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Ramos de Dios, Stephany M., Hass, Jared L., Graham, Danielle L., Kumar, Nivesh, Antony, Aina E., Morton, Martha D., Berkowitz, David B. (2023) Information-Rich, Dual-Function 13C/2H-Isotopic Crosstalk NMR Assay for Human Serine Racemase (hSR) Provides a PLP-Enzyme “Partitioning Fingerprint” and Reveals Disparate Chemotypes for hSR Inhibition. Journal of the American Chemical Society, 145 (5) 3158-3174 doi:10.1021/jacs.2c12774

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Reference TypeJournal (article/letter/editorial)
TitleInformation-Rich, Dual-Function 13C/2H-Isotopic Crosstalk NMR Assay for Human Serine Racemase (hSR) Provides a PLP-Enzyme “Partitioning Fingerprint” and Reveals Disparate Chemotypes for hSR Inhibition
JournalJournal of the American Chemical Society
AuthorsRamos de Dios, Stephany M.Author
Hass, Jared L.Author
Graham, Danielle L.Author
Kumar, NiveshAuthor
Antony, Aina E.Author
Morton, Martha D.Author
Berkowitz, David B.Author
Year2023 (February 8)Volume145
Issue5
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/jacs.2c12774Search in ResearchGate
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Mindat Ref. ID15706819Long-form Identifiermindat:1:5:15706819:3
GUID0
Full ReferenceRamos de Dios, Stephany M., Hass, Jared L., Graham, Danielle L., Kumar, Nivesh, Antony, Aina E., Morton, Martha D., Berkowitz, David B. (2023) Information-Rich, Dual-Function 13C/2H-Isotopic Crosstalk NMR Assay for Human Serine Racemase (hSR) Provides a PLP-Enzyme “Partitioning Fingerprint” and Reveals Disparate Chemotypes for hSR Inhibition. Journal of the American Chemical Society, 145 (5) 3158-3174 doi:10.1021/jacs.2c12774
Plain TextRamos de Dios, Stephany M., Hass, Jared L., Graham, Danielle L., Kumar, Nivesh, Antony, Aina E., Morton, Martha D., Berkowitz, David B. (2023) Information-Rich, Dual-Function 13C/2H-Isotopic Crosstalk NMR Assay for Human Serine Racemase (hSR) Provides a PLP-Enzyme “Partitioning Fingerprint” and Reveals Disparate Chemotypes for hSR Inhibition. Journal of the American Chemical Society, 145 (5) 3158-3174 doi:10.1021/jacs.2c12774
In(2023, February) Journal Of The American Chemical Society Vol. 145 (5) American Chemical Society (ACS)

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