#	Aladdin ID	Assay Type	Description	Organism	Compounds	Reference	BAO Format	Source
1.	ALA749839	B	Affinity for opiate receptors by measuring the inhibition of stereospecific binding of [3H]- naloxone in rat brain homogenates at a drug concentration of 2.0 x 10 E -5 M; Inactive		1		tissue-based format	Scientific Literature
2.	ALA749840	B	50% Inhibition of stereospecific [3H]-naltrexone (10e-9 M) binding towards opiate receptor in rat brain homogenate		7		tissue-based format	Scientific Literature
3.	ALA749841	B	Ability to inhibit the specific binding of [3H]- dihydromorphine to opiate receptors in rat brain membrane preparation by 50%		3		cell membrane format	Scientific Literature
4.	ALA749842	B	Binding affinity against opiate receptor from rat neural membranes, using [3H]dihydromorphine as radioligand		2		assay format	Scientific Literature
5.	ALA749843	B	Concentration required to inhibit opiate receptor using radioligand [3H]- Etorphine		6		protein format	Scientific Literature
6.	ALA749844	B	Concentration required to inhibit opiate receptor using radioligand [3H]- Etorphine; Not tested		1		protein format	Scientific Literature
7.	ALA749845	B	Concentration required to inhibit stereospecific [3H]- naltrexone binding by 50% in rat brain homogenate		5		tissue-based format	Scientific Literature
8.	ALA749846	B	Inhibitory activity against opiate receptor in rat using [3H]naloxone as radioligand		4		assay format	Scientific Literature
9.	ALA749847	B	Inhibition of [3H]dihydromorphine binding to opiate receptor from rat neural membranes after incubation at 20 nM concentration at 37 degree C		3		cell membrane format	Scientific Literature
10.	ALA753916	B	Inhibition of [3H]naloxone binding to opiate receptor from rat neural membranes after incubation at 20 nM concentration at 37 degree C		3		cell membrane format	Scientific Literature
11.	ALA858333	B	Compound was evaluated for binding activity against [3H]sufentanil opiate receptor	Rattus norvegicus	1		protein format	Scientific Literature
12.	ALA753917	B	Ability to displace 50% of (+/-) ethylketocyclazocine (2.8) in rat brain homogenate	Rattus norvegicus	1		tissue-based format	Scientific Literature
13.	ALA753918	B	Ability to inhibit the specific binding of [3H]- dihydromorphine to opiate receptors in rat brain membrane preparation by 50%	Rattus norvegicus	11		cell membrane format	Scientific Literature
14.	ALA753782	B	Compound was evaluated for displacement of 8 nM [3H]dalamid from opioid receptor of rat brain membranes at the concentration of 0 moles		2		cell membrane format	Scientific Literature
15.	ALA753783	B	Compound was evaluated for displacement of 8 nM [3H]-Dalamid from opioid receptor of rat brain membranes at the concentration of 10e-10 moles		2		cell membrane format	Scientific Literature
16.	ALA753784	B	Compound was evaluated for displacement of 8 nM [3H]dalamid from opioid receptor of rat brain membranes at the concentration of 10e-4.2 moles		2		cell membrane format	Scientific Literature
17.	ALA753785	B	Compound was evaluated for displacement of 8 nM [3H]dalamid from opioid receptor of rat brain membranes at the concentration of 10e-4.6 moles		2		cell membrane format	Scientific Literature
18.	ALA753921	B	Compound was evaluated for displacement of 8 nM [3H]dalamid from opioid receptor of rat brain membranes at the concentration of 10e-5 moles		2		cell membrane format	Scientific Literature
19.	ALA753922	B	Compound was evaluated for displacement of 8 nM [3H]dalamid from opioid receptor of rat brain membranes at the concentration of 10e-5.2 moles		2		cell membrane format	Scientific Literature
20.	ALA753923	B	Compound was evaluated for displacement of 8 nM [3H]dalamid from opioid receptor of rat brain membranes at the concentration of 10e-5.6 moles		2		cell membrane format	Scientific Literature