BDBM50001103 (2-(6-amino-9H-purin-9-yl)ethoxy)methylphosphonic acid::(PMEA)[2-(6-Amino-purin-9-yl)-ethoxymethyl]-phosphonic acid::9-(2-(phosphonomethoxy)ethyl)adenine::9-[(2-phosphonylmethoxy)ethyl]adenine::9-[2-(phosphonomethoxy)ethyl]adenine::9-[2-phosphonomethoxyethyl]adenine::9-[3-(Phosphonomethoxy)ethyl]adenine (PMEA)::ADEFOVIR::CHEMBL484::GS-0393::US10071110, Compound Adefovir::[2-(6-Amino-purin-9-yl)-ethoxymethyl]-phosphonic acid::[2-(6-Amino-purin-9-yl)-ethoxymethyl]-phosphonic acid(PMEA)::[2-(6-amino-9H-purin-9-yl)ethoxy]methylphosphonic acid::{[2-(6-AMINO-9H-PURIN-9-YL)ETHOXY]METHYL}PHOSPHONIC ACID
SMILES Nc1ncnc2n(CCOCP(O)(O)=O)cnc12
InChI Key InChIKey=SUPKOOSCJHTBAH-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 13 hits for monomerid = 50001103
Affinity DataKi: >8.00E+5nMAssay Description:Inhibitory activity against adenosine deaminaseMore data for this Ligand-Target Pair
TargetPhosphoribosyl pyrophosphate synthase-associated protein 2(Human)
Academia Sinica
Curated by ChEMBL
Academia Sinica
Curated by ChEMBL
Affinity DataKi: 3.00E+6nMAssay Description:Inhibitory activity against PRPP synthetaseMore data for this Ligand-Target Pair
TargetHIV-1 protease(Human immunodeficiency virus)
The Regents of The University of California
US Patent
The Regents of The University of California
US Patent
Affinity DataEC50: 1.60E+4nMAssay Description:Preliminary experiments in the inhibition of HIV-1 replication by invention compounds were performed as follows. Drug assays were carried out as prev...More data for this Ligand-Target Pair
Affinity DataEC50: 5.50E+4nMAssay Description:Antiviral assays for HCMV DNA were carried out by DNA hybridization as reported by Dankner, W. M., Scholl, D., Stanat, S. C., Martin, M., Souke, R. L...More data for this Ligand-Target Pair
Affinity DataIC50: 2.80E+4nMAssay Description:TP_TRANSPORTER: inhibition of 6-Carboxyfluorescein uptake in OAT1-expressing CHO cellsMore data for this Ligand-Target Pair
Affinity DataEC50: 4.75E+4nMAssay Description:Inhibition of herpes simplex virus type 1 thymidine kinase (HSV-1 TK-) B2006 strainMore data for this Ligand-Target Pair
Affinity DataEC50: 6.58E+4nMAssay Description:Inhibition of varicella zoster virus thymidine kinase (VZV TK+) YS/R strainMore data for this Ligand-Target Pair
Affinity DataEC50: 3.11E+4nMAssay Description:Inhibitory activity against varicella zoster virus thymidine kinase (VZV TK+) OKA strainMore data for this Ligand-Target Pair
Affinity DataEC50: 1.83E+4nMAssay Description:Inhibitory activity against herpes simplex virus type 1 (HSV-1) thymidine kinase (TK) VMW 1837 strainMore data for this Ligand-Target Pair
Affinity DataEC50: 1.97E+4nMAssay Description:Inhibitory activity against varicella zoster virus thymidine kinase (VZV TK+) YS strainMore data for this Ligand-Target Pair
TargetFibroblast growth factor receptor 1(Human)
The Regents of The University of California
US Patent
The Regents of The University of California
US Patent
Affinity DataEC50: 5.50E+4nMAssay Description:Subconfluent human lung fibroblast cells (MRC-5, American Type Culture Collection, Rockville, Md.) in 24-well plates were treated with drugs diluted ...More data for this Ligand-Target Pair
Affinity DataIC50: 3.20E+6nMAssay Description:Inhibitory concentration against Escherichia coli Pyrophosphate Synthetase (PRPP)More data for this Ligand-Target Pair
Affinity DataEC50: 83nMAssay Description:Inhibition of hepatitis B virus capsid assembly infected in human HepG2.215 cells assessed as reduction in viral DNA replication measured on day 7 by...More data for this Ligand-Target Pair