Compile Data Set for Download or QSAR
Found 703 with Last Name = 'inaba' and Initial = 't'
TargetCannabinoid receptor 2(MOUSE)
Japan Tobacco Inc.

Curated by PDSP Ki Database
LigandPNGBDBM21280(5-(4-chloro-3-methylphenyl)-1-[(4-methylphenyl)met...)copy SMILEScopy InChI
Affinity DataKi:  0.0400nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VH5MCTPubMed
TargetCannabinoid receptor 1(Rattus norvegicus (rat))
Japan Tobacco Inc.

Curated by PDSP Ki Database
LigandPNGBDBM21281((11R)-2-methyl-11-(morpholin-4-ylmethyl)-3-(naphth...)copy SMILEScopy InChI
Affinity DataKi:  0.140nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VH5MCTPubMed
TargetCannabinoid receptor 2(Rattus norvegicus (Rat))
Japan Tobacco Inc.

Curated by PDSP Ki Database
LigandPNGBDBM21280(5-(4-chloro-3-methylphenyl)-1-[(4-methylphenyl)met...)copy SMILEScopy InChI
Affinity DataKi:  0.240nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VH5MCTPubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Japan Tobacco Inc.

Curated by PDSP Ki Database
LigandPNGBDBM21281((11R)-2-methyl-11-(morpholin-4-ylmethyl)-3-(naphth...)copy SMILEScopy InChI
Affinity DataKi:  0.290nMMore data for this Ligand-Target Pair
TargetCannabinoid receptor 2(Rattus norvegicus (Rat))
Japan Tobacco Inc.

Curated by PDSP Ki Database
LigandPNGBDBM85739(CHEMBL178372 | JTE-907 | N-(1,3-Benzodioxole-5-ylm...)copy SMILEScopy InChI
Affinity DataKi:  0.380nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VH5MCTPubMed
TargetCannabinoid receptor 1(Mus musculus (Mouse))
Japan Tobacco Inc.

Curated by PDSP Ki Database
LigandPNGBDBM21281((11R)-2-methyl-11-(morpholin-4-ylmethyl)-3-(naphth...)copy SMILEScopy InChI
Affinity DataKi:  0.410nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VH5MCTPubMed
TargetCannabinoid receptor 2(MOUSE)
Japan Tobacco Inc.

Curated by PDSP Ki Database
LigandPNGBDBM21281((11R)-2-methyl-11-(morpholin-4-ylmethyl)-3-(naphth...)copy SMILEScopy InChI
Affinity DataKi:  0.560nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VH5MCTPubMed
TargetCannabinoid receptor 2(Rattus norvegicus (Rat))
Japan Tobacco Inc.

Curated by PDSP Ki Database
LigandPNGBDBM21281((11R)-2-methyl-11-(morpholin-4-ylmethyl)-3-(naphth...)copy SMILEScopy InChI
Affinity DataKi:  1.30nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VH5MCTPubMed
TargetCannabinoid receptor 2(MOUSE)
Japan Tobacco Inc.

Curated by PDSP Ki Database
LigandPNGBDBM85739(CHEMBL178372 | JTE-907 | N-(1,3-Benzodioxole-5-ylm...)copy SMILEScopy InChI
Affinity DataKi:  1.55nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VH5MCTPubMed
TargetCannabinoid receptor 2(MOUSE)
Japan Tobacco Inc.

Curated by PDSP Ki Database
LigandPNGBDBM50000729((+)-6,6,9-Trimethyl-3-pentyl-6a,7,8,10a-tetrahydro...)copy SMILEScopy InChI
Affinity DataKi:  1.73nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VH5MCTPubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Japan Tobacco Inc.

Curated by PDSP Ki Database
LigandPNGBDBM21280(5-(4-chloro-3-methylphenyl)-1-[(4-methylphenyl)met...)copy SMILEScopy InChI
Affinity DataKi:  1.99nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VH5MCTPubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Japan Tobacco Inc.

Curated by PDSP Ki Database
LigandPNGBDBM50000729((+)-6,6,9-Trimethyl-3-pentyl-6a,7,8,10a-tetrahydro...)copy SMILEScopy InChI
Affinity DataKi:  3.13nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VH5MCTPubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
Japan Tobacco Inc.

Curated by PDSP Ki Database
LigandPNGBDBM50000729((+)-6,6,9-Trimethyl-3-pentyl-6a,7,8,10a-tetrahydro...)copy SMILEScopy InChI
Affinity DataKi:  5.05nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VH5MCTPubMed
TargetCannabinoid receptor 2(Rattus norvegicus (Rat))
Japan Tobacco Inc.

