The development of useful chemical probes generally requires careful optimization of initially discovered agent, whether they arise by modifying an existing agent, from high throughput screening or fragment-based methods, or through a computational study. The purpose of Core D is to provide synthetic chemistry support, including the validation of hit compounds obtained through high-throughput screening, quality control and analysis of compounds, synthesis of compounds unavailable commercially but needed by researchers, structure-activity relationship studies based on HTS campaigns, and optimization of fragment binders. Although most libraries used for screening and fragment efforts will continue to be commercially procured, the MC Core will continue ongoing efforts to create novel libraries for screening and fragment work. The work of the MC Core will be integrated into the suite of core lab activities. For example, hit selection and clustering will be done in conjunction with Cores B and C, compound management and storage in close cooperation with the HTS component of Core C, and analog design in collaboration with Core C.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Exploratory Grants (P20)
Project #
5P20GM113117-05
Application #
9935094
Study Section
Special Emphasis Panel (ZGM1)
Project Start
Project End
Budget Start
2020-05-01
Budget End
2021-04-30
Support Year
5
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Kansas Lawrence
Department
Type
DUNS #
076248616
City
Lawrence
State
KS
Country
United States
Zip Code
66045
Roy, Anuradha (2018) Early Probe and Drug Discovery in Academia: A Minireview. High Throughput 7:
Franklin, Meghan Whitney; Nepomnyachiy, Sergey; Feehan, Ryan et al. (2018) Efflux Pumps Represent Possible Evolutionary Convergence onto the ?-Barrel Fold. Structure 26:1266-1274.e2
Mori-Quiroz, Luis M; Hedrick, Sidnee L; De Los Santos, Andrew R et al. (2018) A Unified Strategy for the Syntheses of the Isoquinolinium Alkaloids Berberine, Coptisine, and Jatrorrhizine. Org Lett 20:4281-4284
Franklin, Meghan Whitney; Slusky, Joanna S G (2018) Tight Turns of Outer Membrane Proteins: An Analysis of Sequence, Structure, and Hydrogen Bonding. J Mol Biol 430:3251-3265
Deschamps, Thibaut; Kalamvoki, Maria (2018) Extracellular Vesicles Released by Herpes Simplex Virus 1-Infected Cells Block Virus Replication in Recipient Cells in a STING-Dependent Manner. J Virol 92:
Denler, Melissa C; Wijeratne, Gayan B; Rice, Derek B et al. (2018) MnIII-Peroxo adduct supported by a new tetradentate ligand shows acid-sensitive aldehyde deformylation reactivity. Dalton Trans 47:13442-13458
Kfoury, Najla; Sun, Tao; Yu, Kwanha et al. (2018) Cooperative p16 and p21 action protects female astrocytes from transformation. Acta Neuropathol Commun 6:12
Komiya, Takefumi; Yamamoto, Satomi; Roy, Anuradha et al. (2017) Drug screening to target nuclear orphan receptor NR4A2 for cancer therapeutics. Transl Lung Cancer Res 6:600-610
Cao, Shuai; Realegeno, Susan; Pant, Anil et al. (2017) Suppression of Poxvirus Replication by Resveratrol. Front Microbiol 8:2196
Deschamps, Thibaut; Kalamvoki, Maria (2017) Evasion of the STING DNA-Sensing Pathway by VP11/12 of Herpes Simplex Virus 1. J Virol 91:

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