Found 56 hits with Last Name = 'garau' and Initial = 'g' Target/Host
(Institution) | Ligand | Target/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 | pH | Temp
°C |
|---|
Beta-lactamase
(Aeromonas hydrophila) | BDBM26113
(2,4 PDCA | cid_10365 | pyridine carboxylate, 6a | ...)Show InChI InChI=1S/C7H5NO4/c9-6(10)4-1-2-8-5(3-4)7(11)12/h1-3H,(H,9,10)(H,11,12) | PDB
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| 4.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ de Li£ge
Curated by ChEMBL
| Assay Description
Inhibition of Aeromonas hydrophila beta lactamase CphA by competitive inhibition assay |
Antimicrob Agents Chemother 51: 2136-42 (2007)
Article DOI: 10.1128/aac.00866-06
BindingDB Entry DOI: 10.7270/Q23T9M0P |
More data for this
Ligand-Target Pair | 
3D Structure (crystal) |
Beta-lactamase
(Aeromonas hydrophila) | BDBM50000407
(2-carboxypyridine | CHEMBL72628 | alpha-picolinic ...)Show InChI InChI=1S/C6H5NO2/c8-6(9)5-3-1-2-4-7-5/h1-4H,(H,8,9) | PDB
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| Article
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| 5.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ de Li£ge
Curated by ChEMBL
| Assay Description
Inhibition of Aeromonas hydrophila beta lactamase CphA by competitive inhibition assay |
Antimicrob Agents Chemother 51: 2136-42 (2007)
Article DOI: 10.1128/aac.00866-06
BindingDB Entry DOI: 10.7270/Q23T9M0P |
More data for this
Ligand-Target Pair | |
Beta-lactamase
(Aeromonas hydrophila) | BDBM26113
(2,4 PDCA | cid_10365 | pyridine carboxylate, 6a | ...)Show InChI InChI=1S/C7H5NO4/c9-6(10)4-1-2-8-5(3-4)7(11)12/h1-3H,(H,9,10)(H,11,12) | PDB
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| 1.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ de Li£ge
Curated by ChEMBL
| Assay Description
Inhibition of Aeromonas hydrophila beta lactamase CphA at pH 7.0 |
Antimicrob Agents Chemother 51: 2136-42 (2007)
Article DOI: 10.1128/aac.00866-06
BindingDB Entry DOI: 10.7270/Q23T9M0P |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Beta-lactamase
(Aeromonas hydrophila) | BDBM26113
(2,4 PDCA | cid_10365 | pyridine carboxylate, 6a | ...)Show InChI InChI=1S/C7H5NO4/c9-6(10)4-1-2-8-5(3-4)7(11)12/h1-3H,(H,9,10)(H,11,12) | PDB
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| 3.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ de Li£ge
Curated by ChEMBL
| Assay Description
Inhibition of Aeromonas hydrophila beta lactamase CphA at pH 8.0 |
Antimicrob Agents Chemother 51: 2136-42 (2007)
Article DOI: 10.1128/aac.00866-06
BindingDB Entry DOI: 10.7270/Q23T9M0P |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Beta-lactamase
(Aeromonas hydrophila) | BDBM50000407
(2-carboxypyridine | CHEMBL72628 | alpha-picolinic ...)Show InChI InChI=1S/C6H5NO2/c8-6(9)5-3-1-2-4-7-5/h1-4H,(H,8,9) | PDB
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| 4.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ de Li£ge
Curated by ChEMBL
| Assay Description
Inhibition of Aeromonas hydrophila beta lactamase CphA at pH 7.0 |
Antimicrob Agents Chemother 51: 2136-42 (2007)
Article DOI: 10.1128/aac.00866-06
BindingDB Entry DOI: 10.7270/Q23T9M0P |
More data for this
Ligand-Target Pair | |
Beta-lactamase
(Aeromonas hydrophila) | BDBM50000407
(2-carboxypyridine | CHEMBL72628 | alpha-picolinic ...)Show InChI InChI=1S/C6H5NO2/c8-6(9)5-3-1-2-4-7-5/h1-4H,(H,8,9) | PDB
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| 7.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ de Li£ge
Curated by ChEMBL
| Assay Description
Inhibition of Aeromonas hydrophila beta lactamase CphA at pH 8.0 |
Antimicrob Agents Chemother 51: 2136-42 (2007)
Article DOI: 10.1128/aac.00866-06
BindingDB Entry DOI: 10.7270/Q23T9M0P |
More data for this
Ligand-Target Pair | |
Beta-lactamase
(Aeromonas hydrophila) | BDBM26113
