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BDBM50206067 CHEMBL233228::N-(2-amino-benzothiazol-5-yl)-thiophene-2-carboxamidine

SMILES: NC(=Nc1ccc2sc(N)nc2c1)c1cccs1

InChI Key: InChIKey=PMJLXZQZFUUSKS-UHFFFAOYSA-N

Data: 3 IC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50206067   
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, endothelial


(Homo sapiens (Human))
BDBM50206067
PNG
(CHEMBL233228 | N-(2-amino-benzothiazol-5-yl)-thiop...)
Show SMILES NC(=Nc1ccc2sc(N)nc2c1)c1cccs1
Show InChI InChI=1S/C12H10N4S2/c13-11(10-2-1-5-17-10)15-7-3-4-9-8(6-7)16-12(14)18-9/h1-6H,(H2,13,15)(H2,14,16)
PDB

GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 2.30E+3n/an/an/an/an/an/a



NeurAxon Inc.

Curated by ChEMBL


Assay Description
Inhibition of human endothelial NOS activity


Bioorg Med Chem Lett 17: 2540-4 (2007)


Article DOI: 10.1016/j.bmcl.2007.02.011
BindingDB Entry DOI: 10.7270/Q2WM1F6B
More data for this
Ligand-Target Pair
Nitric oxide synthase, brain


(Homo sapiens (Human))
BDBM50206067
PNG
(CHEMBL233228 | N-(2-amino-benzothiazol-5-yl)-thiop...)
Show SMILES NC(=Nc1ccc2sc(N)nc2c1)c1cccs1
Show InChI InChI=1S/C12H10N4S2/c13-11(10-2-1-5-17-10)15-7-3-4-9-8(6-7)16-12(14)18-9/h1-6H,(H2,13,15)(H2,14,16)
PDB
MMDB

Reactome pathway
KEGG

B.MOAD
DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 200n/an/an/an/an/an/a



NeurAxon Inc.

Curated by ChEMBL


Assay Description
Inhibition of human neuronal NOS activity


Bioorg Med Chem Lett 17: 2540-4 (2007)


Article DOI: 10.1016/j.bmcl.2007.02.011
BindingDB Entry DOI: 10.7270/Q2WM1F6B
More data for this
Ligand-Target Pair
Nitric oxide synthase, inducible


(Homo sapiens (Human))
BDBM50206067
PNG
(CHEMBL233228 | N-(2-amino-benzothiazol-5-yl)-thiop...)
Show SMILES NC(=Nc1ccc2sc(N)nc2c1)c1cccs1
Show InChI InChI=1S/C12H10N4S2/c13-11(10-2-1-5-17-10)15-7-3-4-9-8(6-7)16-12(14)18-9/h1-6H,(H2,13,15)(H2,14,16)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

B.MOAD
DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 7.90E+4n/an/an/an/an/an/a



NeurAxon Inc.

Curated by ChEMBL


Assay Description
Inhibition of human inducible NOS activity


Bioorg Med Chem Lett 17: 2540-4 (2007)


Article DOI: 10.1016/j.bmcl.2007.02.011
BindingDB Entry DOI: 10.7270/Q2WM1F6B
More data for this
Ligand-Target Pair