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SMILES: COc1ccc2[nH]cc(C3CCCN(CCCCn4c(=O)c(c5CCCCn5c4=O)-c4ccccc4C)C3)c2c1

InChI Key: InChIKey=AXHPLUSKGDVRJM-UHFFFAOYSA-N

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50516847   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
5-hydroxytryptamine receptor 1A


(Homo sapiens (Human))
BDBM50516847
PNG
(CHEMBL4458712)
Show SMILES COc1ccc2[nH]cc(C3CCCN(CCCCn4c(=O)c(c5CCCCn5c4=O)-c4ccccc4C)C3)c2c1 |(45.69,-56.48,;44.67,-55.33,;43.16,-55.64,;42.68,-57.1,;41.17,-57.41,;40.15,-56.25,;38.62,-56.24,;38.16,-54.77,;39.41,-53.88,;39.42,-52.34,;40.76,-51.58,;40.78,-50.04,;39.45,-49.26,;38.12,-50.01,;36.79,-49.24,;35.45,-50,;34.12,-49.22,;32.78,-49.98,;31.45,-49.21,;31.46,-47.67,;32.8,-46.9,;30.13,-46.89,;28.8,-47.66,;27.47,-46.88,;26.14,-47.66,;26.14,-49.2,;27.47,-49.96,;28.79,-49.2,;30.12,-49.97,;30.11,-51.51,;30.14,-45.35,;28.81,-44.58,;28.81,-43.05,;30.15,-42.27,;31.48,-43.05,;31.47,-44.59,;32.8,-45.36,;38.1,-51.56,;40.65,-54.8,;42.15,-54.49,)|
Show InChI InChI=1S/C33H40N4O3/c1-23-10-3-4-12-26(23)31-30-13-5-6-18-36(30)33(39)37(32(31)38)19-8-7-16-35-17-9-11-24(22-35)28-21-34-29-15-14-25(40-2)20-27(28)29/h3-4,10,12,14-15,20-21,24,34H,5-9,11,13,16-19,22H2,1-2H3
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
66n/an/an/an/an/an/an/an/a



Medical University of Warsaw

Curated by ChEMBL


Assay Description
Displacement of [3H]8-OH-DPAT from human 5-HT1A receptor expressed in CHO-K1 cell membranes incubated for 60 mins by microbeta scintillation counting...


Eur J Med Chem 180: 383-397 (2019)


Article DOI: 10.1016/j.ejmech.2019.07.027
More data for this
Ligand-Target Pair
Sodium-dependent serotonin transporter


(Rattus norvegicus (rat))
BDBM50516847
PNG
(CHEMBL4458712)
Show SMILES COc1ccc2[nH]cc(C3CCCN(CCCCn4c(=O)c(c5CCCCn5c4=O)-c4ccccc4C)C3)c2c1 |(45.69,-56.48,;44.67,-55.33,;43.16,-55.64,;42.68,-57.1,;41.17,-57.41,;40.15,-56.25,;38.62,-56.24,;38.16,-54.77,;39.41,-53.88,;39.42,-52.34,;40.76,-51.58,;40.78,-50.04,;39.45,-49.26,;38.12,-50.01,;36.79,-49.24,;35.45,-50,;34.12,-49.22,;32.78,-49.98,;31.45,-49.21,;31.46,-47.67,;32.8,-46.9,;30.13,-46.89,;28.8,-47.66,;27.47,-46.88,;26.14,-47.66,;26.14,-49.2,;27.47,-49.96,;28.79,-49.2,;30.12,-49.97,;30.11,-51.51,;30.14,-45.35,;28.81,-44.58,;28.81,-43.05,;30.15,-42.27,;31.48,-43.05,;31.47,-44.59,;32.8,-45.36,;38.1,-51.56,;40.65,-54.8,;42.15,-54.49,)|
Show InChI InChI=1S/C33H40N4O3/c1-23-10-3-4-12-26(23)31-30-13-5-6-18-36(30)33(39)37(32(31)38)19-8-7-16-35-17-9-11-24(22-35)28-21-34-29-15-14-25(40-2)20-27(28)29/h3-4,10,12,14-15,20-21,24,34H,5-9,11,13,16-19,22H2,1-2H3
PDB

KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
98n/an/an/an/an/an/an/an/a



Medical University of Warsaw

Curated by ChEMBL


Assay Description
Displacement of [3H]-citalopram from SERT in rat cortex tissue incubated for 60 mins by microbeta scintillation counting method


Eur J Med Chem 180: 383-397 (2019)


Article DOI: 10.1016/j.ejmech.2019.07.027
More data for this
Ligand-Target Pair