<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Schmidt, Lori E.</style></author><author><style face="normal" font="default" size="100%">Deyrup, Stephen T.</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas</style></author><author><style face="normal" font="default" size="100%">Swenson, Dale C.</style></author><author><style face="normal" font="default" size="100%">Wicklow, Donald T.</style></author><author><style face="normal" font="default" size="100%">Gloer, James B.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Hymenopsins A and B and a macrophorin analog from a fungicolous Hymenopsis sp.</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Natural Products</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">hymenopsin Hymenopsis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2010</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2010///</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society-American Society of Pharmacognosy</style></publisher><volume><style face="normal" font="default" size="100%">73</style></volume><pages><style face="normal" font="default" size="100%">404 - 408</style></pages><isbn><style face="normal" font="default" size="100%">0163-3864</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Hymenopsin A (1), hymenopsin B (2), and a new macrophorin analog, 2',3'-epoxy-13-hydroxy-4'-oxomacrophorin A (3), have been isolated from a fungicolous isolate of Hymenopsis sp. (MYC-1703; NRRL 37638).  The structures and relative configurations of these compds. were assigned on the basis of 2D NMR and MS data, and the identity of 1 was confirmed by X-ray crystallog. anal.  The abs. configuration of 2 was proposed on the basis of CD anal. using both empirical and computational methods.  Compds. 2 and 3 showed antibacterial activity against Staphylococcus aureus and Bacillus subtilis.  Compd. 3 was also active against Aspergillus flavus and Fusarium verticillioides. [on SciFinder(R)]</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><notes><style face="normal" font="default" size="100%">CAPLUS AN 2009:1462186(Journal)</style></notes></record></records></xml>