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Compile Data Set for Download or QSAR

Found 164 hits with Last Name = 'li' and Initial = 'rt'   
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
Neuronal acetylcholine receptor Alpha-4/Beta-2


(Homo sapiens (Human))
BDBM50115808
PNG
(CHEMBL61616 | Dimethyl-[2-(pyridin-3-yloxy)-ethyl]...)
Show SMILES CN(C)CCOc1cccnc1
Show InChI InChI=1S/C9H14N2O/c1-11(2)6-7-12-9-4-3-5-10-8-9/h3-5,8H,6-7H2,1-2H3
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21n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Affinity to alpha-4-beta-2 AChR


Bioorg Med Chem Lett 16: 2013-6 (2006)


Article DOI: 10.1016/j.bmcl.2005.12.073
BindingDB Entry DOI: 10.7270/Q2WD41TH
More data for this
Ligand-Target Pair
Neuronal acetylcholine receptor Alpha-4/Beta-2


(Homo sapiens (Human))
BDBM50115825
PNG
(CHEMBL60792 | Ethyl-methyl-pyridin-3-ylmethyl-amin...)
Show SMILES CCN(C)Cc1cccnc1
Show InChI InChI=1S/C9H14N2/c1-3-11(2)8-9-5-4-6-10-7-9/h4-7H,3,8H2,1-2H3
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28n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Affinity to alpha-4-beta-2 AChR


Bioorg Med Chem Lett 16: 2013-6 (2006)


Article DOI: 10.1016/j.bmcl.2005.12.073
BindingDB Entry DOI: 10.7270/Q2WD41TH
More data for this
Ligand-Target Pair
Neuronal acetylcholine receptor Alpha-4/Beta-2


(Homo sapiens (Human))
BDBM50120586
PNG
(CHEMBL112221 | Methyl-[2-(pyridin-3-yloxy)-ethyl]-...)
Show SMILES CNCCOc1cccnc1
Show InChI InChI=1S/C8H12N2O/c1-9-5-6-11-8-3-2-4-10-7-8/h2-4,7,9H,5-6H2,1H3
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35n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Affinity to alpha-4-beta-2 AChR


Bioorg Med Chem Lett 16: 2013-6 (2006)


Article DOI: 10.1016/j.bmcl.2005.12.073
BindingDB Entry DOI: 10.7270/Q2WD41TH
More data for this
Ligand-Target Pair
Neuronal acetylcholine receptor protein alpha-7 subunit


(Homo sapiens (Human))
BDBM50336020
PNG
(CHEMBL1669092 | N,N,N-trimethyl-1-(4-styrylphenoxy...)
Show SMILES CC(COc1ccc(\C=C/c2ccccc2)cc1)[N+](C)(C)C
Show InChI InChI=1S/C20H26NO/c1-17(21(2,3)4)16-22-20-14-12-19(13-15-20)11-10-18-8-6-5-7-9-18/h5-15,17H,16H2,1-4H3/q+1/b11-10-
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57n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Binding affinity to alpha7 nAChR


Bioorg Med Chem Lett 21: 940-3 (2011)


Article DOI: 10.1016/j.bmcl.2010.12.052
BindingDB Entry DOI: 10.7270/Q2M045Q6
More data for this
Ligand-Target Pair
Neuronal acetylcholine receptor Alpha-4/Beta-2


(Homo sapiens (Human))
BDBM50138489
PNG
(CHEMBL54860 | Methyl-(4-pyridin-3-yl-but-3-ynyl)-a...)
Show SMILES CNCCC#Cc1cccnc1
Show InChI InChI=1S/C10H12N2/c1-11-7-3-2-5-10-6-4-8-12-9-10/h4,6,8-9,11H,3,7H2,1H3
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113n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Affinity to alpha-4-beta-2 AChR


Bioorg Med Chem Lett 16: 2013-6 (2006)


Article DOI: 10.1016/j.bmcl.2005.12.073
BindingDB Entry DOI: 10.7270/Q2WD41TH
More data for this
Ligand-Target Pair
Neuronal acetylcholine receptor protein alpha-4/beta-2 subunit


(Rattus norvegicus (Rat))
BDBM50061567
PNG
(1,1-Dimethyl-4-phenyl-piperazin-1-ium | CHEMBL1347...)
Show SMILES C[N+]1(C)CCN(CC1)c1ccccc1
Show InChI InChI=1S/C12H19N2/c1-14(2)10-8-13(9-11-14)12-6-4-3-5-7-12/h3-7H,8-11H2,1-2H3/q+1
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250n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Binding affinity towards nicotinic receptor in rat brain using [3H]cytisine ligand


Bioorg Med Chem Lett 13: 1729-32 (2003)


Article DOI: 10.1016/s0960-894x(03)00213-0
BindingDB Entry DOI: 10.7270/Q2Q81FK8
More data for this
Ligand-Target Pair
Neuronal acetylcholine receptor Alpha-4/Beta-2


(Homo sapiens (Human))
BDBM50138494
PNG
(CHEMBL150893 | Dimethyl-(4-pyridin-3-yl-but-3-ynyl...)
Show SMILES CN(C)CCC#Cc1cccnc1
Show InChI InChI=1S/C11H14N2/c1-13(2)9-4-3-6-11-7-5-8-12-10-11/h5,7-8,10H,4,9H2,1-2H3
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510n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Affinity to alpha-4-beta-2 AChR


Bioorg Med Chem Lett 16: 2013-6 (2006)


Article DOI: 10.1016/j.bmcl.2005.12.073
BindingDB Entry DOI: 10.7270/Q2WD41TH
More data for this
Ligand-Target Pair
Neuronal acetylcholine receptor Alpha-4/Beta-2


