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Compile Data Set for Download or QSAR

Found 16 hits with Last Name = 'mckenna' and Initial = 'ce'   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Farnesyl pyrophosphate synthase


(Homo sapiens (Human))
BDBM25308
PNG
((1-hydroxy-2-{imidazo[1,2-a]pyridin-3-yl}-1-phosph...)
Show SMILES OC(Cc1cnc2ccccn12)(P(O)(O)=O)P(O)(O)=O
Show InChI InChI=1S/C9H12N2O7P2/c12-9(19(13,14)15,20(16,17)18)5-7-6-10-8-3-1-2-4-11(7)8/h1-4,6,12H,5H2,(H2,13,14,15)(H2,16,17,18)
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n/an/a 3n/an/an/an/an/an/a



University of Southern California

Curated by ChEMBL


Assay Description
Inhibition of human FPPS after 10 mins using [14C]IPP as substrate by liquid scintillation counting


J Med Chem 53: 3454-64 (2010)

Checked by Author
Article DOI: 10.1021/jm900232u
BindingDB Entry DOI: 10.7270/Q21837FJ
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Farnesyl pyrophosphate synthase


(Homo sapiens (Human))
BDBM12576
PNG
(Bisphosphonate 1 | CHEMBL923 | JMC515594 Compound ...)
Show SMILES OC(Cc1cccnc1)(P(O)(O)=O)P(O)(O)=O
Show InChI InChI=1S/C7H11NO7P2/c9-7(16(10,11)12,17(13,14)15)4-6-2-1-3-8-5-6/h1-3,5,9H,4H2,(H2,10,11,12)(H2,13,14,15)
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n/an/a 5.70n/an/an/an/an/an/a



University of Southern California

Curated by ChEMBL


Assay Description
Inhibition of human FPPS


Bioorg Med Chem Lett 18: 2878-82 (2008)


Article DOI: 10.1016/j.bmcl.2008.03.088
BindingDB Entry DOI: 10.7270/Q2WM1F9P
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Farnesyl pyrophosphate synthase


(Homo sapiens (Human))
BDBM50225999
PNG
(1-fluoro-2-(3-pyridinyl)-ethylidene-1,1-bisphospho...)
Show SMILES OP(O)(=O)C(F)(Cc1cccnc1)P(O)(O)=O
Show InChI InChI=1S/C7H10FNO6P2/c8-7(16(10,11)12,17(13,14)15)4-6-2-1-3-9-5-6/h1-3,5H,4H2,(H2,10,11,12)(H2,13,14,15)
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n/an/a 16.4n/an/an/an/an/an/a



University of Southern California

Curated by ChEMBL


Assay Description
Inhibition of human cloned FPPS expressed in Escherichia col BL2 (DE3)


J Med Chem 50: 5967-75 (2007)


Article DOI: 10.1021/jm0702884
BindingDB Entry DOI: 10.7270/Q27944DF
More data for this
Ligand-Target Pair
Farnesyl pyrophosphate synthase


(Homo sapiens (Human))
BDBM50138725
PNG
((1-phosphono-2-pyridin-3-yl-ethyl)-phosphonic acid...)
Show SMILES OP(O)(=O)C(Cc1cccnc1)P(O)(O)=O
Show InChI InChI=1S/C7H11NO6P2/c9-15(10,11)7(16(12,13)14)4-6-2-1-3-8-5-6/h1-3,5,7H,4H2,(H2,9,10,11)(H2,12,13,14)
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n/an/a 34.2n/an/an/an/an/an/a



University of Southern California

Curated by ChEMBL


Assay Description
Inhibition of human cloned FPPS expressed in Escherichia col BL2 (DE3)


J Med Chem 50: 5967-75 (2007)


Article DOI: 10.1021/jm0702884
BindingDB Entry DOI: 10.7270/Q27944DF
More data for this
Ligand-Target Pair
Farnesyl pyrophosphate synthase


(Homo sapiens (Human))
BDBM50225995
PNG
(1-chloro-2-(3-pyridinyl)-ethylidene-1,1-bisphospho...)
Show SMILES OP(O)(=O)C(Cl)(Cc1cccnc1)P(O)(O)=O
Show InChI InChI=1S/C7H10ClNO6P2/c8-7(16(10,11)12,17(13,14)15)4-6-2-1-3-9-5-6/h1-3,5H,4H2,(H2,10,11,12)(H2,13,14,15)
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n/an/a 94.6n/an/an/an/an/an/a



University of Southern California

Curated by ChEMBL


Assay Description
Inhibition of human cloned FPPS expressed in Escherichia col BL2 (DE3)


J Med Chem 50: 5967-75 (2007)


Article DOI: 10.1021/jm0702884
BindingDB Entry DOI: 10.7270/Q27944DF
More data for this
Ligand-Target Pair
Farnesyl pyrophosphate synthase


