Compile Data Set for Download or QSAR
Report error Found 307 of affinity data for UniProtKB/TrEMBL: Q04760
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50402202(CHEMBL2203964)
Affinity DataIC50: 11nMAssay Description:Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50402204(CHEMBL2203978)
Affinity DataIC50: 14nMAssay Description:Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50402206(CHEMBL2203976)
Affinity DataIC50: 40nMAssay Description:Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50402207(CHEMBL2203975)
Affinity DataIC50: 250nMAssay Description:Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50402203(CHEMBL2203963)
Affinity DataIC50: 260nMAssay Description:Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50402208(CHEMBL2203974)
Affinity DataIC50: 280nMAssay Description:Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50402200(CHEMBL2203966)
Affinity DataIC50: 300nMAssay Description:Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50402201(CHEMBL2203965)
Affinity DataIC50: 300nMAssay Description:Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50517468(CHEMBL4559294)
Affinity DataIC50: 370nMAssay Description:Inhibition recombinant human N-terminal 6His-tagged GLO1 (2 to 184 residues) expressed in Escherichia coli using MG as substrate preincubated for 15 ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/22/2021
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50517488(CHEMBL4516514)
Affinity DataIC50: 460nMAssay Description:Inhibition recombinant human N-terminal 6His-tagged GLO1 (2 to 184 residues) expressed in Escherichia coli using MG as substrate preincubated for 15 ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/22/2021
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50402205(CHEMBL2203977)
Affinity DataIC50: 480nMAssay Description:Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50517469(CHEMBL4543065)
Affinity DataIC50: 480nMAssay Description:Inhibition recombinant human N-terminal 6His-tagged GLO1 (2 to 184 residues) expressed in Escherichia coli using MG as substrate preincubated for 15 ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/22/2021
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50517474(CHEMBL4539074)
Affinity DataIC50: 500nMAssay Description:Inhibition recombinant human N-terminal 6His-tagged GLO1 (2 to 184 residues) expressed in Escherichia coli using MG as substrate preincubated for 15 ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/22/2021
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50402199(CHEMBL2203967)
Affinity DataIC50: 510nMAssay Description:Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50517465(CHEMBL4457949)
Affinity DataIC50: 540nMAssay Description:Inhibition recombinant human N-terminal 6His-tagged GLO1 (2 to 184 residues) expressed in Escherichia coli using MG as substrate preincubated for 15 ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/22/2021
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM15236(CHEMBL164 | Cannabiscetin | 3,5,7-trihydroxy-2-(3,...)
Affinity DataIC50: 560nMAssay Description:Inhibition of human recombinant His-tagged Glyoxalase 1 expressed in Sf21-Baculovirus systemMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM15236(CHEMBL164 | Cannabiscetin | 3,5,7-trihydroxy-2-(3,...)
Affinity DataIC50: 560nMAssay Description:Inhibition of recombinant human His-tagged glyoxalase 1 expressed in Escherichia coli BL21 assessed as formation of S-D-lactoylglutathione after 5 mi...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/20/2012
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50517466(CHEMBL4571524)
Affinity DataIC50: 590nMAssay Description:Inhibition recombinant human N-terminal 6His-tagged GLO1 (2 to 184 residues) expressed in Escherichia coli using MG as substrate preincubated for 15 ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/22/2021
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50517473(CHEMBL4573731)
Affinity DataIC50: 640nMAssay Description:Inhibition recombinant human N-terminal 6His-tagged GLO1 (2 to 184 residues) expressed in Escherichia coli using MG as substrate preincubated for 15 ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/22/2021
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50517471(CHEMBL4466017)
Affinity DataIC50: 720nMAssay Description:Inhibition recombinant human N-terminal 6His-tagged GLO1 (2 to 184 residues) expressed in Escherichia coli using MG as substrate preincubated for 15 ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/22/2021
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50045936(CHEMBL69863 | 4-(3,5-dihydroxystyryl)benzene-1,2-d...)
