Drug	Gene	Type	Source
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	AIFM1	Text_Mining(affects(localization))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	AIFM1	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	AKT1	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	AKT1	Text_Mining(increases(phosphorylation))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	ALPL	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	ALPL	Text_Mining(increases(activity))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	APOA1	Text_Mining(increases(expression))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	APOA1	Text_Mining(increases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	APOA1	Text_Mining(increases(secretion))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	APOE	Text_Mining(increases(expression))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	APOE	Text_Mining(increases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	APOE	Text_Mining(increases(secretion))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	BCL2	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	BCL2	Text_Mining(increases(cleavage))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	BIRC2	Text_Mining(decreases(expression))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	BIRC2	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	BIRC3	Text_Mining(decreases(expression))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	BIRC3	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CASP3	Text_Mining(increases(activity))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CASP3	Text_Mining(increases(cleavage))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CASP3	Text_Mining(increases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CASP7	Text_Mining(increases(activity))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CASP7	Text_Mining(increases(cleavage))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CASP7	Text_Mining(increases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CASP9	Text_Mining(increases(activity))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CASP9	Text_Mining(increases(cleavage))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CCL2	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CCL2	Text_Mining(increases(expression))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CCL2	Text_Mining(increases(secretion))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CDKN1A	Text_Mining(increases(expression))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CETP	Text_Mining(increases(expression))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CETP	Text_Mining(increases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CETP	Text_Mining(increases(secretion))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CTNNB1	Text_Mining(affects(binding))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CTNNB1	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CTNNB1	Text_Mining(decreases(localization))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CTNNB1	Text_Mining(decreases(activity))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CTNNB1	Text_Mining(increases(degradation))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CTSD	Text_Mining(increases(expression))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CXCL8	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CXCL8	Text_Mining(increases(expression))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	GCLC	Text_Mining(increases(expression))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	GCLM	Text_Mining(increases(expression))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	HAX1	Text_Mining(decreases(expression))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	HAX1	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	HAX1	Text_Mining(decreases(response to substance))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	HMOX1	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	HMOX1	Text_Mining(increases(expression))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	ICAM1	Text_Mining(decreases(expression))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	IKBKG	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	IKBKG	Text_Mining(increases(phosphorylation))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	IKBKG	Text_Mining(increases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	IL17A	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	IL17A	Text_Mining(increases(activity))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	IL17A	Text_Mining(increases(expression))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	IL1B	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	IL1B	Text_Mining(increases(phosphorylation))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	IL1B	Text_Mining(increases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	IL1B	Text_Mining(increases(activity))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	IL6	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	IL6	Text_Mining(increases(expression))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	IL6	Text_Mining(increases(activity))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	IL6	Text_Mining(increases(phosphorylation))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	ITGAM	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	ITGAM	Text_Mining(increases(localization))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	MMP9	Text_Mining(decreases(activity))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	NFKB1	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	NFKB1	Text_Mining(increases(activity))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	NFKBIA	Text_Mining(decreases(activity))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	NFKBIA	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	NFKBIA	Text_Mining(increases(degradation))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	NFKBIA	Text_Mining(increases(phosphorylation))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	NFKBIA	Text_Mining(decreases(degradation))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	NFKBIA	Text_Mining(decreases(expression))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	NFKBIA	Text_Mining(decreases(phosphorylation))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	NFKBIB	Text_Mining(decreases(phosphorylation))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	NFKBIB	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	NQO1	Text_Mining(increases(expression))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	PARP1	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	PARP1	Text_Mining(increases(cleavage))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	PDPK1	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	PDPK1	Text_Mining(increases(phosphorylation))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	PDPK1	Text_Mining(decreases(activity))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	PLAU	Text_Mining(decreases(expression))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	RELA	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	RELA	Text_Mining(increases(activity))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	RELA	Text_Mining(increases(phosphorylation))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	RELA	Text_Mining(increases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	RELA	Text_Mining(increases(transport))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	RELA	Text_Mining(decreases(activity))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	RELA	Text_Mining(increases(degradation))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	