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Dopaminergics

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PRODUCT NAMECATALOG #DESCRIPTIONCITATIONSRANKING
BTCP maleatesc-200397BTCP maleate is a potent DAT (dopamine transporter) inhibitor. BTCP maleate competitively inhibits the binding of PCP to PCP receptors in the rat cerebellum. CAS # 112726-66-6

2-Chloro-11-(4-methylpiperazino)dibenz[b,f]oxepin maleatesc-205920A high affinity dopamine D4 receptor ligand that is almost 40 times more potent than clozapine.

3-(3,4-Dimethylphenyl)-1-propyl-piperidine hydrochloridesc-202411Highly selective ligand for the D4 dopamine receptor. CAS # 219704-16-2

3-CPMTsc-203777Cocaine analog that binds with high affinity to the dopamine transporter (Ki = 30 nM) and blocks re-uptake of dopamine. However, it is a weak psychomotor stimulant and does not substitute for cocaine in addicted rats. CAS # 14008-79-8

3-Hydroxytyramine, Hydrochloridesc-2024173-Hydroxytyramine, Hydrochloride is a major catecholamine neurotransmitter derived from the amino acid tyrosine. CAS # 62-31-7

1
GBR 12935 dihydrochloridesc-203965GBR 12935 dihydrochloride inhibits DAT (dopamine transporter) (Ki = 21.5 nM) and SLC6A2 (norepinephrine transporter) (Ki = 225 nM). CAS # 67469-81-2

Halopemidesc-221704Halopemide is a dopamine inhibitor and a phospholipase D2 inhibitor. Halopemide may be used as a screen to identify inhibitors of human PLD2 using an in vitro biochemical assay. CAS # 59831-65-1

Mesulergine hydrochloridesc-361251Mesulergine hydrochloride is a D2-like dopamine receptor partial agonist and a SR-2A/SR-2C antagonist. CAS # 64795-35-3

3-Mercaptotyramine, Hydrochloridesc-206656A 3-Mercaptotyramine and the mercapto analog of dopamine which irreversibly inhibits the enzyme, catechol-O-methyltransferase by the formation of an SS bridge to a reactive mercapto group in the reactive site. CAS # 37736-93-9

PG 01037 dihydrochloridesc-361291PG 01037 dihydrochloride is a dopamine D3 receptor (D3DR) antagonist with a higher selectivity for D3DR over D2DR in vivo. CAS # 790658-27-4

Chlorpromazine, Hydrochloridesc-202537Chlorpromazine, Hydrochloride is an inhibitor of calmodulin-dependent stimulation of cyclic nucleotide phosphodiesterase (PDE), D2DR, α-adrenergic action, NOS1, and PLA2. CAS # 69-09-0

Indatraline hydrochloridesc-203605Indatraline hydrochloride is a strong monoamine uptake inhibitor which inhibits the transporters ST (serotonin/SERT), DAT (dopamine), and SLC6A2 (noradrenalin/NET). CAS # 86939-10-8

3'-Fluorobenzylspiperone maleatesc-361079 This compound has been found to be a highly selective and potent ligand for the D2 receptor. It displays a 2.5-fold greater affinity at D2 and a 12-fold lower affinity at 5-HT2 receptors compared with spiperone.

Trifluoperazine·2HCl (Stelazine)sc-201498Trifluoperazine is a phenothiazine compound with antiadrenergic and antidopaminergic effects. CAS # 440-17-5

4-Phenyl-1,2,3,4-tetrahydroisoquinoline hydrochloridesc-203476Inhibitor of release of dopamine induced by methamphetamine. CAS # 75626-12-9

3α-Bis-(4-fluorophenyl) methoxytropane hydrochloridesc-203778A potent inhibitor of dopamine uptake and transport (Ki = 11.8 nM).

