BDBM70894 2-furfuryl-[2-(m-toluidino)quinazolin-4-yl]amine;hydrochloride::4-N-(furan-2-ylmethyl)-2-N-(3-methylphenyl)quinazoline-2,4-diamine;hydrochloride::MLS000662793::N4-(2-furanylmethyl)-N2-(3-methylphenyl)quinazoline-2,4-diamine;hydrochloride::N4-(furan-2-ylmethyl)-N2-(3-methylphenyl)quinazoline-2,4-diamine;hydrochloride::N~4~-(2-furylmethyl)-N~2~-(3-methylphenyl)-2,4-quinazolinediamine hydrochloride::SMR000270242::cid_2910633
SMILES Cc1cccc(Nc2nc(NCc3ccco3)c3ccccc3n2)c1
InChI Key InChIKey=DPRZKNDPFKQQOC-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 70894
TargetCOUP transcription factor 2(Human)
The Scripps Research Institute Molecular Screening Center
Curated by PubChem BioAssay
The Scripps Research Institute Molecular Screening Center
Curated by PubChem BioAssay
Affinity DataEC50: 1.64E+4nMAssay Description:Activation of SOS1 in human HeLa cells assessed as increase in RAS-GTP levels after 30 mins by pull-down assayMore data for this Ligand-Target Pair
TargetTegument protein VP16(HHV-1)
The Scripps Research Institute Molecular Screening Center
Curated by PubChem BioAssay
The Scripps Research Institute Molecular Screening Center
Curated by PubChem BioAssay
Affinity DataIC50: 5.30E+4nMAssay Description:Source (MLPCN Center Name): The Scripps Research Institute Molecular Screening Center Affiliation: The Scripps Research Institute, TSRI Assay Provide...More data for this Ligand-Target Pair
