| tachykinin receptor 2 |
TERFENADINE |
Tachykinin NK2 |
80% |
2.677uM |
.892uM |
View
|
| Sigma-2 Receptor |
THIORIDAZINE |
Sigma2 |
80% |
.845uM |
.52uM |
View
|
| Protein-tyrosine kinase, Fyn |
MONTELUKAST |
Protein Tyrosine Kinase, Fyn |
80% |
4.702uM |
NoneNone |
View
|
| Protein-tyrosine kinase, Fyn |
THIORIDAZINE |
Protein Tyrosine Kinase, Fyn |
80% |
5.05uM |
NoneNone |
View
|
| cholinergic receptor, muscarinic 5 |
METHAPYRILENE |
Muscarinic M5 |
80% |
3.265uM |
2.346uM |
View
|
| solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 |
DIMENHYDRINATE |
Dopamine Transporter |
80% |
2.245uM |
1.784uM |
View
|
| solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 |
METHAPYRILENE |
Dopamine Transporter |
80% |
2.757uM |
2.19uM |
View
|
| dopamine receptor D1A |
FLUNARIZINE |
Dopamine D1 |
80% |
3.874uM |
1.937uM |
View
|
| cytochrome P450, family 3, subfamily a, polypeptide 13 |
CISAPRIDE |
CYP450-3A4 Inhibition |
80% |
.3uM |
NoneNone |
View
|
| Cytochrom P450-2D6 monooxygenase |
METOCLOPRAMIDE |
CYP450-2D6 Inhibition |
80% |
.8uM |
NoneNone |
View
|
| Cytochrom P450-2D6 monooxygenase |
NALTREXONE |
CYP450-2D6 Inhibition |
80% |
1uM |
NoneNone |
View
|
| Cytochrom P450-2D6 monooxygenase |
CLEMASTINE |
CYP450-2D6 Inhibition |
80% |
3uM |
NoneNone |
View
|
| Cytochrom P450-2C19 monooxygenase |
CHLORMADINONE ACETATE |
CYP450-2C19 Inhibition |
80% |
3uM |
NoneNone |
View
|
| solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 |
DOBUTAMINE |
Serotonin Transporter |
80% |
1.895uM |
1.006uM |
View
|
| lymphocyte protein tyrosine kinase (mapped) |
GRAMICIDIN |
Protein Tyrosine Kinase, Lck |
80% |
1.094uM |
NoneNone |
View
|
| solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 |
ETHYLESTRENOL |
Adrenergic, Norepinephrine Transporter |
80% |
2.098uM |
2.08uM |
View
|
| opioid receptor, sigma 1 |
QUETIAPINE |
Sigma1 |
80% |
2.2935uM |
.9639uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 1 |
NITRENDIPINE |
Calcium Channel Type L, Benzothiazepine |
80% |
.001565uM |
.001391uM |
View
|
| calcium channel, voltage-dependent, beta 4 subunit |
NITRENDIPINE |
Calcium Channel Type L, Benzothiazepine |
80% |
.001565uM |
.001391uM |
View
|
| calcium channel, voltage-dependent, beta 3 subunit |
NITRENDIPINE |
Calcium Channel Type L, Benzothiazepine |
80% |
.001565uM |
.001391uM |
View
|
| calcium channel, voltage-dependent, beta 2 subunit |
NITRENDIPINE |
Calcium Channel Type L, Benzothiazepine |
80% |
.001565uM |
.001391uM |
View
|
| calcium channel, voltage-dependent, L type, alpha 1S subunit |
NITRENDIPINE |
Calcium Channel Type L, Benzothiazepine |
80% |
.001565uM |
.001391uM |
View
|
| calcium channel, voltage-dependent, alpha 1F subunit |
NITRENDIPINE |
Calcium Channel Type L, Benzothiazepine |
80% |
.001565uM |
.001391uM |
View
|
| calcium channel, voltage-dependent, L type, alpha 1D subunit |
NITRENDIPINE |
Calcium Channel Type L, Benzothiazepine |
80% |
.001565uM |
.001391uM |
View
|
| calcium channel, voltage-dependent, L type, alpha 1C subunit |
NITRENDIPINE |
Calcium Channel Type L, Benzothiazepine |
80% |
.001565uM |
.001391uM |
View
|
| prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase) |
