sodium channel, voltage-gated, type II, alpha 2 |
MIANSERIN |
Sodium Channel, Site 2 |
80% |
4.194uM |
3.826uM |
View
|
sodium channel, voltage-gated, type I, beta |
MIANSERIN |
Sodium Channel, Site 2 |
80% |
4.194uM |
3.826uM |
View
|
sodium channel, voltage-gated, type I, alpha |
MIANSERIN |
Sodium Channel, Site 2 |
80% |
4.194uM |
3.826uM |
View
|
dopamine receptor 2 |
TIAPRIDE |
Dopamine D2L |
80% |
1.232uM |
.411uM |
View
|
epidermal growth factor receptor |
MITOXANTRONE |
Protein Tyrosine Kinase, EGF Receptor |
80% |
5.3859uM |
NoneNone |
View
|
Protein-tyrosine kinase, Fyn |
ZIRCONIUM(IV) CHLORIDE |
Protein Tyrosine Kinase, Fyn |
80% |
2.921uM |
NoneNone |
View
|
lymphocyte protein tyrosine kinase (mapped) |
LEVODOPA |
Protein Tyrosine Kinase, Lck |
80% |
3.729uM |
NoneNone |
View
|
sodium channel, voltage-gated, type III, alpha |
PIPAMAZINE |
Sodium Channel, Site 2 |
80% |
2.686uM |
2.451uM |
View
|
sodium channel, voltage-gated, type II, beta |
PIPAMAZINE |
Sodium Channel, Site 2 |
80% |
2.686uM |
2.451uM |
View
|
sodium channel, voltage-gated, type II, alpha 2 |
PIPAMAZINE |
Sodium Channel, Site 2 |
80% |
2.686uM |
2.451uM |
View
|
sodium channel, voltage-gated, type I, beta |
PIPAMAZINE |
Sodium Channel, Site 2 |
80% |
2.686uM |
2.451uM |
View
|
sodium channel, voltage-gated, type I, alpha |
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 associated protein 1 |
PIPAMAZINE |
Sodium Channel, Site 2 |
80% |
2.686uM |
2.451uM |
View
|
calcium channel, voltage-dependent, gamma subunit 1 |
DESLORATADINE |
Calcium Channel Type L, Phenylalkylamine |
79% |
2.786uM |
2.708uM |
View
|
calcium channel, voltage-dependent, beta 4 subunit |
DESLORATADINE |
Calcium Channel Type L, Phenylalkylamine |
79% |
2.786uM |
2.708uM |
View
|
Cytochrom P450-2D6 monooxygenase |
CARMOFUR |
CYP450-2D6 Inhibition |
79% |
5uM |
NoneNone |
View
|
Cytochrom P450-2D6 monooxygenase |
RISPERIDONE |
CYP450-2D6 Inhibition |
79% |
5.2734uM |
NoneNone |
View
|
Cytochrom P450-2D6 monooxygenase |
GENTIAN VIOLET |
CYP450-2D6 Inhibition |
79% |
.8244uM |
NoneNone |
View
|
Cytochrom P450-2C19 monooxygenase |
PODOPHYLLOTOXIN |
CYP450-2C19 Inhibition |
79% |
5uM |
NoneNone |
View
|
ATPase, Na+/K+ transporting, alpha 4 polypeptide |
GRAMICIDIN |
ATPase, Na+/K+ |
79% |
5.143uM |
NoneNone |
View
|
ATPase, Na+/K+ transporting, alpha 3 polypeptide |
GRAMICIDIN |
ATPase, Na+/K+ |
79% |
5.143uM |
NoneNone |
View
|
ATPase, Na+/K+ transporting, alpha 2 polypeptide |
GRAMICIDIN |
ATPase, Na+/K+ |
79% |
5.143uM |
NoneNone |
View
|
ATPase, Na+/K+ transporting, alpha 1 polypeptide |
GRAMICIDIN |
ATPase, Na+/K+ |
79% |
5.143uM |
NoneNone |
View
|
ATPase, Na+/K+ transporting, beta 1 polypeptide |
GRAMICIDIN |
ATPase, Na+/K+ |
79% |
5.143uM |
NoneNone |
View
|
ATPase, Na+/K+ transporting, beta 3 polypeptide |
GRAMICIDIN |
ATPase, Na+/K+ |
79% |
5.143uM |
NoneNone |
View
|
ATPase, Na+/K+ transporting, beta 2 polypeptide |
GRAMICIDIN |
ATPase, Na+/K+ |
79% |
5.143uM |
NoneNone |
View
|
ATPase, (Na+)/K+ transporting, beta 4 polypeptide |
GRAMICIDIN |
ATPase, Na+/K+ |
79% |
5.143uM |
NoneNone |
View
|
tachykinin receptor 2 |
GRAMICIDIN |
Tachykinin NK2 |
79% |
4.564uM |
1.521uM |
View
|
cholinergic receptor, muscarinic 1 |
IVERMECTIN |
Muscarinic M1 |
79% |
4.9441uM |
1.1907uM |
View
|
ATPase, Na+/K+ transporting, beta 3 polypeptide |
HEXACHLOROPHENE |
ATPase, Na+/K+ |
78% |
6.1319uM |
NoneNone |
View
|
ATPase, Na+/K+ transporting, beta 2 polypeptide |
HEXACHLOROPHENE |
ATPase, Na+/K+ |
78% |
6.1319uM |
NoneNone |
View
|
ATPase, (Na+)/K+ transporting, beta 4 polypeptide |
HEXACHLOROPHENE |
ATPase, Na+/K+ |
78% |
6.1319uM |
NoneNone |
View
|
ATPase, Na+/K+ transporting, alpha 4 polypeptide |
HEXACHLOROPHENE |
ATPase, Na+/K+ |
78% |
6.1319uM |
NoneNone |
View
|
cholinergic receptor, muscarinic 4 |
SERTRALINE |
Muscarinic M4 |
78% |
2.6309uM |
.3669uM |
View
|
5-hydroxytryptamine (serotonin) receptor 1A |
OXICONAZOLE |
Serotonin 5-HT1A |
78% |
5.5774uM |
3.1871uM |
View
|
5-hydroxytryptamine (serotonin) receptor 1B |
EBASTINE |
Serotonin 5-HT1B |
78% |
2.314uM |
1.4171uM |
View
|
solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 |
CINNARIZINE |
Adrenergic, Norepinephrine Transporter |
78% |
2.832uM |
2.808uM |
View
|
adrenergic receptor, alpha 2b |
PROMETHAZINE |
Adrenergic alpha2C |
78% |
2.431uM |
.353uM |
View
|
adrenergic receptor, alpha 2c (Non-specific probe) |
PROMETHAZINE |
Adrenergic alpha2C |
78% |
2.431uM |
.353uM |
View
|
adrenergic receptor, beta 3 |
4-NONYLPHENOL |
Adrenergic beta3 |
78% |
4.19uM |
3.142uM |
View
|
melanocortin 5 receptor |
CETYLPYRIDINIUM BROMIDE |
Melanocortin MC5 |
78% |
3.726uM |
3.495uM |
View
|
Cytochrom P450-2D6 monooxygenase |
STANOZOLOL |
CYP450-2D6 Inhibition |
78% |
9.274uM |
NoneNone |
View
|
Cytochrome P450, subfamily IIC (mephenytoin 4-hydroxylase) |
RALOXIFENE |
CYP450-2C9 Inhibition |
78% |
2uM |
NoneNone |
View
|
cytochrome P450, family 2, subfamily C, polypeptide 9 |
RALOXIFENE |
CYP450-2C9 Inhibition |
78% |
2uM |
NoneNone |
View
|
opioid receptor, delta 1 |
RALOXIFENE |
Opiate delta |
78% |
6.644uM |
2.342uM |
View
|
5-hydroxytryptamine (serotonin) receptor 2C |
RALOXIFENE |
Serotonin 5-HT2C |
78% |
1.178uM |
.617uM |
View
|
androgen receptor |
LACIDIPINE |
Testosterone |
78% |
3.918uM |
2.612uM |
View
|
solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 |
MODAFINIL |
Dopamine Transporter |
78% |
1.832uM |
1.456uM |
View
|
aldo-keto reductase family 1, member B4 (aldose reductase) |
SULFASALAZINE |
Aldose Reductase |
78% |
17.042uM |
NoneNone |
View
|
aldo-keto reductase family 1, member B1 (aldose reductase) |
SULFASALAZINE |
Aldose Reductase |
78% |
17.042uM |
NoneNone |
View
|
aldo-keto reductase family 7, member A2 (aflatoxin aldehyde reductase) |
SULFASALAZINE |
Aldose Reductase |
78% |
17.042uM |
NoneNone |
View
|
aldo-keto reductase family 7, member A3 (aflatoxin aldehyde reductase) |
SULFASALAZINE |
Aldose Reductase |
78% |
17.042uM |
NoneNone |
View
|
5-hydroxytryptamine (serotonin) receptor 2C |
HALOPROGIN |
Serotonin 5-HT2C |
78% |
2.602uM |
1.363uM |
View
|
solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 |
HALOPROGIN |
Adrenergic, Norepinephrine Transporter |
78% |
2.77uM |
2.747uM |
View
|
5-hydroxytryptamine (serotonin) receptor 2A |
S-(-)-PROPRANOLOL |
Serotonin 5-HT2A |
78% |
1.883uM |
.538uM |
View
|
5-hydroxytryptamine (serotonin) receptor 1B |
DISULFIRAM |
Serotonin 5-HT1B |
78% |
4.72uM |
2.145uM |
View
|
sodium channel, voltage-gated, type IX, alpha |
BROMOCRIPTINE |
Sodium Channel, Site 2 |
78% |
6.692uM |
6.105uM |
View
|
sodium channel, voltage-gated, type VII, alpha |
BROMOCRIPTINE |
Sodium Channel, Site 2 |
78% |
6.692uM |
6.105uM |
View
|
amiloride-sensitive cation channel 5, intestinal |
BROMOCRIPTINE |
Sodium Channel, Site 2 |
78% |
6.692uM |
6.105uM |
View
|
sodium channel, voltage-gated, type III, beta |
BROMOCRIPTINE |
Sodium Channel, Site 2 |
78% |
6.692uM |
6.105uM |
View
|
sodium channel, voltage-gated, type VIII, alpha polypeptide |
BROMOCRIPTINE |
Sodium Channel, Site 2 |
78% |
6.692uM |
6.105uM |
View
|
sodium channel, voltage-gated, type XI, alpha |
BROMOCRIPTINE |
Sodium Channel, Site 2 |
78% |
6.692uM |
6.105uM |
View
|
sodium channel, voltage-gated, type I, beta |
BROMOCRIPTINE |
Sodium Channel, Site 2 |
78% |
6.692uM |
6.105uM |
View
|
sodium channel, voltage-gated, type 10, alpha polypeptide |
BROMOCRIPTINE |
Sodium Channel, Site 2 |
78% |
6.692uM |
6.105uM |
View
|
sodium channel, voltage-gated, type IV, alpha polypeptide |
BROMOCRIPTINE |
Sodium Channel, Site 2 |
78% |
6.692uM |
6.105uM |
View
|
sodium channel, voltage-gated, type V, alpha polypeptide |
BROMOCRIPTINE |
Sodium Channel, Site 2 |
78% |
6.692uM |
6.105uM |
View
|
sodium channel, voltage-gated, type II, beta |
BROMOCRIPTINE |
Sodium Channel, Site 2 |
78% |
6.692uM |
6.105uM |
View
|
calcium channel, voltage-dependent, L type, alpha 1C subunit |
BENZTROPINE |
Calcium Channel Type L, Benzothiazepine |
82% |
3.25uM |
2.889uM |
View
|
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit |
BENZTROPINE |
Calcium Channel Type L, Benzothiazepine |
82% |
3.25uM |
2.889uM |
View
|
calcium channel, voltage-dependent, beta 1 subunit |
BENZTROPINE |
Calcium Channel Type L, Benzothiazepine |
82% |
3.25uM |
2.889uM |
View
|
calcium channel, voltage-dependent, L type, alpha 1E subunit |
BENZTROPINE |
Calcium Channel Type L, Benzothiazepine |
82% |
3.25uM |
2.889uM |
View
|
calcium channel, voltage-dependent, N type, alpha 1B subunit |
BENZTROPINE |
Calcium Channel Type L, Benzothiazepine |
82% |
3.25uM |
2.889uM |
View
|
calcium channel, voltage-dependent, alpha2/delta subunit 1 |
BENZTROPINE |
Calcium Channel Type L, Benzothiazepine |
82% |
3.25uM |
2.889uM |
View
|
cholinergic receptor, muscarinic 3 |
IVERMECTIN |
Muscarinic M3 |
82% |
6.0626uM |
1.285uM |
View
|
Sigma-2 Receptor |
BUTENAFINE |
Sigma2 |
82% |
.2547uM |
.1567uM |
View
|
solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 |
BUTENAFINE |
Serotonin Transporter |
82% |
1.4118uM |
.75uM |
View
|
histamine receptor H 2 |
PROMAZINE |
Histamine H2 |
82% |
2.858uM |
2.81uM |
View
|
adrenergic receptor, alpha 2a |
PYRILAMINE |
Adrenergic alpha2A |
82% |
2.976uM |
1.116uM |
View
|
solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 |
PYRILAMINE |
Dopamine Transporter |
82% |
.879uM |
.699uM |
View
|
cholinergic receptor, muscarinic 5 |
TERCONAZOLE |
Muscarinic M5 |
82% |
4.362uM |
3.134uM |
View
|
solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 |
TACRINE |
Adrenergic, Norepinephrine Transporter |
82% |
.517uM |
.513uM |
View
|
calcium channel, voltage-dependent, beta 4 subunit |
PENTAMIDINE |
Calcium Channel Type L, Benzothiazepine |
82% |
2.208uM |
1.963uM |
View
|
calcium channel, voltage-dependent, beta 3 subunit |
PENTAMIDINE |
Calcium Channel Type L, Benzothiazepine |
82% |
2.208uM |
1.963uM |
View
|
calcium channel, voltage-dependent, beta 2 subunit |
PENTAMIDINE |
Calcium Channel Type L, Benzothiazepine |
82% |
2.208uM |
1.963uM |
View
|
calcium channel, voltage-dependent, L type, alpha 1S subunit |
PENTAMIDINE |
Calcium Channel Type L, Benzothiazepine |
82% |
2.208uM |
1.963uM |
View
|
calcium channel, voltage-dependent, alpha 1F subunit |
PENTAMIDINE |
Calcium Channel Type L, Benzothiazepine |
82% |
2.208uM |
1.963uM |
View
|
calcium channel, voltage-dependent, L type, alpha 1D subunit |
PENTAMIDINE |
Calcium Channel Type L, Benzothiazepine |
82% |
2.208uM |
1.963uM |
View
|
calcium channel, voltage-dependent, L type, alpha 1C subunit |
PENTAMIDINE |
Calcium Channel Type L, Benzothiazepine |
82% |
2.208uM |
1.963uM |
View
|
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit |
PENTAMIDINE |
Calcium Channel Type L, Benzothiazepine |
82% |
2.208uM |
1.963uM |
View
|
calcium channel, voltage-dependent, beta 1 subunit |
PENTAMIDINE |
Calcium Channel Type L, Benzothiazepine |
82% |
2.208uM |
1.963uM |
View
|
calcium channel, voltage-dependent, L type, alpha 1E subunit |
PENTAMIDINE |
Calcium Channel Type L, Benzothiazepine |
82% |
2.208uM |
1.963uM |
View
|
calcium channel, voltage-dependent, N type, alpha 1B subunit |
PENTAMIDINE |
Calcium Channel Type L, Benzothiazepine |
82% |
2.208uM |
1.963uM |
View
|
calcium channel, voltage-dependent, alpha2/delta subunit 1 |
PENTAMIDINE |
Calcium Channel Type L, Benzothiazepine |
82% |
2.208uM |
1.963uM |
View
|
adrenergic receptor, alpha 2a |
METERGOLINE |
Imidazoline I2, Central |
82% |
1.923uM |
1.282uM |
View
|
v-erb-b2 erythroblastic leukemia viral oncogene homolog 2, neuro/glioblastoma derived oncogene homolog (avian) |
ASTEMIZOLE |
Protein Tyrosine Kinase, HER2 Receptor |
81% |
13.084uM |
NoneNone |
View
|
calcium channel, voltage-dependent, gamma subunit 8 |
DROPERIDOL |
Calcium Channel Type L, Phenylalkylamine |
81% |
4.165uM |
4.049uM |
View
|
calcium channel, voltage-dependent, gamma subunit 7 |
DROPERIDOL |
Calcium Channel Type L, Phenylalkylamine |
81% |
4.165uM |
4.049uM |
View
|
calcium channel, voltage-dependent, gamma subunit 6 |
DROPERIDOL |
Calcium Channel Type L, Phenylalkylamine |
81% |
4.165uM |
4.049uM |
View
|
calcium channel, voltage-dependent, gamma subunit 5 |
DROPERIDOL |
Calcium Channel Type L, Phenylalkylamine |
81% |
4.165uM |
4.049uM |
View
|
calcium channel, voltage-dependent, gamma subunit 4 |
DROPERIDOL |
Calcium Channel Type L, Phenylalkylamine |
81% |
4.165uM |
4.049uM |
View
|
calcium channel, voltage-dependent, gamma subunit 3 |
DROPERIDOL |
Calcium Channel Type L, Phenylalkylamine |
81% |
4.165uM |
4.049uM |
View
|
calcium channel, voltage-dependent, gamma subunit 2 |
DROPERIDOL |
Calcium Channel Type L, Phenylalkylamine |
81% |
4.165uM |
4.049uM |
View
|
