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Compile Data Set for Download or QSAR

Found 27 hits of kd data for polymerid = 2236,50000534,5514   
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
Translocator protein


(Rattus norvegicus (rat))
BDBM22032
PNG
(1-(2-chlorophenyl)-N-methyl-N-(1-methylpropyl)isoq...)
Show SMILES CCC(C)N(C)C(=O)c1cc2ccccc2c(n1)-c1ccccc1Cl
Show InChI InChI=1S/C21H21ClN2O/c1-4-14(2)24(3)21(25)19-13-15-9-5-6-10-16(15)20(23-19)17-11-7-8-12-18(17)22/h5-14H,4H2,1-3H3
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n/an/an/a 0.600n/an/an/an/an/a



Brain and Mind Research Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]PK11195 from TSPO in rat cortex


J Med Chem 52: 581-92 (2009)


Article DOI: 10.1021/jm8011678
BindingDB Entry DOI: 10.7270/Q2222VP0
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Translocator protein


(Homo sapiens (Human))
BDBM22040
PNG
(4 -chlorodiazepam | 4' Cl-diazepam | 7-chloro-...)
Show SMILES CN1c2ccc(Cl)cc2C(=NCC1=O)c1ccc(Cl)cc1 |c:10|
Show InChI InChI=1S/C16H12Cl2N2O/c1-20-14-7-6-12(18)8-13(14)16(19-9-15(20)21)10-2-4-11(17)5-3-10/h2-8H,9H2,1H3
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n/an/an/a 1.10n/an/an/an/an/a


TBA

Assay Description
Inhibitory activity against Dihydrofolate reductase of Escherichia coli


Citation and Details
More data for this
Ligand-Target Pair
Translocator protein


(Rattus norvegicus (rat))
BDBM22040
PNG
(4 -chlorodiazepam | 4' Cl-diazepam | 7-chloro-...)
Show SMILES CN1c2ccc(Cl)cc2C(=NCC1=O)c1ccc(Cl)cc1 |c:10|
Show InChI InChI=1S/C16H12Cl2N2O/c1-20-14-7-6-12(18)8-13(14)16(19-9-15(20)21)10-2-4-11(17)5-3-10/h2-8H,9H2,1H3
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n/an/an/a 1.10n/an/an/an/an/a



Brain and Mind Research Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]Ro5-4864 from TSPO in rat kainate lesioned striatum


J Med Chem 52: 581-92 (2009)


Article DOI: 10.1021/jm8011678
BindingDB Entry DOI: 10.7270/Q2222VP0
More data for this
Ligand-Target Pair
Translocator protein


(Homo sapiens (Human))
BDBM22032
PNG
(1-(2-chlorophenyl)-N-methyl-N-(1-methylpropyl)isoq...)
Show SMILES CCC(C)N(C)C(=O)c1cc2ccccc2c(n1)-c1ccccc1Cl
Show InChI InChI=1S/C21H21ClN2O/c1-4-14(2)24(3)21(25)19-13-15-9-5-6-10-16(15)20(23-19)17-11-7-8-12-18(17)22/h5-14H,4H2,1-3H3
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n/an/an/a 2n/an/an/an/an/a



Emory University

Curated by ChEMBL


Assay Description
Binding affinity to human PBR


Bioorg Med Chem 16: 6145-55 (2008)


Article DOI: 10.1016/j.bmc.2008.04.046
BindingDB Entry DOI: 10.7270/Q26Q1Z4G
More data for this
Ligand-Target Pair
Translocator protein


(Homo sapiens (Human))
BDBM50054139
PNG
((R)1-(2-Chloro-phenyl)-isoquinoline-3-carboxylic a...)
Show SMILES CC[C@@H](C)N(C)C(=O)c1cc2ccccc2c(n1)-c1ccccc1Cl
Show InChI InChI=1S/C21H21ClN2O/c1-4-14(2)24(3)21(25)19-13-15-9-5-6-10-16(15)20(23-19)17-11-7-8-12-18(17)22/h5-14H,4H2,1-3H3/t14-/m1/s1
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n/an/an/a 2n/an/an/an/an/a


TBA

Assay Description
Inhibitory activity against dihydrofolate reductase (DHFR) from Escherichia coli


