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Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Thioredoxin reductase 1, cytoplasmic' and Ligand = 'BDBM50236320'   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Thioredoxin reductase 1, cytoplasmic


(Rattus norvegicus)
BDBM50236320
PNG
(CHEMBL4091106)
Show SMILES Cl.NC1=NC2(CCCC2)N(OCCCCOc2cccc(c2)C(=O)\C=C\c2ccccc2)C(N)=N1 |c:35,t:1|
Show InChI InChI=1S/C26H31N5O3/c27-24-29-25(28)31(26(30-24)15-4-5-16-26)34-18-7-6-17-33-22-12-8-11-21(19-22)23(32)14-13-20-9-2-1-3-10-20/h1-3,8-14,19H,4-7,15-18H2,(H4,27,28,29,30)/b14-13+
PDB
MMDB

KEGG

UniProtKB/SwissProt

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

Similars

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



National University of Singapore

Curated by ChEMBL


Assay Description
Inhibition of recombinant rat liver thioredoxin reductase after 60 mins by DTNB reduction assay


J Med Chem 60: 1734-1745 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01253
BindingDB Entry DOI: 10.7270/Q2FJ2K2V
More data for this
Ligand-Target Pair
Thioredoxin reductase 1, cytoplasmic


(Rattus norvegicus)
BDBM50236320
PNG
(CHEMBL4091106)
Show SMILES Cl.NC1=NC2(CCCC2)N(OCCCCOc2cccc(c2)C(=O)\C=C\c2ccccc2)C(N)=N1 |c:35,t:1|
Show InChI InChI=1S/C26H31N5O3/c27-24-29-25(28)31(26(30-24)15-4-5-16-26)34-18-7-6-17-33-22-12-8-11-21(19-22)23(32)14-13-20-9-2-1-3-10-20/h1-3,8-14,19H,4-7,15-18H2,(H4,27,28,29,30)/b14-13+
PDB
MMDB

KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 9.20E+3n/an/an/an/an/an/a



National University of Singapore

Curated by ChEMBL


Assay Description
Affinity towards human M1 receptor expressed in CHO cells using [3H]QNB as radioligand


J Med Chem 60: 1734-1745 (2017)


Article DOI: 10.1021/acs.jmedchem.6b01253
BindingDB Entry DOI: 10.7270/Q2FJ2K2V
More data for this
Ligand-Target Pair