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Compile Data Set for Download or QSAR

Found 271 hits with Last Name = 'ramunno' and Initial = 'a'   
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
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118528
PNG
(CHEMBL135514 | Ethyl-carbamic acid 5-phenyl-6-oxa-...)
Show SMILES CCNC(=O)OC1=C(Oc2ccccc2-n2cccc12)c1ccccc1 |t:6|
Show InChI InChI=1S/C21H18N2O3/c1-2-22-21(24)26-20-17-12-8-14-23(17)16-11-6-7-13-18(16)25-19(20)15-9-4-3-5-10-15/h3-14H,2H2,1H3,(H,22,24)
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0.100n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-Ro-5-4864 binding to mitochondrial rat testis Peripheral type benzodiazepine receptor (PBR)


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118528
PNG
(CHEMBL135514 | Ethyl-carbamic acid 5-phenyl-6-oxa-...)
Show SMILES CCNC(=O)OC1=C(Oc2ccccc2-n2cccc12)c1ccccc1 |t:6|
Show InChI InChI=1S/C21H18N2O3/c1-2-22-21(24)26-20-17-12-8-14-23(17)16-11-6-7-13-18(16)25-19(20)15-9-4-3-5-10-15/h3-14H,2H2,1H3,(H,22,24)
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0.110n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to Peripheral type benzodiazepine receptor (PBR) in rat cortex homogenate by 50%


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118537
PNG
(CHEMBL135391 | Ethyl-carbamic acid 7-chloro-5-phen...)
Show SMILES CCNC(=O)OC1=C(Oc2c(Cl)cccc2-n2cccc12)c1ccccc1 |t:6|
Show InChI InChI=1S/C21H17ClN2O3/c1-2-23-21(25)27-20-17-12-7-13-24(17)16-11-6-10-15(22)19(16)26-18(20)14-8-4-3-5-9-14/h3-13H,2H2,1H3,(H,23,25)
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0.180n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to Peripheral type benzodiazepine receptor (PBR) in rat cortex homogenate by 50%


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118528
PNG
(CHEMBL135514 | Ethyl-carbamic acid 5-phenyl-6-oxa-...)
Show SMILES CCNC(=O)OC1=C(Oc2ccccc2-n2cccc12)c1ccccc1 |t:6|
Show InChI InChI=1S/C21H18N2O3/c1-2-22-21(24)26-20-17-12-8-14-23(17)16-11-6-7-13-18(16)25-19(20)15-9-4-3-5-10-15/h3-14H,2H2,1H3,(H,22,24)
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0.200n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to mitochondrial rat testis Peripheral type benzodiazepine receptor (PBR)


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118539
PNG
(CHEMBL136036 | Diethyl-carbamic acid 5-thiophen-2-...)
Show SMILES CCN(CC)C(=O)OC1=C(Oc2cccnc2-n2cccc12)c1cccs1 |t:8|
Show InChI InChI=1S/C20H19N3O3S/c1-3-22(4-2)20(24)26-17-14-8-6-12-23(14)19-15(9-5-11-21-19)25-18(17)16-10-7-13-27-16/h5-13H,3-4H2,1-2H3
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0.230n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to Peripheral type benzodiazepine receptor (PBR) in rat cortex homogenate by 50%


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118541
PNG
(CHEMBL445583 | Cyclopropyl-carbamic acid 5-phenyl-...)
Show SMILES O=C(NC1CC1)OC1=C(Oc2ccccc2-n2cccc12)c1ccccc1 |t:8|
Show InChI InChI=1S/C22H18N2O3/c25-22(23-16-12-13-16)27-21-18-10-6-14-24(18)17-9-4-5-11-19(17)26-20(21)15-7-2-1-3-8-15/h1-11,14,16H,12-13H2,(H,23,25)
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0.310n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to mitochondrial rat testis Peripheral type benzodiazepine receptor (PBR)


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118534
PNG
(CHEMBL136926 | Dimethyl-carbamic acid 5-p-tolyl-6-...)
Show SMILES CN(C)C(=O)OC1=C(Oc2cccnc2-n2cccc12)c1ccc(C)cc1 |t:6|
Show InChI InChI=1S/C21H19N3O3/c1-14-8-10-15(11-9-14)18-19(27-21(25)23(2)3)16-6-5-13-24(16)20-17(26-18)7-4-12-22-20/h4-13H,1-3H3
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0.440n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to Peripheral type benzodiazepine receptor (PBR) in rat cortex homogenate by 50%


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118541
PNG
(CHEMBL445583 | Cyclopropyl-carbamic acid 5-phenyl-...)
Show SMILES O=C(NC1CC1)OC1=C(Oc2ccccc2-n2cccc12)c1ccccc1 |t:8|
Show InChI InChI=1S/C22H18N2O3/c25-22(23-16-12-13-16)27-21-18-10-6-14-24(18)17-9-4-5-11-19(17)26-20(21)15-7-2-1-3-8-15/h1-11,14,16H,12-13H2,(H,23,25)
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0.470n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-Ro-5-4864 binding to mitochondrial rat testis Peripheral type benzodiazepine receptor (PBR)


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118542
PNG
(CHEMBL335300 | Diethyl-carbamic acid 5-m-tolyl-6-o...)
Show SMILES CCN(CC)C(=O)OC1=C(Oc2cccnc2-n2cccc12)c1cccc(C)c1 |t:8|
Show InChI InChI=1S/C23H23N3O3/c1-4-25(5-2)23(27)29-21-18-11-8-14-26(18)22-19(12-7-13-24-22)28-20(21)17-10-6-9-16(3)15-17/h6-15H,4-5H2,1-3H3
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0.560n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to Peripheral type benzodiazepine receptor (PBR) in rat cortex homogenate by 50%


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118545
PNG
(CHEMBL133144 | Ethyl-carbamic acid 5-p-tolyl-6-oxa...)
Show SMILES CCNC(=O)OC1=C(Oc2ccccc2-n2cccc12)c1ccc(C)cc1 |t:6|
Show InChI InChI=1S/C22H20N2O3/c1-3-23-22(25)27-21-18-8-6-14-24(18)17-7-4-5-9-19(17)26-20(21)16-12-10-15(2)11-13-16/h4-14H,3H2,1-2H3,(H,23,25)
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0.680n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to Peripheral type benzodiazepine receptor (PBR) in rat cortex homogenate by 50%


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118544
PNG
(CHEMBL335085 | Methyl-propyl-carbamic acid 5-pheny...)
Show SMILES CCCN(C)C(=O)OC1=C(Oc2ccccc2-n2cccc12)c1ccccc1 |t:8|
Show InChI InChI=1S/C23H22N2O3/c1-3-15-24(2)23(26)28-22-19-13-9-16-25(19)18-12-7-8-14-20(18)27-21(22)17-10-5-4-6-11-17/h4-14,16H,3,15H2,1-2H3
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0.690n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to Peripheral type benzodiazepine receptor (PBR) in rat cortex homogenate by 50%


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118527
PNG
(CHEMBL336774 | Methyl-carbamic acid 5-phenyl-6-oxa...)
Show SMILES CNC(=O)OC1=C(Oc2ccccc2-n2cccc12)c1ccccc1 |t:5|
Show InChI InChI=1S/C20H16N2O3/c1-21-20(23)25-19-16-11-7-13-22(16)15-10-5-6-12-17(15)24-18(19)14-8-3-2-4-9-14/h2-13H,1H3,(H,21,23)
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0.760n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-Ro-5-4864 binding to mitochondrial rat testis Peripheral type benzodiazepine receptor (PBR)


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118543
PNG
(CHEMBL341455 | Ethyl-methyl-carbamic acid 5-phenyl...)
Show SMILES CCN(C)C(=O)OC1=C(Oc2ccccc2-n2cccc12)c1ccccc1 |t:7|
Show InChI InChI=1S/C22H20N2O3/c1-3-23(2)22(25)27-21-18-13-9-15-24(18)17-12-7-8-14-19(17)26-20(21)16-10-5-4-6-11-16/h4-15H,3H2,1-2H3
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0.780n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to Peripheral type benzodiazepine receptor (PBR) in rat cortex homogenate by 50%


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118535
PNG
(CHEMBL135801 | Propyl-carbamic acid 5-phenyl-6-oxa...)
Show SMILES CCCNC(=O)OC1=C(Oc2ccccc2-n2cccc12)c1ccccc1 |t:7|
Show InChI InChI=1S/C22H20N2O3/c1-2-14-23-22(25)27-21-18-12-8-15-24(18)17-11-6-7-13-19(17)26-20(21)16-9-4-3-5-10-16/h3-13,15H,2,14H2,1H3,(H,23,25)
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0.910n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to Peripheral type benzodiazepine receptor (PBR) in rat cortex homogenate by 50%


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118529
PNG
(Butyl-methyl-carbamic acid 5-phenyl-6-oxa-10b-aza-...)
Show SMILES CCCCN(C)C(=O)OC1=C(Oc2ccccc2-n2cccc12)c1ccccc1 |t:9|
Show InChI InChI=1S/C24H24N2O3/c1-3-4-16-25(2)24(27)29-23-20-14-10-17-26(20)19-13-8-9-15-21(19)28-22(23)18-11-6-5-7-12-18/h5-15,17H,3-4,16H2,1-2H3
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0.920n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to Peripheral type benzodiazepine receptor (PBR) in rat cortex homogenate by 50%