6-Chloromelatoninsc-2034816-Chloromelatonin is a potent MEL-1 (melatonin receptor) agonist with comparable affinity to Melatonin itself. CAS # 63762-74-3

JHW 007 hydrochloridesc-362752 CAS # 202645-74-7

6-Hydroxydopamine hydrochloridesc-2034826-Hydroxydopamine hydrochloride is a selective catecholaminergic neurotoxin. CAS # 28094-15-7

6,7-ADTN·HBrsc-2003936,7-ADTN is a potent dopamine agonist that displays some alpha adrenergic activity as well. CAS # 73304-33-3

2
Paroxetine HClsc-201141Paroxetine HCl, a phenylpiperidine derivative, is a highly potent and selective ST (serotonin transporter/5-HT uptake) inhibitor. CAS # 78246-49-8

7-Hydroxy-DPAT·HBrsc-2004007-Hydroxy-DPAT·HBr is a selective D3DR agonist that is primarily found in neurons of the brain. CAS # 74938-11-7

3
A-77636 hydrochloride hydratesc-239151This is a potent, orally active D1 dopamine receptor agonist. CAS # 145307-34-2 (anhydrous)

7-Hydroxy-PIPAT maleatesc-3610887-Hydroxy-PIPAT maleate is a ligand with high selectivity and affinity for the D3DR receptor. CAS # 159559-71-4

A 68930 hydrochloridesc-203485A 68930 hydrochloride is a potent and selective D1DR(D1-like dopamine receptor) agonist. CAS # 130465-39-3

ABT 724 trihydrochloridesc-203489ABT 724 trihydrochloride is a selective D4DR (dopamine D4 receptor) partial agonist with an EC50=12.4nM. CAS # 70006-24-5

Fluspirilenesc-252832Fluspirilene is a dopamine inhibitor, a calcium channel protein inhibitor, and an antipsychotic. CAS # 1841-19-6

A 77636 hydrochloridesc-203486A 77636 hydrochloride is a selective and potent dopamine D1-like agonist stimulating the release of adenylate cyclase. CAS # 145307-34-2

3
ABT-418 hydrochloridesc-239177Neuronal nicotinic acetylcholine receptor agonist with anxiolytic and cognition enhancing activities. CAS # 147388-83-8

Amantadine Hydrochloridesc-217619NMDA-receptor antagonist. Antiviral antiparkinsonian. CAS # 665-66-7

Graminesc-255191 CAS # 87-52-5

B-HT 920sc-203523B-HT 920 is a dopamine D2 receptor agonist, SR-3 antagonist and α2-adrenoceptor agonist. It also displays antiparkinsonian activity. CAS # 36085-73-1

bis-(4-Methyl-1-homopiperazinylthiocarbonyl)disulfidesc-202502A dopamine β-hydroxylase inhibitor. CAS # 26087-98-9

AJ-76 HCLsc-200394AJ-76 HCL is a selective antagonist of dopamine autoreceptors, which displays a reduction in ventral firing rates of dopaminergic neurons. CAS # 85379-09-5

3
Bromocriptine mesylatesc-200395An agonist of the D2 and D3 dopamine receptors. Demonstrates ten-fold higher affinity at D2 over D3 in recombinant dopamine receptors. CAS # 22260-51-1

AMI-193sc-203509Selective 5-HT antagonist that binds to 5-HT2 sites as potently as spiperone but has lower affinity for 5-HT2C receptors. CAS # 510-74-7

Cabergolinesc-203864Cabergoline is a D2DR (D2-like receptor) agonist, shown to have a high affinity for serotonin receptors. CAS # 81409-90-7

Amisulpridesc-203510Amisulpride is a selective, potent D2DR and D3DR inhibitor. (Ki values are 2.8 and 3.2 nM respectively for human D2DR and D3DR and > 1000 nM for human D1DR, D4DR and D5DR.) CAS # 71675-85-9

Carmoxirole hydrochloridesc-203539Selective,peripherally acting D2-like agonist CAS # 98323-83-2

cis-8-Hydroxy-3-(n-propyl)-1,2,3a,4,5,9b-hexahydro-1H-benz[e]indole hydrobromidesc-300375D3 dopamine receptor agonist.

