Reaction Details |
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Target | Fibroblast growth factor receptor 3 |
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Ligand | BDBM139909 |
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Substrate/Competitor | n/a |
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Meas. Tech. | In Vitro Kinase Inhibitory Activity Assay |
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pH | 7.5±n/a |
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IC50 | 0.78±n/a nM |
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Citation | Berdini, V; Besong, GE; Callaghan, O; Carr, MG; Congreve, MS; Gill, AL; Griffiths-Jones, CM; Madin, A; Murray, CW; Nijjar, RK; O'Brien, MA; Pike, A; Saxty, G; Taylor, RD; Vickerstaffe, E Bicyclic heterocyclic compounds as FGFR inhibitors US Patent US8895745 Publication Date 11/25/2014 |
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More Info.: | Get all data from this article, Solution Info, Assay Method |
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Fibroblast growth factor receptor 3 |
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Name: | Fibroblast growth factor receptor 3 |
Synonyms: | CD_antigen: CD333 | FGFR-3 | FGFR3 | FGFR3_HUMAN | Fibroblast growth factor receptor | Fibroblast growth factor receptor 3 (FGFR3) | JTK4 |
Type: | Protein |
Mol. Mass.: | 87699.57 |
Organism: | Homo sapiens (Human) |
Description: | P22607 |
Residue: | 806 |
Sequence: | MGAPACALALCVAVAIVAGASSESLGTEQRVVGRAAEVPGPEPGQQEQLVFGSGDAVELS
CPPPGGGPMGPTVWVKDGTGLVPSERVLVGPQRLQVLNASHEDSGAYSCRQRLTQRVLCH
FSVRVTDAPSSGDDEDGEDEAEDTGVDTGAPYWTRPERMDKKLLAVPAANTVRFRCPAAG
NPTPSISWLKNGREFRGEHRIGGIKLRHQQWSLVMESVVPSDRGNYTCVVENKFGSIRQT
YTLDVLERSPHRPILQAGLPANQTAVLGSDVEFHCKVYSDAQPHIQWLKHVEVNGSKVGP
DGTPYVTVLKTAGANTTDKELEVLSLHNVTFEDAGEYTCLAGNSIGFSHHSAWLVVLPAE
EELVEADEAGSVYAGILSYGVGFFLFILVVAAVTLCRLRSPPKKGLGSPTVHKISRFPLK
RQVSLESNASMSSNTPLVRIARLSSGEGPTLANVSELELPADPKWELSRARLTLGKPLGE
GCFGQVVMAEAIGIDKDRAAKPVTVAVKMLKDDATDKDLSDLVSEMEMMKMIGKHKNIIN
LLGACTQGGPLYVLVEYAAKGNLREFLRARRPPGLDYSFDTCKPPEEQLTFKDLVSCAYQ
VARGMEYLASQKCIHRDLAARNVLVTEDNVMKIADFGLARDVHNLDYYKKTTNGRLPVKW
MAPEALFDRVYTHQSDVWSFGVLLWEIFTLGGSPYPGIPVEELFKLLKEGHRMDKPANCT
HDLYMIMRECWHAAPSQRPTFKQLVEDLDRVLTVTSTDEYLDLSAPFEQYSPGGQDTPSS
SSSGDDSVFAHDLLPPAPPSSGGSRT
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BDBM139909 |
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n/a |
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Name | BDBM139909 |
Synonyms: | US8895745, 310 |
Type | Small organic molecule |
Emp. Form. | C19H15F3N6OS |
Mol. Mass. | 432.422 |
SMILES | Cc1nnc(s1)-c1ccn2c(cnc2c1)-c1cccc(NC(=O)NCC(F)(F)F)c1 |
Structure |
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