calcium channel, voltage-dependent, gamma subunit 1 |
DROPERIDOL |
Calcium Channel Type L, Phenylalkylamine |
81% |
4.165uM |
4.049uM |
View
|
calcium channel, voltage-dependent, beta 4 subunit |
DROPERIDOL |
Calcium Channel Type L, Phenylalkylamine |
81% |
4.165uM |
4.049uM |
View
|
calcium channel, voltage-dependent, beta 3 subunit |
DROPERIDOL |
Calcium Channel Type L, Phenylalkylamine |
81% |
4.165uM |
4.049uM |
View
|
calcium channel, voltage-dependent, beta 2 subunit |
DROPERIDOL |
Calcium Channel Type L, Phenylalkylamine |
81% |
4.165uM |
4.049uM |
View
|
calcium channel, voltage-dependent, L type, alpha 1S subunit |
DROPERIDOL |
Calcium Channel Type L, Phenylalkylamine |
81% |
4.165uM |
4.049uM |
View
|
calcium channel, voltage-dependent, alpha 1F subunit |
DROPERIDOL |
Calcium Channel Type L, Phenylalkylamine |
81% |
4.165uM |
4.049uM |
View
|
calcium channel, voltage-dependent, L type, alpha 1D subunit |
DROPERIDOL |
Calcium Channel Type L, Phenylalkylamine |
81% |
4.165uM |
4.049uM |
View
|
calcium channel, voltage-dependent, L type, alpha 1C subunit |
DROPERIDOL |
Calcium Channel Type L, Phenylalkylamine |
81% |
4.165uM |
4.049uM |
View
|
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit |
DROPERIDOL |
Calcium Channel Type L, Phenylalkylamine |
81% |
4.165uM |
4.049uM |
View
|
calcium channel, voltage-dependent, beta 1 subunit |
DROPERIDOL |
Calcium Channel Type L, Phenylalkylamine |
81% |
4.165uM |
4.049uM |
View
|
adrenergic receptor, alpha 2c (Non-specific probe) |
AMLODIPINE |
Adrenergic alpha2C |
90% |
1.8uM |
.261uM |
View
|
adrenergic receptor, alpha 2b |
AMLODIPINE |
Adrenergic alpha2C |
90% |
1.8uM |
.261uM |
View
|
sodium channel, nonvoltage-gated 1 gamma |
AMITRIPTYLINE |
Sodium Channel, Site 2 |
90% |
2.288uM |
2.088uM |
View
|
sodium channel, nonvoltage-gated 1 beta |
AMITRIPTYLINE |
Sodium Channel, Site 2 |
90% |
2.288uM |
2.088uM |
View
|
sodium channel, voltage-gated, type 2, alpha 1 polypeptide |
AMITRIPTYLINE |
Sodium Channel, Site 2 |
90% |
2.288uM |
2.088uM |
View
|
sodium channel, voltage-gated, type XI, alpha |
AMITRIPTYLINE |
Sodium Channel, Site 2 |
90% |
2.288uM |
2.088uM |
View
|
sodium channel, nonvoltage-gated 1, gamma |
AMITRIPTYLINE |
Sodium Channel, Site 2 |
90% |
2.288uM |
2.088uM |
View
|
sodium channel, nonvoltage-gated 1, delta |
AMITRIPTYLINE |
Sodium Channel, Site 2 |
90% |
2.288uM |
2.088uM |
View
|
sodium channel, nonvoltage-gated 1, beta (Liddle syndrome) |
AMITRIPTYLINE |
Sodium Channel, Site 2 |
90% |
2.288uM |
2.088uM |
View
|
sodium channel, nonvoltage-gated 1 alpha |
AMITRIPTYLINE |
Sodium Channel, Site 2 |
90% |
2.288uM |
2.088uM |
View
|
sodium channel, voltage-gated, type X, alpha |
AMITRIPTYLINE |
Sodium Channel, Site 2 |
90% |
2.288uM |
2.088uM |
View
|
sodium channel, voltage-gated, type IX, alpha |
AMITRIPTYLINE |
Sodium Channel, Site 2 |
90% |
2.288uM |
2.088uM |
View
|
sodium channel, voltage gated, type VIII, alpha |
AMITRIPTYLINE |
Sodium Channel, Site 2 |
90% |
2.288uM |
2.088uM |
View
|
sodium channel, voltage-gated, type VII, alpha |
AMITRIPTYLINE |
Sodium Channel, Site 2 |
90% |
2.288uM |
2.088uM |
View
|
potassium voltage-gated channel, subfamily H, member 8 |