Clothiapinesc-200404Structurally analogous to quetiapine (sc-219681), clothiapine is an atypical antipsychotic of the dibenzothiazepine chemical class. CAS # 2058-52-8

Clozapinesc-200402Clozapine is a selective antagonist for D4- and D2-dopamine receptors with activity at several serotonin receptors. CAS # 5786-21-0

Cyclo(-Leu-Gly)sc-294123 CAS # 5845-67-0

Diclofensine Hydrochloridesc-207563A stimulant. Inhibits reuptake of dopamine and noradrenaline, is an effective antidepressant. Compound exhibits significant addictive properties. CAS # 34041-84-4

Dopamine-d4 Hydrochloridesc-218267Endogenous catecholamine with α and β-adrenergic activity. Cardiotonic antihypotensive. CAS # 203633-19-6

FAUC 73sc-300690Selective, nonaromatic, potent D3 dopamine receptor agonist.

Thioridazine·HClsc-201149Thioridazine·HCl is a calcium channel protein inhibitor as well as D2DR D4DR inhibitor. Its administration has been associated with hypotension. CAS # 130-61-0

Fenoldopam monohydrobromidesc-215032A selective dopamine agonist that is being considered for the parenteral treatment of systemic hypertension. In both an oral and parenteral form, this compound causes peripheral vasodilation by stimulating dopamine-1 adrenergic receptors. Intravenous fenoldopam may provide advantages over sodium nitroprusside because it can induce both a diuresis and natriuresis. It is not light sensitive, nor is it associated with cyanide toxicity. There is no evidence for rebound hypertension after discontinuation of fenoldopam infusion. CAS # 67287-54-1

CY 208-243sc-361163CY 208-243 is a centrally active D1DR agonist, selective over D2DR sites. CAS # 100999-26-6

GBR 12783 dihydrochloridesc-203587A very potent and selective inhibitor of dopamine uptake (IC50 for inhibition of [3H]-dopamine uptake in rat striatal synaptosomes is 1.8 nM). CAS # 67469-57-2

Domperidonesc-203032Domperidone is a selective inhibitor of the peripheral D2DR. The antidopaminergic effects of Domperidone have been correlated to antiemetic and gastroprokinetic action. CAS # 57808-66-9

GBR 13069 dihydrochloridesc-203966Potent dopamine uptake inhibitor. Systemically active post-administration in vivo. CAS # 77862-93-2

Eticlopride hydrochloridesc-203576Eticlopride hydrochloride is a selective inhibitor of D2DR and D3DR (Ki values are 0.50 and 0.16 nM respectively). Eticlopride is also an antipsychotic. CAS # 97612-24-3

Imipramine Hydrochloridesc-207753A tricyclic antidepressant. Inhibits the serotonin and norepinephrine transporters but has little effect on the dopamine transporter. CAS # 113-52-0

L-3,4-Dihydroxyphenylalanine methyl ester hydrochloridesc-250211A precursor to L-DOPA which crosses the blood-brain barrier; antiparkinsonian agent. CAS # 1421-65-4

Dobutamine Hydrochloridesc-203031Dobutamine Hydrochloride is a derivative of dopamine and has exhibited usage as a β1-AR adrenergic agonist. CAS # 49745-95-1

L-745,870 hydrochloridesc-300864This product is a selective D4 dopamine receptor antagonist.

Fenoldopam hydrochloridesc-279160Fenoldopam hydrochloride is a selective D1-like dopamine receptor partial agonist, but does not readily cross the blood-brain barrier. In addition to being a vasodilator, Fenoldopam hydrochloride is an α2-adrenoceptor antagonist in vitro. CAS # 67227-56-9

L-750,667 trihydrochloridesc-300865This product is a selective D4 dopamine receptor antagonist.

