Capsaicin-d3
(Synonyms: TRANS-辣椒素-D3,(E)-Capsaicin-d3) 目录号 : GC49761
An internal standard for the quantification of capsaicin
Cas No.:1217899-52-9
Sample solution is provided at 25 µL, 10mM.
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)
Cas No. | 1217899-52-9 | SDF | Download SDF |
别名 | TRANS-辣椒素-D3,(E)-Capsaicin-d3 | ||
Canonical SMILES | CC(C)/C=C/CCCCC(NCC1=CC(OC([2H])([2H])[2H])=C(C=C1)O)=O | ||
分子式 | C18H24D3NO3 | 分子量 | 308.4 |
溶解度 | Chloroform: soluble,DMF: soluble,DMSO: soluble,Ethyl Acetate: soluble,Methanol: soluble | 储存条件 | -20°C |
General tips | 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。 为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。 |
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Shipping Condition | 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。 |
制备储备液 | |||
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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 | |||
第二步:请输入动物体内配方组成(配方适用于不溶于水的药物;不同批次药物配方比例不同,请联系GLPBIO为您提供正确的澄清溶液配方) | ||||||||||
% DMSO % % Tween 80 % saline | ||||||||||
计算重置 |
计算结果:
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。
3. 以上所有助溶剂都可在 GlpBio 网站选购。
Quality Control & SDS
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- Purity: >99.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet