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Found 233 Enz. Inhib. hit(s) with Target = 'Pyruvate kinase PKM'
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50455474(CHEMBL4218770)
Affinity DataKi:  50nMAssay Description:Irreversible binding affinity to recombinant human PKM2 expressed in Escherichia coli BL21More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM26664(7-Hydroxy-flavone, 5a | 7-Hydroxyflavone, 11 | 7-h...)
Affinity DataKi:  3.53E+3nMAssay Description:Binding affinity to PKM2 (unknown origin) assessed as oxidation of beta-NADH by spectrophotometry based LDH coupled assayMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50081950(6-Hydroxy-2-phenyl-chromen-4-one | 6-Hydroxyflavon...)
Affinity DataKi:  3.53E+3nMAssay Description:Binding affinity to PKM2 (unknown origin) assessed as oxidation of beta-NADH by spectrophotometry based LDH coupled assayMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50049385(5-Hydroxy-2-phenyl-chromen-4-one | 5-Hydroxyflavon...)
Affinity DataKi:  3.53E+3nMAssay Description:Binding affinity to PKM2 (unknown origin) assessed as oxidation of beta-NADH by spectrophotometry based LDH coupled assayMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50187668(3-Hydroxyflavone | 3-Hydroxyflavone (12) | 3-hydro...)
Affinity DataKi:  3.53E+3nMAssay Description:Binding affinity to PKM2 (unknown origin) assessed as oxidation of beta-NADH by spectrophotometry based LDH coupled assayMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50140257(5,7-Dihydroxy-8-methoxy-2-phenyl-chromen-4-one | 5...)
Affinity DataKi:  3.53E+3nMAssay Description:Binding affinity to PKM2 (unknown origin) assessed as oxidation of beta-NADH by spectrophotometry based LDH coupled assayMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50336799(5,5',5''-[1,3,6-naphthalenetriyltris(sulfonylimino...)
Affinity DataKi:  1.00E+4nMAssay Description:Inhibitory activity against cell free dihydrofolate redutase (DHFR) from Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50336799(5,5',5''-[1,3,6-naphthalenetriyltris(sulfonylimino...)
Affinity DataKi:  1.65E+4nMAssay Description:Inhibitory activity against cell free dihydrofolate redutase (DHFR) from Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Rattus norvegicus)
TBA

Curated by ChEMBL
LigandPNGBDBM50367051(CHEMBL606059)
Affinity DataKi:  5.00E+5nMAssay Description:Inhibition of rat muscle pyruvate kinase (PK-M)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Rattus norvegicus)
TBA

Curated by ChEMBL
LigandPNGBDBM50367051(CHEMBL606059)
Affinity DataKi:  5.00E+5nMAssay Description:Inhibition of rat muscle pyruvate kinase (PK-M)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Rattus norvegicus)
TBA

Curated by ChEMBL
LigandPNGBDBM50367052(CHEMBL605425)
Affinity DataKi:  9.00E+5nMAssay Description:Inhibition of rat muscle pyruvate kinase (PK-M)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Rattus norvegicus)
TBA

Curated by ChEMBL
LigandPNGBDBM50028624(CHEMBL3142978 | [6-(6-amino-9H-purin-9-yl)-2-methy...)
Affinity DataKi:  1.60E+6nMAssay Description:Inhibition of rat muscle pyruvate kinase (PK-M)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Rattus norvegicus)
TBA

Curated by ChEMBL
LigandPNGBDBM50367054(CHEMBL606476)
Affinity DataKi:  3.70E+6nMAssay Description:Inhibition of rat muscle pyruvate kinase (PK-M)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Rattus norvegicus)
TBA

Curated by ChEMBL
LigandPNGBDBM50367053(CHEMBL605428)
Affinity DataKi:  4.30E+6nMAssay Description:Inhibition of rat muscle pyruvate kinase (PK-M)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Rattus norvegicus)
TBA

Curated by ChEMBL
LigandPNGBDBM50367050(CHEMBL606006)
Affinity DataKi:  4.50E+6nMAssay Description:Inhibition of rat muscle pyruvate kinase (PK-M) at 10 mMMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Rattus norvegicus)
TBA

Curated by ChEMBL
LigandPNGBDBM50367050(CHEMBL606006)
Affinity DataKi:  7.00E+6nMAssay Description:Inhibition of rat muscle pyruvate kinase (PK-M) at 6.7 mMMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Rattus norvegicus)
TBA

