#	Aladdin ID	Assay Type	Description	Organism	Compounds	Reference	BAO Format	Source
1.	ALA873411	B	Binding affinity towards mouse Prostanoid EP1 receptor in CHO cells.		17		cell-based format	Scientific Literature
2.	ALA766142	B	Evaluated for its competitive binding affinity towards mouse Prostanoid EP1 receptor in CHO cells expressing prostanoid receptor		20		cell-based format	Scientific Literature
3.	ALA763180	B	Affinity for mouse Prostanoid EP1 receptor expressed in CHO cells	Mus musculus	13		cell-based format	Scientific Literature
4.	ALA828212	B	Binding affinity for mouse Prostanoid EP1 receptor	Mus musculus	13		single protein format	Scientific Literature
5.	ALA830428	B	Ability to inhibit the binding of [3H]PGD-2 radioligand to membranes of CHO cells stably expressing mouse Prostaglandin E receptor EP1	Mus musculus	14		cell-based format	Scientific Literature
6.	ALA2038097	B	Displacement of [3H]PGE2 from mouse EP1 receptor expressed in CHO cells after 20 mins by scintillation counting	Mus musculus	29		cell-based format	Scientific Literature
7.	ALA1815358	B	Displacement of [3H]-PGE2 from mouse EP1 receptor expressed in CHO cells after 20 mins by liquid scintillation counting	Mus musculus	11		cell-based format	Scientific Literature
8.	ALA1821222	B	Displacement of [3H]PGE2 from mouse prostaglandin EP1 receptor expressed in CHO cells after 60 mins by liquid scintillation counting	Mus musculus	11		cell-based format	Scientific Literature
9.	ALA1932308	B	Displacement of [3H]-PGE2 from mouse EP1 receptor expressed in CHO cells after 20 mins by liquid scintillation counter	Mus musculus	27		cell-based format	Scientific Literature
10.	ALA1936147	B	Displacement of [3H]-PGE2 from mouse EP1 receptor expressed in CHO cells after 20 mins by liquid scintillation counting	Mus musculus	16		cell-based format	Scientific Literature
11.	ALA1961330	B	Displacement of [3H]-PGE2 from mouse EP1 receptor expressed in CHO cells after 60 mins by scintillation counting	Mus musculus	22		cell-based format	Scientific Literature
12.	ALA1073243	B	Displacement of [3H]PGE2 from mouse EP1 receptor expressed in CHO cells by liquid scintillation counting	Mus musculus	19		cell-based format	Scientific Literature
13.	ALA1070315	B	Displacement of [3H]PGE2 from mouse EP1 receptor expressed in CHO cell membrane	Mus musculus	6		cell-based format	Scientific Literature
14.	ALA1074318	B	Displacement of [3H]PGE2 from mouse EP1 receptor expressed in CHO cells by liquid scintillation counting	Mus musculus	7		cell-based format	Scientific Literature
15.	ALA1104421	B	Displacement of [3H]PGE2 from mouse EP1 receptor expressed in CHO cells after 60 mins by scintillation counter	Mus musculus	10		cell-based format	Scientific Literature
16.	ALA1117300	B	Displacement of [3H]PGE2 from mouse EP1 receptor expressed in CHO cells after 20 mins by liquid scintillation counting	Mus musculus	23		cell-based format	Scientific Literature
17.	ALA2320396	F	Antagonist activity at mouse EP1 receptor expressed in CHOK1 cells assessed as inhibition of 17PTPGE2-induced calcium influx at >100 uM	Mus musculus	1		cell-based format	Scientific Literature
18.	ALA2320404	F	Antagonist activity at mouse EP1 receptor expressed in CHOK1 cells assessed as inhibition of 17PTPGE2-induced calcium influx	Mus musculus	14		cell-based format	Scientific Literature
19.	ALA3887505	B	Inhibition Assay: The cells expressing mouse EP1 receptor were seeded at 104 cells/well in 96-well plates and cultured for 2 days with 10% Fetal Bovine Serum (FBS)/alpha Modified Eagle Medium (alphaMEM) in the incubator (37° C., 5% CO2). The cells were washed with phosphate buffer, and load buffer (10% FBS/αMEM containing Fura2/AM (5 uM), indomethacin (20 uM) and probenecid (2.5 mM)) was then added to each well and cells were left standing for 1 hour. Load buffer of each well was discarded and assay buffer (Hank's Balanced Salt Solution (HBSS) containing indomethacin (2.5 mM), probenecid (2.5 mM), HEPES-NaOH (10 mM) and 0.1% (w/v) Bovine Serum Albumin (BSA)) was added to each well and plates were left at room temperature in a dark room for 1 hour. Afterwards, compounds of the present invention (10 uL) or PGE2 (10 uL) prepared with assay buffer was added to each well and intracellular calcium concentrations were measured using a Fluorescence Drug Screening System.	Mus musculus	12		cell-based format	BindingDB Database