#	Aladdin ID	Assay Type	Description	Organism	Compounds	Reference	BAO Format	Source
1.	ALA2327429	B	Inhibition of TASK-1 (unknown origin)	Homo sapiens	1		single protein format	Scientific Literature
2.	ALA3215269	F	PubChem BioAssay. SAR Analysis for the identification of inhibitors of the two-pore domain potassium channel TASK1 (KCNK3). (Class of assay: confirmatory)		94		assay format	PubChem BioAssays
3.	ALA3367859	B	Inhibition of TASK-1 (unknown origin) expressed in CHO cells at 3 uM by thallium flux assay	Homo sapiens	56		cell-based format	Scientific Literature
4.	ALA3367860	B	Inhibition of TASK-1 (unknown origin) expressed in CHO cells by thallium flux assay	Homo sapiens	58		cell-based format	Scientific Literature
5.	ALA3367866	B	Inhibition of TASK-1 (unknown origin) at 3 uM by parental cell based thallium flux assay	Homo sapiens	1		cell-based format	Scientific Literature
6.	ALA3367867	B	Inhibition of TASK-1 (unknown origin) by parental cell based thallium flux assay	Homo sapiens	1		cell-based format	Scientific Literature
7.	ALA3367868	B	Inhibition of TASK-1 (unknown origin) expressed in CHO cells by QPatch assay	Homo sapiens	8		cell-based format	Scientific Literature
8.	ALA3705435	B	Inhibition Assay: Human TASK-1 channels were expressed in Xenopus oocytes. For this purpose, oocytes were isolated from Xenopus laevis and defoliculated. Subsequently, TASK- 1 -encoding RNA synthesized in vitro was injected into oocytes. After two days of TASK-1 protein expression, TASK-1 currents were measured by two-microelectrode voltage clamp. Data were acquired and analyzed using a TEC-10cx amplifier (NPI Electronic, Tamm, Germany) connected to an ITC-16 interface (Instrutech Corp., Long Island, USA) and Pulse software (HEKA Elektronik, Lambrecht, Germany). Oocytes were clamped to -90 mV and TASK-1 mediated currents were measured during 500 ms voltage pulses to 40 mV. Oocytes were continuously superfused with ND96 buffer containing: NaCI 96 mM, KCI2 mM, CaCI21.8 mM, MgCI21 mM, HEPES 5 mM (pH adjusted to 7.4 with NaOH).		44		cell-based format	BindingDB Database
9.	ALA3819960	B	Inhibition of of TASK1 (unknown origin) expressed in CHO cells assessed as reduction in channel currents	Homo sapiens	2		cell-based format	Scientific Literature
10.	ALA3887241	B	Biological Assay: Human TASK-1 channels were expressed in Xenopus oocytes. For this purpose, oocytes were isolated from Xenopus laevis and defoliculated. Subsequently, TASK-1-encoding RNA synthesized in vitro was injected into oocytes. After two days of TASK-1 protein expression, TASK-1 currents were measured by two-microelectrode voltage clamp. Data were acquired and analyzed using a TEC-10cx amplifier (NPI Electronic, Tamm, Germany) connected to an ITC-16 interface (Instrutech Corp., Long Island, USA) and Pulse software (HEKA Elektronik, Lambrecht, Germany). Oocytes were clamped to −90 mV and TASK-1 mediated currents were measured during 500 ms voltage pulses to 40 mV. Oocytes were continuously superfused with ND96 buffer containing: NaCl 96 mM, KCl 2 mM, CaCl2 1.8 mM, MgCl2 1 mM, HEPES 5 mM (pH adjusted to 7.4 with NaOH). All experiments were performed at room temperature.		63		cell-based format	BindingDB Database
11.	ALA3888209	B	TASK-1 Inhibiition Assay: Human TASK-1 channels were expressed in Xenopus oocytes. For this purpose, oocytes were isolated from Xenopus laevis and defoliculated. Subsequently, TASK-1-encoding RNA synthesized in vitro was injected into the oocytes. After two days of TASK-1 protein expression, TASK-1 currents were measured by two-microelectrode voltage clamp. Data were acquired and analyzed using a TEC-10cx amplifier (NPI Electronic, Tamm, Germany) connected to an ITC-16 interface (Instrutech Corp., Long Island, USA) and Pulse software (HEKA Elektronik, Lambrecht, Germany). Oocytes were clamped to -90 mV and TASK-1 mediated currents were measured during 500 ms voltage pulses to 40 mV. Oocytes were continuously superfused with ND96 buffer containing 96 mM sodium chloride, 2 mM potassium chloride, 1.8 mM calcium chloride, 1 mM magnesium chloride, 5 mM 4-(2-hydroxyethyl)-piperazine-1-ethanesulfonic acid (HEPES; pH adjusted to 7.4 with sodium hydroxide). All experiments were performed at room temperature.		363		cell-based format	BindingDB Database
12.	ALA4322155	B	Inhibition of human TASK1 expressed in CHO cells by Inside-out macro-patches based electrophysiology assay	Homo sapiens	1		cell-based format	Scientific Literature
13.	ALA4322156	B	Inhibition of human TASK1 expressed in Xenopus oocytes by whole cell voltage clamp assay	Homo sapiens	15		cell-based format	Scientific Literature
14.	ALA4322158	B	Inhibition of human TASK1 by whole cell voltage clamp assay	Homo sapiens	2		single protein format	Scientific Literature
15.	ALA4322160	B	Inhibition of human TASK1 expressed in African green monkey COS7 cells by whole cell patch clamp assay	Homo sapiens	1		cell-based format	Scientific Literature
16.	ALA4322164	B	Inhibition of human TASK1 expressed in African green monkey COS cells at 0.6 mM by whole cell patch clamp assay relative to control	Homo sapiens	1		cell-based format	Scientific Literature
17.	ALA4322167	B	Activation of human TASK1 expressed in African green monkey COS cells at 1 mM by whole cell patch clamp assay relative to control	Homo sapiens	1		cell-based format	Scientific Literature
18.	ALA4322168	B	Activation of human TASK1 expressed in African green monkey COS cells at 2 mM by whole cell patch clamp assay relative to control	Homo sapiens	1		cell-based format	Scientific Literature
19.	ALA4322170	B	Inhibition of human TASK1 expressed in African green monkey COS cells by whole cell patch clamp assay	Homo sapiens	1		cell-based format	Scientific Literature
20.	ALA4322172	B	Inhibition of human TASK1 expressed in CHO cells by Qpatch HT platform based assay	Homo sapiens	1		cell-based format	Scientific Literature