Compile Data Set for Download or QSAR
Found 112 with Last Name = 'hoffmann' and Initial = 'k'
TargetIntestinal-type alkaline phosphatase(Bos taurus (Cattle))
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322604(2-mercaptophenylphosphonic acid | CHEMBL1173336)copy SMILEScopy InChI
Affinity DataKi:  210nMAssay Description:Inhibition of bovine intestinal alkaline phosphataseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase type 2(Aeromonas hydrophila)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322609(CHEMBL1170023 | diisopropyl mercapto(phenyl)methyl...)copy SMILEScopy InChI
Affinity DataKi:  250nMAssay Description:Inhibition of Aeromonas hydrophila cphAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322612(CHEMBL1173797 | alpha-Sulfanyl(2,4-dichlorobenzyl)...)copy SMILEScopy InChI
Affinity DataKi:  400nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in absence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322612(CHEMBL1173797 | alpha-Sulfanyl(2,4-dichlorobenzyl)...)copy SMILEScopy InChI
Affinity DataKi:  400nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in presence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase type 2(Aeromonas hydrophila)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322606(2-(Sulfanylmethyl)phenylphosphonic acid | CHEMBL11...)copy SMILEScopy InChI
Affinity DataKi:  500nMAssay Description:Inhibition of Aeromonas hydrophila cphAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322601(CHEMBL1173800 | alpha-Sulfanyl(4-chlorobenzyl)phos...)copy SMILEScopy InChI
Affinity DataKi:  700nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in presence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase type 2(Aeromonas hydrophila)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322602(CHEMBL1172743 | alpha-Sulfanyl(4-fluorobenzyl)phos...)copy SMILEScopy InChI
Affinity DataKi:  1.00E+3nMAssay Description:Inhibition of Aeromonas hydrophila cphAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322600(CHEMBL1173799 | alpha-Sulfanyl(4-bromobenzyl)phosp...)copy SMILEScopy InChI
Affinity DataKi:  1.70E+3nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in presence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetArginase(Schistosoma mansoni (flatworms))
University of Pennsylvania

LigandPNGBDBM130378(2(S)-amino-6-boronohexanoic acid (ABH))copy SMILEScopy InChI
Affinity DataKi:  1.80E+3nMpH: 8.5Assay Description:Briefly, 0.5-50 mM L-arginine (pH 8.5) was added to a solution of 50 mM 4-(2-hydroxyethyl)piperazine-1-propanesulfonic acid (EPPS) (pH 8.5) and 100 &...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR1WZQPubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322606(2-(Sulfanylmethyl)phenylphosphonic acid | CHEMBL11...)copy SMILEScopy InChI
Affinity DataKi:  2.00E+3nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in absence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase type 2(Aeromonas hydrophila)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322605(CHEMBL1173337 | Diisopropyl 2-(sulfanylmethyl)phen...)copy SMILEScopy InChI
Affinity DataKi:  2.00E+3nMAssay Description:Inhibition of Aeromonas hydrophila cphAMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase type 2(Aeromonas hydrophila)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322607(CHEMBL1173339 | diisopropyl 1-mercaptopropylphosph...)copy SMILEScopy InChI
Affinity DataKi:  2.00E+3nMAssay Description:Inhibition of Aeromonas hydrophila cphAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322605(CHEMBL1173337 | Diisopropyl 2-(sulfanylmethyl)phen...)copy SMILEScopy InChI
Affinity DataKi:  3.00E+3nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in absence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetArginase(Schistosoma mansoni (flatworms))
University of Pennsylvania