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118527
PNG
(CHEMBL336774 | Methyl-carbamic acid 5-phenyl-6-oxa...)
Show SMILES CNC(=O)OC1=C(Oc2ccccc2-n2cccc12)c1ccccc1 |t:5|
Show InChI InChI=1S/C20H16N2O3/c1-21-20(23)25-19-16-11-7-13-22(16)15-10-5-6-12-17(15)24-18(19)14-8-3-2-4-9-14/h2-13H,1H3,(H,21,23)
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0.960n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to mitochondrial rat testis Peripheral type benzodiazepine receptor (PBR)


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118546
PNG
(CHEMBL134781 | Diethyl-carbamic acid 5-m-tolyl-6-o...)
Show SMILES CCN(CC)C(=O)OC1=C(Oc2ccccc2-n2cccc12)c1cccc(C)c1 |t:8|
Show InChI InChI=1S/C24H24N2O3/c1-4-25(5-2)24(27)29-23-20-13-9-15-26(20)19-12-6-7-14-21(19)28-22(23)18-11-8-10-17(3)16-18/h6-16H,4-5H2,1-3H3
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1.20n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to Peripheral type benzodiazepine receptor (PBR) in rat cortex homogenate by 50%


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118547
PNG
(CHEMBL135428 | Diethyl-carbamic acid 5-(3,5-difluo...)
Show SMILES CCN(CC)C(=O)OC1=C(Oc2ccccc2-n2cccc12)c1cc(F)cc(F)c1 |t:8|
Show InChI InChI=1S/C23H20F2N2O3/c1-3-26(4-2)23(28)30-22-19-9-7-11-27(19)18-8-5-6-10-20(18)29-21(22)15-12-16(24)14-17(25)13-15/h5-14H,3-4H2,1-2H3
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1.26n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to Peripheral type benzodiazepine receptor (PBR) in rat cortex homogenate by 50%


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118531
PNG
(CHEMBL135327 | Diethyl-carbamic acid 5-phenyl-6-ox...)
Show SMILES CCN(CC)C(=O)OC1=C(Oc2cccnc2-n2cccc12)c1ccccc1 |t:8|
Show InChI InChI=1S/C22H21N3O3/c1-3-24(4-2)22(26)28-20-17-12-9-15-25(17)21-18(13-8-14-23-21)27-19(20)16-10-6-5-7-11-16/h5-15H,3-4H2,1-2H3
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1.77n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to Peripheral type benzodiazepine receptor (PBR) in rat cortex homogenate by 50%


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118541
PNG
(CHEMBL445583 | Cyclopropyl-carbamic acid 5-phenyl-...)
Show SMILES O=C(NC1CC1)OC1=C(Oc2ccccc2-n2cccc12)c1ccccc1 |t:8|
Show InChI InChI=1S/C22H18N2O3/c25-22(23-16-12-13-16)27-21-18-10-6-14-24(18)17-9-4-5-11-19(17)26-20(21)15-7-2-1-3-8-15/h1-11,14,16H,12-13H2,(H,23,25)
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2.21n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to Peripheral type benzodiazepine receptor (PBR) in rat cortex homogenate by 50%


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118527
PNG
(CHEMBL336774 | Methyl-carbamic acid 5-phenyl-6-oxa...)
Show SMILES CNC(=O)OC1=C(Oc2ccccc2-n2cccc12)c1ccccc1 |t:5|
Show InChI InChI=1S/C20H16N2O3/c1-21-20(23)25-19-16-11-7-13-22(16)15-10-5-6-12-17(15)24-18(19)14-8-3-2-4-9-14/h2-13H,1H3,(H,21,23)
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2.26n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to Peripheral type benzodiazepine receptor (PBR) in rat cortex homogenate by 50%


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM21279
PNG
(1-(2,4-dichlorophenyl)-5-(4-iodophenyl)-4-methyl-N...)
Show SMILES Cc1c(nn(c1-c1ccc(I)cc1)-c1ccc(Cl)cc1Cl)C(=O)NN1CCCCC1
Show InChI InChI=1S/C22H21Cl2IN4O/c1-14-20(22(30)27-28-11-3-2-4-12-28)26-29(19-10-7-16(23)13-18(19)24)21(14)15-5-8-17(25)9-6-15/h5-10,13H,2-4,11-12H2,1H3,(H,27,30)
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2.30n/an/an/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Displacement of [3H]CP-55940 from human recombinant CB1 receptor expressed in HEK cells


