benzamide and threonine

benzamide has been researched along with threonine in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	2 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Amdani, S; Cummings, DF; Ericksen, SS; Schetz, JA; Teer, ME	1
Ding, K; Leng, F; Li, Y; Long, H; Lu, X; Luo, J; Pan, X; Ren, X; Shen, M; Tu, Z; Wen, D; Zhang, F; Zhang, Z	1

Other Studies

2 other study(ies) available for benzamide and threonine

Article	Year
Ring substituents on substituted benzamide ligands indirectly mediate interactions with position 7.39 of transmembrane helix 7 of the D4 dopamine receptor. The Journal of pharmacology and experimental therapeutics, 2012, Volume: 342, Issue:2 Topics: Alanine; Animals; Benzamides; Binding Sites; Cell Line, Transformed; Diethylamines; HEK293 Cells; Humans; Ligands; Membrane Proteins; Mutation; Protein Binding; Protein Structure, Secondary; Rats; Receptors, Dopamine D2; Receptors, Dopamine D4; Salicylamides; Sodium; Structure-Activity Relationship; Threonine	2012
Design, synthesis, and biological evaluation of 3-(1H-1,2,3-triazol-1-yl)benzamide derivatives as Potent Pan Bcr-Abl inhibitors including the threonine(315)→isoleucine(315) mutant. Journal of medicinal chemistry, 2012, Nov-26, Volume: 55, Issue:22 Topics: Benzamides; Blotting, Western; Cell Line, Tumor; Cell Proliferation; Cells, Cultured; Drug Design; Drug Resistance, Neoplasm; Fusion Proteins, bcr-abl; Humans; Imatinib Mesylate; Isoleucine; Leukemia, Myelogenous, Chronic, BCR-ABL Positive; Models, Molecular; Molecular Structure; Mutation; Phosphorylation; Piperazines; Protein Kinase Inhibitors; Pyrimidines; Structure-Activity Relationship; Threonine	2012

Article

Year

Ring substituents on substituted benzamide ligands indirectly mediate interactions with position 7.39 of transmembrane helix 7 of the D4 dopamine receptor.

The Journal of pharmacology and experimental therapeutics, 2012, Volume: 342, Issue:2

Topics: Alanine; Animals; Benzamides; Binding Sites; Cell Line, Transformed; Diethylamines; HEK293 Cells; Humans; Ligands; Membrane Proteins; Mutation; Protein Binding; Protein Structure, Secondary; Rats; Receptors, Dopamine D2; Receptors, Dopamine D4; Salicylamides; Sodium; Structure-Activity Relationship; Threonine

2012

Design, synthesis, and biological evaluation of 3-(1H-1,2,3-triazol-1-yl)benzamide derivatives as Potent Pan Bcr-Abl inhibitors including the threonine(315)→isoleucine(315) mutant.

Journal of medicinal chemistry, 2012, Nov-26, Volume: 55, Issue:22

Topics: Benzamides; Blotting, Western; Cell Line, Tumor; Cell Proliferation; Cells, Cultured; Drug Design; Drug Resistance, Neoplasm; Fusion Proteins, bcr-abl; Humans; Imatinib Mesylate; Isoleucine; Leukemia, Myelogenous, Chronic, BCR-ABL Positive; Models, Molecular; Molecular Structure; Mutation; Phosphorylation; Piperazines; Protein Kinase Inhibitors; Pyrimidines; Structure-Activity Relationship; Threonine

2012