Lisuride maleatesc-361233Lisuride maleate is known to act as a dopamine receptor agonist and anti-Parkinson’s agent. CAS # 19875-60-6

N-[2-(4-(4-Chlorophenyl)piperazin-1-yl)ethyl]-3-methoxybenzamidesc-301260A selective and potent ligand for the D4 dopamine receptor.

N-Methyl-(R)-salsolinol hydrobromidesc-301368On dopaminergic neurons N-Methyl-(R)-salsolinol hydrobromide acts as an endogenous nerotoxin.

NGD 94-1sc-358837High affinity D4 receptor ligand and is selective over D1, D2, D3 and D5 receptors. CAS # 179333-18-7

GR 103691sc-361188GR 103691 is an effective and selective receptor antagonist of the D3DR. CAS # 162408-66-4

Bupropion HClsc-201121Bupropion HCl is a non-selective inhibitor of dopamine and SLC6A2 (Ki values are 1.4 μM for SLC6A2, 2.8 μM for dopamine, and 45 μM for serotonin). CAS # 31677-93-7

Haloperidol hydrochloridesc-203593Haloperidol hydrochloride is a dopamine inhibitor selective for D2DR. Haloperidol is a selective NMDA inhibitor and also an inhibitor of NOS1 (nNOS) (Ki = 31 μM). CAS # 52-86-8

NPEC-caged-dopaminesc-359018NPEC ((N)-1-(2-nitrophenyl)ethyl) is a caged version of dopamine. CAS # 1257326-23-0

OSU 6162 hydrochloridesc-204825Dopamine stabilizer that lacks high in vitro affinity for various neuroreceptors. In vivo, shows high D2 receptor occupancy and is highly active on dopamine synthesis and turnover. Induces stabilizing effects on psychomotor function in behavioral tests without inducing hypolocomotion or catalepsy. CAS # 156907-84-5

Palmatine Chloride Hydratesc-205788A protoberberine alkaloid that is isolated from medicinal herbs like Coptis chinensis Franch. Sedative effect of palmatine is related to its ability to inhibit dopamine generation. It also acts as a selective topoisomerase I and II position and as vasodilator that effectively reduces Ca2+ concentration. CAS # 171869-95-7

L-741,742 hydrochloridesc-361227L-741,742 hydrochloride an effective and selective D4DR antagonist. CAS # 156337-32-5

PD 168077 maleatesc-204165D4 dopamine agonist. >400-fold selectivity over D2 with >300-fold selectivity v.s. D3 subtypes. Generates synaptic translocation of CaMK II to postsynaptic sites in cultured prefrontal cortical neurons. Shown to be centrally active in vivo. CAS # 190383-31-4

Pergolide Mesylatesc-212538An antiparkinsonian agent. A dopaminergic agonist that also decrease plasma prolactin concentrations. CAS # 66104-23-2

LE 300sc-203622LE 300 is a potent and selective D1DR antagonist with Ki values of 0.08-1.9 nM and 6-45 nM for D1DR and D2DR receptors respectively. CAS # 274694-98-3

Piribedil dihydrochloridesc-204198A dopamine agonist reported to have selectivity for D3 subtype receptors with moderate to non-significant affinity for D2 and D1 receptors. CAS # 78213-63-5

Piribedil maleate saltsc-301552A dopamine agonist reported to have selectivity for D3 subtype receptors with moderate to non-significant affinity for D2 and D1 receptors.

Levodopasc-205372Natural form of DOPA used in the treatment of Parkinson's disease. Immediate precursor of dopamine and product of tyrosine hydroxylase. CAS # 59-92-7

PNU 96415Esc-204852PNU 96415E displays highest affinity for dopamine D4 and SR-2A and relatively weak affinity at D2 receptors. CAS # 170856-41-4

Loxapine, Succinatesc-211754Loxapine Succinate is a D2DR and D4DR inhibitor and serotonergic receptor antagonist. It is also a dibenzoxazepine anti-psychotic agent. CAS # 27833-64-3

Quinelorane dihydrochloridesc-255455D2 dopamine receptor agonist; 2-aminopyridine analog of quinpirole. CAS # 97548-97-5

