#	Aladdin ID	Assay Type	Description	Organism	Compounds	Reference	BAO Format	Source
1.	ALA4312819	P	Lipophilicity, logD of the compound at pH 7.4		10		small-molecule physicochemical format	Scientific Literature
2.	ALA4312822	A	Displacement of [3H]BTCP from recombinant human dopamine transporter at 10 uM after 120 mins by scintillation counting analysis relative to control	Homo sapiens	27		single protein format	Scientific Literature
3.	ALA4312823	B	Displacement of Tracer Red from human ERG by fluorescence polarization assay	Homo sapiens	27		single protein format	Scientific Literature
4.	ALA4312824	B	Inhibition of full-length C-terminal his-tagged mouse CHIT1 expressed in CHO-K1 cells assessed as reduction in chitinolytic activity using 4-methylumbelliferyl-beta-D-N,N',N\"-triacetylchitotrioside as substrate after 60 mins by fluorometric assay	Mus musculus	27		cell-based format	Scientific Literature
5.	ALA4312825	B	Inhibition of full-length C-terminal his-tagged mouse acidic mammalian chitinase expressed in CHO-K1 cells assessed as reduction in chitinolytic activity using 4-methylumbelliferyl-beta-D-N,N'-diacetylchitobioside hydrate as substrate after 60 mins by fluorometric assay	Mus musculus	27		cell-based format	Scientific Literature
6.	ALA4312826	B	Inhibition of full-length C-terminal his-tagged human CHIT1 expressed in CHOK1 cells assessed as reduction in chitinolytic activity using 4-methylumbelliferyl-beta-D-N,N',N\"-triacetylchitotrioside as substrate after 60 mins by fluorometric assay	Homo sapiens	27		cell-based format	Scientific Literature
7.	ALA4312827	B	Inhibition of full-length C-terminal his-tagged human acidic mammalian chitinase expressed in CHOK1 cells assessed as reduction in chitinolytic activity using 4-methylumbelliferyl-beta-D-N,N-diacetylchitobioside hydrate as substrate after 60 mins by fluorometric assay	Homo sapiens	27		cell-based format	Scientific Literature
8.	ALA4704014	B	Inhibition of full-length C-terminal his-tagged human recombinant CHIT1 catalytic domain (1 to 386 residues) expressed in HEK293F cells assessed as reduction in chitinolytic activity using 4-methylumbelliferyl-beta-D-N,N',N"-triacetylchitotrioside as substrate after 60 mins by fluorometric assay	Homo sapiens	18		cell-based format	Scientific Literature
9.	ALA4704015	B	Inhibition of recombinant full-length C-terminal his-tagged mouse CHIT1 expressed in CHO-K1 cells assessed as reduction in chitinolytic activity using 4-methylumbelliferyl-beta-D-N,N',N"-triacetylchitotrioside as substrate after 60 mins by fluorometric assay	Mus musculus	18		cell-based format	Scientific Literature
10.	ALA4704017	B	Inhibition of full-length C-terminal his-tagged human AMCase expressed in CHO-K1 cells assessed as reduction in chitinolytic activity using 4-methylumbelliferyl-beta-D-N,N-diacetylchitobioside hydrate as substrate after 60 mins by fluorometric assay	Homo sapiens	18		cell-based format	Scientific Literature
11.	ALA4704018	B	Inhibition of full-length C-terminal his-tagged mouse AMCase expressed in expressed in CHO-K1 cells assessed as reduction in chitinolytic activity using 4-methylumbelliferyl-beta-D-N,N'-diacetylchitobioside hydrate as substrate after 60 mins by fluorometric assay	Mus musculus	18		cell-based format	Scientific Literature
12.	ALA4704019	B	Inhibition of tracer red binding to human ERG expressed in HEK293 cell membranes measured after 2 to 6 hrs by fluorescence polarization assay	Homo sapiens	18		cell membrane format	Scientific Literature
13.	ALA4704020	B	Inhibition of [3H]BTCP binding to human recombinant dopamine transporter at 10 uM measured after 120 mins by scintillation counting method relative to control	Homo sapiens	18		single protein format	Scientific Literature