(Homo sapiens (Human))
BDBM50119559
PNG
(CHEMBL331904 | Dimethyl-pyridin-3-ylmethyl-amine |...)
Show SMILES CN(C)Cc1cccnc1
Show InChI InChI=1S/C8H12N2/c1-10(2)7-8-4-3-5-9-6-8/h3-6H,7H2,1-2H3
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540n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Affinity to alpha-4-beta-2 AChR


Bioorg Med Chem Lett 16: 2013-6 (2006)


Article DOI: 10.1016/j.bmcl.2005.12.073
BindingDB Entry DOI: 10.7270/Q2WD41TH
More data for this
Ligand-Target Pair
Neuronal acetylcholine receptor Alpha-4/Beta-2


(Homo sapiens (Human))
BDBM50138487
PNG
(CHEMBL150948 | Ethyl-methyl-(4-pyridin-3-yl-but-3-...)
Show SMILES CCN(C)CCC#Cc1cccnc1
Show InChI InChI=1S/C12H16N2/c1-3-14(2)10-5-4-7-12-8-6-9-13-11-12/h6,8-9,11H,3,5,10H2,1-2H3
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1.77E+3n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Affinity to alpha-4-beta-2 AChR


Bioorg Med Chem Lett 16: 2013-6 (2006)


Article DOI: 10.1016/j.bmcl.2005.12.073
BindingDB Entry DOI: 10.7270/Q2WD41TH
More data for this
Ligand-Target Pair
Neuronal acetylcholine receptor Alpha-4/Beta-2


(Homo sapiens (Human))
BDBM50138486
PNG
(CHEMBL357101 | Methyl-pyridin-3-ylmethyl-amine | N...)
Show SMILES CNCc1cccnc1
Show InChI InChI=1S/C7H10N2/c1-8-5-7-3-2-4-9-6-7/h2-4,6,8H,5H2,1H3
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>1.00E+4n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Affinity to alpha-4-beta-2 AChR


Bioorg Med Chem Lett 16: 2013-6 (2006)


Article DOI: 10.1016/j.bmcl.2005.12.073
BindingDB Entry DOI: 10.7270/Q2WD41TH
More data for this
Ligand-Target Pair
Neuronal acetylcholine receptor subunit beta-2


(Homo sapiens (Human))
BDBM50336020
PNG
(CHEMBL1669092 | N,N,N-trimethyl-1-(4-styrylphenoxy...)
Show SMILES CC(COc1ccc(\C=C/c2ccccc2)cc1)[N+](C)(C)C
Show InChI InChI=1S/C20H26NO/c1-17(21(2,3)4)16-22-20-14-12-19(13-15-20)11-10-18-8-6-5-7-9-18/h5-15,17H,16H2,1-4H3/q+1/b11-10-
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3.90E+4n/an/an/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Binding affinity to beta2 nAChR


Bioorg Med Chem Lett 21: 940-3 (2011)


Article DOI: 10.1016/j.bmcl.2010.12.052
BindingDB Entry DOI: 10.7270/Q2M045Q6
More data for this
Ligand-Target Pair
Proteasome subunit beta type-1/beta type-5


(Homo sapiens (Human))
BDBM50259656
PNG
(CHEMBL4089402)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)N1CCc2ccccc2C1)B(O)O
Show InChI InChI=1S/C24H32BN3O4/c1-17(2)14-22(25(31)32)27-23(29)21(15-18-8-4-3-5-9-18)26-24(30)28-13-12-19-10-6-7-11-20(19)16-28/h3-11,17,21-22,31-32H,12-16H2,1-2H3,(H,26,30)(H,27,29)/t21-,22-/m0/s1
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n/an/a 0.000200n/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Dissociation constant against galectin-3 using competitive fluorescence polarization


Eur J Med Chem 125: 925-939 (2017)


BindingDB Entry DOI: 10.7270/Q2348NTK
More data for this
Ligand-Target Pair
Proteasome subunit beta type-1/beta type-5


(Homo sapiens (Human))
BDBM50259645
PNG
(CHEMBL4070336)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)NCc1cccc(c1)-c1ccccc1)B(O)O
Show InChI InChI=1S/C28H34BN3O4/c1-20(2)16-26(29(35)36)32-27(33)25(18-21-10-5-3-6-11-21)31-28(34)30-19-22-12-9-15-24(17-22)23-13-7-4-8-14-23/h3-15,17,20,25-26,35-36H,16,18-19H2,1-2H3,(H,32,33)(H2,30,31,34)/t25-,26-/m0/s1
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n/an/a 0.300n/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Inhibition of chymotrypsin-like activity of 20S proteasome in human HL60 cells using Suc-LLVYaminoluciferin as substrate after 2 hrs by fluorescence ...