PROCHLORPERAZINE |
Potassium Channel HERG |
90% |
1.8481uM |
1.5141uM |
View
|
potassium voltage-gated channel, subfamily H (eag-related), member 6 |
PROCHLORPERAZINE |
Potassium Channel HERG |
90% |
1.8481uM |
1.5141uM |
View
|
potassium voltage-gated channel, subfamily H (eag-related), member 7 |
PROCHLORPERAZINE |
Potassium Channel HERG |
90% |
1.8481uM |
1.5141uM |
View
|
potassium voltage-gated channel, subfamily H (eag-related), member 2 |
PROCHLORPERAZINE |
Potassium Channel HERG |
90% |
1.8481uM |
1.5141uM |
View
|
potassium voltage-gated channel, subfamily H (eag-related), member 5 |
PROCHLORPERAZINE |
Potassium Channel HERG |
90% |
1.8481uM |
1.5141uM |
View
|
potassium voltage-gated channel, subfamily H (eag-related), member 3 |
PROCHLORPERAZINE |
Potassium Channel HERG |
90% |
1.8481uM |
1.5141uM |
View
|
potassium voltage-gated channel, subfamily H (eag-related), member 4 |
PROCHLORPERAZINE |
Potassium Channel HERG |
90% |
1.8481uM |
1.5141uM |
View
|
potassium voltage-gated channel, subfamily H (eag-related), member 1 |
PROCHLORPERAZINE |
Potassium Channel HERG |
90% |
1.8481uM |
1.5141uM |
View
|
potassium voltage-gated channel, subfamily H (eag-related), member 1 |
PROCHLORPERAZINE |
Potassium Channel HERG |
90% |
1.8481uM |
1.5141uM |
View
|
adenosine A1 receptor |
ALPHA-NAPHTHOFLAVONE |
Adenosine A1 |
90% |
1.1325uM |
.6606uM |
View
|
solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 |
HEXACHLOROPHENE |
Serotonin Transporter |
90% |
4.3494uM |
2.3106uM |
View
|
Protein-tyrosine kinase, Fyn |
SULOCTIDIL |
Protein Tyrosine Kinase, Fyn |
90% |
.7221uM |
NoneNone |
View
|
dopamine receptor D3 |
SULOCTIDIL |
Dopamine D3 |
90% |
2.1039uM |
.7145uM |
View
|
Sigma-2 Receptor |
FLUNARIZINE |
Sigma2 |
90% |
.062uM |
.038uM |
View
|
5-hydroxytryptamine receptor 6 |
TERFENADINE |
Serotonin 5-HT6 |
90% |
1.306uM |
.606uM |
View
|
5-hydroxytryptamine (serotonin) receptor 2B |
METHAPYRILENE |
Serotonin 5-HT2B |
90% |
.843uM |
.537uM |
View
|
5-hydroxytryptamine (serotonin) receptor 2B |
CINNARIZINE |
Serotonin 5-HT2B |
90% |
.731uM |
.465uM |
View
|
5-hydroxytryptamine (serotonin) receptor 2C |
DIMENHYDRINATE |
Serotonin 5-HT2C |
90% |
.634uM |
.332uM |
View
|
mitogen activated protein kinase 1 |
ZAFIRLUKAST |
Protein Serine/Threonine Kinase, ERK2 |
90% |
.538uM |
NoneNone |
View
|
mitogen-activated protein kinase 1 |
ZAFIRLUKAST |
Protein Serine/Threonine Kinase, ERK2 |
90% |
.538uM |
NoneNone |
View
|
cholinergic receptor, muscarinic 4 |
CYCLIZINE |
Muscarinic M4 |
90% |
.852uM |
.119uM |
View
|
cholinergic receptor, muscarinic 3 |
FLUNARIZINE |
Muscarinic M3 |
90% |
1.479uM |
.313uM |
View
|
calcium channel, voltage-dependent, gamma subunit 8 |
FLUNARIZINE |
Calcium Channel Type L, Dihydropyridine |
90% |
1.012uM |
.65uM |
View
|
calcium channel, voltage-dependent, gamma subunit 7 |
FLUNARIZINE |
Calcium Channel Type L, Dihydropyridine |
90% |
1.012uM |
.65uM |
View
|
calcium channel, voltage-dependent, gamma subunit 6 |
FLUNARIZINE |
Calcium Channel Type L, Dihydropyridine |
90% |
1.012uM |
.65uM |
View
|
calcium channel, voltage-dependent, gamma subunit 5 |
FLUNARIZINE |
