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SMILES: C[C@H]1CN(CCN1Cc1ccc(Cc2ccc3OCOc3c2)cc1)C1CCN(CC1)C(=O)c1c(C)cccc1C

InChI Key: InChIKey=WHOCMELZNZWNHY-SANMLTNESA-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 = 50103084   
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
Muscarinic acetylcholine receptor M2


(Homo sapiens (Human))
BDBM50103084
PNG
(CHEMBL66623 | {4-[(S)-4-(4-Benzo[1,3]dioxol-5-ylme...)
Show SMILES C[C@H]1CN(CCN1Cc1ccc(Cc2ccc3OCOc3c2)cc1)C1CCN(CC1)C(=O)c1c(C)cccc1C
Show InChI InChI=1S/C34H41N3O3/c1-24-5-4-6-25(2)33(24)34(38)35-15-13-30(14-16-35)37-18-17-36(26(3)21-37)22-28-9-7-27(8-10-28)19-29-11-12-31-32(20-29)40-23-39-31/h4-12,20,26,30H,13-19,21-23H2,1-3H3/t26-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
>40n/an/an/an/an/an/an/an/a



Schering-Plough Research Institute

Curated by ChEMBL


Assay Description
Affinity for Muscarinic acetylcholine receptor M2


Bioorg Med Chem Lett 11: 2143-6 (2001)


BindingDB Entry DOI: 10.7270/Q2VQ320K
More data for this
Ligand-Target Pair
C-C chemokine receptor type 5


(Homo sapiens (Human))
BDBM50103084
PNG
(CHEMBL66623 | {4-[(S)-4-(4-Benzo[1,3]dioxol-5-ylme...)
Show SMILES C[C@H]1CN(CCN1Cc1ccc(Cc2ccc3OCOc3c2)cc1)C1CCN(CC1)C(=O)c1c(C)cccc1C
Show InChI InChI=1S/C34H41N3O3/c1-24-5-4-6-25(2)33(24)34(38)35-15-13-30(14-16-35)37-18-17-36(26(3)21-37)22-28-9-7-27(8-10-28)19-29-11-12-31-32(20-29)40-23-39-31/h4-12,20,26,30H,13-19,21-23H2,1-3H3/t26-/m0/s1
PDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
44n/an/an/an/an/an/an/an/a



Schering-Plough Research Institute

Curated by ChEMBL


Assay Description
Inhibition of [125I]-labeled RANTES binding to C-C chemokine receptor type 5


Bioorg Med Chem Lett 11: 2143-6 (2001)


BindingDB Entry DOI: 10.7270/Q2VQ320K
More data for this
Ligand-Target Pair