Compile Data Set for Download or QSAR
Found 510 of ic50 data for polymerid = 1179,1181,1191,50004780
TargetChitinase B(Serratia marcescens)
Kitasato University

Curated by ChEMBL
LigandPNGBDBM10854(4-[(1S,4R,10S,13S,16S,18R)-10-{3-[(acetamidomethan...)copy SMILEScopy InChI
Affinity DataIC50: 3.40nMAssay Description:Binding affinity to Serratia marcescens chitinase BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NG4QCGPubMed
TargetChitinase B(Serratia marcescens)
Kitasato University

Curated by ChEMBL
LigandPNGBDBM50611491(CHEMBL5290116)copy SMILES
Affinity DataIC50: 4.20nMMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50214361(CHEMBL415389)copy SMILEScopy InChI
Affinity DataIC50: 7.53nMAssay Description:Compound was evaluated for inhibitory activity against Trichoderma ChitinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TM7D9XPubMed
TargetChitinase B(Serratia marcescens)
Kitasato University

Curated by ChEMBL
LigandPNGBDBM50611492(CHEMBL5289869)copy SMILES
Affinity DataIC50: 12nMMore data for this Ligand-Target Pair
Ligand Info
In DepthDetails
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM10854(4-[(1S,4R,10S,13S,16S,18R)-10-{3-[(acetamidomethan...)copy SMILEScopy InChI
Affinity DataIC50: 13nMpH: 5.2 T: 2°CAssay Description:The IC50s of inhibitor against the human chitinase were determined using the fluorogenic substrate 4MU-NAG3. The fluorescence of the liberated 4MU wa...More data for this Ligand-Target Pair
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50554342(CHEMBL4776610)copy SMILES
Affinity DataIC50: 14nMAssay Description:Inhibition of full-length C-terminal his-tagged human recombinant CHIT1 catalytic domain (1 to 386 residues) expressed in HEK293F cells assessed as r...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B85CS7PubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50554344(CHEMBL4756869)copy SMILES
Affinity DataIC50: 16nMAssay Description:Inhibition of full-length C-terminal his-tagged human recombinant CHIT1 catalytic domain (1 to 386 residues) expressed in HEK293F cells assessed as r...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B85CS7PubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50214358(CHEMBL318258)copy SMILEScopy InChI
Affinity DataIC50: 16.1nMAssay Description:Compound was evaluated for inhibitory activity against Trichoderma ChitinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TM7D9XPubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50554343(CHEMBL4794014)copy SMILES
Affinity DataIC50: 18nMAssay Description:Inhibition of full-length C-terminal his-tagged human recombinant CHIT1 catalytic domain (1 to 386 residues) expressed in HEK293F cells assessed as r...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B85CS7PubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50504025(CHEMBL4464754)copy SMILEScopy InChI
Affinity DataIC50: 21nMAssay Description:Inhibition of full-length C-terminal his-tagged human CHIT1 expressed in CHOK1 cells assessed as reduction in chitinolytic activity using 4-methylumb...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27H1NTZPubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50554347(CHEMBL4755139)copy SMILES
Affinity DataIC50: 22nMAssay Description:Inhibition of full-length C-terminal his-tagged human recombinant CHIT1 catalytic domain (1 to 386 residues) expressed in HEK293F cells assessed as r...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B85CS7PubMed
TargetChitinase B(Serratia marcescens)
Kitasato University

Curated by ChEMBL
LigandPNGBDBM50462584(CHEMBL4245260)copy SMILEScopy InChI
Affinity DataIC50: 22nMAssay Description:Inhibition of Serratia marcescens chitinase BMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50554345(CHEMBL4789376)copy SMILES
Affinity DataIC50: 22nMAssay Description:Inhibition of full-length C-terminal his-tagged human recombinant CHIT1 catalytic domain (1 to 386 residues) expressed in HEK293F cells assessed as r...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B85CS7PubMed
TargetChitinase B(Serratia marcescens)
Kitasato University

Curated by ChEMBL
LigandPNGBDBM50462584(CHEMBL4245260)copy SMILEScopy InChI
Affinity DataIC50: 22nMAssay Description:Inhibition of Serratia marcescens 6x-His-tagged ChiB after 20 hrs by LCMS-SIR analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50554340(CHEMBL4788866)copy SMILES
Affinity DataIC50: 23nMAssay Description:Inhibition of full-length C-terminal his-tagged human recombinant CHIT1 catalytic domain (1 to 386 residues) expressed in HEK293F cells assessed as r...More data for this Ligand-Target Pair
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50554346(CHEMBL4764430)copy SMILES
Affinity DataIC50: 23nMAssay Description:Inhibition of full-length C-terminal his-tagged human recombinant CHIT1 catalytic domain (1 to 386 residues) expressed in HEK293F cells assessed as r...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B85CS7PubMed
TargetEndochitinase B1(Aspergillus fumigatus)
University of Dundee

