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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
Structure of METHYLNALTREXONE, (17S)-

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

HIDE SMILES / InChI

Molecular Formula C21H25NO4
Molecular Weight 355.4275
Charge 0
Count
Stereochemistry EPIMERIC
Additional Stereochemistry No
Defined Stereocenters 4 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
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

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).

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P35372|||G8XRH8|||Q5TDA1|||Q9UN57
Gene ID: 4988.0
Gene Symbol: OPRM1
Target Organism: Homo sapiens (Human)
70.0 nM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
Relistor

Approved Use

indicated 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 Date

2009
PubMed

PubMed

TitleDatePubMed
Reversal of morphine-induced catalepsy in the rat by narcotic antagonists and their quaternary derivatives.
1983 Mar
Involvement of substance P and central opioid receptors in morphine modulation of the CHS response.
2001 Apr 2
Pharmacokinetic profile of epidurally administered methylnaltrexone, a novel peripheral opioid antagonist in a rabbit model.
2001 Jan
Opioid antagonists in the treatment of opioid-induced constipation and pruritus.
2001 Jan
A review of the potential role of methylnaltrexone in opioid bowel dysfunction.
2001 Nov
Methylnaltrexone mechanisms of action and effects on opioid bowel dysfunction and other opioid adverse effects.
2007 Jun
Methylnaltrexone methobromide: the first peripherally active, centrally inactive opioid receptor-antagonist.
2009 Mar
Patents

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
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).
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:35:40 GMT 2023
Edited
by admin
on Fri Dec 15 16:35:40 GMT 2023
Record UNII
72Q1QQ555V
Record Status Validated (UNII)
Record Version
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Name Type Language
METHYLNALTREXONE, (17S)-
Common Name English
MORPHINAN-17-IUM-6-ONE, 17-(CYCLOPROPYLMETHYL)-4,5-EPOXY-3,14-DIHYDROXY-17-METHYL-, (5.ALPHA.,17S)-
Systematic Name English
MORPHINANIUM, 17-(CYCLOPROPYLMETHYL)-4,5-EPOXY-3,9-DIHYDROXY-17-METHYL-6-OXO-, (17S)-
Systematic Name English
METHYLNALTREXONE CATION, (17S)-
Common Name English
METHYLNALTREXONE ION, (17S)-
Common Name English
Code System Code Type Description
FDA UNII
72Q1QQ555V
Created by admin on Fri Dec 15 16:35:40 GMT 2023 , Edited by admin on Fri Dec 15 16:35:40 GMT 2023
PRIMARY
PUBCHEM
16088038
Created by admin on Fri Dec 15 16:35:40 GMT 2023 , Edited by admin on Fri Dec 15 16:35:40 GMT 2023
PRIMARY
CAS
916045-22-2
Created by admin on Fri Dec 15 16:35:40 GMT 2023 , Edited by admin on Fri Dec 15 16:35:40 GMT 2023
PRIMARY