8 | 2705402-91-9 | Norclozapine-d8 | Desmethylclozapine-d8 | Normethylclozapine-d8 | 氯氮平EP雜質C-d8 | mAChR | Opioid Receptor | Drug Metabolite | Virus Protease | Muscarinic acetylcholine receptor | Inhibitor | inhibitor | inhibit"/>

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  1. GPCR/G Protein Neuronal Signaling Metabolic Enzyme/Protease Anti-infection
  2. mAChR Opioid Receptor Drug Metabolite Virus Protease
  3. N-Desmethylclozapine-d8 hydrochloride

N-Desmethylclozapine-d8 hydrochloride  (Synonyms: N-去甲基氯氮平-d8; Norclozapine-d8 hydrochloride; Desmethylclozapine-d8 hydrochloride; Normethylclozapine-d8 hydrochloride)

目錄號: HY-G0021S1 純度: 99.74%
COA 產品使用指南 技術支持

N-Desmethylclozapine-d8 (hydrochloride) 是 N-Desmethylclozapine hydrochloride 的氘代物。N-Desmethylclozapine hydrochloride 是非典型抗精神病有效劑 Clozapine 的主要活性代謝產物。N-Desmethylclozapine hydrochloride 是一種有效的、變構的部分 M1 受體激動劑 (EC50=115 nM),能通過 M1 受體激活增強海馬 N-methyl-d-aspartate (NMDA) 受體電流。N-Desmethylclozapine hydrochloride 也是 δ-opioid 激動劑。

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N-Desmethylclozapine-d<sub>8</sub> hydrochloride Chemical Structure

N-Desmethylclozapine-d8 hydrochloride Chemical Structure

CAS No. : 2705402-91-9

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Other Forms of N-Desmethylclozapine-d8 hydrochloride:

  • 生物活性

  • 純度 & 產品資料

  • 參考文獻

生物活性

N-Desmethylclozapine-d8 (hydrochloride) is the deuterium labeled N-Desmethylclozapine hydrochloride. N-Desmethylclozapine hydrochloride is a major active metabolite of the atypical antipsychotic agent Clozapine. N-Desmethylclozapine hydrochloride is a potent, allosteric and partial M1 receptors agonist (EC50=115 nM) and is able to potentiate hippocampal N-methyl-d-aspartate (NMDA) receptor currents through M1 receptor activation. N-Desmethylclozapine hydrochloride is also a δ-opioid agonist[1][2][3].

體外研究
(In Vitro)

Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

357.31

Formula

C17H10D8Cl2N4

CAS 號
非標記 CAS
性狀

固體

顏色

Light yellow to yellow

中文名稱

氯氮平EP雜質C-d8

運輸條件

Room temperature in continental US; may vary elsewhere.

儲存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
溶解性數(shù)據(jù)
細胞實驗: 

DMSO 中的溶解度 : ≥ 50 mg/mL (139.93 mM; 吸濕的 DMSO 對產品的溶解度有顯著影響,請使用新開封的 DMSO)

* "≥" means soluble, but saturation unknown.

配制儲備液
濃度 溶劑體積 質量 1 mg 5 mg 10 mg
1 mM 2.7987 mL 13.9935 mL 27.9869 mL
5 mM 0.5597 mL 2.7987 mL 5.5974 mL
查看完整儲備液配制表

* 請根據(jù)產品在不同溶劑中的溶解度選擇合適的溶劑配制儲備液;一旦配成溶液,請分裝保存,避免反復凍融造成的產品失效。
儲備液的保存方式和期限:-80°C, 6 months; -20°C, 1 month。-80°C儲存時,請在6個月內使用,-20°C儲存時,請在1個月內使用。

  • 摩爾計算器

  • 稀釋計算器

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

質量
=
濃度
×
體積
×
分子量 *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

濃度 (start)

C1

×
體積 (start)

V1

=
濃度 (final)

C2

×
體積 (final)

V2

動物溶解方案計算器
請輸入動物實驗的基本信息:

給藥劑量

mg/kg

動物的平均體重

g

每只動物的給藥體積

μL

動物數(shù)量

由于實驗過程有損耗,建議您多配一只動物的量
計算結果
工作液所需濃度 : mg/mL
純度 & 產品資料
參考文獻

完整儲備液配制表

* 請根據(jù)產品在不同溶劑中的溶解度選擇合適的溶劑配制儲備液;一旦配成溶液,請分裝保存,避免反復凍融造成的產品失效。
儲備液的保存方式和期限:-80°C, 6 months; -20°C, 1 month。-80°C儲存時,請在6個月內使用,-20°C儲存時,請在1個月內使用。

可選溶劑 濃度 溶劑體積 質量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 2.7987 mL 13.9935 mL 27.9869 mL 69.9673 mL
5 mM 0.5597 mL 2.7987 mL 5.5974 mL 13.9935 mL
10 mM 0.2799 mL 1.3993 mL 2.7987 mL 6.9967 mL
15 mM 0.1866 mL 0.9329 mL 1.8658 mL 4.6645 mL
20 mM 0.1399 mL 0.6997 mL 1.3993 mL 3.4984 mL
25 mM 0.1119 mL 0.5597 mL 1.1195 mL 2.7987 mL
30 mM 0.0933 mL 0.4664 mL 0.9329 mL 2.3322 mL
40 mM 0.0700 mL 0.3498 mL 0.6997 mL 1.7492 mL
50 mM 0.0560 mL 0.2799 mL 0.5597 mL 1.3993 mL
60 mM 0.0466 mL 0.2332 mL 0.4664 mL 1.1661 mL
80 mM 0.0350 mL 0.1749 mL 0.3498 mL 0.8746 mL
100 mM 0.0280 mL 0.1399 mL 0.2799 mL 0.6997 mL
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產品名稱:
N-Desmethylclozapine-d8 hydrochloride
目錄號:
HY-G0021S1
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