Compile Data Set for Download or QSAR
Found 223 with Last Name = 'iida' and Initial = 't'
TargetNociceptin receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094650(CHEMBL434060 | N-(4-Amino-2-ethyl-quinolin-6-yl)-2...)copy SMILEScopy InChI
Affinity DataKi:  1.80nMAssay Description:Compound was evaluated for its ability to displace [3H]nociceptin ( 0.5 nM ) binding from Opioid receptor like 1 expressed in HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetNociceptin receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094648(CHEMBL139776 | N-(4-Amino-2-methyl-quinolin-6-yl)-...)copy SMILEScopy InChI
Affinity DataKi:  1.80nMAssay Description:Compound was evaluated for its ability to displace [3H]nociceptin ( 0.5 nM ) binding from Opioid receptor like 1 expressed in HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetNociceptin receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094640(CHEMBL140640 | N-(4-Amino-2-propyl-quinolin-6-yl)-...)copy SMILEScopy InChI
Affinity DataKi:  1.80nMAssay Description:Compound was evaluated for its ability to displace [3H]nociceptin ( 0.5 nM ) binding from Opioid receptor like 1 expressed in HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetNociceptin receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094651(CHEMBL342580 | N-(4-Amino-2-methyl-quinolin-6-yl)-...)copy SMILEScopy InChI
Affinity DataKi:  2.20nMAssay Description:Compound was evaluated for its ability to displace [3H]nociceptin ( 0.5 nM ) binding from Opioid receptor like 1 expressed in HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetNociceptin receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094638(CHEMBL337128 | N-(4-Amino-2-methyl-quinolin-6-yl)-...)copy SMILEScopy InChI
Affinity DataKi:  2.30nMAssay Description:Compound was evaluated for its ability to displace [3H]nociceptin ( 0.5 nM ) binding from Opioid receptor like 1 expressed in HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetNociceptin receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094642(CHEMBL142454 | N-(4-Amino-2-methyl-quinolin-6-yl)-...)copy SMILEScopy InChI
Affinity DataKi:  2.60nMAssay Description:Compound was evaluated for its ability to displace [3H]nociceptin ( 0.5 nM ) binding from Opioid receptor like 1 expressed in HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetNociceptin receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094646(CHEMBL139934 | N-(4-Amino-2-methyl-quinolin-6-yl)-...)copy SMILEScopy InChI
Affinity DataKi:  6.5nMAssay Description:Compound was evaluated for its ability to displace [3H]nociceptin ( 0.5 nM ) binding from Opioid receptor like 1 expressed in HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetNociceptin receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094636(CHEMBL140103 | N-(4-Amino-2-methyl-quinolin-6-yl)-...)copy SMILEScopy InChI
Affinity DataKi:  7nMAssay Description:Compound was evaluated for its ability to displace [3H]nociceptin ( 0.5 nM ) binding from Opioid receptor like 1 expressed in HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetNociceptin receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094634(CHEMBL140979 | N-(4-Amino-2-methyl-quinolin-6-yl)-...)copy SMILEScopy InChI
Affinity DataKi:  8.20nMAssay Description:Compound was evaluated for its ability to displace [3H]nociceptin ( 0.5 nM ) binding from Opioid receptor like 1 expressed in HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Amgen, Inc.

