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2-[(2-乙氧基苯氧基)甲基]吗啉盐酸盐

2-[(2-乙氧基苯氧基)甲基]吗啉盐酸盐用途

Viloxazine hydrochloride 是 Viloxazine (HY-W380450) 的非活性异构体,可作为实验中的对照化合物。Viloxazine (Viloxazin) 是一种去甲肾上腺素重摄取 (norepinephrine reuptake) 抑制剂,也是有效的 5-HT2C 激动剂和 5-HT2B 拮抗剂,对 5-HT2C 的 EC50 为 32 μM,对 5-HT2B 的 IC50 为 27 μM。Viloxazine 的作用机制主要涉及血清素能和去甲肾上腺素能通路。Viloxazine 可用于抗抑郁研究。

2-[(2-乙氧基苯氧基)甲基]吗啉盐酸盐名称

[ CAS 号 ]:
35604-67-2

[ 中文名 ]:
2-[(2-乙氧基苯氧基)甲基]吗啉盐酸盐

[ 英文名 ]:
2-[(2-ethoxyphenoxy)methyl]morpholine hydrochloride

[中文别名 ]:

[英文别名 ]:

2-[(2-乙氧基苯氧基)甲基]吗啉盐酸盐生物活性

[ 描述 ]:

Viloxazine hydrochloride 是 Viloxazine (HY-W380450) 的非活性异构体,可作为实验中的对照化合物。Viloxazine (Viloxazin) 是一种去甲肾上腺素重摄取 (norepinephrine reuptake) 抑制剂,也是有效的 5-HT2C 激动剂和 5-HT2B 拮抗剂,对 5-HT2C 的 EC50 为 32 μM,对 5-HT2B 的 IC50 为 27 μM。Viloxazine 的作用机制主要涉及血清素能和去甲肾上腺素能通路。Viloxazine 可用于抗抑郁研究。

[ 相关类别 ]:

信号通路 >> 其他 >> 其他
研究领域 >> 神经疾病

[参考文献]

[1]. Yu C, et al. New Insights into the Mechanism of Action of Viloxazine: Serotonin and Norepinephrine Modulating Properties. J Exp Pharmacol. 2020 Aug 25;12:285-300.  

[2]. Pinder RM, et al. Viloxazine: a review of its pharmacological properties and therapeutic efficacy in depressive illness. Drugs. 1977 Jun;13(6):401-21.  

2-[(2-乙氧基苯氧基)甲基]吗啉盐酸盐物理化学性质

[ 密度 ]:
1.061g/cm3

[ 沸点 ]:
350.5ºC at 760mmHg

[ 分子式 ]:
C13H20ClNO3

[ 分子量 ]:
273.76

[ 闪点 ]:
144.3ºC

[ 精确质量 ]:
273.11300

[ PSA ]:
39.72000

[ LogP ]:
2.58330

2-[(2-乙氧基苯氧基)甲基]吗啉盐酸盐毒性和生态

CHEMICAL IDENTIFICATION

RTECS NUMBER :
QE3950000
CHEMICAL NAME :
Morpholine, 2-((2-ethoxyphenoxy)methyl)-, hydrochloride
CAS REGISTRY NUMBER :
35604-67-2
LAST UPDATED :
199209
DATA ITEMS CITED :
9
MOLECULAR FORMULA :
C13-H19-N-O3.Cl-H
MOLECULAR WEIGHT :
273.79
WISWESSER LINE NOTATION :
T6M DOTJ C1OR BO2 &GH

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Human
DOSE/DURATION :
25 mg/kg/6D
TOXIC EFFECTS :
Behavioral - hallucinations, distorted perceptions Behavioral - convulsions or effect on seizure threshold
REFERENCE :
BMJOAE British Medical Journal. (British Medical Assoc., BMA House, Tavistock Sq., London WC1H 9JR, UK) V.1- 1857- Volume(issue)/page/year: 2,96,1977
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Human - woman
DOSE/DURATION :
30 mg/kg
TOXIC EFFECTS :
Sense Organs and Special Senses (Eye) - mydriasis (pupillary dilation) Behavioral - sleep
REFERENCE :
JIMRBV Journal of International Medical Research. (Cambridge Medical Pub. Ltd., 435/437 Wellingborough Rd., Northampton, NN1 4EZ, UK) V.1- 1972- Volume(issue)/page/year: 4,83,1976
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
2 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JIMRBV Journal of International Medical Research. (Cambridge Medical Pub. Ltd., 435/437 Wellingborough Rd., Northampton, NN1 4EZ, UK) V.1- 1972- Volume(issue)/page/year: 4,83,1976
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
162 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
FRPSAX Farmaco, Edizione Scientifica. (Casella Postale 227, 27100 Pavia, Italy) V.8-43 1953-88 For publisher information, see FRMCE8 Volume(issue)/page/year: 35,812,1980
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
60 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JIMRBV Journal of International Medical Research. (Cambridge Medical Pub. Ltd., 435/437 Wellingborough Rd., Northampton, NN1 4EZ, UK) V.1- 1972- Volume(issue)/page/year: 4,83,1976
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
480 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
DDREDK Drug Development Research. (Alan R. Liss, Inc., 41 E. 11th St., New York, NY 10003) V.1- 1981- Volume(issue)/page/year: 22,385,1991
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
162 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
FRPSAX Farmaco, Edizione Scientifica. (Casella Postale 227, 27100 Pavia, Italy) V.8-43 1953-88 For publisher information, see FRMCE8 Volume(issue)/page/year: 35,812,1980
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
60 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JIMRBV Journal of International Medical Research. (Cambridge Medical Pub. Ltd., 435/437 Wellingborough Rd., Northampton, NN1 4EZ, UK) V.1- 1972- Volume(issue)/page/year: 4,83,1976 *** REVIEWS *** TOXICOLOGY REVIEW DRUGAY Drugs. International Journal of Current Therapeutics and Applied Pharmacology Reviews. (ADIS Press International Inc., Suite B-30, Oxford Ct. Business Center, 582 Middletown Blvd., Langhorne, PA 19047) V.1- 1971- Volume(issue)/page/year: 13,401,1977

2-[(2-乙氧基苯氧基)甲基]吗啉盐酸盐安全信息

[ 海关编码 ]:
2934999090

2-[(2-乙氧基苯氧基)甲基]吗啉盐酸盐上下游产品

2-[(2-乙氧基苯氧基)甲基]吗啉盐酸盐上游产品

2-[(2-乙氧基苯氧基)甲基]吗啉盐酸盐下游产品

2-[(2-乙氧基苯氧基)甲基]吗啉盐酸盐海关

[ 海关编码 ]: 2934999090

[ 中文概述 ]:
2934999090. 其他杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%

[ 申报要素 ]: 品名, 成分含量, 用途

[ Summary ]:
2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

推荐生产厂家/供应商:

公司名:上海阿拉丁生化科技股份有限公司

区域:上海市浦东新区

价格:
¥2099.0/1mg ¥需询单/1g ¥需询单/1g ¥需询单/1g

联系人:阿拉丁李高志

产品详情:盐酸拉氯嗪


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