TENOXICAM |
Cyclooxygenase COX-1 |
83% |
1.14uM |
NoneNone |
View
|
| adrenergic receptor, alpha 1d (Non-specific probe) |
CYCLIZINE |
Adrenergic alpha1D |
83% |
1.215uM |
.597uM |
View
|
| Cytochrom P450-2D6 monooxygenase |
PAROXETINE |
CYP450-2D6 Inhibition |
83% |
1uM |
NoneNone |
View
|
| adrenergic receptor, alpha 2a |
PENTAMIDINE |
Adrenergic alpha2A |
83% |
1.375uM |
.516uM |
View
|
| solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 |
PENTAMIDINE |
Adrenergic, Norepinephrine Transporter |
83% |
2.214uM |
2.196uM |
View
|
| cholinergic receptor, muscarinic 3 |
PROCHLORPERAZINE |
Muscarinic M3 |
83% |
1.514uM |
.321uM |
View
|
| potassium voltage-gated channel, subfamily H, member 8 |
DOXAZOSIN |
Potassium Channel HERG |
83% |
2.2155uM |
1.8151uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 6 |
DOXAZOSIN |
Potassium Channel HERG |
83% |
2.2155uM |
1.8151uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 7 |
DOXAZOSIN |
Potassium Channel HERG |
83% |
2.2155uM |
1.8151uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 2 |
DOXAZOSIN |
Potassium Channel HERG |
83% |
2.2155uM |
1.8151uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 5 |
DOXAZOSIN |
Potassium Channel HERG |
83% |
2.2155uM |
1.8151uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 3 |
DOXAZOSIN |
Potassium Channel HERG |
83% |
2.2155uM |
1.8151uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 4 |
DOXAZOSIN |
Potassium Channel HERG |
83% |
2.2155uM |
1.8151uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 1 |
DOXAZOSIN |
Potassium Channel HERG |
83% |
2.2155uM |
1.8151uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 1 |
DOXAZOSIN |
Potassium Channel HERG |
83% |
2.2155uM |
1.8151uM |
View
|
| potassium voltage-gated channel, subfamily H, member 8 |
PERPHENAZINE |
Potassium Channel HERG |
83% |
4.216uM |
3.4541uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 6 |
PERPHENAZINE |
Potassium Channel HERG |
83% |
4.216uM |
3.4541uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 7 |
PERPHENAZINE |
Potassium Channel HERG |
83% |
4.216uM |
3.4541uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 2 |
PERPHENAZINE |
Potassium Channel HERG |
83% |
4.216uM |
3.4541uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 5 |
PERPHENAZINE |
Potassium Channel HERG |
83% |
4.216uM |
3.4541uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 3 |
PERPHENAZINE |
Potassium Channel HERG |
83% |
4.216uM |
3.4541uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 4 |
PERPHENAZINE |
Potassium Channel HERG |
83% |
4.216uM |
3.4541uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 1 |
PERPHENAZINE |
Potassium Channel HERG |
83% |
4.216uM |
3.4541uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 1 |
PERPHENAZINE |
Potassium Channel HERG |
83% |
4.216uM |
3.4541uM |
View
|
| leukotriene B4 receptor 2 |
SULOCTIDIL |
Leukotriene B4 |
83% |
1.4405uM |
.3655uM |
View
|
| leukotriene B4 receptor |
SULOCTIDIL |
Leukotriene B4 |
83% |
1.4405uM |
.3655uM |
View
|
| leukotriene B4 receptor |
SULOCTIDIL |
Leukotriene B4 |
83% |
1.4405uM |
.3655uM |
View
|