Bioorg Med Chem 16: 7510-5 (2008)


Article DOI: 10.1016/j.bmc.2008.06.001
BindingDB Entry DOI: 10.7270/Q2C53MSN
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118540
PNG
(Acetic acid 5-m-tolyl-6-oxa-10b-aza-benzo[e]azulen...)
Show SMILES CC(=O)OC1=C(Oc2ccccc2-n2cccc12)c1cccc(C)c1 |t:4|
Show InChI InChI=1S/C21H17NO3/c1-14-7-5-8-16(13-14)20-21(24-15(2)23)18-10-6-12-22(18)17-9-3-4-11-19(17)25-20/h3-13H,1-2H3
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2.5n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to Peripheral type benzodiazepine receptor (PBR) in rat cortex homogenate by 50%


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118530
PNG
(Azetidine-1-carboxylic acid 5-phenyl-6-oxa-10b-aza...)
Show SMILES O=C(OC1=C(Oc2ccccc2-n2cccc12)c1ccccc1)N1CCC1 |t:3|
Show InChI InChI=1S/C22H18N2O3/c25-22(23-13-7-14-23)27-21-18-11-6-15-24(18)17-10-4-5-12-19(17)26-20(21)16-8-2-1-3-9-16/h1-6,8-12,15H,7,13-14H2
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4.30n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-Ro-5-4864 binding to mitochondrial rat testis Peripheral type benzodiazepine receptor (PBR)


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50180022
PNG
(5-(4-chloro-3-methyl-phenyl)-1-(4-methyl-benzyl)-1...)
Show SMILES Cc1ccc(Cn2nc(cc2-c2ccc(Cl)c(C)c2)C(=O)NC2C3(C)CCC(C3)C2(C)C)cc1 |THB:21:22:26.25:28|
Show InChI InChI=1S/C29H34ClN3O/c1-18-6-8-20(9-7-18)17-33-25(21-10-11-23(30)19(2)14-21)15-24(32-33)26(34)31-27-28(3,4)22-12-13-29(27,5)16-22/h6-11,14-15,22,27H,12-13,16-17H2,1-5H3,(H,31,34)
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5.40n/an/an/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Displacement of [3H]CP-55940 from human recombinant CB2 receptor expressed in HEK cells


Bioorg Med Chem 16: 7510-5 (2008)


Article DOI: 10.1016/j.bmc.2008.06.001
BindingDB Entry DOI: 10.7270/Q2C53MSN
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118533
PNG
(CHEMBL336903 | Diethyl-carbamic acid 5-phenyl-6H-b...)
Show SMILES CCN(CC)C(=O)OC1=C(Cc2ccccc2-n2cccc12)c1ccccc1 |t:8|
Show InChI InChI=1S/C24H24N2O2/c1-3-25(4-2)24(27)28-23-20(18-11-6-5-7-12-18)17-19-13-8-9-14-21(19)26-16-10-15-22(23)26/h5-16H,3-4,17H2,1-2H3
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5.70n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to Peripheral type benzodiazepine receptor (PBR) in rat cortex homogenate by 50%


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118530
PNG
(Azetidine-1-carboxylic acid 5-phenyl-6-oxa-10b-aza...)
Show SMILES O=C(OC1=C(Oc2ccccc2-n2cccc12)c1ccccc1)N1CCC1 |t:3|
Show InChI InChI=1S/C22H18N2O3/c25-22(23-13-7-14-23)27-21-18-11-6-15-24(18)17-10-4-5-12-19(17)26-20(21)16-8-2-1-3-9-16/h1-6,8-12,15H,7,13-14H2
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6n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to mitochondrial rat testis Peripheral type benzodiazepine receptor (PBR)


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118530
PNG
(Azetidine-1-carboxylic acid 5-phenyl-6-oxa-10b-aza...)
Show SMILES O=C(OC1=C(Oc2ccccc2-n2cccc12)c1ccccc1)N1CCC1 |t:3|
Show InChI InChI=1S/C22H18N2O3/c25-22(23-13-7-14-23)27-21-18-11-6-15-24(18)17-10-4-5-12-19(17)26-20(21)16-8-2-1-3-9-16/h1-6,8-12,15H,7,13-14H2
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6.03n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to Peripheral type benzodiazepine receptor (PBR) in rat cortex homogenate by 50%