Curated by ChEMBL
LigandPNGBDBM50028625(CHEMBL3142968 | [5-(6-amino-9H-purin-9-yl)-4-hydro...)
Affinity DataKi:  9.30E+6nMAssay Description:Inhibition of rat muscle pyruvate kinase (PK-M)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM36609(Rapamycin C-7, analog 4 | SIROLIMUS | US11603377, ...)
Affinity DataIC50:  50nMAssay Description:Inhibitory activity against cell free dihydrofolate redutase (DHFR) from Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50033731((R)-5,8-dihydroxy-2-(1-hydroxy-4-methylpent-3-enyl...)
Affinity DataIC50:  500nMAssay Description:Inhibition of recombinant human N-terminal His6/SUMO-tagged PKM2 expressed in Escherichia coli BL21 using PEP as substrate incubated for 30 mins in p...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50597717(CHEMBL3609603)
Affinity DataIC50:  650nMAssay Description:Inhibitory activity against cell free dihydrofolate redutase (DHFR) from Mycobacterium lufuMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50597717(CHEMBL3609603)
Affinity DataIC50:  650nMAssay Description:Inhibition of recombinant PKM2 (unknown origin) Ser205, Asp177, Asp178, Lys207, Hie78, Gly128, Gly52, Ile51, Asn75, Hie84, Ser77, Lys367 residuesMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50033731((R)-5,8-dihydroxy-2-(1-hydroxy-4-methylpent-3-enyl...)
Affinity DataIC50:  800nMAssay Description:Inhibition of PKM2 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50135169((-)-Catechin gallate | (2S,3R)-2-(3,4-dihydroxyphe...)
Affinity DataIC50:  850nMAssay Description:Inhibition of recombinant PKM2 (unknown origin) Ser362, Ser205, Gly128, Lys207, Asp177, Hie84, Arg120, Ile51, Lys367 residuesMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50135164(3,4,5-Trihydroxy-benzoic acid (2S,3S)-2-(3,4-dihyd...)
Affinity DataIC50:  850nMAssay Description:Inhibitory activity against cell free dihydrofolate reductase (DHFR) from Candida albicansMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50597697(ALKANNIN | CHEBI:2578 | E103)
Affinity DataIC50:  900nMAssay Description:Inhibition of PKM2 (unknown origin) Hie78, Lys207, Asn75, Ile51, Ser362, Ser205, Gly128 residuesMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50597697(ALKANNIN | CHEBI:2578 | E103)
Affinity DataIC50:  900nMAssay Description:Inhibition of PKM2 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM7457(2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-4H-chromen-4...)
Affinity DataIC50:  900nMAssay Description:Inhibitory activity against cell free dihydrofolate redutase (DHFR) from Mycobacterium lufuMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM7457(2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-4H-chromen-4...)
Affinity DataIC50:  900nMAssay Description:Inhibition of recombinant PKM2 (unknown origin) Gly128, Asp177, Asp178, Ser362, Hie78, Be51, Asn75 residuesMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50597706(CHEMBL5189727)
Affinity DataIC50:  960nMAssay Description:Inhibition of human N-terminal His tagged PKM2 expressed in Escherichia coli Gly128, Ser205, Lys367, Gly208, Ile335, Gly363, Asn75, Ser362, lle51 res...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM7458(5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one...)
Affinity DataIC50:  990nMAssay Description:Inhibition of recombinant PKM2 (unknown origin) Asp177, Asp178, Asn75, Ile51, Gly128, Hie78, Lys367 residuesMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM7458(5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one...)
Affinity DataIC50:  990nMAssay Description:Inhibitory activity against cell free dihydrofolate redutase (DHFR) from Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM7458(5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one...)
Affinity DataIC50:  990nMAssay Description:Allosteric inhibition of PKM2 (unknown origin) assessed as oxidation of beta-NADH per minuteMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50084980((+)-taxifolin | (-)-Epicatechol | (2R,3R)-(-)-Epic...)
Affinity DataIC50:  1.16E+3nMAssay Description:Inhibition of recombinant PKM2 (unknown origin) Asp178, Asp177, Hie78, Lys367, Asn75, Il61, Ser362, Gly128 residuesMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50084980((+)-taxifolin | (-)-Epicatechol | (2R,3R)-(-)-Epic...)
