#	Aladdin ID	Assay Type	Description	Organism	Compounds	Reference	BAO Format	Source
1.	ALA1024879	F	Inhibition of Vaccinia virus DNA synthesis in by rapid plate assay	Vaccinia virus	93		organism-based format	Scientific Literature
2.	ALA1024880	F	Antiviral activity against Vaccinia virus WR in BSC1 cells assessed as reduction in plaque formation after 20 hrs	Vaccinia virus	60		organism-based format	Scientific Literature
3.	ALA1024882	A	Cytotoxicity against african green monkey BSC1 cells after 20 hrs WST-1 based assay	Chlorocebus aethiops	75		cell-based format	Scientific Literature
4.	ALA1837681	B	Inhibition of His6-tagged Escherichia coli DH5alpha CDP-ME kinase assessed as ADP production after 30 mins by Kinase Glo luminescence-based assay or standard pyruvate kinase/lactate dehydrogenase-coupled absorbance-based assay	Escherichia coli DH5[alpha]	6		assay format	Scientific Literature
5.	ALA1838042	B	Inhibition of His6-tagged Yersinia pestis KIM6 CDP-ME kinase assessed as ADP production after 30 mins by Kinase Glo luminescence-based assay or standard pyruvate kinase/lactate dehydrogenase-coupled absorbance-based assay	Yersinia pestis	6		single protein format	Scientific Literature
6.	ALA1838043	F	Antimicrobial activity against Escherichia coli DH5[alpha] assessed as growth inhibition at 50 uM up to 6 hrs	Escherichia coli	1		organism-based format	Scientific Literature
7.	ALA1838044	F	Antimicrobial activity against Escherichia coli DH5[alpha] assessed as growth inhibition at 50 uM after overnight incubation	Escherichia coli	1		organism-based format	Scientific Literature
8.	ALA2020225	B	Inhibition of human galactosidase after 30 mins by Kinase-GloTM assay	Homo sapiens	13		single protein format	Scientific Literature
9.	ALA3705442	B	FP Assay: The FP assay was then adapted for HTS and used to screen ~120,000 small molecule library for compounds that displaced probe 5 from the T4 binding of TTR. The FP assay was performed in 384-well plate using very low concentration of probe 5 (1.5 nM) and TTR (50 nM) in a 10 μL assay volume. A detergent (0.01% Triton-X100) was added to the assay buffer to avoid any false positive hits from promiscuous, aggregate-based inhibitors. The assay demonstrated robust performance, with a very good dynamic range (−70-230 mP) and a Z′ factor in the range of 0.57-0.78 (FIGS. 4A and 4B). "Hits" were defined as compounds that resulted in at least 50% decrease in fluorescence polarization and demonstrated relative fluorescence between 70 and 130%. Many fluorescence quenchers and enhancers having less than 70% and greater than 130% total fluorescence relative to a control, respectively, were excluded from the hit list. 200 compounds were designated as positive hits (0.167% hit rate).		33		single protein format	BindingDB Database
10.	ALA4477063	B	Inhibition of His6-tagged recombinant human GALK expressed in Escherichia coli HMS174 (DE3) incubated for 60 mins using galactose and ATP by Kinase-Glo reagent based assay	Homo sapiens	34		assay format	Patent Bioactivity Data
11.	ALA4477064	B	Inhibition of Bacillus stearothermophilus glucokinase	Geobacillus stearothermophilus	34		assay format	Patent Bioactivity Data
12.	ALA4477065	B	Inhibition of Saccharomyces cerevisiae hexokinase	Saccharomyces cerevisiae	34		assay format	Patent Bioactivity Data