(2,4 PDCA | cid_10365 | pyridine carboxylate, 6a | ...)Show InChI InChI=1S/C7H5NO4/c9-6(10)4-1-2-8-5(3-4)7(11)12/h1-3H,(H,9,10)(H,11,12) | PDB
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| 1.60E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ de Li£ge
Curated by ChEMBL
| Assay Description
Inhibition of Aeromonas hydrophila beta lactamase CphA at pH 9.0 |
Antimicrob Agents Chemother 51: 2136-42 (2007)
Article DOI: 10.1128/aac.00866-06
BindingDB Entry DOI: 10.7270/Q23T9M0P |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Beta-lactamase
(Aeromonas hydrophila) | BDBM26115
(CHEMBL286204 | Quinolinate | Quinolinic acid | pyr...)Show InChI InChI=1S/C7H5NO4/c9-6(10)4-2-1-3-8-5(4)7(11)12/h1-3H,(H,9,10)(H,11,12) | PDB
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| 2.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ de Li£ge
Curated by ChEMBL
| Assay Description
Inhibition of Aeromonas hydrophila beta lactamase CphA by competitive inhibition assay |
Antimicrob Agents Chemother 51: 2136-42 (2007)
Article DOI: 10.1128/aac.00866-06
BindingDB Entry DOI: 10.7270/Q23T9M0P |
More data for this
Ligand-Target Pair | |
Beta-lactamase
(Aeromonas hydrophila) | BDBM26114
(CHEMBL88972 | pyridine carboxylate, 6b | pyridine-...)Show InChI InChI=1S/C7H5NO4/c9-6(10)4-1-2-5(7(11)12)8-3-4/h1-3H,(H,9,10)(H,11,12) | PDB
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| 4.20E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ de Li£ge
Curated by ChEMBL
| Assay Description
Inhibition of Aeromonas hydrophila beta lactamase CphA by competitive inhibition assay |
Antimicrob Agents Chemother 51: 2136-42 (2007)
Article DOI: 10.1128/aac.00866-06
BindingDB Entry DOI: 10.7270/Q23T9M0P |
More data for this
Ligand-Target Pair | |
Beta-lactamase
(Aeromonas hydrophila) | BDBM50000407
(2-carboxypyridine | CHEMBL72628 | alpha-picolinic ...)Show InChI InChI=1S/C6H5NO2/c8-6(9)5-3-1-2-4-7-5/h1-4H,(H,8,9) | PDB
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| 4.40E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ de Li£ge
Curated by ChEMBL
| Assay Description
Inhibition of Aeromonas hydrophila beta lactamase CphA at pH 9.0 |
Antimicrob Agents Chemother 51: 2136-42 (2007)
Article DOI: 10.1128/aac.00866-06
BindingDB Entry DOI: 10.7270/Q23T9M0P |
More data for this
Ligand-Target Pair | |
Beta-lactamase
(Aeromonas hydrophila) | BDBM26113
(2,4 PDCA | cid_10365 | pyridine carboxylate, 6a | ...)Show InChI InChI=1S/C7H5NO4/c9-6(10)4-1-2-8-5(3-4)7(11)12/h1-3H,(H,9,10)(H,11,12) | PDB
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| PDB
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| 5.20E+5 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ de Li£ge
Curated by ChEMBL
| Assay Description
Inhibition of Aeromonas hydrophila beta lactamase CphA at pH 10.0 |
Antimicrob Agents Chemother 51: 2136-42 (2007)
Article DOI: 10.1128/aac.00866-06
BindingDB Entry DOI: 10.7270/Q23T9M0P |
More data for this
Ligand-Target Pair |
3D Structure (crystal) |
Beta-lactamase
(Aeromonas hydrophila) | BDBM26117
(pyridine carboxylate, 6e | pyridine-3,4-dicarboxyl...)Show InChI InChI=1S/C7H5NO4/c9-6(10)4-1-2-8-3-5(4)7(11)12/h1-3H,(H,9,10)(H,11,12) | PDB
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| 1.10E+6 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ de Li£ge
Curated by ChEMBL
| Assay Description
Inhibition of Aeromonas hydrophila beta lactamase CphA by competitive inhibition assay |
Antimicrob Agents Chemother 51: 2136-42 (2007)
Article DOI: 10.1128/aac.00866-06
BindingDB Entry DOI: 10.7270/Q23T9M0P |
More data for this
Ligand-Target Pair | |
Beta-lactamase
(Aeromonas hydrophila) | BDBM50000407
(2-carboxypyridine | CHEMBL72628 | alpha-picolinic ...)Show InChI InChI=1S/C6H5NO2/c8-6(9)5-3-1-2-4-7-5/h1-4H,(H,8,9) | PDB
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| 1.10E+6 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ de Li£ge
Curated by ChEMBL
| Assay Description
