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BDBM19674 (2S)-N-[(1S)-1-cyclopropyl-2-{[4-(trifluoromethoxy)phenyl]amino}ethyl]-4-(morpholin-4-yl)-4-oxo-2-[4-(trifluoromethyl)phenyl]butanamide::succinamide peptidomimetic, 40

SMILES: FC(F)(F)Oc1ccc(NC[C@@H](NC(=O)[C@@H](CC(=O)N2CCOCC2)c2ccc(cc2)C(F)(F)F)C2CC2)cc1

InChI Key: InChIKey=SCMZSMNINRMDKK-XZOQPEGZSA-N

Data: 3 KI

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 19674   
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 S


(Homo sapiens (Human))
BDBM19674
PNG
((2S)-N-[(1S)-1-cyclopropyl-2-{[4-(trifluoromethoxy...)
Show SMILES FC(F)(F)Oc1ccc(NC[C@@H](NC(=O)[C@@H](CC(=O)N2CCOCC2)c2ccc(cc2)C(F)(F)F)C2CC2)cc1 |r|
Show InChI InChI=1S/C27H29F6N3O4/c28-26(29,30)19-5-3-17(4-6-19)22(15-24(37)36-11-13-39-14-12-36)25(38)35-23(18-1-2-18)16-34-20-7-9-21(10-8-20)40-27(31,32)33/h3-10,18,22-23,34H,1-2,11-16H2,(H,35,38)/t22-,23+/m0/s1
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Article
PubMed
616n/an/an/an/an/an/an/an/a



GNF



Assay Description
The recombinant human cathepsin enzyme was preincubated with inhibitor for 20 minutes prior to addition of substrate. The substrate hydrolysis was mo...


Bioorg Med Chem Lett 17: 2899-903 (2007)


Article DOI: 10.1016/j.bmcl.2007.02.049
BindingDB Entry DOI: 10.7270/Q2K64GBR
More data for this
Ligand-Target Pair
Procathepsin L


(Homo sapiens (Human))
BDBM19674
PNG
((2S)-N-[(1S)-1-cyclopropyl-2-{[4-(trifluoromethoxy...)
Show SMILES FC(F)(F)Oc1ccc(NC[C@@H](NC(=O)[C@@H](CC(=O)N2CCOCC2)c2ccc(cc2)C(F)(F)F)C2CC2)cc1 |r|
Show InChI InChI=1S/C27H29F6N3O4/c28-26(29,30)19-5-3-17(4-6-19)22(15-24(37)36-11-13-39-14-12-36)25(38)35-23(18-1-2-18)16-34-20-7-9-21(10-8-20)40-27(31,32)33/h3-10,18,22-23,34H,1-2,11-16H2,(H,35,38)/t22-,23+/m0/s1
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Article
PubMed
>1.00E+5n/an/an/an/an/an/an/an/a



GNF



Assay Description
The recombinant human cathepsin enzyme was preincubated with inhibitor for 20 minutes prior to addition of substrate. The substrate hydrolysis was mo...


Bioorg Med Chem Lett 17: 2899-903 (2007)


Article DOI: 10.1016/j.bmcl.2007.02.049
BindingDB Entry DOI: 10.7270/Q2K64GBR
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM19674
PNG
((2S)-N-[(1S)-1-cyclopropyl-2-{[4-(trifluoromethoxy...)
Show SMILES FC(F)(F)Oc1ccc(NC[C@@H](NC(=O)[C@@H](CC(=O)N2CCOCC2)c2ccc(cc2)C(F)(F)F)C2CC2)cc1 |r|
Show InChI InChI=1S/C27H29F6N3O4/c28-26(29,30)19-5-3-17(4-6-19)22(15-24(37)36-11-13-39-14-12-36)25(38)35-23(18-1-2-18)16-34-20-7-9-21(10-8-20)40-27(31,32)33/h3-10,18,22-23,34H,1-2,11-16H2,(H,35,38)/t22-,23+/m0/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Patents


Similars

Article
PubMed
>1.00E+5n/an/an/an/an/an/an/an/a



GNF



Assay Description
The recombinant human cathepsin enzyme was preincubated with inhibitor for 20 minutes prior to addition of substrate. The substrate hydrolysis was mo...


Bioorg Med Chem Lett 17: 2899-903 (2007)


Article DOI: 10.1016/j.bmcl.2007.02.049
BindingDB Entry DOI: 10.7270/Q2K64GBR
More data for this
Ligand-Target Pair