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118536
PNG
(4-Methyl-piperazine-1-carboxylic acid 5-phenyl-6-o...)
Show SMILES CN1CCN(CC1)C(=O)OC1=C(Oc2ccccc2-n2cccc12)c1ccccc1 |t:11|
Show InChI InChI=1S/C24H23N3O3/c1-25-14-16-26(17-15-25)24(28)30-23-20-11-7-13-27(20)19-10-5-6-12-21(19)29-22(23)18-8-3-2-4-9-18/h2-13H,14-17H2,1H3
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7.20n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to Peripheral type benzodiazepine receptor (PBR) in rat cortex homogenate by 50%


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM21278
PNG
(5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl...)
Show SMILES Cc1c(nn(c1-c1ccc(Cl)cc1)-c1ccc(Cl)cc1Cl)C(=O)NN1CCCCC1
Show InChI InChI=1S/C22H21Cl3N4O/c1-14-20(22(30)27-28-11-3-2-4-12-28)26-29(19-10-9-17(24)13-18(19)25)21(14)15-5-7-16(23)8-6-15/h5-10,13H,2-4,11-12H2,1H3,(H,27,30)
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8n/an/an/an/an/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Displacement of [3H]CP-55940 from human recombinant CB1 receptor expressed in HEK cells


Bioorg Med Chem 16: 7510-5 (2008)


Article DOI: 10.1016/j.bmc.2008.06.001
BindingDB Entry DOI: 10.7270/Q2C53MSN
More data for this
Ligand-Target Pair
Human immunodeficiency virus type 1 reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50102265
PNG
(1-(5-Bromo-pyridin-2-yl)-3-[2-(6-fluoro-4-oxo-4H-p...)
Show SMILES Fc1cccc2c1n(CCNC(=S)Nc1ccc(Br)cn1)c(=O)c1cccn21
Show InChI InChI=1S/C19H15BrFN5OS/c20-12-6-7-16(23-11-12)24-19(28)22-8-10-26-17-13(21)3-1-4-14(17)25-9-2-5-15(25)18(26)27/h1-7,9,11H,8,10H2,(H2,22,23,24,28)
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9n/an/an/an/an/an/an/an/a



Universita' degli Studi di Salerno

Curated by ChEMBL


Assay Description
Inhibition of HIV-1 wild-type RT


J Med Chem 44: 305-15 (2001)


BindingDB Entry DOI: 10.7270/Q2HX1DD9
More data for this
Ligand-Target Pair
Human immunodeficiency virus type 1 reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50102271
PNG
(1-(5-Bromo-pyridin-2-yl)-3-[2-(4-oxo-4H-5,9,9b-tri...)
Show SMILES Brc1ccc(NC(=S)NCCn2c3cccnc3n3cccc3c2=O)nc1
Show InChI InChI=1S/C18H15BrN6OS/c19-12-5-6-15(22-11-12)23-18(27)21-8-10-25-13-3-1-7-20-16(13)24-9-2-4-14(24)17(25)26/h1-7,9,11H,8,10H2,(H2,21,22,23,27)
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9n/an/an/an/an/an/an/an/a



Universita' degli Studi di Salerno

Curated by ChEMBL


Assay Description
Inhibition of HIV-1 wild-type RT


J Med Chem 44: 305-15 (2001)


BindingDB Entry DOI: 10.7270/Q2HX1DD9
More data for this
Ligand-Target Pair
Human immunodeficiency virus type 1 reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50082061
PNG
((+/-)-5-ethyl-5-(3-methoxy-phenyl)-6-oxa-10b-aza-b...)
Show SMILES CCC1(Oc2ccccc2-n2cccc2C1=O)c1cccc(OC)c1
Show InChI InChI=1S/C21H19NO3/c1-3-21(15-8-6-9-16(14-15)24-2)20(23)18-11-7-13-22(18)17-10-4-5-12-19(17)25-21/h4-14H,3H2,1-2H3
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10n/an/an/an/an/an/an/an/a



Universita' degli Studi di Salerno

Curated by ChEMBL


Assay Description
In vitro inhibitory activity of the compound against HIV-1 mutant Reverse transcriptase containing the single amino acid substitution V106A


J Med Chem 42: 4462-70 (1999)


BindingDB Entry DOI: 10.7270/Q20R9NMJ
More data for this
Ligand-Target Pair
Human immunodeficiency virus type 1 reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50082061
PNG
((+/-)-5-ethyl-5-(3-methoxy-phenyl)-6-oxa-10b-aza-b...)
Show SMILES CCC1(Oc2ccccc2-n2cccc2C1=O)c1cccc(OC)c1
Show InChI InChI=1S/C21H19NO3/c1-3-21(15-8-6-9-16(14-15)24-2)20(23)18-11-7-13-22(18)17-10-4-5-12-19(17)25-21/h4-14H,3H2,1-2H3
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11n/an/an/an/an/an/an/an/a



