ANALYSIS OF 25-DIALKYL HYDROQUINONES AS NOVEL ENZYME INHIBITORS

$17,024P20FY2009RRNIH

University Of Louisville, Louisville KY

Investigators

Linked publications & trials

Paper 39094954 Paper 36194009 Paper 34890772 Paper 31687925 Paper 30931350 Paper 29614295 Paper 29497912 Paper 29382671 Paper 29319823 Paper 29197979 Paper 27277141 Paper 27264359 Paper 27081652 Paper 27076424 Paper 27010837 Paper 26981369 Paper 26762836 Paper 26713731 Paper 26697387 Paper 26583908 Paper 26542393 Paper 26515323 Paper 26279602 Paper 26256519 Paper 26107351 Paper 25999268 Paper 25875294 Paper 25681180 Paper 25632406 Paper 25483336 Paper 25303335 Paper 25293549 Paper 25210480 Paper 25077036 Paper 25040590 Paper 24863475 Paper 24808906 Paper 24782501 Paper 24745005 Paper 24709747 Paper 24641478 Paper 24625056 Paper 24569806 Paper 24406899 Paper 24404440 Paper 24361506 Paper 24048286 Paper 24035030 Paper 23995634 Paper 23922931 Paper 23893078 Paper 23850071 Paper 23826173 Paper 23817991 Paper 23750695 Paper 23747862 Paper 23744053 Paper 23742275 Paper 23667718 Paper 23643898 Paper 23533589 Paper 23468653 Paper 23461570 Paper 23384094 Paper 23316162 Paper 23285269 Paper 22971005 Paper 22967011 Paper 22935098 Paper 22803786 Paper 22724427 Paper 22720090 Paper 22719926 Paper 22697494 Paper 22649077 Paper 22444875 Paper 22373349 Paper 22368389 Paper 22258284 Paper 22140580 Paper 22119580 Paper 22117008 Paper 22084302 Paper 22045191 Paper 22023670 Paper 22023227 Paper 21999392 Paper 21981824 Paper 21909303 Paper 21888654 Paper 21848957 Paper 21840976 Paper 21840085 Paper 21829638 Paper 21827812 Paper 21824971 Paper 21789473 Paper 21783437 Paper 21731731 Paper 21720950

Abstract

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The overall goal of the proposed research is to initiate the development of novel inhibitors of the enzyme sarco-endoplasmic reticulum calcium ATPase (SERCA) using a combination of experimental and computational techniques. Not only are SERCA inhibitors powerful tools for the study of the enzyme's function, but they are also believed to be of potential medicinal value for cancer chemotherapy.

View original record on NIH RePORTER →