Drug	Gene	Type	Source
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	CES1	Text_Mining(Inhibitor)	TTD
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	ALDH1A1	Potency=0.0501(uM)	D4 PubChem
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	ALDH1A1	Potency=0.0794(uM)	D4 PubChem
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	ALDH1A1	Potency=79.4(nM)	D4 ChEMBL
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	ALDH1A1	Potency=50.1(nM)	D4 ChEMBL
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	ALOX15	Potency=10.0(uM)	D4 PubChem
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	ALOX15	Potency=10000.0(nM)	D4 ChEMBL
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	ALOX15B	Potency=7943.3(nM)	D4 ChEMBL
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	APAF1	IC50_Mean=34.0(uM)	D4 PubChem
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	CASP3	IC50_Mean=22.7(uM)	D4 PubChem
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	CASP9	IC50_Mean=22.7(uM)	D4 PubChem
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	CYP1A2	None=None(uM)	D4 PubChem
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	CYP1A2	AC50=12589.2(nM)	D4 ChEMBL
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	CYP2D6	Potency=3.9811(uM)	D4 PubChem
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	CYP2D6	None=None(uM)	D4 PubChem
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	CYP2D6	Potency=3981.1(nM)	D4 ChEMBL
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	CYP2D6	AC50=3981.07(nM)	D4 ChEMBL
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	MAPT	Potency=14.1254(uM)	D4 PubChem
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	MAPT	None=None(uM)	D4 PubChem
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	MAPT	Potency=14125.4(nM)	D4 ChEMBL
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	STK33	None=None(uM)	D4 PubChem
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	TDP1	Potency=1.8837(uM)	D4 PubChem
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	TDP1	Potency=2.6609(uM)	D4 PubChem
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	TP53	Potency=6.3096(uM)	D4 PubChem
1-(3,4-Dichlorobenzyl)-1H-indole-2,3-dione	TP53	Potency=6309.6(nM)	D4 ChEMBL