Modular assembly of cytotoxic acetogenin mimetics by click linkage with nitrogen functionalities

Linear annonaceous acetogenin mimetic AA005 has been found to exhibit potent antitumor activity and significant selectivity between human normal and cancerous cells. Utilizing the concept of Click chemistry, a convergent modular fragment-assembly approach has been newly developed and successfully applied to the synthesis of three representative AA005-like molecules via formation of small nitrogen-containing heterocycles or amide bond. These nitrogen-containing analogues were found to exhibit low micromolar inhibitory activities against the growth of several cancer cell lines.

[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 .