Inhibition of Aeromonas hydrophila beta lactamase CphA at pH 10.0 |
Antimicrob Agents Chemother 51: 2136-42 (2007)
Article DOI: 10.1128/aac.00866-06
BindingDB Entry DOI: 10.7270/Q23T9M0P |
More data for this
Ligand-Target Pair | |
N-acylethanolamine-hydrolyzing acid amidase
(Homo sapiens (Human)) | BDBM50389023
(CHEMBL2064166 | US9353075, 6)Show SMILES C[C@@H]1OC(=O)[C@@H]1NC(=O)OCCCCCc1ccccc1 |r| Show InChI InChI=1S/C16H21NO4/c1-12-14(15(18)21-12)17-16(19)20-11-7-3-6-10-13-8-4-2-5-9-13/h2,4-5,8-9,12,14H,3,6-7,10-11H2,1H3,(H,17,19)/t12-,14+/m0/s1 | PDB
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| n/a | n/a | 7.30 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged NAAA expressed in HEK293 cells using 10-cis-heptadecenoylethanolamide as substrate after 30 mins by UPLC/... |
ACS Med Chem Lett 3: 422-426 (2012)
Article DOI: 10.1021/ml300056y
BindingDB Entry DOI: 10.7270/Q29W0GKS |
More data for this
Ligand-Target Pair | |
Aurora kinase A
(Homo sapiens (Human)) | BDBM50185000
(CHEMBL3823844 | US10351548, Compound SA16)Show SMILES Fc1ccc(Cn2cccc(C(=O)N[C@@H](C(=O)Nc3ccc4NC(=O)\C(=C/c5cnc[nH]5)c4c3)c3ccccc3)c2=O)cc1F |r| Show InChI InChI=1S/C33H24F2N6O4/c34-26-10-8-19(13-27(26)35)17-41-12-4-7-23(33(41)45)30(42)40-29(20-5-2-1-3-6-20)32(44)38-21-9-11-28-24(14-21)25(31(43)39-28)15-22-16-36-18-37-22/h1-16,18,29H,17H2,(H,36,37)(H,38,44)(H,39,43)(H,40,42)/b25-15-/t29-/m1/s1 | PDB
MMDB
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| Article
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| n/a | n/a | 35 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of recombinant full length human His-tagged AURA expressed in Baculovirus expression system in presence of ATP measured by Bradford protei... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2021.113895
BindingDB Entry DOI: 10.7270/Q2J1072Q |
More data for this
Ligand-Target Pair | |
Fatty-acid amide hydrolase 1 [33-574]
(Rattus norvegicus (Rat)) | BDBM108250
(3‐(3‐carbamoylphenyl)‐4‐me...)Show SMILES Cc1ccc(OC(=O)NC2CCCCC2)cc1-c1cccc(c1)C(N)=O Show InChI InChI=1S/C21H24N2O3/c1-14-10-11-18(26-21(25)23-17-8-3-2-4-9-17)13-19(14)15-6-5-7-16(12-15)20(22)24/h5-7,10-13,17H,2-4,8-9H2,1H3,(H2,22,24)(H,23,25) | PDB
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| PC cid
PC sid
UniChem
Similars
| Article
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| n/a | n/a | 60 | n/a | n/a | n/a | n/a | n/a | n/a |
Fondazione Istituto Italiano di Tecnologia, Via Morego 30, 16163 Genova (Italy).
| |
Chembiochem 14: 1611-9 (2013)
Article DOI: 10.1002/cbic.201300347
BindingDB Entry DOI: 10.7270/Q2DB80G3 |
More data for this
Ligand-Target Pair | |
Aurora kinase A
(Homo sapiens (Human)) | BDBM50582136
(CHEMBL5085987)Show SMILES Cc1ccc(C(=O)N[C@@H](C(=O)Nc2ccc3NC(=O)\C(=C/c4cnc[nH]4)c3c2)c2ccccc2)c(=O)n1Cc1ccc(F)c(F)c1 |r| | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
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GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 70 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of recombinant full length human His-tagged AURA expressed in Baculovirus expression system in presence of ATP measured by Bradford protei... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2021.113895
BindingDB Entry DOI: 10.7270/Q2J1072Q |
More data for this
Ligand-Target Pair | |
Fatty-acid amide hydrolase 1 [33-574]
(Rattus norvegicus (Rat)) | BDBM108251
(2,3‐dichloro‐N‐{1H‐pyrrolo...)Show InChI InChI=1S/C14H9Cl2N3O/c15-11-3-1-2-10(12(11)16)14(20)19-9-6-8-4-5-17-13(8)18-7-9/h1-7H,(H,17,18)(H,19,20) | PDB
MMDB
UniProtKB/SwissProt
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GoogleScholar
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| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 95 | n/a | n/a | n/a | n/a | n/a | n/a |
Fondazione Istituto Italiano di Tecnologia, Via Morego 30, 16163 Genova (Italy).
