2016 - Fellow of the American Academy of Arts and Sciences
2007 - Fellow of the American Association for the Advancement of Science (AAAS)
His main research concerns Biochemistry, Fatty acid amide hydrolase, Anandamide, Endocannabinoid system and Cannabinoid receptor. Biochemistry is closely attributed to In vivo in his research. Benjamin F. Cravatt interconnects AM404, Hydrolase, Neocortex, Fatty acid and URB597 in the investigation of issues within Fatty acid amide hydrolase.
Benjamin F. Cravatt combines subjects such as Fatty acid amide, Cannabinoid, Endogeny, JZL184 and Pharmacology with his study of Anandamide. Benjamin F. Cravatt studies Endocannabinoid system, namely Monoacylglycerol lipase. His Proteome study combines topics from a wide range of disciplines, such as Amino acid, Molecular probe, Proteomics, Cysteine and Small molecule.
Benjamin F. Cravatt mainly investigates Biochemistry, Fatty acid amide hydrolase, Endocannabinoid system, Anandamide and Enzyme. His study connects In vivo and Biochemistry. His research integrates issues of Oleamide, Amidase, Fatty acid, Stereochemistry and URB597 in his study of Fatty acid amide hydrolase.
His Endocannabinoid system research is multidisciplinary, relying on both Endocrinology, Pharmacology and Cannabinoid receptor. His research in Cannabinoid receptor intersects with topics in Cannabinoid and Neuroscience. The study incorporates disciplines such as Cysteine, Activity-based proteomics and Cell biology in addition to Proteome.
Cell biology, Biochemistry, Endocannabinoid system, Monoacylglycerol lipase and Pharmacology are his primary areas of study. His Biochemistry study focuses mostly on Enzyme, Cysteine, Serine, In vitro and Metabolism. His work carried out in the field of Endocannabinoid system brings together such families of science as Fatty acid amide hydrolase, Anandamide, Cannabinoid receptor type 1 and Cannabinoid receptor.
Internal medicine covers Benjamin F. Cravatt research in Fatty acid amide hydrolase. His Cannabinoid receptor research includes elements of Cannabinoid and Neuroscience. The various areas that Benjamin F. Cravatt examines in his Pharmacology study include Proinflammatory cytokine, Neuroinflammation and Nicotine.
Benjamin F. Cravatt spends much of his time researching Cell biology, Biochemistry, Cysteine, Endocannabinoid system and Monoacylglycerol lipase. His Cell biology study combines topics in areas such as Receptor, Caenorhabditis elegans and Immune system. His Biochemistry study frequently links to related topics such as Biomarker.
His studies in Endocannabinoid system integrate themes in fields like Anandamide, Endocrinology, Fatty acid amide hydrolase and AM251. His Anandamide study is related to the wider topic of Cannabinoid receptor. His Monoacylglycerol lipase research is multidisciplinary, incorporating perspectives in Inflammation and Pharmacology.
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Molecular characterization of an enzyme that degrades neuromodulatory fatty-acid amides
Benjamin F. Cravatt;Dan K. Giang;Stephen P. Mayfield;Dale L. Boger.
Supersensitivity to anandamide and enhanced endogenous cannabinoid signaling in mice lacking fatty acid amide hydrolase
Benjamin F. Cravatt;Kristin Demarest;Matthew P. Patricelli;Michael H. Bracey.
Proceedings of the National Academy of Sciences of the United States of America (2001)
Activity-based protein profiling: The serine hydrolases
Yongsheng Liu;Matthew P. Patricelli;Benjamin F. Cravatt.
Proceedings of the National Academy of Sciences of the United States of America (1999)
Activity-Based Protein Profiling in Vivo Using a Copper(I)-Catalyzed Azide-Alkyne [3 + 2] Cycloaddition
Anna E. Speers;Gregory C. Adam;Benjamin F. Cravatt.
Journal of the American Chemical Society (2003)
Noxious compounds activate TRPA1 ion channels through covalent modification of cysteines
Lindsey J. Macpherson;Adrienne E. Dubin;Michael J. Evans;Felix Marr;Felix Marr.
Quantitative reactivity profiling predicts functional cysteines in proteomes
Eranthie Weerapana;Chu Wang;Gabriel M. Simon;Florian Richter.
A Comprehensive Profile of Brain Enzymes that Hydrolyze the Endocannabinoid 2-Arachidonoylglycerol
Jacqueline Lorayne Blankman;Gabriel M. Simon;Benjamin F. Cravatt.
Chemistry & Biology (2007)
Activity-Based Protein Profiling: From Enzyme Chemistry to Proteomic Chemistry
Benjamin F. Cravatt;Aaron T. Wright;John W. Kozarich.
Annual Review of Biochemistry (2008)
Profiling Enzyme Activities In Vivo Using Click Chemistry Methods
Anna E Speers;Benjamin F Cravatt.
Chemistry & Biology (2004)
Selective blockade of 2-arachidonoylglycerol hydrolysis produces cannabinoid behavioral effects
Jonathan Z Long;Weiwei Li;Lamont Booker;James J Burston.
Nature Chemical Biology (2009)
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