| gamma-aminobutyric acid (GABA-C) receptor, subunit rho 1 |
TROPISETRON |
GABAA, Agonist Site |
71% |
3.025uM |
2.395uM |
View
|
| gamma-aminobutyric acid A receptor, delta |
TROPISETRON |
GABAA, Agonist Site |
71% |
3.025uM |
2.395uM |
View
|
| gamma-aminobutyric acid (GABA-A) receptor, subunit alpha 3 |
TROPISETRON |
GABAA, Agonist Site |
71% |
3.025uM |
2.395uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 8 |
KETOTIFEN |
Calcium Channel Type L, Benzothiazepine |
71% |
2.305uM |
2.049uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 7 |
KETOTIFEN |
Calcium Channel Type L, Benzothiazepine |
71% |
2.305uM |
2.049uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 6 |
KETOTIFEN |
Calcium Channel Type L, Benzothiazepine |
71% |
2.305uM |
2.049uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 5 |
KETOTIFEN |
Calcium Channel Type L, Benzothiazepine |
71% |
2.305uM |
2.049uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 4 |
KETOTIFEN |
Calcium Channel Type L, Benzothiazepine |
71% |
2.305uM |
2.049uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 3 |
KETOTIFEN |
Calcium Channel Type L, Benzothiazepine |
71% |
2.305uM |
2.049uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 2 |
KETOTIFEN |
Calcium Channel Type L, Benzothiazepine |
71% |
2.305uM |
2.049uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 1 |
KETOTIFEN |
Calcium Channel Type L, Benzothiazepine |
71% |
2.305uM |
2.049uM |
View
|
| sodium channel associated protein 1 |
KETOCONAZOLE |
Sodium Channel, Site 2 |
70% |
23.911uM |
21.438uM |
View
|
| sodium channel associated protein 2 |
KETOCONAZOLE |
Sodium Channel, Site 2 |
70% |
23.911uM |
21.438uM |
View
|
| sodium channel, voltage-gated, type III, beta |
KETOCONAZOLE |
Sodium Channel, Site 2 |
70% |
23.911uM |
21.438uM |
View
|
| sodium channel, voltage-gated, type I, alpha |
KETOCONAZOLE |
Sodium Channel, Site 2 |
70% |
23.911uM |
21.438uM |
View
|
| sodium channel, voltage-gated, type IX, alpha |
KETOCONAZOLE |
Sodium Channel, Site 2 |
70% |
23.911uM |
21.438uM |
View
|
| sodium channel, voltage-gated, type VII, alpha |
KETOCONAZOLE |
Sodium Channel, Site 2 |
70% |
23.911uM |
21.438uM |
View
|
| thromboxane A synthase 1 |
KETOCONAZOLE |
Thromboxane Synthetase |
70% |
2.165uM |
NoneNone |
View
|
| thromboxane A synthase 1 (platelet, cytochrome P450, family 5, subfamily A) |
KETOCONAZOLE |
Thromboxane Synthetase |
70% |
2.165uM |
NoneNone |
View
|
| adrenergic receptor, beta 3 |
CIGLITAZONE |
Adrenergic beta3 |
70% |
17.871uM |
13.403uM |
View
|
| aldo-keto reductase family 1, member B4 (aldose reductase) |
KETOROLAC |
Aldose Reductase |
70% |
6.109uM |
NoneNone |
View
|
| aldo-keto reductase family 1, member B1 (aldose reductase) |
KETOROLAC |
Aldose Reductase |
70% |
6.109uM |
NoneNone |
View
|
| aldo-keto reductase family 7, member A2 (aflatoxin aldehyde reductase) |
KETOROLAC |
Aldose Reductase |
70% |
6.109uM |
NoneNone |
View
|
| aldo-keto reductase family 7, member A3 (aflatoxin aldehyde reductase) |
KETOROLAC |
Aldose Reductase |
70% |
6.109uM |
NoneNone |
View
|
| monoamine oxidase A |
NOCODAZOLE |
Monoamine Oxidase MAOA |
70% |
24.099uM |
NoneNone |
View
|
| monoamine oxidase A |
NOCODAZOLE |
Monoamine Oxidase MAOA |
70% |
24.099uM |
NoneNone |
View
|
| adenosine A2a receptor |
NOCODAZOLE |
Adenosine A2A |
70% |
7.509uM |
4.219uM |
View
|
| opioid receptor, sigma 1 |
PROGESTERONE |
Sigma1 |
70% |
3.055uM |
1.284uM |
View
|
| adrenergic receptor, alpha 2a |
AMOXAPINE |
Imidazoline I2, Central |
70% |
3.466uM |
2.31uM |
View
|
| adrenergic receptor, alpha 2c (Non-specific probe) |
AMOXAPINE |
Imidazoline I2, Central |
70% |
3.466uM |
2.31uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 8 |
CLOTRIMAZOLE |
Calcium Channel Type L, Benzothiazepine |
70% |
28.499uM |
25.332uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 7 |
CLOTRIMAZOLE |
Calcium Channel Type L, Benzothiazepine |
70% |
28.499uM |
25.332uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 6 |
CLOTRIMAZOLE |
Calcium Channel Type L, Benzothiazepine |
70% |
28.499uM |
25.332uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 5 |
CLOTRIMAZOLE |
Calcium Channel Type L, Benzothiazepine |
70% |
28.499uM |
25.332uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 4 |
CLOTRIMAZOLE |
Calcium Channel Type L, Benzothiazepine |
70% |
28.499uM |
25.332uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 3 |
CLOTRIMAZOLE |
Calcium Channel Type L, Benzothiazepine |
70% |
28.499uM |
25.332uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 2 |
CLOTRIMAZOLE |
Calcium Channel Type L, Benzothiazepine |
70% |
28.499uM |
25.332uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 1 |
CLOTRIMAZOLE |
Calcium Channel Type L, Benzothiazepine |
70% |
28.499uM |
25.332uM |
View
|
| calcium channel, voltage-dependent, beta 4 subunit |
CLOTRIMAZOLE |
Calcium Channel Type L, Benzothiazepine |
70% |
28.499uM |
25.332uM |
View
|
| calcium channel, voltage-dependent, beta 3 subunit |
CLOTRIMAZOLE |
Calcium Channel Type L, Benzothiazepine |
70% |
28.499uM |
25.332uM |
View
|
| solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 |
BW-723C86 |
Serotonin Transporter |
70% |
4.785uM |
2.542uM |
View
|
| cholinergic receptor, muscarinic 3 |
SULOCTIDIL |
Muscarinic M3 |
70% |
4.6238uM |
.98uM |
View
|
| opioid receptor, sigma 1 |
DIMENHYDRINATE |
Sigma1 |
70% |
1.158uM |
.487uM |
View
|
| mu-opioid receptor MOR |
CINNARIZINE |
Opiate mu |
70% |
2.272uM |
.922uM |
View
|
| opioid receptor, kappa 1 |
DOMPERIDONE |
Opiate kappa |
70% |
6.994uM |
2.798uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 8 |
VALETHAMATE BROMIDE |
Calcium Channel Type L, Benzothiazepine |
70% |
3.389uM |
3.013uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 7 |
VALETHAMATE BROMIDE |
Calcium Channel Type L, Benzothiazepine |
70% |
3.389uM |
3.013uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 6 |
VALETHAMATE BROMIDE |
Calcium Channel Type L, Benzothiazepine |
70% |
3.389uM |
3.013uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 5 |
VALETHAMATE BROMIDE |
Calcium Channel Type L, Benzothiazepine |
70% |
3.389uM |
3.013uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 4 |
VALETHAMATE BROMIDE |
Calcium Channel Type L, Benzothiazepine |
70% |
3.389uM |
3.013uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 3 |
VALETHAMATE BROMIDE |
Calcium Channel Type L, Benzothiazepine |
70% |
3.389uM |
3.013uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 2 |