Eur J Med Chem 125: 925-939 (2017)


BindingDB Entry DOI: 10.7270/Q2348NTK
More data for this
Ligand-Target Pair
ITGAV/ITGB3


(Homo sapiens (Human))
BDBM50237601
PNG
(CHEMBL411941 | CycloRGDfV | [(2S,5R,8S,11S)-5-Benz...)
Show SMILES CC(C)[C@@H]1NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCN=C(N)N)NC1=O
Show InChI InChI=1S/C26H38N8O7/c1-14(2)21-25(41)32-16(9-6-10-29-26(27)28)22(38)30-13-19(35)31-18(12-20(36)37)23(39)33-17(24(40)34-21)11-15-7-4-3-5-8-15/h3-5,7-8,14,16-18,21H,6,9-13H2,1-2H3,(H,30,38)(H,31,35)(H,32,41)(H,33,39)(H,34,40)(H,36,37)(H4,27,28,29)/t16-,17+,18-,21-/m0/s1
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n/an/a 0.487n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of human alpha-v-beta-3 integrin receptor by ELISA


Bioorg Med Chem Lett 16: 6178-80 (2006)


BindingDB Entry DOI: 10.7270/Q2C25069
More data for this
Ligand-Target Pair
Cytochrome P450 11B1


(Homo sapiens (Human))
BDBM50464579
PNG
(CHEMBL4281975)
Show SMILES COc1cncc(Cc2ccc(nc2)-c2ccccc2F)c1
Show InChI InChI=1S/C18H15FN2O/c1-22-15-9-14(10-20-12-15)8-13-6-7-18(21-11-13)16-4-2-3-5-17(16)19/h2-7,9-12H,8H2,1H3
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n/an/a 0.800n/an/an/an/an/an/a



Saarland University

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B1 expressed in hamster V79MZ cells using [1,2-3H]-11-deoxycorticosterone as substrate after 6 hrs by HPTLC analysis


Eur J Med Chem 143: 591-597 (2018)


BindingDB Entry DOI: 10.7270/Q2SF2ZTB
More data for this
Ligand-Target Pair
Neuronal acetylcholine receptor Alpha-4/Beta-2


(Homo sapiens (Human))
BDBM50049757
PNG
(()-2-(6-Chloro-pyridin-3-yl)-7-aza-bicyclo[2.2.1]h...)
Show SMILES Clc1ccc(cn1)C1CC2CCC1N2
Show InChI InChI=1S/C11H13ClN2/c12-11-4-1-7(6-13-11)9-5-8-2-3-10(9)14-8/h1,4,6,8-10,14H,2-3,5H2
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n/an/a 1.10n/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Inhibition of alpha-4-beta-2 nAChR


Bioorg Med Chem Lett 17: 6245-9 (2007)


Article DOI: 10.1016/j.bmcl.2007.09.026
BindingDB Entry DOI: 10.7270/Q24J0GBN
More data for this
Ligand-Target Pair
Sodium-dependent dopamine transporter


(Rattus norvegicus (rat))
BDBM50006774
PNG
((2S,3S)-methyl 3-(4-iodophenyl)-8-methyl-8-aza-bic...)
Show SMILES COC(=O)[C@@H]1C2CC[C@H](C[C@@H]1c1ccc(I)cc1)N2C
Show InChI InChI=1S/C16H20INO2/c1-18-12-7-8-14(18)15(16(19)20-2)13(9-12)10-3-5-11(17)6-4-10/h3-6,12-15H,7-9H2,1-2H3/t12-,13-,14?,15+/m1/s1
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n/an/a 1.60n/an/an/an/an/an/a



Research Biochemicals Inc.

Curated by ChEMBL


Assay Description
Compound was tested for binding affinity to dopamine reuptake sites in the tissue homogenates prepared from primate rat striatum using [3H]CFT as rad...


J Med Chem 34: 3144-6 (1991)


Article DOI: 10.1021/jm00114a027
BindingDB Entry DOI: 10.7270/Q23R0TGB
More data for this
Ligand-Target Pair
Proteasome subunit beta type-1/beta type-5


(Homo sapiens (Human))
BDBM50259657
PNG
(CHEMBL4068221)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)N(C)Cc1ccccc1)B(O)O
Show InChI InChI=1S/C23H32BN3O4/c1-17(2)14-21(24(30)31)26-22(28)20(15-18-10-6-4-7-11-18)25-23(29)27(3)16-19-12-8-5-9-13-19/h4-13,17,20-21,30-31H,14-16H2,1-3H3,(H,25,29)(H,26,28)/t20-,21-/m0/s1
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n/an/a 2n/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Dissociation constant against galectin-3 using competitive fluorescence polarization


Eur J Med Chem 125: 925-939 (2017)


BindingDB Entry DOI: 10.7270/Q2348NTK
More data for this
Ligand-Target Pair
Proteasome subunit beta type-1/beta type-5


(Homo sapiens (Human))
BDBM50259647
PNG
(CHEMBL4100727)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)NCc1ccc(F)c(F)c1)B(O)O
Show InChI InChI=1S/C22H28BF2N3O4/c1-14(2)10-20(23(31)32)28-21(29)19(12-15-6-4-3-5-7-15)27-22(30)26-13-16-8-9-17(24)18(25)11-16/h3-9,11,14,19-20,31-32H,10,12-13H2,1-2H3,(H,28,29)(H2,26,27,30)/t19-,20-/m0/s1
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n/an/a 2n/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Inhibition of chymotrypsin-like activity of 20S proteasome in human HL60 cells using Suc-LLVYaminoluciferin as substrate after 2 hrs by fluorescence ...


