Compile Data Set for Download or QSAR
Found 35 with Last Name = 'aucagne' and Initial = 'v'
TargetCathepsin K(Homo sapiens (Human))
CNRS UPR 4301

Curated by ChEMBL
LigandPNGBDBM50255753(CHEMBL481611 | MK-0822 | Odanacatib)copy SMILEScopy InChI
Affinity DataKi:  0.180nMAssay Description:Inhibition of human cathepsin KMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP55ZMPubMed
TargetCathepsin K(Homo sapiens (Human))
CNRS UPR 4301

Curated by ChEMBL
LigandPNGBDBM50464766(CHEMBL4292287)copy SMILEScopy InChI
Affinity DataKi:  3nMAssay Description:Reversible competitive inhibition of human cathepsin K using fluorogenic AMC-derived peptide substrate assessed as reduction in residual activity pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP55ZMPubMed
TargetProcathepsin L(Homo sapiens (Human))
CNRS UPR 4301

Curated by ChEMBL
LigandPNGBDBM50464766(CHEMBL4292287)copy SMILEScopy InChI
Affinity DataKi:  5nMAssay Description:Reversible competitive inhibition of human cathepsin L using fluorogenic AMC-derived peptide substrate assessed as reduction in residual activity pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP55ZMPubMed
TargetCathepsin K(Homo sapiens (Human))
CNRS UPR 4301

Curated by ChEMBL
LigandPNGBDBM50464764(CHEMBL4287663)copy SMILEScopy InChI
Affinity DataKi:  9nMAssay Description:Reversible competitive inhibition of human cathepsin K using fluorogenic AMC-derived peptide substrate assessed as reduction in residual activity pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP55ZMPubMed
TargetCathepsin S(Homo sapiens (Human))
CNRS UPR 4301

Curated by ChEMBL
LigandPNGBDBM50464766(CHEMBL4292287)copy SMILEScopy InChI
Affinity DataKi:  17nMAssay Description:Reversible competitive inhibition of human cathepsin S using fluorogenic AMC-derived peptide substrate assessed as reduction in residual activity at ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP55ZMPubMed
TargetCathepsin S(Homo sapiens (Human))
CNRS UPR 4301

Curated by ChEMBL
LigandPNGBDBM50464766(CHEMBL4292287)copy SMILEScopy InChI
Affinity DataKi:  26nMAssay Description:Reversible competitive inhibition of human cathepsin S using fluorogenic AMC-derived peptide substrate assessed as reduction in residual activity at ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP55ZMPubMed
TargetCathepsin K(Homo sapiens (Human))
CNRS UPR 4301

Curated by ChEMBL
LigandPNGBDBM50464765(CHEMBL4279759)copy SMILEScopy InChI
Affinity DataKi:  800nMAssay Description:Reversible competitive inhibition of human cathepsin K using fluorogenic AMC-derived peptide substrate assessed as reduction in residual activity pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP55ZMPubMed
TargetPro-cathepsin H(Homo sapiens (Human))
CNRS UPR 4301

Curated by ChEMBL
LigandPNGBDBM50464764(CHEMBL4287663)copy SMILEScopy InChI
Affinity DataKi:  1.30E+3nMAssay Description:Reversible competitive inhibition of human cathepsin H using fluorogenic AMC-derived peptide substrate assessed as reduction in residual activity pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP55ZMPubMed
TargetProcathepsin L(Homo sapiens (Human))
CNRS UPR 4301

Curated by ChEMBL
LigandPNGBDBM50464764(CHEMBL4287663)copy SMILEScopy InChI
Affinity DataKi:  2.00E+3nMAssay Description:Reversible competitive inhibition of human cathepsin L using fluorogenic AMC-derived peptide substrate assessed as reduction in residual activity pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP55ZMPubMed
TargetPro-cathepsin H(Homo sapiens (Human))
CNRS UPR 4301

