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AB120074

Naloxone hydrochloride, Opioid antagonist

Naloxone hydrochloride, Opioid antagonist

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(6 Publications)

MW 363.8 Da, Purity >98%. Competitive opioid antagonist. Achieve your results faster with highly validated, pure and trusted compounds.

查看别名

D-OR-1, Delta type opioid receptor DOR 1, Delta-type opioid receptor, K-OR-1, Kappa opioid receptor, Kappa-type opioid receptor, LMOR, M-OR-1, MOR, Mu opiate receptor, Mu opioid receptor, Mu-type opioid receptor, Nbor, OPRD 1, OPRD_HUMAN, OPRK 1, OPRK_HUMAN, OPRM1, OPRM_HUMAN, Opiate receptor kappa 1, Opioid receptor delta 1, Opioid receptor mu 1, Opioid receptor, kappa 1, Oprk2, R21, hMOP, mDOR

1 Images
Chemical Structure - Naloxone hydrochloride, Opioid antagonist (AB120074)
  • Chemical Structure

Lab

Chemical Structure - Naloxone hydrochloride, Opioid antagonist (AB120074)

2D chemical structure image of ab120074, Naloxone hydrochloride, Opioid antagonist

关键信息

CAS 号

357-08-4

纯度

>98%

形式

Solid

form

分子量

363.8 Da

分子式

C<sub>1</sub><sub>9</sub>H<sub>2</sub><sub>2</sub>ClNO<sub>4</sub>

PubChem

5464092

属性

Synthetic

溶解度

Soluble in water to 100 mM

生化试剂名称

Naloxone hydrochloride

生物学描述

Competitive opioid antagonist.

经典 SMILES

C=CCN1CCC23C4C(=O)CCC2(C1CC5=C3C(=C(C=C5)O)O4)O.Cl

同分异构的 SMILES

C=CCN1CC[C@]23[C@@H]4C(=O)CC[C@]2([C@H]1CC5=C3C(=C(C=C5)O)O4)O.Cl

InChi

InChI=1S/C19H21NO4.ClH/c1-2-8-20-9-7-18-15-11-3-4-12(21)16(15)24-17(18)13(22)5-6-19(18,23)14(20)10-11;/h2-4,14,17,21,23H,1,5-10H2;1H/t14-,17+,18+,19-;/m1./s1

InChiKey

RGPDIGOSVORSAK-STHHAXOLSA-N

IUPAC 名

(4R,4aS,7aR,12bS)-4a,9-dihydroxy-3-prop-2-enyl-2,4,5,6,7a,13-hexahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinolin-7-one;hydrochloride

性能和储存信息

运输条件
Ambient - Can Ship with Ice
推荐的短期储存条件
+4°C
推荐的长期储存条件
+4°C
储存信息
Store under desiccating conditions|The product can be stored for up to 12 months

补充信息

This supplementary information is collated from multiple sources and compiled automatically.

The Delta Opioid Receptor Kappa Opioid Receptor and Mu Opioid Receptor also known as DOR KOR and MOR are part of the opioid receptor family. These receptors are G-protein coupled receptors (GPCRs) that respond to endogenous opioids like endorphins and enkephalins as well as synthetic opioids. Each receptor type has a mass of approximately 40 kDa. Opioid receptors are mainly expressed in the central and peripheral nervous systems where they modulate pain perception mood and stress. Distinctions arise in their distribution: Delta and Mu receptors are common in the brain whereas Kappa receptors can be found in larger numbers in the spinal cord.
Biological function summary

Opioid receptors are integral to the modulation of pain and reward systems. They exist as monomers or dimers and can form higher-order complexes with each other or with other GPCRs to influence signal transduction pathways. When activated by their ligands they inhibit cyclic adenosine monophosphate (cAMP) production which reduces neuronal excitability. By interacting with ligand molecules like herkinorin dermorphin and Mu agonists these receptors contribute to the analgesic and euphoric effects typical of opioid ligands.

Pathways

Delta Kappa and Mu receptors play key roles in the endogenous opioid signaling pathways and the dopaminergic reward pathway. These pathways influence neurotransmitter release and neuronal activity often associated with the sensation of pain relief and reward. The dopaminergic pathway also involves proteins like the dopamine transporter protein which works alongside these opioid receptors to regulate dopamine levels in synaptic clefts. Opioid antagonists like naloxone interact with these pathways by blocking the opioid receptors to reverse opioid-induced effects.

The dysregulation of Delta Kappa and Mu opioid receptors associates with chronic pain and addiction. Mu opioid receptors in particular are linked to the development of opioid use disorder due to their involvement in reward processing. Delta receptors have been associated with mood disorders influencing symptoms through their complex interactions with other nervous system proteins. Researchers use compounds like naloxone hydrochloride an opioid antagonist to mitigate conditions related to these receptors. It serves not just as a therapeutic agent but also as a research tool to understand the roles of these receptors in disease contexts.

产品实验方案

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文献 (6)

Recent publications for all applications. Explore the full list and refine your search

Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics 21:e00377 PubMed38777742

2024

A synthetic peptide exerts nontolerance-forming antihyperalgesic and antidepressant effects in mice.

Applications

Unspecified application

Species

Unspecified reactive species

Yongjiang Wu,Xiaofei Song,YanZhe Ji,Gang Chen,Long Zhao

Science advances 9:eadf6521 PubMed37224253

2023

Transcriptomics reveals amygdala neuron regulation by fasting and ghrelin thereby promoting feeding.

Applications

Unspecified application

Species

Unspecified reactive species

Christian Peters,Songwei He,Federica Fermani,Hansol Lim,Wenyu Ding,Christian Mayer,Rüdiger Klein

European journal of oral sciences 127:408-416 PubMed31365768

2019

Effect of endomorphin-2 on orofacial pain induced by orthodontic tooth movement in rats.

Applications

Unspecified application

Species

Unspecified reactive species

Sixin Liu,Lu Liu,Yanlu Jiang,Jing Zhou,Huimin Hu,Zhouqiang Wu,Hu Long,Wenli Lai

eLife 8: PubMed31099753

2019

Synapse-specific opioid modulation of thalamo-cortico-striatal circuits.

Applications

Unspecified application

Species

Unspecified reactive species

William T Birdsong,Bart C Jongbloets,Kim A Engeln,Dong Wang,Grégory Scherrer,Tianyi Mao

eLife 7: PubMed29589831

2018

Cellular tolerance at the µ-opioid receptor is phosphorylation dependent.

Applications

Unspecified application

Species

Unspecified reactive species

Seksiri Arttamangkul,Daniel A Heinz,James R Bunzow,Xianqiang Song,John T Williams

Molecular pain 6:96 PubMed21172011

2010

Abnormal nociception and opiate sensitivity of STOP null mice exhibiting elevated levels of the endogenous alkaloid morphine.

Applications

Unspecified application

Species

Unspecified reactive species

Alexandre Charlet,Arnaud H Muller,Alexis Laux,Véronique Kemmel,Annie Schweitzer,Jean-Christophe Deloulme,Denise Stuber,François Delalande,Enrica Bianchi,Alain Van Dorsselaer,Dominique Aunis,Annie Andrieux,Pierrick Poisbeau,Yannick Goumon
View all publications

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