Eur J Med Chem 125: 925-939 (2017)


BindingDB Entry DOI: 10.7270/Q2348NTK
More data for this
Ligand-Target Pair
Proteasome subunit beta type-1/beta type-5


(Homo sapiens (Human))
BDBM50259659
PNG
(CHEMBL4076838)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)NCc1cccc(c1)[N+]([O-])=O)B(O)O
Show InChI InChI=1S/C22H29BN4O6/c1-15(2)11-20(23(30)31)26-21(28)19(13-16-7-4-3-5-8-16)25-22(29)24-14-17-9-6-10-18(12-17)27(32)33/h3-10,12,15,19-20,30-31H,11,13-14H2,1-2H3,(H,26,28)(H2,24,25,29)/t19-,20-/m0/s1
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n/an/a 3n/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Dissociation constant against galectin-3 using competitive fluorescence polarization


Eur J Med Chem 125: 925-939 (2017)


BindingDB Entry DOI: 10.7270/Q2348NTK
More data for this
Ligand-Target Pair
Sodium-dependent serotonin transporter


(Rattus norvegicus (rat))
BDBM50006774
PNG
((2S,3S)-methyl 3-(4-iodophenyl)-8-methyl-8-aza-bic...)
Show SMILES COC(=O)[C@@H]1C2CC[C@H](C[C@@H]1c1ccc(I)cc1)N2C
Show InChI InChI=1S/C16H20INO2/c1-18-12-7-8-14(18)15(16(19)20-2)13(9-12)10-3-5-11(17)6-4-10/h3-6,12-15H,7-9H2,1-2H3/t12-,13-,14?,15+/m1/s1
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n/an/a 3.80n/an/an/an/an/an/a



Research Biochemicals Inc.

Curated by ChEMBL


Assay Description
Compound was tested for binding affinity to Serotonin transporter sites in homogenates prepared from rat cortical membranes using [3H]paroxetine as r...


J Med Chem 34: 3144-6 (1991)


Article DOI: 10.1021/jm00114a027
BindingDB Entry DOI: 10.7270/Q23R0TGB
More data for this
Ligand-Target Pair
Proteasome subunit beta type-1/beta type-5


(Homo sapiens (Human))
BDBM50259642
PNG
(CHEMBL4077037)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)NCc1cccc(C)c1C)B(O)O
Show InChI InChI=1S/C24H34BN3O4/c1-16(2)13-22(25(31)32)28-23(29)21(14-19-10-6-5-7-11-19)27-24(30)26-15-20-12-8-9-17(3)18(20)4/h5-12,16,21-22,31-32H,13-15H2,1-4H3,(H,28,29)(H2,26,27,30)/t21-,22-/m0/s1
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n/an/a 4n/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Inhibition of chymotrypsin-like activity of 20S proteasome in human HL60 cells using Suc-LLVYaminoluciferin as substrate after 2 hrs by fluorescence ...


Eur J Med Chem 125: 925-939 (2017)


BindingDB Entry DOI: 10.7270/Q2348NTK
More data for this
Ligand-Target Pair
Proteasome subunit beta type-1/beta type-5


(Homo sapiens (Human))
BDBM50069989
PNG
((R)-3-methyl-1-((S)-3-phenyl-2-(pyrazine-2-carboxa...)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)c1cnccn1)B(O)O
Show InChI InChI=1S/C19H25BN4O4/c1-13(2)10-17(20(27)28)24-18(25)15(11-14-6-4-3-5-7-14)23-19(26)16-12-21-8-9-22-16/h3-9,12-13,15,17,27-28H,10-11H2,1-2H3,(H,23,26)(H,24,25)/t15-,17-/m0/s1
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n/an/a 4n/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Inhibition of chymotrypsin-like activity of 20S proteasome in human HL60 cells using Suc-LLVYaminoluciferin as substrate after 2 hrs by fluorescence ...


Eur J Med Chem 125: 925-939 (2017)


BindingDB Entry DOI: 10.7270/Q2348NTK
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Matrix metalloproteinase 2/9


(Homo sapiens (Human))
BDBM50063140
PNG
((2R)-[(4-biphenylylsulfonyl) amino]-N-hydroxy-3-ph...)
Show SMILES ONC(=O)[C@@H](Cc1ccccc1)NS(=O)(=O)c1ccc(cc1)-c1ccccc1
Show InChI InChI=1S/C21H20N2O4S/c24-21(22-25)20(15-16-7-3-1-4-8-16)23-28(26,27)19-13-11-18(12-14-19)17-9-5-2-6-10-17/h1-14,20,23,25H,15H2,(H,22,24)/t20-/m1/s1
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n/an/a 7.06n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of human MMP9 by quenched fluorescense assay


Bioorg Med Chem Lett 16: 6178-80 (2006)


BindingDB Entry DOI: 10.7270/Q2C25069
More data for this
Ligand-Target Pair
Proteasome subunit beta type-1/beta type-5


(Homo sapiens (Human))
BDBM50259641
PNG
(CHEMBL484701)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)NCc1ccccc1)B(O)O
Show InChI InChI=1S/C22H30BN3O4/c1-16(2)13-20(23(29)30)26-21(27)19(14-17-9-5-3-6-10-17)25-22(28)24-15-18-11-7-4-8-12-18/h3-12,16,19-20,29-30H,13-15H2,1-2H3,(H,26,27)(H2,24,25,28)/t19-,20-/m0/s1
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n/an/a 10n/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Inhibition of chymotrypsin-like activity of 20S proteasome in human HL60 cells using Suc-LLVYaminoluciferin as substrate after 2 hrs by fluorescence ...


Eur J Med Chem 125: 925-939 (2017)


BindingDB Entry DOI: 10.7270/Q2348NTK
More data for this
Ligand-Target Pair
Proteasome subunit beta type-1/beta type-5


(Homo sapiens (Human))
BDBM50259655
PNG
(CHEMBL4080306)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)N[C@H](C)c1ccccc1)B(O)O
Show InChI InChI=1S/C23H32BN3O4/c1-16(2)14-21(24(30)31)27-22(28)20(15-18-10-6-4-7-11-18)26-23(29)25-17(3)19-12-8-5-9-13-19/h4-13,16-17,20-21,30-31H,14-15H2,1-3H3,(H,27,28)(H2,25,26,29)/t17-,20+,21+/m1/s1
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n/an/a 10n/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Dissociation constant against galectin-3 using competitive fluorescence polarization


