物质信息

ID:1058

名称和标识
商标名
NarconNaloneNarcanNarcanti
别名
N-AllylnoroxymorphoneEN 1530 BaseNalossone [Dcit]Naloxonum [INN-Latin]NaloxoneNaloxona [INN-Spanish]L-NaloxoneNaloxone HCl
IUPAC传统名
naloxone
IUPAC标准名
(1S,5R,13R,17S)-10,17-dihydroxy-4-(prop-2-en-1-yl)-12-oxa-4-azapentacyclo[9.6.1.0^{1,13}.0^{5,17}.0^{7,18}]octadeca-7(18),8,10-trien-14-one
数据登录号
PubChem SID
PubChem CID
CAS号
化合物性质
理化性质
疏水性(logP)
0.6
溶解度
Soluble
描述信息
Drug Groups
approved
Description
A specific opiate antagonist that has no agonist activity. It is a competitive antagonist at mu, delta, and kappa opioid receptors. [PubChem]
Indication
For the complete or partial reversal of narcotic depression, including respiratory depression, induced by opioids including natural and synthetic narcotics, propoxyphene, methadone and the narcotic-antagonist analgesics: nalbuphine, pentazocine and butorphanol.
Pharmacology
Naloxone is an opiate antagonist and prevents or reverses the effects of opioids including respiratory depression, sedation and hypotension. Also, it can reverse the psychotomimetic and dysphoric effects of agonist-antagonists such as pentazocine. Naloxone is an essentially pure narcotic antagonist, i.e., it does not possess the "agonistic" or morphine-like properties characteristic of other narcotic antagonists; naloxone does not produce respiratory depression, psychotomimetic effects or pupillary constriction. In the absence of narcotics or agonistic effects of other narcotic antagonists, it exhibits essentially no pharmacologic activity.
Affected Organisms
Humans and other mammals
Biotransformation
Hepatic.
Absorption
Well absorbed following intramuscular injection.
Half Life
30-81 minutes
External Links
分子图谱
暂无数据
点击上传数据
参考文献
暂无数据
点击上传数据