(Homo sapiens (Human))
BDBM50225997
PNG
(1-bromo-2-(3-pyridinyl)-ethylidene-1,1-bisphosphon...)
Show SMILES OP(O)(=O)C(Br)(Cc1cccnc1)P(O)(O)=O
Show InChI InChI=1S/C7H10BrNO6P2/c8-7(16(10,11)12,17(13,14)15)4-6-2-1-3-9-5-6/h1-3,5H,4H2,(H2,10,11,12)(H2,13,14,15)
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n/an/a 340n/an/an/an/an/an/a



University of Southern California

Curated by ChEMBL


Assay Description
Inhibition of human cloned FPPS expressed in Escherichia col BL2 (DE3)


J Med Chem 50: 5967-75 (2007)


Article DOI: 10.1021/jm0702884
BindingDB Entry DOI: 10.7270/Q27944DF
More data for this
Ligand-Target Pair
Farnesyl pyrophosphate synthase


(Homo sapiens (Human))
BDBM50377836
PNG
(CHEMBL317573)
Show SMILES OC(C1CCc2ccncc12)(P(O)(O)=O)P(O)(O)=O
Show InChI InChI=1S/C9H13NO7P2/c11-9(18(12,13)14,19(15,16)17)8-2-1-6-3-4-10-5-7(6)8/h3-5,8,11H,1-2H2,(H2,12,13,14)(H2,15,16,17)
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n/an/a 630n/an/an/an/an/an/a



University of Southern California

Curated by ChEMBL


Assay Description
Inhibition of human FPPS


Bioorg Med Chem Lett 18: 2878-82 (2008)


Article DOI: 10.1016/j.bmcl.2008.03.088
BindingDB Entry DOI: 10.7270/Q2WM1F9P
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Geranylgeranyl pyrophosphate synthase


(Homo sapiens (Human))
BDBM25308
PNG
((1-hydroxy-2-{imidazo[1,2-a]pyridin-3-yl}-1-phosph...)
Show SMILES OC(Cc1cnc2ccccn12)(P(O)(O)=O)P(O)(O)=O
Show InChI InChI=1S/C9H12N2O7P2/c12-9(19(13,14)15,20(16,17)18)5-7-6-10-8-3-1-2-4-11(7)8/h1-4,6,12H,5H2,(H2,13,14,15)(H2,16,17,18)
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n/an/a 670n/an/an/an/an/an/a



University of Southern California

Curated by ChEMBL


Assay Description
Inhibition of GGPPS after 10 mins using [14C]IPP as substrate by liquid scintillation counting


J Med Chem 53: 3454-64 (2010)

Checked by Author
Article DOI: 10.1021/jm900232u
BindingDB Entry DOI: 10.7270/Q21837FJ
More data for this
Ligand-Target Pair
Farnesyl pyrophosphate synthase


(Homo sapiens (Human))
BDBM50318032
PNG
((+)-2-hydroxy-3-imidazo[1,2-a]pyridin-3-yl-2-phosp...)
Show SMILES OC(=O)C(O)(Cc1cnc2ccccn12)P(O)(O)=O
Show InChI InChI=1S/C10H11N2O6P/c13-9(14)10(15,19(16,17)18)5-7-6-11-8-3-1-2-4-12(7)8/h1-4,6,15H,5H2,(H,13,14)(H2,16,17,18)
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of Southern California

Curated by ChEMBL


Assay Description
Inhibition of human FPPS after 10 mins using [14C]IPP as substrate by liquid scintillation counting


J Med Chem 53: 3454-64 (2010)

Checked by Author
Article DOI: 10.1021/jm900232u
BindingDB Entry DOI: 10.7270/Q21837FJ
More data for this
Ligand-Target Pair
Farnesyl pyrophosphate synthase


(Homo sapiens (Human))
BDBM50226001
PNG
(2-bromo-3-(3-pyridinyl)-2-phosphonopropionic acid ...)
Show SMILES OC(=O)C(Br)(Cc1cccnc1)P(O)(O)=O |w:3.3|
Show InChI InChI=1S/C8H9BrNO5P/c9-8(7(11)12,16(13,14)15)4-6-2-1-3-10-5-6/h1-3,5H,4H2,(H,11,12)(H2,13,14,15)
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n/an/a>6.00E+4n/an/an/an/an/an/a



University of Southern California

Curated by ChEMBL


Assay Description
Inhibition of human cloned FPPS expressed in Escherichia col BL2 (DE3)


J Med Chem 50: 5967-75 (2007)


Article DOI: 10.1021/jm0702884
BindingDB Entry DOI: 10.7270/Q27944DF
More data for this
Ligand-Target Pair
Farnesyl pyrophosphate synthase


(Homo sapiens (Human))
BDBM50226002
PNG
((R)-2-hydroxy-2-phosphono-3-(pyridin-3-yl)propanoi...)
Show SMILES OC(=O)C(O)(Cc1cccnc1)P(O)(O)=O
Show InChI InChI=1S/C8H10NO6P/c10-7(11)8(12,16(13,14)15)4-6-2-1-3-9-5-6/h1-3,5,12H,4H2,(H,10,11)(H2,13,14,15)
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n/an/a 2.54E+5n/an/an/an/an/an/a



University of Southern California

Curated by ChEMBL


Assay Description
Inhibition of human cloned FPPS expressed in Escherichia col BL2 (DE3)