VALETHAMATE BROMIDE |
Calcium Channel Type L, Benzothiazepine |
70% |
3.389uM |
3.013uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 1 |
VALETHAMATE BROMIDE |
Calcium Channel Type L, Benzothiazepine |
70% |
3.389uM |
3.013uM |
View
|
| calcium channel, voltage-dependent, beta 4 subunit |
VALETHAMATE BROMIDE |
Calcium Channel Type L, Benzothiazepine |
70% |
3.389uM |
3.013uM |
View
|
| ATPase, Na+/K+ transporting, beta 2 polypeptide |
CLADRIBINE |
ATPase, Na+/K+ |
13% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, beta 3 subunit |
VALETHAMATE BROMIDE |
Calcium Channel Type L, Benzothiazepine |
70% |
3.389uM |
3.013uM |
View
|
| calcium channel, voltage-dependent, beta 2 subunit |
VALETHAMATE BROMIDE |
Calcium Channel Type L, Benzothiazepine |
70% |
3.389uM |
3.013uM |
View
|
| calcium channel, voltage-dependent, L type, alpha 1S subunit |
VALETHAMATE BROMIDE |
Calcium Channel Type L, Benzothiazepine |
70% |
3.389uM |
3.013uM |
View
|
| calcium channel, voltage-dependent, alpha 1F subunit |
VALETHAMATE BROMIDE |
Calcium Channel Type L, Benzothiazepine |
70% |
3.389uM |
3.013uM |
View
|
| calcium channel, voltage-dependent, L type, alpha 1D subunit |
VALETHAMATE BROMIDE |
Calcium Channel Type L, Benzothiazepine |
70% |
3.389uM |
3.013uM |
View
|
| calcium channel, voltage-dependent, L type, alpha 1C subunit |
VALETHAMATE BROMIDE |
Calcium Channel Type L, Benzothiazepine |
70% |
3.389uM |
3.013uM |
View
|
| calcium channel, voltage-dependent, L type, alpha 1E subunit |
OXICONAZOLE |
Calcium Channel Type L, Benzothiazepine |
67% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, N type, alpha 1B subunit |
OXICONAZOLE |
Calcium Channel Type L, Benzothiazepine |
67% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, alpha2/delta subunit 1 |
OXICONAZOLE |
Calcium Channel Type L, Benzothiazepine |
67% |
NoneNone |
NoneNone |
View
|
| cholinergic receptor, muscarinic 5 |
OXICONAZOLE |
Muscarinic M5 |
67% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, gamma subunit 5 |
OXYMETAZOLINE |
Calcium Channel Type L, Benzothiazepine |
67% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, gamma subunit 4 |
OXYMETAZOLINE |
Calcium Channel Type L, Benzothiazepine |
67% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, gamma subunit 3 |
OXYMETAZOLINE |
Calcium Channel Type L, Benzothiazepine |
67% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, gamma subunit 2 |
OXYMETAZOLINE |
Calcium Channel Type L, Benzothiazepine |
67% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, gamma subunit 1 |
OXYMETAZOLINE |
Calcium Channel Type L, Benzothiazepine |
67% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, beta 4 subunit |
OXYMETAZOLINE |
Calcium Channel Type L, Benzothiazepine |
67% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, beta 3 subunit |
OXYMETAZOLINE |
Calcium Channel Type L, Benzothiazepine |
67% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, beta 2 subunit |
OXYMETAZOLINE |
Calcium Channel Type L, Benzothiazepine |
67% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, L type, alpha 1S subunit |
OXYMETAZOLINE |
Calcium Channel Type L, Benzothiazepine |
67% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, alpha 1F subunit |
OXYMETAZOLINE |
