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Shared Resource 10: Medicinal Chemistry (MCSR)

$113,775P30FY2022CANIH

Ohio State University, Columbus OH

Investigators

Linked publications, trials & patents

Trial NCT04662645Trial NCT04602026Trial NCT04567706Trial NCT04454086Trial NCT04439006Trial NCT04329962Trial NCT04269837Trial NCT04267874Trial NCT04233567Trial NCT04229381Trial NCT04220684Trial NCT04205903Trial NCT04205240Trial NCT04205071Trial NCT04164069Trial NCT04140513Trial NCT04120454Trial NCT04116970Trial NCT04115163Trial NCT04063410Trial NCT04049539Trial NCT04032106Trial NCT03975231Trial NCT03943342Trial NCT03892044Trial NCT03868423Trial NCT03858855Trial NCT03824327Trial NCT03798639Trial NCT03786354Trial NCT03749018Trial NCT03728361Trial NCT03719092Trial NCT03715959Trial NCT03711890Trial NCT03691350Trial NCT03665675Trial NCT03656835Trial NCT03654638Trial NCT03631641Trial NCT03611205Trial NCT03583424Trial NCT03568526Trial NCT03537599Trial NCT03532581Trial NCT03525925Trial NCT03513562Trial NCT03463460Trial NCT03460483Trial NCT03447808Trial NCT03409432Trial NCT03372720Trial NCT03333746Trial NCT03328936Trial NCT03307044Trial NCT03287453Trial NCT02960100Trial NCT02950220Trial NCT02942524Trial NCT02940301Trial NCT02927899Trial NCT02835755Trial NCT02831582Trial NCT02812693Trial NCT02795104Trial NCT02791737Trial NCT02760030Trial NCT02439255Trial NCT02303392Trial NCT02101944Trial NCT02015117Trial NCT01964924Trial NCT01955499Trial NCT01861314Trial NCT01841723Trial NCT01811212Trial NCT01533194Trial NCT01519414Trial NCT01515176Trial NCT01468896Trial NCT01425879Trial NCT01351896Trial NCT01281124Trial NCT01280058Trial NCT01254617Trial NCT01254578Trial NCT01251874Trial NCT01249430Trial NCT01238133Trial NCT01132586Trial NCT01130506Trial NCT01129193Trial NCT01126502Trial NCT01076556Trial NCT01017640Trial NCT00735930Trial NCT00703300Trial NCT00602277Trial NCT00563290Trial NCT00499473

Abstract

PROJECT SUMMARY – MEDICINAL CHEMISTRY SHARED RESOURCE (MCSR) The MCSR supports scientific endeavors of OSUCCC members to create chemical probes to disrupt molecular pathways implicated in tumor growth, and to work with investigators to identify and create targeted agents against novel therapeutic moieties selected for properties important for preclinical and clinical development. The MCSR was established as a developing shared resource in 2011, and became a full CCSG shared resource in 2015. The MCSR supports investigators conducting preclinical in vitro and in vivo studies by integrating the expertise of multiple disciplines, including medicinal chemistry, process chemistry, computational chemistry, structural biology and molecular pharmacology. Key services are custom synthesis and lead optimization, including structure activity relationship analysis and structure-based optimization. Overall, the MCSR provides a crucial niche service for investigators identifying new therapeutic compounds. The Specific Aims of the MCSR are: 1) enable researchers to develop chemical probes of cancer biology; 2) Optimize hit and lead molecules through the design and synthesis of analogs with improved drug-like properties for translational development as cancer therapeutics; and 3) as a developing aim, enable screening of small molecules against proteins and whole-cell assays to identify new compounds for further preclinical testing. For this Developing Aim, Dr. Blake Peterson (TT) has been added as co-Director of the MCSR, and the OSUCCC will invest $3M in small molecule screening; these new capabilities will require hiring additional staff and a technical director, purchasing of equipment to conduct screens, and renovation of space. Over the current grant cycle, the MCSR supported 34 investigators (79% OSUCCC members) from all five research programs, including members at Nationwide Children's Hospital, and provided 7,625 hours of service (81.7% to OSUCCC members). The MCSR also contributed to 29 publications (9 > 10 impact factor), 34 users, and 7 NCI grants, including 1 K12, 1 U01, 1 R35, 1 R01, 2 P01s, and 1 P50. Over the next grant cycle, the MCSR will directly support the OSUCCC's strategic priorities for immuno-oncology and translational genomics. It will also support the development of drugs with potential for cancer prevention. The major thrust for the MCSR will be to implement small molecule screening and build the user base to identify novel compounds, and targets by phenotypic screening against cancer pathways, thereby identifying mechanisms of cancer initiation and progression that are central to goals of CB and MCC. The annual budget of the MCSR is $930,296, yet the CCSG request is $80,063. As such, the MCSR seeks only 8.6% budgetary support from CCSG funds.

View original record on NIH RePORTER →