Compile Data Set for Download or QSAR
Found 77 with Last Name = 'barnes' and Initial = 't'
TargetNociceptin receptor(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50475328(CHEMBL414782)copy SMILEScopy InChI
Affinity DataKi:  0.00500nMAssay Description:Receptor binding affinity for recombinant human N/OFQ peptide receptor (NOP) expressed in chinese hamster ovary cellsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J38WBWPubMed
TargetNociceptin receptor(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50475327(CHEMBL410653)copy SMILEScopy InChI
Affinity DataKi:  0.00700nMAssay Description:Receptor binding affinity for recombinant human N/OFQ peptide receptor (NOP) expressed in chinese hamster ovary cellsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J38WBWPubMed
TargetNociceptin receptor(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50475330(CHEMBL442297)copy SMILEScopy InChI
Affinity DataKi:  0.0200nMAssay Description:Receptor binding affinity for recombinant human N/OFQ peptide receptor (NOP) expressed in chinese hamster ovary cellsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J38WBWPubMed
TargetNociceptin receptor(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM86660(OFQ/N UFP-102)copy SMILEScopy InChI
Affinity DataKi:  0.0210nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2222SC4PubMed
TargetNociceptin receptor(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50475333(CHEMBL264846)copy SMILEScopy InChI
Affinity DataKi:  0.0220nMAssay Description:Receptor binding affinity for recombinant human N/OFQ peptide receptor (NOP) expressed in chinese hamster ovary cellsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J38WBWPubMed
TargetNociceptin receptor(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50475331(CHEMBL411649)copy SMILEScopy InChI
Affinity DataKi:  0.0250nMAssay Description:Receptor binding affinity for recombinant human N/OFQ peptide receptor (NOP) expressed in chinese hamster ovary cellsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J38WBWPubMed
TargetNociceptin receptor(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50475325(CHEMBL262544)copy SMILEScopy InChI
Affinity DataKi:  0.0320nMAssay Description:Receptor binding affinity for recombinant human N/OFQ peptide receptor (NOP) expressed in chinese hamster ovary cellsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J38WBWPubMed
TargetNociceptin receptor(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50475329(CHEMBL263588)copy SMILEScopy InChI
Affinity DataKi:  0.0480nMAssay Description:Receptor binding affinity for recombinant human N/OFQ peptide receptor (NOP) expressed in chinese hamster ovary cellsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J38WBWPubMed
TargetNociceptin receptor(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50004178(Nociceptin | Nociceptin/orphanin FQ | ORPHANIN FQ)copy SMILEScopy InChI
Affinity DataKi:  0.0490nMAssay Description:Binding affinity for recombinant human N/OFQ peptide receptor (NOP) expressed in chinese hamster ovary cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J38WBWPubMed
TargetNociceptin receptor(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM86660(OFQ/N UFP-102)copy SMILEScopy InChI
Affinity DataKi:  0.0680nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2222SC4PubMed
TargetNociceptin receptor(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM86660(OFQ/N UFP-102)copy SMILEScopy InChI
Affinity DataKi:  0.0760nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2222SC4PubMed
TargetNociceptin receptor(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50472747(CHEMBL414767)copy SMILEScopy InChI
Affinity DataKi:  0.129nMAssay Description:Receptor binding affinity for recombinant human N/OFQ peptide receptor (NOP) expressed in chinese hamster ovary cellsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J38WBWPubMed
TargetNociceptin receptor(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50475326(CHEMBL410145)copy SMILEScopy InChI
Affinity DataKi:  0.129nMAssay Description:Receptor binding affinity for recombinant human N/OFQ peptide receptor (NOP) expressed in chinese hamster ovary cellsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J38WBWPubMed
TargetNociceptin receptor(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM85822(Demethyl-AMPA | OFQ/N | OFQ/N (1-11) | OFQ/N (1-11...)copy SMILEScopy InChI
Affinity DataKi:  0.140nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2222SC4PubMed
TargetNociceptin receptor(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50475332(CHEMBL413944)copy SMILEScopy InChI
Affinity DataKi:  0.240nMAssay Description:Receptor binding affinity for recombinant human N/OFQ peptide receptor (NOP) expressed in chinese hamster ovary cellsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J38WBWPubMed
TargetNociceptin receptor(MOUSE)
Section of Pharmacology

Curated by PDSP Ki Database
LigandPNGBDBM86660(OFQ/N UFP-102)copy SMILEScopy InChI
Affinity DataKi:  0.360nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2222SC4PubMed
TargetNociceptin receptor(MOUSE)
Section of Pharmacology

Curated by PDSP Ki Database
LigandPNGBDBM86660(OFQ/N UFP-102)copy SMILEScopy InChI
Affinity DataKi:  0.380nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2222SC4PubMed
TargetNociceptin receptor(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50472746(CHEMBL411621)copy SMILEScopy InChI
Affinity DataKi:  0.417nMAssay Description:Receptor binding affinity for recombinant human N/OFQ peptide receptor (NOP) expressed in chinese hamster ovary cellsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J38WBWPubMed
TargetNociceptin receptor(GUINEA PIG)
Section of Pharmacology

Curated by PDSP Ki Database
LigandPNGBDBM86660(OFQ/N UFP-102)copy SMILEScopy InChI
Affinity DataKi:  0.580nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2222SC4PubMed
TargetNociceptin receptor(MOUSE)
Section of Pharmacology

Curated by PDSP Ki Database
LigandPNGBDBM86660(OFQ/N UFP-102)copy SMILEScopy InChI
Affinity DataKi:  0.650nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2222SC4PubMed
TargetNociceptin receptor(MOUSE)
Section of Pharmacology

Curated by PDSP Ki Database
LigandPNGBDBM85822(Demethyl-AMPA | OFQ/N | OFQ/N (1-11) | OFQ/N (1-11...)copy SMILEScopy InChI
Affinity DataKi:  1.20nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2222SC4PubMed
TargetNociceptin receptor(MOUSE)
Section of Pharmacology

Curated by PDSP Ki Database
LigandPNGBDBM85822(Demethyl-AMPA | OFQ/N | OFQ/N (1-11) | OFQ/N (1-11...)copy SMILEScopy InChI
Affinity DataKi:  2.29nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2222SC4PubMed
TargetNociceptin receptor(RAT)
Section of Pharmacology

Curated by PDSP Ki Database
LigandPNGBDBM86660(OFQ/N UFP-102)copy SMILEScopy InChI
Affinity DataKi:  2.69nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2222SC4PubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
Section of Pharmacology

Curated by PDSP Ki Database
LigandPNGBDBM86660(OFQ/N UFP-102)copy SMILEScopy InChI
Affinity DataKi:  4.79nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2222SC4PubMed
TargetNociceptin receptor(GUINEA PIG)
Section of Pharmacology

Curated by PDSP Ki Database
LigandPNGBDBM85822(Demethyl-AMPA | OFQ/N | OFQ/N (1-11) | OFQ/N (1-11...)copy SMILEScopy InChI
Affinity DataKi:  11.5nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2222SC4PubMed
TargetNociceptin receptor(MOUSE)
Section of Pharmacology

Curated by PDSP Ki Database
LigandPNGBDBM85822(Demethyl-AMPA | OFQ/N | OFQ/N (1-11) | OFQ/N (1-11...)copy SMILEScopy InChI
Affinity DataKi:  17.4nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2222SC4PubMed
TargetNociceptin receptor(RAT)
Section of Pharmacology

Curated by PDSP Ki Database
LigandPNGBDBM85822(Demethyl-AMPA | OFQ/N | OFQ/N (1-11) | OFQ/N (1-11...)copy SMILEScopy InChI
Affinity DataKi:  57.5nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2222SC4PubMed
TargetMu-type opioid receptor(Homo sapiens (Human))
Section of Pharmacology

Curated by PDSP Ki Database
LigandPNGBDBM86660(OFQ/N UFP-102)copy SMILEScopy InChI
Affinity DataKi:  70.8nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2222SC4PubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))
Section of Pharmacology

Curated by PDSP Ki Database
LigandPNGBDBM86660(OFQ/N UFP-102)copy SMILEScopy InChI
Affinity DataKi:  380nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2222SC4PubMed
TargetHeat shock protein HSP 90-beta(Homo sapiens (Human))
University of California

Curated by ChEMBL
LigandPNGBDBM227589(Radicicol)copy SMILEScopy InChI
Affinity DataIC50: 19nMAssay Description:Inhibition of HSP90 (unknown origin)More data for this Ligand-Target Pair
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
Gilead Sciences Inc.

LigandPNGBDBM33410(CHEMBL16755 | N-hydroxyisoquinolinedione, 2)copy SMILEScopy InChI
Affinity DataIC50: 135nMpH: 8.0 T: 2°CAssay Description:Enzyme activity was measuring substrate hydrolysis of RNase H. The intact substrate has a low background fluorescent signal and provides up to 50-fol...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM78F2PubMed
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
Gilead Sciences Inc.

LigandPNGBDBM33419(pyrimidinol carboxylic acid, 11)copy SMILEScopy InChI
Affinity DataIC50: 175nMpH: 8.0 T: 2°CAssay Description:Enzyme activity was measuring substrate hydrolysis of RNase H. The intact substrate has a low background fluorescent signal and provides up to 50-fol...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM78F2PubMed
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
Gilead Sciences Inc.

LigandPNGBDBM33411(β-Thujaplicinol | hydroxytropolone, 3)copy SMILEScopy InChI
Affinity DataIC50: 660nMpH: 8.0 T: 2°CAssay Description:Enzyme activity was measuring substrate hydrolysis of RNase H. The intact substrate has a low background fluorescent signal and provides up to 50-fol...More data for this Ligand-Target Pair
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
Gilead Sciences Inc.

LigandPNGBDBM33418(pyrimidinol carboxylic acid, 10)copy SMILEScopy InChI
Affinity DataIC50: 1.15E+3nMpH: 8.0 T: 2°CAssay Description:Enzyme activity was measuring substrate hydrolysis of RNase H. The intact substrate has a low background fluorescent signal and provides up to 50-fol...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM78F2PubMed
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
Gilead Sciences Inc.

LigandPNGBDBM33417(pyrimidinol carboxylic acid, 9)copy SMILEScopy InChI
Affinity DataIC50: 1.45E+3nMpH: 8.0 T: 2°CAssay Description:Enzyme activity was measuring substrate hydrolysis of RNase H. The intact substrate has a low background fluorescent signal and provides up to 50-fol...More data for this Ligand-Target Pair
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
Gilead Sciences Inc.

LigandPNGBDBM33415(CHEMBL204900 | pyrimidinol carboxylic acid, 7)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+3nMpH: 8.0 T: 2°CAssay Description:Enzyme activity was measuring substrate hydrolysis of RNase H. The intact substrate has a low background fluorescent signal and provides up to 50-fol...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM78F2PubMed
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
Gilead Sciences Inc.

LigandPNGBDBM33412(CHEMBL183852 | N-hydroxy quinazolinedione, 4 | US1...)copy SMILEScopy InChI
Affinity DataIC50: 6.00E+3nMpH: 8.0 T: 2°CAssay Description:Enzyme activity was measuring substrate hydrolysis of RNase H. The intact substrate has a low background fluorescent signal and provides up to 50-fol...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM78F2PubMed
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
Gilead Sciences Inc.

LigandPNGBDBM33409(alpha, gamma-diketo acid, 1)copy SMILEScopy InChI
Affinity DataIC50: 9.85E+3nMpH: 8.0 T: 2°CAssay Description:Enzyme activity was measuring substrate hydrolysis of RNase H. The intact substrate has a low background fluorescent signal and provides up to 50-fol...More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM78F2PubMed
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
Gilead Sciences Inc.

LigandPNGBDBM33416(pyrimidinol carboxylic acid, 8)copy SMILEScopy InChI
Affinity DataIC50: 1.02E+4nMpH: 8.0 T: 2°CAssay Description:Enzyme activity was measuring substrate hydrolysis of RNase H. The intact substrate has a low background fluorescent signal and provides up to 50-fol...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM78F2PubMed
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
Gilead Sciences Inc.

LigandPNGBDBM33414(CHEMBL440562 | pyrimidinol carboxylic acid, 6)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+4nMpH: 8.0 T: 2°CAssay Description:Enzyme activity was measuring substrate hydrolysis of RNase H. The intact substrate has a low background fluorescent signal and provides up to 50-fol...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM78F2PubMed
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
Gilead Sciences Inc.