| |
Chembiochem 14: 1611-9 (2013)
Article DOI: 10.1002/cbic.201300347
BindingDB Entry DOI: 10.7270/Q2DB80G3 |
More data for this
Ligand-Target Pair | |
[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial
(Homo sapiens (Human)) | BDBM50582135
(CHEMBL5087446)Show SMILES Cc1ccc(C(=O)NCC(=O)Nc2ccc3NC(=O)\C(=C/c4cnc[nH]4)c3c2)c(=O)n1Cc1ccc(F)c(F)c1 | PDB
KEGG
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| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 103 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of recombinant full length human His-tagged PDK1 expressed in Baculovirus expression system in presence of ATP measured by Bradford protei... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2021.113895
BindingDB Entry DOI: 10.7270/Q2J1072Q |
More data for this
Ligand-Target Pair | |
[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial
(Homo sapiens (Human)) | BDBM405827
(US10351548, Compound DD21)Show SMILES Fc1ccc(Cn2cccc(C(=O)NCCC(=O)Nc3ccc4NC(=O)\C(=C/c5cnc[nH]5)c4c3)c2=O)cc1F Show InChI InChI=1S/C28H22F2N6O4/c29-22-5-3-16(10-23(22)30)14-36-9-1-2-19(28(36)40)26(38)32-8-7-25(37)34-17-4-6-24-20(11-17)21(27(39)35-24)12-18-13-31-15-33-18/h1-6,9-13,15H,7-8,14H2,(H,31,33)(H,32,38)(H,34,37)(H,35,39)/b21-12- | PDB
KEGG
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B.MOAD
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GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 103 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of recombinant full length human His-tagged PDK1 expressed in Baculovirus expression system in presence of ATP measured by Bradford protei... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2021.113895
BindingDB Entry DOI: 10.7270/Q2J1072Q |
More data for this
Ligand-Target Pair | |
Aurora kinase A
(Homo sapiens (Human)) | BDBM50582138
(CHEMBL5092990)Show SMILES Cc1c(Br)cc(C(=O)N[C@@H](C(=O)Nc2ccc3NC(=O)\C(=C/c4cnc[nH]4)c3c2)c2ccccc2)c(=O)n1Cc1ccc(F)c(F)c1 |r| | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
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GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 118 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of recombinant full length human His-tagged AURA expressed in Baculovirus expression system in presence of ATP measured by Bradford protei... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2021.113895
BindingDB Entry DOI: 10.7270/Q2J1072Q |
More data for this
Ligand-Target Pair | |
[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial
(Homo sapiens (Human)) | BDBM50582137
(CHEMBL5078188)Show SMILES Cc1c(Br)cc(C(=O)NCC(=O)Nc2ccc3NC(=O)\C(=C/c4cnc[nH]4)c3c2)c(=O)n1Cc1ccc(F)c(F)c1 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 134 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of recombinant full length human His-tagged PDK1 expressed in Baculovirus expression system in presence of ATP measured by Bradford protei... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2021.113895
BindingDB Entry DOI: 10.7270/Q2J1072Q |
More data for this
Ligand-Target Pair | |
Fatty-acid amide hydrolase 1 [33-574]
(Rattus norvegicus (Rat)) | BDBM50437232
(3‐(3‐carbamoylphenyl)‐4‐me...)Show SMILES COc1ccc(OC(=O)NC2CCCCC2)cc1-c1cccc(c1)C(N)=O Show InChI InChI=1S/C21H24N2O4/c1-26-19-11-10-17(27-21(25)23-16-8-3-2-4-9-16)13-18(19)14-6-5-7-15(12-14)20(22)24/h5-7,10-13,16H,2-4,8-9H2,1H3,(H2,22,24)(H,23,25) | PDB
MMDB
UniProtKB/SwissProt
B.MOAD
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
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| Article
PubMed
| n/a | n/a | 137 | n/a | n/a | n/a | n/a | n/a | n/a |
Fondazione Istituto Italiano di Tecnologia, Via Morego 30, 16163 Genova (Italy).
| |
Chembiochem 14: 1611-9 (2013)
Article DOI: 10.1002/cbic.201300347
BindingDB Entry DOI: 10.7270/Q2DB80G3 |
More data for this
Ligand-Target Pair | |
[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial
(Homo sapiens (Human)) | BDBM50582136
(CHEMBL5085987)Show SMILES Cc1ccc(C(=O)N[C@@H](C(=O)Nc2ccc3NC(=O)\C(=C/c4cnc[nH]4)c3c2)c2ccccc2)c(=O)n1Cc1ccc(F)c(F)c1 |r| | PDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
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| PC cid
PC sid
UniChem
| Article
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| n/a | n/a | 148 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of recombinant full length human His-tagged PDK1 expressed in Baculovirus expression system in presence of ATP measured by Bradford protei... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2021.113895
BindingDB Entry DOI: 10.7270/Q2J1072Q |
More data for this
Ligand-Target Pair | |
Aurora kinase A
(Homo sapiens (Human)) | BDBM50582135
(CHEMBL5087446)Show SMILES Cc1ccc(C(=O)NCC(=O)Nc2ccc3NC(=O)\C(=C/c4cnc[nH]4)c3c2)c(=O)n1Cc1ccc(F)c(F)c1 | PDB
MMDB
NCI pathway
Reactome pathway
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UniProtKB/SwissProt
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| PC cid
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UniChem