Eur J Med Chem 125: 925-939 (2017)


BindingDB Entry DOI: 10.7270/Q2348NTK
More data for this
Ligand-Target Pair
Proteasome subunit beta type-1/beta type-5


(Homo sapiens (Human))
BDBM50259646
PNG
(CHEMBL4075225)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)NCc1ccc2ccccc2c1)B(O)O
Show InChI InChI=1S/C26H32BN3O4/c1-18(2)14-24(27(33)34)30-25(31)23(16-19-8-4-3-5-9-19)29-26(32)28-17-20-12-13-21-10-6-7-11-22(21)15-20/h3-13,15,18,23-24,33-34H,14,16-17H2,1-2H3,(H,30,31)(H2,28,29,32)/t23-,24-/m0/s1
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n/an/a 12n/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Inhibition of chymotrypsin-like activity of 20S proteasome in human HL60 cells using Suc-LLVYaminoluciferin as substrate after 2 hrs by fluorescence ...


Eur J Med Chem 125: 925-939 (2017)


BindingDB Entry DOI: 10.7270/Q2348NTK
More data for this
Ligand-Target Pair
Sodium-dependent dopamine transporter


(Rattus norvegicus (rat))
BDBM50451132
PNG
(CHEMBL2079586 | WIN-35428)
Show SMILES COC(=O)[C@@H]1[C@H]2CC[C@H](C[C@@H]1c1ccc(F)cc1)N2C
Show InChI InChI=1S/C16H20FNO2/c1-18-12-7-8-14(18)15(16(19)20-2)13(9-12)10-3-5-11(17)6-4-10/h3-6,12-15H,7-9H2,1-2H3/t12-,13-,14-,15+/m1/s1
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n/an/a 15n/an/an/an/an/an/a



Research Biochemicals Inc.

Curated by ChEMBL


Assay Description
Compound was tested for binding affinity to dopamine reuptake sites in the tissue homogenates prepared from primate rat striatum using [3H]CFT as rad...


J Med Chem 34: 3144-6 (1991)


Article DOI: 10.1021/jm00114a027
BindingDB Entry DOI: 10.7270/Q23R0TGB
More data for this
Ligand-Target Pair
Cytochrome P450 11B1


(Homo sapiens (Human))
BDBM50028166
PNG
(CHEMBL934 | METYRAPONE | US9138393, Metyrapone | U...)
Show SMILES CC(C)(C(=O)c1cccnc1)c1cccnc1
Show InChI InChI=1S/C14H14N2O/c1-14(2,12-6-4-8-16-10-12)13(17)11-5-3-7-15-9-11/h3-10H,1-2H3
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n/an/a 15n/an/an/an/an/an/a



Saarland University

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B1 expressed in hamster V79MZ cells using [1,2-3H]-11-deoxycorticosterone as substrate after 6 hrs by HPTLC analysis


Eur J Med Chem 143: 591-597 (2018)


BindingDB Entry DOI: 10.7270/Q2SF2ZTB
More data for this
Ligand-Target Pair
Cytochrome P450 11B1


(Homo sapiens (Human))
BDBM50464575
PNG
(CHEMBL4282375)
Show SMILES Cn1nc(cc1Cc1cncc(O)c1)-c1ccccc1
Show InChI InChI=1S/C16H15N3O/c1-19-14(7-12-8-15(20)11-17-10-12)9-16(18-19)13-5-3-2-4-6-13/h2-6,8-11,20H,7H2,1H3
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n/an/a 17n/an/an/an/an/an/a



Saarland University

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B1 expressed in hamster V79MZ cells using [1,2-3H]-11-deoxycorticosterone as substrate after 6 hrs by HPTLC analysis


Eur J Med Chem 143: 591-597 (2018)


BindingDB Entry DOI: 10.7270/Q2SF2ZTB
More data for this
Ligand-Target Pair
Beta-lactamase


(Enterobacter cloacae)
BDBM50129566
PNG
((2S,5R,6R)-2'-(tert-Butyl-dimethyl-silanyl-oxy)-3,...)
Show SMILES CC(C)(C)[Si](C)(C)O[C@H]1C[C@@]11[C@@H]2N([C@@H](C(O)=O)C(C)(C)S2(=O)=O)C1=O
Show InChI InChI=1S/C16H27NO6SSi/c1-14(2,3)25(6,7)23-9-8-16(9)12(20)17-10(11(18)19)15(4,5)24(21,22)13(16)17/h9-10,13H,8H2,1-7H3,(H,18,19)/t9-,10-,13+,16+/m0/s1
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n/an/a 20n/an/an/an/an/an/a



Wyeth Research

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against Beta-lactamase AmpC of class C enzyme


J Med Chem 46: 2569-71 (2003)


Article DOI: 10.1021/jm034056q
BindingDB Entry DOI: 10.7270/Q2W66K59
More data for this
Ligand-Target Pair
Proteasome subunit beta type-1/beta type-5


(Homo sapiens (Human))
BDBM50259658
PNG
(CHEMBL4096371)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)NCc1ccco1)B(O)O
Show InChI InChI=1S/C20H28BN3O5/c1-14(2)11-18(21(27)28)24-19(25)17(12-15-7-4-3-5-8-15)23-20(26)22-13-16-9-6-10-29-16/h3-10,14,17-18,27-28H,11-13H2,1-2H3,(H,24,25)(H2,22,23,26)/t17-,18-/m0/s1
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n/an/a 20n/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Dissociation constant against galectin-3 using competitive fluorescence polarization


Eur J Med Chem 125: 925-939 (2017)


BindingDB Entry DOI: 10.7270/Q2348NTK
More data for this
Ligand-Target Pair
Proteasome subunit beta type-1/beta type-5