LigandPNGBDBM33413(benzo[7]annulene-8-carboxylic acid, 5)copy SMILEScopy InChI
Affinity DataIC50: 2.32E+4nMpH: 8.0 T: 2°CAssay Description:Enzyme activity was measuring substrate hydrolysis of RNase H. The intact substrate has a low background fluorescent signal and provides up to 50-fol...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM78F2PubMed
TargetRibonuclease H1(Homo sapiens (Human))
Gilead Sciences Inc.

LigandPNGBDBM33419(pyrimidinol carboxylic acid, 11)copy SMILEScopy InChI
Affinity DataIC50: 4.85E+4nMpH: 8.0 T: 2°CAssay Description:Enzyme activity was measuring substrate hydrolysis of RNase H. The intact substrate has a low background fluorescent signal and provides up to 50-fol...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM78F2PubMed
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
Gilead Sciences Inc.

LigandPNGBDBM33420(pyrimidinol carboxylic acid, 12)copy SMILEScopy InChI
Affinity DataIC50: 7.20E+4nMpH: 8.0 T: 2°CAssay Description:Enzyme activity was measuring substrate hydrolysis of RNase H. The intact substrate has a low background fluorescent signal and provides up to 50-fol...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM78F2PubMed
TargetRibonuclease H1(Homo sapiens (Human))
Gilead Sciences Inc.

LigandPNGBDBM33418(pyrimidinol carboxylic acid, 10)copy SMILEScopy InChI
Affinity DataIC50: 7.40E+4nMpH: 8.0 T: 2°CAssay Description:Enzyme activity was measuring substrate hydrolysis of RNase H. The intact substrate has a low background fluorescent signal and provides up to 50-fol...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM78F2PubMed
TargetRibonuclease H1(Homo sapiens (Human))
Gilead Sciences Inc.

LigandPNGBDBM33414(CHEMBL440562 | pyrimidinol carboxylic acid, 6)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMpH: 8.0 T: 2°CAssay Description:Enzyme activity was measuring substrate hydrolysis of RNase H. The intact substrate has a low background fluorescent signal and provides up to 50-fol...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM78F2PubMed
TargetRibonuclease H1(Homo sapiens (Human))
Gilead Sciences Inc.

LigandPNGBDBM33415(CHEMBL204900 | pyrimidinol carboxylic acid, 7)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMpH: 8.0 T: 2°CAssay Description:Enzyme activity was measuring substrate hydrolysis of RNase H. The intact substrate has a low background fluorescent signal and provides up to 50-fol...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM78F2PubMed
TargetRibonuclease H1(Homo sapiens (Human))
Gilead Sciences Inc.

LigandPNGBDBM33416(pyrimidinol carboxylic acid, 8)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMpH: 8.0 T: 2°CAssay Description:Enzyme activity was measuring substrate hydrolysis of RNase H. The intact substrate has a low background fluorescent signal and provides up to 50-fol...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM78F2PubMed
TargetRibonuclease H1(Homo sapiens (Human))
Gilead Sciences Inc.

LigandPNGBDBM33417(pyrimidinol carboxylic acid, 9)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMpH: 8.0 T: 2°CAssay Description:Enzyme activity was measuring substrate hydrolysis of RNase H. The intact substrate has a low background fluorescent signal and provides up to 50-fol...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TM78F2PubMed
TargetNociceptin receptor(MOUSE)
Section of Pharmacology

Curated by PDSP Ki Database
LigandPNGBDBM50004178(Nociceptin | Nociceptin/orphanin FQ | ORPHANIN FQ)copy SMILEScopy InChI
Affinity DataEC50:  5.40nMAssay Description:Inhibition of electrically evoked contraction of mouse vas deferensMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J38WBWPubMed
TargetNociceptin receptor(Homo sapiens (Human))
University of Ferrara

Curated by ChEMBL
LigandPNGBDBM50475331(CHEMBL411649)copy SMILEScopy InChI
Affinity DataEC50:  4.90nMAssay Description:Inhibition of forskolin stimulated cAMP levels in CHO cell membranes expressing the human NOP receptor (CHOhNOP)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J38WBWPubMed
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