Details
| Stereochemistry | RACEMIC |
| 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 |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Nonlinear elimination of methyprylon (noludar) in an overdosed patient: correlation of clinical effects with plasma concentration. | 1991-08 |
|
| Pharmacokinetics of methyprylon following a single oral dose. | 1985-09 |
|
| Hypnotic efficacy of triazolam and methyprylon ininsomniac in-patients. | 1976 |
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
Mon Mar 31 18:30:15 GMT 2025
by
admin
on
Mon Mar 31 18:30:15 GMT 2025
|
| Record UNII |
CUT48I42ON
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
WHO-VATC |
QN05CE02
Created by
admin on Mon Mar 31 18:30:15 GMT 2025 , Edited by admin on Mon Mar 31 18:30:15 GMT 2025
|
||
|
NCI_THESAURUS |
C29756
Created by
admin on Mon Mar 31 18:30:15 GMT 2025 , Edited by admin on Mon Mar 31 18:30:15 GMT 2025
|
||
|
DEA NO. |
2575
Created by
admin on Mon Mar 31 18:30:15 GMT 2025 , Edited by admin on Mon Mar 31 18:30:15 GMT 2025
|
||
|
WHO-ATC |
N05CE02
Created by
admin on Mon Mar 31 18:30:15 GMT 2025 , Edited by admin on Mon Mar 31 18:30:15 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
6910
Created by
admin on Mon Mar 31 18:30:15 GMT 2025 , Edited by admin on Mon Mar 31 18:30:15 GMT 2025
|
PRIMARY | RxNorm | ||
|
DTXSID7023306
Created by
admin on Mon Mar 31 18:30:15 GMT 2025 , Edited by admin on Mon Mar 31 18:30:15 GMT 2025
|
PRIMARY | |||
|
3128
Created by
admin on Mon Mar 31 18:30:15 GMT 2025 , Edited by admin on Mon Mar 31 18:30:15 GMT 2025
|
PRIMARY | |||
|
C66122
Created by
admin on Mon Mar 31 18:30:15 GMT 2025 , Edited by admin on Mon Mar 31 18:30:15 GMT 2025
|
PRIMARY | |||
|
30442
Created by
admin on Mon Mar 31 18:30:15 GMT 2025 , Edited by admin on Mon Mar 31 18:30:15 GMT 2025
|
PRIMARY | |||
|
4162
Created by
admin on Mon Mar 31 18:30:15 GMT 2025 , Edited by admin on Mon Mar 31 18:30:15 GMT 2025
|
PRIMARY | |||
|
287
Created by
admin on Mon Mar 31 18:30:15 GMT 2025 , Edited by admin on Mon Mar 31 18:30:15 GMT 2025
|
PRIMARY | |||
|
METHYPRYLON
Created by
admin on Mon Mar 31 18:30:15 GMT 2025 , Edited by admin on Mon Mar 31 18:30:15 GMT 2025
|
PRIMARY | |||
|
SUB08879MIG
Created by
admin on Mon Mar 31 18:30:15 GMT 2025 , Edited by admin on Mon Mar 31 18:30:15 GMT 2025
|
PRIMARY | |||
|
CHEMBL1200790
Created by
admin on Mon Mar 31 18:30:15 GMT 2025 , Edited by admin on Mon Mar 31 18:30:15 GMT 2025
|
PRIMARY | |||
|
1774
Created by
admin on Mon Mar 31 18:30:15 GMT 2025 , Edited by admin on Mon Mar 31 18:30:15 GMT 2025
|
PRIMARY | |||
|
DB01107
Created by
admin on Mon Mar 31 18:30:15 GMT 2025 , Edited by admin on Mon Mar 31 18:30:15 GMT 2025
|
PRIMARY | |||
|
204-745-4
Created by
admin on Mon Mar 31 18:30:15 GMT 2025 , Edited by admin on Mon Mar 31 18:30:15 GMT 2025
|
PRIMARY | |||
|
m7482
Created by
admin on Mon Mar 31 18:30:15 GMT 2025 , Edited by admin on Mon Mar 31 18:30:15 GMT 2025
|
PRIMARY | Merck Index | ||
|
7238
Created by
admin on Mon Mar 31 18:30:15 GMT 2025 , Edited by admin on Mon Mar 31 18:30:15 GMT 2025
|
PRIMARY | |||
|
125-64-4
Created by
admin on Mon Mar 31 18:30:15 GMT 2025 , Edited by admin on Mon Mar 31 18:30:15 GMT 2025
|
PRIMARY | |||
|
100000080891
Created by
admin on Mon Mar 31 18:30:15 GMT 2025 , Edited by admin on Mon Mar 31 18:30:15 GMT 2025
|
PRIMARY | |||
|
CUT48I42ON
Created by
admin on Mon Mar 31 18:30:15 GMT 2025 , Edited by admin on Mon Mar 31 18:30:15 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
METABOLITE -> PARENT |
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |