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Almorexant hydrochloride ( ACT-078573 hydrochloride)

    
99.7%

(R)-2-((R)-6,7-diMethoxy-1-(4-(trifluoroMethyl)phenethyl)-3,4-dihydroisoquinolin-2(1H)-yl)-N-Methyl-2-phenylacetaMide

源葉(MedMol)
S81095 一鍵復制產品信息
913358-93-7
C29H31F3N2O3
512.5632496
阿莫倫特鹽酸鹽;(ALPHAR,1S)-3,4-二氫-6,7-二甲氧基-N-甲基-ALPHA-苯基-1-[2-[4-(三氟甲基)苯基]乙基]-2(1H)-異喹啉乙酰胺單鹽酸鹽;鹽酸阿莫倫特;AlMorexant (hydrochloride);(alphaR,1S)-3,4-Dihydro-6,7-dimethoxy-N-methyl-alpha-phenyl-1-[2-[4-(trifluoro
貨號 規格 價格 上海 北京 武漢 南京 購買數量
S81095-5mg
99.7% ¥440.00 >10 - - -
S81095-10mg
99.7% ¥590.00 10 - - -
S81095-50mg
99.7% ¥790.00 5 - - -
S81095-100mg
99.7% ¥1500.00 4 - - -
產品介紹 參考文獻 質檢證書(COA) 摩爾濃度計算器 相關產品

產品介紹

Almorexant (ACT 078573) hydrochloride is an orally active, potent and competitive dual orexin receptor antagonist, with Kd values of 1.3 nM (OX1) and 0.17 nM (OX2), respectively. Almorexant hydrochloride reversibly blocks signaling of orexin-A and orexin-B peptides. Almorexant hydrochloride totally blocked the intracellular Ca2+ signal pathway. Almorexant hydrochloride stimulates caspase-3 activity in AsPC-1 cells and induces apoptosis

產品描述: Almorexant (ACT 078573) hydrochloride is an orally active, potent and competitive dual orexin receptor antagonist, with Kd values of 1.3 nM (OX1) and 0.17 nM (OX2), respectively. Almorexant hydrochloride reversibly blocks signaling of orexin-A and orexin-B peptides. Almorexant hydrochloride totally blocked the intracellular Ca2+ signal pathway. Almorexant hydrochloride stimulates caspase-3 activity in AsPC-1 cells and induces apoptosis
靶點: human OX2R:0.17 nM (Kd);human OX1R:1.3 nM (Kd);Caspase-3 ;OXReceptor
體內研究: Almorexant hydrochloride (1.8 μmol/kg, 100 μL; IP, daily) reduces the volume of tumors. Almorexant hydrochloride (300 mg/kg, PO, once) can help rats to be fully capable of spatial and avoidance learning. Almorexant hydrochloride (30-300 mg/kg) dose-dependently increases rapid eye movement (REM) and non-REM (NREM) sleep and decreases wakefulness apparently without inducing either cataplexy18 or deficits in next-day performance.
參考文獻: 1. Dayot S, et al. In vitro, in vivo and ex vivo demonstration of the antitumoral role of hypocretin-1/orexin-A and almorexant in pancreatic ductal adenocarcinoma. Oncotarget. 2018 Jan 9;9(6):6952-6967. 2. Malherbe P, et al. Biochemical and electrophysiological characterization of almorexant, a dual orexin 1 receptor (OX1)/orexin 2 receptor (OX2) antagonist: comparison with selective OX1 and OX2 antagonists. Mol Pharmacol. 2009 Sep;76(3):618-31. 3. Black SW, et al. Almorexant promotes sleep and exacerbates cataplexy in a murine model of narcolepsy. Sleep. 2013 Mar 1;36(3):325-36. 4. Dietrich H, et al. Intact learning and memory in rats following treatment with the dual orexin receptor antagonist almorexant. Psychopharmacology (Berl). 2010 Oct;212(2):145-54.
溶解性: DMSO  :  ≥  46  mg/mL  (83.79  mM)    H2O  :  <  0.1  mg/mL  (ultrasonic;warming;heat  to  60°C)  (insoluble)
保存條件: RT
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 1.951 ml 9.755 ml 19.51 ml
5 mM 0.39 ml 1.951 ml 3.902 ml
10 mM 0.195 ml 0.975 ml 1.951 ml
50 mM 0.039 ml 0.195 ml 0.39 ml
注意: 部分產品我司僅能提供部分信息,我司不保證所提供信息的權威性,僅供客戶參考交流研究之用。

參考文獻

質檢證書(COA)

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批號:JS298415 貨號:S20001-25g
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摩爾濃度計算器

質量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)

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