Citation and Details
More data for this
Ligand-Target Pair
Translocator protein


(Rattus norvegicus (rat))
BDBM22032
PNG
(1-(2-chlorophenyl)-N-methyl-N-(1-methylpropyl)isoq...)
Show SMILES CCC(C)N(C)C(=O)c1cc2ccccc2c(n1)-c1ccccc1Cl
Show InChI InChI=1S/C21H21ClN2O/c1-4-14(2)24(3)21(25)19-13-15-9-5-6-10-16(15)20(23-19)17-11-7-8-12-18(17)22/h5-14H,4H2,1-3H3
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n/an/an/a 2n/an/an/an/an/a



Universit£ di Ferrara

Curated by ChEMBL


Assay Description
Binding affinity constant for peripheral (mitochondrial) Benzodiazepine receptor


J Med Chem 38: 4730-8 (1995)


BindingDB Entry DOI: 10.7270/Q2ZW1MJ8
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Translocator protein


(Rattus norvegicus (rat))
BDBM50255226
PNG
((7-chloro-N,N,5-trimethyl-4-oxo-3-phenyl-3,5-dihyd...)
Show SMILES CN(C)C(=O)Cc1nn(-c2ccccc2)c(=O)c2n(C)c3cc(Cl)ccc3c12
Show InChI InChI=1S/C21H19ClN4O2/c1-24(2)18(27)12-16-19-15-10-9-13(22)11-17(15)25(3)20(19)21(28)26(23-16)14-7-5-4-6-8-14/h4-11H,12H2,1-3H3
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n/an/an/a 3n/an/an/an/an/a



Brain and Mind Research Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]SSR180575 from TSPO in rat cortex


J Med Chem 52: 581-92 (2009)


Article DOI: 10.1021/jm8011678
BindingDB Entry DOI: 10.7270/Q2222VP0
More data for this
Ligand-Target Pair
Translocator protein


(Rattus norvegicus (rat))
BDBM50316600
PNG
(CHEMBL1097176 | N,N-Dipropyl-[5-isothiocyanato-2-p...)
Show SMILES CCCN(CCC)C(=O)C(=O)c1c([nH]c2ccc(cc12)N=C=S)-c1ccccc1
Show InChI InChI=1S/C23H23N3O2S/c1-3-12-26(13-4-2)23(28)22(27)20-18-14-17(24-15-29)10-11-19(18)25-21(20)16-8-6-5-7-9-16/h5-11,14,25H,3-4,12-13H2,1-2H3
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n/an/an/a 3.17n/an/an/an/an/a



Universit£ di Pisa

Curated by ChEMBL


Assay Description
Irreversible binding affinity to TSPO in rat kidney mitochondrial membrane


J Med Chem 53: 4085-93 (2010)


Article DOI: 10.1021/jm100100q
BindingDB Entry DOI: 10.7270/Q2XG9R9C
More data for this
Ligand-Target Pair
Translocator protein


(Rattus norvegicus (rat))
BDBM22040
PNG
(4 -chlorodiazepam | 4' Cl-diazepam | 7-chloro-...)
Show SMILES CN1c2ccc(Cl)cc2C(=NCC1=O)c1ccc(Cl)cc1 |c:10|
Show InChI InChI=1S/C16H12Cl2N2O/c1-20-14-7-6-12(18)8-13(14)16(19-9-15(20)21)10-2-4-11(17)5-3-10/h2-8H,9H2,1H3
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n/an/an/a 3.5n/an/an/an/an/a



University of Kansas

Curated by ChEMBL


Assay Description
Binding affinity constant for Benzodiazepine receptor in rat RG-2 glioma cells


J Med Chem 40: 1726-30 (1997)


Article DOI: 10.1021/jm960592p
BindingDB Entry DOI: 10.7270/Q2X929DZ
More data for this
Ligand-Target Pair
Translocator protein


(Homo sapiens (Human))
BDBM50255226
PNG
((7-chloro-N,N,5-trimethyl-4-oxo-3-phenyl-3,5-dihyd...)
Show SMILES CN(C)C(=O)Cc1nn(-c2ccccc2)c(=O)c2n(C)c3cc(Cl)ccc3c12
Show InChI InChI=1S/C21H19ClN4O2/c1-24(2)18(27)12-16-19-15-10-9-13(22)11-17(15)25(3)20(19)21(28)26(23-16)14-7-5-4-6-8-14/h4-11H,12H2,1-3H3
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n/an/an/a 3.5n/an/an/an/an/a



