Reaction Details
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Tyrosine-protein kinase SYK [360-635]
Ligand
BDBM295281
Substrate
n/a
Meas. Tech.
SYK Assa
pH
7.5±n/a
IC50
7.00±n/a nM
Comments
extracted
Citation
Bhagirath, N; Kennedy-Smith, J; Le, NT; Lucas, MC; Padilla, F; Soth, M Inhibitors of SYK US Patent US10112928 Publication Date 10/30/2018 More Info.:
Target
Name:
Tyrosine-protein kinase SYK [360-635]
Synonyms:
KSYK_HUMAN | SYK | SYK RPA purified, truncated construct of Spleen Tyrosine Kinase (aa 360-635) | Tyrosine-protein kinase SYK | recombinant human SYK(aa 360-635)
Type:
n/a
Mol. Mass.:
31987.15
Organism:
Homo sapiens (Human)
Description:
Human MetAP2 protein from a culture superatant of insect cells (sf9) infected with MetAP2 recombinant baculovirus
Residue:
276
Sequence:
PKEVYLDRKLLTLEDKELGSGNFGTVKKGYYQMKKVVKTVAVKILKNEANDPALKDELLAEANVMQQLDNPYIVRMIGICEAESWMLVMEMAELGPLNKYLQQNRHVKDKNIIELVHQVSMGMKYLEESNFVHRDLAARNVLLVTQHYAKISDFGLSKALRADENYYKAQTHGKWPVKWYAPECINYYKFSSKSDVWSFGVLMWEAFSYGQKPYRGMKGSEVTAMLEKGERMGCPAGCPREMYDLMNLCWTYDVENRPGFAAVELRLRNYYYDVVN
Inhibitor
Name:
BDBM295281
Synonyms:
6-(2- aminoethylamino)-4- (6-(trifluoromethyl) pyridin-2- ylamino)pyridazine- 3-carboxamide | US10112928, Compound I-25
Type:
Small organic molecule
Emp. Form.:
C13H14F3N7O
Mol. Mass.:
341.2918
SMILES:
NCCNc1cc(Nc2cccc(n2)C(F)(F)F)c(nn1)C(N)=O
Structure:
