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Found 73 with Last Name = 'di bugno' and Initial = 'c'
TargetSubstance-K receptor(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50472916(CHEMBL223221 | MEN-11690)
Affinity DataKi:  0.100nMAssay Description:Binding affinity towards Tachykinin receptor 2More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Menarini Ricerche

Curated by ChEMBL
LigandPNGBDBM50366377(CHEMBL334721 | MEN-10627)
Affinity DataKi:  0.631nMAssay Description:Binding affinity towards Tachykinin receptor 2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Menarini Ricerche

Curated by ChEMBL
LigandPNGBDBM50472917(CHEMBL323884 | MEN-11749)
Affinity DataKi:  1.60nMAssay Description:Binding affinity towards Tachykinin receptor 2More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Menarini Ricerche

Curated by ChEMBL
LigandPNGBDBM50404020(CHEMBL435324 | MEN-11558)
Affinity DataKi:  2nMAssay Description:Binding affinity towards Tachykinin receptor 2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Menarini Ricerche

Curated by ChEMBL
LigandPNGBDBM50472911(CHEMBL407782 | MEN-11420)
Affinity DataKi:  2.5nMAssay Description:Binding affinity towards Tachykinin receptor 2More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Menarini Ricerche

Curated by ChEMBL
LigandPNGBDBM50472912(CHEMBL116564 | MEN-11712)
Affinity DataKi:  7.90nMAssay Description:Binding affinity towards Tachykinin receptor 2More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Menarini Ricerche

Curated by ChEMBL
LigandPNGBDBM50472910(CHEMBL263194)
Affinity DataKi:  10nMAssay Description:Binding affinity towards Tachykinin receptor 2More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Menarini Ricerche

Curated by ChEMBL
LigandPNGBDBM50472908(CHEMBL336053)
Affinity DataKi:  10nMAssay Description:Binding affinity towards Tachykinin receptor 2More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Menarini Ricerche

Curated by ChEMBL
LigandPNGBDBM50472913(CHEMBL2112675)
Affinity DataKi:  20nMAssay Description:Binding affinity towards Tachykinin receptor 2More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Menarini Ricerche

Curated by ChEMBL
LigandPNGBDBM50472914(CHEMBL114442 | MEN-11667)
Affinity DataKi:  316nMAssay Description:Binding affinity towards Tachykinin receptor 2More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Menarini Ricerche

Curated by ChEMBL
LigandPNGBDBM50472919(CHEMBL337628)
Affinity DataKi:  631nMAssay Description:Binding affinity towards Tachykinin receptor 2More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Menarini Ricerche

Curated by ChEMBL
LigandPNGBDBM50472915(CHEMBL114036 | MEN-11540)
Affinity DataKi:  794nMAssay Description:Binding affinity towards Tachykinin receptor 2More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Menarini Ricerche

Curated by ChEMBL
LigandPNGBDBM50472918(CHEMBL324804 | MEN-11970)
Affinity DataKi:  1.26E+3nMAssay Description:Binding affinity towards Tachykinin receptor 2More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Menarini Ricerche

Curated by ChEMBL
LigandPNGBDBM50472906(CHEMBL2111858)
Affinity DataKi:  1.26E+3nMAssay Description:Binding affinity towards Tachykinin receptor 2More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Menarini Ricerche

Curated by ChEMBL
LigandPNGBDBM50472907(CHEMBL131024)
Affinity DataKi:  1.26E+3nMAssay Description:Binding affinity towards Tachykinin receptor 2More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetSubstance-K receptor(Homo sapiens (Human))
Menarini Ricerche

Curated by ChEMBL
LigandPNGBDBM50472909(CHEMBL2112669)
Affinity DataKi:  1.26E+3nMAssay Description:Binding affinity towards Tachykinin receptor 2More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM21642((2S)-1-[(2S)-2-methyl-3-sulfanylpropanoyl]pyrrolid...)
Affinity DataIC50:  3nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046641(1R,2R-trans-2-(Ethyl-hydroxycarbamoylmethyl-carbam...)
Affinity DataIC50:  14nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Menarini Ricerche

Curated by ChEMBL
LigandPNGBDBM50070307((1R,2S)-2-(2-Methylamino-3-naphthalen-2-yl-propion...)
Affinity DataIC50:  22nMAssay Description:Compound was evaluated for the inhibition of thrombin using the synthetic substrate chromozym THMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046633(1R,2R-trans-2-(Hydroxycarbamoylmethyl-methyl-carba...)
Affinity DataIC50:  45nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046633(1R,2R-trans-2-(Hydroxycarbamoylmethyl-methyl-carba...)
Affinity DataIC50:  45nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Menarini Ricerche