| leukotriene B4 receptor 2 |
SULOCTIDIL |
Leukotriene B4 |
83% |
1.4405uM |
.3655uM |
View
|
| aldo-keto reductase family 1, member B4 (aldose reductase) |
PIRINIXIC ACID |
Aldose Reductase |
83% |
2.8169uM |
NoneNone |
View
|
| aldo-keto reductase family 1, member B1 (aldose reductase) |
PIRINIXIC ACID |
Aldose Reductase |
83% |
2.8169uM |
NoneNone |
View
|
| aldo-keto reductase family 7, member A2 (aflatoxin aldehyde reductase) |
PIRINIXIC ACID |
Aldose Reductase |
83% |
2.8169uM |
NoneNone |
View
|
| aldo-keto reductase family 7, member A3 (aflatoxin aldehyde reductase) |
PIRINIXIC ACID |
Aldose Reductase |
83% |
2.8169uM |
NoneNone |
View
|
| opioid receptor, sigma 1 |
THIORIDAZINE |
Sigma1 |
83% |
.363uM |
.153uM |
View
|
| opioid receptor, sigma 1 |
1,3-DIPHENYLGUANIDINE |
Sigma1 |
83% |
1.696uM |
.713uM |
View
|
| mitogen activated protein kinase 3 |
IODOQUINOL |
Protein Serine/Threonine Kinase, ERK1 |
83% |
5.264uM |
NoneNone |
View
|
| mitogen-activated protein kinase 3 |
IODOQUINOL |
Protein Serine/Threonine Kinase, ERK1 |
83% |
5.264uM |
NoneNone |
View
|
| opioid receptor, kappa 1 |
THIORIDAZINE |
Opiate kappa |
83% |
2.49uM |
.996uM |
View
|
| solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 |
PROPAFENONE |
Dopamine Transporter |
83% |
1.868uM |
1.484uM |
View
|
| calcium channel, voltage-dependent, L type, alpha 1D subunit |
CINNARIZINE |
Calcium Channel Type L, Phenylalkylamine |
83% |
.624uM |
.607uM |
View
|
| calcium channel, voltage-dependent, L type, alpha 1C subunit |
CINNARIZINE |
Calcium Channel Type L, Phenylalkylamine |
83% |
.624uM |
.607uM |
View
|
| calcium channel, voltage-dependent, P/Q type, alpha 1A subunit |
CINNARIZINE |
Calcium Channel Type L, Phenylalkylamine |
83% |
.624uM |
.607uM |
View
|
| calcium channel, voltage-dependent, beta 1 subunit |
CINNARIZINE |
Calcium Channel Type L, Phenylalkylamine |
83% |
.624uM |
.607uM |
View
|
| calcium channel, voltage-dependent, L type, alpha 1E subunit |
CINNARIZINE |
Calcium Channel Type L, Phenylalkylamine |
83% |
.624uM |
.607uM |
View
|
| calcium channel, voltage-dependent, N type, alpha 1B subunit |
CINNARIZINE |
Calcium Channel Type L, Phenylalkylamine |
83% |
.624uM |
.607uM |
View
|
| calcium channel, voltage-dependent, alpha2/delta subunit 1 |
CINNARIZINE |
Calcium Channel Type L, Phenylalkylamine |
83% |
.624uM |
.607uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 8 |
CINNARIZINE |
Calcium Channel Type L, Phenylalkylamine |
83% |
.624uM |
.607uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 7 |
CINNARIZINE |
Calcium Channel Type L, Phenylalkylamine |
83% |
.624uM |
.607uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 6 |
CINNARIZINE |
Calcium Channel Type L, Phenylalkylamine |
83% |
.624uM |
.607uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 5 |
CINNARIZINE |
Calcium Channel Type L, Phenylalkylamine |
83% |
.624uM |
.607uM |
View
|
| sodium channel, nonvoltage-gated 1, beta (Liddle syndrome) |
TETRACAINE |
Sodium Channel, Site 2 |
81% |
1.7uM |
1.551uM |
View
|
| sodium channel, nonvoltage-gated 1 alpha |
TETRACAINE |
Sodium Channel, Site 2 |
81% |
1.7uM |
1.551uM |
View
|
