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Compile Data Set for Download or QSAR

Found 8 hits of kd for drug = Combivir   
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
Reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50138406
PNG
(3TC Triphosphate | CHEMBL1230 | LAMIVUDINE | Lamiv...)
Show SMILES Nc1ccn([C@@H]2CS[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O2)c(=O)n1 |r|
Show InChI InChI=1S/C8H14N3O12P3S/c9-5-1-2-11(8(12)10-5)6-4-27-7(21-6)3-20-25(16,17)23-26(18,19)22-24(13,14)15/h1-2,6-7H,3-4H2,(H,16,17)(H,18,19)(H2,9,10,12)(H2,13,14,15)/t6-,7+/m0/s1
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n/an/an/a 130n/an/an/an/an/a



Veterans Affairs Medical Center

Curated by ChEMBL


Assay Description
Binding affinity to HIV1 reverse transcriptase assessed as L-3'-azido-NTP incorporation in nascent DNA


Eur J Med Chem 46: 3832-44 (2011)


Article DOI: 10.1016/j.ejmech.2011.05.051
BindingDB Entry DOI: 10.7270/Q2RN3BQP
More data for this
Ligand-Target Pair
Reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50138406
PNG
(3TC Triphosphate | CHEMBL1230 | LAMIVUDINE | Lamiv...)
Show SMILES Nc1ccn([C@@H]2CS[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O2)c(=O)n1 |r|
Show InChI InChI=1S/C8H14N3O12P3S/c9-5-1-2-11(8(12)10-5)6-4-27-7(21-6)3-20-25(16,17)23-26(18,19)22-24(13,14)15/h1-2,6-7H,3-4H2,(H,16,17)(H,18,19)(H2,9,10,12)(H2,13,14,15)/t6-,7+/m0/s1
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n/an/an/a 370n/an/an/an/an/a



University of Pittsburgh School of Medicine

Curated by ChEMBL


Assay Description
Binding affinity to HIV1 reverse transcriptase


Antimicrob Agents Chemother 53: 3715-9 (2009)


Article DOI: 10.1128/AAC.00392-09
BindingDB Entry DOI: 10.7270/Q2KD21R2
More data for this
Ligand-Target Pair
Reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50138406
PNG
(3TC Triphosphate | CHEMBL1230 | LAMIVUDINE | Lamiv...)
Show SMILES Nc1ccn([C@@H]2CS[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O2)c(=O)n1 |r|
Show InChI InChI=1S/C8H14N3O12P3S/c9-5-1-2-11(8(12)10-5)6-4-27-7(21-6)3-20-25(16,17)23-26(18,19)22-24(13,14)15/h1-2,6-7H,3-4H2,(H,16,17)(H,18,19)(H2,9,10,12)(H2,13,14,15)/t6-,7+/m0/s1
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n/an/an/a 370n/an/an/an/an/a



University of Pittsburgh School of Medicine

Curated by ChEMBL


Assay Description
Binding affinity to wild type HIV1 LAI reverse transcriptase


Antimicrob Agents Chemother 52: 157-63 (2008)


Article DOI: 10.1128/aac.00904-07
BindingDB Entry DOI: 10.7270/Q2CV4MK7
More data for this
Ligand-Target Pair
Reverse transcriptase protein


(Human immunodeficiency virus 1)
BDBM50138406
PNG
(3TC Triphosphate | CHEMBL1230 | LAMIVUDINE | Lamiv...)
Show SMILES Nc1ccn([C@@H]2CS[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O2)c(=O)n1 |r|
Show InChI InChI=1S/C8H14N3O12P3S/c9-5-1-2-11(8(12)10-5)6-4-27-7(21-6)3-20-25(16,17)23-26(18,19)22-24(13,14)15/h1-2,6-7H,3-4H2,(H,16,17)(H,18,19)(H2,9,10,12)(H2,13,14,15)/t6-,7+/m0/s1
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n/an/an/a 430n/an/an/an/an/a



University of Pittsburgh School of Medicine

Curated by ChEMBL


Assay Description
Binding affinity to HIV1 LAI reverse transcriptase M41L/L210W/T215Y mutant


Antimicrob Agents Chemother 52: 157-63 (2008)


Article DOI: 10.1128/aac.00904-07
BindingDB Entry DOI: 10.7270/Q2CV4MK7
More data for this
Ligand-Target Pair
Reverse transcriptase protein


