Naltrexone methylbromide

Naltrexone methylbromide Structure
CAS No.
73232-52-7
Chemical Name:
Naltrexone methylbromide
Synonyms
MNTX;Moa-728;Relistor;Unii-rfo6il3D3m;Adamantane Impurity 52;Naltrexone methobromide;Methylnaltrexone bromide;Naltrexone methylbromide;Methyhaaltrexone broMide;N-Methyl Naltrexone BroMide
CBNumber:
CB11105859
Molecular Formula:
C21H26BrNO4
Molecular Weight:
436.35
MOL File:
73232-52-7.mol
Modify Date:
2024/3/19 15:37:50

Naltrexone methylbromide Properties

Melting point 237-239°C
storage temp. -20°C
solubility H2O: ≥5mg/mL
form powder
color white to beige
Stability Hygroscopic

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS06,GHS09
Signal word  Danger
Hazard statements  H301-H400
Precautionary statements  P273-P301+P310
Hazard Codes  T,N
Risk Statements  25-50
Safety Statements  45-61
RIDADR  UN 2811 6.1 / PGIII
WGK Germany  3
RTECS  QD0188550
HS Code  2934990002
NFPA 704
0
3 0

Naltrexone methylbromide Chemical Properties,Uses,Production

Description

The widespread efficacy of opioids in treating patients with moderate to severe acute and chronic pain is often accompanied by untoward side effects. In particular, opioid-induced bowel dysfunction is one of the more common and debilitating consequences afflicting up to 50% of patients. To counteract the peripherally-mediated adverse effects, opioid antagonists such as naloxone, naltrexone, and nalmephene are sometimes prescribed. The latest market entry exploits a strategic modification of naltrexone to lower its lipid solubility and increase its polarity: quaternization of the amine of naltrexone by methylation (methyl bromide) prevents crossing of the blood–brain barrier thereby creating an effective peripheral antagonist. Despite a loss of potency upon methylation, methylnaltrexone antagonizes opioid binding at m-opioid receptors with an IC50 of 70 nM. Its affinity for k-opioid receptors is approximately eightfold less (IC50= 575 nM) with no significant binding to d-opioid, orphanin, or non-opioid receptors. Methylnaltrexone bromide has been approved for the treatment of opioid-induced constipation in patients with advanced illness receiving palliative care.Regarding metabolism, methylnaltrexone bromide is eliminated primarily as intact drug (85% based on administered radioactivity) by slightly more renal than hepatic clearance.
The most common adverse events were abdominal pain and flatulence followed by nausea, dizziness, and diarrhea.

Chemical Properties

Pale Pink Solid

Uses

A metabolite of Naltrexone (N285750). Methylnaltrexone (MNTX), a selective μ-opioid receptor antagonist, functions as a peripherally acting receptor antagonist in tissues of the gastrointestinal tract.

General Description

Methylnaltrexone does not cross blood brain barrier and does not affect the opioid effects in the brain, such as analgesia. It is used to treat opioid-induced constipation (OIC).

Naltrexone methylbromide Preparation Products And Raw materials

Raw materials

Preparation Products

Naltrexone methylbromide Suppliers

Global( 74)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
Rusan Pharma Ltd +91-2228687035 +91-9690022465 Maharashtra, India 14 58 Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
Pharmaffiliates Analytics and Synthetics P. Ltd +91-172-5066494 Haryana, India 6773 58 Inquiry
Henan Tianfu Chemical Co.,Ltd. +86-0371-55170693 +86-19937530512 China 21667 55 Inquiry
Shenzhen Nexconn Pharmatechs Ltd +86-755-89396905 +86-15013857715 China 10311 58 Inquiry
CONIER CHEM AND PHARMA LIMITED +8618523575427 China 49392 58 Inquiry
SIMAGCHEM CORP +86-13806087780 China 17367 58 Inquiry
TargetMol Chemicals Inc. +1-781-999-5354 +1-00000000000 United States 19892 58 Inquiry
Career Henan Chemica Co +86-0371-86658258 +8613203830695 China 30250 58 Inquiry
Win-Win chemical CO., Limited +86-0086-577-64498589 +86-15355981851 China 14351 58 Inquiry

73232-52-7(Naltrexone methylbromide)Related Search:

Naltrexone methobromide Naltrexone methylbromide Moa-728 Morphinanium, 17-(cyclopropylmethyl)-4,5-epoxy-3,14-dihydroxy-17-methyl-6-oxo-, bromide, (5alpha)- Relistor Unii-rfo6il3D3m Methylnaltrexone bromide (5alpha)-17-(Cyclopropylmethyl)-4,5-epoxy-3,14-dihydroxy-17-methyl-6-oxomorphinanium bromide N-Methyl Naltrexone BroMide (5α)-17-(CyclopropylMethyl)-4,5-epoxy-3,14-dihydroxy-17-Methyl-6-oxoMorphinaniuM BroMide N-CyclopropylMethyl-noroxyMorphone MethobroMide Methyhaaltrexone broMide 17-(CyclopropylMethyl)-4,5-epoxy-3,14-dihydroxy-17-Methyl-6-oxoMorphinaniuM broMide MNTX Quaternary ammonium naltrexone 17-(Cyclopropylmethyl)-4,5A-Epoxy-3,14-Dihydroxy-17-Methyl-6-Oxomorphinanium Bromide Methylnaltrexone Peak Identification Mixture Cll (4R,4aS,7aR,12bS)-3-(cyclopropylmethyl)-4a,9-dihydroxy-3-methyl-2,4,5,6,7a,13-hexahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline-3-ium-7-one,bromide Methylnaltrexone iodide salt N-Methyl Naltrexone Bromide (1.0mg/ml in DMSO) Methylnaltrexone Bromide (1430735) inhibit,Opioid Receptor,suppression,gastrointestinal,Methylnaltrexone bromide,blood-brain,tract,peripheral,barrier,analgesia,Inhibitor Adamantane Impurity 52 73232-52-7 C21H26NO4Br Aromatics Heterocycles Intermediates & Fine Chemicals Metabolites & Impurities Pharmaceuticals