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Dopamine Receptor

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Dopamine Receptor

Chemical Structure Cat. No. Product Name CAS No.
Ocaperidone Chemical Structure
 BCP32651 Ocaperidone 129029-23-8
Ocaperidone is an effective antipsychotic agent, acting as a potent 5-HT2 and dopamine D2 antagonist, and a 5-HT1A agonist, with Kis of 0.14 nM, 0.46 nM, 0.75 nM, 1.6 nM and 5.4 nM for 5-HT2, a1-adrenergic receptor, dopamine D2, histamine H1 and a2-adrenergic receptor, respectively, and a pEC50 and pKi of 7.60 and 8.08 for h5-HT1A.
Fupentixol dihydrochloride Chemical Structure
 BCP12120 Fupentixol dihydrochloride 2413-38-9
Flupenthixol dihydrochloride is a dopamine receptor antagonist used as an antipsychotic drug for schizophrenia treatment.
SCH-23390 maleate Chemical Structure
 BCP28944 SCH-23390 maleate 87134-87-0
SCH 23390 is a potent dopamine receptor D1 antagonist with Ki values of 0.2 and 0.3 nM for the D1 and D5.
WAY-100635 Maleate Chemical Structure
 BCP29013 WAY-100635 Maleate 1092679-51-0
WAY100635 Maleate is a potent, silent antagonist of serotonin 5-HT1A receptors.
Sarizotan Chemical Structure
 BCP32062 Sarizotan 177975-08-5
Sarizotan, also known as EMD-128130, is a Dopamine D2 receptor partial agonist and Serotonin 1A receptor agonist.
PD-168077 maleate Chemical Structure
 BCP31168 PD-168077 maleate 630117-19-0
PD-168077 maleate is a selective dopamine D4 receptor agonist, with a Ki of 9 nM.
BHT 958 Chemical Structure
 BCP27640 BHT 958 83718-64-3
B-HT 958 is a Dopamine D2 receptor agonist, α2-adrenoceptor partial agonist
Odapipam Chemical Structure
 BCP27610 Odapipam 131796-63-9
Odapipam is a potent dopamine D1 antagonist.
Nepicastat HCl Chemical Structure
 BCP06517 Nepicastat HCl 170151-24-3
Nepicastat (SYN-117) HCl is a potent and selective inhibitor of both bovine and human dopamine-β-hydroxylase with IC50 of 8.5 nM and 9 nM, with negligible affinity for twelve other enzymes and thirteen neurotransmitter receptors.
SKF 38393 hydrobromide Chemical Structure
 BCP30804 SKF 38393 hydrobromide 20012-10-6
SKF 38393 hydrobromide is a selective dopamine D1-like receptor partial agonist (Ki = 1, ~ 0.5, ~ 150, ~ 5000 and ~ 1000 nM for D1, D5, D2, D3 and D4 receptors, respectively).
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