Calcium Channel Type L, Dihydropyridine |
90% |
1.012uM |
.65uM |
View
|
calcium channel, voltage-dependent, gamma subunit 4 |
FLUNARIZINE |
Calcium Channel Type L, Dihydropyridine |
90% |
1.012uM |
.65uM |
View
|
calcium channel, voltage-dependent, gamma subunit 3 |
FLUNARIZINE |
Calcium Channel Type L, Dihydropyridine |
90% |
1.012uM |
.65uM |
View
|
calcium channel, voltage-dependent, gamma subunit 2 |
FLUNARIZINE |
Calcium Channel Type L, Dihydropyridine |
90% |
1.012uM |
.65uM |
View
|
calcium channel, voltage-dependent, gamma subunit 1 |
FLUNARIZINE |
Calcium Channel Type L, Dihydropyridine |
90% |
1.012uM |
.65uM |
View
|
calcium channel, voltage-dependent, beta 4 subunit |
FLUNARIZINE |
Calcium Channel Type L, Dihydropyridine |
90% |
1.012uM |
.65uM |
View
|
calcium channel, voltage-dependent, beta 3 subunit |
FLUNARIZINE |
Calcium Channel Type L, Dihydropyridine |
90% |
1.012uM |
.65uM |
View
|
calcium channel, voltage-dependent, beta 2 subunit |
FLUNARIZINE |
Calcium Channel Type L, Dihydropyridine |
90% |
1.012uM |
.65uM |
View
|
calcium channel, voltage-dependent, L type, alpha 1S subunit |
FLUNARIZINE |
Calcium Channel Type L, Dihydropyridine |
90% |
1.012uM |
.65uM |
View
|
calcium channel, voltage-dependent, alpha 1F subunit |
FLUNARIZINE |
Calcium Channel Type L, Dihydropyridine |
90% |
1.012uM |
.65uM |
View
|
calcium channel, voltage-dependent, L type, alpha 1D subunit |
FLUNARIZINE |
Calcium Channel Type L, Dihydropyridine |
90% |
1.012uM |
.65uM |
View
|
calcium channel, voltage-dependent, gamma subunit 4 |
PERHEXILINE |
Calcium Channel Type L, Benzothiazepine |
89% |
1.0569uM |
.9394uM |
View
|
calcium channel, voltage-dependent, gamma subunit 3 |
PERHEXILINE |
Calcium Channel Type L, Benzothiazepine |
89% |
1.0569uM |
.9394uM |
View
|
calcium channel, voltage-dependent, gamma subunit 2 |
PERHEXILINE |
Calcium Channel Type L, Benzothiazepine |
89% |
1.0569uM |
.9394uM |
View
|
calcium channel, voltage-dependent, gamma subunit 1 |
PERHEXILINE |
Calcium Channel Type L, Benzothiazepine |
89% |
1.0569uM |
.9394uM |
View
|
calcium channel, voltage-dependent, beta 4 subunit |
PERHEXILINE |
Calcium Channel Type L, Benzothiazepine |
89% |
1.0569uM |
.9394uM |
View
|
calcium channel, voltage-dependent, beta 3 subunit |
PERHEXILINE |
Calcium Channel Type L, Benzothiazepine |
89% |
1.0569uM |
.9394uM |
View
|
calcium channel, voltage-dependent, beta 2 subunit |
PERHEXILINE |
Calcium Channel Type L, Benzothiazepine |
89% |
1.0569uM |
.9394uM |
View
|
calcium channel, voltage-dependent, L type, alpha 1S subunit |
PERHEXILINE |
Calcium Channel Type L, Benzothiazepine |
89% |
1.0569uM |
.9394uM |
View
|
calcium channel, voltage-dependent, alpha 1F subunit |
PERHEXILINE |
Calcium Channel Type L, Benzothiazepine |
89% |
1.0569uM |
.9394uM |
View
|
calcium channel, voltage-dependent, L type, alpha 1D subunit |
PERHEXILINE |
Calcium Channel Type L, Benzothiazepine |
89% |
1.0569uM |
.9394uM |
View
|
calcium channel, voltage-dependent, L type, alpha 1C subunit |
PERHEXILINE |
Calcium Channel Type L, Benzothiazepine |
89% |
1.0569uM |
.9394uM |
View
|
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit |
PERHEXILINE |
