Nefazodone-d6 (hydrochloride)
(Synonyms: BMY-13754-d6; MJ-13754-1-d6) 目录号 : GC49204
An internal standard for the quantification of nefazodone
Cas No.:1330236-06-0
Sample solution is provided at 25 µL, 10mM.
Nefazodone-d6 (hydrochloride) is intended for use as an internal standard for the quantification of nefazodone by GC- or LC-MS. Nefazodone is a serotonin (5-HT), norepinephrine, and dopamine reuptake inhibitor (SNDRI; Kis = 137, 570, 2,380 nM, respectively, in rat brain synaptosomes).1 It is also an antagonist of 5-HT2A, 5-HT1A, and histamine H1 receptors, as well as α1- and α2-adrenergic receptors (α2-ARs; Kis = 7.1, 52, 30, 5.5, and 84 nM, respectively).2 Nefazodone (100 mg/kg) reduces immobility time in the tail suspension test in gerbils.3 However, it is toxic to isolated human hepatocytes in a cultured sandwich hepatocyte preparation when used at a concentration of 30 µM.4 Formulations containing nefazodone have previously been used in the treatment of depression.
1.Carlier, P.R., Lo, M.M.-C., Lo, P.C.-K., et al.Synthesis of a potent wide-spectrum serotonin-, norepinephrine-, dopamine-reuptake inhibitor (SNDRI) and a species-selective dopamine-reuptake inhibitor based on the gamma-amino alcohol functional groupBioorg. Med. Chem. Lett.8(5)487-492(1998) 2.Owens, M.J., Neal, W., Plott, S.J., et al.Neurotransmitter receptor and transporter binding profile of antidepressants and their metabolitesJ. Pharmacol. Exp. Ther.283(3)1305-1322(1997) 3.Varty, G.B., Cohen-Williams, M.E., and Hunter, J.C.The antidepressant-like effects of neurokinin NK1 receptor antagonists in a gerbil tail suspension testBehav. Pharmacol.14(1)87-95(2003) 4.Kostrubsky, S.E., Strom, S.C., Kalgutkar, A.S., et al.Inhibition of hepatobiliary transport as a predictive method for clinical hepatotoxicity of nefazodoneToxicol. Sci.90(2)451-459(2006)
Cas No. | 1330236-06-0 | SDF | |
别名 | BMY-13754-d6; MJ-13754-1-d6 | ||
Canonical SMILES | O=C1N(CCOC2=CC=CC=C2)C(CC)=NN1C([2H])([2H])C([2H])([2H])C([2H])([2H])N3CCN(C4=CC(Cl)=CC=C4)CC3.Cl | ||
分子式 | C25H26ClD6N5O2·HCl | 分子量 | 512.5 |
溶解度 | DMSO: 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 | 1.9512 mL | 9.7561 mL | 19.5122 mL |
5 mM | 0.3902 mL | 1.9512 mL | 3.9024 mL |
10 mM | 0.1951 mL | 0.9756 mL | 1.9512 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
- View current batch:
- Purity: >99.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet