null

SMILES NCCc1cnc[nH]1

InChI Key InChIKey=NTYJJOPFIAHURM-UHFFFAOYSA-N

PDB links: 8 PDB IDs match this monomer. 50 PDB IDs contain this monomer as substructures. 50 PDB IDs contain inhibitors having a similarity of 90% to this monomer.

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 117 hits for monomerid = 7966   

TargetHistamine receptor H4(GUINEA PIG)
SmithKline Beecham Pharmaceuticals

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  0.140nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z899ZRPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  2.32nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ866CPubMedDrugBank
TargetHistamine H4 receptor(Homo sapiens (Human))
SmithKline Beecham Pharmaceuticals

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  2.5nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z899ZRPubMedDrugBank
TargetHrh3 protein(RAT)
Glaxo Research & Development Ltd.

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  2.51nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6QSDPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  2.61nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ866CPubMedDrugBank
TargetHrh3 protein(RAT)
Glaxo Research & Development Ltd.

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  2.66nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ866CPubMed
TargetHrh3 protein(RAT)
Glaxo Research & Development Ltd.

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  4.90nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ866CPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  5.20nMAssay Description:Displacement of [3H[N-alpha-methylhistamine form human recombinant histamine H3 receptor expressed in CHO cells after 1 hr by liquid scintillation co...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21Z44KCPubMedDrugBank
TargetHrh3 protein(RAT)
Glaxo Research & Development Ltd.

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  5.30nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23X8556PubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  5.40nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26Q1VSRPubMedDrugBank
TargetHistamine H3 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  6.31nMAssay Description:Displacement of [3H]histamine from human H3 receptor expressed in HEK293 cells after 1 to 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2JDXPubMedDrugBank
TargetHrh3 protein(RAT)
Glaxo Research & Development Ltd.

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  7.30nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23X8556PubMed
TargetHistamine H4 receptor(Homo sapiens (Human))
SmithKline Beecham Pharmaceuticals

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  8.10nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26Q1VSRPubMedDrugBank
TargetHistamine H4 receptor(Homo sapiens (Human))
SmithKline Beecham Pharmaceuticals

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  9nMAssay Description:Displacement of [3H]histamine from human H4 receptor expressed in HEK cell membranesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D79BT2PubMedDrugBank
TargetHistamine H3 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  10nMAssay Description:Ligand displacement assays were performed on The SK-N-MC/hH3R cell homogenates. Retained radioactivity was determined by liquid scintillation countin...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KD1W6VPubMedDrugBank
TargetHrh3 protein(RAT)
Glaxo Research & Development Ltd.

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  10nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6QSDPubMed
TargetHrh3 protein(RAT)
Glaxo Research & Development Ltd.

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  11nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X63KF2PubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  11.8nMAssay Description:Displacement of [3H]N-alpha-methylhistamine from human histamine H3 receptor expressed in HEK293 cells after 60 mins by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20G3MDDPubMedDrugBank
TargetHrh3 protein(RAT)
Glaxo Research & Development Ltd.

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  12nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2348HX8PubMed
TargetHistamine H4 receptor(Homo sapiens (Human))
SmithKline Beecham Pharmaceuticals

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  12.0nMAssay Description:Displacement of [3H]histamine from human histamine H4 receptor expressed in HEK293T cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44RJ4PubMedDrugBank
TargetHistamine H4 receptor(Homo sapiens (Human))
SmithKline Beecham Pharmaceuticals

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  12.0nMAssay Description:Displacement of [3H]histamine from human histamine H4 receptor expressed in HEK293 cells after 60 mins by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20G3MDDPubMedDrugBank
TargetHrh3 protein(RAT)
Glaxo Research & Development Ltd.

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  13.2nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2348HX8PubMed
TargetHistamine H4 receptor(Homo sapiens (Human))
SmithKline Beecham Pharmaceuticals

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  13.4nMAssay Description:Displacement of [3H]histamine from human histamine H4 receptor expressed in SK-NM-C cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M046BPPubMedDrugBank
TargetHistamine H3 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  15.2nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2348HX8PubMedDrugBank
TargetHistamine H4 receptor(Homo sapiens (Human))
SmithKline Beecham Pharmaceuticals

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  15.8nMAssay Description:Displacement of [3H]histamine from human H4 receptor expressed in HEK293 cells after 1 to 1.5 hrs by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2JDXPubMedDrugBank
TargetHistamine H4 receptor(Homo sapiens (Human))
SmithKline Beecham Pharmaceuticals

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  16nM ΔG°:  -11.1kcal/molepH: 7.4 T: 2°CAssay Description:Ligand displacement assays were performed on The SK-N-MC/hH4R cell homogenates. Retained radioactivity was determined by liquid scintillation countin...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KD1W6VPubMedDrugBank
TargetHistamine H2 receptor(RAT)
Boehringer Ingelheim Italia

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  17nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Q52N48PubMed
TargetHistamine H4 receptor(Homo sapiens (Human))
SmithKline Beecham Pharmaceuticals

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  17nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z899ZRPubMedDrugBank
TargetHrh3 protein(RAT)
Glaxo Research & Development Ltd.

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  25.1nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6QSDPubMed
TargetHistamine H4 receptor(Homo sapiens (Human))
SmithKline Beecham Pharmaceuticals

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  39.8nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ866CPubMedDrugBank
TargetHistamine H4 receptor(Homo sapiens (Human))
SmithKline Beecham Pharmaceuticals

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  60nMAssay Description:Displacement of [3H]histamine from human recombinant histamine H4 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3D4ZPubMedDrugBank
TargetHrh3 protein(RAT)
Glaxo Research & Development Ltd.

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  62nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23X8556PubMed
TargetHistamine H3 receptor(Mus musculus)
Tsukuba Research Institute

Curated by ChEMBL
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  68nMAssay Description:Displacement of 3-([1,1,1-3H]methyl)-2-(4-{[3-(1-pyrrolidinyl)propyl]oxy}phenyl)-4(3H)-quinazolinone from mouse histamine H3 receptor expressed in HE...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GQ6XSZPubMed
TargetHistamine H2 receptor(Cavia porcellus (domestic guinea pig))
Queen's Medical Centre

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  100nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX99KHPubMed
TargetHrh3 protein(RAT)
Glaxo Research & Development Ltd.

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  100nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22R3Q5WPubMed
TargetHistamine H3 receptor(GUINEA PIG)
Unité 109

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  100nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22R3Q5WPubMed
TargetHistamine H1 receptor(Cavia porcellus (domestic guinea pig))
Queen's Medical Centre

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  100nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX99KHPubMed
TargetHistamine H3 receptor(GUINEA PIG)
Unité 109

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  100nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX99KHPubMed
TargetHistamine receptor H4(GUINEA PIG)
SmithKline Beecham Pharmaceuticals

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  104nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z899ZRPubMed
TargetHrh3 protein(RAT)
Glaxo Research & Development Ltd.

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  158nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZG6QSDPubMed
TargetHistamine H1 receptor(Homo sapiens (Human))
University of Kansas

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  190nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X63KHZPubMedDrugBank
Target5-hydroxytryptamine receptor 7(Rattus norvegicus (rat))
National Institute of Neurological Disorders and Stroke

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  1.00E+3nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2V1239RPubMed
Target5-hydroxytryptamine receptor 7(Rattus norvegicus (rat))
National Institute of Neurological Disorders and Stroke

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  1.00E+3nMMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2V1239RPubMed
TargetHistamine H2 receptor(Homo sapiens (Human))
University of Kansas

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  1.20E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X63KHZPubMedDrugBank
TargetHistamine H2 receptor(Cavia porcellus (domestic guinea pig))
Queen's Medical Centre

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  1.20E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X63KHZPubMed
TargetHistamine H1 receptor(Homo sapiens (Human))
University of Kansas

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  1.26E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H70DB4PubMedDrugBank
TargetHistamine H1 receptor(Homo sapiens (Human))
University of Kansas

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  1.26E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PZ57BRPubMedDrugBank
TargetHistamine H1 receptor(Homo sapiens (Human))
University of Kansas

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  1.26E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D50KJ8PubMedDrugBank
TargetHistamine H1 receptor(Homo sapiens (Human))
University of Kansas

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  2.06E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2HM5708PubMedDrugBank
TargetTrace amine-associated receptor 1(Homo sapiens (Human))
Synaptic Pharmaceutical Corporation

Curated by PDSP Ki Database
LigandPNGBDBM7966(2-(1H-imidazol-4-yl)ethan-1-amine | CHEMBL544208 |...)copy SMILEScopy InChI
Affinity DataKi:  3.11E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G15ZD5PubMed
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