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SMILES: Cc1c(Sc2ccccc2[N+]([O-])=O)n(COCCO)c(=O)[nH]c1=O

InChI Key: InChIKey=FHUSIFJQECQBMI-UHFFFAOYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50008305   
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
Reverse transcriptase/RNaseH


(Human immunodeficiency virus 1)
BDBM50008305
PNG
(1-(2-Hydroxy-ethoxymethyl)-5-methyl-6-(2-nitro-phe...)
Show SMILES Cc1c(Sc2ccccc2[N+]([O-])=O)n(COCCO)c(=O)[nH]c1=O
Show InChI InChI=1S/C14H15N3O6S/c1-9-12(19)15-14(20)16(8-23-7-6-18)13(9)24-11-5-3-2-4-10(11)17(21)22/h2-5,18H,6-8H2,1H3,(H,15,19,20)
PDB
MMDB

UniProtKB/TrEMBL

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PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/an/an/a 1.40E+5n/an/an/an/a



Université d'Orléans

Curated by ChEMBL


Assay Description
Inhibitory concentration against HIV-1 reverse transcriptase


J Med Chem 40: 4257-64 (1998)


Article DOI: 10.1021/jm970110p
BindingDB Entry DOI: 10.7270/Q2WS8SC3
More data for this
Ligand-Target Pair