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BDBM50524273 CHEMBL4447840

SMILES: CCCCCCC(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)[C@@]1(CO)CO1

InChI Key: InChIKey=HPAGFWZVTGGUPS-YZVOILCLSA-N

Data: 2 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 2 hits for monomerid = 50524273   
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
Proteasome subunit beta type-1/beta type-5


(Homo sapiens (Human))
BDBM50524273
PNG
(CHEMBL4447840)
Show SMILES CCCCCCC(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)[C@@]1(CO)CO1 |r|
Show InChI InChI=1S/C19H34N2O5/c1-5-6-7-8-9-16(23)20-14(4)18(25)21-15(10-13(2)3)17(24)19(11-22)12-26-19/h13-15,22H,5-12H2,1-4H3,(H,20,23)(H,21,25)/t14-,15-,19+/m0/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 1.70E+3n/an/an/an/an/an/a



University of Kentucky

Curated by ChEMBL


Assay Description
Inhibition of 20S proteasome beta5 subunit in human RPMI8226 cell lysate using Suc-LLVY-AMC as substrate pretreated for 1 hr followed by substrate ad...


J Med Chem 62: 4444-4455 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01943
More data for this
Ligand-Target Pair
Proteasome subunit beta type-9


(Homo sapiens (Human))
BDBM50524273
PNG
(CHEMBL4447840)
Show SMILES CCCCCCC(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)[C@@]1(CO)CO1 |r|
Show InChI InChI=1S/C19H34N2O5/c1-5-6-7-8-9-16(23)20-14(4)18(25)21-15(10-13(2)3)17(24)19(11-22)12-26-19/h13-15,22H,5-12H2,1-4H3,(H,20,23)(H,21,25)/t14-,15-,19+/m0/s1
PDB

KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
DrugBank
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 36n/an/an/an/an/an/a



University of Kentucky

Curated by ChEMBL


Assay Description
Inhibition of purified human 20S immunoproteasome beta1 subunit using Ac-Pro-Ala-Leu-AMC as substrate pretreated for 1 hr followed by substrate addit...


J Med Chem 62: 4444-4455 (2019)


Article DOI: 10.1021/acs.jmedchem.8b01943
More data for this
Ligand-Target Pair