Affinity DataIC50: 760nMAssay Description:Inhibition of human N-terminal His6-tagged GLO1 expressed in baculovirus infected sf21 cells assessed as reduction in S-D-lactoylglutathione formatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/21/2019
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50517437(CHEMBL4514413)
Affinity DataIC50: 790nMAssay Description:Inhibition recombinant human N-terminal 6His-tagged GLO1 (2 to 184 residues) expressed in Escherichia coli using MG as substrate preincubated for 15 ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/22/2021
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50517463(CHEMBL4532036)
Affinity DataIC50: 790nMAssay Description:Inhibition recombinant human N-terminal 6His-tagged GLO1 (2 to 184 residues) expressed in Escherichia coli using MG as substrate preincubated for 15 ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/22/2021
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50517467(CHEMBL4580349)
Affinity DataIC50: 1.04E+3nMAssay Description:Inhibition recombinant human N-terminal 6His-tagged GLO1 (2 to 184 residues) expressed in Escherichia coli using MG as substrate preincubated for 15 ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/22/2021
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50560159(CHEMBL4752509)
Affinity DataIC50: 1.13E+3nMAssay Description:Inhibition of recombinant human N-terminal Met and 6-His-tagged Glyoxalase-1 (Ala2 to Met184 residues) using glutathione and methylglyoxal as substra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/28/2022
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50402215(CHEMBL1624076)
Affinity DataIC50: 1.19E+3nMAssay Description:Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50517461(CHEMBL4575972)
Affinity DataIC50: 1.19E+3nMAssay Description:Inhibition recombinant human N-terminal 6His-tagged GLO1 (2 to 184 residues) expressed in Escherichia coli using MG as substrate preincubated for 15 ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/22/2021
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50241121(S-p-bromobenzyl glutatione | S-p-bromobenzylglutat...)
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50517462(CHEMBL4467660)
Affinity DataIC50: 1.21E+3nMAssay Description:Inhibition recombinant human N-terminal 6His-tagged GLO1 (2 to 184 residues) expressed in Escherichia coli using MG as substrate preincubated for 15 ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/22/2021
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50560166(CHEMBL4799336)
Affinity DataIC50: 1.22E+3nMAssay Description:Inhibition of recombinant human N-terminal Met and 6-His-tagged Glyoxalase-1 (Ala2 to Met184 residues) using glutathione and methylglyoxal as substra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/28/2022
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50560150(CHEMBL4779039)
Affinity DataIC50: 1.28E+3nMAssay Description:Inhibition of recombinant human N-terminal Met and 6-His-tagged Glyoxalase-1 (Ala2 to Met184 residues) using glutathione and methylglyoxal as substra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/28/2022
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50517483(CHEMBL3981698)
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibition recombinant human N-terminal 6His-tagged GLO1 (2 to 184 residues) expressed in Escherichia coli using MG as substrate preincubated for 15 ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/22/2021
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50517489(CHEMBL4454726)
Affinity DataIC50: 1.32E+3nMAssay Description:Inhibition recombinant human N-terminal 6His-tagged GLO1 (2 to 184 residues) expressed in Escherichia coli using MG as substrate preincubated for 15 ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/22/2021
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50560167(CHEMBL4749730)
Affinity DataIC50: 1.36E+3nMAssay Description:Inhibition of recombinant human N-terminal Met and 6-His-tagged Glyoxalase-1 (Ala2 to Met184 residues) using glutathione and methylglyoxal as substra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/28/2022
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50402214(CHEMBL2203968)
Affinity DataIC50: 1.52E+3nMAssay Description:Inhibition of human recombinant GLO1 expressed in Escherichia coli BL21 assessed as decrease in reduced glutathione level after 1 hr by Ellman's meth...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50326997(CHEMBL590878 | Delphinidin)
Affinity DataIC50: 1.90E+3nMAssay Description:Inhibition of human recombinant glyoxalase 1 assessed as S-D-lactoylglutathione after 15 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/12/2011
