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BDBM50386551 CHEMBL2048237

SMILES: OP(O)(=O)C(Cc1cncc(c1)-c1ccccc1)P(O)(O)=O

InChI Key: InChIKey=ZJOQFOORZUSDPB-UHFFFAOYSA-N

Data: 2 IC50

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

Found 2 hits for monomerid = 50386551   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Farnesyl diphosphate synthase


(Homo sapiens (Human))
BDBM50386551
PNG
(CHEMBL2048237)
Show SMILES OP(O)(=O)C(Cc1cncc(c1)-c1ccccc1)P(O)(O)=O
Show InChI InChI=1S/C13H15NO6P2/c15-21(16,17)13(22(18,19)20)7-10-6-12(9-14-8-10)11-4-2-1-3-5-11/h1-6,8-9,13H,7H2,(H2,15,16,17)(H2,18,19,20)
PDB
MMDB

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CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 164n/an/an/an/an/an/a



McGill University

Curated by ChEMBL


Assay Description
Inhibition of human recombinant N-terminal-His6 tagged FPPS expressed in Escherichia coli BL21 using [14C]IPP and GPP as substrate incubated for 10 m...


J Med Chem 55: 3201-15 (2012)


Article DOI: 10.1021/jm201657x
BindingDB Entry DOI: 10.7270/Q29024V1
More data for this
Ligand-Target Pair
Farnesyl diphosphate synthase


(Homo sapiens (Human))
BDBM50386551
PNG
(CHEMBL2048237)
Show SMILES OP(O)(=O)C(Cc1cncc(c1)-c1ccccc1)P(O)(O)=O
Show InChI InChI=1S/C13H15NO6P2/c15-21(16,17)13(22(18,19)20)7-10-6-12(9-14-8-10)11-4-2-1-3-5-11/h1-6,8-9,13H,7H2,(H2,15,16,17)(H2,18,19,20)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 164n/an/an/an/an/an/a



McGill University

Curated by ChEMBL


Assay Description
Inhibition of human His6-tagged recombinant FPPS expressed in Escherichia coli BL21(DE3) using GPP and [3H]IPP as substrate incubated for 5 mins prio...


Bioorg Med Chem 20: 5583-91 (2012)


Article DOI: 10.1016/j.bmc.2012.07.019
BindingDB Entry DOI: 10.7270/Q2J67J6M
More data for this
Ligand-Target Pair