產(chǎn)品描述: | Tegaserod maleate (SDZ-HTF-919) is an orally active?serotonin receptor 4?(HTR4;?5-HT4R) agonist and a?5-HT2B?receptor antagonist. Tegaserod maleate has pKis of 7.5, 8.4 and 7.0 for human recombinant 5-HT2A, 5-HT2B?and 5-HT2C?receptors, respectively. Tegaserod maleate causes tumor cell?apoptosis, blunts?PI3K/Akt/mTOR?signaling and decreases S6 phosphorylation. Tegaserod maleate has anti-tumor activity and has the potential for irritable bowel syndrome (IBS) research |
靶點(diǎn): |
5-HT4?Receptor;5-HT2B Receptor;5-HTReceptor |
體內(nèi)研究: |
馬來(lái)酸替加色羅 (SDZ-HTF-919; 5 mg/kg/天; 腹腔注射; 連續(xù)五天) 在體內(nèi)延遲腫瘤生長(zhǎng)、減少轉(zhuǎn)移、增加存活率并抑制 p-S6。 馬來(lái)酸替加色羅 (0.1-2.0 mg/kg; 胃負(fù)荷前 15 分鐘腹腔注射) 顯著加速 db/db 小鼠的胃葡萄糖排空率,在 0.1mg/kg 的情況下將 30 分鐘時(shí)留在胃中的膳食部分減少80% . |
參考文獻(xiàn): |
1. Wei Liu, et al. Repurposing the serotonin agonist Tegaserod as an anticancer agent in melanoma: molecular mechanisms and clinical implications. J Exp Clin Cancer Res. 2020 Feb 21;39(1):38. 2. M D Crowell, et al. The effects of tegaserod, a 5-HT receptor agonist, on gastric emptying in a murine model of diabetes mellitus. Neurogastroenterol Motil. 2005 Oct;17(5):738-43. 3. D T Beattie, et al. The 5-HT4 receptor agonist, tegaserod, is a potent 5-HT2B receptor antagonist in vitro and in vivo. Br J Pharmacol. 2004 Nov;143(5):549-60. |
溶解性: |
DMSO : ≥ 35 mg/mL (83.84 mM) H2O : 1 mg/mL (2.40 mM; Need ultrasonic) |
保存條件: |
-20℃ |
配置溶液濃度參考: |
|
1mg |
5mg |
10mg |
1 mM |
2.395 ml |
11.977 ml |
23.954 ml |
5 mM |
0.479 ml |
2.395 ml |
4.791 ml |
10 mM |
0.24 ml |
1.198 ml |
2.395 ml |
50 mM |
0.048 ml |
0.24 ml |
0.479 ml |
|
注意: |
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