LigandPNGBDBM10853((2R,5S,8S,11S,15S)-8-benzyl-2,7-dimethyl-5-[3-({[(...)copy SMILEScopy InChI
Affinity DataIC50: 27nMpH: 5.5Assay Description:Inhibition of argifin and other peptide derivatives against AfchiB1 and hCHT.More data for this Ligand-Target Pair
TargetEndochitinase B1(Aspergillus fumigatus)
University of Dundee

LigandPNGBDBM50559069(CHEMBL4756641)copy SMILES
Affinity DataIC50: 27nMAssay Description:Inhibition of Aspergillus fumigatus chitinase B1 expressed in Escherichia coli using 4MU-GlcNAc2 as substrate by fluorescence methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348Q30PubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50504017(CHEMBL4541831)copy SMILEScopy InChI
Affinity DataIC50: 27nMAssay Description:Inhibition of full-length C-terminal his-tagged human CHIT1 expressed in CHOK1 cells assessed as reduction in chitinolytic activity using 4-methylumb...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27H1NTZPubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50554348(CHEMBL4749391)copy SMILES
Affinity DataIC50: 32nMAssay Description:Inhibition of full-length C-terminal his-tagged human recombinant CHIT1 catalytic domain (1 to 386 residues) expressed in HEK293F cells assessed as r...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B85CS7PubMed
TargetChitinase B(Serratia marcescens)
Kitasato University

Curated by ChEMBL
LigandPNGBDBM50089857(Argadin)copy SMILES
Affinity DataIC50: 33nMAssay Description:Inhibition of Serratia marcescens chitinase ChiBMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VT1TV5PubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50243685(CHEMBL4084573)copy SMILEScopy InChI
Affinity DataIC50: 36nMAssay Description:Inhibition of human recombinant full length C-terminal His-tagged chitotriosidase expressed in CHO-K1 cells using 4-methylumbelliferyl-beta-D-N,N',N\...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J105J5PubMed
TargetChitinase B(Serratia marcescens)
Kitasato University