Calcium Channel Type L, Benzothiazepine |
89% |
1.0569uM |
.9394uM |
View
|
calcium channel, voltage-dependent, beta 1 subunit |
PERHEXILINE |
Calcium Channel Type L, Benzothiazepine |
89% |
1.0569uM |
.9394uM |
View
|
calcium channel, voltage-dependent, L type, alpha 1E subunit |
PERHEXILINE |
Calcium Channel Type L, Benzothiazepine |
89% |
1.0569uM |
.9394uM |
View
|
calcium channel, voltage-dependent, N type, alpha 1B subunit |
PERHEXILINE |
Calcium Channel Type L, Benzothiazepine |
89% |
1.0569uM |
.9394uM |
View
|
calcium channel, voltage-dependent, alpha2/delta subunit 1 |
PERHEXILINE |
Calcium Channel Type L, Benzothiazepine |
89% |
1.0569uM |
.9394uM |
View
|
Cytochrome P450, subfamily IIC (mephenytoin 4-hydroxylase) |
ZAFIRLUKAST |
CYP450-2C9 Inhibition |
89% |
2.2575uM |
NoneNone |
View
|
cytochrome P450, family 2, subfamily C, polypeptide 9 |
ZAFIRLUKAST |
CYP450-2C9 Inhibition |
89% |
2.2575uM |
NoneNone |
View
|
adrenergic receptor, alpha 2b |
SULOCTIDIL |
Adrenergic alpha2C |
89% |
3.446uM |
.5007uM |
View
|
adrenergic receptor, alpha 2c (Non-specific probe) |
SULOCTIDIL |
Adrenergic alpha2C |
89% |
3.446uM |
.5007uM |
View
|
Sigma-2 Receptor |
CINNARIZINE |
Sigma2 |
89% |
.161uM |
.099uM |
View
|
arachidonate 15-lipoxygenase, second type |
INDAPAMIDE |
Lipoxygenase 15-LO |
89% |
2.918uM |
NoneNone |
View
|
arachidonate 15-lipoxygenase |
INDAPAMIDE |
Lipoxygenase 15-LO |
89% |
2.918uM |
NoneNone |
View
|
arachidonate 15-lipoxygenase |
INDAPAMIDE |
Lipoxygenase 15-LO |
89% |
2.918uM |
NoneNone |
View
|
solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 |
CINNARIZINE |
Dopamine Transporter |
89% |
1.641uM |
1.304uM |
View
|
solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 |
MONTELUKAST |
Dopamine Transporter |
89% |
2.601uM |
2.067uM |
View
|
solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 |
THIORIDAZINE |
Dopamine Transporter |
89% |
2.376uM |
1.888uM |
View
|
prostaglandin-endoperoxide synthase 1 |
FELBINAC |
Cyclooxygenase COX-1 |
89% |
.894uM |
NoneNone |
View
|
prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase) |
FELBINAC |
Cyclooxygenase COX-1 |
89% |
.894uM |
NoneNone |
View
|
cytochrome P450, family 3, subfamily a, polypeptide 13 |
ERGOCORNINE |
CYP450-3A4 Inhibition |
89% |
.5uM |
NoneNone |
View
|
cytochrome P450, family 3, subfamily a, polypeptide 13 |
ALPHA-ERGOCRYPTINE |
CYP450-3A4 Inhibition |
89% |
.6uM |
NoneNone |
View
|
cytochrome P450, family 3, subfamily a, polypeptide 13 |
TACROLIMUS |
CYP450-3A4 Inhibition |
89% |
1uM |
NoneNone |
View
|
Cytochrome P450, subfamily IIC (mephenytoin 4-hydroxylase) |
CANDESARTAN |
CYP450-2C9 Inhibition |
89% |
3uM |
NoneNone |
View
|
cytochrome P450, family 2, subfamily C, polypeptide 9 |
CANDESARTAN |
CYP450-2C9 Inhibition |
89% |
3uM |
NoneNone |
View
|
Cytochrome P450, subfamily IIC (mephenytoin 4-hydroxylase) |
NOSCAPINE |
CYP450-2C9 Inhibition |
89% |
8.1773uM |
NoneNone |
View
|
cytochrome P450, family 2, subfamily C, polypeptide 9 |
NOSCAPINE |
CYP450-2C9 Inhibition |
89% |
8.1773uM |
NoneNone |
View
|
Cytochrome P450, subfamily IIC (mephenytoin 4-hydroxylase) |
CLOSANTEL |
CYP450-2C9 Inhibition |
89% |
2uM |
NoneNone |
View
|