Curated by PDSP Ki Database
LigandPNGBDBM50000729((+)-6,6,9-Trimethyl-3-pentyl-6a,7,8,10a-tetrahydro...)copy SMILEScopy InChI
Affinity DataKi:  6.80nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VH5MCTPubMed
TargetCannabinoid receptor 1(Mus musculus (Mouse))
Japan Tobacco Inc.

Curated by PDSP Ki Database
LigandPNGBDBM50000729((+)-6,6,9-Trimethyl-3-pentyl-6a,7,8,10a-tetrahydro...)copy SMILEScopy InChI
Affinity DataKi:  8.33nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VH5MCTPubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
Japan Tobacco Inc.

Curated by PDSP Ki Database
LigandPNGBDBM21281((11R)-2-methyl-11-(morpholin-4-ylmethyl)-3-(naphth...)copy SMILEScopy InChI
Affinity DataKi:  9.87nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VH5MCTPubMed
TargetCannabinoid receptor 1(Rattus norvegicus (rat))
Japan Tobacco Inc.

Curated by PDSP Ki Database
LigandPNGBDBM50000729((+)-6,6,9-Trimethyl-3-pentyl-6a,7,8,10a-tetrahydro...)copy SMILEScopy InChI
Affinity DataKi:  13.5nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VH5MCTPubMed
TargetCannabinoid receptor 1(Mus musculus (Mouse))
Japan Tobacco Inc.

Curated by PDSP Ki Database
LigandPNGBDBM21280(5-(4-chloro-3-methylphenyl)-1-[(4-methylphenyl)met...)copy SMILEScopy InChI
Affinity DataKi:  20.1nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VH5MCTPubMed
TargetCannabinoid receptor 1(Rattus norvegicus (rat))
Japan Tobacco Inc.

Curated by PDSP Ki Database
LigandPNGBDBM21280(5-(4-chloro-3-methylphenyl)-1-[(4-methylphenyl)met...)copy SMILEScopy InChI
Affinity DataKi:  27.6nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VH5MCTPubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Japan Tobacco Inc.

Curated by PDSP Ki Database
LigandPNGBDBM85739(CHEMBL178372 | JTE-907 | N-(1,3-Benzodioxole-5-ylm...)copy SMILEScopy InChI
Affinity DataKi:  35.9nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VH5MCTPubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
Japan Tobacco Inc.

Curated by PDSP Ki Database
LigandPNGBDBM21280(5-(4-chloro-3-methylphenyl)-1-[(4-methylphenyl)met...)copy SMILEScopy InChI
Affinity DataKi:  50.3nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VH5MCTPubMed
TargetCannabinoid receptor 1(Rattus norvegicus (rat))
Japan Tobacco Inc.

Curated by PDSP Ki Database
LigandPNGBDBM85739(CHEMBL178372 | JTE-907 | N-(1,3-Benzodioxole-5-ylm...)copy SMILEScopy InChI
Affinity DataKi:  1.05E+3nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VH5MCTPubMed
TargetCannabinoid receptor 1(Mus musculus (Mouse))
Japan Tobacco Inc.

Curated by PDSP Ki Database
LigandPNGBDBM85739(CHEMBL178372 | JTE-907 | N-(1,3-Benzodioxole-5-ylm...)copy SMILEScopy InChI
Affinity DataKi:  1.06E+3nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2VH5MCTPubMed
TargetA disintegrin and metalloproteinase with thrombospondin motifs 4(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50167609((2R,5R)-1-[4-(2,4-Dichloro-benzyloxy)-benzenesulfo...)copy SMILEScopy InChI
Affinity DataIC50: 1.10nMAssay Description:Inhibition of human recombinant aggrecanase 1 after 150 mins by fluorescence plate readerMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87B3DPubMed
TargetMatrix metalloproteinase-14(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50341824((1S,2R,3R)-2-Methyl-1-[5-(4-methylpyrazol-1-yl)thi...)copy SMILEScopy InChI
Affinity DataIC50: 1.20nMAssay Description:Inhibition of human recombinant MMP14 after 60 mins by fluorescence plate readerMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87B3DPubMed
TargetMatrix metalloproteinase-14(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50341816((1S,2R,3R)-1-[5-(4-Methoxypyrazol-1-yl)thiophene-2...)copy SMILEScopy InChI
Affinity DataIC50: 1.30nMAssay Description:Inhibition of human recombinant MMP14 after 60 mins by fluorescence plate readerMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87B3DPubMed
TargetA disintegrin and metalloproteinase with thrombospondin motifs 5(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50167609((2R,5R)-1-[4-(2,4-Dichloro-benzyloxy)-benzenesulfo...)copy SMILEScopy InChI
Affinity DataIC50: 1.40nMAssay Description:Inhibition of human recombinant aggrecanase 2 after 150 mins by fluorescence plate readerMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87B3DPubMed
TargetProtein kinase C beta type(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50153465(2-{3-[3-(2,5-Dioxo-4-phenylamino-2,5-dihydro-1H-py...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C beta 2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VDJPubMed
TargetStearoyl-CoA desaturase(Homo sapiens (Human))
Japan Tobacco Inc.