| sodium channel, voltage-gated, type X, alpha |
TETRACAINE |
Sodium Channel, Site 2 |
81% |
1.7uM |
1.551uM |
View
|
| sodium channel, voltage-gated, type IX, alpha |
TETRACAINE |
Sodium Channel, Site 2 |
81% |
1.7uM |
1.551uM |
View
|
| sodium channel, voltage gated, type VIII, alpha |
TETRACAINE |
Sodium Channel, Site 2 |
81% |
1.7uM |
1.551uM |
View
|
| sodium channel, voltage-gated, type VII, alpha |
TETRACAINE |
Sodium Channel, Site 2 |
81% |
1.7uM |
1.551uM |
View
|
| sodium channel, voltage-gated, type V, alpha (long QT syndrome 3) |
TETRACAINE |
Sodium Channel, Site 2 |
81% |
1.7uM |
1.551uM |
View
|
| sodium channel, voltage-gated, type IV, beta |
TETRACAINE |
Sodium Channel, Site 2 |
81% |
1.7uM |
1.551uM |
View
|
| sodium channel, voltage-gated, type IV, alpha |
TETRACAINE |
Sodium Channel, Site 2 |
81% |
1.7uM |
1.551uM |
View
|
| sodium channel, voltage-gated, type III, alpha |
TETRACAINE |
Sodium Channel, Site 2 |
81% |
1.7uM |
1.551uM |
View
|
| sodium channel, voltage-gated, type II, beta |
TETRACAINE |
Sodium Channel, Site 2 |
81% |
1.7uM |
1.551uM |
View
|
| sodium channel, voltage-gated, type II, alpha 2 |
TETRACAINE |
Sodium Channel, Site 2 |
81% |
1.7uM |
1.551uM |
View
|
| sodium channel, voltage-gated, type I, beta |
TETRACAINE |
Sodium Channel, Site 2 |
81% |
1.7uM |
1.551uM |
View
|
| sodium channel, voltage-gated, type I, alpha |
TETRACAINE |
Sodium Channel, Site 2 |
81% |
1.7uM |
1.551uM |
View
|
| cholinergic receptor, muscarinic 2 |
GALLAMINE TRIETHIODIDE |
Muscarinic M2 |
81% |
1.999uM |
.711uM |
View
|
| solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 |
THIMEROSAL |
Adrenergic, Norepinephrine Transporter |
81% |
.931uM |
.923uM |
View
|
| dopamine receptor D1A |
BENZOTHIAZYL DISULFIDE |
Dopamine D1 |
81% |
1.189uM |
.595uM |
View
|
| aldo-keto reductase family 1, member B4 (aldose reductase) |
CAFFEIC ACID PHENETHYL ESTER |
Aldose Reductase |
81% |
1.414uM |
NoneNone |
View
|
| aldo-keto reductase family 1, member B1 (aldose reductase) |
CAFFEIC ACID PHENETHYL ESTER |
Aldose Reductase |
81% |
1.414uM |
NoneNone |
View
|
| aldo-keto reductase family 7, member A2 (aflatoxin aldehyde reductase) |
CAFFEIC ACID PHENETHYL ESTER |
Aldose Reductase |
81% |
1.414uM |
NoneNone |
View
|
| aldo-keto reductase family 7, member A3 (aflatoxin aldehyde reductase) |
CAFFEIC ACID PHENETHYL ESTER |
Aldose Reductase |
81% |
1.414uM |
NoneNone |
View
|
| prostaglandin-endoperoxide synthase 1 |
CAPSAICIN |
Cyclooxygenase COX-1 |
81% |
1.551uM |
NoneNone |
View
|
| prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase) |
CAPSAICIN |
Cyclooxygenase COX-1 |
81% |
1.551uM |
NoneNone |
View
|
| solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 |
LABETALOL |
Adrenergic, Norepinephrine Transporter |
81% |
3.354uM |
3.326uM |
View
|
| adrenergic receptor, alpha 2c (Non-specific probe) |
TRAZODONE |
Adrenergic alpha2C |
81% |
1.942uM |
.282uM |
View
|
| adrenergic receptor, alpha 2b |
TRAZODONE |
Adrenergic alpha2C |
81% |
1.942uM |
.282uM |
View
|
| Sigma-2 Receptor |
TRAZODONE |
Sigma2 |
81% |
1.342uM |
.826uM |
View
|
| aldo-keto reductase family 1, member B4 (aldose reductase) |
TICRYNAFEN |
Aldose Reductase |
81% |
3.206uM |
NoneNone |
View
|
| aldo-keto reductase family 1, member B1 (aldose reductase) |
TICRYNAFEN |
Aldose Reductase |
81% |
3.206uM |
NoneNone |
View
|
| aldo-keto reductase family 7, member A2 (aflatoxin aldehyde reductase) |
TICRYNAFEN |
Aldose Reductase |
81% |
3.206uM |
NoneNone |
View
|
| aldo-keto reductase family 7, member A3 (aflatoxin aldehyde reductase) |
TICRYNAFEN |
Aldose Reductase |
81% |
3.206uM |
NoneNone |
View
|
| adrenergic receptor, alpha 2a |
MOSAPRIDE |
Adrenergic alpha2A |
81% |
3.6794uM |
1.3798uM |
View
|
| adrenergic receptor, alpha 1a |
CITALOPRAM |
Adrenergic alpha1A |
81% |
1.756uM |
.711uM |
View
|
| adrenergic receptor, alpha 2b |
LYSERGOL |
Adrenergic alpha2C |
81% |
1.61uM |
.234uM |
View
|
| adrenergic receptor, alpha 2c (Non-specific probe) |
LYSERGOL |
Adrenergic alpha2C |
81% |
1.61uM |
.234uM |
View
|
| Cytochrome P450, subfamily IIC (mephenytoin 4-hydroxylase) |
1-(2-CHLOROBENZOYL)-4-(PHENYLMETHYL)-PIPERIDINE |
CYP450-2C9 Inhibition |
81% |
2uM |
NoneNone |
View
|
| sodium channel, voltage-gated, type II, beta |
CYCLIZINE |
Sodium Channel, Site 2 |
81% |
3.091uM |
2.82uM |
View
|
| sodium channel, voltage-gated, type II, alpha 2 |
CYCLIZINE |
Sodium Channel, Site 2 |
81% |
3.091uM |
2.82uM |
View
|
| sodium channel, voltage-gated, type I, beta |
CYCLIZINE |
Sodium Channel, Site 2 |
81% |
3.091uM |
2.82uM |
View
|
| sodium channel, voltage-gated, type I, alpha |
CYCLIZINE |
Sodium Channel, Site 2 |
81% |
3.091uM |
2.82uM |
View
|
| cholinergic receptor, muscarinic 2 |
HYDROXYCHLOROQUINE |
Muscarinic M2 |
81% |
2.951uM |
1.049uM |
View
|
| Cytochrome P450, subfamily IIC (mephenytoin 4-hydroxylase) |
PHENELZINE |
CYP450-2C9 Inhibition |
81% |
4uM |
NoneNone |
View
|
| cytochrome P450, family 2, subfamily C, polypeptide 9 |
PHENELZINE |
CYP450-2C9 Inhibition |
81% |
4uM |
NoneNone |
View
|
| Cytochrom P450-2C19 monooxygenase |
NORETHINDRONE ACETATE |
CYP450-2C19 Inhibition |
81% |
.8uM |
NoneNone |
View
|
| adrenergic receptor, alpha 2a |
BERBERINE CHLORIDE |
Imidazoline I2, Central |
81% |
1.278uM |
.852uM |
View
|
| adrenergic receptor, alpha 2c (Non-specific probe) |
BERBERINE CHLORIDE |
Imidazoline I2, Central |
81% |
1.278uM |
.852uM |
View
|
| mu-opioid receptor MOR |
BITHIONOL |
Opiate mu |
81% |
5.507uM |
2.236uM |
View
|
| 5-hydroxytryptamine (serotonin) receptor 1A |
BITHIONOL |
Serotonin 5-HT1A |
81% |
5.515uM |
3.152uM |
View
|
| thromboxane A synthase 1 |
VINBLASTINE |
Thromboxane Synthetase |
81% |
1.87uM |
NoneNone |
View
|
| thromboxane A synthase 1 (platelet, cytochrome P450, family 5, subfamily A) |
VINBLASTINE |
Thromboxane Synthetase |
81% |
1.87uM |
NoneNone |
View
|
| Sigma-2 Receptor |
DOBUTAMINE |
Sigma2 |
81% |
2.6uM |
1.6uM |
View
|
| solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 |
BENZTROPINE |
Adrenergic, Norepinephrine Transporter |
81% |
1.391uM |
1.379uM |
View
|
| 5-hydroxytryptamine (serotonin) receptor 2A |
BUSPIRONE |
Serotonin 5-HT2A |
81% |
2.286uM |
.653uM |
View
|
| calcium channel, voltage-dependent, P/Q type, alpha 1A subunit |
NITRENDIPINE |
