Reaction Details |
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Target | Proto-oncogene tyrosine-protein kinase receptor Ret [658-1114,G810R] |
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Ligand | BDBM296788 |
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Substrate/Competitor | n/a |
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Meas. Tech. | RET G810R Mutant Assay |
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IC50 | 473±n/a nM |
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Citation | Andrews, SW; Aronow, S; Blake, JF; Brandhuber, BJ; Cook, A; Haas, J; Jiang, Y; Kolakowski, GR; McFaddin, EA; McKenney, ML; McNulty, OT; Metcalf, AT; Moreno, DA; Tang, TP; Ren, L Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors US Patent US10555944 Publication Date 2/11/2020 |
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More Info.: | Get all data from this article, Assay Method |
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Proto-oncogene tyrosine-protein kinase receptor Ret [658-1114,G810R] |
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Name: | Proto-oncogene tyrosine-protein kinase receptor Ret [658-1114,G810R] |
Synonyms: | CDHF12 | CDHR16 | PTC | Proto-oncogene tyrosine-protein kinase receptor Ret (G810R) | RET | RET51 | RET_HUMAN |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 51635.31 |
Organism: | Homo sapiens (Human) |
Description: | P07949[658-1114,G810R] |
Residue: | 457 |
Sequence: | HCYHKFAHKPPISSAEMTFRRPAQAFPVSYSSSGARRPSLDSMENQVSVDAFKILEDPKW
EFPRKNLVLGKTLGEGEFGKVVKATAFHLKGRAGYTTVAVKMLKENASPSELRDLLSEFN
VLKQVNHPHVIKLYGACSQDGPLLLIVEYAKYRSLRGFLRESRKVGPGYLGSGGSRNSSS
LDHPDERALTMGDLISFAWQISQGMQYLAEMKLVHRDLAARNILVAEGRKMKISDFGLSR
DVYEEDSYVKRSQGRIPVKWMAIESLFDHIYTTQSDVWSFGVLLWEIVTLGGNPYPGIPP
ERLFNLLKTGHRMERPDNCSEEMYRLMLQCWKQEPDKRPVFADISKDLEKMMVKRRDYLD
LAASTPSDSLIYDDGLSEEETPLVDCNNAPLPRALPSTWIENKLYGMSDPNWPGESPVPL
TRADGTNTGFPRYPNDSVYANWMLSPSAAKLMDTFDS
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BDBM296788 |
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n/a |
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Name | BDBM296788 |
Synonyms: | US10112942, Example 523 | US10137124, Example 523 | US10172851, Example 523 | US10555944, Example 523 | US10953005, Example 523 |
Type | Small organic molecule |
Emp. Form. | C23H26N6O |
Mol. Mass. | 402.4921 |
SMILES | CCOc1cc(-c2ccc(nc2)N2CC[C@@]3(C2)CCCNC3)c2c(cnn2c1)C#N |r| |
Structure |
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