#	Aladdin ID	Assay Type	Description	Organism	Compounds	Reference	BAO Format	Source
1.	ALA1697855	ADME	Literature-mined public compounds from Kruhlak et al phospholipidosis modelling dataset		484	ALA1697821	assay format	Scientific Literature
2.	ALA5291723	Functional	Compound was evaluated for inhibition of human ACHE in an vitro cell free assay measured by absorbance method		927	ALA5291721	assay format	Scientific Literature
3.	ALA5291725	Binding	Binding affinity towards human ADORA1 (agonistic activity) in an in vitro assay with cellular components measured by scintillation counting		227	ALA5291721	single protein format	Scientific Literature
4.	ALA5291728	Binding	Binding affinity towards human ADORA3 (agonistic activity) in an in vitro assay with cellular components measured by scintillation counting		754	ALA5291721	single protein format	Scientific Literature
5.	ALA5291730	Functional	Agonist activity at human ADRA1A in an in vitro cell-based assay (CRO assay) measured by fluorescence spectroscopy		845	ALA5291721	cell-based format	Scientific Literature
6.	ALA5291731	Functional	Antagonist activity at human ADRA1A in an in vitro cell-based assay measured by fluorescence spectroscopy		800	ALA5291721	cell-based format	Scientific Literature
7.	ALA5291736	Binding	Binding affinity towards human ADRA2A in an in vitro assay with cellular components measured by scintillation counting		927	ALA5291721	single protein format	Scientific Literature
8.	ALA5291749	Binding	Binding affinity towards human AR in an in vitro assay with cellular components measured by scintillation counting		927	ALA5291721	single protein format	Scientific Literature
9.	ALA5291759	Functional	Agonist activity at human CHRM1 in an in vitro cell-based assay (CRO assay) measured by fluorescence spectroscopy		842	ALA5291721	cell-based format	Scientific Literature
10.	ALA5291761	Functional	Antagonist activity human CHRM1 in an in vitro cell-based assay measured by fluorescence spectroscopy		812	ALA5291721	cell-based format	Scientific Literature
11.	ALA5291766	Binding	Binding affinity towards human CHRM2 in an in vitro assay with cellular components measured by scintillation counting		927	ALA5291721	single protein format	Scientific Literature
12.	ALA5291779	Binding	Binding affinity towards human DRD1 in an in vitro assay with cellular components (NIBR assay) measured by scintillation counting		927	ALA5291721	single protein format	Scientific Literature
13.	ALA5291782	Binding	Binding affinity towards human DRD3 in an in vitro assay with cellular components measured by scintillation counting		896	ALA5291721	single protein format	Scientific Literature
14.	ALA5291792	Binding	Binding affinity towards human ESR1 in an in vitro cell free assay (CRO assay) measured by membrane filtration		927	ALA5291721	assay format	Scientific Literature
15.	ALA5291794	Functional	Compound was evaluated for inhibition of human F2 in an in vitro cell free assay measured by fluorescence spectroscopy		927	ALA5291721	assay format	Scientific Literature
16.	ALA5291800	Binding	Binding affinity towards rat Gabra1 in an in vitro assay with cellular components measured by scintillation counting		532	ALA5291721	single protein format	Scientific Literature
17.	ALA5291812	Binding	Binding affinity towards human HRH3 in an in vitro assay with cellular components measured by scintillation counting		927	ALA5291721	single protein format	Scientific Literature
18.	ALA5291815	Binding	Binding affinity towards human HTR1A in an in vitro assay with cellular components measured by scintillation counting		927	ALA5291721	single protein format	Scientific Literature
19.	ALA5291820	Functional	Agonist activity at human HTR2B in an in vitro cell-based assay (CRO assay) measured by time-resolved fluorescence resonance energy transfer method		927	ALA5291721	cell-based format	Scientific Literature
20.	ALA5291829	Functional	Compound was evaluated for inhibition of human KDR in an in vitro cell free assay measured by time-resolved fluorescence resonance energy transfer method		692	ALA5291721	assay format	Scientific Literature