Curated by ChEMBL
LigandPNGBDBM50089847(CHEMBL3577620)copy SMILEScopy InChI
Affinity DataIC50: 36nMAssay Description:Inhibition of Serratia marcescens chitinase ChiB assessed as reduction in chitinolytic activity using 4MU-(GlcNAc)2 substrate by fluorescence based a...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VT1TV5PubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50504019(CHEMBL4580568)copy SMILEScopy InChI
Affinity DataIC50: 41nMAssay Description:Inhibition of full-length C-terminal his-tagged human recombinant CHIT1 catalytic domain (1 to 386 residues) expressed in HEK293F cells assessed as r...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B85CS7PubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50504019(CHEMBL4580568)copy SMILEScopy InChI
Affinity DataIC50: 41nMAssay Description:Inhibition of full-length C-terminal his-tagged human CHIT1 expressed in CHOK1 cells assessed as reduction in chitinolytic activity using 4-methylumb...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27H1NTZPubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50214357(CHEMBL319102)copy SMILEScopy InChI
Affinity DataIC50: 41nMAssay Description:Compound was evaluated for inhibitory activity against Trichoderma ChitinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TM7D9XPubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50214360(CHEMBL327266)copy SMILEScopy InChI
Affinity DataIC50: 41.1nMAssay Description:Compound was evaluated for inhibitory activity against Trichoderma ChitinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TM7D9XPubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50504037(CHEMBL4470253)copy SMILEScopy InChI
Affinity DataIC50: 44nMAssay Description:Inhibition of full-length C-terminal his-tagged human CHIT1 expressed in CHOK1 cells assessed as reduction in chitinolytic activity using 4-methylumb...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27H1NTZPubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50504028(CHEMBL4520755)copy SMILEScopy InChI
Affinity DataIC50: 44nMAssay Description:Inhibition of full-length C-terminal his-tagged human CHIT1 expressed in CHOK1 cells assessed as reduction in chitinolytic activity using 4-methylumb...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27H1NTZPubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50504016(CHEMBL4537828)copy SMILEScopy InChI
Affinity DataIC50: 47nMAssay Description:Inhibition of full-length C-terminal his-tagged human CHIT1 expressed in CHOK1 cells assessed as reduction in chitinolytic activity using 4-methylumb...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27H1NTZPubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50504024(CHEMBL4461925)copy SMILEScopy InChI
Affinity DataIC50: 48nMAssay Description:Inhibition of full-length C-terminal his-tagged human recombinant CHIT1 catalytic domain (1 to 386 residues) expressed in HEK293F cells assessed as r...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B85CS7PubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50504024(CHEMBL4461925)copy SMILEScopy InChI
Affinity DataIC50: 48nMAssay Description:Inhibition of full-length C-terminal his-tagged human CHIT1 expressed in CHOK1 cells assessed as reduction in chitinolytic activity using 4-methylumb...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27H1NTZPubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50541930(CHEMBL4637417)copy SMILEScopy InChI
Affinity DataIC50: 49nMAssay Description:Inhibition of full length recombinant C-terminal His-taged human CHIT1 expressed in CHOK1 cells assessed as reduction in chitinolytic activity using ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6PX3PubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50504034(CHEMBL4588384)copy SMILEScopy InChI
Affinity DataIC50: 59nMAssay Description:Inhibition of full-length C-terminal his-tagged human CHIT1 expressed in CHOK1 cells assessed as reduction in chitinolytic activity using 4-methylumb...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27H1NTZPubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50541931(CHEMBL4634943)copy SMILEScopy InChI
Affinity DataIC50: 79nMAssay Description:Inhibition of full length recombinant C-terminal His-taged human CHIT1 expressed in CHOK1 cells assessed as reduction in chitinolytic activity using ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6PX3PubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50214359(CHEMBL103401)copy SMILEScopy InChI
Affinity DataIC50: 80nMAssay Description:Compound was evaluated for inhibitory activity against Trichoderma ChitinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TM7D9XPubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50504039(CHEMBL4442663)copy SMILEScopy InChI
Affinity DataIC50: 82nMAssay Description:Inhibition of full-length C-terminal his-tagged human CHIT1 expressed in CHOK1 cells assessed as reduction in chitinolytic activity using 4-methylumb...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27H1NTZPubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50504031(CHEMBL4521547)copy SMILEScopy InChI
Affinity DataIC50: 84nMAssay Description:Inhibition of full-length C-terminal his-tagged human CHIT1 expressed in CHOK1 cells assessed as reduction in chitinolytic activity using 4-methylumb...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27H1NTZPubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50504014(CHEMBL4547227)copy SMILEScopy InChI
Affinity DataIC50: 87nMAssay Description:Inhibition of full-length C-terminal his-tagged human CHIT1 expressed in CHOK1 cells assessed as reduction in chitinolytic activity using 4-methylumb...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27H1NTZPubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM50541933(CHEMBL4646309)copy SMILEScopy InChI
Affinity DataIC50: 90nMAssay Description:Inhibition of full length recombinant C-terminal His-taged human CHIT1 expressed in CHOK1 cells assessed as reduction in chitinolytic activity using ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6PX3PubMed
TargetChitinase B(Serratia marcescens)
Kitasato University

Curated by ChEMBL
LigandPNGBDBM50331851(Allosamidin | CHEMBL1230997)copy SMILEScopy InChI
Affinity DataIC50: 90nMAssay Description:Inhibition of Serratia marcescens chitinase ChiB assessed as reduction in chitinolytic activity using 4MU-(GlcNAc)2 substrate by fluorescence based a...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VT1TV5PubMedDrugBank
TargetChitinase B(Serratia marcescens)
Kitasato University

Curated by ChEMBL
LigandPNGBDBM50257241(CHEMBL506684 | N-Ac-D-Ala-Arg{N-omega-(N-methylcar...)copy SMILEScopy InChI
Affinity DataIC50: 91nMAssay Description:Displacement of 4-methylumbelliferydiacetyl-chitobiose from Serratia marcescens ChiBMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR7VVMPubMed
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM601600(US11638707, Example 5.)copy SMILES
Affinity DataIC50: 100nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DV1PTC
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM601601(US11638707, Example 6.)copy SMILES
Affinity DataIC50: 100nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DV1PTC
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM601602(US11638707, Example 7.)copy SMILES
Affinity DataIC50: 100nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DV1PTC
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM601603(US11638707, Example 8.)copy SMILES
Affinity DataIC50: 100nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DV1PTC
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM601604(US11638707, Example 9.)copy SMILES
Affinity DataIC50: 100nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DV1PTC
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM601605(US11638707, Example 10.)copy SMILES
Affinity DataIC50: 100nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DV1PTC
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM601606(US11638707, Example 11.)copy SMILES
Affinity DataIC50: 100nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DV1PTC
TargetChitotriosidase-1(Homo sapiens (Human))
University of Tokyo

Curated by ChEMBL
LigandPNGBDBM601607(US11638707, Example 12.)copy SMILES
Affinity DataIC50: 100nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2DV1PTC
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