Mesoridazine besylatesc-201133Mesoridazine besylate is a phenothiazine dopamine receptor anatagonist. Mesoridazine is described to demonstrate inhibition for D2DR and D4DR. CAS # 32672-69-8

4
R (+)-Eticlopride hydrochloridesc-296183The inactive enantiomer of the dopamine D2 antagonist S(-)-Eticlopride CAS # 84226-12-0

R(+)-6-Bromo-APB hydrobromidesc-301656This product is the more potent D1 Dopamine receptor agonist enantiomer. CAS # 139689-19-3

rac-trans-Sertralinesc-212762Used in the treatment of menopause and mood, anxiety, and cognitive disorders CAS # 79836-45-6

N-Allyl-(±)-SKF-38393 hydrobromidesc-224127N-Allyl-(±)-SKF-38393 hydrobromide is a selective dopamine D1-like receptor partial agonist. CAS # 300561-58-4

RBI 257 maleate saltsc-311521A high affinity D4 dopamine receptor ligand.

Nafadotridesc-361269Nafadotride is a highly potent and competitive D3DR antagonist, with efficacy against D2DR and D4DR as well. CAS # 149649-22-9

Nemonapridesc-204123Nemonapride is a highly selective D2DR antagonist and potent SR-1A agonist. CAS # 75272-39-8

3
Ro 10-5824 dihydrochloridesc-204886Selective dopamine D4 receptor partial agonist that binds with high affinity (Ki = 5.2 nM). Displays 250-fold selectivity over D3 receptors and > 1000-fold selectivity over D2, D1 and D5 receptors. CAS # 189744-46-5

NGB 2904sc-204127NGB 2904 is a highly-selective D3DR antagonist, with antagonistic effects against quinpirole-stimulated mitogenesis. CAS # 189060-98-8

Ropinirole Hydrochloridesc-205843A dopamine receptor agonist commonly used to treat restless legs sydrome and Parkinson disease. CAS # 91374-20-8

S(-)-DS 121 hydrochloridesc-311528Dopamine autoreceptor antagonist with selectivity for the D3 dopamine receptor.

Paliperidonesc-204828Paliperidone is a serotonin (5-HT2) receptor antagonist and D2DR inhibitor. CAS # 144598-75-4

SKF-75670 hydrobromidesc-301809Atypical D1 dopamine receptor agonist. Displays antagonist activity in vitro and agonist activity in vivo. CAS # 62717-63-9

SKF-89145 hydrobromidesc-301811D1 dopamine receptor agonist.

(+)-PD 128907 HYDROCHLORIDEsc-204162(+)-PD 128907 hydrochloride is a potent D3DR (D3 dopamine receptor) agonist. CAS # 300576-59-4

ST-148sc-301838ST-148 is a D2 dopamine receptor antagonist. Compared to haloperidol and (S)-nafodotride, ST-148 exhibits improved selectivity for hD2L receptors. ST-148 has a pKi = 7.85 at hD2L receptors.

Tetrabenazinesc-204338Potent inhibitor of vesicular monoamine uptake; depletes stores of serotonin, dopamine and noradrenalin. CAS # 58-46-8

PD 168568 dihydrochloridesc-204167Selective D4 antagonist. Reverses amphetamine-stimulated movement in vivo and is orally active. CAS # 210688-56-5

U-101958 Maleatesc-222396Selective D4 dopamine receptor antagonist.

U-99194A maleatesc-202373D3 dopamine receptor agonist. CAS # 153570-58-2

PG01037 dihydrochloride hydratesc-364578PG01037 dihydrochloride is a selective dopamine D3 receptor (D3DR) antagonist. has a selectivity ratio for D2DR/D3DR of 867 and a D4DR/D3DR selectivity ratio of 13,000. CAS # 675599-62-9

Pimozidesc-203662Pimozide is a D2DR inhibitor and antipsychotic which binds with very high affinity and inhibits SR-7 (Ki = 0.5 nM). Pimozide is a calcium channel protein inhibitor. CAS # 2062-78-4

(+)-UH 232 maleatesc-203717D2-likeautoreceptor antagonist and D3 partial agonist. CAS # 95999-12-5

PNU 177864 hydrochloridesc-204205PNU 177864 hydrochloride is a highly selective dopamine D3 receptor (D3DR) antagonist. CAS # 250266-51-4

Quetiapine Fumaratesc-219681Quetiapine fumarate is an inhibitor of D2DR and SR-2A. CAS # 111974-72-2

Dihydroergocristine mesylatesc-201117Dihydroergocristine mesylate demonstrates antagonism at serotonin receptors (SR) and partial agonism/antagonism of dopaminergic and adrenergic receptors. CAS # 24730-10-7

2
(R)-(-)-Apomorphine hydrochloridesc-203675(R)-(-)-Apomorphine hydrochloride is a prototypical dopamine agonist that has been shown to produce biphasic effects on locomotor acitivity, displays antiparkinsonian, and neuroprotective actions. CAS # 314-19-2

Raclopridesc-204229Raclopride is a potent and selective D2DR/D3DR antagonist. CAS # 84225-95-6

Remoxipride Hydrochloridesc-200410Remoxipride Hydrochloride, a substituted benzamide, is an atypical antipsychotic agent, as well as, a selective and potent D2DR antagonist. CAS # 73220-03-8

Roxindole hydrochloridesc-203685Selective and potent presynaptic D-2 dopamine autoreceptor agonist. Inhibits serotonin (5-HT) uptake. CAS # 112192-04-8

(RS)-(±)-Sulpiridesc-205494(RS)-(±)-Sulpiride is a selective postsynaptic D2DR inhibitor. CAS # 15676-16-1

(S)-(-)-Sulpiridesc-258111(S)-(-)-Sulpiride is a D2DR inhibitor. CAS # 23672-07-3

SB 277011A dihydrochloridesc-364608SB 277011A is a selective and potent D3DR antagonist CAS # 1226917-67-4

SCH 23390sc-200408A selective and highly effective dopamine D1 (D1DR) and D5 (D5DR) antagonist. In vitro studies reveal its ability to bind to the serotonin receptors 5-HT2 and 5-HT1C. CAS # 125941-87-9

SCH 39166 hydrobromidesc-204270SCH 39166 hydrobromide is a high affinity dopamine D1DR/D5DR antagonist.

SKF 38393 HClsc-203264SKF 38393 HCl is a selective dopamine D1DR agonist that seems to be correlated to induced desynchronization of electroencephalographic activity in rats. CAS # 81633-77-4

SKF 81297 hydrobromidesc-204283SKF 81297 hydrobromide is a full D1-like dopamine receptor agonist used in the study of the effects of d-amphetamine. CAS # 71636-61-8

SKF 83566 hydrobromidesc-361360SKF 83566 hydrobromide has been reported to be a selective and potent D1-like dopamine receptor antagonist. As well as an antagonist at the vascular 5-HT2 receptor. CAS # 108179-91-5

SKF 83822 hydrobromidesc-204284SKF 83822 hydrobromide is a high affinity, selective dopamine D1-like agonist. SKF 83822 hydrobromide also stimulates adenylyl cyclase. CAS # 74115-08-5

SKF 83959sc-204285SKF 83959 is a D1-like partial agonist. CAS # 80751-85-5

Sonepiprazolesc-364623Sonepiprazole is a selective and potent dopamine D4 antagonist with a Ki value of 10 nM. It shows low efficacy towards other monoamine receptors. CAS # 170858-33-0

U 99194 maleatesc-204365U 99194 maleate is a potent and selective D3DR antagonist with a Ki value of 160 nM. CAS # 83598-46-3

Zotepinesc-360895Zotepine is a SR-2A and D2DR inhibitor (Ki values are 0.69 and 2.3 nM respectively). Zotepine is also a potent histamine H1 receptor antagonist (IC50 = 8.0 nM). CAS # 26615-21-4

