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BDBM50455105 CHEMBL4218384

SMILES: Cc1cc(no1)C(=O)N[C@H]1C\C=C\CO[C@H]2CCN(C2)C(=O)CC[C@H](NC(=O)[C@H](Cc2ccc(F)cc2)NC1=O)C=O

InChI Key: InChIKey=BYVGYYMLWXAQPH-WXJHPKIDSA-N

Data: 1 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50455105   
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
Genome polyprotein


(Human rhinovirus 14)
BDBM50455105
PNG
(CHEMBL4218384)
Show SMILES Cc1cc(no1)C(=O)N[C@H]1C\C=C\CO[C@H]2CCN(C2)C(=O)CC[C@H](NC(=O)[C@H](Cc2ccc(F)cc2)NC1=O)C=O |r,t:12|
Show InChI InChI=1S/C29H34FN5O7/c1-18-14-25(34-42-18)29(40)32-23-4-2-3-13-41-22-11-12-35(16-22)26(37)10-9-21(17-36)31-28(39)24(33-27(23)38)15-19-5-7-20(30)8-6-19/h2-3,5-8,14,17,21-24H,4,9-13,15-16H2,1H3,(H,31,39)(H,32,40)(H,33,38)/b3-2+/t21-,22-,23-,24-/m0/s1
PDB

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 3n/an/an/an/an/an/a



Novartis Institutes for BioMedical Research

Curated by ChEMBL


Assay Description
Inhibition of Human rhinovirus serotype 14 3C protease preincubated for 1 hr followed by Cys(PT14M)-Ala-Ile-Phe-Gln'Gly-Pro-Asp-Phe(4-NH2)-OH substra...


Bioorg Med Chem Lett 28: 906-909 (2018)


Article DOI: 10.1016/j.bmcl.2018.01.064
BindingDB Entry DOI: 10.7270/Q2TF00Z3
More data for this
Ligand-Target Pair