null

SMILES CCOC(=O)C(=O)CC(=O)C=Cc1cccn1Cc1ccc(F)cc1

InChI Key InChIKey=JYAXIESQUNGIMN-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 9 hits for monomerid = 50142734   

TargetIntegrase(Human immunodeficiency virus 1)
Università degli Studi di Roma 'La Sapienza'

Curated by ChEMBL
LigandPNGBDBM50142734((E)-6-[1-(4-Fluoro-benzyl)-1H-pyrrol-2-yl]-2,4-dio...)copy SMILEScopy InChI
Affinity DataIC50: 9.50E+4nMAssay Description:Inhibitory activity against HIV-1 integrase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B56J61PubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
University of Cagliari

Curated by ChEMBL
LigandPNGBDBM50142734((E)-6-[1-(4-Fluoro-benzyl)-1H-pyrrol-2-yl]-2,4-dio...)copy SMILEScopy InChI
Affinity DataIC50: 9.20E+3nMAssay Description:Inhibition of HIV1 reverse transcriptase Lys103Asn mutant-associated DNA polymerase-independent RNase H activity after 1 hrMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BG2QPZPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
University of Cagliari

Curated by ChEMBL
LigandPNGBDBM50142734((E)-6-[1-(4-Fluoro-benzyl)-1H-pyrrol-2-yl]-2,4-dio...)copy SMILEScopy InChI
Affinity DataIC50: 9.60E+3nMAssay Description:Inhibition of HIV1 reverse transcriptase Tyr181Cys mutant-associated DNA polymerase-independent RNase H activity after 1 hrMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BG2QPZPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
University of Cagliari

Curated by ChEMBL
LigandPNGBDBM50142734((E)-6-[1-(4-Fluoro-benzyl)-1H-pyrrol-2-yl]-2,4-dio...)copy SMILEScopy InChI
Affinity DataIC50: 1.01E+4nMAssay Description:Inhibition of HIV1 reverse transcriptase-associated DNA polymerase-independent RNase H activity after 1 hrMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BG2QPZPubMed
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
University of Cagliari

Curated by ChEMBL
LigandPNGBDBM50142734((E)-6-[1-(4-Fluoro-benzyl)-1H-pyrrol-2-yl]-2,4-dio...)copy SMILEScopy InChI
Affinity DataIC50: 1.12E+4nMAssay Description:Inhibition of His6-tagged HIV-1 reverse transcriptase RNase H using 5'-GTTTTCTTTTCCCCCCTGAC-3'-Fluorescein-labeled RNA/5'-CAAAAGAAAAGGGGGGACUG-3'-Dab...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NK3JDHPubMed
TargetIntegrase(Human immunodeficiency virus 1)
"Sapienza" Universit£ di Roma

Curated by ChEMBL
LigandPNGBDBM50142734((E)-6-[1-(4-Fluoro-benzyl)-1H-pyrrol-2-yl]-2,4-dio...)copy SMILEScopy InChI
Affinity DataIC50: 9.80E+4nMAssay Description:Inhibition of strand transfer activity of recombinant HIV1 integrase using 5'-end-labeled 21-mer double-stranded DNA as substrate after 60 mins by el...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BZ690CPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
University of Cagliari

Curated by ChEMBL
LigandPNGBDBM50142734((E)-6-[1-(4-Fluoro-benzyl)-1H-pyrrol-2-yl]-2,4-dio...)copy SMILEScopy InChI
Affinity DataIC50: 8.00E+3nMAssay Description:Inhibition of RNase H activity of recombinant HIV1 reverse transcriptase using poly(dC)-[3H]poly(rG) as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BZ690CPubMed
TargetReverse transcriptase(Human immunodeficiency virus 1)
University of Cagliari

Curated by ChEMBL
LigandPNGBDBM50142734((E)-6-[1-(4-Fluoro-benzyl)-1H-pyrrol-2-yl]-2,4-dio...)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+4nMAssay Description:Inhibition of HIV1 reverse transcriptase RNase H activityMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1PRSPubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università degli Studi di Roma 'La Sapienza'

Curated by ChEMBL
LigandPNGBDBM50142734((E)-6-[1-(4-Fluoro-benzyl)-1H-pyrrol-2-yl]-2,4-dio...)copy SMILEScopy InChI
Affinity DataIC50: 8.70E+4nMAssay Description:Inhibitory activity against HIV-1 integrase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B56J61PubMed