| Cat. No. |
Product Name |
Information |
| PC-22633 |
FOB02-04
D3R agonist
|
FOB02-04 is a potent, selective dopamine D3 receptor (D3R) agonist with Ki of 2.84 nM, weak affinity with Ki of 106 nM for D2R. |
| PC-22235 |
Raclopride
Dopamine D2/D3 antagonist
|
Raclopride (FLA 870) is a potent, selective dopamine D2/D3 receptor antagonist, binds to D2 and D3 receptors with Ki of 1.8 nM and 3.5 nM, respectively. |
| PC-22227 |
A-77636 hydrochloride
Dopamine D1 agonist
|
A-77636 hydrochloride is a potent, selective, orally active and long acting dopamine D1 receptor agonist with Ki of 39.8 nM. |
| PC-22147 |
SCH23390 hydrochloride
Dopamine Receptor antagonist
|
SCH23390 hydrochloride is a potent and selective dopamine D1-like receptor antagonist with Kis of 0.2 nM and 0.3 nM for the D1 and D5 receptor, respectively. |
| PC-21488 |
NGD-94-1
D4R inhibitor
|
NGD-94-1 is a highly potent, selective dopamine D4 receptor antagonist with Ki of 3.6 nM. |
| PC-21105 |
CAB-01-019
D4R inhibitor
|
CAB-01-019 is potent, selective dopamine D4 receptor (D4R) full antagonist with binding Ki of 2.2 nM, >500-fold selectivity over D2R and D3R. |
| PC-20978 |
ZINC621433144
D4 agonist
|
ZINC621433144 is a Gi-biased, high-affinity full agonist of dopamine D4 receptor with Ki of 4.3 nM and cAMP EC50 of 0.18 nM. |
| PC-20864 |
CJB 090
D3 receptor agonist
|
CJB 090 (CJB090) is a selective partial agonist of dopamine D3 receptor with binding Ki of 0.6 nM, CJB 090 is 97-fold selective for D3 receptors over D2. |
| PC-43162 |
Apomorphine hydrochloride hemihydrate
|
Apomorphine hydrochloride hemihydrate is a non-selective dopamine agonist which activates both D1-likeand D2-like receptors, with some preference for the latter subtypes.. |
| PC-63114 |
SKF-38393 hydrobromide
|
SKF-38393 is a potent, selective D1/D5 receptor partial agonist with Ki of 1 and 0.5 nM, respectively. |
| PC-63037 |
Bromocriptine
|
Bromocriptine (2-Bromoergocriptine. |
| PC-60615 |
L 741742 hydrochloride
|
A potent and highly selective D4 dopamine receptor antagonist with Ki of 3.5 nM, >200-fold selectivity over D2 and D3 receptors. |