Affinity DataIC50:  1.16E+3nMAssay Description:Inhibitory activity against cell free dihydrofolate reductase (DHFR) from Candida albicansMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50081950(6-Hydroxy-2-phenyl-chromen-4-one | 6-Hydroxyflavon...)
Affinity DataIC50:  1.24E+3nMAssay Description:Inhibition of recombinant PKM2 (unknown origin) Gly128, Lys207, Hie78, Asn75, Ile51, Lys367, Gly79 residuesMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50260539(CHEMBL80941)
Affinity DataIC50:  1.33E+3nMAssay Description:Inhibitory activity against cell free dihydrofolate reductase (DHFR) from Candida albicansMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM23417(α-CA inhibitor, 4 | (-)-Epicatechin | (2R,3R)...)
Affinity DataIC50:  1.33E+3nMAssay Description:Inhibition of recombinant PKM2 (unknown origin) Asp177, Ser77, Gly52, Gly128 residuesMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50049385(5-Hydroxy-2-phenyl-chromen-4-one | 5-Hydroxyflavon...)
Affinity DataIC50:  1.39E+3nMAssay Description:Inhibition of recombinant PKM2 (unknown origin) Thr129, Ser205, Hie78, Lys367, Ala366, Gly52 residuesMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50384788(LAPACHOL)
Affinity DataIC50:  1.40E+3nMAssay Description:Inhibitory activity against cell free dihydrofolate reductase (DHFR) from Candida albicansMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50271046(CHEMBL4127005)
Affinity DataIC50:  1.40E+3nMAssay Description:Inhibition of recombinant human N-terminal His-tagged PKM2 expressed in Escherichia coli BL21 preincubated for 15 mins followed by PEP/NADH addition ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50009353(1,5,10-triazadecane | 4-azaoctamethylenediamine | ...)
Affinity DataIC50:  1.41E+3nMAssay Description:Inhibition of PKM2 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50033731((R)-5,8-dihydroxy-2-(1-hydroxy-4-methylpent-3-enyl...)
Affinity DataIC50:  1.42E+3nMAssay Description:Inhibitory activity against cell free dihydrofolate reductase (DHFR) from Candida albicansMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50271056(CHEMBL4127111)
Affinity DataIC50:  1.74E+3nMAssay Description:Inhibition of recombinant human N-terminal His-tagged PKM2 expressed in Escherichia coli BL21 preincubated for 15 mins followed by PEP/NADH addition ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50187668(3-Hydroxyflavone | 3-Hydroxyflavone (12) | 3-hydro...)
Affinity DataIC50:  1.75E+3nMAssay Description:Inhibition of PKM2 (unknown origin) Gly128, Hie78, Hie84, Lys207, Asp177, Lys367, Ile51 residuesMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50597715(CHEMBL4877010)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibitory activity against cell free dihydrofolate redutase (DHFR) from Mycobacterium lufuMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50597715(CHEMBL4877010)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibition of PKM2 (unknown origin) Hie78, Gln329, Asp178, Ser362, Asn75, Ile51 residuesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50140257(5,7-Dihydroxy-8-methoxy-2-phenyl-chromen-4-one | 5...)
Affinity DataIC50:  2.01E+3nMAssay Description:Inhibition of PKM2 (unknown origin) Ser205, Lys207, Hie78, Lys367, Asn75, Ile51, Thr129 residuesMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM26664(7-Hydroxy-flavone, 5a | 7-Hydroxyflavone, 11 | 7-h...)
Affinity DataIC50:  2.12E+3nMAssay Description:Inhibition of recombinant PKM2 (unknown origin) Ile335, Lys367, Lys207, Thr129, Lys206, Lys207, Asn75, Hie78 residuesMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50271044(CHEMBL4125726)
Affinity DataIC50:  2.21E+3nMAssay Description:Inhibition of recombinant human N-terminal His-tagged PKM2 expressed in Escherichia coli BL21 preincubated for 15 mins followed by PEP/NADH addition ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPyruvate kinase PKM(Homo sapiens (Human))
Nankai University

Curated by ChEMBL
LigandPNGBDBM50271058(CHEMBL4128346)
Affinity DataIC50:  2.58E+3nMAssay Description:Inhibition of recombinant human N-terminal His-tagged PKM2 expressed in Escherichia coli BL21 preincubated for 15 mins followed by PEP/NADH addition ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
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