Curated by ChEMBL
LigandPNGBDBM50467599(CHEMBL4282070)copy SMILEScopy InChI
Affinity DataIC50: 2.80nMAssay Description:Inhibition of recombinant human SCD1 expressed in baculovirus expression system assessed as reduction in [3H]H2O production using stearoyl [9,10-3H]C...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5HN5PubMed
TargetA disintegrin and metalloproteinase with thrombospondin motifs 5(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50341819((1S,2R,3R)-1-(6-Chloro-4H-thieno[3,2-b]indole-2-su...)copy SMILEScopy InChI
Affinity DataIC50: 2.90nMAssay Description:Inhibition of human recombinant aggrecanase 2 after 150 mins by fluorescence plate readerMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87B3DPubMed
TargetStearoyl-CoA desaturase(Homo sapiens (Human))
Japan Tobacco Inc.

Curated by ChEMBL
LigandPNGBDBM50467583(CHEMBL4295170)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of recombinant human SCD1 expressed in baculovirus expression system assessed as reduction in [3H]H2O production using stearoyl [9,10-3H]C...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5HN5PubMed
TargetStearoyl-CoA desaturase(Homo sapiens (Human))
Japan Tobacco Inc.

Curated by ChEMBL
LigandPNGBDBM50467595(CHEMBL4277121)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of recombinant human SCD1 expressed in baculovirus expression system assessed as reduction in [3H]H2O production using stearoyl [9,10-3H]C...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5HN5PubMed
TargetDiacylglycerol O-acyltransferase 1(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50003815(CHEMBL3235321)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of DGAT1 (unknown origin) by cell-based assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23X886WPubMed
TargetA disintegrin and metalloproteinase with thrombospondin motifs 4(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50104963((2S,3R)-2-(cyclopropylmethylamino)-N1-hydroxy-N4-(...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of human recombinant aggrecanase 1 after 150 mins by fluorescence plate readerMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87B3DPubMed
TargetStearoyl-CoA desaturase(Homo sapiens (Human))
Japan Tobacco Inc.

Curated by ChEMBL
LigandPNGBDBM50467619(CHEMBL4278602)copy SMILEScopy InChI
Affinity DataIC50: 3.20nMAssay Description:Inhibition of recombinant human SCD1 expressed in baculovirus expression system assessed as reduction in [3H]H2O production using stearoyl [9,10-3H]C...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5HN5PubMed
TargetCollagenase 3(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50311088(CHEMBL1078281 | cis-rac-1-(5-(4-chloro-1H-pyrazol-...)copy SMILEScopy InChI
Affinity DataIC50: 3.40nMAssay Description:Inhibition of human recombinant MMP13 after 60 mins by fluorescence plate readerMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87B3DPubMed
TargetMatrix metalloproteinase-14(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50311088(CHEMBL1078281 | cis-rac-1-(5-(4-chloro-1H-pyrazol-...)copy SMILEScopy InChI
Affinity DataIC50: 3.40nMAssay Description:Inhibition of human recombinant MMP14 after 60 mins by fluorescence plate readerMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87B3DPubMed
TargetAcyl-CoA desaturase 1(Mus musculus)
Japan Tobacco Inc.

Curated by ChEMBL
LigandPNGBDBM50467593(CHEMBL4284259)copy SMILEScopy InChI
Affinity DataIC50: 3.80nMAssay Description:Inhibition of mouse liver microsome SCD assessed as reduction in [3H]H2O production using stearoyl [9,10-3H]CoA as substrate in presence of NADH incu...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5HN5PubMed
TargetStearoyl-CoA desaturase(Homo sapiens (Human))
Japan Tobacco Inc.