Melperone hydrochloridesc-204074Melperone hydrochloride is an atypical neuroleptic; 5-HT2A receptor antagonist and D2DR inhibitor. CAS # 1622-79-3

Memantine hydrochloridesc-203628An antagonist at the NMDA receptor, binding to the ion channel site. Used in the treatment of Parkinsonism. CAS # 41100-52-1

(-)-Butaclamol hydrochloridesc-252526(-)-Butaclamol hydrochloride is a dopamine inhibitor. The (-) form is the less active enantiomer. CAS # 55528-08-0

Olanzapinesc-212469Olanzapine is a Serotonin 5-HT2A and D2DR inhibitor with anti-cholinergic activity. CAS # 132539-06-1

FAUC 213sc-252820A highly selective D4 dopamine receptor full antagonist. CAS # 337972-47-1

(+)-Bulbocapnine hydrochloridesc-257199(+)-Bulbocapnine hydrochloride is a dopamine inhibitor that is also the water-soluble form of (+)-Bulbocapnine. CAS # 632-47-3

Octoclothepin maleate saltsc-253215Octoclothepin maleate salt is an SR-2A inhibitor as well as a D2DR inhibitor. CAS # 4789-68-8

(-)-Quinpirole hydrochloridesc-253339(-)-Quinpirole • HCl is an agonist of D2-like dopamine receptors. Stimulation of D2 receptors demonstrates a neuroprotective effect against glutamate excitotoxicity and oxidative damage. CAS # 85798-08-9

R(+)-7-Hydroxy-DPAT hydrobromidesc-253356R(+)-7-Hydroxy-DPAT hydrobromide is an active enantiomer of (±)-7-hydroxy-DPAT and acts as a selective D3DR dopamine receptor agonist. CAS # 82730-72-1

S(+)-Propylnorapomorphine hydrochloridesc-253463S(+)-Propylnorapomorphine hydrochloride is a limbic-selective dopamine antagonist. CAS # 79703-31-4

(S)-(+)-Apomorphine hydrochloride hydratesc-253505(S)-(+)-Apomorphine hydrochloride hydrate is a dopamine inhibitor. (S)-(+)-Apomorphine is inactive as an agonist. CAS # 41035-30-7 (anhydrous)

Trifluperidol hydrochloridesc-253757Trifluperidol hydrochloride is a dopamine inhibitor and antipsychotic. CAS # 2062-77-3

Acepromazine Maleatesc-207247Acepromazine maleate is thought to be a dopamine inhibitor in the brain, and inhibit ABCG2 transport protein whose overexpression in tumors is associated with drug resistance. CAS # 3598-37-6

Bicifadine Hydrochloridesc-210918Bicifadine Hydrochloride is a potent inhibitor of SLC6A2 (noradrenalin transporter) (IC50 = 55 nM). Bicifadine also displays inhibition of the 5-HT and dopamine transporters. CAS # 66504-75-4

cis-(Z)-Flupentixol Dihydrochloridesc-211102cis-(Z)-Flupentixol Dihydrochloride is the hydrochloride salt preparation of cis-(Z)-Flupentixol, a thioxanthene-derived nonselective dopamine inhibitor. CAS # 51529-01-2

Rotigotine Hydrochloridesc-212790Rotigotine Hydrochloride is a Dopamine D2DR and D3DR agonist that shows a significant affinity for 5-HT1A and adrenergic α2B receptors. Rotigotine Hydrochloride shows antiparkinsonian activity. CAS # 125572-93-2

(S)-Pramipexole Dihydrochloridesc-212895(S)-Pramipexole Dihydrochloride is a D2DR and D3DR agonist. CAS # 104632-25-9

GSK 789472 hydrochloridesc-358242GSK 789472 hydrochloride is a specific D3DR antagonist, D2DR partial agonist, and D4DR selectivity in vitro.