Emory University

Curated by ChEMBL


Assay Description
Binding affinity to human PBR


Bioorg Med Chem 16: 6145-55 (2008)


Article DOI: 10.1016/j.bmc.2008.04.046
BindingDB Entry DOI: 10.7270/Q26Q1Z4G
More data for this
Ligand-Target Pair
Translocator protein


(Rattus norvegicus (rat))
CHEMBL5282701
PNG
Show SMILES OC1CCN(CC1)C1CN(CCC2(CCC(=O)N(Cc3ccccc3)C2)c2ccc(Cl)c(Cl)c2)C1
Show InChI InChI=1S/C28H35Cl2N3O2/c29-25-7-6-22(16-26(25)30)28(11-8-27(35)33(20-28)17-21-4-2-1-3-5-21)12-15-31-18-23(19-31)32-13-9-24(34)10-14-32/h1-7,16,23-24,34H,8-15,17-20H2
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n/an/an/a 3.80n/an/an/an/an/a


TBA

Assay Description
Inhibitory activity against dihydrofolate reductase (DHFR) from rat liver


Citation and Details
More data for this
Ligand-Target Pair
Translocator protein


(Homo sapiens (Human))
BDBM50045877
PNG
(2-(2-(4-fluorophenyl)-1H-indol-3-yl)-N,N-dihexylac...)
Show SMILES CCCCCCN(CCCCCC)C(=O)Cc1c([nH]c2ccccc12)-c1ccc(F)cc1
Show InChI InChI=1S/C28H37FN2O/c1-3-5-7-11-19-31(20-12-8-6-4-2)27(32)21-25-24-13-9-10-14-26(24)30-28(25)22-15-17-23(29)18-16-22/h9-10,13-18,30H,3-8,11-12,19-21H2,1-2H3
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n/an/an/a 4n/an/an/an/an/a



Emory University

Curated by ChEMBL


Assay Description
Binding affinity to human PBR


Bioorg Med Chem 16: 6145-55 (2008)


Article DOI: 10.1016/j.bmc.2008.04.046
BindingDB Entry DOI: 10.7270/Q26Q1Z4G
More data for this
Ligand-Target Pair
Translocator protein


(Rattus norvegicus (rat))
BDBM50316601
PNG
(CHEMBL1097503 | N,N-Dihexyl-[5-isothiocyanato-2-ph...)
Show SMILES CCCCCCN(CCCCCC)C(=O)C(=O)c1c([nH]c2ccc(cc12)N=C=S)-c1ccccc1
Show InChI InChI=1S/C29H35N3O2S/c1-3-5-7-12-18-32(19-13-8-6-4-2)29(34)28(33)26-24-20-23(30-21-35)16-17-25(24)31-27(26)22-14-10-9-11-15-22/h9-11,14-17,20,31H,3-8,12-13,18-19H2,1-2H3
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n/an/an/a 5.07n/an/an/an/an/a



Universit£ di Pisa

Curated by ChEMBL


Assay Description
Irreversible binding affinity to TSPO in rat kidney mitochondrial membrane


J Med Chem 53: 4085-93 (2010)


Article DOI: 10.1021/jm100100q
BindingDB Entry DOI: 10.7270/Q2XG9R9C
More data for this
Ligand-Target Pair
Translocator protein


(Homo sapiens (Human))
BDBM22040
PNG
(4 -chlorodiazepam | 4' Cl-diazepam | 7-chloro-...)
Show SMILES CN1c2ccc(Cl)cc2C(=NCC1=O)c1ccc(Cl)cc1 |c:10|
Show InChI InChI=1S/C16H12Cl2N2O/c1-20-14-7-6-12(18)8-13(14)16(19-9-15(20)21)10-2-4-11(17)5-3-10/h2-8H,9H2,1H3
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n/an/an/a 6n/an/an/an/an/a



Emory University

Curated by ChEMBL


Assay Description
Binding affinity to human PBR


Bioorg Med Chem 16: 6145-55 (2008)