Calcium Channel Type L, Benzothiazepine |
80% |
.001565uM |
.001391uM |
View
|
| calcium channel, voltage-dependent, beta 1 subunit |
NITRENDIPINE |
Calcium Channel Type L, Benzothiazepine |
80% |
.001565uM |
.001391uM |
View
|
| calcium channel, voltage-dependent, L type, alpha 1E subunit |
NITRENDIPINE |
Calcium Channel Type L, Benzothiazepine |
80% |
.001565uM |
.001391uM |
View
|
| calcium channel, voltage-dependent, N type, alpha 1B subunit |
NITRENDIPINE |
Calcium Channel Type L, Benzothiazepine |
80% |
.001565uM |
.001391uM |
View
|
| calcium channel, voltage-dependent, alpha2/delta subunit 1 |
NITRENDIPINE |
Calcium Channel Type L, Benzothiazepine |
80% |
.001565uM |
.001391uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 8 |
NITRENDIPINE |
Calcium Channel Type L, Benzothiazepine |
80% |
.001565uM |
.001391uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 7 |
NITRENDIPINE |
Calcium Channel Type L, Benzothiazepine |
80% |
.001565uM |
.001391uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 6 |
NITRENDIPINE |
Calcium Channel Type L, Benzothiazepine |
80% |
.001565uM |
.001391uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 5 |
NITRENDIPINE |
Calcium Channel Type L, Benzothiazepine |
80% |
.001565uM |
.001391uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 4 |
NITRENDIPINE |
Calcium Channel Type L, Benzothiazepine |
80% |
.001565uM |
.001391uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 3 |
NITRENDIPINE |
Calcium Channel Type L, Benzothiazepine |
80% |
.001565uM |
.001391uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 2 |
NITRENDIPINE |
Calcium Channel Type L, Benzothiazepine |
80% |
.001565uM |
.001391uM |
View
|
| solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 |
NELFINAVIR |
Adrenergic, Norepinephrine Transporter |
80% |
8.852uM |
8.779uM |
View
|
| nuclear receptor subfamily 3, group C, member 1 |
17-METHYLTESTOSTERONE |
Glucocorticoid |
80% |
1.843uM |
.838uM |
View
|
| adrenergic receptor, alpha 1b |
TERFENADINE |
Adrenergic alpha1B |
80% |
3.335uM |
1.846uM |
View
|
| progesterone receptor |
FLUOROMETHOLONE |
Progesterone |
80% |
.815uM |
.106uM |
View
|
| progesterone receptor |
FLUOROMETHOLONE |
Progesterone |
80% |
.815uM |
.106uM |
View
|
| adrenergic receptor, alpha 2a |
PERGOLIDE |
Imidazoline I2, Central |
80% |
3.075uM |
2.05uM |
View
|
| adrenergic receptor, alpha 2c (Non-specific probe) |
PERGOLIDE |
Imidazoline I2, Central |
80% |
3.075uM |
2.05uM |
View
|
| thromboxane A synthase 1 |
GW-1929 |
Thromboxane Synthetase |
80% |
2.953uM |
NoneNone |
View
|
| thromboxane A synthase 1 (platelet, cytochrome P450, family 5, subfamily A) |
GW-1929 |
Thromboxane Synthetase |
80% |
2.953uM |
NoneNone |
View
|
| sodium channel, voltage-gated, type V, alpha (long QT syndrome 3) |
PIPAMAZINE |
Sodium Channel, Site 2 |
80% |
2.686uM |
2.451uM |
View
|
| sodium channel, voltage-gated, type IV, beta |
PIPAMAZINE |
Sodium Channel, Site 2 |
80% |
2.686uM |
2.451uM |
View
|
| sodium channel, voltage-gated, type IV, alpha |
PIPAMAZINE |
Sodium Channel, Site 2 |
80% |
2.686uM |
2.451uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 7 |
