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SMILES: CN(C[C@H]1Cc2c(CN1)cccc2N[C@H]1CC[C@H](N)CC1)[C@H]1CCCc2cccnc12

InChI Key:

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 3 hits for monomerid = 50579575   
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
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50579575
PNG
(CHEMBL4864332)
Show SMILES CN(C[C@H]1Cc2c(CN1)cccc2N[C@H]1CC[C@H](N)CC1)[C@H]1CCCc2cccnc12 |r,wU:3.2,17.19,wD:21.23,14.15,(6.81,-26.81,;5.48,-26.03,;4.14,-26.8,;4.14,-28.34,;5.47,-29.11,;5.46,-30.65,;4.12,-31.41,;2.79,-30.64,;2.8,-29.1,;4.11,-32.95,;5.44,-33.73,;6.78,-32.96,;6.78,-31.42,;8.12,-30.66,;9.45,-31.43,;9.45,-32.97,;10.77,-33.74,;12.11,-32.98,;13.44,-33.76,;12.12,-31.44,;10.79,-30.66,;5.48,-24.49,;6.83,-23.72,;6.83,-22.17,;5.49,-21.38,;4.15,-22.16,;2.81,-21.4,;1.48,-22.17,;1.48,-23.72,;2.81,-24.49,;4.14,-23.72,)|
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 755n/an/an/an/an/an/a


TBA

Assay Description
Antagonist activity at CXCR4 receptor in human CCRF-CEM cells assessed as inhibition of SDF-1alpha-induced calcium release preincubated for 25 mins f...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00449
BindingDB Entry DOI: 10.7270/Q23N277W
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM50579575
PNG
(CHEMBL4864332)
Show SMILES CN(C[C@H]1Cc2c(CN1)cccc2N[C@H]1CC[C@H](N)CC1)[C@H]1CCCc2cccnc12 |r,wU:3.2,17.19,wD:21.23,14.15,(6.81,-26.81,;5.48,-26.03,;4.14,-26.8,;4.14,-28.34,;5.47,-29.11,;5.46,-30.65,;4.12,-31.41,;2.79,-30.64,;2.8,-29.1,;4.11,-32.95,;5.44,-33.73,;6.78,-32.96,;6.78,-31.42,;8.12,-30.66,;9.45,-31.43,;9.45,-32.97,;10.77,-33.74,;12.11,-32.98,;13.44,-33.76,;12.12,-31.44,;10.79,-30.66,;5.48,-24.49,;6.83,-23.72,;6.83,-22.17,;5.49,-21.38,;4.15,-22.16,;2.81,-21.4,;1.48,-22.17,;1.48,-23.72,;2.81,-24.49,;4.14,-23.72,)|
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a>2.00E+4n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of CYP3A4 (unknown origin)


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00449
BindingDB Entry DOI: 10.7270/Q23N277W
More data for this
Ligand-Target Pair
Cytochrome P450 2D6


(Homo sapiens (Human))
BDBM50579575
PNG
(CHEMBL4864332)
Show SMILES CN(C[C@H]1Cc2c(CN1)cccc2N[C@H]1CC[C@H](N)CC1)[C@H]1CCCc2cccnc12 |r,wU:3.2,17.19,wD:21.23,14.15,(6.81,-26.81,;5.48,-26.03,;4.14,-26.8,;4.14,-28.34,;5.47,-29.11,;5.46,-30.65,;4.12,-31.41,;2.79,-30.64,;2.8,-29.1,;4.11,-32.95,;5.44,-33.73,;6.78,-32.96,;6.78,-31.42,;8.12,-30.66,;9.45,-31.43,;9.45,-32.97,;10.77,-33.74,;12.11,-32.98,;13.44,-33.76,;12.12,-31.44,;10.79,-30.66,;5.48,-24.49,;6.83,-23.72,;6.83,-22.17,;5.49,-21.38,;4.15,-22.16,;2.81,-21.4,;1.48,-22.17,;1.48,-23.72,;2.81,-24.49,;4.14,-23.72,)|
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a>2.00E+4n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of human recombinant CYP2D6 expressed in insect cells using AMMC as substrate preincubated for 30 mins followed by NADPH regenerating syst...


Citation and Details

Article DOI: 10.1021/acsmedchemlett.1c00449
BindingDB Entry DOI: 10.7270/Q23N277W
More data for this
Ligand-Target Pair