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MedChemexpress LLC
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Product Name:Alosetron (Hydrochloride(1:X))
CAS:132414-02-9
Purity:>98% Package:474RMB/10mg
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LETOPHARM LIMITED
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+86-21-5821 5861 |
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sales@letopharm.com |
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Product Name:Alosetron (Hydrochloride(1:X))
CAS:132414-02-9
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Musechem
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+1-800-259-7612 |
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info@musechem.com |
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Product Name:Alosetron Hydrochloride(1:X)
CAS:132414-02-9
Purity:>98% HPLC Package:10mg;100mg;1g Remarks:Reagent Grade
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Fan De(Beijing) Biotechnology Co., Ltd.
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15911056312 |
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Product Name:2,3,4,5-Tetrahydro-5-methyl-2-[(4-methyl-1H-imidazol-5-yl)methyl]-1H-pyrido[4,3-b]indol-1-one hydrochloride
CAS:132414-02-9
Purity:97.0% Package:5mg
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Absin Bioscience Inc.
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021-38015121 15000105423 |
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chenjw@absin.cn |
| Products Intro: |
Product Name:Alosetron Hydrochloride(1:X)
CAS:132414-02-9
Package:10mg;50mg Remarks: 见爱必信官网
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| | 2,3,4,5-Tetrahydro-5-methyl-2-[(4-methyl-1H-imidazol-5-yl)methyl]-1H-pyrido[4,3-b]indol-1-one hydrochloride Basic information |
| | 2,3,4,5-Tetrahydro-5-methyl-2-[(4-methyl-1H-imidazol-5-yl)methyl]-1H-pyrido[4,3-b]indol-1-one hydrochloride Chemical Properties |
| storage temp. | Store at -20°C | | solubility | Soluble in DMSO |
| | 2,3,4,5-Tetrahydro-5-methyl-2-[(4-methyl-1H-imidazol-5-yl)methyl]-1H-pyrido[4,3-b]indol-1-one hydrochloride Usage And Synthesis |
| Description | Alosetron was launched in March 2000 in the US as a new oral treatment for diarrheapredominant
irritable bowel syndrome in women. This structurally-related analog of
ondansetron is prepared by alkylation of the pyrido[4,3-b]indol-1-one skeleton with the
appropriate trityl-protected chloromethylimidazole. Although its mechanism of action is not
fully understood, alosetron is known to be a potent and selective 5-HT3 antagonist with a
superior pharmacodynamic profile than its predecessor ondansetron. Besides being
present in the central nervous system, 5-HT3 receptors are located on neurons of both
enteric and sensory nervous systems. Alosetron may act on several of these sites leading
to the regulation of intestinal secretion, gastrointestinal contractility and gastric emptying.
Clinically, it has been found that a twice-daily dose of Img of alosetron not only improves
bowel function, stool frequency and stool consistency but also affects the pain severity and
sense of urgency in IBS. Despite its short half-life (1.5h) and extensive metabolism (at
least 12 metabolites have been identified in urine), alosetron shows a long duration (10h)
of inhibition of the serotonin-induced skin flare response in man. Due to reported cases of
constipation and ischemic colitis as well as rare fatalities of patients under treatment with
Lotronex, Glaxo-Wellcome withdrew the drug from the US market in November and is
currently running further clinical trials. | | Originator | Glaxo-Wellcome (UK) | | Brand name | Lotronex | | Biological Activity | Alosetron(GR68755)Hydrochloride(1:X) is a potent and selective 5-HT3 receptor (5-HT3receptor) antagonist. AlosetronHydrochloride(1:X) for the study of irritable bowel syndrome (IBS). AChemicalbooklosetronHydrochloride (1:X) blocks 5HT3-mediated rapid depolarization of guinea pig intermuscular and submucosal neurons with IC50 at ~55nM. AlosetronHydrochloride (1:X) attenuates visceral nociceptive effects of rectal distension in awake or anesthetized dogs. Has anti-inflammatory activity. | | in vivo | Dexamethasone and Alosetron-treated (1 mg/kg; ip; daily for 6 days) rats exhibits a significant decrease in the diarrhea index, in comparison with TNBS-control group, especially after the initial 2 days of treatment following the induction of colitis. |
| | 2,3,4,5-Tetrahydro-5-methyl-2-[(4-methyl-1H-imidazol-5-yl)methyl]-1H-pyrido[4,3-b]indol-1-one hydrochloride Preparation Products And Raw materials |
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