Calcium Channel Type L, Benzothiazepine |
67% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, L type, alpha 1D subunit |
OXYMETAZOLINE |
Calcium Channel Type L, Benzothiazepine |
67% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, L type, alpha 1C subunit |
OXYMETAZOLINE |
Calcium Channel Type L, Benzothiazepine |
67% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, P/Q type, alpha 1A subunit |
OXYMETAZOLINE |
Calcium Channel Type L, Benzothiazepine |
67% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, beta 1 subunit |
OXYMETAZOLINE |
Calcium Channel Type L, Benzothiazepine |
67% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, L type, alpha 1E subunit |
OXYMETAZOLINE |
Calcium Channel Type L, Benzothiazepine |
67% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, N type, alpha 1B subunit |
OXYMETAZOLINE |
Calcium Channel Type L, Benzothiazepine |
67% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, alpha2/delta subunit 1 |
OXYMETAZOLINE |
Calcium Channel Type L, Benzothiazepine |
67% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, gamma subunit 8 |
OXYMETAZOLINE |
Calcium Channel Type L, Benzothiazepine |
67% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, gamma subunit 7 |
OXYMETAZOLINE |
Calcium Channel Type L, Benzothiazepine |
67% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, gamma subunit 6 |
OXYMETAZOLINE |
Calcium Channel Type L, Benzothiazepine |
67% |
NoneNone |
NoneNone |
View
|
| Cytochrom P450-2C19 monooxygenase |
FELODIPINE |
CYP450-2C19 Inhibition |
67% |
NoneNone |
NoneNone |
View
|
| dopamine receptor D3 |
CANDESARTAN |
Dopamine D3 |
67% |
NoneNone |
NoneNone |
View
|
| cholinergic receptor, muscarinic 2 |
RALOXIFENE |
Muscarinic M2 |
67% |
NoneNone |
NoneNone |
View
|
| 5-hydroxytryptamine (serotonin) receptor 5B |
SB-203580 |
Serotonin 5-HT4 |
67% |
10.553uM |
1.759uM |
View
|
| 5-hydroxytryptamine (serotonin) receptor 4 |
SB-203580 |
Serotonin 5-HT4 |
67% |
10.553uM |
1.759uM |
View
|
| adrenergic receptor, beta 2 |
ATENOLOL |
Adrenergic beta2 |
67% |
14.634uM |
10.061uM |
View
|
| lymphocyte protein tyrosine kinase (mapped) |
CLOMIPHENE |
Protein Tyrosine Kinase, Lck |
67% |
NoneNone |
NoneNone |
View
|
| mu-opioid receptor MOR |
DROPERIDOL |
Opiate mu |
67% |
NoneNone |
NoneNone |
View
|
| Cytochrome P450, subfamily IIC (mephenytoin 4-hydroxylase) |
ANTIMYCIN A |
CYP450-2C9 Inhibition |
67% |
NoneNone |
NoneNone |
View
|
| cytochrome P450, family 2, subfamily C, polypeptide 9 |
ANTIMYCIN A |
CYP450-2C9 Inhibition |
67% |
NoneNone |
NoneNone |
View
|
| neuropeptide Y receptor Y2 |
DIHYDROERGOCRISTINE MESYLATE |
Neuropeptide Y2 |
67% |
NoneNone |
NoneNone |
View
|
| adrenergic receptor, beta 3 |
NELFINAVIR |
Adrenergic beta3 |
67% |
34.08uM |
25.566uM |
View
|
| opioid receptor, sigma 1 |
STANOLONE |
Sigma1 |
67% |
NoneNone |
NoneNone |
View
|
| leukotriene C4 synthase |
6-METHOXY-2-NAPHTHYLACETIC ACID |
Leukotriene C4 Synthetase |
67% |
49.66uM |
NoneNone |
View
|
| leukotriene C4 synthase |
6-METHOXY-2-NAPHTHYLACETIC ACID |
Leukotriene C4 Synthetase |
67% |
49.66uM |
NoneNone |
View
|
| adrenergic receptor, alpha 2a |
PROCHLORPERAZINE |
Imidazoline I2, Central |
67% |
NoneNone |
NoneNone |
View
|
