16 Results for "

Short-duration

" in MedChemExpress (MCE) Product Catalog:
Products (16)

16 Results for "Short-duration" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-B0546
CAS No.: 59-46-1
Procaine is a DNA-demethylating agent. Procaine acts through multiple targets and has a slow onset and a short duration of action .
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2
2 Cited Publications
Cat. No.: HY-B0546A
CAS No.: 51-05-8
Procaine hydrochloride is a DNA-demethylating agent. Procaine hydrochloride acts through multiple targets and has a slow onset and a short duration of action .
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Cat. No.: HY-B1700A
CAS No.: 106861-44-3
Target:  

nAChR

Research Areas:  

Neurological Disease

Mivacurium dichloride is a benzylisoquinoline derivative and is a short-acting non-depolarizing neuromuscular blocking agent and skeletal muscle relaxant. Mivacurium dichloride couples with the nAChR to reduce or inhibit the depolarizing effect of acetylcholine on the terminal disc of the muscle cell .
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Cat. No.: HY-105656
CAS No.: 6000-74-4
Purity:  99.11%
Synonyms: Hydrocortisone 21-phosphate sodium; Cortisol 21-phosphate sodium
Target:  

Phosphatase

Research Areas:  

Infection

Hydrocortisone phosphate sodium is a soft steroid with low anti-inflammatory properties and a short duration of action. Hydrocortisone phosphate sodium can be used for the research for several ocular conditions and gastric ulcers .
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Cat. No.: HY-B0546AR
CAS No.: 51-05-8
Procaine (hydrochloride) (Standard) is the analytical standard of Procaine (hydrochloride). This product is intended for research and analytical applications. Procaine hydrochloride is a DNA-demethylating agent. Procaine hydrochloride acts through multiple targets and has a slow onset and a short duration of action .
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Cat. No.: HY-B0546AS
Procaine-d4 (hydrochloride) is the deuterium labeled Procaine hydrochloride. Procaine hydrochloride is a DNA-demethylating agent. Procaine hydrochloride acts through multiple targets and has a slow onset and a short duration of action .
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Cat. No.: HY-W704876
Procaine hydrochloride-d4 is the deuterium labeled Procaine hydrochloride (HY-B0546A). Procaine hydrochloride is a DNA-demethylating agent. Procaine hydrochloride acts through multiple targets and has a slow onset and a short duration of action .
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Cat. No.: HY-129451
CAS No.: 805326-00-5
Target:  

GABA Receptor

Research Areas:  

Others

HIE-124 is a potent ultra-short acting hypnotic that exhibits a rapid onset of action and a shorter duration of action with no acute tolerance or noticeable side effects. HIE-124 is promising for research of preanesthetic medication and anesthesia inducer .
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Cat. No.: HY-106018A
CAS No.: 154802-96-7
Synonyms: GM 611 fumarate
Target:  

Motilin Receptor

Research Areas:  

Others

Mitemcinal fumarate is an oral motilium agonist. Studies in rabbits and dogs have shown that it can promote defecation without causing severe diarrhea, increase stool weight without increasing water content in the rabbit constipation model, and reduce the time to first defecation in dogs. Mitemcinal fumarate may be a constipation suppressant due to its early onset and short duration of action.
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Cat. No.: HY-106018
CAS No.: 154738-42-8
Synonyms: GM 611
Target:  

Motilin Receptor

Research Areas:  

Others

Mitemcinal (GM 611) is an oral motilin receptor agonist. Studies in rabbits and dogs have shown that it can promote defecation without causing severe diarrhea, increase stool weight without increasing water content in the rabbit constipation model, and reduce the time to first defecation in dogs. Mitemcinal may be a constipation suppressant due to its early onset and short duration of action .
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Cat. No.: HY-108204
CAS No.: 579494-66-9
Synonyms: THRX 918661
Target:  

GABA Receptor

Research Areas:  

Others

AZD 3043 (THRX 918661) is a positive allosteric modulator of GABA(A) receptors with sedative and hypnotic activity. AZD 3043 can enhance GABA(A) receptor-mediated chloride currents in vitro and produce hypnotic and electroencephalographic inhibitory effects in vivo. Due to its esterase-dependent metabolic pathway, it has a short duration of action and can be quickly cleared even after long-term infusion, which may have clinical application potential.
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Cat. No.: HY-B1700AR
CAS No.: 106861-44-3
Research Areas:  

Neurological Disease

Mivacurium (dichloride) (Standard) is the analytical standard of Mivacurium (dichloride). This product is intended for research and analytical applications. Mivacurium dichloride is a benzylisoquinoline derivative and is a short-acting non-depolarizing neuromuscular blocking agent and skeletal muscle relaxant. Mivacurium dichloride couples with the nAChR to reduce or inhibit the depolarizing effect of acetylcholine on the terminal disc of the muscle cell .
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Cat. No.: HY-182537
CAS No.: 119302-18-0
Target:  

Drug Derivative

Research Areas:  

Neurological Disease

Org 9616 bromide is a non-depolarizing neuromuscular blocker with a structure similar to Pancuroniam. Org 9616 bromide induces rapid-onset, short-duration neuromuscular blockade .
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Cat. No.: HY-B1778C
CAS No.: 541-19-5
Synonyms: Suxamethonium iodide
Target:  

nAChR mAChR

Research Areas:  

Neurological Disease

Succinylcholine iodide (Suxamethonium iodide) is a depolarizing neuromuscular blocker with rapid onset and short duration of action. Succinylcholine iodide also acts as an agonist of the Acetylcholine receptor. Succinylcholine iodide is used for emergency airway management .
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Cat. No.: HY-105656R
CAS No.: 6000-74-4
Synonyms: Hydrocortisone 21-phosphate sodium (Standard); Cortisol 21-phosphate sodium (Standard)
Research Areas:  

Infection

Hydrocortisone phosphate sodium (Standard) is the analytical standard of Hydrocortisone phosphate sodium (HY-105656). This product is intended for research and analytical applications. Hydrocortisone phosphate sodium is a soft steroid with low anti-inflammatory properties and a short duration of action. Hydrocortisone phosphate sodium can be used for the research for several ocular conditions and gastric ulcers .
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Cat. No.: HY-182301
CAS No.: 112227-15-3
Target:  

Renin

Research Areas:  

Cardiovascular Disease

CP 71362 is a renin inhibitor, a highly potent substrate-analog transition state mimic with antihypertensive properties. CP 71362 exhibits significant inhibitory activity against plasma renin from rats, dogs, and humans (IC50 values are 3 nM, 0.0033 nM, and 20 nM, respectively). CP 71362 reduces the mean arterial pressure of anesthetized and conscious sodium-depleted animals in a dose-dependent manner, and has pharmacokinetic characteristics of rapid elimination and short duration of action. CP 71362 can be used in research related to hypertension and congestive heart failure .
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