Microbial transformation of some triterpenoids of Guayule resin by Chaetomium sp.
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E. Wijeratne | Chandrashekhar Madasu | M. C. Inácio | A. L. Gunatilaka | Weimao Zhong | István Gábor Molnár | Ya-Ming Xu
[1] I. Molnár,et al. Semi-synthesis and cytotoxicity evaluation of pyrimidine, thiazole, and indole analogues of argentatins A–C from guayule (Parthenium argentatum) resin , 2021, Medicinal Chemistry Research.
[2] Jason C. Quinn,et al. Guayule (Parthenium argentatum) resin: A review of chemistry, extraction techniques, and applications , 2021, Industrial Crops and Products.
[3] D. Dierig,et al. Cycloartane- and Lanostane-Type Triterpenoids from the Resin of Parthenium argentatum AZ-2, a Byproduct of Guayule Rubber Production , 2021, ACS omega.
[4] F. Chemat,et al. Guayule (Parthenium argentatum A. Gray), a Renewable Resource for Natural Polyisoprene and Resin: Composition, Processes and Applications , 2021, Molecules.
[5] Feng Cheng,et al. Characterization and evaluation of guayule processing residues as potential feedstock for biofuel and chemical production , 2020 .
[6] L. Rocha-Zavaleta,et al. A Higher Frequency Administration of the Nontoxic Cycloartane-Type Triterpene Argentatin A Improved Its Anti-Tumor Activity , 2020, Molecules.
[7] E. Ratovitski,et al. Argentatin B derivatives induce cell cycle arrest and DNA damage in human colon cancer cells through p73/p53 regulation , 2018, Medicinal Chemistry Research.
[8] R. López-Marure,et al. Argentatin B Inhibits Proliferation of Prostate and Colon Cancer Cells by Inducing Cell Senescence , 2015, Molecules.
[9] Usama A. Mahalel,et al. Microbial biotransformation as a tool for drug development based on natural products from mevalonic acid pathway: A review , 2014, Journal of advanced research.
[10] Juliane Steingroewer,et al. Biotransformation of triterpenes , 2011 .
[11] M. Martínez-Vázquez,et al. Anti-inflammatory and Cytotoxic Cycloartanes from Guayule (Parthenium Argentatum) , 2008 .
[12] Kenji Watanabe,et al. Biotransformation of cycloartane-type triterpenes by the fungus Glomerella fusarioides. , 2006, Journal of natural products.
[13] P. Ostrosky-Wegman,et al. Evaluation of the cytotoxicity, cytostaticity and genotoxicity of argentatins A and B from Parthenium argentatum (Gray). , 2005, Life sciences.
[14] G. Maatooq. Microbiological and Chemical Transformations of Argentatin B , 2003, Zeitschrift fur Naturforschung. C, Journal of biosciences.
[15] J. Hoffmann,et al. Microbial Transformation of a Mixture of Argentatin A and Incanilin , 2002, Zeitschrift fur Naturforschung. C, Journal of biosciences.
[16] K. Katoh,et al. Ring-A cleavage of 3-oxo-olean-12-en-28-oic acid by the fungus Chaetomium longirostre , 1996 .
[17] S. Gaskell,et al. Spectroscopic methods of steroid analysis , 1995 .
[18] L V Rubinstein,et al. Comparison of in vitro anticancer-drug-screening data generated with a tetrazolium assay versus a protein assay against a diverse panel of human tumor cell lines. , 1990, Journal of the National Cancer Institute.
[19] Felix J. Parodi. Structure Elucidation of Natural Products From Asteraceae by Modern NMR Techniques and Biomimetic Transformations of 11,13-Dihydroparthenolide. , 1988 .
[20] E. C. Gregg,et al. Identification of guayule triterpenes by two‐dimensional and multipulse NMR techniques , 1986 .