Microbial transformation of some triterpenoids of Guayule resin by Chaetomium sp.

[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 .