Universita' degli Studi di Salerno

Curated by ChEMBL


Assay Description
In vitro inhibitory activity of the compound against HIV-1 mutant Reverse transcriptase containing the single amino acid substitution L100I


J Med Chem 42: 4462-70 (1999)


BindingDB Entry DOI: 10.7270/Q20R9NMJ
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118531
PNG
(CHEMBL135327 | Diethyl-carbamic acid 5-phenyl-6-ox...)
Show SMILES CCN(CC)C(=O)OC1=C(Oc2cccnc2-n2cccc12)c1ccccc1 |t:8|
Show InChI InChI=1S/C22H21N3O3/c1-3-24(4-2)22(26)28-20-17-12-9-15-25(17)21-18(13-8-14-23-21)27-19(20)16-10-6-5-7-11-16/h5-15H,3-4H2,1-2H3
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11n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to mitochondrial rat testis Peripheral type benzodiazepine receptor (PBR)


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118538
PNG
(CHEMBL135663 | Diethyl-carbamic acid 5-thiophen-2-...)
Show SMILES CCN(CC)C(=O)OC1=C(Oc2ccccc2-n2cccc12)c1cccs1 |t:8|
Show InChI InChI=1S/C21H20N2O3S/c1-3-22(4-2)21(24)26-19-16-10-7-13-23(16)15-9-5-6-11-17(15)25-20(19)18-12-8-14-27-18/h5-14H,3-4H2,1-2H3
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11.5n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to Peripheral type benzodiazepine receptor (PBR) in rat cortex homogenate by 50%


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118532
PNG
(Acetic acid 5-p-tolyl-6-oxa-10,10b-diaza-benzo[e]a...)
Show SMILES CC(=O)OC1=C(Oc2cccnc2-n2cccc12)c1ccc(C)cc1 |t:4|
Show InChI InChI=1S/C20H16N2O3/c1-13-7-9-15(10-8-13)18-19(24-14(2)23)16-5-4-12-22(16)20-17(25-18)6-3-11-21-20/h3-12H,1-2H3
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13.5n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to Peripheral type benzodiazepine receptor (PBR) in rat cortex homogenate by 50%


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Human immunodeficiency virus type 1 reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50102268
PNG
(1-(5-Bromo-pyridin-2-yl)-3-[2-(5-oxo-pyrazolo[1,5-...)
Show SMILES Brc1ccc(NC(=S)NCCn2c3ccccc3c3ccnn3c2=O)nc1
Show InChI InChI=1S/C18H15BrN6OS/c19-12-5-6-16(21-11-12)23-17(27)20-9-10-24-14-4-2-1-3-13(14)15-7-8-22-25(15)18(24)26/h1-8,11H,9-10H2,(H2,20,21,23,27)
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15n/an/an/an/an/an/an/an/a



Universita' degli Studi di Salerno

Curated by ChEMBL


Assay Description
Inhibition of HIV-1 wild-type RT


J Med Chem 44: 305-15 (2001)


BindingDB Entry DOI: 10.7270/Q2HX1DD9
More data for this
Ligand-Target Pair
Human immunodeficiency virus type 1 reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50102265
PNG
(1-(5-Bromo-pyridin-2-yl)-3-[2-(6-fluoro-4-oxo-4H-p...)
Show SMILES Fc1cccc2c1n(CCNC(=S)Nc1ccc(Br)cn1)c(=O)c1cccn21
Show InChI InChI=1S/C19H15BrFN5OS/c20-12-6-7-16(23-11-12)24-19(28)22-8-10-26-17-13(21)3-1-4-14(17)25-9-2-5-15(25)18(26)27/h1-7,9,11H,8,10H2,(H2,22,23,24,28)
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15n/an/an/an/an/an/an/an/a



Universita' degli Studi di Salerno

Curated by ChEMBL


Assay Description
Inhibition of HIV-1 Mutant HIV-1 RT enzymes containing the single amino acid substitution V106A


J Med Chem 44: 305-15 (2001)


BindingDB Entry DOI: 10.7270/Q2HX1DD9
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118536
PNG
(4-Methyl-piperazine-1-carboxylic acid 5-phenyl-6-o...)
Show SMILES CN1CCN(CC1)C(=O)OC1=C(Oc2ccccc2-n2cccc12)c1ccccc1 |t:11|
Show InChI InChI=1S/C24H23N3O3/c1-25-14-16-26(17-15-25)24(28)30-23-20-11-7-13-27(20)19-10-5-6-12-21(19)29-22(23)18-8-3-2-4-9-18/h2-13H,14-17H2,1H3
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15n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-Ro-5-4864 binding to mitochondrial rat testis Peripheral type benzodiazepine receptor (PBR)


