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K Mattson

Showing results (181-190 of 190) with videos related to

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Bioorganic & Medicinal Chemistry|May 16, 2006
Synthesis and evaluation of 5,5-diphenylimidazolones as potent human neuropeptide Y5 receptor antagonistsKevin W Gillman, Mendi A Higgins, Graham S Poindexter, et al.
Bioorganic & Medicinal Chemistry Letters|June 30, 2009
Conformationally restricted homotryptamines. Part 5: 3-(trans-2-aminomethylcyclopentyl)indoles as potent selective serotonin reuptake inhibitorsDerek J Denhart, Jeffrey A Deskus, Jonathan L Ditta, et al.
Journal of Medicinal Chemistry|October 19, 2010
Conformationally restricted homotryptamines. Part 7: 3-cis-(3-aminocyclopentyl)indoles as potent selective serotonin reuptake inhibitorsH Dalton King, Zhaoxing Meng, Jeffrey A Deskus, et al.
European Journal of Cancer (Oxford, England : 1990)|February 21, 1998
Etoposide in malignant pleural mesothelioma: two phase II trials of the EORTC Lung Cancer Cooperative GroupT Sahmoud, P E Postmus, C van Pottelsberghe, et al.
Bioorganic & Medicinal Chemistry Letters|March 30, 2007
Conformationally restricted homotryptamines 3. Indole tetrahydropyridines and cyclohexenylamines as selective serotonin reuptake inhibitorsJeffrey A Deskus, James R Epperson, Charles P Sloan, et al.
Journal of Medicinal Chemistry|September 16, 2005
Conformationally restricted homotryptamines. 2. Indole cyclopropylmethylamines as selective serotonin reuptake inhibitorsRonald J Mattson, John D Catt, Derek J Denhart, et al.
Bioorganic & Medicinal Chemistry Letters|September 4, 2007
Conformationally restricted homotryptamines. Part 4: Heterocyclic and naphthyl analogs of a potent selective serotonin reuptake inhibitorH Dalton King, Derek J Denhart, Jeffrey A Deskus, et al.
ACS Medicinal Chemistry Letters|April 21, 2016
Discovery and Optimization of Macrocyclic Quinoxaline-pyrrolo-dihydropiperidinones as Potent Pim-1/2 Kinase InhibitorsVictor J Cee, Frank Chavez, Bradley Herberich, et al.
Bioorganic & Medicinal Chemistry Letters|September 27, 2012
[18F](R)-5-chloro-1-(1-cyclopropyl-2-methoxyethyl)-3-(4-(2-fluoroethoxy)-2,5-dimethyl phenylamino)pyrazin-2(1H)-one: introduction of N3-phenylpyrazinones as potential CRF-R1 PET imaging agentsJeffrey A Deskus, Douglas D Dischino, Ronald J Mattson, et al.
Journal of Medicinal Chemistry|June 26, 2009
Synthesis, structure-activity relationships, and in vivo evaluation of N3-phenylpyrazinones as novel corticotropin-releasing factor-1 (CRF1) receptor antagonistsRichard A Hartz, Vijay T Ahuja, Argyrios G Arvanitis, et al.
Pageof 19

Showing results (181-190 of 190) with videos related to

Sort By:
Pageof 19
You have reached the last page of results.This site can display upto 190 results.
Bioorganic & Medicinal Chemistry|May 16, 2006
Synthesis and evaluation of 5,5-diphenylimidazolones as potent human neuropeptide Y5 receptor antagonistsKevin W Gillman, Mendi A Higgins, Graham S Poindexter, et al.
Bioorganic & Medicinal Chemistry Letters|June 30, 2009
Conformationally restricted homotryptamines. Part 5: 3-(trans-2-aminomethylcyclopentyl)indoles as potent selective serotonin reuptake inhibitorsDerek J Denhart, Jeffrey A Deskus, Jonathan L Ditta, et al.
Journal of Medicinal Chemistry|October 19, 2010
Conformationally restricted homotryptamines. Part 7: 3-cis-(3-aminocyclopentyl)indoles as potent selective serotonin reuptake inhibitorsH Dalton King, Zhaoxing Meng, Jeffrey A Deskus, et al.
European Journal of Cancer (Oxford, England : 1990)|February 21, 1998
Etoposide in malignant pleural mesothelioma: two phase II trials of the EORTC Lung Cancer Cooperative GroupT Sahmoud, P E Postmus, C van Pottelsberghe, et al.
Bioorganic & Medicinal Chemistry Letters|March 30, 2007
Conformationally restricted homotryptamines 3. Indole tetrahydropyridines and cyclohexenylamines as selective serotonin reuptake inhibitorsJeffrey A Deskus, James R Epperson, Charles P Sloan, et al.
Journal of Medicinal Chemistry|September 16, 2005
Conformationally restricted homotryptamines. 2. Indole cyclopropylmethylamines as selective serotonin reuptake inhibitorsRonald J Mattson, John D Catt, Derek J Denhart, et al.
Bioorganic & Medicinal Chemistry Letters|September 4, 2007
Conformationally restricted homotryptamines. Part 4: Heterocyclic and naphthyl analogs of a potent selective serotonin reuptake inhibitorH Dalton King, Derek J Denhart, Jeffrey A Deskus, et al.
ACS Medicinal Chemistry Letters|April 21, 2016
Discovery and Optimization of Macrocyclic Quinoxaline-pyrrolo-dihydropiperidinones as Potent Pim-1/2 Kinase InhibitorsVictor J Cee, Frank Chavez, Bradley Herberich, et al.
Bioorganic & Medicinal Chemistry Letters|September 27, 2012
[18F](R)-5-chloro-1-(1-cyclopropyl-2-methoxyethyl)-3-(4-(2-fluoroethoxy)-2,5-dimethyl phenylamino)pyrazin-2(1H)-one: introduction of N3-phenylpyrazinones as potential CRF-R1 PET imaging agentsJeffrey A Deskus, Douglas D Dischino, Ronald J Mattson, et al.
Journal of Medicinal Chemistry|June 26, 2009
Synthesis, structure-activity relationships, and in vivo evaluation of N3-phenylpyrazinones as novel corticotropin-releasing factor-1 (CRF1) receptor antagonistsRichard A Hartz, Vijay T Ahuja, Argyrios G Arvanitis, et al.
Pageof 19