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BDBM27024 2-[(3S,13S,16S,17R,19S)-3-({[(2S)-3,3-dimethyl-1-[methyl(pyridine-2-)sulfonamido]butan-2-yl]carbamoyl}amino)-18,18-dimethyl-2,15-dioxo-1,14-diazatricyclo[14.4.0.0^{17,19}]icosan-13-yl]-2-oxo-N-(prop-2-en-1-yl)acetamide::ketoamide derived macrocyclic inhibitor, 48

SMILES: CN(C[C@@H](NC(=O)N[C@H]1CCCCCCCCC[C@H](NC(=O)[C@@H]2[C@@H]3[C@H](CN2C1=O)C3(C)C)C(=O)C(=O)NCC=C)C(C)(C)C)S(=O)(=O)c1ccccn1

InChI Key: InChIKey=FKDGZQHWVGYKRP-AVWBUSPOSA-N

Data: 1 KI

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 27024   
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
HCV NS3-NS4A Serine Proteinase


(Hepatitis C virus (HCV genotype 1a, isolate H))
BDBM27024
PNG
(2-[(3S,13S,16S,17R,19S)-3-({[(2S)-3,3-dimethyl-1-[...)
Show SMILES CN(C[C@@H](NC(=O)N[C@H]1CCCCCCCCC[C@H](NC(=O)[C@@H]2[C@@H]3[C@H](CN2C1=O)C3(C)C)C(=O)C(=O)NCC=C)C(C)(C)C)S(=O)(=O)c1ccccn1 |r|
Show InChI InChI=1S/C38H59N7O7S/c1-8-21-40-34(48)32(46)26-18-14-12-10-9-11-13-15-19-27(35(49)45-23-25-30(38(25,5)6)31(45)33(47)41-26)42-36(50)43-28(37(2,3)4)24-44(7)53(51,52)29-20-16-17-22-39-29/h8,16-17,20,22,25-28,30-31H,1,9-15,18-19,21,23-24H2,2-7H3,(H,40,48)(H,41,47)(H2,42,43,50)/t25-,26-,27-,28+,30-,31-/m0/s1
PDB
MMDB

UniProtKB/SwissProt

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DrugBank
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PC cid
PC sid
UniChem

Patents

Article
PubMed
7n/an/an/an/an/an/an/an/a



Schering-Plough Research Institute



Assay Description
Proteolytic cleavage of the ester linkage between the Nva (L-norvaline) and the chromophore (PAP) was monitored for change in absorbance at 370 nm. I...


J Med Chem 52: 336-46 (2009)


Article DOI: 10.1021/jm800940u
BindingDB Entry DOI: 10.7270/Q2639N17
More data for this
Ligand-Target Pair