null

SMILES Cc1c[nH]c(n1)-c1[nH]c2ccc(Cl)cc2c1S(=O)(=O)c1ccccc1

InChI Key InChIKey=YZEAJCOIBSMIOB-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50230553   

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
TBA

Curated by ChEMBL
LigandPNGBDBM50230553(3-Benzenesulfonyl-5-chloro-2-(5-methyl-1H-imidazol...)copy SMILEScopy InChI
Affinity DataIC50: 9nMAssay Description:Inhibitory activity against K103N mutant of HIV-1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28052KF
TargetReverse transcriptase protein(Human immunodeficiency virus 1)
Merck & Co.

Curated by ChEMBL
LigandPNGBDBM50230553(3-Benzenesulfonyl-5-chloro-2-(5-methyl-1H-imidazol...)copy SMILEScopy InChI
Affinity DataIC50: 9nMAssay Description:Inhibition of HIV NL43 recombinant reverse transcriptase K103N mutant by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76GBMPubMed
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
TBA

Curated by ChEMBL
LigandPNGBDBM50230553(3-Benzenesulfonyl-5-chloro-2-(5-methyl-1H-imidazol...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+5nMAssay Description:Inhibitory activity against K103N mutant of HIV-1 reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28052KF
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandPNGBDBM50230553(3-Benzenesulfonyl-5-chloro-2-(5-methyl-1H-imidazol...)copy SMILEScopy InChI
Affinity DataIC50: 4.70nMAssay Description:Inhibitory activity against HIV-1 RT with poly.rC-oligo.dG template primerMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28052KF