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Human immunodeficiency virus type 1 reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50102276
PNG
(1-(5-Bromo-pyridin-2-yl)-3-[2-(7-chloro-4-oxo-4H-p...)
Show SMILES Clc1ccc2c(c1)n(CCNC(=S)Nc1ccc(Br)cn1)c(=O)c1cccn21
Show InChI InChI=1S/C19H15BrClN5OS/c20-12-3-6-17(23-11-12)24-19(28)22-7-9-26-16-10-13(21)4-5-14(16)25-8-1-2-15(25)18(26)27/h1-6,8,10-11H,7,9H2,(H2,22,23,24,28)
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20n/an/an/an/an/an/an/an/a



Universita' degli Studi di Salerno

Curated by ChEMBL


Assay Description
Inhibition of HIV-1 wild-type RT


J Med Chem 44: 305-15 (2001)


BindingDB Entry DOI: 10.7270/Q2HX1DD9
More data for this
Ligand-Target Pair
Human immunodeficiency virus type 1 reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50102276
PNG
(1-(5-Bromo-pyridin-2-yl)-3-[2-(7-chloro-4-oxo-4H-p...)
Show SMILES Clc1ccc2c(c1)n(CCNC(=S)Nc1ccc(Br)cn1)c(=O)c1cccn21
Show InChI InChI=1S/C19H15BrClN5OS/c20-12-3-6-17(23-11-12)24-19(28)22-7-9-26-16-10-13(21)4-5-14(16)25-8-1-2-15(25)18(26)27/h1-6,8,10-11H,7,9H2,(H2,22,23,24,28)
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20n/an/an/an/an/an/an/an/a



Universita' degli Studi di Salerno

Curated by ChEMBL


Assay Description
Inhibition of HIV-1 Mutant HIV-1 RT enzymes containing the single amino acid substitution V106A


J Med Chem 44: 305-15 (2001)


BindingDB Entry DOI: 10.7270/Q2HX1DD9
More data for this
Ligand-Target Pair
Human immunodeficiency virus type 1 reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50102268
PNG
(1-(5-Bromo-pyridin-2-yl)-3-[2-(5-oxo-pyrazolo[1,5-...)
Show SMILES Brc1ccc(NC(=S)NCCn2c3ccccc3c3ccnn3c2=O)nc1
Show InChI InChI=1S/C18H15BrN6OS/c19-12-5-6-16(21-11-12)23-17(27)20-9-10-24-14-4-2-1-3-13(14)15-7-8-22-25(15)18(24)26/h1-8,11H,9-10H2,(H2,20,21,23,27)
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21n/an/an/an/an/an/an/an/a



Universita' degli Studi di Salerno

Curated by ChEMBL


Assay Description
Inhibition of HIV-1 Mutant HIV-1 RT enzymes containing the single amino acid substitution K103N


J Med Chem 44: 305-15 (2001)


BindingDB Entry DOI: 10.7270/Q2HX1DD9
More data for this
Ligand-Target Pair
Human immunodeficiency virus type 1 reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50082055
PNG
(5-Ethyl-5-m-tolyl-6-oxa-10,10b-diaza-benzo[e]azule...)
Show SMILES CCC1(Oc2cccnc2-n2cccc2C1=O)c1cccc(C)c1
Show InChI InChI=1S/C20H18N2O2/c1-3-20(15-8-4-7-14(2)13-15)18(23)16-9-6-12-22(16)19-17(24-20)10-5-11-21-19/h4-13H,3H2,1-2H3
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21n/an/an/an/an/an/an/an/a



Universita' degli Studi di Salerno

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against HIV-1 wild type reverse transcriptase (RT)


J Med Chem 42: 4462-70 (1999)


BindingDB Entry DOI: 10.7270/Q20R9NMJ
More data for this
Ligand-Target Pair
Human immunodeficiency virus type 1 reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50082060
PNG
(5-Ethyl-5-phenyl-6-oxa-10,10b-diaza-benzo[e]azulen...)
Show SMILES CCC1(Oc2cccnc2-n2cccc2C1=O)c1ccccc1
Show InChI InChI=1S/C19H16N2O2/c1-2-19(14-8-4-3-5-9-14)17(22)15-10-7-13-21(15)18-16(23-19)11-6-12-20-18/h3-13H,2H2,1H3
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22n/an/an/an/an/an/an/an/a



Universita' degli Studi di Salerno

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against HIV-1 wild type reverse transcriptase (RT)


J Med Chem 42: 4462-70 (1999)


