Found 357 with Last Name = 'haupenthal' and Initial = 'j' Target72 kDa type IV collagenase(Homo sapiens (Human))
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Affinity DataKi: 9nMAssay Description:Inhibition of human MMP-2 assessed as inhibition constant using AcProLeuGly-S-LeuLeuGlyOEt as substrate by spectrophotometer analysisMore data for this Ligand-Target Pair
TargetNeutrophil collagenase(Homo sapiens (Human))
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Affinity DataKi: 13nMAssay Description:Inhibition of human MMP-8 assessed as inhibition constant using AcProLeuGly-S-LeuLeuGlyOEt as substrate by spectrophotometer analysisMore data for this Ligand-Target Pair
TargetElastase(Pseudomonas aeruginosa)
Helmholtz Institute For Pharmaceutical Research Saarland (Hips) - Helmholtz Centre For Infection Research (Hzi
Curated by ChEMBL
Helmholtz Institute For Pharmaceutical Research Saarland (Hips) - Helmholtz Centre For Infection Research (Hzi
Curated by ChEMBL
Affinity DataKi: 41nMAssay Description:Inhibition of Pseudomonas aeruginosa LasB using aminobenzoyl-Ala-Gly-Leu-Ala-p-nitro-benzyl-amide as fluorogenic substrate by fluorimetric assayMore data for this Ligand-Target Pair
TargetCollagenase ColQ1(Bacillus cereus (strain Q1))
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Affinity DataKi: 100nMAssay Description:Inhibition of Bacillus cereus ATCC 14579 collagenase unit of ColQ1 assessed as inhibition constant incubated for 144 seconds by FRET based assayMore data for this Ligand-Target Pair
TargetNeutrophil collagenase(Homo sapiens (Human))
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Affinity DataKi: 100nMAssay Description:Inhibition of human MMP-8 assessed as inhibition constant using AcProLeuGly-S-LeuLeuGlyOEt as substrate by spectrophotometer analysisMore data for this Ligand-Target Pair
TargetCollagenase ColH(Hathewaya histolytica)
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Affinity DataKi: 200nMAssay Description:Inhibition of Clostridium histolyticum CoLH assessed as inhibition constant using M MOCAcPro-Leu-Gly-Leu-A2pr-(DNP)Ala-Arg-NH2 as substrate incubated...More data for this Ligand-Target Pair
TargetCollagenase ColQ1(Bacillus cereus (strain Q1))
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Affinity DataKi: 820nMAssay Description:Inhibition of Bacillus cereus ATCC 14579 collagenase unit of ColQ1 assessed as inhibition constant incubated for 144 seconds by FRET based assayMore data for this Ligand-Target Pair
TargetCollagenase ColH(Hathewaya histolytica)
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Affinity DataKi: 1.70E+3nMAssay Description:Inhibition of Clostridium histolyticum peptidase unit of ColH assessed as inhibition constant incubated for 144 seconds by FRET based assayMore data for this Ligand-Target Pair
Target72 kDa type IV collagenase(Homo sapiens (Human))
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Affinity DataKi: 2.00E+3nMAssay Description:Inhibition of human MMP-2 assessed as inhibition constant using AcProLeuGly-S-LeuLeuGlyOEt as substrate by spectrophotometer analysisMore data for this Ligand-Target Pair
TargetCollagenase ColA(Bacillus cereus (strain ATCC 14579 / DSM 31 / CCUG...)
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Affinity DataKi: 3.40E+3nMAssay Description:Inhibition of Bacillus cereus ATCC 14579 collagenase unit of ColA assessed as inhibition constant incubated for 144 seconds by FRET based assayMore data for this Ligand-Target Pair
TargetCollagenase ColA(Bacillus cereus (strain ATCC 14579 / DSM 31 / CCUG...)
