Details
Stereochemistry | UNKNOWN |
Molecular Formula | C10H17NO2 |
Molecular Weight | 183.2475 |
Optical Activity | ( + ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC1(CC)C(=O)NCC(C)C1=O
InChI
InChIKey=SIDLZWOQUZRBRU-UHFFFAOYSA-N
InChI=1S/C10H17NO2/c1-4-10(5-2)8(12)7(3)6-11-9(10)13/h7H,4-6H2,1-3H3,(H,11,13)
Molecular Formula | C10H17NO2 |
Molecular Weight | 183.2475 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
DescriptionSources: https://www.drugs.com/mmx/methyprylon.html
Sources: https://www.drugs.com/mmx/methyprylon.html
Methyprylon (brand name Noludar) is a sedative agent, which used to treat insomnia. But then the drug was replaced in the market by another drugs with less side effects. The precise mechanism of action is not known, but was made suggestion, that methyprylon increases the effects of gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter in the brain.
CNS Activity
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL2093872 Sources: https://www.ncbi.nlm.nih.gov/pubmed/16792 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | NOLUDAR Approved UseUnknown |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
5.62 mg/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/2866242 |
300 mg single, oral dose: 300 mg route of administration: Oral experiment type: SINGLE co-administered: |
METHYPRYLON plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
AUC
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
74.75 mg × h/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/2866242 |
300 mg single, oral dose: 300 mg route of administration: Oral experiment type: SINGLE co-administered: |
METHYPRYLON plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
9.2 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/2866242 |
300 mg single, oral dose: 300 mg route of administration: Oral experiment type: SINGLE co-administered: |
METHYPRYLON plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
Doses
Dose | Population | Adverse events |
---|---|---|
30 g single, oral Overdose Dose: 30 g Route: oral Route: single Dose: 30 g Co-administed with:: dimenhydrinate(one hundred 50-mg capsules) Sources: |
unhealthy, 36 years n = 1 Health Status: unhealthy Age Group: 36 years Sex: F Population Size: 1 Sources: |
Other AEs: Comatose... |
AEs
AE | Significance | Dose | Population |
---|---|---|---|
Comatose | 1 patient | 30 g single, oral Overdose Dose: 30 g Route: oral Route: single Dose: 30 g Co-administed with:: dimenhydrinate(one hundred 50-mg capsules) Sources: |
unhealthy, 36 years n = 1 Health Status: unhealthy Age Group: 36 years Sex: F Population Size: 1 Sources: |
PubMed
Title | Date | PubMed |
---|---|---|
Hypnotic efficacy of triazolam and methyprylon ininsomniac in-patients. | 1976 |
|
Pharmacokinetics of methyprylon following a single oral dose. | 1985 Sep |
|
Nonlinear elimination of methyprylon (noludar) in an overdosed patient: correlation of clinical effects with plasma concentration. | 1991 Aug |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/16792
300 mg once a day before bedtime.
Route of Administration:
Oral
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 10:40:59 GMT 2023
by
admin
on
Sat Dec 16 10:40:59 GMT 2023
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Record UNII |
P66Z3UR32T
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Record Status |
Validated (UNII)
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Record Version |
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-
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