4 Results for "

contractile potency

" in MedChemExpress (MCE) Product Catalog:
Products (4)

4 Results for "contractile potency" in MCE Product Catalog:

Cat. No.: HY-P3591
CAS No.: 83903-32-6
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

YMRF-NH2 is a neuropeptide. YMRF-NH2 binds to FMRFa-R with an EC50 value of 31 nM .
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Cat. No.: HY-123459
CAS No.: 137431-04-0
Synonyms: ABT-232; NS-49; PNO-49B
Target:  

Adrenergic Receptor

Research Areas:  

Endocrinology

Garomefrine hydrochlorid (ABT-232) is an α1A-adrenergic agonist with the potential to inhibit urinary incontinence. Garomefrine hydrochlorid showed the greatest contractility in pig nasal mucosal vessels. The biological activity of Garomefrine hydrochlorid has been shown to give it a competitive advantage compared to other drugs. The potency of Garomefrine hydrochlorid makes it a valuable research object in related research .
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Cat. No.: HY-A0252A
CAS No.: 15148-80-8
Target:  

Adrenergic Receptor

Research Areas:  

Cancer

Bupranolol hydrochloride is a non-selective β-adrenergic blocker with potent membrane stabilizing activity. Bupranolol hydrochloride is able to significantly modulate the contractile activity of the non-pregnant human uterus. Bupranolol hydrochloride showed significant effects on spontaneous uterine contractions in an in vitro study in patients with ovarian cancer. Bupranolol hydrochloride is similar in potency to propranolol, another β-adrenergic blocker. Bupranolol hydrochloride is rapidly and completely absorbed in vivo, and its major metabolite is carboxybupranolol .
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Cat. No.: HY-19279A
CAS No.: 171277-06-8
Target:  

Adrenergic Receptor

Research Areas:  

Endocrinology

JTH-601 Free base is a novel alpha1-adrenoceptor antagonist that exhibits potent activity in inhibiting phenylephrine-induced contractions in lower urinary tract tissues. JTH-601 Free base competitively antagonizes alpha1-adrenoceptor-mediated contractile responses, demonstrating greater potency than prazosin or tamsulosin. JTH-601 Free base is anticipated to be effective in treating urinary outlet obstruction associated with benign prostatic hyperplasia.
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