| Article
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| n/a | n/a | 193 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of recombinant full length human His-tagged AURA expressed in Baculovirus expression system in presence of ATP measured by Bradford protei... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2021.113895
BindingDB Entry DOI: 10.7270/Q2J1072Q |
More data for this
Ligand-Target Pair | |
[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial
(Homo sapiens (Human)) | BDBM405829
(US10351548, Compound DF8)Show SMILES Fc1ccc(Cn2cccc(C(=O)NCCCC(=O)Nc3ccc4NC(=O)\C(=C/c5cnc[nH]5)c4c3)c2=O)cc1F Show InChI InChI=1S/C29H24F2N6O4/c30-23-7-5-17(11-24(23)31)15-37-10-2-3-20(29(37)41)27(39)33-9-1-4-26(38)35-18-6-8-25-21(12-18)22(28(40)36-25)13-19-14-32-16-34-19/h2-3,5-8,10-14,16H,1,4,9,15H2,(H,32,34)(H,33,39)(H,35,38)(H,36,40)/b22-13- | PDB
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antibodypedia
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| PC cid
PC sid
UniChem
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| n/a | n/a | 245 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of recombinant full length human His-tagged PDK1 expressed in Baculovirus expression system in presence of ATP measured by Bradford protei... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2021.113895
BindingDB Entry DOI: 10.7270/Q2J1072Q |
More data for this
Ligand-Target Pair | |
[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial
(Homo sapiens (Human)) | BDBM405828
(US10351548, Compound DD40)Show SMILES Fc1ccc(Cn2cccc(C(=O)Nc3cccc(c3)C(=O)Nc3ccc4NC(=O)\C(=C/c5cnc[nH]5)c4c3)c2=O)cc1F Show InChI InChI=1S/C32H22F2N6O4/c33-26-8-6-18(11-27(26)34)16-40-10-2-5-23(32(40)44)30(42)38-20-4-1-3-19(12-20)29(41)37-21-7-9-28-24(13-21)25(31(43)39-28)14-22-15-35-17-36-22/h1-15,17H,16H2,(H,35,36)(H,37,41)(H,38,42)(H,39,43)/b25-14- | PDB
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antibodypedia
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| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 245 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of recombinant full length human His-tagged PDK1 expressed in Baculovirus expression system in presence of ATP measured by Bradford protei... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2021.113895
BindingDB Entry DOI: 10.7270/Q2J1072Q |
More data for this
Ligand-Target Pair | |
N-acylethanolamine-hydrolyzing acid amidase
(Homo sapiens (Human)) | BDBM50389607
(CHEMBL2069631)Show SMILES C[C@@H]1OC(=O)[C@@H]1NC(=O)CCCCCCc1ccccc1 |r| Show InChI InChI=1S/C17H23NO3/c1-13-16(17(20)21-13)18-15(19)12-8-3-2-5-9-14-10-6-4-7-11-14/h4,6-7,10-11,13,16H,2-3,5,8-9,12H2,1H3,(H,18,19)/t13-,16+/m0/s1 | PDB
UniProtKB/SwissProt
antibodypedia
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| CHEMBL
PC cid
PC sid
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Similars
| Article
PubMed
| n/a | n/a | 314 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant His6-tagged NAAA expressed in HEK293 cells using 10-cis-heptadecenoylethanolamide as substrate after 30 mins by UPLC/... |
ACS Med Chem Lett 3: 422-426 (2012)
Article DOI: 10.1021/ml300056y
BindingDB Entry DOI: 10.7270/Q29W0GKS |
More data for this
Ligand-Target Pair | |
[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial
(Homo sapiens (Human)) | BDBM50185000
(CHEMBL3823844 | US10351548, Compound SA16)Show SMILES Fc1ccc(Cn2cccc(C(=O)N[C@@H](C(=O)Nc3ccc4NC(=O)\C(=C/c5cnc[nH]5)c4c3)c3ccccc3)c2=O)cc1F |r| Show InChI InChI=1S/C33H24F2N6O4/c34-26-10-8-19(13-27(26)35)17-41-12-4-7-23(33(41)45)30(42)40-29(20-5-2-1-3-6-20)32(44)38-21-9-11-28-24(14-21)25(31(43)39-28)15-22-16-36-18-37-22/h1-16,18,29H,17H2,(H,36,37)(H,38,44)(H,39,43)(H,40,42)/b25-15-/t29-/m1/s1 | PDB
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PC cid
PC sid
UniChem
Similars
| Article
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| n/a | n/a | 416 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of recombinant full length human His-tagged PDK1 expressed in Baculovirus expression system in presence of ATP measured by Bradford protei... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2021.113895
BindingDB Entry DOI: 10.7270/Q2J1072Q |
More data for this
Ligand-Target Pair | |
[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial
(Homo sapiens (Human)) | BDBM50582134
(CHEMBL5092987)Show SMILES Fc1ccc(Cn2cccc(C(=O)NCCC(=O)Nc3ccc4NC(=O)\C(=C/c5ncc[nH]5)c4c3)c2=O)cc1F | PDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
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| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 455 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of recombinant full length human His-tagged PDK1 expressed in Baculovirus expression system in presence of ATP measured by Bradford protei... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2021.113895
BindingDB Entry DOI: 10.7270/Q2J1072Q |
More data for this
Ligand-Target Pair | |
