Dopamine Receptor

Dopamine Receptor

In the central nervous system (CNS) of vertebrates, dopamine receptors are a class of G protein-coupled receptors that are widely distributed. The main endogenous ligand for dopamine receptors is the neurotransmitter dopamine. Numerous neurological functions, including motivation, pleasure, cognition, memory, learning, and fine motor control, as well as the modulation of neuroendocrine signaling, are associated with dopamine receptors.Numerous neuropsychiatric disorders have abnormal dopamine receptor signaling and dopaminergic nerve function at their core. Dopamine receptors are therefore typical neurologic drug targets; psychostimulants are typically indirect agonists of dopamine receptors, whereas antipsychotics are frequently dopamine receptor antagonists. Dopamine receptors come in at least five different subtypes: D1, D2, D3, D4, and D5. The D2, D3, and D4 dopamine receptors are members of the D2-like family, whereas the D1 and D5 receptors belong to the D1-like family.

Dopamine Receptor related products

Structure Cat No. Product Name CAS No. Product Description
V15137 Spiperone 749-02-0 Spiperone (E-525; R-5147; Spiroperidol) is a novel and potent antipsychotic agent acting as adopamine D2, serotonin 5-HT1A, and serotonin 5-HT2A antagonist with the potential for neurology diseases.
V15138 Spiperone HCl 2022-29-9 Spiperone HCl (NSC-170983; E-525; R-5147; Spiroperidol) is a novel and potent antipsychotic agent acting as a dopamine D2, serotonin 5-HT1A, and serotonin 5-HT2A antagonist with the potential for neurology diseases.
V15535 Sumanirole maleate 179386-44-8 Sumanirole maleate (U-95666E; PNU-95666), the maleate salt of Sumanirole, is a first-in-class and highly selective D2 receptor full agonist (ED50 = ~46 nM) with antiparkinsonian effects.
V15792 Tavapadon (PF6649751; CVL751) 1643489-24-0 Tavapadon (PF-6649751; CVL-751) is a partial dopamine receptor agonist with the potential to be used in the treatment of Parkinsons disease and Alzheimers.
V1247 Tetracaine HCl 136-47-0 Tetracaine HCl (also called Amethocalne; Butylocaine; Curtacain; Decicain; Gingicain; PantocaineM; Intercaine; Leocaine; Menonasal; Niphanoid), thehydrochloride salt form of tetracaine, is a local anaesthetic and a channel function allosteric inhibitor.
V30298 Tetrahydroberberine 522-97-4 Tetrahydroberberine is a natural isoquinoline alkaloid extractedfrom corydalis tuber with micromolar affinity for dopamine D(2) (pK(i) = 6.08) and 5-HT(1A) (pK(i) = 5.38) receptors but moderate to no affinity for other relevant serotonin receptors (5-HT(1B), 5-HT(1D), 5-HT(3), and 5-HT(4); pK(i) < 5.00).
V60107 Tetrahydropalmatine hydrochloride 6024-85-7 Tetrahydropalmatine (also known as DL-Tetrahydropalmatine) hydrochloride has analgesic properties. Tetrahydropalmatine hydrochloride prevents a rat epileptic seizure by blocking the release of dopamine from amygdaloid.
V71735 Trazpiroben (TAK-906) 1352993-39-5 Trazpiroben (Taku-906) is a dopamine D2/D3 receptor blocker (antagonist) indicated for the study of chronic moderate to severe gastroparesis.
V71781 Trimethobenzamide (Ro 2-9578 free base) 138-56-7 Trimethobenzamide (Ro 2-9578 free base) is a dopamine D2 receptor antagonist (blocker) that is used as an antiemetic to prevent nausea and vomiting.
V2067 Trimethobenzamide HCl (Ro 2-9578) 554-92-7 rimethobenzamide (also known as Ro 2-9578; trade names Tebamide, Tigan), a blocker of the D2 receptor, is a potent antiemetic that is used to prevent nausea and vomiting.
V71726 UCM-1306 (2-(Fluoromethoxy)-4'-(S-methylsulfonimidoyl)-1,1'-biphenyl) 2258608-78-3 UCM-1306 is an orally bioavailable allosteric modulator (PAM) of the human dopamine D1 receptor.
V71740 Vanicoside E 208707-91-9 Vanicoside E is an antioxidant and anticancer agent.
V71207 Zicronapine fumarate (Lu 31-130 fumarate) 170381-17-6 Zicronapine (Lu 31-130) fumarate is an antipsychotic drug with strong precognitive effects in animal models and may be used to treat many neurological and psychiatric disorders.
V71782 Zuclopenthixol-d4 succinate 1246833-97-5 Zuclopenthixol-d4 (succinate) is the deuterium labelled form of Zuclopenthixol.
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