LigandPNGBDBM130379(N-hydroxy-L-arginine (NOHA))copy SMILEScopy InChI
Affinity DataKi:  3.70E+3nMpH: 8.5Assay Description:Briefly, 0.5-50 mM L-arginine (pH 8.5) was added to a solution of 50 mM 4-(2-hydroxyethyl)piperazine-1-propanesulfonic acid (EPPS) (pH 8.5) and 100 &...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RR1WZQPubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322601(CHEMBL1173800 | alpha-Sulfanyl(4-chlorobenzyl)phos...)copy SMILEScopy InChI
Affinity DataKi:  3.80E+3nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in absence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322611(5-Fluoro-2-sulfanyl-phenylphosphonic acid | CHEMBL...)copy SMILEScopy InChI
Affinity DataKi:  4.00E+3nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in presence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322613(CHEMBL1173798 | alpha-Sulfanyl(2-methoxybenzyl)pho...)copy SMILEScopy InChI
Affinity DataKi:  4.00E+3nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in presence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase type 2(Aeromonas hydrophila)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322612(CHEMBL1173797 | alpha-Sulfanyl(2,4-dichlorobenzyl)...)copy SMILEScopy InChI
Affinity DataKi:  5.00E+3nMAssay Description:Inhibition of Aeromonas hydrophila cphAMore data for this Ligand-Target Pair
TargetMetallo-beta-lactamase type 2(Aeromonas hydrophila)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322604(2-mercaptophenylphosphonic acid | CHEMBL1173336)copy SMILEScopy InChI
Affinity DataKi:  7.00E+3nMAssay Description:Inhibition of Aeromonas hydrophila cphAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322600(CHEMBL1173799 | alpha-Sulfanyl(4-bromobenzyl)phosp...)copy SMILEScopy InChI
Affinity DataKi:  8.40E+3nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in absence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322613(CHEMBL1173798 | alpha-Sulfanyl(2-methoxybenzyl)pho...)copy SMILEScopy InChI
Affinity DataKi:  9.00E+3nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in absence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322604(2-mercaptophenylphosphonic acid | CHEMBL1173336)copy SMILEScopy InChI
Affinity DataKi:  9.00E+3nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in absence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase type 2(Aeromonas hydrophila)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322610(CHEMBL1170424 | alpha-Sulfanylbenzylphosphonic aci...)copy SMILEScopy InChI
Affinity DataKi:  1.10E+4nMAssay Description:Inhibition of Aeromonas hydrophila cphAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322604(2-mercaptophenylphosphonic acid | CHEMBL1173336)copy SMILEScopy InChI
Affinity DataKi:  1.20E+4nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in presence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase type 2(Aeromonas hydrophila)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322600(CHEMBL1173799 | alpha-Sulfanyl(4-bromobenzyl)phosp...)copy SMILEScopy InChI
Affinity DataKi:  1.30E+4nMAssay Description:Inhibition of Aeromonas hydrophila cphAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322605(CHEMBL1173337 | Diisopropyl 2-(sulfanylmethyl)phen...)copy SMILEScopy InChI
Affinity DataKi:  1.40E+4nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in presence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase type 2(Aeromonas hydrophila)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322608(CHEMBL1172388 | alpha-Sulfanylpropylphosphonic aci...)copy SMILEScopy InChI
Affinity DataKi:  1.50E+4nMAssay Description:Inhibition of Aeromonas hydrophila cphAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase type 2(Aeromonas hydrophila)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322613(CHEMBL1173798 | alpha-Sulfanyl(2-methoxybenzyl)pho...)copy SMILEScopy InChI
Affinity DataKi:  1.50E+4nMAssay Description:Inhibition of Aeromonas hydrophila cphAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322609(CHEMBL1170023 | diisopropyl mercapto(phenyl)methyl...)copy SMILEScopy InChI
Affinity DataKi:  1.60E+4nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in presence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322602(CHEMBL1172743 | alpha-Sulfanyl(4-fluorobenzyl)phos...)copy SMILEScopy InChI
Affinity DataKi:  1.80E+4nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in presence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322602(CHEMBL1172743 | alpha-Sulfanyl(4-fluorobenzyl)phos...)copy SMILEScopy InChI
Affinity DataKi: >2.00E+4nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in absence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322609(CHEMBL1170023 | diisopropyl mercapto(phenyl)methyl...)copy SMILEScopy InChI
Affinity DataKi:  2.00E+4nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in absence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase type 2(Aeromonas hydrophila)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322601(CHEMBL1173800 | alpha-Sulfanyl(4-chlorobenzyl)phos...)copy SMILEScopy InChI
Affinity DataKi:  2.40E+4nMAssay Description:Inhibition of Aeromonas hydrophila cphAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322610(CHEMBL1170424 | alpha-Sulfanylbenzylphosphonic aci...)copy SMILEScopy InChI
Affinity DataKi:  3.20E+4nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in presence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322607(CHEMBL1173339 | diisopropyl 1-mercaptopropylphosph...)copy SMILEScopy InChI
Affinity DataKi: >4.00E+4nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in presence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase type 2(Aeromonas hydrophila)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322611(5-Fluoro-2-sulfanyl-phenylphosphonic acid | CHEMBL...)copy SMILEScopy InChI
Affinity DataKi: >4.00E+4nMAssay Description:Inhibition of Aeromonas hydrophila cphAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322611(5-Fluoro-2-sulfanyl-phenylphosphonic acid | CHEMBL...)copy SMILEScopy InChI
Affinity DataKi:  4.00E+4nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in absence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322608(CHEMBL1172388 | alpha-Sulfanylpropylphosphonic aci...)copy SMILEScopy InChI
Affinity DataKi: >4.00E+4nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in presence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322607(CHEMBL1173339 | diisopropyl 1-mercaptopropylphosph...)copy SMILEScopy InChI
Affinity DataKi: >4.00E+4nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in absence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322606(2-(Sulfanylmethyl)phenylphosphonic acid | CHEMBL11...)copy SMILEScopy InChI
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in presence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322608(CHEMBL1172388 | alpha-Sulfanylpropylphosphonic aci...)copy SMILEScopy InChI
Affinity DataKi: >8.00E+4nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in absence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322610(CHEMBL1170424 | alpha-Sulfanylbenzylphosphonic aci...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in absence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase type 2(Aeromonas hydrophila)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322603(CHEMBL1172387 | diisopropyl 2-mercaptophenylphosph...)copy SMILEScopy InChI
Affinity DataKi: >2.50E+5nMAssay Description:Inhibition of Aeromonas hydrophila cphAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322603(CHEMBL1172387 | diisopropyl 2-mercaptophenylphosph...)copy SMILEScopy InChI
Affinity DataKi: >2.50E+5nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in presence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetMetallo-beta-lactamase L1 type 3(Stenotrophomonas maltophilia)
University of Li£ge