| adrenergic receptor, alpha 2c (Non-specific probe) |
PROCHLORPERAZINE |
Imidazoline I2, Central |
67% |
NoneNone |
NoneNone |
View
|
| adrenergic receptor, alpha 1d (Non-specific probe) |
PENTAMIDINE |
Adrenergic alpha1D |
67% |
NoneNone |
NoneNone |
View
|
| Sigma-2 Receptor |
CYPROHEPTADINE |
Sigma2 |
67% |
NoneNone |
NoneNone |
View
|
| opioid receptor, sigma 1 |
METOCLOPRAMIDE |
Sigma1 |
67% |
NoneNone |
NoneNone |
View
|
| 5-hydroxytryptamine (serotonin) receptor 1B |
ECONAZOLE |
Serotonin 5-HT1B |
67% |
22.034uM |
10.016uM |
View
|
| Sigma-2 Receptor |
MICONAZOLE |
Sigma2 |
67% |
3.305uM |
2.034uM |
View
|
| adrenergic receptor, alpha 2a |
KETOCONAZOLE |
Adrenergic alpha2A |
67% |
19.783uM |
7.419uM |
View
|
| progesterone receptor |
CIGLITAZONE |
Progesterone |
67% |
29.118uM |
3.798uM |
View
|
| progesterone receptor |
CIGLITAZONE |
Progesterone |
67% |
29.118uM |
3.798uM |
View
|
| thromboxane A synthase 1 |
AURANOFIN |
Thromboxane Synthetase |
67% |
NoneNone |
NoneNone |
View
|
| thromboxane A synthase 1 (platelet, cytochrome P450, family 5, subfamily A) |
AURANOFIN |
Thromboxane Synthetase |
67% |
NoneNone |
NoneNone |
View
|
| opioid receptor, kappa 1 |
SULCONAZOLE |
Opiate kappa |
67% |
NoneNone |
NoneNone |
View
|
| lymphocyte protein tyrosine kinase (mapped) |
4-OCTYLPHENOL |
Protein Tyrosine Kinase, Lck |
67% |
22.054uM |
NoneNone |
View
|
| acetylcholinesterase (YT blood group) |
4-OCTYLPHENOL |
Acetylcholinesterase |
67% |
11.471uM |
NoneNone |
View
|
| collagen-like tail subunit (single strand of homotrimer) of asymmetric acetylcholinesterase |
4-OCTYLPHENOL |
Acetylcholinesterase |
67% |
11.471uM |
NoneNone |
View
|
| calcium channel, voltage-dependent, beta 4 subunit |
KETOTIFEN |
Calcium Channel Type L, Benzothiazepine |
71% |
2.305uM |
2.049uM |
View
|
| calcium channel, voltage-dependent, beta 3 subunit |
KETOTIFEN |
Calcium Channel Type L, Benzothiazepine |
71% |
2.305uM |
2.049uM |
View
|
| calcium channel, voltage-dependent, beta 2 subunit |
KETOTIFEN |
Calcium Channel Type L, Benzothiazepine |
71% |
2.305uM |
2.049uM |
View
|
| calcium channel, voltage-dependent, L type, alpha 1S subunit |
KETOTIFEN |
Calcium Channel Type L, Benzothiazepine |
71% |
2.305uM |
2.049uM |
View
|
| calcium channel, voltage-dependent, alpha 1F subunit |
KETOTIFEN |
Calcium Channel Type L, Benzothiazepine |
71% |
2.305uM |
2.049uM |
View
|
| calcium channel, voltage-dependent, L type, alpha 1D subunit |
KETOTIFEN |
Calcium Channel Type L, Benzothiazepine |
71% |
2.305uM |
2.049uM |
View
|
| calcium channel, voltage-dependent, L type, alpha 1C subunit |
KETOTIFEN |
Calcium Channel Type L, Benzothiazepine |
71% |
2.305uM |
2.049uM |
View
|
| calcium channel, voltage-dependent, P/Q type, alpha 1A subunit |
KETOTIFEN |
Calcium Channel Type L, Benzothiazepine |
71% |
2.305uM |
2.049uM |
View
|
| calcium channel, voltage-dependent, beta 1 subunit |
KETOTIFEN |
Calcium Channel Type L, Benzothiazepine |
71% |
2.305uM |
2.049uM |
View
|
| calcium channel, voltage-dependent, L type, alpha 1E subunit |
KETOTIFEN |
Calcium Channel Type L, Benzothiazepine |
71% |
2.305uM |
2.049uM |
View
|
| calcium channel, voltage-dependent, N type, alpha 1B subunit |
KETOTIFEN |
Calcium Channel Type L, Benzothiazepine |