Curated by ChEMBL
LigandPNGBDBM50464766(CHEMBL4292287)copy SMILEScopy InChI
Affinity DataKi:  7.00E+3nMAssay Description:Reversible competitive inhibition of human cathepsin H using fluorogenic AMC-derived peptide substrate assessed as reduction in residual activity pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP55ZMPubMed
TargetCathepsin K(Homo sapiens (Human))
CNRS UPR 4301

Curated by ChEMBL
LigandPNGBDBM50464763(CHEMBL4292973)copy SMILEScopy InChI
Affinity DataKi:  1.00E+4nMAssay Description:Reversible competitive inhibition of human cathepsin K using fluorogenic AMC-derived peptide substrate assessed as reduction in residual activity pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP55ZMPubMed
TargetCathepsin S(Homo sapiens (Human))
CNRS UPR 4301

Curated by ChEMBL
LigandPNGBDBM50464763(CHEMBL4292973)copy SMILEScopy InChI
Affinity DataKi:  1.50E+4nMAssay Description:Reversible competitive inhibition of human cathepsin S using fluorogenic AMC-derived peptide substrate assessed as reduction in residual activity at ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP55ZMPubMed
TargetProcathepsin L(Homo sapiens (Human))
CNRS UPR 4301

Curated by ChEMBL
LigandPNGBDBM50464765(CHEMBL4279759)copy SMILEScopy InChI
Affinity DataKi:  2.20E+4nMAssay Description:Reversible competitive inhibition of human cathepsin L using fluorogenic AMC-derived peptide substrate assessed as reduction in residual activity pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP55ZMPubMed
TargetProcathepsin L(Homo sapiens (Human))
CNRS UPR 4301

Curated by ChEMBL
LigandPNGBDBM50464763(CHEMBL4292973)copy SMILEScopy InChI
Affinity DataKi:  3.00E+4nMAssay Description:Reversible competitive inhibition of human cathepsin L using fluorogenic AMC-derived peptide substrate assessed as reduction in residual activity pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP55ZMPubMed
TargetCathepsin S(Homo sapiens (Human))
CNRS UPR 4301

Curated by ChEMBL
LigandPNGBDBM50464763(CHEMBL4292973)copy SMILEScopy InChI
Affinity DataKi:  4.20E+4nMAssay Description:Reversible competitive inhibition of human cathepsin S using fluorogenic AMC-derived peptide substrate assessed as reduction in residual activity at ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP55ZMPubMed
TargetKiSS-1 receptor(Homo sapiens (Human))
UMR7247; Universit£ Fran£ois Rabelais Tours; IFCE)

Curated by ChEMBL
LigandPNGBDBM50082077(CHEMBL3422410)copy SMILES
Affinity DataEC50:  120nMAssay Description:Agonist activity at human wild-type KISS1R expressed in HEK293 cells assessed as induction of intracellular Ca2+ mobilization after 30 mins by Fluo4 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD4ZHJPubMed
TargetKiSS-1 receptor(Homo sapiens (Human))
UMR7247; Universit£ Fran£ois Rabelais Tours; IFCE)

Curated by ChEMBL
LigandPNGBDBM50082078(CHEMBL3422411)copy SMILES
Affinity DataEC50:  0.00600nMAssay Description:Agonist activity at human wild-type KISS1R expressed in HEK293 cells assessed as induction of intracellular Ca2+ mobilization after 30 mins by Fluo4 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD4ZHJPubMed
TargetKiSS-1 receptor(Homo sapiens (Human))
UMR7247; Universit£ Fran£ois Rabelais Tours; IFCE)

Curated by ChEMBL
LigandPNGBDBM50082079(CHEMBL3422412)copy SMILES
Affinity DataEC50:  0.900nMAssay Description:Agonist activity at human wild-type KISS1R expressed in HEK293 cells assessed as induction of intracellular Ca2+ mobilization after 30 mins by Fluo4 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD4ZHJPubMed
TargetKiSS-1 receptor(Homo sapiens (Human))
UMR7247; Universit£ Fran£ois Rabelais Tours; IFCE)