Curated by ChEMBL
LigandPNGBDBM28681(5-[(4-{2-[methyl(pyridin-2-yl)amino]ethoxy}phenyl)...)copy SMILEScopy InChI
Affinity DataKi:  10nMAssay Description:Displacement of [3H]-rosiglitazone from GST-tagged PPARgammaLBD (unknown origin) after 1 hr by scintillation proximity assayMore data for this Ligand-Target Pair
TargetNociceptin receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094644(CHEMBL140519 | N-(4-Amino-2-methyl-quinolin-6-yl)-...)copy SMILEScopy InChI
Affinity DataKi:  12nMAssay Description:Compound was evaluated for its ability to displace [3H]nociceptin ( 0.5 nM ) binding from Opioid receptor like 1 expressed in HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetNociceptin receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094639(CHEMBL142999 | N-(4-Amino-2-methyl-quinolin-6-yl)-...)copy SMILEScopy InChI
Affinity DataKi:  13nMAssay Description:Compound was evaluated for its ability to displace [3H]nociceptin ( 0.5 nM ) binding from Opioid receptor like 1 expressed in HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetNociceptin receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094647(CHEMBL143605 | N-(4-Amino-2-methyl-quinolin-6-yl)-...)copy SMILEScopy InChI
Affinity DataKi:  20nMAssay Description:Compound was evaluated for its ability to displace [3H]nociceptin ( 0.5 nM ) binding from Opioid receptor like 1 expressed in HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetNociceptin receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094649(CHEMBL140580 | N-(1-Amino-3-methyl-isoquinolin-7-y...)copy SMILEScopy InChI
Affinity DataKi:  37nMAssay Description:Compound was evaluated for its ability to displace [3H]nociceptin ( 0.5 nM ) binding from Opioid receptor like 1 expressed in HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetNociceptin receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094637(CHEMBL139566 | N-(4-Amino-2-methyl-quinolin-6-yl)-...)copy SMILEScopy InChI
Affinity DataKi:  47nMAssay Description:Compound was evaluated for its ability to displace [3H]nociceptin ( 0.5 nM ) binding from Opioid receptor like 1 expressed in HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetNociceptin receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094635(CHEMBL336238 | N-(4-Amino-2-methyl-quinolin-6-yl)-...)copy SMILEScopy InChI
Affinity DataKi:  51nMAssay Description:Compound was evaluated for its ability to displace [3H]-nociceptin ( 0.5 nM ) binding from Opioid receptor like 1 expressed in HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetNAD-dependent protein deacetylase sirtuin-2(Homo sapiens (Human))
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50513317(CHEMBL4465620)copy SMILEScopy InChI
Affinity DataKi:  68nMAssay Description:Inhibition of human N-terminal His-tagged SIRT2 expressed in Escherichia coli using p53 (Gln-Pro-Lys-Lys(Ac)) (317 to 320 residues) as substrate incu...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JH3QJRPubMed
TargetNociceptin receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094643(CHEMBL358306 | N-(4-Amino-2-methyl-quinolin-6-yl)-...)copy SMILEScopy InChI
Affinity DataKi:  80nMAssay Description:Compound was evaluated for its ability to displace [3H]-nociceptin ( 0.5 nM ) binding from Opioid receptor like 1 expressed in HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetNociceptin receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094641(CHEMBL422641 | N-(4-Amino-2-methyl-quinolin-6-yl)-...)copy SMILEScopy InChI
Affinity DataKi:  82nMAssay Description:Compound was evaluated for its ability to displace [3H]nociceptin ( 0.5 nM ) binding from Opioid receptor like 1 expressed in HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetNociceptin receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094645(CHEMBL143243 | N-(4-Amino-quinolin-6-yl)-2-(4-chlo...)copy SMILEScopy InChI
Affinity DataKi:  86nMAssay Description:Compound was evaluated for its ability to displace [3H]nociceptin ( 0.5 nM ) binding from Opioid receptor like 1 expressed in HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetNociceptin receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094652(CHEMBL343424 | N-(4-Amino-2-methyl-quinolin-6-yl)-...)copy SMILEScopy InChI
Affinity DataKi:  89nMAssay Description:Compound was evaluated for its ability to displace [3H]nociceptin ( 0.5 nM ) binding from Opioid receptor like 1 expressed in HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094634(CHEMBL140979 | N-(4-Amino-2-methyl-quinolin-6-yl)-...)copy SMILEScopy InChI
Affinity DataKi:  103nMAssay Description:Inhibition of [3H]diprenorphine (0.33 nM) binding from human Opioid receptor mu 1 expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetNociceptin receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094653(CHEMBL141078 | N-(4-Amino-2-methyl-quinolin-6-yl)-...)copy SMILEScopy InChI
Affinity DataKi:  121nMAssay Description:Compound was evaluated for its ability to displace [3H]nociceptin ( 0.5 nM ) binding from Opioid receptor like 1 expressed in HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetNociceptin receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094654(Biphenyl-2-carboxylic acid (4-amino-2-methyl-quino...)copy SMILEScopy InChI
Affinity DataKi:  369nMAssay Description:Compound was evaluated for its ability to displace [3H]nociceptin ( 0.5 nM ) binding from Opioid receptor like 1 expressed in HeLa cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetNAD-dependent protein deacetylase sirtuin-2(Homo sapiens (Human))
Kyoto Prefectural University of Medicine