71% |
2.305uM |
2.049uM |
View
|
| calcium channel, voltage-dependent, alpha2/delta subunit 1 |
KETOTIFEN |
Calcium Channel Type L, Benzothiazepine |
71% |
2.305uM |
2.049uM |
View
|
| AT hook, DNA binding motif, containing 1 (DBSS) |
NORETHINDRONE |
GABAA, Benzodiazepine, Central |
71% |
13.343uM |
10.872uM |
View
|
| gamma-aminobutyric acid A receptor, theta |
NORETHINDRONE |
GABAA, Benzodiazepine, Central |
71% |
13.343uM |
10.872uM |
View
|
| gamma-aminobutyric acid A receptor, gamma 2 |
NORETHINDRONE |
GABAA, Benzodiazepine, Central |
71% |
13.343uM |
10.872uM |
View
|
| gamma-aminobutyric acid (GABA-A) receptor, subunit alpha 6 |
NORETHINDRONE |
GABAA, Benzodiazepine, Central |
71% |
13.343uM |
10.872uM |
View
|
| gamma-aminobutyric acid (GABA-A) receptor, subunit alpha 5 |
NORETHINDRONE |
GABAA, Benzodiazepine, Central |
71% |
13.343uM |
10.872uM |
View
|
| gamma-aminobutyric acid A receptor, alpha 2 |
NORETHINDRONE |
GABAA, Benzodiazepine, Central |
71% |
13.343uM |
10.872uM |
View
|
| gamma-aminobutyric acid A receptor, alpha 1 |
NORETHINDRONE |
GABAA, Benzodiazepine, Central |
71% |
13.343uM |
10.872uM |
View
|
| gamma-aminobutyric acid (GABA-C) receptor, subunit rho 2 |
NORETHINDRONE |
GABAA, Benzodiazepine, Central |
71% |
13.343uM |
10.872uM |
View
|
| gamma-aminobutyric acid (GABA-C) receptor, subunit rho 1 |
NORETHINDRONE |
GABAA, Benzodiazepine, Central |
71% |
13.343uM |
10.872uM |
View
|
| gamma-aminobutyric acid A receptor, delta |
NORETHINDRONE |
GABAA, Benzodiazepine, Central |
71% |
13.343uM |
10.872uM |
View
|
| gamma-aminobutyric acid (GABA-A) receptor, subunit alpha 3 |
NORETHINDRONE |
GABAA, Benzodiazepine, Central |
71% |
13.343uM |
10.872uM |
View
|
| gamma-aminobutyric acid (GABA-A) receptor, subunit alpha 4 |
NORETHINDRONE |
GABAA, Benzodiazepine, Central |
71% |
13.343uM |
10.872uM |
View
|
| gamma-aminobutyric acid A receptor, gamma 1 |
NORETHINDRONE |
GABAA, Benzodiazepine, Central |
71% |
13.343uM |
10.872uM |
View
|
| gamma-aminobutyric acid A receptor, pi |
NORETHINDRONE |
GABAA, Benzodiazepine, Central |
71% |
13.343uM |
10.872uM |
View
|
| solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 |
PROPAFENONE |
Adrenergic, Norepinephrine Transporter |
71% |
3.016uM |
2.991uM |
View
|
| progesterone receptor |
STANOZOLOL |
Progesterone |
71% |
3.705uM |
.483uM |
View
|
| progesterone receptor |
STANOZOLOL |
Progesterone |
71% |
3.705uM |
.483uM |
View
|
| solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 |
SIBUTRAMINE |
Serotonin Transporter |
71% |
2.085uM |
1.108uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 5 |
RALOXIFENE |
Calcium Channel Type L, Dihydropyridine |
71% |
.388uM |
.249uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 4 |
RALOXIFENE |
Calcium Channel Type L, Dihydropyridine |
71% |
.388uM |
.249uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 3 |
RALOXIFENE |
Calcium Channel Type L, Dihydropyridine |
71% |
.388uM |
.249uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 2 |
RALOXIFENE |
Calcium Channel Type L, Dihydropyridine |
71% |
.388uM |
.249uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 1 |
RALOXIFENE |
Calcium Channel Type L, Dihydropyridine |
71% |
.388uM |
.249uM |
View
|