Curated by ChEMBL
LigandPNGBDBM50082073(CHEMBL3422407)copy SMILES
Affinity DataEC50:  0.0700nMAssay Description:Agonist activity at human wild-type KISS1R expressed in HEK293 cells assessed as induction of intracellular Ca2+ mobilization after 30 mins by Fluo4 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD4ZHJPubMed
TargetKiSS-1 receptor(Homo sapiens (Human))
UMR7247; Universit£ Fran£ois Rabelais Tours; IFCE)

Curated by ChEMBL
LigandPNGBDBM50082076(CHEMBL3422409)copy SMILES
Affinity DataEC50:  0.600nMAssay Description:Agonist activity at human wild-type KISS1R expressed in HEK293 cells assessed as induction of intracellular Ca2+ mobilization after 30 mins by Fluo4 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD4ZHJPubMed
TargetKiSS-1 receptor(Homo sapiens (Human))
UMR7247; Universit£ Fran£ois Rabelais Tours; IFCE)

Curated by ChEMBL
LigandPNGBDBM50082074(CHEMBL3422408)copy SMILES
Affinity DataEC50:  0.0700nMAssay Description:Agonist activity at human wild-type KISS1R expressed in HEK293 cells assessed as induction of intracellular Ca2+ mobilization after 30 mins by Fluo4 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD4ZHJPubMed
TargetKiSS-1 receptor(Homo sapiens (Human))
UMR7247; Universit£ Fran£ois Rabelais Tours; IFCE)

Curated by ChEMBL
LigandPNGBDBM50082075(CHEMBL3422406)copy SMILES
Affinity DataEC50:  2.5nMAssay Description:Agonist activity at human wild-type KISS1R expressed in HEK293 cells assessed as induction of intracellular Ca2+ mobilization after 30 mins by Fluo4 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD4ZHJPubMed
TargetNeuropeptide FF receptor 1(Homo sapiens (Human))
UMR7247; Universit£ Fran£ois Rabelais Tours; IFCE)

Curated by ChEMBL
LigandPNGBDBM50082065(CHEMBL3422516)copy SMILES
Affinity DataEC50:  222nMAssay Description:Agonist activity at human NPFF1R expressed in CHO cells assessed as effect on forskolin-induced cAMP accumulation after 15 mins by luminescence based...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD4ZHJPubMed
TargetNeuropeptide FF receptor 1(Homo sapiens (Human))
UMR7247; Universit£ Fran£ois Rabelais Tours; IFCE)

Curated by ChEMBL
LigandPNGBDBM50082074(CHEMBL3422408)copy SMILES
Affinity DataEC50: >5.00E+3nMAssay Description:Agonist activity at human NPFF1R expressed in CHO cells assessed as effect on forskolin-induced cAMP accumulation after 15 mins by luminescence based...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD4ZHJPubMed
TargetNeuropeptide FF receptor 1(Homo sapiens (Human))
UMR7247; Universit£ Fran£ois Rabelais Tours; IFCE)

Curated by ChEMBL
LigandPNGBDBM50082073(CHEMBL3422407)copy SMILES
Affinity DataEC50: >5.00E+3nMAssay Description:Agonist activity at human NPFF1R expressed in CHO cells assessed as effect on forskolin-induced cAMP accumulation after 15 mins by luminescence based...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD4ZHJPubMed
TargetKiSS-1 receptor(Homo sapiens (Human))
UMR7247; Universit£ Fran£ois Rabelais Tours; IFCE)

Curated by ChEMBL
LigandPNGBDBM50082072(CHEMBL3422513)copy SMILEScopy InChI
Affinity DataEC50: >500nMAssay Description:Agonist activity at human wild-type KISS1R expressed in HEK293 cells assessed as induction of intracellular Ca2+ mobilization after 30 mins by Fluo4 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD4ZHJPubMed
TargetKiSS-1 receptor(Homo sapiens (Human))
UMR7247; Universit£ Fran£ois Rabelais Tours; IFCE)

Curated by ChEMBL
LigandPNGBDBM50082071(CHEMBL3422512)copy SMILES
Affinity DataEC50:  182nMAssay Description:Agonist activity at human wild-type KISS1R expressed in HEK293 cells assessed as induction of intracellular Ca2+ mobilization after 30 mins by Fluo4 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD4ZHJPubMed
TargetKiSS-1 receptor(Homo sapiens (Human))
UMR7247; Universit£ Fran£ois Rabelais Tours; IFCE)

