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Target
Receptor-type tyrosine-protein kinase FLT3 [564-710,762-958]
Ligand
BDBM538619
Substrate
n/a
Meas. Tech.
Kinase Assay
Kd
1.90±n/a nM
Citation
 Starczynowski, DT; Thomas, CJ; Rhyasen, G; Melgar, K; Walker, MM; Jiang, J Substituted Imidazo[1,2-a]-pyridines as IRAK 1/4 and FLT3 inhibitors US Patent  US11542261 Publication Date 1/3/2023 
Target
Name:
Receptor-type tyrosine-protein kinase FLT3 [564-710,762-958]
Synonyms:
CD135 | FLK2 | FLT3 | FLT3-autoinhibited | FLT3_HUMAN | STK1
Type:
Enzyme
Mol. Mass.:
39747.92
Organism:
Homo sapiens (Human)
Description:
P36888[564-710,762-958]
Residue:
344
Sequence:
HKYKKQFRYESQLQMVQVTGSSDNEYFYVDFREYEYDLKWEFPRENLEFGKVLGSGAFGKVMNATAYGISKTGVSIQVAVKMLKEKADSSEREALMSELKMMTQLGSHENIVNLLGACTLSGPIYLIFEYCCYGDLLNYLRSKREKFSEDEIEYENQKRLEEEEDLNVLTFEDLLCFAYQVAKGMEFLEFKSCVHRDLAARNVLVTHGKVVKICDFGLARDIMSDSNYVVRGNARLPVKWMAPESLFEGIYTIKSDVWSYGILLWEIFSLGVNPYPGIPVDANFYKLIQNGFKMDQPFYATEEIYIIMQSCWAFDSRKRPSFPNLTSFLGCQLADAEEAMYQNV
  
Inhibitor
Name:
BDBM538619
Synonyms:
NCGC 00371479 | US11254667, Compound I-22 | US11542261, Compound I-22
Type:
Small organic molecule
Emp. Form.:
C22H22N6O
Mol. Mass.:
386.4497
SMILES:
COc1cc2ncc(-c3cccc(NC4CCNC4)n3)n2cc1-c1cccnc1
Structure:
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