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Affinity DataKi: 4.70E+3nMAssay Description:Inhibition of Bacillus cereus ATCC 14579 collagenase unit of ColA assessed as inhibition constant incubated for 144 seconds by FRET based assayMore data for this Ligand-Target Pair
TargetCollagenase ColH(Hathewaya histolytica)
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Affinity DataKi: 1.16E+4nMAssay Description:Inhibition of Clostridium histolyticum peptidase unit of ColH assessed as inhibition constant incubated for 144 seconds by FRET based assayMore data for this Ligand-Target Pair
TargetCollagenase ColG(Clostridium histolyticum)
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Affinity DataKi: 1.84E+4nMAssay Description:Inhibition of Clostridium histolyticum collagenase unit of ColG assessed as inhibition constant incubated for 144 seconds by FRET based assayMore data for this Ligand-Target Pair
TargetCollagenase ColG(Clostridium histolyticum)
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Affinity DataKi: 3.10E+4nMAssay Description:Inhibition of Clostridium histolyticum collagenase unit of ColG assessed as inhibition constant incubated for 144 seconds by FRET based assayMore data for this Ligand-Target Pair
3D Structure (crystal)
Affinity DataIC50: 0.100nMAssay Description:Inhibition of human CYP11B2 expressed in hamster V79 MZ cells using [3H] 11 deoxycorticosterone as substrate by HPLC radioflow detectorMore data for this Ligand-Target Pair
Affinity DataIC50: 0.5nMAssay Description:Inhibition of human CYP11B1 expressed in hamster V79 MZ cells using [3H] 11 deoxycorticosterone as substrate by HPLC radioflow detectorMore data for this Ligand-Target Pair
TargetCollagenase ColH(Hathewaya histolytica)
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Affinity DataIC50: 10nMAssay Description:Inhibition of Clostridium histolyticum CoLHMore data for this Ligand-Target Pair
Affinity DataIC50: 15nMAssay Description:Inhibition of human CYP11B1 expressed in hamster V79 MZ cells using [3H] 11 deoxycorticosterone as substrate by HPLC radioflow detectorMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
University Institute Of Pharmaceutical Sciences
Curated by ChEMBL
University Institute Of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataIC50: 16nMAssay Description:Inhibition of human 5alpha-2 reductase expressed in HEK293 cells assessed as suppression of conversion of [3]androstenedione incubated for 30 mins by...More data for this Ligand-Target Pair
Affinity DataIC50: 16nMAssay Description:Inhibition of human CYP11B1 expressed in hamster V79 MZ cells using [3H] 11 deoxycorticosterone as substrate by HPLC radioflow detectorMore data for this Ligand-Target Pair
TargetCollagenase ColH(Hathewaya histolytica)
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Affinity DataIC50: 17nMAssay Description:Inhibition of Clostridium histolyticum CoLHMore data for this Ligand-Target Pair
TargetCollagenase ColH(Hathewaya histolytica)
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Affinity DataIC50: 17nMAssay Description:Inhibition of Clostridium histolyticum ColH peptidase domain expressed in Escherichia coli BL21(DE3) cells using Mca-Ala-Gly-Pro-Pro-Gly-Pro-Dpa-Gly-...More data for this Ligand-Target Pair
Affinity DataIC50: 17nMAssay Description:Inhibition of human CYP11B1 expressed in hamster V79 MZ cells using [3H] 11 deoxycorticosterone as substrate by HPLC radioflow detectorMore data for this Ligand-Target Pair
TargetCollagenase ColH(Hathewaya histolytica)
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Affinity DataIC50: 21nMAssay Description:Inhibition of Clostridium histolyticum CoLH using M MOCAcPro-Leu-Gly-Leu-A2pr-(DNP)Ala-Arg-NH2 as substrate incubated for 10 mins by fluorescence spe...More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
University Institute Of Pharmaceutical Sciences
Curated by ChEMBL
University Institute Of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataIC50: 22.1nMAssay Description:Inhibition of human type-2 5-alpha reductase expressed in HEK293 cells using [3H]-androstenedione as substrate after 30 mins by HPLC analysisMore data for this Ligand-Target Pair
TargetCollagenase ColH(Hathewaya histolytica)
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Affinity DataIC50: 24nMAssay Description:Inhibition of Clostridium histolyticum CoLH using M MOCAcPro-Leu-Gly-Leu-A2pr-(DNP)Ala-Arg-NH2 as substrate incubated for 10 mins by fluorescence spe...More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
University Institute Of Pharmaceutical Sciences
Curated by ChEMBL
University Institute Of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataIC50: 26.5nMAssay Description:Inhibition of human type-2 5-alpha reductase expressed in HEK293 cells using [3H]-androstenedione as substrate after 30 mins by HPLC analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 29nMAssay Description:Inhibition of human CYP11B1 expressed in hamster V79 MZ cells using [3H] 11 deoxycorticosterone as substrate by HPLC radioflow detectorMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
University Institute Of Pharmaceutical Sciences
Curated by ChEMBL
University Institute Of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataIC50: 30.3nMAssay Description:Inhibition of human type-2 5-alpha reductase expressed in HEK293 cells using [3H]-androstenedione as substrate after 30 mins by HPLC analysisMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
University Institute Of Pharmaceutical Sciences
Curated by ChEMBL
