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| Product | Description | |
|---|---|---|
| Pirenzepine | Pirenzepine (LS 519 free base) is a selective M1 mAChR ( muscarinic acetylcholine receptor ) antagonist. Pirenzepine reduces gastric acid secretion and reduces muscle spasm, can be used in peptic ulcers research. Pirenzepine shows anti-proliferative activity to cancer cells [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LS 519 free base; Pirenzepin; Gastrozepin. CAS No. 28797-61-7. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 500 mg. Product ID: HY-17037A. |  |
| Pirenzepine dihydrochloride | ?98% (TLC), powder. Group: Fluorescence/luminescence spectroscopy. |  |
| Pirenzepine dihydrochloride | Pirenzepine (LS 519) dihydrochloride is a selective M1 mAChR ( muscarinic acetylcholine receptor ) antagonist. Pirenzepine dihydrochloride reduces gastric acid secretion and reduces muscle spasm, can be used in peptic ulcers research. Pirenzepine dihydrochloride shows anti-proliferative activity to cancer cells [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: LS 519; Pirenzepin dihydrochloride; Gastrozepin dihydrochloride. CAS No. 29868-97-1. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g. Product ID: HY-17037. | |
| Pirenzepine, dihydrochloride | Pirenzepine, dihydrochloride. Group: Biochemicals. Alternative Names: 5,11-Dihydro-11-[2-(4-methyl-1-piperazinyl)acetyl]-6H-pyrido[2,3-b][1,4]benzo-diazepin-6-one dihydrochloride; Duogastral; Durapirenz. Grades: Highly Purified. CAS No. 29868-97-1. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. Molecular Formula: C19H23Cl2N5O2. US Biological Life Sciences. |  Worldwide |
| Pirenzepine Dihydrochloride | An antagonist selective for mAChR subtype M1. Used for studying the functional roles of M1 receptors in both central and peripheral nervous systems. Group: Biochemicals. Grades: Highly Purified. CAS No. 28797-61-7. Pack Sizes: 100mg. Molecular Formula: C??H??N?O? 2HCl. US Biological Life Sciences. | Worldwide |
| Pirenzepine, Dihydrochloride (Duogastral, Durapirenz, Gasteril, Gastrozepin, Leblon, Maghen, Renzepin, Tabe, Ulcuforton, Ulcosan) | An antiulcerative. Group: Biochemicals. Alternative Names: Duogastral, Durapirenz, Gasteril, Gastrozepin, Leblon, Maghen, Renzepin, Tabe, Ulcuforton, Ulcosan. Grades: Highly Purified. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Pirenzepine hydrochloride | Pirenzepine hydrochloride is an antiulcerative that acts via suppressing gastric secretion. Pirenzepine is a selective muscarinic M1 receptor antagonist. Uses: M1 muscarinic receptor selective antagonist. Synonyms: Pirenzepine dihydrochloride; Pirenzepine HCl; Bisvanil; 11-[2-(4-methylpiperazin-1-yl)acetyl]-5-H-pyrido[2,3-b][1,4]benzodiazepin-6-one dihydrochloride. Grades: >98%. CAS No. 29868-97-1. Molecular formula: C19H23Cl2N5O2. Mole weight: 424.33. |  |
| N-Desmethyl pirenzepine | N-Desmethyl pirenzepine. Group: Biochemicals. Alternative Names: 5,11-Dihydro-11-(1-piperazinylacetyl)-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one; LS 822. Grades: Highly Purified. CAS No. 63257-31-8. Pack Sizes: 1mg, 2mg, 5mg, 10mg. Molecular Formula: C18H19N5O2. US Biological Life Sciences. | Worldwide |
| 11, 11'- (2, 2'- (Piperazine-1, 4-diyl)bis (acetyl))bis (5H-benzo[e]pyrido[3, 2-b][1, 4]diazepin-6 (11H)-one)-d8 | 11, 11'- (2, 2'- (Piperazine-1, 4-diyl)bis (acetyl))bis (5H-benzo[e]pyrido[3, 2-b][1, 4]diazepin-6 (11H)-one)-d8 is an labelled dimer impurity of labelled Pirenzepine (P508502), an antiulcerative agent. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 5mg. Molecular Formula: C32H20D8N8O4, Molecular Weight: 596.669999999999. US Biological Life Sciences. | Worldwide |
| Coluracetam | MKC-231 (10(-10)-10(-6) moll) significantly increased high affinity choline uptake (HACU) when it was incubated with the hippocampal synaptosomes of ethylcholine mustard aziridinium ion (AF64A) treated rats, but not of normal rats. MKC-231 did not affect the AChE activity, [3H]- quinuclidinyl benzilate binding, and [3H]-pirenzepine binding. Oral administration of MKC-231 (1-10 mg/kg) significantly improved the learning deficits in the Morris' water maze of AF64A-treated rats, but it did not produce any significant side effects, like tremor, salivation or hypothermia, which were observed in rats treated with high doses of tacrine [1]. In acute behavioral experiments, MKC-231 and THA had no significant effect on AF64A-induced memory deficits at any doses tested (0.3, 1.0 and 3.0 mg/kg), whereas Dup 996, at a dose of 1.0 mg/kg, significantly improved memory deficits. In chronic experiments, MKC-231 improved memory deficit at all doses tested (0.3, 1.0, or 3.0 mg/kg p.o., once daily for 11 days) and Dup 996 did so only at a dose of 3.0 mg/kg, whereas THA did not improve memory deficit at any doses tested. Synonyms: Coluracetam; BCI-540; MKC-231; BCI 540; MKC 231; BCI540; MKC231. Grades: >98%. CAS No. 135463-81-9. Molecular formula: C19H23N3O3. Mole weight: 341.4. | |
| Nuvenzepine | Nuvenzepine, a new pirenzepine-analog, is an mAChR antagonist, administered intraduodenally, displayed a long-lasting and dose-dependent inhibition of neostigmine-induced intestinal motility in anaesthetized cats. Synonyms: 11-(1-methylpiperidine-4-carbonyl)-6H-pyrido[3,2-c][1,5]benzodiazepin-5-one; 11-(N-methylisonipecotyl)-6,11-dihydro-5H-pyrido(2,3-b)(1,5)benzodiazepin-5-one; DF 545; DF-545; nuvenzepine. CAS No. 96487-37-5. Molecular formula: C19H20N4O2. Mole weight: 336.39. | |
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