null

SMILES Cc1cn([C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)c(=O)n(CC(O)=O)c1=O

InChI Key InChIKey=QRBGBJXBTGHYMS-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50106903   

TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
Instituto de Química Médica (C.S.I.C.)

Curated by ChEMBL
LigandPNGBDBM50106903(CHEMBL3142817 | {3-[4-(tert-Butyl-dimethyl-silanyl...)copy SMILEScopy InChI
Affinity DataIC50: 3.35E+5nMAssay Description:The compound was evaluated for inhibition of HIV-1 mutant GluL38-Lys recombinant reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QC02S2PubMed
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
Instituto de Química Médica (C.S.I.C.)

Curated by ChEMBL
LigandPNGBDBM50106903(CHEMBL3142817 | {3-[4-(tert-Butyl-dimethyl-silanyl...)copy SMILEScopy InChI
Affinity DataEC50:  1.80E+3nMAssay Description:Effective concentration required to inhibit HIV-1 induced cytopathicity by 50% in CEM cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QC02S2PubMed
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
Instituto de Química Médica (C.S.I.C.)

Curated by ChEMBL
LigandPNGBDBM50106903(CHEMBL3142817 | {3-[4-(tert-Butyl-dimethyl-silanyl...)copy SMILEScopy InChI
Affinity DataIC50: 2.07E+5nMAssay Description:The compound was evaluated for inhibition of HIV-1 mutant GluL38-Lys recombinant reverse transcriptaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QC02S2PubMed