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Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Renin' and Ligand = 'BDBM50365568'   
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
Renin


(Homo sapiens (Human))
BDBM50365568
PNG
(CHEMBL1957795)
Show SMILES CC(=O)NCCc1ccccc1-c1ccc([C@H]2CNCC[C@]2(O)c2ccc(F)c(F)c2)c(C)c1 |r|
Show InChI InChI=1S/C28H30F2N2O2/c1-18-15-21(24-6-4-3-5-20(24)11-13-32-19(2)33)7-9-23(18)25-17-31-14-12-28(25,34)22-8-10-26(29)27(30)16-22/h3-10,15-16,25,31,34H,11-14,17H2,1-2H3,(H,32,33)/t25-,28+/m1/s1
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Article
PubMed
n/an/a 0.5n/an/an/an/an/an/a



Merck Frosst Center for Therapeutic Research

Curated by ChEMBL


Assay Description
Inhibition of human recombinant renin using DNP-Lys-His-Pro-Phe-His-Leu-Val-Ile-His-D,L-Amp as substrate after 3 hrs by fluorimetry


Bioorg Med Chem Lett 22: 1953-7 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.044
BindingDB Entry DOI: 10.7270/Q22F7NXB
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50365568
PNG
(CHEMBL1957795)
Show SMILES CC(=O)NCCc1ccccc1-c1ccc([C@H]2CNCC[C@]2(O)c2ccc(F)c(F)c2)c(C)c1 |r|
Show InChI InChI=1S/C28H30F2N2O2/c1-18-15-21(24-6-4-3-5-20(24)11-13-32-19(2)33)7-9-23(18)25-17-31-14-12-28(25,34)22-8-10-26(29)27(30)16-22/h3-10,15-16,25,31,34H,11-14,17H2,1-2H3,(H,32,33)/t25-,28+/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Patents

Article
PubMed
n/an/a 4.95n/an/an/an/an/an/a



Merck Frosst Center for Therapeutic Research

Curated by ChEMBL


Assay Description
Inhibition of human recombinant renin using QXL520-Lys-His-Pro-Phe-His-Leu-Val-Ile-His-Lys-(5-FAM) as substrate preincubated for 10 mins prior to sub...


Bioorg Med Chem Lett 22: 1953-7 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.044
BindingDB Entry DOI: 10.7270/Q22F7NXB
More data for this
Ligand-Target Pair