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Lercanidipine hydrochloride hemihydrate

    
99.8%

Lercanidipine hydrochloride hemihydrate

源葉(MedMol)
S82849 一鍵復(fù)制產(chǎn)品信息
132866-11-6
C36H41N3O6 · HCl · 0.5H2O
657.2
MFCD07773089
鹽酸樂(lè)卡地平;1,4-二氫-2,6-二甲基-4-(3-硝基苯基)-3,5-吡啶二羧酸 2-[(3,3-二苯丙基)甲基氨基]-1,1-二甲基乙基甲酯鹽酸鹽; 樂(lè)卡地平鹽酸鹽; 樂(lè)卡地平鹽酸鹽;;Lercanidipine hydrochloride hemihydrate; Lercanidipine hydrochloride;
貨號(hào) 規(guī)格 價(jià)格 上海 北京 武漢 南京 購(gòu)買(mǎi)數(shù)量
S82849-10mg
99.8% ¥60.00 >10 - - -
S82849-50mg
99.8% ¥120.00 >10 - - -
S82849-100mg
99.8% ¥180.00 >10 - - -
S82849-1g
≥99% ¥350.00 >10 - - -
產(chǎn)品介紹 參考文獻(xiàn) 質(zhì)檢證書(shū)(COA) 摩爾濃度計(jì)算器 相關(guān)產(chǎn)品

產(chǎn)品介紹

Lercanidipine is a calcium channel blocker of the dihydropyridine class.

產(chǎn)品描述: Lercanidipine is a calcium channel blocker of the dihydropyridine class.
靶點(diǎn): Calcium Channel;CalciumChannel
體內(nèi)研究: In chronically catheterised dogs with experimental renovascular hypertension, lercanidipine decreases diastolic blood pressure in a dose-dependent manner (ED25 = 0.9 mg/kg p.o). In the same animals, long term application of lercanidipine showed permanent decrease of diastolic blood pressure indicating no tolerance of the antihypertensive effect. Lercanidipine possesses significant anticonvulsant effect. It does not affect the muscle coordination or locomotor activity in mice[5]. In clinical studies, lercanidipine has a 24-hour antihypertensive effect and causes no significant increase in heart rate. Lercanidipine has been shown to be effective in a wide range of hypertensive patients, including mild-to-moderate hypertension, severe hypertension, the elderly, and those with isolated systolic hypertension. It is associated with a low rate of adverse events
細(xì)胞實(shí)驗(yàn): Cells are incubated for 24 hours in DMEM+EFAF 0.2% and lercanidipine, then with lercanidipine and AcLDL for 24 hours. In the last 2 hours [14C]-oleic acid albumin complex is added for the determination of cholesterol esterification (ACAT activity). (Only for Reference)
參考文獻(xiàn): 1.Shereen M. Tawakkol, et al. Analytical Chemistry Letters. 2014, 4:255-266. 2.Epstein M, et al. Heart Dis. 2001, 3(6):398-407. 3.Selvaraj N, et al. J Clin Diagn Res. 2015, 9(11):FF01-5. 4.Gasser R, et al. Journal of Clinical and Basic Cardiology. 1999, 2(2):169-174. 5.Canavesi M, et al. J Cardiovasc Pharmacol. 2004, 44(4):416-422.
溶解性: DMSO:64.8  mg/mL  (100  mM)    Ethanol:6.5  mg/mL  (10  mM)
保存條件: 2-8℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 1.522 ml 7.608 ml 15.216 ml
5 mM 0.304 ml 1.522 ml 3.043 ml
10 mM 0.152 ml 0.761 ml 1.522 ml
50 mM 0.03 ml 0.152 ml 0.304 ml
注意: 部分產(chǎn)品我司僅能提供部分信息,我司不保證所提供信息的權(quán)威性,僅供客戶參考交流研究之用。

參考文獻(xiàn)

質(zhì)檢證書(shū)(COA)

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請(qǐng)輸入貨號(hào)和一個(gè)與之匹配的批號(hào)。
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批號(hào):JS298415 貨號(hào):S20001-25g
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摩爾濃度計(jì)算器

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

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