Article DOI: 10.1016/j.bmc.2008.04.046
BindingDB Entry DOI: 10.7270/Q26Q1Z4G
More data for this
Ligand-Target Pair
Translocator protein


(Rattus norvegicus (rat))
BDBM50316602
PNG
(CHEMBL1099012 | N-(5-Isothiocyanato-2-phenylindol-...)
Show SMILES [O-][N+](=O)c1ccc(NCCCCCCNC(=O)C(=O)c2c([nH]c3ccc(cc23)N=C=S)-c2ccccc2)c2nonc12
Show InChI InChI=1S/C29H25N7O5S/c37-28(24-20-16-19(32-17-42)10-11-21(20)33-25(24)18-8-4-3-5-9-18)29(38)31-15-7-2-1-6-14-30-22-12-13-23(36(39)40)27-26(22)34-41-35-27/h3-5,8-13,16,30,33H,1-2,6-7,14-15H2,(H,31,38)
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n/an/an/a 8.31n/an/an/an/an/a



Universit£ di Pisa

Curated by ChEMBL


Assay Description
Irreversible binding affinity to TSPO in rat kidney mitochondrial membrane


J Med Chem 53: 4085-93 (2010)


Article DOI: 10.1021/jm100100q
BindingDB Entry DOI: 10.7270/Q2XG9R9C
More data for this
Ligand-Target Pair
Translocator protein


(Homo sapiens (Human))
BDBM50378901
PNG
(CHEMBL1672418)
Show SMILES CCC(C)N(C)C(=O)c1cc2ccccc2c(n1)-c1ccccc1I
Show InChI InChI=1S/C21H21IN2O/c1-4-14(2)24(3)21(25)19-13-15-9-5-6-10-16(15)20(23-19)17-11-7-8-12-18(17)22/h5-14H,4H2,1-3H3
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n/an/an/a 10n/an/an/an/an/a


TBA

Assay Description
Inhibitory activity against dihydrofolate reductase (DHFR) from Escherichia coli


Citation and Details
More data for this
Ligand-Target Pair
Translocator protein


(Rattus norvegicus (rat))
BDBM50021058
PNG
(7-Chloro-1-methyl-5-phenyl-2,3-dihydro-1H-benzo[e]...)
Show SMILES CN1CCN=C(c2ccccc2)c2cc(Cl)ccc12 |t:4|
Show InChI InChI=1S/C16H15ClN2/c1-19-10-9-18-16(12-5-3-2-4-6-12)14-11-13(17)7-8-15(14)19/h2-8,11H,9-10H2,1H3
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Universit£ di Ferrara

Curated by ChEMBL


Assay Description
Binding affinity constant for peripheral (mitochondrial) Benzodiazepine receptor


J Med Chem 38: 4730-8 (1995)


BindingDB Entry DOI: 10.7270/Q2ZW1MJ8
More data for this
Ligand-Target Pair
Translocator protein


(Homo sapiens (Human))
BDBM22032
PNG
(1-(2-chlorophenyl)-N-methyl-N-(1-methylpropyl)isoq...)
Show SMILES CCC(C)N(C)C(=O)c1cc2ccccc2c(n1)-c1ccccc1Cl
Show InChI InChI=1S/C21H21ClN2O/c1-4-14(2)24(3)21(25)19-13-15-9-5-6-10-16(15)20(23-19)17-11-7-8-12-18(17)22/h5-14H,4H2,1-3H3
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n/an/an/a 11n/an/an/an/an/a



Korea Institute of Science and Technology (KIST)

Curated by ChEMBL


Assay Description
Inhibition concentration against human adenosine kinase


Eur J Med Chem 141: 240-256 (2017)


Article DOI: 10.1016/j.ejmech.2017.09.033
BindingDB Entry DOI: 10.7270/Q2ZG6VRM
More data for this
Ligand-Target Pair
Translocator protein


(Homo sapiens (Human))
BDBM22032
PNG
(1-(2-chlorophenyl)-N-methyl-N-(1-methylpropyl)isoq...)
Show SMILES CCC(C)N(C)C(=O)c1cc2ccccc2c(n1)-c1ccccc1Cl
Show InChI InChI=1S/C21H21ClN2O/c1-4-14(2)24(3)21(25)19-13-15-9-5-6-10-16(15)20(23-19)17-11-7-8-12-18(17)22/h5-14H,4H2,1-3H3
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n/an/an/a 11n/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Binding affinity to recombinant human TSPO by SPR assay