University Institute Of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataIC50: 40nMAssay Description:Inhibition of human 5alpha-2 reductase expressed in HEK293 cells assessed as suppression of conversion of [3]androstenedione incubated for 30 mins by...More data for this Ligand-Target Pair
Affinity DataIC50: 40nMAssay Description:Inhibition of human CYP11B1 expressed in hamster V79 MZ cells using [3H] 11 deoxycorticosterone as substrate by HPLC radioflow detectorMore data for this Ligand-Target Pair
Affinity DataIC50: 42nMAssay Description:Inhibition of human CYP11B1 expressed in hamster V79 MZ cells using [3H] 11 deoxycorticosterone as substrate by HPLC radioflow detectorMore data for this Ligand-Target Pair
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Homo sapiens (Human))
Saarland University
Curated by ChEMBL
Saarland University
Curated by ChEMBL
Affinity DataIC50: 52nMAssay Description:Inhibition of human CYP17 expressed in Escherichia coliMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
University Institute Of Pharmaceutical Sciences
Curated by ChEMBL
University Institute Of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataIC50: 54.1nMAssay Description:Inhibition of human type-2 5-alpha reductase expressed in HEK293 cells using [3H]-androstenedione as substrate after 30 mins by HPLC analysisMore data for this Ligand-Target Pair
TargetCollagenase ColH(Hathewaya histolytica)
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Helmholtz Center For Infection Research (Hzi)
Curated by ChEMBL
Affinity DataIC50: 60nMAssay Description:Inhibition of Clostridium histolyticum ColH peptidase domain expressed in Escherichia coli BL21(DE3) cells using Mca-Ala-Gly-Pro-Pro-Gly-Pro-Dpa-Gly-...More data for this Ligand-Target Pair
Affinity DataIC50: 61nMAssay Description:Inhibition of human CYP11B1 expressed in hamster V79 MZ cells using [3H] 11 deoxycorticosterone as substrate by HPLC radioflow detectorMore data for this Ligand-Target Pair
Affinity DataIC50: 62nMAssay Description:Inhibition of human CYP11B1 expressed in hamster V79 MZ cells using [3H] 11 deoxycorticosterone as substrate by HPLC radioflow detectorMore data for this Ligand-Target Pair
Affinity DataIC50: 67nMAssay Description:Inhibition of human CYP11B2 expressed in hamster V79 MZ cells using [3H] 11 deoxycorticosterone as substrate by HPLC radioflow detectorMore data for this Ligand-Target Pair
Affinity DataIC50: 72nMAssay Description:Inhibition of human CYP11B2 expressed in hamster V79 MZ cells using [3H] 11 deoxycorticosterone as substrate by HPLC radioflow detectorMore data for this Ligand-Target Pair
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Homo sapiens (Human))
Saarland University
Curated by ChEMBL
Saarland University
Curated by ChEMBL
Affinity DataIC50: 72nMAssay Description:Inhibition of human CYP17 expressed in Escherichia coliMore data for this Ligand-Target Pair
Affinity DataIC50: 72nMAssay Description:Inhibition of human CYP11B1 expressed in hamster V79 MZ cells using [3H] 11 deoxycorticosterone as substrate by HPLC radioflow detectorMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
University Institute Of Pharmaceutical Sciences
Curated by ChEMBL
University Institute Of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataIC50: 72.8nMAssay Description:Inhibition of human type-2 5-alpha reductase expressed in HEK293 cells using [3H]-androstenedione as substrate after 30 mins by HPLC analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 73nMAssay Description:Inhibition of human CYP11B1 expressed in hamster V79 MZ cells using [3H] 11 deoxycorticosterone as substrate by HPLC radioflow detectorMore data for this Ligand-Target Pair
Affinity DataIC50: 75nMAssay Description:Inhibition of human CYP11B1 expressed in hamster V79 MZ cells using [3H] 11 deoxycorticosterone as substrate by HPLC radioflow detectorMore data for this Ligand-Target Pair
Affinity DataIC50: 76nMAssay Description:Inhibition of human CYP11B1 expressed in hamster V79 MZ cells using [3H] 11 deoxycorticosterone as substrate by HPLC radioflow detectorMore data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
University Institute Of Pharmaceutical Sciences
Curated by ChEMBL
University Institute Of Pharmaceutical Sciences
Curated by ChEMBL
Affinity DataIC50: 84nMAssay Description:Inhibition of human 5alpha-2 reductase expressed in HEK293 cells assessed as suppression of conversion of [3]androstenedione incubated for 30 mins by...More data for this Ligand-Target Pair
Affinity DataIC50: 95nMAssay Description:Inhibition of human CYP11B1 expressed in hamster V79 MZ cells using [3H] 11 deoxycorticosterone as substrate by HPLC radioflow detectorMore data for this Ligand-Target Pair
TargetSteroid 17-alpha-hydroxylase/17,20 lyase(Homo sapiens (Human))
Saarland University
Curated by ChEMBL
Saarland University
Curated by ChEMBL
Affinity DataIC50: 97nMAssay Description:Inhibition of human CYP17 expressed in Escherichia coliMore data for this Ligand-Target Pair
TargetVIM-1 metallo-beta-lactamase(Klebsiella pneumoniae)
Helmholtz Institute For Pharmaceutical Research Saarland
Curated by ChEMBL
Helmholtz Institute For Pharmaceutical Research Saarland
Curated by ChEMBL
Affinity DataIC50: 100nMAssay Description:Inhibition of Escherichia coli VIM-1 using fluorocillin as substrate incubated for 30 mins by fluorescence based assayMore data for this Ligand-Target Pair
TargetVIM-1 metallo-beta-lactamase(Klebsiella pneumoniae)
Helmholtz Institute For Pharmaceutical Research Saarland
Curated by ChEMBL
Helmholtz Institute For Pharmaceutical Research Saarland
Curated by ChEMBL
Affinity DataIC50: 100nMAssay Description:Inhibition of Escherichia coli VIM-1 using fluorocillin as substrate incubated for 30 mins by fluorescence based assayMore data for this Ligand-Target Pair