RISPERIDONE |
Potassium Channel HERG |
80% |
4.1901uM |
3.4328uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 2 |
RISPERIDONE |
Potassium Channel HERG |
80% |
4.1901uM |
3.4328uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 5 |
RISPERIDONE |
Potassium Channel HERG |
80% |
4.1901uM |
3.4328uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 3 |
RISPERIDONE |
Potassium Channel HERG |
80% |
4.1901uM |
3.4328uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 4 |
RISPERIDONE |
Potassium Channel HERG |
80% |
4.1901uM |
3.4328uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 1 |
RISPERIDONE |
Potassium Channel HERG |
80% |
4.1901uM |
3.4328uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 1 |
RISPERIDONE |
Potassium Channel HERG |
80% |
4.1901uM |
3.4328uM |
View
|
| potassium voltage-gated channel, subfamily H, member 8 |
RISPERIDONE |
Potassium Channel HERG |
80% |
4.1901uM |
3.4328uM |
View
|
| potassium voltage-gated channel, subfamily H (eag-related), member 6 |
RISPERIDONE |
Potassium Channel HERG |
80% |
4.1901uM |
3.4328uM |
View
|
| sodium channel, voltage-gated, type IV, beta |
BW-723C86 |
Sodium Channel, Site 2 |
80% |
2.1739uM |
1.9833uM |
View
|
| sodium channel, voltage-gated, type IV, alpha |
BW-723C86 |
Sodium Channel, Site 2 |
80% |
2.1739uM |
1.9833uM |
View
|
| sodium channel, voltage-gated, type III, alpha |
BW-723C86 |
Sodium Channel, Site 2 |
80% |
2.1739uM |
1.9833uM |
View
|
| sodium channel, voltage-gated, type II, beta |
BW-723C86 |
Sodium Channel, Site 2 |
80% |
2.1739uM |
1.9833uM |
View
|
| sodium channel, voltage-gated, type II, alpha 2 |
BW-723C86 |
Sodium Channel, Site 2 |
80% |
2.1739uM |
1.9833uM |
View
|
| sodium channel, voltage-gated, type I, beta |
BW-723C86 |
Sodium Channel, Site 2 |
80% |
2.1739uM |
1.9833uM |
View
|
| sodium channel, voltage-gated, type I, alpha |
BW-723C86 |
Sodium Channel, Site 2 |
80% |
2.1739uM |
1.9833uM |
View
|
| sodium channel, voltage-gated, type IV, beta |
BW-723C86 |
Sodium Channel, Site 2 |
80% |
2.1739uM |
1.9833uM |
View
|
| sodium channel associated protein 1 |
BW-723C86 |
Sodium Channel, Site 2 |
80% |
2.1739uM |
1.9833uM |
View
|
| sodium channel associated protein 2 |
BW-723C86 |
Sodium Channel, Site 2 |
80% |
2.1739uM |
1.9833uM |
View
|
| sodium channel, voltage-gated, type III, beta |
BW-723C86 |
Sodium Channel, Site 2 |
80% |
2.1739uM |
1.9833uM |
View
|
| sodium channel, voltage-gated, type I, alpha |
BW-723C86 |
Sodium Channel, Site 2 |
80% |
2.1739uM |
1.9833uM |
View
|
| sodium channel, voltage-gated, type IX, alpha |
BW-723C86 |
Sodium Channel, Site 2 |
80% |
2.1739uM |
1.9833uM |
View
|
| sodium channel, voltage-gated, type VII, alpha |
BW-723C86 |
Sodium Channel, Site 2 |
80% |
2.1739uM |
1.9833uM |
View
|
| amiloride-sensitive cation channel 5, intestinal |
BW-723C86 |
Sodium Channel, Site 2 |
80% |
2.1739uM |
1.9833uM |
View
|
| sodium channel, voltage-gated, type III, beta |
BW-723C86 |
Sodium Channel, Site 2 |
80% |
2.1739uM |
1.9833uM |
View
|
| sodium channel, voltage-gated, type VIII, alpha polypeptide |
BW-723C86 |
Sodium Channel, Site 2 |
80% |
2.1739uM |
