Compile Data Set for Download or QSAR
Found 14 with Last Name = 'asai' and Initial = 'k'
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by PDSP Ki Database
LigandPNGBDBM50091652(CHEMBL269503 | PYY | PYY, rat | Peptide YY(PYY)(YP...)copy SMILEScopy InChI
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25Q4TPTPubMed
TargetNeuropeptide Y receptor type 1(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by PDSP Ki Database
LigandPNGBDBM50091652(CHEMBL269503 | PYY | PYY, rat | Peptide YY(PYY)(YP...)copy SMILEScopy InChI
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25Q4TPTPubMed
TargetNeuropeptide Y receptor type 2(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by PDSP Ki Database
LigandPNGBDBM50091652(CHEMBL269503 | PYY | PYY, rat | Peptide YY(PYY)(YP...)copy SMILEScopy InChI
Affinity DataKi:  2.10nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25Q4TPTPubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by PDSP Ki Database
LigandPNGBDBM86732(3-(5,6,7,8-tetrahydro-9-isopropyl-carbazol-3-yl)-1...)copy SMILEScopy InChI
Affinity DataKi:  4.30nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25Q4TPTPubMed
TargetNeuropeptide Y receptor type 5(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by PDSP Ki Database
LigandPNGBDBM86733(5,5-DIMETHYL-2-(2,3,4,9-TETRAHYDRO-3,3-DIMETHYL-1O...)copy SMILEScopy InChI
Affinity DataKi:  25nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25Q4TPTPubMed
TargetNeuropeptide Y receptor type 2(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by PDSP Ki Database
LigandPNGBDBM86733(5,5-DIMETHYL-2-(2,3,4,9-TETRAHYDRO-3,3-DIMETHYL-1O...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25Q4TPTPubMed
TargetNeuropeptide Y receptor type 2(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by PDSP Ki Database
LigandPNGBDBM86732(3-(5,6,7,8-tetrahydro-9-isopropyl-carbazol-3-yl)-1...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25Q4TPTPubMed
TargetNeuropeptide Y receptor type 1(Homo sapiens (Human))
Meiji Seika Kaisha, Ltd.

Curated by PDSP Ki Database
LigandPNGBDBM86733(5,5-DIMETHYL-2-(2,3,4,9-TETRAHYDRO-3,3-DIMETHYL-1O...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25Q4TPTPubMed
TargetKynurenine/alpha-aminoadipate aminotransferase, mitochondrial(Homo sapiens (Human))
University of Piemonte Orientale Amedeo Avogadro

Curated by ChEMBL
LigandPNGBDBM50324539((S)-(-)-9-(4-aminopiperazin-1-yl)-8-fluoro-3-methy...)copy SMILEScopy InChI
Affinity DataIC50: 910nMAssay Description:Inhibition of human recombinant MBP-KAT2 expressed in HEK293 cells assessed as conversion of L-kynurenine to kynurenic acid after 1 hrMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HM58N6PubMedMMDB
TargetKynurenine/alpha-aminoadipate aminotransferase, mitochondrial(Rattus norvegicus)
University of Piemonte Orientale Amedeo Avogadro

Curated by ChEMBL
LigandPNGBDBM50324539((S)-(-)-9-(4-aminopiperazin-1-yl)-8-fluoro-3-methy...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of rat brain KAT2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HM58N6PubMed
TargetKynurenine/alpha-aminoadipate aminotransferase, mitochondrial(Homo sapiens (Human))
University of Piemonte Orientale Amedeo Avogadro

Curated by ChEMBL
LigandPNGBDBM50324539((S)-(-)-9-(4-aminopiperazin-1-yl)-8-fluoro-3-methy...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of KAT2 in human prefrontal cortex homogenatesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HM58N6PubMedMMDB
TargetKynurenine/alpha-aminoadipate aminotransferase, mitochondrial(Homo sapiens (Human))
University of Piemonte Orientale Amedeo Avogadro

Curated by ChEMBL
LigandPNGBDBM50416560(CHEMBL1215660)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+3nMAssay Description:Inhibition of human recombinant MBP-KAT2 expressed in HEK293 cells assessed as conversion of L-kynurenine to kynurenic acid after 1 hrMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HM58N6PubMed
TargetKynurenine--oxoglutarate transaminase 1(Homo sapiens (Human))
University of Piemonte Orientale Amedeo Avogadro

Curated by ChEMBL
LigandPNGBDBM50324539((S)-(-)-9-(4-aminopiperazin-1-yl)-8-fluoro-3-methy...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of KAT1 in human prefrontal cortex homogenatesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HM58N6PubMed
TargetKynurenine--oxoglutarate transaminase 1(Homo sapiens (Human))
University of Piemonte Orientale Amedeo Avogadro

Curated by ChEMBL
LigandPNGBDBM50324539((S)-(-)-9-(4-aminopiperazin-1-yl)-8-fluoro-3-methy...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human recombinant MBP-KAT1 expressed in HEK293 cells assessed as conversion of L-kynurenine to kynurenic acid after 1 hrMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HM58N6PubMed