Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Jean E. Patterson"'
Publikováno v:
Tetrahedron Letters. 44:5137-5140
Polycyclic indolic compounds containing the [6,5,6,5,6] ring system were prepared via an intramolecular furan Diels–Alder reaction of α,β-unsaturated amides generated by the N-acylation of 1-(2-furyl)-β-tetrahydrocarbolines. This chemistry can p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0d9b91454167af1f5d7b27a2bd39841
https://doi.org/10.1016/s0040-4039(03)01179-1
https://doi.org/10.1016/s0040-4039(03)01179-1
Autor:
Alexander S. Asser, Lawrence King, John J. Robleski, Benjamin J. Wilcox, Megan A. Baumgart, Matthias E. Henz, Kimberly J. Ritenour-Rodgers, Laura E. Baumgart, Uta Glufke, Mitchell A. deLong, Dale L. Boger, Kathleen A. Merkler, Jean E. Patterson, David J. Merkler, Jodi L. DeBlassio, John C. Vederas
Publikováno v:
Biochemistry. 38:3235-3245
Bifunctional peptidylglycine alpha-amidating enzyme (alpha-AE) catalyzes the O2-dependent conversion of C-terminal glycine-extended prohormones to the active, C-terminal alpha-amidated peptide and glyoxylate. We show that alpha-AE will also catalyze
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c66c32ff42c9ce640adc3700d5860e2
https://doi.org/10.1021/bi982255j
https://doi.org/10.1021/bi982255j
Autor:
Dale L. Boger, Norton B. Gilula, Richard A. Lerner, Benjamin F. Cravatt, Jean E. Patterson, Xiaojun Guan
Publikováno v:
Proceedings of the National Academy of Sciences. 95:4810-4815
Oleamide is an endogenous fatty acid primary amide that possesses sleep-inducing properties in animals and has been shown to effect serotonergic systems and block gap junction communication in a structurally specific manner. Herein, the structural fe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::181ab780a38d501c0659e1df3229e0de
https://doi.org/10.1073/pnas.95.9.4810
https://doi.org/10.1073/pnas.95.9.4810
Publikováno v:
Proceedings of the National Academy of Sciences. 95:4102-4107
Oleamide is an endogenous fatty acid primary amide that possesses sleep-inducing properties in animals and that has been shown to effect serotonergic receptor responses and block gap junction communication. Herein, the potentiation of the 5-HT 1A rec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89bc77a2caa736af0a80ec6e78f09e92
https://doi.org/10.1073/pnas.95.8.4102
https://doi.org/10.1073/pnas.95.8.4102
Autor:
Dale L. Boger, Richard A. Lerner, Jean E. Patterson, Benjamin F. Cravatt, Ian R. Ollmann, Chi-Huey Wong
Publikováno v:
Journal of the American Chemical Society. 118:5938-5945
Oleamide (1, cis-9-octadecenamide) is a naturally occurring brain constituent that has been shown to accumulate and disappear under conditions of sleep deprivation and sleep recovery, respectively. Synthetic 1 has been found to induce sleep in a stru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c8cdc6996b61300442c82f6ed473f88
https://doi.org/10.1021/ja954064z
https://doi.org/10.1021/ja954064z
Autor:
Richard A. Lerner, Dale L. Boger, Benjamin F. Cravatt, Chi-Huey Wong, Jean E. Patterson, Ian R. Ollmann
Publikováno v:
ChemInform. 27
Oleamide (1, cis-9-octadecenamide) is a naturally occurring brain constituent that has been shown to accumulate and disappear under conditions of sleep deprivation and sleep recovery, respectively. Synthetic 1 has been found to induce sleep in a stru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d38e5b8739d8071dc098fa130a10c84f
https://doi.org/10.1002/chin.199640217
https://doi.org/10.1002/chin.199640217
Autor:
Jay Parker, Jean E. Patterson, Diglio A. Simoni, Tom Cwik, N. Jacobi, Paulett C. Liewer, Robert Ferraro, Gregory A. Lyzenga, Thomas Lockhart
Publikováno v:
Electromagnetics. 10:21-39
We have been applying the computational power of parallel processing to the solution of large-scale electromagnetic scattering and radiation problems. Several analysis codes have been implemented on the Jet Propulsion Laboratory/California Institute
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0bddf272b047a6d4f66554dc96f71de
https://doi.org/10.1080/02726349008908227
https://doi.org/10.1080/02726349008908227
Publikováno v:
Digest on Antennas and Propagation Society International Symposium.
A method for constructing a Green's function for an arbitrary scatterer or antenna consisting of multiple parts is presented. By exploiting the partitioning of the impedance matrix that naturally develops in a method-of-moments (MM) formulation when
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebcfdc464598c0a2f72b7c12b294d28d
https://doi.org/10.1109/aps.1989.134754
https://doi.org/10.1109/aps.1989.134754
Autor:
Robert A. Fecik, Jean E. Patterson, Matthew P. Patricelli, Dale L. Boger, Benjamin F. Cravatt, Hiroshi Miyauchi
Publikováno v:
Bioorganicmedicinal chemistry letters. 10(23)
Fatty acid amide hydrolase (FAAH), also referred to as oleamide hydrolase and anandamide amidohydrolase, is a serine hydrolase responsible for the degradation of endogenous oleamide and anandamide, fatty acid amides that function as chemical messenge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::220161909ae22c8d4344e7435c290502
https://pubmed.ncbi.nlm.nih.gov/11128635
https://pubmed.ncbi.nlm.nih.gov/11128635
Autor:
Matthew P. Patricelli, Dale L. Boger, Benjamin F. Cravatt, Aaron E. Lerner, Jean E. Patterson, Bryce J. Austin, Haruhiko Sato
Publikováno v:
Bioorganicmedicinal chemistry letters. 9(2)
The examination of a series of trifluoromethyl ketone inhibitors of Fatty Acid Amide Hydrolase (FAAH, oleamide hydrolase, anandamide amidohydrolase) is detailed in efforts that define structural and conformational properties that contribute to enzyme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9623ba6cc0f991be908979479b5b70c8
https://pubmed.ncbi.nlm.nih.gov/10021942
https://pubmed.ncbi.nlm.nih.gov/10021942