Found 28 hits for monomerid = 50031299 Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
Dihydrofolate reductase
(Escherichia coli) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/TrEMBL
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Patents
| Article PubMed
| 1.52E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Georgia Institute of Technology
Curated by ChEMBL
| Assay Description Inhibition of Escherichia coli DHFR assessed as NADP formation by quadratic Morrison plot analysis |
Eur J Med Chem 103: 600-14 (2015)
Article DOI: 10.1016/j.ejmech.2015.08.021 BindingDB Entry DOI: 10.7270/Q2DR2ZGJ |
More data for this Ligand-Target Pair | |
Voltage-gated sodium channel subunit alpha Nav1.4 (Nav1.4)
(Homo sapiens (Human)) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB
Reactome pathway
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Patents
| Article PubMed
| 1.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Purdue Pharma LP
Curated by ChEMBL
| Assay Description Affinity for inactive human SkM1 sodium channel expressed in HEK293 cells |
J Med Chem 47: 1547-52 (2004)
Article DOI: 10.1021/jm030498q BindingDB Entry DOI: 10.7270/Q2SX6F0Q |
More data for this Ligand-Target Pair | |
Sodium channel protein type 2 alpha subunit
(Homo sapiens (Human)) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB
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Patents
| Article PubMed
| n/a | n/a | 1.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc
Curated by ChEMBL
| Assay Description Inhibition of human Nav1.2 expressed in SHSY5Y cells assessed as reduction in blue fluorescent signal by VSP-FRET assay |
ACS Med Chem Lett 6: 650-4 (2015)
Article DOI: 10.1021/acsmedchemlett.5b00059 BindingDB Entry DOI: 10.7270/Q23R0VMJ |
More data for this Ligand-Target Pair | |
Voltage-gated sodium channel subunit alpha Nav1.3 (Nav1.3)
(Homo sapiens (Human)) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB
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Patents
| Article PubMed
| n/a | n/a | 1.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc
Curated by ChEMBL
| Assay Description Inhibition of human Nav1.3 expressed in SHSY5Y cells assessed as reduction in blue fluorescent signal by VSP-FRET assay |
ACS Med Chem Lett 6: 650-4 (2015)
Article DOI: 10.1021/acsmedchemlett.5b00059 BindingDB Entry DOI: 10.7270/Q23R0VMJ |
More data for this Ligand-Target Pair | |
Sodium channel protein type 9 subunit alpha
(Homo sapiens (Human)) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB
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Patents
| Article PubMed
| n/a | n/a | 1.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc
Curated by ChEMBL
| Assay Description Inhibition of human Nav1.7 expressed in SHSY5Y cells assessed as reduction in blue fluorescent signal by VSP-FRET assay |
ACS Med Chem Lett 6: 650-4 (2015)
Article DOI: 10.1021/acsmedchemlett.5b00059 BindingDB Entry DOI: 10.7270/Q23R0VMJ |
More data for this Ligand-Target Pair | |
Sodium channel protein type 10 subunit alpha
(Homo sapiens (Human)) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB
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Patents
| Article PubMed
| n/a | n/a | 9.80E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Pfizer Inc
Curated by ChEMBL
| Assay Description Inhibition of human Nav1.8 expressed in HEK293 cells assessed as reduction in blue fluorescent signal by VSP-FRET assay |
ACS Med Chem Lett 6: 650-4 (2015)
Article DOI: 10.1021/acsmedchemlett.5b00059 BindingDB Entry DOI: 10.7270/Q23R0VMJ |
More data for this Ligand-Target Pair | |
Calcium channel (Type L)
(Homo sapiens (Human)) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB
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Patents
| Article PubMed
| n/a | n/a | 1.58E+6 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Oxford
Curated by ChEMBL
| Assay Description Inhibition of long-lasting type calcium current (hICa) in Chinese Hamster Ovary (CHO) cells expressing hCav1.2 measured using IonWorks Quattro automa... |
J Pharmacol Toxicol Methods 70: 246-54 (2014)
Article DOI: 10.1016/j.vascn.2014.07.002 BindingDB Entry DOI: 10.7270/Q2J104W7 |
More data for this Ligand-Target Pair | |
Sodium channel protein type 5 subunit alpha
(Homo sapiens (Human)) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB
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Patents
| Article PubMed
| n/a | n/a | 3.98E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Oxford
Curated by ChEMBL
| Assay Description Inhibition of fast sodium current (INa) in HEK293 cells transfected with human Nav1.5 measured using IonWorks Quattro automated patch clamp platform |
J Pharmacol Toxicol Methods 70: 246-54 (2014)
Article DOI: 10.1016/j.vascn.2014.07.002 BindingDB Entry DOI: 10.7270/Q2J104W7 |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily H member 2
(Homo sapiens (Human)) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB MMDB
Reactome pathway KEGG
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Patents
| Article PubMed
| n/a | n/a | 3.98E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Oxford
Curated by ChEMBL
| Assay Description Inhibition of rapid delayed inward rectifying potassium current (IKr) in Chinese hamster ovary (CHO) K1 cells stably expressing hERG measured using I... |
J Pharmacol Toxicol Methods 70: 246-54 (2014)
Article DOI: 10.1016/j.vascn.2014.07.002 BindingDB Entry DOI: 10.7270/Q2J104W7 |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily H member 2
(Homo sapiens (Human)) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB MMDB
Reactome pathway KEGG
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Patents
| Article PubMed
| n/a | n/a | 2.51E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Oxford
Curated by ChEMBL
| Assay Description Inhibition of rapid delayed inward rectifying potassium current (IKr) measured using manual patch clamp assay |
J Pharmacol Toxicol Methods 70: 246-54 (2014)
Article DOI: 10.1016/j.vascn.2014.07.002 BindingDB Entry DOI: 10.7270/Q2J104W7 |
More data for this Ligand-Target Pair | |
Sodium channel protein type 5 subunit alpha
(Homo sapiens (Human)) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB
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Patents
| Article PubMed
| n/a | n/a | 1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Oxford
Curated by ChEMBL
| Assay Description Inhibition of fast sodium current (INa) in Chinese Hamster Ovary (CHO) K1 cells transfected with human Nav1.5 measured using IonWorks Quattro automat... |
J Pharmacol Toxicol Methods 70: 246-54 (2014)
Article DOI: 10.1016/j.vascn.2014.07.002 BindingDB Entry DOI: 10.7270/Q2J104W7 |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily H member 2
(Homo sapiens (Human)) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB MMDB
Reactome pathway KEGG
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Patents
| Article PubMed
| n/a | n/a | 2.51E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Oxford
Curated by ChEMBL
| Assay Description Inhibition of rapid delayed inward rectifying potassium current (IKr) in Chinese hamster ovary (CHO) cells stable expressing hERG measured using IonW... |
J Pharmacol Toxicol Methods 70: 246-54 (2014)
Article DOI: 10.1016/j.vascn.2014.07.002 BindingDB Entry DOI: 10.7270/Q2J104W7 |
More data for this Ligand-Target Pair | |
Calcium channel (Type L)
(Homo sapiens (Human)) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB
Reactome pathway
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Patents
| Article PubMed
| n/a | n/a | 1.26E+6 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Oxford
Curated by ChEMBL
| Assay Description Inhibition of long-lasting type calcium current (ICaL) in HEK293 cells (alpha1C/beta2a/alpha2delta1) cells measured using IonWorks Barracuda automat... |
J Pharmacol Toxicol Methods 70: 246-54 (2014)
Article DOI: 10.1016/j.vascn.2014.07.002 BindingDB Entry DOI: 10.7270/Q2J104W7 |
More data for this Ligand-Target Pair | |
Voltage-gated sodium channel subunit alpha Nav1.8
(Rattus norvegicus (Rat)) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB
Reactome pathway KEGG
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Patents
| Article PubMed
| n/a | n/a | 2.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Blockade of Nav1.8 channel in rat dorsal root ganglion neurons assessed as inhibition of TTX-R current by whole cell patch clamp technique |
Bioorg Med Chem 16: 6379-86 (2008)
Article DOI: 10.1016/j.bmc.2008.05.003 BindingDB Entry DOI: 10.7270/Q2VH5NNT |
More data for this Ligand-Target Pair | |