Curated by ChEMBL
LigandPNGBDBM50513318(CHEMBL4516553)copy SMILEScopy InChI
Affinity DataKi:  470nMAssay Description:Inhibition of human N-terminal His-tagged SIRT2 expressed in Escherichia coli using p53 (Gln-Pro-Lys-Lys(Ac)) (317 to 320 residues) as substrate incu...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JH3QJRPubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094634(CHEMBL140979 | N-(4-Amino-2-methyl-quinolin-6-yl)-...)copy SMILEScopy InChI
Affinity DataKi:  1.06E+3nMAssay Description:Inhibition of [3H]naltrindole (0.55 nM) binding from human Opioid receptor kappa 1More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
Central Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50094634(CHEMBL140979 | N-(4-Amino-2-methyl-quinolin-6-yl)-...)copy SMILEScopy InChI
Affinity DataKi:  8.65E+3nMAssay Description:Inhibition of [3H]naltrindole (0.55 nM) binding from human Opioid receptor delta 1 expressed in CHO-K1 cells.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2NK3D9HPubMed
TargetSodium/glucose cotransporter 1(Homo sapiens (Human))
Japan Tobacco Inc.

US Patent
LigandPNGBDBM493926(US10988462, Example 37)copy SMILEScopy InChI
Affinity DataIC50: 0.980nMAssay Description:Human SGLT1-stably-expressing cell lines were seeded at 5×104 cells/well on BioCoat™ Poly-D-Lysine 96 well plate with Lid (Becton, Dickinson and Comp...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TH8QV5US Patent
TargetCytochrome P450 3A4(Homo sapiens (Human))
Amgen, Inc.

Curated by ChEMBL
LigandPNGBDBM50428877(CHEMBL2338480)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of CYP3A4 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23F4R13PubMed
TargetSodium/glucose cotransporter 1(Homo sapiens (Human))
Japan Tobacco Inc.

US Patent
LigandPNGBDBM493894(US10988462, Example 10)copy SMILEScopy InChI
Affinity DataIC50: 1.20nMAssay Description:Human SGLT1-stably-expressing cell lines were seeded at 5×104 cells/well on BioCoat™ Poly-D-Lysine 96 well plate with Lid (Becton, Dickinson and Comp...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TH8QV5US Patent
TargetSodium/glucose cotransporter 1(Homo sapiens (Human))
Japan Tobacco Inc.

US Patent
LigandPNGBDBM493906(US10988462, Example 21)copy SMILEScopy InChI
Affinity DataIC50: 1.20nMAssay Description:Human SGLT1-stably-expressing cell lines were seeded at 5×104 cells/well on BioCoat™ Poly-D-Lysine 96 well plate with Lid (Becton, Dickinson and Comp...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TH8QV5US Patent
TargetSodium/glucose cotransporter 1(Homo sapiens (Human))
Japan Tobacco Inc.

US Patent
LigandPNGBDBM493905(US10988462, Example 20)copy SMILEScopy InChI
Affinity DataIC50: 1.20nMAssay Description:Human SGLT1-stably-expressing cell lines were seeded at 5×104 cells/well on BioCoat™ Poly-D-Lysine 96 well plate with Lid (Becton, Dickinson and Comp...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TH8QV5US Patent
TargetSodium/glucose cotransporter 1(Homo sapiens (Human))
Japan Tobacco Inc.

