Capsaicin-d3
(Synonyms: TRANS-辣椒素-D3,(E)-Capsaicin-d3) 目录号 : GC49761An internal standard for the quantification of capsaicin
Cas No.:1217899-52-9
Sample solution is provided at 25 µL, 10mM.
Quality Control & SDS
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- Purity: >99.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
Capsaicin-d3 is intended for use as an internal standard for the quantification of capsaicin by GC- or LC-MS. Capsaicin is a terpene alkaloid that has been found in Capsicum and has diverse biological activities.1,2,3,4 It induces inward currents in HEK293 cells expressing rat transient receptor potential vanilloid 1 (TRPV1; EC50 = 0.64 µM at neutral pH), an effect that can be blocked by the TRPV1 inhibitor A-425619.1 Capsaicin (10 and 50 µM) decreases LPS-induced prostaglandin E2 production, as well as reduces LPS- and IFN-induced nitric oxide (NO) release in isolated mouse peritoneal macrophages.2 Capsaicin induces substance P release in rat spinal cord slices with an EC50 value of 2.3 µM.3 It reduces acetylcholine- or phenylquinone-induced writhing (ED50s = 1.33 and 1.38 mg/kg, respectively, s.c.) but has no effect on the latency to paw withdrawal in the hot plate test in mice (ED50 = >20 mg/kg, s.c.).4 Formulations containing capsaicin have been used in the treatment of nerve pain associated with shingles.
1.Neelands, T.R., Jarvis, M.F., Han, P., et al.Acidification of rat TRPVI alters the kinetics of capsaicin responsesMol. Pain128(2005) 2.Kim, C.-S., Kawada, T., Kim, B.-S., et al.Capsaicin exhibits anti-inflammatory property by inhibiting IkB-a degradation in LPS-stimulated peritoneal macrophagesCell. Signal.15(3)299-306(2003) 3.MarvizÓn, J.C.G., Wang, X., Matsuka, Y., et al.Relationship between capsaicin-evoked substance P release and neurokinin 1 receptor internalization in the rat spinal cordNeuroscience118(2)535-545(2003) 4.Hayes, A.G., Skingle, M., and Tyers, M.B.Effects of single doses of capsaicin on nociceptive thresholds in the rodentNeuropharmacology20(5)505-511(1981)
制备储备液 | |||
1 mg | 5 mg | 10 mg | |
1 mM | 3.2425 mL | 16.2127 mL | 32.4254 mL |
5 mM | 0.6485 mL | 3.2425 mL | 6.4851 mL |
10 mM | 0.3243 mL | 1.6213 mL | 3.2425 mL |
第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量) | ||||||||||
给药剂量 | mg/kg | 动物平均体重 | g | 每只动物给药体积 | ul | 动物数量 | 只 | |||
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% DMSO % % Tween 80 % saline | ||||||||||
计算重置 |
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工作液浓度: mg/ml;
DMSO母液配制方法: mg 药物溶于 μL DMSO溶液(母液浓度 mg/mL,
体内配方配制方法:取 μL DMSO母液,加入 μL PEG300,混匀澄清后加入μL Tween 80,混匀澄清后加入 μL saline,混匀澄清。
1. 首先保证母液是澄清的;
2.
一定要按照顺序依次将溶剂加入,进行下一步操作之前必须保证上一步操作得到的是澄清的溶液,可采用涡旋、超声或水浴加热等物理方法助溶。
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