(Homo sapiens (Human))
BDBM50259649
PNG
(CHEMBL4077282)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)NCCc1ccccc1)B(O)O
Show InChI InChI=1S/C23H32BN3O4/c1-17(2)15-21(24(30)31)27-22(28)20(16-19-11-7-4-8-12-19)26-23(29)25-14-13-18-9-5-3-6-10-18/h3-12,17,20-21,30-31H,13-16H2,1-2H3,(H,27,28)(H2,25,26,29)/t20-,21-/m0/s1
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n/an/a 20n/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Dissociation constant against galectin-3 using competitive fluorescence polarization


Eur J Med Chem 125: 925-939 (2017)


BindingDB Entry DOI: 10.7270/Q2348NTK
More data for this
Ligand-Target Pair
Proteasome component C5


(Homo sapiens (Human))
BDBM50259656
PNG
(CHEMBL4089402)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)N1CCc2ccccc2C1)B(O)O
Show InChI InChI=1S/C24H32BN3O4/c1-17(2)14-22(25(31)32)27-23(29)21(15-18-8-4-3-5-9-18)26-24(30)28-13-12-19-10-6-7-11-20(19)16-28/h3-11,17,21-22,31-32H,12-16H2,1-2H3,(H,26,30)(H,27,29)/t21-,22-/m0/s1
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n/an/a 20n/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Inhibition of caspase-like activity of 20S proteasome in human HL60 cells using Z-nLPnLDaminoluciferin as substrate after 2 hrs by fluorescence analy...


Eur J Med Chem 125: 925-939 (2017)


BindingDB Entry DOI: 10.7270/Q2348NTK
More data for this
Ligand-Target Pair
Cytochrome P450 11B1


(Homo sapiens (Human))
BDBM50464576
PNG
(CHEMBL4290660)
Show SMILES Oc1cncc(Cc2ccc(nc2)-c2ccccc2F)c1
Show InChI InChI=1S/C17H13FN2O/c18-16-4-2-1-3-15(16)17-6-5-12(10-20-17)7-13-8-14(21)11-19-9-13/h1-6,8-11,21H,7H2
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n/an/a 29n/an/an/an/an/an/a



Saarland University

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B1 expressed in hamster V79MZ cells using [1,2-3H]-11-deoxycorticosterone as substrate after 6 hrs by HPTLC analysis


Eur J Med Chem 143: 591-597 (2018)


BindingDB Entry DOI: 10.7270/Q2SF2ZTB
More data for this
Ligand-Target Pair
Proteasome component C5


(Homo sapiens (Human))
BDBM50259657
PNG
(CHEMBL4068221)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)N(C)Cc1ccccc1)B(O)O
Show InChI InChI=1S/C23H32BN3O4/c1-17(2)14-21(24(30)31)26-22(28)20(15-18-10-6-4-7-11-18)25-23(29)27(3)16-19-12-8-5-9-13-19/h4-13,17,20-21,30-31H,14-16H2,1-3H3,(H,25,29)(H,26,28)/t20-,21-/m0/s1
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n/an/a 30n/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Inhibition of caspase-like activity of 20S proteasome in human HL60 cells using Z-nLPnLDaminoluciferin as substrate after 2 hrs by fluorescence analy...


Eur J Med Chem 125: 925-939 (2017)


BindingDB Entry DOI: 10.7270/Q2348NTK
More data for this
Ligand-Target Pair
Proteasome component C5


(Homo sapiens (Human))
BDBM50069989
PNG
((R)-3-methyl-1-((S)-3-phenyl-2-(pyrazine-2-carboxa...)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)c1cnccn1)B(O)O
Show InChI InChI=1S/C19H25BN4O4/c1-13(2)10-17(20(27)28)24-18(25)15(11-14-6-4-3-5-7-14)23-19(26)16-12-21-8-9-22-16/h3-9,12-13,15,17,27-28H,10-11H2,1-2H3,(H,23,26)(H,24,25)/t15-,17-/m0/s1
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n/an/a 30n/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Inhibition of caspase-like activity of 20S proteasome in human HL60 cells using Z-nLPnLDaminoluciferin as substrate after 2 hrs by fluorescence analy...


Eur J Med Chem 125: 925-939 (2017)


BindingDB Entry DOI: 10.7270/Q2348NTK
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Beta-lactamase


(Enterobacter cloacae)
BDBM50129564
PNG
((2S,5R,6R)-2'-(cyclohexyloxy)-3,3-dimethyl-7-oxo-4...)
Show SMILES CC1(C)[C@@H](N2[C@@H]([C@@]3(C[C@@H]3OC3CCCCC3)C2=O)S1(=O)=O)C(O)=O
Show InChI InChI=1S/C16H23NO6S/c1-15(2)11(12(18)19)17-13(20)16(14(17)24(15,21)22)8-10(16)23-9-6-4-3-5-7-9/h9-11,14H,3-8H2,1-2H3,(H,18,19)/t10-,11-,14+,16+/m0/s1
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Wyeth Research

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against Beta-lactamase AmpC of class C enzyme


J Med Chem 46: 2569-71 (2003)


Article DOI: 10.1021/jm034056q
BindingDB Entry DOI: 10.7270/Q2W66K59
More data for this
Ligand-Target Pair
Proteasome subunit beta type-1/beta type-5


(Homo sapiens (Human))
BDBM50259644
PNG
(CHEMBL4091983)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)NCc1cc(Cl)ccc1Cl)B(O)O
Show InChI InChI=1S/C22H28BCl2N3O4/c1-14(2)10-20(23(31)32)28-21(29)19(11-15-6-4-3-5-7-15)27-22(30)26-13-16-12-17(24)8-9-18(16)25/h3-9,12,14,19-20,31-32H,10-11,13H2,1-2H3,(H,28,29)(H2,26,27,30)/t19-,20-/m0/s1
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n/an/a 40n/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Inhibition of chymotrypsin-like activity of 20S proteasome in human HL60 cells using Suc-LLVYaminoluciferin as substrate after 2 hrs by fluorescence ...