US Patent
LigandPNGBDBM493901(US10988462, Example 17)copy SMILEScopy InChI
Affinity DataIC50: 1.30nMAssay Description:Human SGLT1-stably-expressing cell lines were seeded at 5×104 cells/well on BioCoat™ Poly-D-Lysine 96 well plate with Lid (Becton, Dickinson and Comp...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TH8QV5US Patent
TargetSodium/glucose cotransporter 1(Homo sapiens (Human))
Japan Tobacco Inc.

US Patent
LigandPNGBDBM493879(US10988462, Example 1)copy SMILEScopy InChI
Affinity DataIC50: 1.90nMAssay Description:Human SGLT1-stably-expressing cell lines were seeded at 5×104 cells/well on BioCoat™ Poly-D-Lysine 96 well plate with Lid (Becton, Dickinson and Comp...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TH8QV5US Patent
TargetSodium/glucose cotransporter 1(Homo sapiens (Human))
Japan Tobacco Inc.

US Patent
LigandPNGBDBM493925(US10988462, Example 36)copy SMILEScopy InChI
Affinity DataIC50: 1.90nMAssay Description:Human SGLT1-stably-expressing cell lines were seeded at 5×104 cells/well on BioCoat™ Poly-D-Lysine 96 well plate with Lid (Becton, Dickinson and Comp...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TH8QV5US Patent
TargetSodium/glucose cotransporter 1(Homo sapiens (Human))
Japan Tobacco Inc.

US Patent
LigandPNGBDBM493917(US10988462, Example 30)copy SMILEScopy InChI
Affinity DataIC50: 2.70nMAssay Description:Human SGLT1-stably-expressing cell lines were seeded at 5×104 cells/well on BioCoat™ Poly-D-Lysine 96 well plate with Lid (Becton, Dickinson and Comp...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TH8QV5US Patent
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
TargetSodium/glucose cotransporter 1(Homo sapiens (Human))
Japan Tobacco Inc.

US Patent
LigandPNGBDBM493897(US10988462, Example 13)copy SMILEScopy InChI
Affinity DataIC50: 2.90nMAssay Description:Human SGLT1-stably-expressing cell lines were seeded at 5×104 cells/well on BioCoat™ Poly-D-Lysine 96 well plate with Lid (Becton, Dickinson and Comp...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TH8QV5US Patent
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
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
TargetSodium/glucose cotransporter 1(Homo sapiens (Human))
Japan Tobacco Inc.

US Patent
LigandPNGBDBM493907(US10988462, Example 22)copy SMILEScopy InChI
Affinity DataIC50: 3.40nMAssay Description:Human SGLT1-stably-expressing cell lines were seeded at 5×104 cells/well on BioCoat™ Poly-D-Lysine 96 well plate with Lid (Becton, Dickinson and Comp...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TH8QV5US Patent
TargetSodium/glucose cotransporter 1(Homo sapiens (Human))
Japan Tobacco Inc.

US Patent
LigandPNGBDBM493898(US10988462, Example 14)copy SMILEScopy InChI
Affinity DataIC50: 3.70nMAssay Description:Human SGLT1-stably-expressing cell lines were seeded at 5×104 cells/well on BioCoat™ Poly-D-Lysine 96 well plate with Lid (Becton, Dickinson and Comp...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TH8QV5US Patent
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
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
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
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
TargetSodium/glucose cotransporter 1(Homo sapiens (Human))
Japan Tobacco Inc.

US Patent
LigandPNGBDBM493927(US10988462, Example 38)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Human SGLT1-stably-expressing cell lines were seeded at 5×104 cells/well on BioCoat™ Poly-D-Lysine 96 well plate with Lid (Becton, Dickinson and Comp...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2TH8QV5US Patent
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
Displayed 1 to 50 (of 223 total ) | Next | Last >>
Jump to: