Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C21H26NO4 |
Molecular Weight | 356.4354 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 5 / 5 |
E/Z Centers | 0 |
Charge | 1 |
SHOW SMILES / InChI
SMILES
[H][C@]12OC3=C4C(C[C@]5([H])[C@](O)(CCC1=O)[C@]24CC[N@@+]5(C)CC6CC6)=CC=C3O
InChI
InChIKey=JVLBPIPGETUEET-UGTAXJHQSA-O
InChI=1S/C21H25NO4/c1-22(11-12-2-3-12)9-8-20-17-13-4-5-14(23)18(17)26-19(20)15(24)6-7-21(20,25)16(22)10-13/h4-5,12,16,19,25H,2-3,6-11H2,1H3/p+1/t16-,19+,20+,21-,22+/m1/s1
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/17504835Curator's Comment: Description was created using several sources including:
http://www.accessdata.fda.gov/drugsatfda_docs/label/2009/021964s006lbl.pdf
Sources: https://www.ncbi.nlm.nih.gov/pubmed/17504835
Curator's Comment: Description was created using several sources including:
http://www.accessdata.fda.gov/drugsatfda_docs/label/2009/021964s006lbl.pdf
Methylnaltrexone bromide, (17s)- (methylnaltrexone bromide), a quaternary amine of the pure narcotic antagonist naltrexone, is a peripherally-acting selective mu-opioid antagonist. Methylnaltrexone antagonizes opioid binding at mu-opioid receptors, half-maximal inhibitory concentration (IC50) of 70 nM. It has a relatively lower affinity for κ-opioid receptors (IC50 575 nM), and it does not interact with δ-receptors or orphanin FQ receptors. Approved by FDA in the United States under the trade name Relistor, methylnaltrexone bromide is indicated for the treatment of opioid-induced constipation in patients with advanced illness who are receiving palliative care, when the response to laxative therapy has not been sufficient. Restricted ability to cross the blood-brain barrier allows methylnaltrexone bromide to function in tissues such as the gastrointestinal tract, decreasing the constipating effects of opioids without impacting opioid-mediated analgesic effects on the central nervous system.
CNS Activity
Sources: https://www.ncbi.nlm.nih.gov/pubmed/19555136 | https://www.ncbi.nlm.nih.gov/pubmed/17504835
Curator's Comment: Methylnaltrexone in clinical doses, is unable to cross the blood brain barrier. Therefore, it can reverse the effect of opioids in the peripheral nervous system and relieve constipation without reversing the analgesic effect of opioids in the central nervous system (CNS).
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: P35372|||G8XRH8|||Q5TDA1|||Q9UN57 Gene ID: 4988.0 Gene Symbol: OPRM1 Target Organism: Homo sapiens (Human) |
70.0 nM [IC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Palliative | Relistor Approved Useindicated for the treatment of opioid-induced constipation in patients with advanced illness who are receiving palliative care, when response to laxative therapy has not been sufficient. Launch Date2009 |
PubMed
Title | Date | PubMed |
---|---|---|
Reversal of morphine-induced catalepsy in the rat by narcotic antagonists and their quaternary derivatives. | 1983 Mar |
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Involvement of substance P and central opioid receptors in morphine modulation of the CHS response. | 2001 Apr 2 |
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Pharmacokinetic profile of epidurally administered methylnaltrexone, a novel peripheral opioid antagonist in a rabbit model. | 2001 Jan |
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Opioid antagonists in the treatment of opioid-induced constipation and pruritus. | 2001 Jan |
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A review of the potential role of methylnaltrexone in opioid bowel dysfunction. | 2001 Nov |
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Methylnaltrexone mechanisms of action and effects on opioid bowel dysfunction and other opioid adverse effects. | 2007 Jun |
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Methylnaltrexone methobromide: the first peripherally active, centrally inactive opioid receptor-antagonist. | 2009 Mar |
Sample Use Guides
The recommended dose of Relistor, methylnaltrexone bromide, is 8 mg for patients weighing 38 to less than 62 kg (84 to less than 136 lb) or 12 mg for patients weighing 62 to 114 kg (136 to 251 lb). Patients whose weight falls outside of these ranges should be dosed at 0.15 mg/kg. The usual schedule is one dose every other day, as needed, but no more frequently than one dose in a 24-hour period.
Route of Administration:
Other
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/7781680
In the guinea-pig ileum preparation, methylnaltrexone at 30, 100 and 300 nM blocked 25 +/- 10.5%, 74 +/- 7.2% and 89 +/- 9.9% of morphine-induced (300 nM) inhibition, respectively. In the human intestine preparation, methylnaltrexone at the same concentrations blocked 57 +/- 10.9%, 74 +/- 12.9% and 92 +/- 7.2% of morphine-induced (100 nM) inhibition, respectively. The relative ratio of methylnaltrexone to morphine was higher in human intestine (1:1) than in the guinea-pig ileum preparation (1:3).
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16088038
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916045-22-2
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SUBSTANCE RECORD