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. Background: The Sourcing and Acquisition core is designed to interface natural products and related compounds with CORE-NPN investigators. The National Center for Natural Products Research (NCNPR) was created to bring together an alliance of academia (The University of Mississippi), government, and the pharmaceutical and agrochemical industries to integrate research, development, and commercialization of potentially useful natural products. The NCNPR is the nation's only university-affiliated research center devoted to discovering, developing and commercializing new Pharmaceuticals and agrochemicals derived from natural products. This complements the chemistry core (Core B) which interfaces between the medicinal chemistry and pharmacognosy investigators associated with CORE-NPN and other researchers in the college of pharmacy and NCNPR. In comparison to the plant extracts held in the biomas:; collections and prepared extracts, i.e. the NCNPR Repositories, pharmacognosy investigators have numerous compounds from aquatic species while medicinal chemists have numerous compounds built around natural product (or synthetic) templates. Together there are over 10,000 extracts or pure compounds in-hous& Objectives: The Sourcing and Acquisition Core will provide two services to CORE-NPN investigators. The primary function of the core will be to provide a gateway resource to the extensive repositories that already reside in-house. Specifically, the core will update the existing stand-alone relational management database for the NCNPR to one that allows for network access and is capable of handling chemical structures. Core A will also provide the technical staff and expertise to train investigators on its use and maintain its function. The Sourcing and Acquisition Core's staff will also provide CORE-NPN investigators rapid access to the material extracts that reside in the NCNPR and Core B repositories as well as access to collections that reside with collaborators. The second mission of the Sourcing and Acquisition Core is to provide for the re-acquisition of compounds that investigators have exhausted from the repository. The following diagram displays the current methodology used by both the NCNPR and the department of Pharmacognosy.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
1P20RR021929-01
Application #
7382241
Study Section
Special Emphasis Panel (ZRR1-RI-8 (02))
Project Start
2006-09-04
Project End
2007-06-30
Budget Start
2006-09-04
Budget End
2007-06-30
Support Year
1
Fiscal Year
2006
Total Cost
$195,516
Indirect Cost
Name
University of Mississippi
Department
Pharmacology
Type
Schools of Pharmacy
DUNS #
067713560
City
University
State
MS
Country
United States
Zip Code
38677
Mohamed, Shaymaa M M; Elokely, Khaled M; Bachkeet, Enaam Y et al. (2015) New Glycosides and Trypanocidal Metabolites from Vangueria edulis. Nat Prod Commun 10:1897-900
Radwan, Mohamed M; ElSohly, Mahmoud A; El-Alfy, Abir T et al. (2015) Isolation and Pharmacological Evaluation of Minor Cannabinoids from High-Potency Cannabis sativa. J Nat Prod 78:1271-6
Tabrizian, Tahmineh; Hataway, Felicia; Murray, David et al. (2015) Prolylcarboxypeptidase gene expression in the heart and kidney: Effects of obesity and diabetes. Cardiovasc Hematol Agents Med Chem 13:113-23
Ahmed, Safwat A; Ross, Samir A; Slade, Desmond et al. (2015) Minor oxygenated cannabinoids from high potency Cannabis sativa L. Phytochemistry 117:194-9
Gómez-Betancur, Isabel; Cortés, Natalie; Benjumea, Dora et al. (2015) Antinociceptive activity of extracts and secondary metabolites from wild growing and micropropagated plants of Renealmia alpinia. J Ethnopharmacol 165:191-7
Maddineni, Sindhuri; Battu, Sunil Kumar; Morott, Joe et al. (2015) Influence of process and formulation parameters on dissolution and stability characteristics of Kollidon® VA 64 hot-melt extrudates. AAPS PharmSciTech 16:444-54
Morgan, J Brian; Liu, Yang; Coothankandaswamy, Veena et al. (2015) Kalkitoxin inhibits angiogenesis, disrupts cellular hypoxic signaling, and blocks mitochondrial electron transport in tumor cells. Mar Drugs 13:1552-68
Malak, Lourin G; Ibrahim, Mohamed Ali; Bishay, Daoud W et al. (2014) Antileishmanial metabolites from Geosmithia langdonii. J Nat Prod 77:1987-91
Tarawneh, Amer H; León, Francisco; Ibrahim, Mohammed A et al. (2014) Flavanones from Miconia prasina. Phytochem Lett 7:130-132
Chatterjee, Arindam; Cutler, Stephen J; Doerksen, Robert J et al. (2014) Discovery of thienoquinolone derivatives as selective and ATP non-competitive CDK5/p25 inhibitors by structure-based virtual screening. Bioorg Med Chem 22:6409-21

Showing the most recent 10 out of 134 publications