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4YNE

(R)-2-Phenylpyrrolidine Substitute Imidazopyridazines: a New Class of Potent and Selective Pan-TRK Inhibitors

Summary for 4YNE
Entry DOI10.2210/pdb4yne/pdb
DescriptorHigh affinity nerve growth factor receptor, 6-[(2R)-2-(3-fluorophenyl)pyrrolidin-1-yl]-3-(pyridin-2-yl)imidazo[1,2-b]pyridazine, SULFATE ION, ... (5 entities in total)
Functional Keywordskinase, trk, inhibitor, oncology, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceHomo sapiens (Human)
Cellular locationCell membrane ; Single-pass type I membrane protein : P04629
Total number of polymer chains1
Total formula weight35193.42
Authors
Kreusch, A.,Rucker, P.,Molteni, V.,Loren, J. (deposition date: 2015-03-09, release date: 2015-06-03, Last modification date: 2023-09-27)
Primary citationChoi, H.S.,Rucker, P.V.,Wang, Z.,Fan, Y.,Albaugh, P.,Chopiuk, G.,Gessier, F.,Sun, F.,Adrian, F.,Liu, G.,Hood, T.,Li, N.,Jia, Y.,Che, J.,McCormack, S.,Li, A.,Li, J.,Steffy, A.,Culazzo, A.,Tompkins, C.,Phung, V.,Kreusch, A.,Lu, M.,Hu, B.,Chaudhary, A.,Prashad, M.,Tuntland, T.,Liu, B.,Harris, J.,Seidel, H.M.,Loren, J.,Molteni, V.
(R)-2-Phenylpyrrolidine Substituted Imidazopyridazines: A New Class of Potent and Selective Pan-TRK Inhibitors.
Acs Med.Chem.Lett., 6:562-567, 2015
Cited by
PubMed: 26005534
DOI: 10.1021/acsmedchemlett.5b00050
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.0229 Å)
Structure validation

218500

数据于2024-04-17公开中

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