J Med Chem 50: 5967-75 (2007)


Article DOI: 10.1021/jm0702884
BindingDB Entry DOI: 10.7270/Q27944DF
More data for this
Ligand-Target Pair
Farnesyl pyrophosphate synthase


(Homo sapiens (Human))
BDBM50225998
PNG
(2-chloro-3-(3-pyridinyl)-2-phosphonopropionic acid...)
Show SMILES OC(=O)C(Cl)(Cc1cccnc1)P(O)(O)=O |w:3.3|
Show InChI InChI=1S/C8H9ClNO5P/c9-8(7(11)12,16(13,14)15)4-6-2-1-3-10-5-6/h1-3,5H,4H2,(H,11,12)(H2,13,14,15)
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n/an/a>6.00E+5n/an/an/an/an/an/a



University of Southern California

Curated by ChEMBL


Assay Description
Inhibition of human cloned FPPS expressed in Escherichia col BL2 (DE3)


J Med Chem 50: 5967-75 (2007)


Article DOI: 10.1021/jm0702884
BindingDB Entry DOI: 10.7270/Q27944DF
More data for this
Ligand-Target Pair
Farnesyl pyrophosphate synthase


(Homo sapiens (Human))
BDBM50226000
PNG
(2-fluoro-3-(3-pyridinyl)-2-phosphonopropionic acid...)
Show SMILES OC(=O)C(F)(Cc1cccnc1)P(O)(O)=O |w:3.3|
Show InChI InChI=1S/C8H9FNO5P/c9-8(7(11)12,16(13,14)15)4-6-2-1-3-10-5-6/h1-3,5H,4H2,(H,11,12)(H2,13,14,15)
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n/an/a>6.00E+5n/an/an/an/an/an/a



University of Southern California

Curated by ChEMBL


Assay Description
Inhibition of human cloned FPPS expressed in Escherichia col BL2 (DE3)


J Med Chem 50: 5967-75 (2007)


Article DOI: 10.1021/jm0702884
BindingDB Entry DOI: 10.7270/Q27944DF
More data for this
Ligand-Target Pair
Geranylgeranyl pyrophosphate synthase


(Homo sapiens (Human))
BDBM50318032
PNG
((+)-2-hydroxy-3-imidazo[1,2-a]pyridin-3-yl-2-phosp...)
Show SMILES OC(=O)C(O)(Cc1cnc2ccccn12)P(O)(O)=O
Show InChI InChI=1S/C10H11N2O6P/c13-9(14)10(15,19(16,17)18)5-7-6-11-8-3-1-2-4-12(7)8/h1-4,6,15H,5H2,(H,13,14)(H2,16,17,18)
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n/an/a>1.00E+6n/an/an/an/an/an/a



University of Southern California

Curated by ChEMBL


Assay Description
Inhibition of GGPPS after 10 mins using [14C]IPP as substrate by liquid scintillation counting


J Med Chem 53: 3454-64 (2010)

Checked by Author
Article DOI: 10.1021/jm900232u
BindingDB Entry DOI: 10.7270/Q21837FJ
More data for this
Ligand-Target Pair
Geranylgeranyl pyrophosphate synthase


(Homo sapiens (Human))
BDBM50318032
PNG
((+)-2-hydroxy-3-imidazo[1,2-a]pyridin-3-yl-2-phosp...)
Show SMILES OC(=O)C(O)(Cc1cnc2ccccn12)P(O)(O)=O
Show InChI InChI=1S/C10H11N2O6P/c13-9(14)10(15,19(16,17)18)5-7-6-11-8-3-1-2-4-12(7)8/h1-4,6,15H,5H2,(H,13,14)(H2,16,17,18)
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n/an/a>1.00E+6n/an/an/an/an/an/a



University of Southern California

Curated by ChEMBL


Assay Description
Inhibition of GGPPS after 10 mins using [14C]IPP as substrate by liquid scintillation counting


J Med Chem 53: 3454-64 (2010)

Checked by Author
Article DOI: 10.1021/jm900232u
BindingDB Entry DOI: 10.7270/Q21837FJ
More data for this
Ligand-Target Pair
Farnesyl pyrophosphate synthase


(Homo sapiens (Human))
BDBM50226002
PNG
((R)-2-hydroxy-2-phosphono-3-(pyridin-3-yl)propanoi...)
Show SMILES OC(=O)C(O)(Cc1cccnc1)P(O)(O)=O
Show InChI InChI=1S/C8H10NO6P/c10-7(11)8(12,16(13,14)15)4-6-2-1-3-9-5-6/h1-3,5,12H,4H2,(H,10,11)(H2,13,14,15)
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n/an/a>1.00E+6n/an/an/an/an/an/a



University of Southern California

Curated by ChEMBL


Assay Description
Inhibition of human FPPS after 10 mins using [14C]IPP as substrate by liquid scintillation counting


J Med Chem 53: 3454-64 (2010)

Checked by Author
Article DOI: 10.1021/jm900232u
BindingDB Entry DOI: 10.7270/Q21837FJ
More data for this
Ligand-Target Pair