(Human immunodeficiency virus 1)
BDBM50138406
PNG
(3TC Triphosphate | CHEMBL1230 | LAMIVUDINE | Lamiv...)
Show SMILES Nc1ccn([C@@H]2CS[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O2)c(=O)n1 |r|
Show InChI InChI=1S/C8H14N3O12P3S/c9-5-1-2-11(8(12)10-5)6-4-27-7(21-6)3-20-25(16,17)23-26(18,19)22-24(13,14)15/h1-2,6-7H,3-4H2,(H,16,17)(H,18,19)(H2,9,10,12)(H2,13,14,15)/t6-,7+/m0/s1
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n/an/an/a 8.20E+3n/an/an/an/an/a



University of Pittsburgh School of Medicine

Curated by ChEMBL


Assay Description
Binding affinity to HIV1 LAI reverse transcriptase M184V mutant


Antimicrob Agents Chemother 52: 157-63 (2008)


Article DOI: 10.1128/aac.00904-07
BindingDB Entry DOI: 10.7270/Q2CV4MK7
More data for this
Ligand-Target Pair
Reverse transcriptase protein


(Human immunodeficiency virus 1)
BDBM50138406
PNG
(3TC Triphosphate | CHEMBL1230 | LAMIVUDINE | Lamiv...)
Show SMILES Nc1ccn([C@@H]2CS[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O2)c(=O)n1 |r|
Show InChI InChI=1S/C8H14N3O12P3S/c9-5-1-2-11(8(12)10-5)6-4-27-7(21-6)3-20-25(16,17)23-26(18,19)22-24(13,14)15/h1-2,6-7H,3-4H2,(H,16,17)(H,18,19)(H2,9,10,12)(H2,13,14,15)/t6-,7+/m0/s1
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n/an/an/a 9.80E+3n/an/an/an/an/a



University of Pittsburgh School of Medicine

Curated by ChEMBL


Assay Description
Binding affinity to HIV1 LAI reverse transcriptase M41L/L210W/T215Y/M184V mutant


Antimicrob Agents Chemother 52: 157-63 (2008)


Article DOI: 10.1128/aac.00904-07
BindingDB Entry DOI: 10.7270/Q2CV4MK7
More data for this
Ligand-Target Pair
Reverse transcriptase/RNaseH


(Human immunodeficiency virus 1)
BDBM50138406
PNG
(3TC Triphosphate | CHEMBL1230 | LAMIVUDINE | Lamiv...)
Show SMILES Nc1ccn([C@@H]2CS[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O2)c(=O)n1 |r|
Show InChI InChI=1S/C8H14N3O12P3S/c9-5-1-2-11(8(12)10-5)6-4-27-7(21-6)3-20-25(16,17)23-26(18,19)22-24(13,14)15/h1-2,6-7H,3-4H2,(H,16,17)(H,18,19)(H2,9,10,12)(H2,13,14,15)/t6-,7+/m0/s1
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n/an/an/a 1.50E+4n/an/an/an/an/a



The University of Georgia

Curated by ChEMBL


Assay Description
Equilibrium binding constant at the active site of HIV-1 reverse transcriptase


Bioorg Med Chem Lett 14: 437-40 (2003)


BindingDB Entry DOI: 10.7270/Q2RX9BGK
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Reverse transcriptase protein


(Human immunodeficiency virus 1)
BDBM50138406
PNG
(3TC Triphosphate | CHEMBL1230 | LAMIVUDINE | Lamiv...)
Show SMILES Nc1ccn([C@@H]2CS[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O2)c(=O)n1 |r|
Show InChI InChI=1S/C8H14N3O12P3S/c9-5-1-2-11(8(12)10-5)6-4-27-7(21-6)3-20-25(16,17)23-26(18,19)22-24(13,14)15/h1-2,6-7H,3-4H2,(H,16,17)(H,18,19)(H2,9,10,12)(H2,13,14,15)/t6-,7+/m0/s1
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n/an/an/a 1.80E+4n/an/an/an/an/a



Veterans Affairs Medical Center

Curated by ChEMBL


Assay Description
Binding affinity to HIV1 reverse transcriptase M184V mutant assessed as L-3'-azido-NTP incorporation in nascent DNA


Eur J Med Chem 46: 3832-44 (2011)


Article DOI: 10.1016/j.ejmech.2011.05.051
BindingDB Entry DOI: 10.7270/Q2RN3BQP
More data for this
Ligand-Target Pair