1.9833uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 4 |
CINNARIZINE |
Calcium Channel Type L, Phenylalkylamine |
83% |
.624uM |
.607uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 3 |
CINNARIZINE |
Calcium Channel Type L, Phenylalkylamine |
83% |
.624uM |
.607uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 2 |
CINNARIZINE |
Calcium Channel Type L, Phenylalkylamine |
83% |
.624uM |
.607uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 1 |
CINNARIZINE |
Calcium Channel Type L, Phenylalkylamine |
83% |
.624uM |
.607uM |
View
|
| sodium channel, voltage-gated, type IX, alpha |
PUROMYCIN |
Sodium Channel, Site 2 |
12% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, beta 4 subunit |
CINNARIZINE |
Calcium Channel Type L, Phenylalkylamine |
83% |
.624uM |
.607uM |
View
|
| calcium channel, voltage-dependent, beta 3 subunit |
CINNARIZINE |
Calcium Channel Type L, Phenylalkylamine |
83% |
.624uM |
.607uM |
View
|
| calcium channel, voltage-dependent, beta 2 subunit |
CINNARIZINE |
Calcium Channel Type L, Phenylalkylamine |
83% |
.624uM |
.607uM |
View
|
| calcium channel, voltage-dependent, L type, alpha 1S subunit |
CINNARIZINE |
Calcium Channel Type L, Phenylalkylamine |
83% |
.624uM |
.607uM |
View
|
| calcium channel, voltage-dependent, alpha 1F subunit |
CINNARIZINE |
Calcium Channel Type L, Phenylalkylamine |
83% |
.624uM |
.607uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 8 |
FLUNARIZINE |
Calcium Channel Type L, Benzothiazepine |
83% |
1.12uM |
.995uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 7 |
FLUNARIZINE |
Calcium Channel Type L, Benzothiazepine |
83% |
1.12uM |
.995uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 6 |
FLUNARIZINE |
Calcium Channel Type L, Benzothiazepine |
83% |
1.12uM |
.995uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 5 |
FLUNARIZINE |
Calcium Channel Type L, Benzothiazepine |
83% |
1.12uM |
.995uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 4 |
FLUNARIZINE |
Calcium Channel Type L, Benzothiazepine |
83% |
1.12uM |
.995uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 3 |
FLUNARIZINE |
Calcium Channel Type L, Benzothiazepine |
83% |
1.12uM |
.995uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 2 |
FLUNARIZINE |
Calcium Channel Type L, Benzothiazepine |
83% |
1.12uM |
.995uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 1 |
FLUNARIZINE |
Calcium Channel Type L, Benzothiazepine |
83% |
1.12uM |
.995uM |
View
|
| calcium channel, voltage-dependent, beta 4 subunit |
FLUNARIZINE |
Calcium Channel Type L, Benzothiazepine |
83% |
1.12uM |
.995uM |
View
|
| calcium channel, voltage-dependent, beta 3 subunit |
FLUNARIZINE |
Calcium Channel Type L, Benzothiazepine |
83% |
1.12uM |
.995uM |
View
|
| calcium channel, voltage-dependent, beta 2 subunit |
FLUNARIZINE |
Calcium Channel Type L, Benzothiazepine |
83% |
1.12uM |
.995uM |
View
|
| calcium channel, voltage-dependent, L type, alpha 1S subunit |
FLUNARIZINE |
Calcium Channel Type L, Benzothiazepine |
83% |
1.12uM |
.995uM |
View
|
| cytochrome P450, family 3, subfamily a, polypeptide 13 |
VINORELBINE |
CYP450-3A4 Inhibition |
82.5% |
1uM |
NoneNone |
View
|