Curated by ChEMBL
LigandPNGBDBM50322603(CHEMBL1172387 | diisopropyl 2-mercaptophenylphosph...)copy SMILEScopy InChI
Affinity DataKi: >2.50E+5nMAssay Description:Inhibition of Stenotrophomonas maltophilia beta lactamase L1 in absence of Zn+ chelatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2057G34PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Homo sapiens (Human))
Saarland University

Curated by ChEMBL
LigandPNGBDBM50272209(1-((9H-Fluoren-2-yl)ethyl)-1H-imidazole | CHEMBL50...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Inhibition of CYP17 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2222TK7PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Homo sapiens (Human))
Saarland University

Curated by ChEMBL
LigandPNGBDBM25458((1S,2R,5S,10R,11S,15S)-2,15-dimethyl-14-(pyridin-3...)copy SMILEScopy InChI
Affinity DataIC50: 72nMAssay Description:Inhibition of human CYP17 expressed in Escherichia coli coexpressed with cytochrome P450 reductaseMore data for this Ligand-Target Pair
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Homo sapiens (Human))
Saarland University

Curated by ChEMBL
LigandPNGBDBM25458((1S,2R,5S,10R,11S,15S)-2,15-dimethyl-14-(pyridin-3...)copy SMILEScopy InChI
Affinity DataIC50: 72nMAssay Description:Inhibition of human CYP17 expressed in Escherichia coli co-expressed with NADPH-P450 reductaseMore data for this Ligand-Target Pair
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Homo sapiens (Human))
Saarland University

Curated by ChEMBL
LigandPNGBDBM50272156(7-(1-(1H-imidazol-1-yl)ethyl)-9H-fluoren-2-ol | CH...)copy SMILEScopy InChI
Affinity DataIC50: 99nMAssay Description:Inhibition of human CYP17 expressed in Escherichia coli coexpressed with cytochrome P450 reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2222TK7PubMed
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Homo sapiens (Human))
Saarland University

Curated by ChEMBL
LigandPNGBDBM50272209(1-((9H-Fluoren-2-yl)ethyl)-1H-imidazole | CHEMBL50...)copy SMILEScopy InChI
Affinity DataIC50: 112nMAssay Description:Inhibition of human CYP17 expressed in Escherichia coli coexpressed with cytochrome P450 reductaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2222TK7PubMed
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