| S3044 |
Lurasidone HCl |
Lurasidone is an atypical antipsychotic, inhibits Dopamine D2, 5-HT2A, 5-HT7, 5-HT1A and noradrenaline α2C with IC50 of 1.68 nM, 2.03 nM, 0.495 nM, 6.75 nM and 10.8 nM, respectively. |
Selective |
D2 receptor, IC50: 1.68 nM |
| S3189 |
Ropinirole HCl |
Ropinirole a selective dopamine D2 receptors agonist with Ki of 29 nM. |
Selective |
D2 receptor, Ki: 29 nM |
| S4289 |
Metoclopramide HCl |
Metoclopramide HCl is a selective dopamine D2 receptor antagonist, used for the treatment of nausea and vomiting.
|
Selective |
|
| S4251 |
Phenothiazine |
Phenothiazine is a dopamine-2 (D2) receptor antagonist therefore decreases the effect of dopamine in the brain. |
Selective |
|
| S2104 |
Levosulpiride |
Levosulpiride is a selective antagonist for D2 dopamine receptors used as an antipsychotic and prokinetic agent. |
Selective |
|
| S2493 |
Olanzapine |
Olanzapine is a high affinity for 5-HT2 serotonin and D2 dopamine receptor antagonist. |
Selective |
|
| S2460 |
Pramipexole |
Pramipexole is a partial/full D2S, D2L, D3, D4 receptor agonist with a Ki of 3.9, 2.2, 0.5 and 5.1 nM for D2S, D2L, D3, D4 receptor, respectively. |
Pan |
D2S Receptor, Ki: 3.9 nM; D2L Receptor, Ki: 2.2 nM |
| S2011 |
Pramipexole 2HCl Monohydrate |
Pramipexole 2HCl Monohydrate is a partial/full D2S, D2L, D3, D4, receptor agonist with a Ki of 3.9, 2.2, 0.5, 5.1 nM. |
Pan |
D2S Receptor, Ki: 3.9 nM; D2L Receptor, Ki: 2.2 nM |
| S1771 |
Chlorprothixene |
Chlorprothixene has strong binding affinities to dopamine and histamine receptors, such as D1, D2, D3, D5, H1, 5-HT2, 5-HT6 and 5-HT7, with Ki of 18 nM, 2.96 nM, 4.56 nM, 9 nM, 3.75 nM, 9.4 nM, 3 nM and 5.6 nM, respectively. |
Pan |
D2 receptor, Ki: 2.96 nM |
| S4086 |
Loxapine Succinate |
Loxapine Succinate is a D2DR and D4DR inhibitor, serotonergic receptor antagonist and also a dibenzoxazepine anti-psychotic agent. |
Pan |
D2 receptor (bovine), Ki: 26 nM; D2 receptor (Human), Ki: 24 nM; D2 receptor (human), Ki: 24 nM |
| S2437 |
Rotundine |
Rotundine (L-tetrahydropalmatine, L-THP) is a selective dopamine D1 receptor antagonist with IC50 of 166 nM. |
Pan |
D2 receptor, IC50: 1.47 μM |