BindingDB logo
myBDB logout

BDBM50397135 CHEMBL2169908

SMILES: C[C@@H]1CN(CCN1C(=O)[C@@H]1CCCC[C@H]1C(=O)NC1(CC1)C#N)c1ccc2c(C)noc2c1

InChI Key: InChIKey=MVLVSSYWLGSAFE-MAODMQOUSA-N

Data: 4 IC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50397135   
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
Cathepsin B


(Homo sapiens (Human))
BDBM50397135
PNG
(CHEMBL2169908)
Show SMILES C[C@@H]1CN(CCN1C(=O)[C@@H]1CCCC[C@H]1C(=O)NC1(CC1)C#N)c1ccc2c(C)noc2c1 |r|
Show InChI InChI=1S/C25H31N5O3/c1-16-14-29(18-7-8-19-17(2)28-33-22(19)13-18)11-12-30(16)24(32)21-6-4-3-5-20(21)23(31)27-25(15-26)9-10-25/h7-8,13,16,20-21H,3-6,9-12,14H2,1-2H3,(H,27,31)/t16-,20-,21-/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 603n/an/an/an/an/an/a



AstraZeneca

Curated by ChEMBL


Assay Description
Inhibition of human recombinant cathepsin-B using Z-Arg-Arg-AMC as substrate preincubated for 15 mins measured after 1 hr by QFRET assay


J Med Chem 55: 8827-37 (2012)


Article DOI: 10.1021/jm301119s
BindingDB Entry DOI: 10.7270/Q2HX1DS7
More data for this
Ligand-Target Pair
Procathepsin L


(Homo sapiens (Human))
BDBM50397135
PNG
(CHEMBL2169908)
Show SMILES C[C@@H]1CN(CCN1C(=O)[C@@H]1CCCC[C@H]1C(=O)NC1(CC1)C#N)c1ccc2c(C)noc2c1 |r|
Show InChI InChI=1S/C25H31N5O3/c1-16-14-29(18-7-8-19-17(2)28-33-22(19)13-18)11-12-30(16)24(32)21-6-4-3-5-20(21)23(31)27-25(15-26)9-10-25/h7-8,13,16,20-21H,3-6,9-12,14H2,1-2H3,(H,27,31)/t16-,20-,21-/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a>1.00E+4n/an/an/an/an/an/a



AstraZeneca

Curated by ChEMBL


Assay Description
Inhibition of human recombinant cathepsin-L using Z-Phe-Arg-AMC as substrate preincubated for 15 mins measured after 1 hr by QFRET assay


J Med Chem 55: 8827-37 (2012)


Article DOI: 10.1021/jm301119s
BindingDB Entry DOI: 10.7270/Q2HX1DS7
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50397135
PNG
(CHEMBL2169908)
Show SMILES C[C@@H]1CN(CCN1C(=O)[C@@H]1CCCC[C@H]1C(=O)NC1(CC1)C#N)c1ccc2c(C)noc2c1 |r|
Show InChI InChI=1S/C25H31N5O3/c1-16-14-29(18-7-8-19-17(2)28-33-22(19)13-18)11-12-30(16)24(32)21-6-4-3-5-20(21)23(31)27-25(15-26)9-10-25/h7-8,13,16,20-21H,3-6,9-12,14H2,1-2H3,(H,27,31)/t16-,20-,21-/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 16n/an/an/an/an/an/a



AstraZeneca

Curated by ChEMBL


Assay Description
Inhibition of human recombinant cathepsin-k using Z-Phe-Arg-AMC as substrate preincubated for 15 mins measured after 1 hr by QFRET assay


J Med Chem 55: 8827-37 (2012)


Article DOI: 10.1021/jm301119s
BindingDB Entry DOI: 10.7270/Q2HX1DS7
More data for this
Ligand-Target Pair
Cathepsin S


(Homo sapiens (Human))
BDBM50397135
PNG
(CHEMBL2169908)
Show SMILES C[C@@H]1CN(CCN1C(=O)[C@@H]1CCCC[C@H]1C(=O)NC1(CC1)C#N)c1ccc2c(C)noc2c1 |r|
Show InChI InChI=1S/C25H31N5O3/c1-16-14-29(18-7-8-19-17(2)28-33-22(19)13-18)11-12-30(16)24(32)21-6-4-3-5-20(21)23(31)27-25(15-26)9-10-25/h7-8,13,16,20-21H,3-6,9-12,14H2,1-2H3,(H,27,31)/t16-,20-,21-/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 807n/an/an/an/an/an/a



AstraZeneca

Curated by ChEMBL


Assay Description
Inhibition of human recombinant cathepsin-S using Z-Val-Val-Arg-AMC as substrate preincubated for 15 mins measured after 1 hr by QFRET assay


J Med Chem 55: 8827-37 (2012)


Article DOI: 10.1021/jm301119s
BindingDB Entry DOI: 10.7270/Q2HX1DS7
More data for this
Ligand-Target Pair