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纳曲酮

更新时间:2025-08-20 22:32:14

纳曲酮结构式
纳曲酮结构式
品牌特惠专场
常用名 纳曲酮 英文名 naltrexone
CAS号 16590-41-3 分子量 341.40
密度 1.5±0.1 g/cm3 沸点 558.1±50.0 °C at 760 mmHg
分子式 C20H23NO4 熔点 168-170ºC
MSDS N/A 闪点 291.4±30.1 °C
符号 GHS02 GHS06 GHS08
GHS02, GHS06, GHS08
信号词 Danger

 纳曲酮用途


Naltrexone 是 Opioid receptor 的拮抗剂。Naltrexone 在体内抑制细胞增殖。Naltrexone 通过干扰细胞信号和改变免疫系统来抑制肿瘤生长。

 纳曲酮名称

中文名 纳曲酮
英文名 naltrexone
中文别名 17-(环丙甲基)-4,5-环氧-3,14-二羟基吗啡烷-6-酮 | 纳屈酮
英文别名 更多

 纳曲酮物理化学性质

密度 1.5±0.1 g/cm3
沸点 558.1±50.0 °C at 760 mmHg
熔点 168-170ºC
分子式 C20H23NO4
分子量 341.40
闪点 291.4±30.1 °C
精确质量 341.162720
PSA 70.00000
LogP 1.80
InChIKey DQCKKXVULJGBQN-XFWGSAIBSA-N
SMILES O=C1CCC2(O)C3Cc4ccc(O)c5c4C2(CCN3CC2CC2)C1O5
蒸汽压 0.0±1.6 mmHg at 25°C
折射率 1.709
储存条件 库房通风低温干燥,与氧化剂,食品分开储运

 纳曲酮毒性和生态

 纳曲酮安全信息

符号 GHS02 GHS06 GHS08
GHS02, GHS06, GHS08
信号词 Danger
危害声明 H225-H301 + H311 + H331-H370
警示性声明 P210-P260-P280-P301 + P310-P311
危害码 (欧洲) F,T
风险声明 (欧洲) 11-23/24/25-39/23/24/25
安全声明 (欧洲) 16-36/37-45
危险品运输编码 UN1230 - class 3 - PG 2 - Methanol, solution

 纳曲酮合成线路

 纳曲酮文献62

更多文献
Novel orally available salvinorin A analog PR-38 inhibits gastrointestinal motility and reduces abdominal pain in mouse models mimicking irritable bowel syndrome.

J. Pharmacol. Exp. Ther. 350(1) , 69-78, (2014)

The opioid and cannabinoid systems play a crucial role in multiple physiological processes in the central nervous system and in the periphery. Selective opioid as well as cannabinoid (CB) receptor ago...

Desensitization of functional µ-opioid receptors increases agonist off-rate.

Mol. Pharmacol. 86(1) , 52-61, (2014)

Desensitization of µ-opioid receptors (MORs) develops over 5-15 minutes after the application of some, but not all, opioid agonists and lasts for tens of minutes after agonist removal. The decrease in...

Treatment of alcohol dependence: recent progress and reduction of consumption.

Minerva Med. 105(6) , 447-66, (2014)

Alcohol dependence (AD) is a major public health problem. Currently, three drugs for the treatment of AD have been approved by both the European Medicines Agency (EMA) and the Food and Drug Administra...

 纳曲酮靶点实验

查看更多实验

实验名称:Permeability coefficient, Kp in human Caco2 cells
来源:ChEMBL
靶标:N/A
External Id:CHEMBL4411126
实验名称:Primary qHTS assay for inhibitors of alpha-synuclein gene (SNCA) expression
来源:NCGC
External Id:SNCA-p-activity-luciferase
实验名称:Displacement of [3H]-DPN from recombinant human mu opioid receptor expressed in CHO-K...
来源:ChEMBL
靶标:Mu-type opioid receptor
External Id:CHEMBL4411118
实验名称:Displacement of [3H]-DPN from recombinant human delta opioid receptor expressed in CH...
来源:ChEMBL
靶标:Delta-type opioid receptor
External Id:CHEMBL4411119
实验名称:Displacement of [3H]-DPN from guinea pig kappa opioid receptor expressed in CHO-K1 ce...
来源:ChEMBL
靶标:Kappa-type opioid receptor
External Id:CHEMBL4411120
实验名称:Antagonist activity at human recombinant mu opioid receptor expressed in CHO-K1 cell ...
来源:ChEMBL
靶标:Mu-type opioid receptor
External Id:CHEMBL4411121
实验名称:Half life in rat liver microsomes at 3 uM
来源:ChEMBL
靶标:N/A
External Id:CHEMBL4411123
实验名称:Quantitative High-Throughput drug screen in 47 multiple myeloma cell lines against th...
来源:NCGC
靶标:N/A
External Id:s-my-keats_OPM1-m4-1
实验名称:Quantitative High-Throughput drug screen in 47 multiple myeloma cell lines against th...
来源:NCGC
靶标:N/A
External Id:s-my-OC1MY5-m4-1
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 纳曲酮英文别名

Trexonil
NeMexin
(1S,5R,13R,17S)-4-(Cyclopropylmethyl)-10,17-dihydroxy-12-oxa-4-azapentacyclo[9.6.1.0.0.0]octadeca-7(18),8,10-trien-14-on
Depotrex
ReVia
en1939
Naltrel
en1639
Naltrexone
Vivitrol
(5α)-17-(Cyclopropylmethyl)-3,14-dihydroxy-4,5-epoxymorphinan-6-one
Antaxone
trexan
(1S,5R,13R,17S)-4-(cyclopropylmethyl)-10,17-dihydroxy-12-oxa-4-azapentacyclo[9.6.1.0.0.0]octadeca-7(18),8,10-trien-14-one
(1S,5R,13R,17S)-4-(cyclopropylméthyl)-10,17-dihydroxy-12-oxa-4-azapentacyclo[9.6.1.0.0.0]octadéca-7(18),8,10-trién-14-one
celupan
En 1639A
Um-792
(5a)-17-(Cyclopropylmethyl)-4,5-epoxy-3,14-dihydroxymorphinan-6-one
Nalorex
Depade
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