Curated by ChEMBL
LigandPNGBDBM50082070(CHEMBL3422511)copy SMILES
Affinity DataEC50:  7.20nMAssay Description:Agonist activity at human wild-type KISS1R expressed in HEK293 cells assessed as induction of intracellular Ca2+ mobilization after 30 mins by Fluo4 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD4ZHJPubMed
TargetKiSS-1 receptor(Homo sapiens (Human))
UMR7247; Universit£ Fran£ois Rabelais Tours; IFCE)

Curated by ChEMBL
LigandPNGBDBM50082069(CHEMBL3422510)copy SMILES
Affinity DataEC50:  14nMAssay Description:Agonist activity at human wild-type KISS1R expressed in HEK293 cells assessed as induction of intracellular Ca2+ mobilization after 30 mins by Fluo4 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD4ZHJPubMed
TargetKiSS-1 receptor(Homo sapiens (Human))
UMR7247; Universit£ Fran£ois Rabelais Tours; IFCE)

Curated by ChEMBL
LigandPNGBDBM50082068(CHEMBL3422414)copy SMILEScopy InChI
Affinity DataEC50:  0.0800nMAssay Description:Agonist activity at human wild-type KISS1R expressed in HEK293 cells assessed as induction of intracellular Ca2+ mobilization after 30 mins by Fluo4 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD4ZHJPubMed
TargetKiSS-1 receptor(Homo sapiens (Human))
UMR7247; Universit£ Fran£ois Rabelais Tours; IFCE)

Curated by ChEMBL
LigandPNGBDBM50082067(CHEMBL3422413)copy SMILES
Affinity DataEC50:  0.100nMAssay Description:Agonist activity at human wild-type KISS1R expressed in HEK293 cells assessed as induction of intracellular Ca2+ mobilization after 30 mins by Fluo4 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD4ZHJPubMed
TargetKiSS-1 receptor(Homo sapiens (Human))
UMR7247; Universit£ Fran£ois Rabelais Tours; IFCE)

Curated by ChEMBL
LigandPNGBDBM50082066(CHEMBL3422517)copy SMILEScopy InChI
Affinity DataEC50:  216nMAssay Description:Agonist activity at human wild-type KISS1R expressed in HEK293 cells assessed as induction of intracellular Ca2+ mobilization after 30 mins by Fluo4 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD4ZHJPubMed
TargetKiSS-1 receptor(Homo sapiens (Human))
UMR7247; Universit£ Fran£ois Rabelais Tours; IFCE)

Curated by ChEMBL
LigandPNGBDBM50082065(CHEMBL3422516)copy SMILES
Affinity DataEC50:  1.60nMAssay Description:Agonist activity at human wild-type KISS1R expressed in HEK293 cells assessed as induction of intracellular Ca2+ mobilization after 30 mins by Fluo4 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD4ZHJPubMed
TargetKiSS-1 receptor(Homo sapiens (Human))
UMR7247; Universit£ Fran£ois Rabelais Tours; IFCE)

Curated by ChEMBL
LigandPNGBDBM50082051(CHEMBL3422514)copy SMILEScopy InChI
Affinity DataEC50:  2.90nMAssay Description:Agonist activity at human wild-type KISS1R expressed in HEK293 cells assessed as induction of intracellular Ca2+ mobilization after 30 mins by Fluo4 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD4ZHJPubMed
TargetKiSS-1 receptor(Homo sapiens (Human))
UMR7247; Universit£ Fran£ois Rabelais Tours; IFCE)

Curated by ChEMBL
LigandPNGBDBM50082064(CHEMBL3422515)copy SMILEScopy InChI
Affinity DataEC50:  24nMAssay Description:Agonist activity at human wild-type KISS1R expressed in HEK293 cells assessed as induction of intracellular Ca2+ mobilization after 30 mins by Fluo4 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JD4ZHJPubMed