81 Results for "

amphetamine

" in MedChemExpress (MCE) Product Catalog:
Products (81)

81 Results for "amphetamine" in MCE Product Catalog:

Cat. No.: HY-W704752
CAS No.: 2469242-68-8
Z-Doxepin-d3 hydrochloride is the deuterium labeled 7-Hydroxychlorpromazine hydrochloride (HY-W704749). 7-Hydroxychlorpromazine hydrochloride is the active metabolite of Chlorpromazine (HY-12708). 7-Hydroxychlorpromazine hydrochloride can increase prolactin levels in rats. 7-Hydroxychlorpromazine hydrochloride can increase dopamine turnover and has a sedative effect. In addition, 7-Hydroxychlorpromazine hydrochloride can effectively inhibit amphetamine-induced stereotyped behavior in rats and is used in the study of psychosis .
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Cat. No.: HY-173032
Target:  

mGluR

Research Areas:  

Neurological Disease

VU6033685 is the orally active positive allosteric modulator (PAM) for mGlu1 that positively modulates human mGlu1 and human mGlu5 with EC50 of 39 nM and 3960 nM. VU6033685 also inhibits CYP1A2, CYP2C9 and CYP2D6 with IC50 of 26, 22.3 and 23.8 μM, respectively. VU6033685 reverses amphetamine-induced rats hyperlocomotion, protects rats from MK-801 (HY-15084B)-induced cognitive impairment. VU6033685 exhibits good pharmacokinetics characteristics in rats with an oral bioavailability of 42.8% .
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Cat. No.: HY-111136
CAS No.: 916898-61-8
BL-1020 mesylate is the mesylate salt form of BL-1020. BL-1020 mesylate is an antipsychotic agent. BL-1020 mesylate is inhibitor for dopamine receptor and serotonin receptor (5-HT receptor), with Ki of 0.066, 0.062 and 0.21 nM, for D2L, D2S and 5-HT2A receptors, respectively. BL-1020 mesylate is agonist for GABAA receptor with Ki of 3.74 μM, and enhances the GABA release. BL-1020 mesylate exhibits high affinity with histamine receptor (Ki is 0.47 nM). BL-1020 mesylate reduces Amphetamine-induced hyperactivity, with lower catalepsy and sedation. BL-1020 mesylate is blood-brain barrier penetrate .
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Cat. No.: HY-B1751S1
Quinidine- 13C, d2 hydrochloride is the 13C, d2 labeled Quinidine hydrochloride (HY-W115674). Quinidine hydrochloride is an orally active antiarrhythmic agent. Quinidine hydrochloride reduces the expression level of P-gp, inhibits P-gp-mediated efflux, increases the intracellular accumulation of P-gp substrates, induces PARP cleavage and Caspase-3 activation, and elevates the proportion of Apoptotic cells at the sub-G1 phase. Quinidine hydrochloride exerts sustained block and open-channel block effects on IK(f). Quinidine hydrochloride alters the urinary metabolic ratio of Amphetamine, modulates the Pentylenetetrazol-induced seizure threshold, and regulates the anticonvulsant effect of Dextromethorphan. Quinidine hydrochloride can be used in studies related to uterine sarcoma and seizures .
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Cat. No.: HY-W748758
Synonyms: NSC 108165-d8; Navan-d8; Navane-d8
(Z)-Thiothixene-d8 (NSC 108165-d8; Navan-d8; Navane-d8) is the deuterium labeled Thiothixene (HY-A0139). Thiothixene is a typical antipsychotic. It selectively binds to dopamine D2 over D1, D3, and D4 receptors (Kis=0.417, 338, 186.2, and 363.1 nM, respectively). Thiothixene also binds to various serotonin (5-HT), histamine H1, α1- and α2-adrenergic, muscarinic acetylcholine, and sigma receptors (Kis=15-5,754 nM) as well as the dopamine, norepinephrine, and serotonin transporters (Kis=3.16-30 μM). In vivo, thiothixene reduces spontaneous and amphetamine-induced locomotor activity in rats. It enhances latent inhibition, as measured by a decreased lick latency in response to light and foot shock stimuli, which is a measure of selective attention in rats.3 Thiothixene also increases competitive behavior in submissive mice, indicating antidepressant-like behavior.
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Cat. No.: HY-P74351
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: CARTPT; Cocaine- And amphetamine-Regulated Transcript Protein; CART Prepropeptide; Cocaine And amphetamine Regulated Transcript; CART
Species:  
Human
Source:  
HEK293
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Cat. No.: HY-P74350
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: CARTPT; Cocaine- And amphetamine-Regulated Transcript Protein; CART Prepropeptide; Cocaine And amphetamine Regulated Transcript; CART
Species:  
Human
Source:  
HEK293
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Cat. No.: HY-170735
CAS No.: 54779-54-3
Target:  

Drug Derivative

Research Areas:  

Neurological Disease

4-Chloroethamphetamine hydrochloride is an amphetamine.
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Cat. No.: HY-170732
CAS No.: 5556-75-2
Target:  

Drug Derivative

Research Areas:  

