null

SMILES [Na+].COC(=O)P([O-])(=O)OCCCn1c(=O)c(C)cn([C@@H]2O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@]3(OS(=O)(=O)C=C3N)[C@H]2O[Si](C)(C)C(C)(C)C)c1=O

InChI Key InChIKey=VAWQHGBUNNNRMH-UHFFFAOYSA-M

  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 2 hits for monomerid = 50148762   

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

Curated by ChEMBL
LigandPNGBDBM50148762(CHEMBL3142917 | [1-[2',5'-Bis-O-(tert-butyldimethy...)copy SMILEScopy InChI
Affinity DataIC50: 4.70E+3nMAssay Description:Inhibitory concentration against wild type HIV-1 reverse transcriptase (RT) using poly rC.dG as the template or primerMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B857KWPubMed
TargetReverse transcriptase/RNaseH(Human immunodeficiency virus 1)
Instituto de Química Médica (C.S.I.C.)

Curated by ChEMBL
LigandPNGBDBM50148762(CHEMBL3142917 | [1-[2',5'-Bis-O-(tert-butyldimethy...)copy SMILEScopy InChI
Affinity DataIC50: 3.94E+5nMAssay Description:Inhibitory concentration against wild type HIV-1/138Lys reverse transcriptase (RT) using [3H]dGTP as a radioligandMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B857KWPubMed