Eur J Med Chem 125: 925-939 (2017)


BindingDB Entry DOI: 10.7270/Q2348NTK
More data for this
Ligand-Target Pair
Cathepsin K


(Homo sapiens (Human))
BDBM50213272
PNG
(CHEBI:6426 | LEUPEPTIN | Leupeptin)
Show SMILES CC(C)C[C@H](NC(C)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C=O
Show InChI InChI=1S/C20H38N6O4/c1-12(2)9-16(24-14(5)28)19(30)26-17(10-13(3)4)18(29)25-15(11-27)7-6-8-23-20(21)22/h11-13,15-17H,6-10H2,1-5H3,(H,24,28)(H,25,29)(H,26,30)(H4,21,22,23)/t15-,16-,17-/m0/s1
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n/an/a 42.2n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of human Cathepsin K


Bioorg Med Chem Lett 16: 6178-80 (2006)


BindingDB Entry DOI: 10.7270/Q2C25069
More data for this
Ligand-Target Pair
Estradiol 17-beta-dehydrogenase 1


(Homo sapiens (Human))
BDBM50130177
PNG
(2,6,8-Trihydroxy-10,11-dioxa-benzo[b]fluoren-5-one...)
Show SMILES Oc1ccc2c(c1)oc1oc3cc(O)cc(O)c3c(=O)c21
Show InChI InChI=1S/C15H8O6/c16-6-1-2-8-10(4-6)20-15-12(8)14(19)13-9(18)3-7(17)5-11(13)21-15/h1-5,16-18H
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n/an/a 49n/an/an/an/an/an/a



University of Basel

Curated by ChEMBL


Assay Description
Inhibition of human 17beta-HSD1 expressed in HEK293 cell lysates incubated for 10 mins using [2,4,6,7-3H]-estrone and NADPH by scintillation counting...


J Nat Prod 80: 965-974 (2017)


BindingDB Entry DOI: 10.7270/Q2XD148R
More data for this
Ligand-Target Pair
Proteasome subunit beta type-1/beta type-5


(Homo sapiens (Human))
BDBM50259643
PNG
(CHEMBL4065491)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)NCc1cnccn1)B(O)O
Show InChI InChI=1S/C20H28BN5O4/c1-14(2)10-18(21(29)30)26-19(27)17(11-15-6-4-3-5-7-15)25-20(28)24-13-16-12-22-8-9-23-16/h3-9,12,14,17-18,29-30H,10-11,13H2,1-2H3,(H,26,27)(H2,24,25,28)/t17-,18-/m0/s1
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n/an/a 50n/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Inhibition of chymotrypsin-like activity of 20S proteasome in human HL60 cells using Suc-LLVYaminoluciferin as substrate after 2 hrs by fluorescence ...


Eur J Med Chem 125: 925-939 (2017)


BindingDB Entry DOI: 10.7270/Q2348NTK
More data for this
Ligand-Target Pair
Proteasome component C5


(Homo sapiens (Human))
BDBM50259655
PNG
(CHEMBL4080306)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)N[C@H](C)c1ccccc1)B(O)O
Show InChI InChI=1S/C23H32BN3O4/c1-16(2)14-21(24(30)31)27-22(28)20(15-18-10-6-4-7-11-18)26-23(29)25-17(3)19-12-8-5-9-13-19/h4-13,16-17,20-21,30-31H,14-15H2,1-3H3,(H,27,28)(H2,25,26,29)/t17-,20+,21+/m1/s1
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n/an/a 70n/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Inhibition of caspase-like activity of 20S proteasome in human HL60 cells using Z-nLPnLDaminoluciferin as substrate after 2 hrs by fluorescence analy...


Eur J Med Chem 125: 925-939 (2017)


BindingDB Entry DOI: 10.7270/Q2348NTK
More data for this
Ligand-Target Pair
Trypsin


(Homo sapiens (Human))
BDBM50339540
PNG
(CHEMBL4176792)
Show SMILES CC[C@H](C)[C@@H]1NC(=O)[C@H](Cc2ccc(OC)c(Br)c2)N(C)C(=O)[C@H]([C@H](C)CC)N2[C@H](O)CC[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](COS(O)(=O)=O)OC)C(C)C)[C@@H](C)OC1=O)C2=O
Show InChI InChI=1S/C47H75BrN8O16S/c1-11-25(5)37-47(65)72-27(7)38(54-43(61)36(24(3)4)52-42(60)34(70-10)23-71-73(66,67)68)44(62)50-30(15-13-14-20-49)40(58)51-31-17-19-35(57)56(45(31)63)39(26(6)12-2)46(64)55(8)32(41(59)53-37)22-28-16-18-33(69-9)29(48)21-28/h16,18,21,24-27,30-32,34-39,57H,11-15,17,19-20,22-23,49H2,1-10H3,(H,50,62)(H,51,58)(H,52,60)(H,53,59)(H,54,61)(H,66,67,68)/t25-,26+,27+,30-,31-,32-,34+,35+,36-,37-,38-,39-/m0/s1
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n/an/a 72n/an/an/an/an/an/a



Oregon State University

Curated by ChEMBL


Assay Description
Inhibition of trypsin (unknown origin) assessed as reduction in conversion of N-benzoyl-L-arginine ethyl ester hydrochloride to N-benzoyl-L-arginine ...


