erlotinib has been researched along with 3-(1-(3-(biphenyl-4-ylamino)-3-oxopropyl)-1h-1,2,3-triazol-4-yl)-6-hydroxy-1-methyl-2-phenyl-1h-indole-5-carboxylic acid in 1 studies
Studies (erlotinib) | Trials (erlotinib) | Recent Studies (post-2010) (erlotinib) | Studies (3-(1-(3-(biphenyl-4-ylamino)-3-oxopropyl)-1h-1,2,3-triazol-4-yl)-6-hydroxy-1-methyl-2-phenyl-1h-indole-5-carboxylic acid) | Trials (3-(1-(3-(biphenyl-4-ylamino)-3-oxopropyl)-1h-1,2,3-triazol-4-yl)-6-hydroxy-1-methyl-2-phenyl-1h-indole-5-carboxylic acid) | Recent Studies (post-2010) (3-(1-(3-(biphenyl-4-ylamino)-3-oxopropyl)-1h-1,2,3-triazol-4-yl)-6-hydroxy-1-methyl-2-phenyl-1h-indole-5-carboxylic acid) |
---|---|---|---|---|---|
221 | 0 | 180 | 9 | 0 | 8 |
Protein | Taxonomy | erlotinib (IC50) | 3-(1-(3-(biphenyl-4-ylamino)-3-oxopropyl)-1h-1,2,3-triazol-4-yl)-6-hydroxy-1-methyl-2-phenyl-1h-indole-5-carboxylic acid (IC50) |
---|---|---|---|
Tyrosine-protein phosphatase non-receptor type 11 | Homo sapiens (human) | 6.0833 |
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 | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Chen, CH; Chen, YN; Chen, Z; Deng, Z; Fekkes, P; Firestone, B; Fodor, M; Fortin, PD; Fridrich, C; Garcia Fortanet, J; Grunenfelder, D; Ho, S; Kang, ZB; Karki, R; Kato, M; Keen, N; LaBonte, LR; LaMarche, MJ; Larrow, J; Lenoir, F; Liu, G; Liu, S; Lombardo, F; Majumdar, D; Meyer, MJ; Palermo, M; Perez, L; Pu, M; Ramsey, T; Sellers, WR; Shultz, MD; Stams, T; Towler, C; Wang, P; Williams, SL; Zhang, JH | 1 |
1 other study(ies) available for erlotinib and 3-(1-(3-(biphenyl-4-ylamino)-3-oxopropyl)-1h-1,2,3-triazol-4-yl)-6-hydroxy-1-methyl-2-phenyl-1h-indole-5-carboxylic acid
Article | Year |
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Allosteric Inhibition of SHP2: Identification of a Potent, Selective, and Orally Efficacious Phosphatase Inhibitor.
Topics: Administration, Oral; Allosteric Regulation; Allosteric Site; Animals; Antineoplastic Agents; Cell Line, Tumor; Crystallography, X-Ray; Drug Design; Female; Heterografts; High-Throughput Screening Assays; Humans; Male; Mice, Inbred C57BL; Mice, Nude; Models, Molecular; Neoplasm Transplantation; Piperidines; Protein Conformation; Protein Tyrosine Phosphatase, Non-Receptor Type 11; Pyrazines; Pyrimidines; Structure-Activity Relationship | 2016 |