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BDBM50451337 CHEMBL4204601

SMILES: [H][C@]1(CCCN(C1)C(=O)[C@@H]1CC[C@H](N)C1)C(O)(CCCNC(=O)OC)c1cccc(F)c1-c1cccc(CC)c1

InChI Key: InChIKey=OHJSSMZLPUXQMI-RLWNMZDESA-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 = 50451337   
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
Renin


(Homo sapiens (Human))
BDBM50451337
PNG
(CHEMBL4204601)
Show SMILES [H][C@]1(CCCN(C1)C(=O)[C@@H]1CC[C@H](N)C1)C(O)(CCCNC(=O)OC)c1cccc(F)c1-c1cccc(CC)c1 |r|
Show InChI InChI=1S/C31H42FN3O4/c1-3-21-8-4-9-22(18-21)28-26(11-5-12-27(28)32)31(38,15-7-16-34-30(37)39-2)24-10-6-17-35(20-24)29(36)23-13-14-25(33)19-23/h4-5,8-9,11-12,18,23-25,38H,3,6-7,10,13-17,19-20,33H2,1-2H3,(H,34,37)/t23-,24-,25+,31?/m1/s1
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PC sid
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n/an/a 3.30n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibition of renin in human plasma using angiotensinogen as substrate measured for 90 mins by [125I]-angiotensin based radioimmunoassay


Bioorg Med Chem Lett 27: 4838-4843 (2017)


Article DOI: 10.1016/j.bmcl.2017.09.046
BindingDB Entry DOI: 10.7270/Q2Z60RN0
More data for this
Ligand-Target Pair
Renin


(Homo sapiens (Human))
BDBM50451337
PNG
(CHEMBL4204601)
Show SMILES [H][C@]1(CCCN(C1)C(=O)[C@@H]1CC[C@H](N)C1)C(O)(CCCNC(=O)OC)c1cccc(F)c1-c1cccc(CC)c1 |r|
Show InChI InChI=1S/C31H42FN3O4/c1-3-21-8-4-9-22(18-21)28-26(11-5-12-27(28)32)31(38,15-7-16-34-30(37)39-2)24-10-6-17-35(20-24)29(36)23-13-14-25(33)19-23/h4-5,8-9,11-12,18,23-25,38H,3,6-7,10,13-17,19-20,33H2,1-2H3,(H,34,37)/t23-,24-,25+,31?/m1/s1
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PC cid
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UniChem
Article
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n/an/a 0.600n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibition of trypsin-activated recombinant human Fc-tagged renin expressed in BacMam virus infected HEK-F cells using Arg-Glu-Lys(5-Fam)-Ile-His-Pro...


Bioorg Med Chem Lett 27: 4838-4843 (2017)


Article DOI: 10.1016/j.bmcl.2017.09.046
BindingDB Entry DOI: 10.7270/Q2Z60RN0
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM50451337
PNG
(CHEMBL4204601)
Show SMILES [H][C@]1(CCCN(C1)C(=O)[C@@H]1CC[C@H](N)C1)C(O)(CCCNC(=O)OC)c1cccc(F)c1-c1cccc(CC)c1 |r|
Show InChI InChI=1S/C31H42FN3O4/c1-3-21-8-4-9-22(18-21)28-26(11-5-12-27(28)32)31(38,15-7-16-34-30(37)39-2)24-10-6-17-35(20-24)29(36)23-13-14-25(33)19-23/h4-5,8-9,11-12,18,23-25,38H,3,6-7,10,13-17,19-20,33H2,1-2H3,(H,34,37)/t23-,24-,25+,31?/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 90n/an/an/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
Inhibition of human CYP3A4 expressed in Escherichia coli co-expressing CYP-reductase using diethoxyfluorescein as substrate measured after 10 mins by...


Bioorg Med Chem Lett 27: 4838-4843 (2017)


Article DOI: 10.1016/j.bmcl.2017.09.046
BindingDB Entry DOI: 10.7270/Q2Z60RN0
More data for this
Ligand-Target Pair