Eur J Med Chem 125: 1172-1192 (2017)


Article DOI: 10.1016/j.ejmech.2016.11.017
BindingDB Entry DOI: 10.7270/Q25Q4Z83
More data for this
Ligand-Target Pair
Translocator protein


(Homo sapiens (Human))
BDBM50336914
PNG
(3-[(21S,22S)-16-ethenyl-11-ethyl-12,17,21,26-tetra...)
Show SMILES CCc1c(C)c2cc3[nH]c(cc4[nH]c(c(CCC(=O)NCCCCCCNC(=O)c5cc6ccccc6c(n5)-c5ccccc5I)c4C)c4cc(O)c5c(C)c(cc1[nH]2)[nH]c45)c(C)c3C=C
Show InChI InChI=1S/C55H56IN7O3/c1-7-35-30(3)42-27-44-32(5)37(52(61-44)40-26-49(64)51-33(6)45(62-54(40)51)29-47-36(8-2)31(4)43(60-47)28-46(35)59-42)21-22-50(65)57-23-15-9-10-16-24-58-55(66)48-25-34-17-11-12-18-38(34)53(63-48)39-19-13-14-20-41(39)56/h7,11-14,17-20,25-29,59-62,64H,1,8-10,15-16,21-24H2,2-6H3,(H,57,65)(H,58,66)/b42-27-,43-28-,44-27-,45-29-,46-28-,47-29-,52-40-
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n/an/an/a 40n/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Binding affinity to PBR


ACS Med Chem Lett 2: 136-141 (2011)


Article DOI: 10.1021/ml100211g
BindingDB Entry DOI: 10.7270/Q2F76DJG
More data for this
Ligand-Target Pair
Translocator protein


(Homo sapiens (Human))
BDBM50279019
PNG
(CHEMBL1315992)
Show SMILES CCc1nnc(SCC(=O)N(C)c2ccccc2)c2cc3sccc3n12
Show InChI InChI=1S/C19H18N4OS2/c1-3-17-20-21-19(15-11-16-14(23(15)17)9-10-25-16)26-12-18(24)22(2)13-7-5-4-6-8-13/h4-11H,3,12H2,1-2H3
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n/an/an/a 40n/an/an/an/an/a



Korea Institute of Science and Technology (KIST)

Curated by ChEMBL


Assay Description
Binding affinity to C-terminal DDK-tagged human recombinant full-length TSPO expressed in HEK293 cells by SPR assay


Eur J Med Chem 141: 240-256 (2017)


Article DOI: 10.1016/j.ejmech.2017.09.033
BindingDB Entry DOI: 10.7270/Q2ZG6VRM
More data for this
Ligand-Target Pair
Translocator protein


(Rattus norvegicus (rat))
BDBM22040
PNG
(4 -chlorodiazepam | 4' Cl-diazepam | 7-chloro-...)
Show SMILES CN1c2ccc(Cl)cc2C(=NCC1=O)c1ccc(Cl)cc1 |c:10|
Show InChI InChI=1S/C16H12Cl2N2O/c1-20-14-7-6-12(18)8-13(14)16(19-9-15(20)21)10-2-4-11(17)5-3-10/h2-8H,9H2,1H3
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KEGG

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n/an/an/a 58n/an/an/an/an/a



Universit£ di Ferrara

Curated by ChEMBL


Assay Description
Binding affinity constant for peripheral (mitochondrial) Benzodiazepine receptor


J Med Chem 38: 4730-8 (1995)


BindingDB Entry DOI: 10.7270/Q2ZW1MJ8
More data for this
Ligand-Target Pair
Translocator protein


(Homo sapiens (Human))
BDBM50279015
PNG
(CHEMBL4174207)
Show SMILES CCc1nnc(SCC(=O)N(C)c2ccccc2)c2cc3sc(C)cc3n12
Show InChI InChI=1S/C20H20N4OS2/c1-4-18-21-22-20(16-11-17-15(24(16)18)10-13(2)27-17)26-12-19(25)23(3)14-8-6-5-7-9-14/h5-11H,4,12H2,1-3H3
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n/an/an/a 61n/an/an/an/an/a