[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial
(Homo sapiens (Human)) | BDBM50582138
(CHEMBL5092990)Show SMILES Cc1c(Br)cc(C(=O)N[C@@H](C(=O)Nc2ccc3NC(=O)\C(=C/c4cnc[nH]4)c3c2)c2ccccc2)c(=O)n1Cc1ccc(F)c(F)c1 |r| | PDB
KEGG
UniProtKB/SwissProt
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antibodypedia
GoogleScholar
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| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 475 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of recombinant full length human His-tagged PDK1 expressed in Baculovirus expression system in presence of ATP measured by Bradford protei... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2021.113895
BindingDB Entry DOI: 10.7270/Q2J1072Q |
More data for this
Ligand-Target Pair | |
Aurora kinase A
(Homo sapiens (Human)) | BDBM405829
(US10351548, Compound DF8)Show SMILES Fc1ccc(Cn2cccc(C(=O)NCCCC(=O)Nc3ccc4NC(=O)\C(=C/c5cnc[nH]5)c4c3)c2=O)cc1F Show InChI InChI=1S/C29H24F2N6O4/c30-23-7-5-17(11-24(23)31)15-37-10-2-3-20(29(37)41)27(39)33-9-1-4-26(38)35-18-6-8-25-21(12-18)22(28(40)36-25)13-19-14-32-16-34-19/h2-3,5-8,10-14,16H,1,4,9,15H2,(H,32,34)(H,33,39)(H,35,38)(H,36,40)/b22-13- | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 611 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of recombinant full length human His-tagged AURA expressed in Baculovirus expression system in presence of ATP measured by Bradford protei... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2021.113895
BindingDB Entry DOI: 10.7270/Q2J1072Q |
More data for this
Ligand-Target Pair | |
[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial
(Homo sapiens (Human)) | BDBM50582133
(CHEMBL5091846)Show SMILES Fc1ccc(Cn2cccc(C(=O)NCCC(=O)Nc3ccc4NC(=O)C(=Cc5cccs5)c4c3)c2=O)cc1F | PDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 1.34E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of recombinant full length human His-tagged PDK1 expressed in Baculovirus expression system in presence of ATP measured by Bradford protei... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2021.113895
BindingDB Entry DOI: 10.7270/Q2J1072Q |
More data for this
Ligand-Target Pair | |
Aurora kinase A
(Homo sapiens (Human)) | BDBM405827
(US10351548, Compound DD21)Show SMILES Fc1ccc(Cn2cccc(C(=O)NCCC(=O)Nc3ccc4NC(=O)\C(=C/c5cnc[nH]5)c4c3)c2=O)cc1F Show InChI InChI=1S/C28H22F2N6O4/c29-22-5-3-16(10-23(22)30)14-36-9-1-2-19(28(36)40)26(38)32-8-7-25(37)34-17-4-6-24-20(11-17)21(27(39)35-24)12-18-13-31-15-33-18/h1-6,9-13,15H,7-8,14H2,(H,31,33)(H,32,38)(H,34,37)(H,35,39)/b21-12- | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 2.47E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of recombinant full length human His-tagged AURA expressed in Baculovirus expression system in presence of ATP measured by Bradford protei... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2021.113895
BindingDB Entry DOI: 10.7270/Q2J1072Q |
More data for this
Ligand-Target Pair | |
Fatty-acid amide hydrolase 1 [33-574]
(Rattus norvegicus (Rat)) | BDBM108234
(2‐(trifluoromethyl)‐7H,8H,9H‐[1,...)Show InChI InChI=1S/C10H7F3N4O/c11-10(12,13)8-15-9-14-4-5-6(17(9)16-8)2-1-3-7(5)18/h4H,1-3H2 | PDB
MMDB
UniProtKB/SwissProt
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GoogleScholar
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| Purchase
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 3.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Fondazione Istituto Italiano di Tecnologia, Via Morego 30, 16163 Genova (Italy).
| |
Chembiochem 14: 1611-9 (2013)
Article DOI: 10.1002/cbic.201300347
BindingDB Entry DOI: 10.7270/Q2DB80G3 |
More data for this
Ligand-Target Pair | |
Fatty-acid amide hydrolase 1 [33-574]
(Rattus norvegicus (Rat)) | BDBM50437217
(2‐(3‐carbamoylphenyl)‐4‐ [...)Show SMILES NC(=O)c1cccc(c1)-c1cc(OC(=O)NC2CCCCC2)ccc1C(O)=O Show InChI InChI=1S/C21H22N2O5/c22-19(24)14-6-4-5-13(11-14)18-12-16(9-10-17(18)20(25)26)28-21(27)23-15-7-2-1-3-8-15/h4-6,9-12,15H,1-3,7-8H2,(H2,22,24)(H,23,27)(H,25,26) | PDB
MMDB
UniProtKB/SwissProt
B.MOAD
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 4.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Fondazione Istituto Italiano di Tecnologia, Via Morego 30, 16163 Genova (Italy).
| |
Chembiochem 14: 1611-9 (2013)
Article DOI: 10.1002/cbic.201300347
BindingDB Entry DOI: 10.7270/Q2DB80G3 |
More data for this
Ligand-Target Pair | |
Fatty-acid amide hydrolase 1 [33-574]
(Rattus norvegicus (Rat)) | BDBM108233
(1‐[2‐(trifluoromethyl)phenyl]piperazin...)Show InChI InChI=1S/C11H13F3N2/c12-11(13,14)9-3-1-2-4-10(9)16-7-5-15-6-8-16/h1-4,15H,5-8H2 | PDB
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UniProtKB/SwissProt
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GoogleScholar
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PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 4.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Fondazione Istituto Italiano di Tecnologia, Via Morego 30, 16163 Genova (Italy).
