15 Results for "

non-sedating

" in MedChemExpress (MCE) Product Catalog:
Products (15)

15 Results for "non-sedating" in MCE Product Catalog:

Cat. No.: HY-19505
CAS No.: 425377-76-0
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

TPA-023B is a high-affinity and orally active GABAA receptor α2/α3 subtype (Kis of 0.73 nM/2 nM) partial agonist and a α1 subtype (Ki of 1.8 nM) antagonist. TPA-023B has non-sedating anxiolytic-like properties .
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Cat. No.: HY-101869
CAS No.: 233275-76-8
Purity:  99.69%
Synonyms: MRK-409
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

MK0343 (MRK-409) is an orally bioavailable GABAA receptor subtype-selective partial agonist. MK0343 is a non-sedating anxiolytic .
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Cat. No.: HY-119832B
Purity:  99.72%
Synonyms: (S)-EGIS-2062 free acid; (S)-EGYT-2062 free acid
Target:  

Histamine Receptor

Research Areas:  

Inflammation/Immunology

(S)-Setastine ((S)-EGIS-2062 free acid) is a non-sedating, highly potent antagonist of H1 receptor-mediated responses. (S)-Setastine has a long-lasting antihistamine effect and good oral efficacy. (S)-Setastine can be used in the research of allergic diseases .
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Cat. No.: HY-B0539S3
CAS No.: 1020719-34-9
Synonyms: Sch34117-d5
Desloratadine-d5 is deuterium labeled Desloratadine. Desloratadine (Sch34117) is the orally active major metabolite of the nonsedating H1-antihistamine Loratadine. Desloratadine is a selective H1-receptor antagonist that has anti-allergic and anti-inflammatory activities .
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Cat. No.: HY-101869R
CAS No.: 233275-76-8
Synonyms: MRK-409 (Standard)
Research Areas:  

Neurological Disease

MK-0343 (Standard) is the analytical standard of MK-0343. This product is intended for research and analytical applications. MK0343 (MRK-409) is an orally bioavailable GABAA receptor subtype-selective partial agonist. MK0343 is a non-sedating anxiolytic .
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Cat. No.: HY-123525
CAS No.: 550310-04-8
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

COR628 is a positive allosteric modulator of GABA(B) receptors with the activity of enhancing GABA-induced GTPγS stimulation. COR628 showed significant activity in in vitro studies but did not exhibit endogenous agonist activity. COR628 has shown efficacy in experiments in mice by enhancing the sedation/hypnosis induced by baclofen, shortening the onset time and extending the duration of loss of righting reflex when combined with non-sedating doses of baclofen . The cytotoxic effect of COR628 is comparable to or higher than that of GS39783 or BHF177 in concentration .
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Cat. No.: HY-118910
CAS No.: 119810-68-3
Target:  

Histamine Receptor

Research Areas:  

Inflammation/Immunology

AHR-14310C is a potent, long-acting, nonsedating H1-antihistamine that prevents antigen-induced mucus formation in sensitive rats .
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Cat. No.: HY-B0539S1
CAS No.: 1795024-82-6
Synonyms: Sch34117-d9
Desloratadine-d9 is the deuterium labeled Desloratadine. Desloratadine (Sch34117) is the orally active major metabolite of the nonsedating H1-antihistamine Loratadine. Desloratadine is a selective H1-receptor antagonist that has anti-allergic and anti-inflammatory activities .
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Cat. No.: HY-B0539S
CAS No.: 381727-29-3
Synonyms: Sch34117-d4
Desloratadine-d4 is the deuterium labeled Desloratadine. Desloratadine (Sch34117) is the orally active major metabolite of the nonsedating H1-antihistamine Loratadine. Desloratadine is a selective H1-receptor antagonist that has anti-allergic and anti-inflammatory activities[1][2].
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Cat. No.: HY-B0539R
CAS No.: 100643-71-8
Synonyms: Sch34117 (Standard)
Desloratadine (Standard) is the analytical standard of Desloratadine. This product is intended for research and analytical applications. Desloratadine (Sch34117) is the orally active major metabolite of the nonsedating H1-antihistamine Loratadine. Desloratadine is a selective H1-receptor antagonist that has anti-allergic and anti-inflammatory activities .
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Cat. No.: HY-B0539S4
Synonyms: Sch34117-d4 hydrobromide
Desloratadine-d4 hydrobromide is deuterated labeled Desloratadine (HY-B0539). Desloratadine (Sch34117) is the orally active major metabolite of the nonsedating H1-antihistamine Loratadine. Desloratadine is a selective H1-receptor antagonist that has anti-allergic and anti-inflammatory activities .
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Cat. No.: HY-B0539S2
CAS No.: 2713301-38-1
Desloratadine-3,3,5,5-d4 is the deuterium labeled Desloratadine. Desloratadine (Sch34117) is the orally active major metabolite of the nonsedating H1-antihistamine Loratadine. Desloratadine is a selective H1-receptor antagonist that has anti-allergic and anti-inflammatory activities[1][2].
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Cat. No.: HY-14939A
CAS No.: 279253-83-7
Target:  

Histamine Receptor

Research Areas:  

Inflammation/Immunology

Vapitadine hydrochloride (Compound 3a) is a selective, orally active and nonsedating antihistamine agent, which exhibits a good binding affinity with human cloned histamine H1 receptor with a Ki of 19 nM. Vapitadine hydrochloride decreases the histamine-induced lethality (ED50 is 0.056-1.2 mg/kg), antagonizes the cutaneous reactions to histamine (ED50 is 0.51-1.4 mg/kg) in rats .
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Cat. No.: HY-W665882
CAS No.: 34580-20-6
Norketotifen is the active metabolite of Ketotifen (HY-B0157). Norketotifen exhibits skin anti-inflammatory activity, anti-malarial activity, and antipruritic activity against non-histamine-mediated dog itching in mice. Norketotifen effectively inhibits TNF-α release without causing any sedative side effects. Norketotifen can be used for research on non-sedating anti-inflammatory agents .
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Cat. No.: HY-182548
CAS No.: 165383-52-8
BTS 72664 is a broad-spectrum, non-sedating, orally effective anticonvulsant. Its anticonvulsant effect mainly arises from enhancing GABAA receptor (GABAA receptor)-mediated chloride channel currents, while it exerts weak blocking effects on Na + channels (Ki = 350 μM) and NMDA receptors (NMDA receptor) (IC50 = 43 μM). BTS 72664 prevents the elevation of extracellular glutamate, glycine and serine concentrations in neurons, reduces cerebral infarct size, promotes functional recovery, prevents multiple types of epileptic seizures, and has low sedative potential. BTS 72664 can be used for the research of epilepsy, stroke and migraine .
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