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Marvin Carmack grad student 1970 Indiana University
 (Part A: Synthesis and reactions of α-halo sulfones. Part B: 1, 4-dithio-Lg-threitol)
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Alasmari M, Bӧhlke M, Kelley C, et al. (2018) Inhibition of Fatty Acid Amide Hydrolase (FAAH) by Macamides. Molecular Neurobiology
Chuong MC, Kelley CJ, Muhammad Y, et al. (2018) Investigating effect of water of hydration on active pharmaceutical ingredients in a water-sensitive dosage form Journal of Analytical Science and Technology. 9: 1-8
Hall J, Bedregal S, Kelley C, et al. (2016) Isolation of an anti‐tumor compound from the leaves of Annnona muricata and pharmacological characterization in PC‐3 cells The Faseb Journal. 30
Wu H, Kelley CJ, Pino-Figueroa A, et al. (2013) Macamides and their synthetic analogs: evaluation of in vitro FAAH inhibition. Bioorganic & Medicinal Chemistry. 21: 5188-97
Almukadi H, Wu H, Böhlke M, et al. (2013) The macamide N-3-methoxybenzyl-linoleamide is a time-dependent fatty acid amide hydrolase (FAAH) inhibitor. Molecular Neurobiology. 48: 333-9
Pino-Figueroa AJ, Bohlke M, Wu H, et al. (2011) An approach to standardize Lepidium meyenii (Maca) extracts by evaluating macamide content with an LC-MS/MS method The Faseb Journal. 25
Mehanna AS, Belani JD, Kelley CJ, et al. (2007) Design, synthesis and biological evaluation of a series of thioamides as non-nucleoside reverse transcriptase inhibitors. Medicinal Chemistry (ShāRiqah (United Arab Emirates)). 3: 513-9
Froimowitz M, Gu Y, Dakin LA, et al. (2007) Slow-onset, long-duration, alkyl analogues of methylphenidate with enhanced selectivity for the dopamine transporter. Journal of Medicinal Chemistry. 50: 219-32
Froimowitz M, Gu Y, Dakin LA, et al. (2005) Vinylogous amide analogs of methylphenidate. Bioorganic & Medicinal Chemistry Letters. 15: 3044-7
Bischoff TA, Kelley CJ, Karchesy Y, et al. (2004) Antimalarial activity of lactucin and lactucopicrin: sesquiterpene lactones isolated from Cichorium intybus L. Journal of Ethnopharmacology. 95: 455-7
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