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50355547(CHEMBL1910548)
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of recombinant human His-tagged glyoxalase 1 expressed in Escherichia coli BL21 assessed as formation of S-D-lactoylglutathione after 5 mi...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/20/2012
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50569120(CHEMBL4861582)
Affinity DataIC50: 2.30E+3nMAssay Description:Inhibition of Glyoxalase-1 (unknown origin) assessed as inhibition of S-D-lactoylglutathione formation using MG and reduced glutathione as substrate ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2022
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50569128(CHEMBL4853249)
Affinity DataIC50: 2.30E+3nMAssay Description:Inhibition of Glyoxalase-1 (unknown origin) assessed as inhibition of S-D-lactoylglutathione formation using MG and reduced glutathione as substrate ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2022
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50569133(CHEMBL4875229)
Affinity DataIC50: 2.80E+3nMAssay Description:Inhibition of Glyoxalase-1 (unknown origin) assessed as inhibition of S-D-lactoylglutathione formation using MG and reduced glutathione as substrate ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2022
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50569134(CHEMBL4863408)
Affinity DataIC50: 2.90E+3nMAssay Description:Inhibition of Glyoxalase-1 (unknown origin) assessed as inhibition of S-D-lactoylglutathione formation using MG and reduced glutathione as substrate ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2022
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50569131(CHEMBL4852940)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of Glyoxalase-1 (unknown origin) assessed as inhibition of S-D-lactoylglutathione formation using MG and reduced glutathione as substrate ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2022
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM7460(2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-chromone;...)
Affinity DataIC50: 3.20E+3nMAssay Description:Inhibition of human recombinant His-tagged Glyoxalase 1 expressed in Sf21-Baculovirus systemMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50569129(CHEMBL4851336)
Affinity DataIC50: 3.20E+3nMAssay Description:Inhibition of Glyoxalase-1 (unknown origin) assessed as inhibition of S-D-lactoylglutathione formation using MG and reduced glutathione as substrate ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2022
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50569125(CHEMBL4871220)
Affinity DataIC50: 3.30E+3nMAssay Description:Inhibition of Glyoxalase-1 (unknown origin) assessed as inhibition of S-D-lactoylglutathione formation using MG and reduced glutathione as substrate ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2022
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM15236(CHEMBL164 | Cannabiscetin | 3,5,7-trihydroxy-2-(3,...)
Affinity DataIC50: 3.38E+3nMAssay Description:Inhibition of recombinant human N-terminal Met and 6-His-tagged Glyoxalase-1 (Ala2 to Met184 residues) using glutathione and methylglyoxal as substra...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/28/2022
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50569130(CHEMBL1303934)
Affinity DataIC50: 3.40E+3nMAssay Description:Inhibition of Glyoxalase-1 (unknown origin) assessed as inhibition of S-D-lactoylglutathione formation using MG and reduced glutathione as substrate ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2022
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50517447(CHEMBL3392484)
Affinity DataIC50: 3.60E+3nMAssay Description:Inhibition recombinant human N-terminal 6His-tagged GLO1 (2 to 184 residues) expressed in Escherichia coli using MG as substrate preincubated for 15 ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/22/2021
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50560173(CHEMBL4747412)
Affinity DataIC50: 3.65E+3nMAssay Description:Inhibition of recombinant human N-terminal Met and 6-His-tagged Glyoxalase-1 (Ala2 to Met184 residues) using methylglyoxal and reduced glutathione as...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/28/2022
Entry Details Article
PubMed
TargetLactoylglutathione lyase(Human)
Chugai Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50069024(2-Amino-4-[1-(carboxymethyl-carbamoyl)-3-(hydroxy-...)
Affinity DataIC50: 3.90E+3nMAssay Description:Compound was evaluated for inhibition of Saccharomyces cerevisiae glyoxalase-I, activity is determined with 0.5 mM substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
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