| |
Chembiochem 14: 1611-9 (2013)
Article DOI: 10.1002/cbic.201300347
BindingDB Entry DOI: 10.7270/Q2DB80G3 |
More data for this
Ligand-Target Pair | |
[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial
(Homo sapiens (Human)) | BDBM405830
(US10351548, Compound DF9)Show SMILES Fc1ccc(Cn2cccc(C(=O)NCCCC(=O)Nc3ccc4NC(=O)C(=Cc5cccs5)c4c3)c2=O)cc1F |w:28.28| Show InChI InChI=1S/C30H24F2N4O4S/c31-24-9-7-18(14-25(24)32)17-36-12-2-5-21(30(36)40)28(38)33-11-1-6-27(37)34-19-8-10-26-22(15-19)23(29(39)35-26)16-20-4-3-13-41-20/h2-5,7-10,12-16H,1,6,11,17H2,(H,33,38)(H,34,37)(H,35,39)/b23-16- | PDB
KEGG
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B.MOAD
antibodypedia
GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 5.88E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of recombinant full length human His-tagged PDK1 expressed in Baculovirus expression system in presence of ATP measured by Bradford protei... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2021.113895
BindingDB Entry DOI: 10.7270/Q2J1072Q |
More data for this
Ligand-Target Pair | |
Aurora kinase A
(Homo sapiens (Human)) | BDBM405828
(US10351548, Compound DD40)Show SMILES Fc1ccc(Cn2cccc(C(=O)Nc3cccc(c3)C(=O)Nc3ccc4NC(=O)\C(=C/c5cnc[nH]5)c4c3)c2=O)cc1F Show InChI InChI=1S/C32H22F2N6O4/c33-26-8-6-18(11-27(26)34)16-40-10-2-5-23(32(40)44)30(42)38-20-4-1-3-19(12-20)29(41)37-21-7-9-28-24(13-21)25(31(43)39-28)14-22-15-35-17-36-22/h1-15,17H,16H2,(H,35,36)(H,37,41)(H,38,42)(H,39,43)/b25-14- | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of recombinant full length human His-tagged AURA expressed in Baculovirus expression system in presence of ATP measured by Bradford protei... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2021.113895
BindingDB Entry DOI: 10.7270/Q2J1072Q |
More data for this
Ligand-Target Pair | |
Aurora kinase A
(Homo sapiens (Human)) | BDBM50582137
(CHEMBL5078188)Show SMILES Cc1c(Br)cc(C(=O)NCC(=O)Nc2ccc3NC(=O)\C(=C/c4cnc[nH]4)c3c2)c(=O)n1Cc1ccc(F)c(F)c1 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Inhibition of recombinant full length human His-tagged AURA expressed in Baculovirus expression system in presence of ATP measured by Bradford protei... |
Citation and Details
Article DOI: 10.1016/j.ejmech.2021.113895
BindingDB Entry DOI: 10.7270/Q2J1072Q |
More data for this
Ligand-Target Pair | |
Fatty-acid amide hydrolase 1 [33-574]
(Rattus norvegicus (Rat)) | BDBM108235
(1‐(4‐chlorophenyl)‐2,2,2‐t...)Show InChI InChI=1S/C8H4ClF3O/c9-6-3-1-5(2-4-6)7(13)8(10,11)12/h1-4H | PDB
MMDB
UniProtKB/SwissProt
B.MOAD
GoogleScholar
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| Purchase
MCE
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 2.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Fondazione Istituto Italiano di Tecnologia, Via Morego 30, 16163 Genova (Italy).
| |
Chembiochem 14: 1611-9 (2013)
Article DOI: 10.1002/cbic.201300347
BindingDB Entry DOI: 10.7270/Q2DB80G3 |
More data for this
Ligand-Target Pair | |
Fatty-acid amide hydrolase 1 [33-574]
(Rattus norvegicus (Rat)) | BDBM108238
(5‐phenyl‐3‐(trifluoromethyl)R...)Show InChI InChI=1S/C10H9F3N2O/c11-10(12,13)9(16)6-8(14-15-9)7-4-2-1-3-5-7/h1-5,8,16H,6H2 | PDB
MMDB
UniProtKB/SwissProt
B.MOAD
GoogleScholar
AffyNet
| PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 3.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Fondazione Istituto Italiano di Tecnologia, Via Morego 30, 16163 Genova (Italy).
| |
Chembiochem 14: 1611-9 (2013)
Article DOI: 10.1002/cbic.201300347
BindingDB Entry DOI: 10.7270/Q2DB80G3 |
More data for this
Ligand-Target Pair | |
Fatty-acid amide hydrolase 1 [33-574]
(Rattus norvegicus (Rat)) | BDBM108236
(2‐fluoro‐4‐methanesulfonylanilin...)Show InChI InChI=1S/C7H8FNO2S/c1-12(10,11)5-2-3-7(9)6(8)4-5/h2-4H,9H2,1H3 | PDB
MMDB
UniProtKB/SwissProt
B.MOAD
GoogleScholar
AffyNet
| Purchase
MCE
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 5.80E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Fondazione Istituto Italiano di Tecnologia, Via Morego 30, 16163 Genova (Italy).
