#	Aladdin ID	Assay Type	Description	Organism	Compounds	Reference	BAO Format	Source
1.	ALA2014776	B	Inhibition of Plasmodium falciparum DHODH after 20 mins by 2,6-dichloroindophenol-reduction based assay	Plasmodium falciparum	41		single protein format	Scientific Literature
2.	ALA2014777	B	Inhibition of human DHODH after 20 mins by 2,6-dichloroindophenol-reduction based assay	Homo sapiens	19		single protein format	Scientific Literature
3.	ALA2014780	F	Antiplasmodial activity against Plasmodium falciparum 3D7 infected in human renal proximal tubule cells after 72 hrs by SYBR green assay	Plasmodium falciparum	41		organism-based format	Scientific Literature
4.	ALA2014781	F	Antiplasmodial activity against Plasmodium falciparum Dd2 infected in human renal proximal tubule cells after 72 hrs by SYBR green assay	Plasmodium falciparum	41		organism-based format	Scientific Literature
5.	ALA2014782	A	Cytotoxicity against human RPTEC after 4 days by alamar blue assay	Homo sapiens	11		cell-based format	Scientific Literature
6.	ALA3706206	B	Enzymatic Assays: Type 2 DHODH activity was monitored with either the direct assay measuring the formation of orotate or via a chromogen reduction assay using DCIP. Although the extinction coefficient and absorption wavelength are preferable for the chromogen reduction assay, the inorganic electron acceptor DCIP can be utilized by DHODH as the final electron acceptor in lieu of CoQn when the endogenous substrate is at a low concentration. As such, the direct assay was used to measure the binding affinity of pfDHODH to CoQD and L-DHO. The enzymatic reaction was performed by varying the L-DHO concentration (1-400 μM) or CoQD concentration (1-200 μM) while keeping the other substrate constant and in excess. Inhibition of DHODH by small molecules was evaluated using the chromogen based assay with a final substrate concentration of 200 μM L-DHO, 18 μM CoQD, and 100 μM DCIP, unless otherwise noted.	Plasmodium falciparum	95		single protein format	BindingDB Database