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BDBM50135829 (Bis-phosphono-methyl)-nonyl-ammonium::(Nonylamino-phosphono-methyl)-phosphonic acid::(nonylamino)methylenediphosphonic acid::CHEMBL417549::N-nonyl-aminomethylene-1,1-bisphosphonate

SMILES: CCCCCCCCCN=C(P(O)(O)O)P(O)(O)=O

InChI Key: InChIKey=IKCHRDRLWTXZKU-UHFFFAOYSA-N

Data: 1 KI  4 IC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50135829   
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))
BDBM50135829
PNG
((Bis-phosphono-methyl)-nonyl-ammonium | (Nonylamin...)
Show SMILES CCCCCCCCCN=C(P(O)(O)O)P(O)(O)=O |w:9.8|
Show InChI InChI=1S/C10H25NO6P2/c1-2-3-4-5-6-7-8-9-11-10(18(12,13)14)19(15,16)17/h12-14,18H,2-9H2,1H3,(H2,15,16,17)
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Article
PubMed
86n/an/an/an/an/an/an/an/a



University of Illinois at Urbana-Champaign

Curated by ChEMBL


Assay Description
Binding affinity towards farnesyl Pyrophosphate Synthase using [14C]- isopentenyl pyrophosphate as radioligand


J Med Chem 46: 5171-83 (2003)


Article DOI: 10.1021/jm0302344
BindingDB Entry DOI: 10.7270/Q24M93Z8
More data for this
Ligand-Target Pair
Farnesyl diphosphate synthase


(Homo sapiens (Human))
BDBM50135829
PNG
((Bis-phosphono-methyl)-nonyl-ammonium | (Nonylamin...)
Show SMILES CCCCCCCCCN=C(P(O)(O)O)P(O)(O)=O |w:9.8|
Show InChI InChI=1S/C10H25NO6P2/c1-2-3-4-5-6-7-8-9-11-10(18(12,13)14)19(15,16)17/h12-14,18H,2-9H2,1H3,(H2,15,16,17)
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Article
PubMed
n/an/a 891n/an/an/an/an/an/a



University of Illinois at Urbana-Champaign

Curated by ChEMBL


Assay Description
Inhibitory activity against farnesyl Pyrophosphate Synthase expressed as #NAME? (M)


J Med Chem 46: 5171-83 (2003)


Article DOI: 10.1021/jm0302344
BindingDB Entry DOI: 10.7270/Q24M93Z8
More data for this
Ligand-Target Pair
Vacuolar-type proton translocating pyrophosphatase 1


(Trypanosoma brucei)
BDBM50135829
PNG
((Bis-phosphono-methyl)-nonyl-ammonium | (Nonylamin...)
Show SMILES CCCCCCCCCN=C(P(O)(O)O)P(O)(O)=O |w:9.8|
Show InChI InChI=1S/C10H25NO6P2/c1-2-3-4-5-6-7-8-9-11-10(18(12,13)14)19(15,16)17/h12-14,18H,2-9H2,1H3,(H2,15,16,17)
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Article
PubMed
n/an/a 5.67E+4n/an/an/an/an/an/a



University of Illinois at Urbana-Champaign

Curated by ChEMBL


Assay Description
Inhibition of recombinant Trypanosoma brucei soluble vacuolar pyrophosphatase expressed in Escherichia coli


J Med Chem 48: 6128-39 (2005)


Article DOI: 10.1021/jm058220g
BindingDB Entry DOI: 10.7270/Q2F47PX2
More data for this
Ligand-Target Pair
Farnesyl diphosphate synthase


(Homo sapiens (Human))
BDBM50135829
PNG
((Bis-phosphono-methyl)-nonyl-ammonium | (Nonylamin...)
Show SMILES CCCCCCCCCN=C(P(O)(O)O)P(O)(O)=O |w:9.8|
Show InChI InChI=1S/C10H25NO6P2/c1-2-3-4-5-6-7-8-9-11-10(18(12,13)14)19(15,16)17/h12-14,18H,2-9H2,1H3,(H2,15,16,17)
PDB
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Article
PubMed
n/an/a 900n/an/an/an/an/an/a



University of Illinois at Urbana-Champaign

Curated by ChEMBL


Assay Description
Inhibitory activity against farnesyl Pyrophosphate Synthase was determined


J Med Chem 46: 5171-83 (2003)


Article DOI: 10.1021/jm0302344
BindingDB Entry DOI: 10.7270/Q24M93Z8
More data for this
Ligand-Target Pair
Farnesyl pyrophosphate synthase


(Plasmodium falciparum (isolate 3D7))
BDBM50135829
PNG
((Bis-phosphono-methyl)-nonyl-ammonium | (Nonylamin...)
Show SMILES CCCCCCCCCN=C(P(O)(O)O)P(O)(O)=O |w:9.8|
Show InChI InChI=1S/C10H25NO6P2/c1-2-3-4-5-6-7-8-9-11-10(18(12,13)14)19(15,16)17/h12-14,18H,2-9H2,1H3,(H2,15,16,17)
PDB

KEGG

UniProtKB/TrEMBL

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 900n/an/an/an/an/an/a



University of Illinois at Urbana-Champaign

Curated by ChEMBL


Assay Description
Inhibitory activity against Leishmania major Farnesyl diphosphate synthase


J Med Chem 47: 175-87 (2003)


Article DOI: 10.1021/jm030084x
BindingDB Entry DOI: 10.7270/Q2FN15N5
More data for this
Ligand-Target Pair