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BDBM50062134 6-Cyclohexylmethyl-piperidin-(2Z)-ylideneamine::CHEMBL269560

SMILES: NC1=NC(CC2CCCCC2)CCC1

InChI Key: InChIKey=GFAXMTCFGXNOQD-UHFFFAOYSA-N

Data: 3 IC50

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   Substructure
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50062134   
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
Nitric oxide synthase, brain


(Homo sapiens (Human))
BDBM50062134
PNG
(6-Cyclohexylmethyl-piperidin-(2Z)-ylideneamine | C...)
Show SMILES NC1=NC(CC2CCCCC2)CCC1 |t:1|
Show InChI InChI=1S/C12H22N2/c13-12-8-4-7-11(14-12)9-10-5-2-1-3-6-10/h10-11H,1-9H2,(H2,13,14)
PDB
MMDB

Reactome pathway
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UniProtKB/SwissProt
UniProtKB/TrEMBL

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antibodypedia
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CHEMBL
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PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 2.80E+4n/an/an/an/an/an/a



G. D. Searle Research and Development

Curated by ChEMBL


Assay Description
Inhibition of human Neuronal nitric oxide synthase


J Med Chem 41: 96-101 (1998)


Article DOI: 10.1021/jm9705059
BindingDB Entry DOI: 10.7270/Q2GM86D2
More data for this
Ligand-Target Pair
Nitric oxide synthase, endothelial


(Homo sapiens (Human))
BDBM50062134
PNG
(6-Cyclohexylmethyl-piperidin-(2Z)-ylideneamine | C...)
Show SMILES NC1=NC(CC2CCCCC2)CCC1 |t:1|
Show InChI InChI=1S/C12H22N2/c13-12-8-4-7-11(14-12)9-10-5-2-1-3-6-10/h10-11H,1-9H2,(H2,13,14)
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 3.75E+5n/an/an/an/an/an/a



G. D. Searle Research and Development

Curated by ChEMBL


Assay Description
inhibition of human endothelial constitutive Endothelial nitric oxide synthase (heNOS)


J Med Chem 41: 96-101 (1998)


Article DOI: 10.1021/jm9705059
BindingDB Entry DOI: 10.7270/Q2GM86D2
More data for this
Ligand-Target Pair
Nitric oxide synthase, inducible


(Homo sapiens (Human))
BDBM50062134
PNG
(6-Cyclohexylmethyl-piperidin-(2Z)-ylideneamine | C...)
Show SMILES NC1=NC(CC2CCCCC2)CCC1 |t:1|
Show InChI InChI=1S/C12H22N2/c13-12-8-4-7-11(14-12)9-10-5-2-1-3-6-10/h10-11H,1-9H2,(H2,13,14)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

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

Patents


Similars

Article
PubMed
n/an/a 5.90E+3n/an/an/an/an/an/a



G. D. Searle Research and Development

Curated by ChEMBL


Assay Description
Inhibition of human Inducible nitric oxide synthase


J Med Chem 41: 96-101 (1998)


Article DOI: 10.1021/jm9705059
BindingDB Entry DOI: 10.7270/Q2GM86D2
More data for this
Ligand-Target Pair