RELA	Text_Mining(decreases(expression))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	STAT3	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	STAT3	Text_Mining(increases(activity))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	STAT3	Text_Mining(increases(phosphorylation))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	STS	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	STS	Text_Mining(increases(activity))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	TCF4	Text_Mining(affects(binding))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	TCF4	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	TGFB1	Text_Mining(decreases(expression))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	TGFB1	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	TGFB1	Text_Mining(increases(phosphorylation))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	TNF	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	TNF	Text_Mining(increases(expression))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	TNF	Text_Mining(increases(activity))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	TNF	Text_Mining(increases(transport))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	TNF	Text_Mining(decreases(activity))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	TNF	Text_Mining(increases(degradation))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	TNF	Text_Mining(increases(phosphorylation))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	TP53	Text_Mining(decreases(phosphorylation))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	TP53	Text_Mining(increases(activity))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	TP53	Text_Mining(increases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	TP53	Text_Mining(increases(response to substance))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	VCAM1	Text_Mining(decreases(expression))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	XIAP	Text_Mining(decreases(reaction))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	XIAP	Text_Mining(increases(cleavage))	CTD
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	ABHD5	IC50=1.868(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	ABHD5	IC50=1.901(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	ABHD5	None=None(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	ADRB2	None=None(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	ALDH1A1	Potency=0.3981(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	ALDH1A1	Potency=0.4467(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	ALDH1A1	Potency=0.7943(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	ALDH1A1	Potency=1.0(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	ALDH1A1	Potency=398.1(nM)	D4 ChEMBL
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	ALDH1A1	Potency=446.7(nM)	D4 ChEMBL
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	ALDH1A1	Potency=794.3(nM)	D4 ChEMBL
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	ALDH1A1	Potency=1000.0(nM)	D4 ChEMBL
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	ATAD5	Potency=14.575(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	ATAD5	Potency=16.3601(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	ATAD5	Potency=16360.1(nM)	D4 ChEMBL
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	ATXN2	Potency=22.3872(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	ATXN2	Potency=31.6228(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CFTR	None=None(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CYP1A2	None=None(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CYP1A2	AC50=12589.2(nM)	D4 ChEMBL
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CYP2C19	Potency=10.0(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CYP2C19	None=None(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CYP2C19	AC50=10000.0(nM)	D4 ChEMBL
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CYP2C19	Potency=10000.0(nM)	D4 ChEMBL
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CYP2C9	Potency=19.9526(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CYP2C9	None=None(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CYP2C9	AC50=19952.6(nM)	D4 ChEMBL
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CYP2C9	Potency=19952.6(nM)	D4 ChEMBL
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CYP3A4	Potency=3.1623(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CYP3A4	None=None(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CYP3A4	AC50=3162.28(nM)	D4 ChEMBL
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	CYP3A4	Potency=3162.3(nM)	D4 ChEMBL
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	GFER	None=None(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	GMNN	Potency=2.3109(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	GMNN	Potency=9.2(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	GSTO1	None=None(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	HIF1A	Potency=25.1189(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	HIF1A	Potency=25118.9(nM)	D4 ChEMBL
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	HNF4A	None=None(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	HPGD	Potency=19.9526(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	HPGD	Potency=19952.6(nM)	D4 ChEMBL
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	IL1B	None=None(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	MDM2	None=None(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	MDM4	None=None(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	NFE2L2	Potency=18.3564(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	NFE2L2	Potency=18356.4(nM)	D4 ChEMBL
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	NOD1	EC50=None(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	NPSR1	Potency=19.9526(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	NPSR1	Potency=19952.6(nM)	D4 ChEMBL
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	PADI4	None=None(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	PAFAH1B2	None=None(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	PLIN1	IC50=1.868(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	PLIN1	None=None(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	PLIN5	IC50=1.901(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	PLIN5	None=None(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	RGS4	Potency=7.5193(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	STK33	None=None(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	TDP1	Potency=2.5929(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	TDP1	Potency=5.1735(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	THPO	Potency=10.0(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	THPO	Potency=10000.0(nM)	D4 ChEMBL
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	TP53	Potency=3.1623(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	TP53	Potency=6.3096(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	TP53	Potency=6309.6(nM)	D4 ChEMBL
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	TP53	Potency=3162.3(nM)	D4 ChEMBL
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	USP1	Potency=44.6684(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	USP1	Potency=46.945(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	VDR	Potency=2.8184(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	VDR	Potency=5.6234(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	VDR	Potency=7.0795(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	VDR	Potency=9.4662(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	VDR	Potency=18.3564(uM)	D4 PubChem
TOSYLPHENYLALANYL CHLOROMETHYL KETONE	VDR	Potency=25.1189(uM)	D4 PubChem