Curated by ChEMBL
LigandPNGBDBM50228863((S)-1-((R)-2-Methylamino-3-phenyl-propionyl)-pyrro...)
Affinity DataIC50:  46nMAssay Description:Compound was evaluated for the inhibition of thrombin using the synthetic substrate chromozym THMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046632(CHEMBL159829 | Cis-2-(Hydroxycarbamoylmethyl-propy...)
Affinity DataIC50:  400nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046632(CHEMBL159829 | Cis-2-(Hydroxycarbamoylmethyl-propy...)
Affinity DataIC50:  400nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046621(CHEMBL352453 | Trans-2-(Hydroxycarbamoylmethyl-iso...)
Affinity DataIC50:  500nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046629(1-(3-Hydroxycarbamoyl-2-methyl-propionyl)-pyrrolid...)
Affinity DataIC50:  600nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046628(CHEMBL434293 | Trans-2-(Hydroxycarbamoylmethyl-met...)
Affinity DataIC50:  1.40E+3nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046631(CHEMBL159791 | Cis-2-(3-Mercapto-propionyl)-cycloh...)
Affinity DataIC50:  1.70E+3nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046631(CHEMBL159791 | Cis-2-(3-Mercapto-propionyl)-cycloh...)
Affinity DataIC50:  1.70E+3nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046641(1R,2R-trans-2-(Ethyl-hydroxycarbamoylmethyl-carbam...)
Affinity DataIC50:  2.90E+3nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046634(CHEMBL161968 | Cis-2-(Hydroxycarbamoylmethyl-carba...)
Affinity DataIC50:  3.00E+3nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046634(CHEMBL161968 | Cis-2-(Hydroxycarbamoylmethyl-carba...)
Affinity DataIC50:  3.00E+3nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Menarini Ricerche

Curated by ChEMBL
LigandPNGBDBM50070306((1R,2R)-2-(2-Methylamino-3-phenyl-propionylamino)-...)
Affinity DataIC50:  4.00E+3nMAssay Description:Compound was evaluated for the inhibition of thrombin using the synthetic substrate chromozym THMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046638(CHEMBL163601 | Cis-2-(2-Mercapto-ethylcarbamoyl)-c...)
Affinity DataIC50:  1.10E+4nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Menarini Ricerche

Curated by ChEMBL
LigandPNGBDBM50070305((1R,2S)-Cyclohexane-1,2-dicarboxylic acid 1-[((R)-...)
Affinity DataIC50:  1.20E+4nMAssay Description:Compound was evaluated for the inhibition of thrombin using the synthetic substrate chromozym THMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046630(1-(3-Carboxy-butyryl)-pyrrolidine-2-carboxylic aci...)
Affinity DataIC50:  5.20E+4nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046626(CHEMBL163568 | Cis-2-(Carboxymethyl-ethyl-carbamoy...)
Affinity DataIC50:  7.50E+4nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046626(CHEMBL163568 | Cis-2-(Carboxymethyl-ethyl-carbamoy...)
Affinity DataIC50:  7.50E+4nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Menarini Ricerche

Curated by ChEMBL
LigandPNGBDBM50070304(CHEMBL281784 | Cyclohexane-1,2-dicarboxylic acid 1...)
Affinity DataIC50:  8.40E+4nMAssay Description:Compound was evaluated for the inhibition of thrombin using the synthetic substrate chromozym THMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046636(CHEMBL159996 | Cis-2-[(Benzyloxycarbamoyl-methyl)-...)
Affinity DataIC50: >1.50E+5nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046640(CHEMBL163549 | Cis-2-(2-Mercapto-ethylcarbamoyl)-c...)
Affinity DataIC50: >1.50E+5nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046627(CHEMBL161552 | Cis-2-[(Benzyloxycarbamoyl-methyl)-...)
Affinity DataIC50: >1.50E+5nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046636(CHEMBL159996 | Cis-2-[(Benzyloxycarbamoyl-methyl)-...)
Affinity DataIC50: >1.50E+5nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046640(CHEMBL163549 | Cis-2-(2-Mercapto-ethylcarbamoyl)-c...)
Affinity DataIC50: >1.50E+5nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046627(CHEMBL161552 | Cis-2-[(Benzyloxycarbamoyl-methyl)-...)
Affinity DataIC50: >1.50E+5nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046624(1R,2R-trans-2-[(Benzoyloxycarbamoyl-methyl)-ethyl-...)
Affinity DataIC50: >1.50E+5nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046620(CHEMBL159956 | Cis-2-[(Benzyloxycarbamoyl-methyl)-...)
Affinity DataIC50: >1.50E+5nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046625(1R,2R-trans-2-[(Benzoyloxycarbamoyl-methyl)-carbam...)
Affinity DataIC50: >1.50E+5nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046622(CHEMBL159995 | Trans-2-[(Benzyloxycarbamoyl-methyl...)
Affinity DataIC50: >1.50E+5nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAngiotensin-converting enzyme(Rattus norvegicus)
Laboratori Guidotti

Curated by ChEMBL
LigandPNGBDBM50046635(CHEMBL159973 | Cis-2-(Carboxymethyl-carbamoyl)-cyc...)
Affinity DataIC50: >1.50E+5nMAssay Description:In vitro inhibitory activity against rat serum angiotensin I converting enzyme using hippuryl-glycyl-glycine as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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