Sodium channel protein type 10 subunit alpha
(Homo sapiens (Human)) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB
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Patents
| Article PubMed
| n/a | n/a | 9.60E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Nav1.8 channel expressed in HEK293 cells by whole cell voltage clamp technique |
Bioorg Med Chem 16: 6379-86 (2008)
Article DOI: 10.1016/j.bmc.2008.05.003 BindingDB Entry DOI: 10.7270/Q2VH5NNT |
More data for this Ligand-Target Pair | |
Sodium channel protein type 2 alpha subunit
(Homo sapiens (Human)) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB
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Patents
| Article PubMed
| n/a | n/a | 1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Nav1.2 channel expressed in HEK293 cells by whole cell voltage clamp technique |
Bioorg Med Chem 16: 6379-86 (2008)
Article DOI: 10.1016/j.bmc.2008.05.003 BindingDB Entry DOI: 10.7270/Q2VH5NNT |
More data for this Ligand-Target Pair | |
Sodium channel protein type 5 subunit alpha
(Homo sapiens (Human)) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB
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Patents
| Article PubMed
| n/a | n/a | 6.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Abbott Laboratories
Curated by ChEMBL
| Assay Description Inhibition of human recombinant Nav1.5 channel expressed in HEK293 cells by whole cell voltage clamp technique |
Bioorg Med Chem 16: 6379-86 (2008)
Article DOI: 10.1016/j.bmc.2008.05.003 BindingDB Entry DOI: 10.7270/Q2VH5NNT |
More data for this Ligand-Target Pair | |
Sodium channel protein type 2 alpha subunit
(Homo sapiens (Human)) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB
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Patents
| Article PubMed
| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Università degli Studi di Parma
Curated by ChEMBL
| Assay Description Inhibition of human Nav1.2 channel expressed in HEK cells by patch-clamp electrophysiology method |
Bioorg Med Chem 17: 3642-8 (2009)
Article DOI: 10.1016/j.bmc.2009.03.067 BindingDB Entry DOI: 10.7270/Q2GQ6XN5 |
More data for this Ligand-Target Pair | |
Sigma non-opioid intracellular receptor 1
(RAT) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB
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Patents
| Article PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Pharmacia & Upjohn
Curated by ChEMBL
| Assay Description Inhibition of [3H]pentazocine binding to Opioid receptor sigma 1 |
Bioorg Med Chem Lett 9: 2521-4 (1999)
Article DOI: 10.1016/s0960-894x(99)00415-1 BindingDB Entry DOI: 10.7270/Q29887HT |
More data for this Ligand-Target Pair | |
Sodium channel protein type I I alpha subunit
(Rattus norvegicus) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB
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Patents
| Article PubMed
| n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Pharmacia & Upjohn
Curated by ChEMBL
| Assay Description Inhibition of [3H]saxitoxin binding to rat brain sodium channel |
Bioorg Med Chem Lett 9: 2521-4 (1999)
Article DOI: 10.1016/s0960-894x(99)00415-1 BindingDB Entry DOI: 10.7270/Q29887HT |
More data for this Ligand-Target Pair | |
Sodium channel protein type II alpha subunit
(Rattus norvegicus) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB MMDB
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Patents
| Article PubMed
| n/a | n/a | 3.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Johnson & Johnson Pharmaceutical Research & Development
Curated by ChEMBL
| Assay Description Inhibition of rat Nav1.2 channel expressed in chinese hamster CHL1610 cells at preconditioning pulse of -67 mV after 2 to 3 mins by whole-cell patch-... |
J Med Chem 52: 7528-36 (2009)
Article DOI: 10.1021/jm801432r BindingDB Entry DOI: 10.7270/Q21J9BQD |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily H member 2
(Homo sapiens (Human)) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB MMDB
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Patents
| Article PubMed
| n/a | n/a | 2.29E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ di Pisa
Curated by ChEMBL
| Assay Description Inhibition of human ERG channel in HEK293 cells by voltage-clamp method |
Eur J Med Chem 43: 2479-88 (2008)