Curated by ChEMBL
LigandPNGBDBM50467579(CHEMBL4289946)copy SMILEScopy InChI
Affinity DataIC50: 3.80nMAssay Description:Inhibition of recombinant human SCD1 expressed in baculovirus expression system assessed as reduction in [3H]H2O production using stearoyl [9,10-3H]C...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5HN5PubMed
TargetStearoyl-CoA desaturase(Homo sapiens (Human))
Japan Tobacco Inc.

Curated by ChEMBL
LigandPNGBDBM50467602(CHEMBL4277371)copy SMILEScopy InChI
Affinity DataIC50: 3.80nMAssay Description:Inhibition of recombinant human SCD1 expressed in baculovirus expression system assessed as reduction in [3H]H2O production using stearoyl [9,10-3H]C...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5HN5PubMed
TargetStearoyl-CoA desaturase(Homo sapiens (Human))
Japan Tobacco Inc.

Curated by ChEMBL
LigandPNGBDBM50467578(CHEMBL4293631)copy SMILEScopy InChI
Affinity DataIC50: 3.90nMAssay Description:Inhibition of recombinant human SCD1 expressed in baculovirus expression system assessed as reduction in [3H]H2O production using stearoyl [9,10-3H]C...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5HN5PubMed
TargetA disintegrin and metalloproteinase with thrombospondin motifs 4(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50311088(CHEMBL1078281 | cis-rac-1-(5-(4-chloro-1H-pyrazol-...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Inhibition of human recombinant aggrecanase 1 after 150 mins by fluorescence plate readerMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N87B3DPubMed
TargetDiacylglycerol O-acyltransferase 1(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM50003815(CHEMBL3235321)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Inhibition of human liver flag-tagged DGAT1 expressed in baculovirus infected insect cells after 2 hrs by SPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23X886WPubMed
TargetDiacylglycerol O-acyltransferase 1(Homo sapiens (Human))
Amgen Inc.

Curated by ChEMBL
LigandPNGBDBM27947(2-[4-(4-{4-amino-7,7-dimethyl-7H-pyrimido[4,5-b][1...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Inhibition of DGAT1 (unknown origin) by cell-based assayMore data for this Ligand-Target Pair
TargetStearoyl-CoA desaturase(Homo sapiens (Human))
Japan Tobacco Inc.

Curated by ChEMBL
LigandPNGBDBM50467624(CHEMBL4282359)copy SMILEScopy InChI
Affinity DataIC50: 4.10nMAssay Description:Inhibition of recombinant human SCD1 expressed in baculovirus expression system assessed as reduction in [3H]H2O production using stearoyl [9,10-3H]C...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5HN5PubMed
TargetStearoyl-CoA desaturase(Homo sapiens (Human))
Japan Tobacco Inc.

Curated by ChEMBL
LigandPNGBDBM50467621(CHEMBL4288013)copy SMILEScopy InChI
Affinity DataIC50: 4.20nMAssay Description:Inhibition of recombinant human SCD1 expressed in baculovirus expression system assessed as reduction in [3H]H2O production using stearoyl [9,10-3H]C...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5HN5PubMed
TargetStearoyl-CoA desaturase(Homo sapiens (Human))
Japan Tobacco Inc.

Curated by ChEMBL
LigandPNGBDBM50467597(CHEMBL4283141)copy SMILEScopy InChI
Affinity DataIC50: 4.30nMAssay Description:Inhibition of recombinant human SCD1 expressed in baculovirus expression system assessed as reduction in [3H]H2O production using stearoyl [9,10-3H]C...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5HN5PubMed
TargetStearoyl-CoA desaturase(Homo sapiens (Human))
Japan Tobacco Inc.

Curated by ChEMBL
LigandPNGBDBM50467618(CHEMBL4287233)copy SMILEScopy InChI
Affinity DataIC50: 4.5nMAssay Description:Inhibition of recombinant human SCD1 expressed in baculovirus expression system assessed as reduction in [3H]H2O production using stearoyl [9,10-3H]C...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5HN5PubMed
TargetStearoyl-CoA desaturase(Homo sapiens (Human))
Japan Tobacco Inc.

Curated by ChEMBL
LigandPNGBDBM50467586(CHEMBL4285765)copy SMILEScopy InChI
Affinity DataIC50: 4.5nMAssay Description:Inhibition of recombinant human SCD1 expressed in baculovirus expression system assessed as reduction in [3H]H2O production using stearoyl [9,10-3H]C...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21V5HN5PubMed
TargetProtein kinase C beta type(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM17055((18S)-18-[(dimethylamino)methyl]-17-oxa-4,14,21-tr...)copy SMILEScopy InChI
Affinity DataIC50: 4.70nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C beta 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35VDJPubMed
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