BindingDB Entry DOI: 10.7270/Q20R9NMJ
More data for this
Ligand-Target Pair
Human immunodeficiency virus type 1 reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50102277
PNG
(1-(5-Bromo-pyridin-2-yl)-3-[2-(7,9-difluoro-4-oxo-...)
Show SMILES Fc1cc(F)c2c(c1)n(CCNC(=S)Nc1ccc(Br)cn1)c(=O)c1cccn21
Show InChI InChI=1S/C19H14BrF2N5OS/c20-11-3-4-16(24-10-11)25-19(29)23-5-7-27-15-9-12(21)8-13(22)17(15)26-6-1-2-14(26)18(27)28/h1-4,6,8-10H,5,7H2,(H2,23,24,25,29)
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22n/an/an/an/an/an/an/an/a



Universita' degli Studi di Salerno

Curated by ChEMBL


Assay Description
Inhibition of HIV-1 wild-type RT


J Med Chem 44: 305-15 (2001)


BindingDB Entry DOI: 10.7270/Q2HX1DD9
More data for this
Ligand-Target Pair
Human immunodeficiency virus type 1 reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50082061
PNG
((+/-)-5-ethyl-5-(3-methoxy-phenyl)-6-oxa-10b-aza-b...)
Show SMILES CCC1(Oc2ccccc2-n2cccc2C1=O)c1cccc(OC)c1
Show InChI InChI=1S/C21H19NO3/c1-3-21(15-8-6-9-16(14-15)24-2)20(23)18-11-7-13-22(18)17-10-4-5-12-19(17)25-21/h4-14H,3H2,1-2H3
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22n/an/an/an/an/an/an/an/a



Universita' degli Studi di Salerno

Curated by ChEMBL


Assay Description
In vitro inhibitory activity of the compound against HIV-1 mutant Reverse transcriptase containing the single amino acid substitution K103N


J Med Chem 42: 4462-70 (1999)


BindingDB Entry DOI: 10.7270/Q20R9NMJ
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118531
PNG
(CHEMBL135327 | Diethyl-carbamic acid 5-phenyl-6-ox...)
Show SMILES CCN(CC)C(=O)OC1=C(Oc2cccnc2-n2cccc12)c1ccccc1 |t:8|
Show InChI InChI=1S/C22H21N3O3/c1-3-24(4-2)22(26)28-20-17-12-9-15-25(17)21-18(13-8-14-23-21)27-19(20)16-10-6-5-7-11-16/h5-15H,3-4H2,1-2H3
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22n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-Ro-5-4864 binding to mitochondrial rat testis Peripheral type benzodiazepine receptor (PBR)


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
Human immunodeficiency virus type 1 reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50102266
PNG
(1-(5-Bromo-pyridin-2-yl)-3-[2-(7-fluoro-4-oxo-4H-p...)
Show SMILES Fc1ccc2c(c1)n(CCNC(=S)Nc1ccc(Br)cn1)c(=O)c1cccn21
Show InChI InChI=1S/C19H15BrFN5OS/c20-12-3-6-17(23-11-12)24-19(28)22-7-9-26-16-10-13(21)4-5-14(16)25-8-1-2-15(25)18(26)27/h1-6,8,10-11H,7,9H2,(H2,22,23,24,28)
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29n/an/an/an/an/an/an/an/a



Universita' degli Studi di Salerno

Curated by ChEMBL


Assay Description
Inhibition of HIV-1 wild-type RT


J Med Chem 44: 305-15 (2001)


BindingDB Entry DOI: 10.7270/Q2HX1DD9
More data for this
Ligand-Target Pair
Peripheral-Type Benzodiazepine Receptor


(Rattus norvegicus (rat))
BDBM50118536
PNG
(4-Methyl-piperazine-1-carboxylic acid 5-phenyl-6-o...)
Show SMILES CN1CCN(CC1)C(=O)OC1=C(Oc2ccccc2-n2cccc12)c1ccccc1 |t:11|
Show InChI InChI=1S/C24H23N3O3/c1-25-14-16-26(17-15-25)24(28)30-23-20-11-7-13-27(20)19-10-5-6-12-21(19)29-22(23)18-8-3-2-4-9-18/h2-13H,14-17H2,1H3
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29n/an/an/an/an/an/an/an/a



Universita' degli Studi di Siena

Curated by ChEMBL


Assay Description
Inhibition of [3H]-PK11195 binding to mitochondrial rat testis Peripheral type benzodiazepine receptor (PBR)


J Med Chem 45: 4276-81 (2002)


BindingDB Entry DOI: 10.7270/Q20Z72MT
More data for this
Ligand-Target Pair
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