Article DOI: 10.1016/j.ejmech.2007.12.025 BindingDB Entry DOI: 10.7270/Q2542PTB |
More data for this Ligand-Target Pair | |
Sodium channel protein type I I alpha subunit
(Rattus norvegicus) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB
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Patents
| Article PubMed
| n/a | n/a | 3.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institut Henri Beaufour
Curated by ChEMBL
| Assay Description Concentration required to inhibit [3H]BTX binding to Sodium channel of rat brain |
Bioorg Med Chem Lett 14: 3521-3 (2004)
Article DOI: 10.1016/j.bmcl.2004.04.059 BindingDB Entry DOI: 10.7270/Q2474D2N |
More data for this Ligand-Target Pair | |
Bile salt export pump
(Homo sapiens (Human)) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB
Reactome pathway
UniProtKB/SwissProt
antibodypedia GoogleScholar
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CHEBI CHEMBL DrugBank MCE PC cid PC sid UniChem
Patents
| Article PubMed
| n/a | n/a | 1.33E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Amgen Inc
Curated by ChEMBL
| Assay Description Inhibition of human BSEP overexpressed in Sf9 cell membrane vesicles assessed as uptake of [3H]-taurocholate in presence of ATP measured after 15 to ... |
Toxicol Sci 136: 216-41 (2013)
Article DOI: 10.1093/toxsci/kft176 BindingDB Entry DOI: 10.7270/Q2JM2D2D |
More data for this Ligand-Target Pair | |
Sodium channel protein type I I alpha subunit
(Rattus norvegicus) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB
Reactome pathway
UniProtKB/SwissProt
GoogleScholar
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CHEBI CHEMBL DrugBank MCE PC cid PC sid UniChem
Patents
| Article PubMed
| n/a | n/a | 1.14E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Howard University
Curated by ChEMBL
| Assay Description Inhibition of [3H]BTX-B binding to neurotoxin site 2 of sodium channel of rat cerebral cortex synaptoneurosomes |
J Med Chem 38: 4033-43 (1995)
Article DOI: 10.1021/jm00020a019 BindingDB Entry DOI: 10.7270/Q2DV1NM8 |
More data for this Ligand-Target Pair | |
Dihydrofolate reductase
(Escherichia coli) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/TrEMBL
GoogleScholar
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CHEBI CHEMBL DrugBank MCE PC cid PC sid UniChem
Patents
| Article PubMed
| n/a | n/a | 3.49E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Georgia Institute of Technology
Curated by ChEMBL
| Assay Description Inhibition of Escherichia coli DHFR assessed as NADP formation |
Eur J Med Chem 103: 600-14 (2015)
Article DOI: 10.1016/j.ejmech.2015.08.021 BindingDB Entry DOI: 10.7270/Q2DR2ZGJ |
More data for this Ligand-Target Pair | |
Sodium channel protein type I I alpha subunit
(Rattus norvegicus) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB
Reactome pathway
UniProtKB/SwissProt
GoogleScholar
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CHEBI CHEMBL DrugBank MCE PC cid PC sid UniChem
Patents
| Article PubMed
| n/a | n/a | 1.86E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Pharmacia & Upjohn
Curated by ChEMBL
| Assay Description Inhibition of [3H]batrachotoxin binding to rat brain sodium channel |
Bioorg Med Chem Lett 9: 2521-4 (1999)
Article DOI: 10.1016/s0960-894x(99)00415-1 BindingDB Entry DOI: 10.7270/Q29887HT |
More data for this Ligand-Target Pair | |
Voltage-gated potassium channel beta subunit Mink/subunit Kv7.1
(Homo sapiens (Human)) | BDBM50031299
(6-(2,3-Dichloro-phenyl)-[1,2,4]triazine-3,5-diamin...)Show InChI InChI=1S/C9H7Cl2N5/c10-5-3-1-2-4(6(5)11)7-8(12)14-9(13)16-15-7/h1-3H,(H4,12,13,14,16) | PDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
DrugBank antibodypedia antibodypedia GoogleScholar
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CHEBI CHEMBL DrugBank MCE PC cid PC sid UniChem
Patents
| Article PubMed
| n/a | n/a | 1.58E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
University of Oxford
Curated by ChEMBL
| Assay Description Inhibition of slow delayed inward rectifying potassium current (Iks) in Chinese Hamster Ovary (CHO) cells expressing hKvLQT1/hminK measured using Ion... |
J Pharmacol Toxicol Methods 70: 246-54 (2014)
Article DOI: 10.1016/j.vascn.2014.07.002 BindingDB Entry DOI: 10.7270/Q2J104W7 |
More data for this Ligand-Target Pair | |