Neurological Disease

2,3,6-Trimethoxyamphetamine hydrochloride is an amphetamine .
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Cat. No.: HY-172077
CAS No.: 2749298-47-1
Target:  

Drug Derivative

Research Areas:  

Neurological Disease

4-MA-NBOMe hydrochloride is structurally categorized as an amphetamine.
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Cat. No.: HY-168832
CAS No.: 2980-07-6
Target:  

Drug Derivative

Research Areas:  

Neurological Disease

N-Benzyl-3,4-DMA hydrochloride is an amphetamine.
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Cat. No.: HY-170742
CAS No.: 70932-19-3
Synonyms: 3,4-Dimethoxydimethylamphetamine hydrochloride
Target:  

Drug Derivative

Research Areas:  

Neurological Disease

N,N-Dimethyl-3,4-DMA (3,4-Dimethoxydimethylamphetamine) hydrochloride is an amphetamine.
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Cat. No.: HY-W706595
CAS No.: 29805-52-5
Target:  

Drug Derivative

Research Areas:  

Neurological Disease

N,α-Diethylphenethylamine hydrochloride is an N-substituted amphetamine with an ethyl group attached to the amine. N,α-Diethylphenethylamine hydrochloride is an anorectic.
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Cat. No.: HY-170741
CAS No.: 70932-27-3
Synonyms: N-Ethyl-3,4-dimethoxyamphetamine hydrochloride
Target:  

Drug Derivative

Research Areas:  

Neurological Disease

N-Ethyl-3,4-DMA (N-Ethyl-3,4-dimethoxyamphetamine) hydrochloride is an amphetamine.
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Cat. No.: HY-105760
CAS No.: 40594-09-0
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

Flucindole is an orally active dopamine receptor inhibitor (IC50 = 240 nM) that also exhibits affinity for S2 receptors. Flucindole inhibits amphetamine-induced stereotyped behaviors in rats, and increases the levels of dopamine metabolites in the striatum of rats and mice. Flucindole can be used in the research of psychosis .
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Cat. No.: HY-137935
CAS No.: 42021-34-1
Synonyms: Centbutindole
Research Areas:  

Neurological Disease

Biriperone is a D1, D2, and 5-HT2A receptor antagonist with pKi values of 6.372, 7.88 and 7.619. Biriperone blocks amphetamine-induced hyperactivity and stereotypy in rodents. Biriperone blocks secondary conditioned avoidance responses in rodents. Biriperone can be used for the research of schizophrenia .
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Cat. No.: HY-182631
CAS No.: 1086378-73-5
Target:  

iGluR

Research Areas:  

Neurological Disease

CX1763 is an AMPAR allosteric modulator. CX1763 allosterically potentiates glutamate-evoked currents, accelerates channel opening, and increases the surface levels of AMPAR containing Glur2 (R). CX1763 enhances synaptic transmission in the rat hippocampus. CX1763 improves attention in rats and attenuates amphetamine-induced hyperactivity in mice. CX1763 can be used in studies related to attention deficit hyperactivity disorder and opioid-induced respiratory depression .
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Cat. No.: HY-114833
CAS No.: 27591-01-1
Synonyms: (Rac)-Bunolol; dl-Bunolol
Bunolol ((Rac)-Bunolol) is a β-adrenergic receptor blocker. Bunolol antagonizes the β-receptor agonist activity induced by Isoproterenol (HY-B0468) and Dichloroisoproterenol. Bunolol reduces the heart rate and mean blood pressure of anesthetized dogs. Bunolol decreases spontaneous motor activity and Amphetamine-induced hyperactivity in rats, potentiates Pentobarbital-induced hypnosis in mice, and protects rats from extensor tonic convulsions induced by maximal electroshock .
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Cat. No.: HY-100822R
CAS No.: 123931-04-4
Synonyms: (+)-HA-966 (Standard)
Research Areas:  

Neurological Disease

(R)-(+)-HA-966 (Standard) is the analytical standard of (R)-(+)-HA-966 (HY-100822). This product is intended for research and analytical applications. (R)-(+)-HA-966 ((+)-HA-966) is a partial agonist/antagonist of glycine site of the N-methyl-D-aspartate (NMDA) receptor complex. (R)-(+)-HA-966 selectively blocks the activation of the mesolimbic dopamine system by amphetamine . (R)-(+)-HA-966 can cross the blood-brain barrier and has the potential for neuropathic and acute pain .
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Cat. No.: HY-181559S
Synonyms: AG06827
Target:  

mAChR

Research Areas:  

Neurological Disease

VU6025733 (AG06827) is a highly selective, orally active and blood-brain barrier-penetrant positive allosteric modulator of the muscarinic acetylcholine receptor subtype M4 (M4 mAChR). VU6025733 exerts a potentiating effect on acetylcholine-induced receptor activation with an EC50 of 23 nM for hM4 and 55 nM for rM4. VU6025733 shows high selectivity over other muscarinic acetylcholine receptor subtypes, dose-dependently reduces amphetamine-induced hyperlocomotion in rats. VU6025733 is applicable to the research of schizophrenia, Parkinson's disease, and Alzheimer's disease .
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