,6′R)-diepihimbacine, 4-epihimbacine, and novel himbacine congeners , 2002 .
[26] Luke G Green,et al. A stepwise huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes. , 2002, Angewandte Chemie.
[27] Z. Yao,et al. Mimicry of annonaceous acetogenins: enantioselective synthesis of a (4R)-hydroxy analogue having potent antitumor activity. , 2002, The Journal of organic chemistry.
[28] P. Taylor,et al. Click chemistry in situ: acetylcholinesterase as a reaction vessel for the selective assembly of a femtomolar inhibitor from an array of building blocks. , 2002, Angewandte Chemie.
[29] M. G. Finn,et al. Click Chemistry: Diverse Chemical Function from a Few Good Reactions. , 2001, Angewandte Chemie.
[30] Yu,et al. Enantiopure Simple Analogues of Annonaceous Acetogenins with Remarkable Selective Cytotoxicity towards Tumor Cell Lines This work was supported by the Chinese Academy of Sciences (nos. KJ951-A1-504-04, and KJ952-S1-503), the National Natural Science Foundation of China (nos. 29472070, 29790126, and , 2000, Angewandte Chemie.
[31] Z. Yao,et al. Polyether mimics of naturally occurring cytotoxic annonaceous acetogenins. , 2000, Journal of medicinal chemistry.
[32] Z. Yao,et al. Synthetic studies toward mono-THF annonaceous acetogenins: A diastereoselective and convergent approach to corossolone and (10RS)-corossoline , 1995 .
[33] Z. Yao,et al. Total synthesis of (10ξ,15R,16S,19S,20S,34R)-Corossoline , 1994 .
[34] J. Wilt,et al. Reaction of 2-(.DELTA.3-cyclopentenyl)ethyl bromide with tri-n-butyltin hydride. Cyclization to norbornane , 1970 .