| calcium channel, voltage-dependent, beta 4 subunit |
RALOXIFENE |
Calcium Channel Type L, Dihydropyridine |
71% |
.388uM |
.249uM |
View
|
| calcium channel, voltage-dependent, beta 3 subunit |
RALOXIFENE |
Calcium Channel Type L, Dihydropyridine |
71% |
.388uM |
.249uM |
View
|
| ATPase, Na+/K+ transporting, beta 1 polypeptide |
CHLORMADINONE ACETATE |
ATPase, Na+/K+ |
71% |
4.5696uM |
NoneNone |
View
|
| ATPase, Na+/K+ transporting, beta 3 polypeptide |
CHLORMADINONE ACETATE |
ATPase, Na+/K+ |
71% |
4.5696uM |
NoneNone |
View
|
| ATPase, Na+/K+ transporting, beta 2 polypeptide |
CHLORMADINONE ACETATE |
ATPase, Na+/K+ |
71% |
4.5696uM |
NoneNone |
View
|
| ATPase, (Na+)/K+ transporting, beta 4 polypeptide |
CHLORMADINONE ACETATE |
ATPase, Na+/K+ |
71% |
4.5696uM |
NoneNone |
View
|
| nuclear receptor subfamily 3, group C, member 1 |
CORTISONE ACETATE |
Glucocorticoid |
71% |
3.911uM |
1.778uM |
View
|
| 5-hydroxytryptamine (serotonin) receptor 2B |
BENZBROMARONE |
Serotonin 5-HT2B |
71% |
1.804uM |
1.148uM |
View
|
| tachykinin receptor 2 |
FLUPHENAZINE |
Tachykinin NK2 |
71% |
22.484uM |
7.495uM |
View
|
| Sigma-2 Receptor |
DOXEPIN |
Sigma2 |
71% |
2.143uM |
1.319uM |
View
|
| mitogen activated protein kinase 1 |
DICUMAROL |
Protein Serine/Threonine Kinase, ERK2 |
71% |
4.426uM |
NoneNone |
View
|
| mitogen-activated protein kinase 1 |
DICUMAROL |
Protein Serine/Threonine Kinase, ERK2 |
71% |
4.426uM |
NoneNone |
View
|
| cholinergic receptor, muscarinic 5 |
HALOPERIDOL |
Muscarinic M5 |
71% |
3.89uM |
2.795uM |
View
|
| opioid receptor, sigma 1 |
TRAZODONE |
Sigma1 |
71% |
2.203uM |
.926uM |
View
|
| calcium channel, voltage-dependent, P/Q type, alpha 1A subunit |
VALETHAMATE BROMIDE |
Calcium Channel Type L, Benzothiazepine |
70% |
3.389uM |
3.013uM |
View
|
| calcium channel, voltage-dependent, beta 1 subunit |
VALETHAMATE BROMIDE |
Calcium Channel Type L, Benzothiazepine |
70% |
3.389uM |
3.013uM |
View
|
| calcium channel, voltage-dependent, L type, alpha 1E subunit |
VALETHAMATE BROMIDE |
Calcium Channel Type L, Benzothiazepine |
70% |
3.389uM |
3.013uM |
View
|
| calcium channel, voltage-dependent, N type, alpha 1B subunit |
VALETHAMATE BROMIDE |
Calcium Channel Type L, Benzothiazepine |
70% |
3.389uM |
3.013uM |
View
|
| calcium channel, voltage-dependent, alpha2/delta subunit 1 |
VALETHAMATE BROMIDE |
Calcium Channel Type L, Benzothiazepine |
70% |
3.389uM |
3.013uM |
View
|
| cytochrome P450, family 3, subfamily a, polypeptide 13 |
CLOSANTEL |
CYP450-3A4 Inhibition |
70% |
5uM |
NoneNone |
View
|
| cytochrome P450, family 3, subfamily a, polypeptide 13 |
IDEBENONE |
CYP450-3A4 Inhibition |
70% |
7uM |
NoneNone |
View
|
| Cytochrom P450-2D6 monooxygenase |
BAMBUTEROL |
CYP450-2D6 Inhibition |
70% |
2uM |
NoneNone |
View
|
| Cytochrome P450, subfamily IIC (mephenytoin 4-hydroxylase) |
LOSARTAN |
CYP450-2C9 Inhibition |
70% |
2.882uM |
NoneNone |
View
|
| cytochrome P450, family 2, subfamily C, polypeptide 9 |
LOSARTAN |
CYP450-2C9 Inhibition |
70% |
2.882uM |
NoneNone |
View
|
| adrenergic receptor, alpha 1a |
PROPAFENONE |
Adrenergic alpha1A |
70% |
6.147uM |
2.488uM |
View
|
| adrenergic receptor, alpha 2a |
DOMPERIDONE |
Adrenergic alpha2A |
70% |
2.74uM |
1.027uM |
View
|
| solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 |
IVERMECTIN |
Dopamine Transporter |
70% |
4.4552uM |
3.5397uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 8 |
SPIRADOLINE |
Calcium Channel Type L, Benzothiazepine |
70% |
8.513uM |
7.567uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 7 |
SPIRADOLINE |
Calcium Channel Type L, Benzothiazepine |
70% |
8.513uM |
7.567uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 6 |
SPIRADOLINE |
Calcium Channel Type L, Benzothiazepine |
70% |
8.513uM |
7.567uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 5 |
SPIRADOLINE |
Calcium Channel Type L, Benzothiazepine |
70% |
8.513uM |
7.567uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 4 |
SPIRADOLINE |
Calcium Channel Type L, Benzothiazepine |
70% |
8.513uM |
7.567uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 3 |
SPIRADOLINE |
Calcium Channel Type L, Benzothiazepine |
70% |
8.513uM |
7.567uM |
View
|
| ATPase, (Na+)/K+ transporting, beta 4 polypeptide |
CLADRIBINE |
ATPase, Na+/K+ |
13% |
NoneNone |
NoneNone |
View
|
| calcium channel, voltage-dependent, gamma subunit 2 |
SPIRADOLINE |
Calcium Channel Type L, Benzothiazepine |
70% |
8.513uM |
7.567uM |
View
|
| calcium channel, voltage-dependent, gamma subunit 1 |
SPIRADOLINE |
Calcium Channel Type L, Benzothiazepine |
70% |
8.513uM |
7.567uM |
View
|
| calcium channel, voltage-dependent, beta 4 subunit |
SPIRADOLINE |
Calcium Channel Type L, Benzothiazepine |
70% |
8.513uM |
7.567uM |
View
|
| calcium channel, voltage-dependent, beta 3 subunit |
SPIRADOLINE |
Calcium Channel Type L, Benzothiazepine |
70% |
8.513uM |
7.567uM |
View
|
| calcium channel, voltage-dependent, beta 2 subunit |
SPIRADOLINE |
Calcium Channel Type L, Benzothiazepine |
70% |
8.513uM |
7.567uM |
View
|
| calcium channel, voltage-dependent, L type, alpha 1S subunit |
SPIRADOLINE |
Calcium Channel Type L, Benzothiazepine |
70% |
8.513uM |
7.567uM |
View
|
| calcium channel, voltage-dependent, alpha 1F subunit |
SPIRADOLINE |
Calcium Channel Type L, Benzothiazepine |
70% |
8.513uM |
7.567uM |
View
|
| calcium channel, voltage-dependent, L type, alpha 1D subunit |
SPIRADOLINE |
Calcium Channel Type L, Benzothiazepine |
70% |
8.513uM |
7.567uM |
View
|
| calcium channel, voltage-dependent, L type, alpha 1C subunit |
SPIRADOLINE |
Calcium Channel Type L, Benzothiazepine |
70% |
8.513uM |
7.567uM |
View
|
| calcium channel, voltage-dependent, P/Q type, alpha 1A subunit |
SPIRADOLINE |
Calcium Channel Type L, Benzothiazepine |
70% |
8.513uM |
7.567uM |
View
|
| calcium channel, voltage-dependent, beta 1 subunit |
SPIRADOLINE |
Calcium Channel Type L, Benzothiazepine |
70% |
8.513uM |
7.567uM |
View
|
| calcium channel, voltage-dependent, L type, alpha 1E subunit |
SPIRADOLINE |
Calcium Channel Type L, Benzothiazepine |
70% |
8.513uM |
7.567uM |
View
|
| calcium channel, voltage-dependent, N type, alpha 1B subunit |
SPIRADOLINE |
Calcium Channel Type L, Benzothiazepine |
70% |
8.513uM |
7.567uM |
View
|
| calcium channel, voltage-dependent, alpha2/delta subunit 1 |
SPIRADOLINE |
Calcium Channel Type L, Benzothiazepine |
70% |
8.513uM |
7.567uM |
View
|
| adrenergic receptor, alpha 2a |
BUTENAFINE |
Adrenergic alpha2A |
70% |
3.6443uM |
1.3666uM |
View
|