5 Results for "

peristaltic

" in MedChemExpress (MCE) Product Catalog:
Products (5)

5 Results for "peristaltic" in MCE Product Catalog:

Cat. No.: HY-101222
CAS No.: 207572-69-8
Purity:  99.94%
SB-203186 hydrochloride is a potent, selective and competitive 5-HT4 antagonist. SB-203186 hydrochloride antagonizes the 5-HT4 receptor-mediated relaxations of the carbachol-contracted rat isolated oesophagus against 5-HT with pKB values of 10.9 (rat oesophagus), 9.5 (guinea-pig ileum), and 9.0 (human colon) respectively .
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Cat. No.: HY-103212A
CAS No.: 147663-20-5
Purity:  95.35%
Synonyms: B-HT 933 hydrochloride; Oxazoloazepin hydrochloride
Target:  

Adrenergic Receptor

Research Areas:  

Cardiovascular Disease

Azepexole hydrochloride (B-HT 933 dihydrochloride; Oxazoloazepin dihydrochloride) is a selective agonist for α 2-adrenoceptor, with pKi of 8.3, 7.6, and 7.5 for α2A-, α2B- and α2C-adrenoceptor subtypes, resepctively. Azepexole dihydrochloride causes concentration-dependent inhibition of peristaltic contractions with IC50 of 78.72 nM. Azepexole hydrochloride exhibits antitussive and analgesic efficacy .
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Cat. No.: HY-103212
CAS No.: 36067-72-8
Synonyms: B-HT 933 dihydrochloride; Oxazoloazepin dihydrochloride
Target:  

Adrenergic Receptor

Azepexole (B-HT 933) dihydrochloride is a potent and selective alpha 2-adrenoceptor agonist with pKis of 8.3, 7.6, and 7.5 for α2A-, α2B- and α2C-adrenoceptor subtypes, resepctively . Azepexole dihydrochloride causes concentration-dependent inhibition of peristaltic contractions (IC50= 78.72 nM) .
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Cat. No.: HY-N3136
CAS No.: 53823-02-2
Onitin is a natural product, that can be isolated from Onychium siliculosum. Onitin is also a non-competitive antagonist of histamine. Onitin shows activity in blocking the peristaltic reflex of the guinea-pig ileum, in inhibition of the responses of guinea-pig ileum to histamine and of inhibition of the responses of guinea-pig tracheal muscle to histamine .
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Cat. No.: HY-176193
Target:  

P-glycoprotein

Research Areas:  

Cancer

P-gp modulator-7 (Compound 9e) is a P-glycoprotein (P-gp) inhibitor. P-gp modulator-7 occupies the channel entrance of P-gp with a unique T-shaped configuration, hindering the peristaltic extrusion mechanism of transmembrane domains TM12 and TM9, thereby inhibiting P-gp from pumping drugs out of cells and reversing the multidrug resistance (MDR) of tumor cells. P-gp modulator-7 is promising for research of cancers .
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