J Nat Prod 81: 1417-1425 (2018)


BindingDB Entry DOI: 10.7270/Q25T3P19
More data for this
Ligand-Target Pair
Cytochrome P450 11B1


(Homo sapiens (Human))
BDBM50464578
PNG
(CHEMBL4280014)
Show SMILES Oc1cncc(Cc2cnc(s2)-c2ccccc2)c1
Show InChI InChI=1S/C15H12N2OS/c18-13-6-11(8-16-9-13)7-14-10-17-15(19-14)12-4-2-1-3-5-12/h1-6,8-10,18H,7H2
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n/an/a 77n/an/an/an/an/an/a



Saarland University

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B1 expressed in hamster V79MZ cells using [1,2-3H]-11-deoxycorticosterone as substrate after 6 hrs by HPTLC analysis


Eur J Med Chem 143: 591-597 (2018)


BindingDB Entry DOI: 10.7270/Q2SF2ZTB
More data for this
Ligand-Target Pair
Proteasome component C5


(Homo sapiens (Human))
BDBM50259658
PNG
(CHEMBL4096371)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)NCc1ccco1)B(O)O
Show InChI InChI=1S/C20H28BN3O5/c1-14(2)11-18(21(27)28)24-19(25)17(12-15-7-4-3-5-8-15)23-20(26)22-13-16-9-6-10-29-16/h3-10,14,17-18,27-28H,11-13H2,1-2H3,(H,24,25)(H2,22,23,26)/t17-,18-/m0/s1
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n/an/a 80n/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Dissociation constant against galectin-3 using competitive fluorescence polarization


Eur J Med Chem 125: 925-939 (2017)


BindingDB Entry DOI: 10.7270/Q2348NTK
More data for this
Ligand-Target Pair
Sodium-dependent dopamine transporter


(Rattus norvegicus (rat))
BDBM50010195
PNG
((3S,5R)-methyl 3-(4-iodophenyl)-8-methyl-8-aza-bic...)
Show SMILES COC(=O)C1C2CCC(CC1c1ccc(I)cc1)N2C
Show InChI InChI=1S/C16H20INO2/c1-18-12-7-8-14(18)15(16(19)20-2)13(9-12)10-3-5-11(17)6-4-10/h3-6,12-15H,7-9H2,1-2H3
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n/an/a 88n/an/an/an/an/an/a



Research Biochemicals Inc.

Curated by ChEMBL


Assay Description
Compound was tested for binding affinity to dopamine reuptake sites in the tissue homogenates prepared from primate rat striatum using [3H]CFT as rad...


J Med Chem 34: 3144-6 (1991)


Article DOI: 10.1021/jm00114a027
BindingDB Entry DOI: 10.7270/Q23R0TGB
More data for this
Ligand-Target Pair
Beta-lactamase


(Enterobacter cloacae)
BDBM50053173
PNG
((2S,3S,5R)-3-Methyl-4,4,7-trioxo-3-[1,2,3]triazol-...)
Show SMILES C[C@]1(Cn2ccnn2)[C@@H](N2[C@@H](CC2=O)S1(=O)=O)C(O)=O
Show InChI InChI=1S/C10H12N4O5S/c1-10(5-13-3-2-11-12-13)8(9(16)17)14-6(15)4-7(14)20(10,18)19/h2-3,7-8H,4-5H2,1H3,(H,16,17)/t7-,8+,10+/m1/s1
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n/an/a 100n/an/an/an/an/an/a



Wyeth Research

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against Beta-lactamase TEM-1 of class A enzyme


J Med Chem 46: 2569-71 (2003)


Article DOI: 10.1021/jm034056q
BindingDB Entry DOI: 10.7270/Q2W66K59
More data for this
Ligand-Target Pair
Proteasome component C5


(Homo sapiens (Human))
BDBM50259647
PNG
(CHEMBL4100727)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)NCc1ccc(F)c(F)c1)B(O)O
Show InChI InChI=1S/C22H28BF2N3O4/c1-14(2)10-20(23(31)32)28-21(29)19(12-15-6-4-3-5-7-15)27-22(30)26-13-16-8-9-17(24)18(25)11-16/h3-9,11,14,19-20,31-32H,10,12-13H2,1-2H3,(H,28,29)(H2,26,27,30)/t19-,20-/m0/s1
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n/an/a 110n/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Dissociation constant against galectin-3 using competitive fluorescence polarization


Eur J Med Chem 125: 925-939 (2017)


BindingDB Entry DOI: 10.7270/Q2348NTK
More data for this
Ligand-Target Pair
Proteasome component C5


(Homo sapiens (Human))
BDBM50259646
PNG
(CHEMBL4075225)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)NCc1ccc2ccccc2c1)B(O)O
Show InChI InChI=1S/C26H32BN3O4/c1-18(2)14-24(27(33)34)30-25(31)23(16-19-8-4-3-5-9-19)29-26(32)28-17-20-12-13-21-10-6-7-11-22(21)15-20/h3-13,15,18,23-24,33-34H,14,16-17H2,1-2H3,(H,30,31)(H2,28,29,32)/t23-,24-/m0/s1
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n/an/a 120n/an/an/an/an/an/a



Peking University

Curated by ChEMBL


Assay Description
Dissociation constant against galectin-3 using competitive fluorescence polarization


Eur J Med Chem 125: 925-939 (2017)


BindingDB Entry DOI: 10.7270/Q2348NTK
More data for this
Ligand-Target Pair
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