| |
Chembiochem 14: 1611-9 (2013)
Article DOI: 10.1002/cbic.201300347
BindingDB Entry DOI: 10.7270/Q2DB80G3 |
More data for this
Ligand-Target Pair | |
Fatty-acid amide hydrolase 1 [33-574]
(Rattus norvegicus (Rat)) | BDBM108247
(5‐phenyl‐7‐(trifluoromethyl)R...)Show InChI InChI=1S/C12H7F3N4/c13-12(14,15)10-6-9(8-4-2-1-3-5-8)18-11-16-7-17-19(10)11/h1-7H | PDB
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| n/a | n/a | 1.10E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Fondazione Istituto Italiano di Tecnologia, Via Morego 30, 16163 Genova (Italy).
| |
Chembiochem 14: 1611-9 (2013)
Article DOI: 10.1002/cbic.201300347
BindingDB Entry DOI: 10.7270/Q2DB80G3 |
More data for this
Ligand-Target Pair | |
Fatty-acid amide hydrolase 1 [33-574]
(Rattus norvegicus (Rat)) | BDBM108242
(4‐oxo‐6‐(trifluoromethyl)pyran&#...)Show InChI InChI=1S/C7H3F3O4/c8-7(9,10)5-2-3(11)1-4(14-5)6(12)13/h1-2H,(H,12,13) | PDB
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UniChem
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| n/a | n/a | 1.37E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Fondazione Istituto Italiano di Tecnologia, Via Morego 30, 16163 Genova (Italy).
| |
Chembiochem 14: 1611-9 (2013)
Article DOI: 10.1002/cbic.201300347
BindingDB Entry DOI: 10.7270/Q2DB80G3 |
More data for this
Ligand-Target Pair | |
Fatty-acid amide hydrolase 1 [33-574]
(Rattus norvegicus (Rat)) | BDBM108243
(1‐(4‐chlorophenyl)‐2,2,2‐t...)Show InChI InChI=1S/C8H6ClF3O/c9-6-3-1-5(2-4-6)7(13)8(10,11)12/h1-4,7,13H | PDB
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| n/a | n/a | 1.43E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Fondazione Istituto Italiano di Tecnologia, Via Morego 30, 16163 Genova (Italy).
| |
Chembiochem 14: 1611-9 (2013)
Article DOI: 10.1002/cbic.201300347
BindingDB Entry DOI: 10.7270/Q2DB80G3 |
More data for this
Ligand-Target Pair | |
Fatty-acid amide hydrolase 1 [33-574]
(Rattus norvegicus (Rat)) | BDBM108239
([3‐(trifluoromethyl)pyrazol‐1‐yl...)Show InChI InChI=1S/C6H5F3N2O2/c7-6(8,9)4-1-2-11(10-4)3-5(12)13/h1-2H,3H2,(H,12,13) | PDB
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| n/a | n/a | 1.47E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Fondazione Istituto Italiano di Tecnologia, Via Morego 30, 16163 Genova (Italy).
| |
Chembiochem 14: 1611-9 (2013)
Article DOI: 10.1002/cbic.201300347
BindingDB Entry DOI: 10.7270/Q2DB80G3 |
More data for this
Ligand-Target Pair | |
Fatty-acid amide hydrolase 1 [33-574]
(Rattus norvegicus (Rat)) | BDBM85507
(CAS_4394-00-7 | NSC_4488 | Niflumic acid | Niflumi...)Show InChI InChI=1S/C13H9F3N2O2/c14-13(15,16)8-3-1-4-9(7-8)18-11-10(12(19)20)5-2-6-17-11/h1-7H,(H,17,18)(H,19,20) | PDB
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| n/a | n/a | 1.62E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Fondazione Istituto Italiano di Tecnologia, Via Morego 30, 16163 Genova (Italy).
| |
Chembiochem 14: 1611-9 (2013)
Article DOI: 10.1002/cbic.201300347
BindingDB Entry DOI: 10.7270/Q2DB80G3 |
More data for this
Ligand-Target Pair | |
Fatty-acid amide hydrolase 1 [33-574]
(Rattus norvegicus (Rat)) | BDBM108240
([3‐(trifluoromethyl)phenyl]methanamine (Hit ...)Show InChI InChI=1S/C8H8F3N/c9-8(10,11)7-3-1-2-6(4-7)5-12/h1-4H,5,12H2 | PDB
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UniChem
| Article
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| n/a | n/a | 2.70E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Fondazione Istituto Italiano di Tecnologia, Via Morego 30, 16163 Genova (Italy).
| |
Chembiochem 14: 1611-9 (2013)
Article DOI: 10.1002/cbic.201300347
BindingDB Entry DOI: 10.7270/Q2DB80G3 |
More data for this
Ligand-Target Pair | |
Fatty-acid amide hydrolase 1 [33-574]
(Rattus norvegicus (Rat)) | BDBM108246
(1‐(1,2,3‐benzotriazol‐2‐yl...)Show InChI InChI=1S/C8H4F3N3O/c9-8(10,11)7(15)14-12-5-3-1-2-4-6(5)13-14/h1-4H | PDB
MMDB
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B.MOAD
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| PC cid
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UniChem
| Article
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| n/a | n/a | 4.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Fondazione Istituto Italiano di Tecnologia, Via Morego 30, 16163 Genova (Italy).
| |
Chembiochem 14: 1611-9 (2013)
Article DOI: 10.1002/cbic.201300347
BindingDB Entry DOI: 10.7270/Q2DB80G3 |
More data for this
Ligand-Target Pair | |
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