Korea Institute of Science and Technology (KIST)

Curated by ChEMBL


Assay Description
Binding affinity to C-terminal DDK-tagged human recombinant full-length TSPO expressed in HEK293 cells by SPR assay


Eur J Med Chem 141: 240-256 (2017)


Article DOI: 10.1016/j.ejmech.2017.09.033
BindingDB Entry DOI: 10.7270/Q2ZG6VRM
More data for this
Ligand-Target Pair
Translocator protein


(Homo sapiens (Human))
BDBM50210940
PNG
(CHEMBL3948914)
Show SMILES CC(C)c1ccc(C)c(NC(=O)Cn2c(Cc3c(Cl)cccc3Cl)nc3ccccc23)c1
Show InChI InChI=1S/C26H25Cl2N3O/c1-16(2)18-12-11-17(3)23(13-18)30-26(32)15-31-24-10-5-4-9-22(24)29-25(31)14-19-20(27)7-6-8-21(19)28/h4-13,16H,14-15H2,1-3H3,(H,30,32)
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n/an/an/a 108n/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Binding affinity to recombinant human TSPO by SPR assay


Eur J Med Chem 125: 1172-1192 (2017)


Article DOI: 10.1016/j.ejmech.2016.11.017
BindingDB Entry DOI: 10.7270/Q25Q4Z83
More data for this
Ligand-Target Pair
Translocator protein


(Rattus norvegicus (rat))
BDBM50000766
PNG
(CHEMBL12 | DIAZEPAM | US9271961, Diazepam)
Show SMILES CN1c2ccc(Cl)cc2C(=NCC1=O)c1ccccc1 |c:10|
Show InChI InChI=1S/C16H13ClN2O/c1-19-14-8-7-12(17)9-13(14)16(18-10-15(19)20)11-5-3-2-4-6-11/h2-9H,10H2,1H3
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KEGG

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n/an/an/a 213n/an/an/an/an/a



Universit£ di Ferrara

Curated by ChEMBL


Assay Description
Binding affinity constant for peripheral (mitochondrial) Benzodiazepine receptor


J Med Chem 38: 4730-8 (1995)


BindingDB Entry DOI: 10.7270/Q2ZW1MJ8
More data for this
Ligand-Target Pair
Translocator protein


(Rattus norvegicus (rat))
BDBM22040
PNG
(4 -chlorodiazepam | 4' Cl-diazepam | 7-chloro-...)
Show SMILES CN1c2ccc(Cl)cc2C(=NCC1=O)c1ccc(Cl)cc1 |c:10|
Show InChI InChI=1S/C16H12Cl2N2O/c1-20-14-7-6-12(18)8-13(14)16(19-9-15(20)21)10-2-4-11(17)5-3-10/h2-8H,9H2,1H3
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KEGG

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n/an/an/a 1.30E+3n/an/an/an/an/a



University of Kansas

Curated by ChEMBL


Assay Description
Binding affinity constant for Benzodiazepine receptor in normal rat brain homogenate


J Med Chem 40: 1726-30 (1997)


Article DOI: 10.1021/jm960592p
BindingDB Entry DOI: 10.7270/Q2X929DZ
More data for this
Ligand-Target Pair
Translocator protein


(Rattus norvegicus (rat))
BDBM22040
PNG
(4 -chlorodiazepam | 4' Cl-diazepam | 7-chloro-...)
Show SMILES CN1c2ccc(Cl)cc2C(=NCC1=O)c1ccc(Cl)cc1 |c:10|
Show InChI InChI=1S/C16H12Cl2N2O/c1-20-14-7-6-12(18)8-13(14)16(19-9-15(20)21)10-2-4-11(17)5-3-10/h2-8H,9H2,1H3
PDB

KEGG

UniProtKB/SwissProt

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n/an/an/a 4.00E+3n/an/an/an/an/a



University of Kansas

Curated by ChEMBL


Assay Description
Binding affinity constant for Benzodiazepine receptor in rat C6 glioma cells


J Med Chem 40: 1726-30 (1997)


Article DOI: 10.1021/jm960592p
BindingDB Entry DOI: 10.7270/Q2X929DZ
More data for this
Ligand-Target Pair