BDBM50105629 CHEMBL54893::N-(4-chloro-3-(3-methylbut-2-enyloxy)phenyl)-2-methylfuran-3-carbothioamide::N-{4-chloro-3-[(3-methylbut-2-enyl)oxy]phenyl}-2-methylfuran-3-carbothioamide::UC-781

SMILES [#6]\[#6](-[#6])=[#6]/[#6]-[#8]-c1cc(-[#7]-[#6](=S)-c2ccoc2-[#6])ccc1Cl

InChI Key InChIKey=YZHIXLCGPOTQNB-UHFFFAOYSA-N

Data  3 IC50  2 EC50

PDB links: 4 PDB IDs match this monomer.

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Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50105629   

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
Yale University

Curated by ChEMBL
LigandPNGBDBM50105629(CHEMBL54893 | N-(4-chloro-3-(3-methylbut-2-enyloxy...)
Affinity DataEC50:  9nMAssay Description:Effective concentration required against wild type HIV-1 reverse transcriptaseMore data for this Ligand-Target Pair
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
Yale University

Curated by ChEMBL
LigandPNGBDBM50105629(CHEMBL54893 | N-(4-chloro-3-(3-methylbut-2-enyloxy...)
Affinity DataEC50:  24nMAssay Description:Effective concentration required against L100I mutant HIV-1 reverse transcriptase (as per ref 7 in the article)More data for this Ligand-Target Pair
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
Yale University

Curated by ChEMBL
LigandPNGBDBM50105629(CHEMBL54893 | N-(4-chloro-3-(3-methylbut-2-enyloxy...)
Affinity DataIC50:  20.8nMAssay Description:Inhibitory activity against R172A mutant reverse transcriptaseMore data for this Ligand-Target Pair
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
Yale University

Curated by ChEMBL
LigandPNGBDBM50105629(CHEMBL54893 | N-(4-chloro-3-(3-methylbut-2-enyloxy...)
Affinity DataIC50:  23.8nMAssay Description:Inhibitory activity against wild-type HIV-1 reverse transcriptaseMore data for this Ligand-Target Pair
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
Yale University

Curated by ChEMBL
LigandPNGBDBM50105629(CHEMBL54893 | N-(4-chloro-3-(3-methylbut-2-enyloxy...)
Affinity DataIC50:  226nMAssay Description:Inhibitory activity against E138K mutant reverse transcriptaseMore data for this Ligand-Target Pair