#	Aladdin ID	Assay Type	Description	Organism	Compounds	Reference	BAO Format	Source
1.	ALA4388122	Binding	Inhibition of recombinant human N-terminal TEV cleavage site-fused/FLAG-poly his-tagged TNKS SAM-PARP domain (1024 to 1327 residues) expressed in Escherichia coli assessed as reduction in auto-PARylation preincubated for 10 mins followed by biotinylated-NAD+ addition and measured after 45 mins by ELISA	Homo sapiens	57	ALA4387706	assay format	Scientific Literature
2.	ALA4388123	Binding	Inhibition of recombinant human N-terminal TEV cleavage site-fused/FLAG-poly his-tagged TNKS2 SAM-PARP domain (613 to 1166 residues) expressed in Escherichia coli assessed as reduction in auto-PARylation preincubated for 10 mins followed by biotinylated-NAD+ addition and measured after 45 mins by ELISA	Homo sapiens	57	ALA4387706	assay format	Scientific Literature
3.	ALA4388124	ADME	Inhibition of recombinant human PARP1 expressed in Escherichia coli assessed as reduction in auto-PARylation using histone as substrate measured after 45 mins in presence of biotinylated-NAD+ by ELISA	Homo sapiens	34	ALA4387706	assay format	Scientific Literature
4.	ALA4388125	Binding	Inhibition of TNKS/TNKS2 (unknown origin) expressed in human DLD1 cells assessed as reduction in Wnt-signaling measured after 24 hrs by TCF-luciferase reporter gene assay	Homo sapiens	57	ALA4387706	cell-based format	Scientific Literature
5.	ALA4388126	Functional	Antiproliferative activity against human COLO320DM cells assessed as inhibition of cell growth measured after 4 days by CellTiter-Glo assay	Homo sapiens	51	ALA4387706	cell-based format	Scientific Literature
6.	ALA4388128	Physicochemical	Aqueous solubility of the compound in pH 7.4 phosphate buffer at 200 uM incubated for 1 hr under shaking condition by UV spectra analysis		56	ALA4387706	small-molecule physicochemical format	Scientific Literature