Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C16H26N2.2ClH |
| Molecular Weight | 319.313 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.Cl.CN(C)CCN1CCC(CC2=CC=CC=C2)CC1
InChI
InChIKey=XZRWNULNYWMWBM-UHFFFAOYSA-N
InChI=1S/C16H26N2.2ClH/c1-17(2)12-13-18-10-8-16(9-11-18)14-15-6-4-3-5-7-15;;/h3-7,16H,8-14H2,1-2H3;2*1H
| Molecular Formula | C16H26N2 |
| Molecular Weight | 246.391 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Pimetine has been reported to be an antiatherogenic agent of particular interest since its activities are unrelated to blood cholesterol levels. Pimetine hydrochloride (IN 379) alters the production and utilization of acid mucopolysaeeharides and may block the formation of atherosclerotic plaque. The initial clinical evaluation of pimetine in neuropsychiatric disorders was performed in hospitalized patients with the diagnosis of "chronic brain syndrome". Behavioral effects of pimetine were increased alertness, interest and sociability with improvement in organization of thought processes. In patients suffering from chronic organic diseases, pimetine was reported to produce a feeling of "more energy", a general feeling of "well being" and mild insomnia was reported as a non-limiting side effect. Pimetine was found to be a less active stimulant than amphetamine.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6082309
Curator's Comment: Mongrel dogs data
Single dose - 1, 3 or 10 mg/kg
Route of Administration:
Intravenous
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:55:55 GMT 2025
by
admin
on
Mon Mar 31 18:55:55 GMT 2025
|
| Record UNII |
L9C364S02D
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Code | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
528880
Created by
admin on Mon Mar 31 18:55:55 GMT 2025 , Edited by admin on Mon Mar 31 18:55:55 GMT 2025
|
PRIMARY | |||
|
DTXSID80964474
Created by
admin on Mon Mar 31 18:55:55 GMT 2025 , Edited by admin on Mon Mar 31 18:55:55 GMT 2025
|
PRIMARY | |||
|
300000055522
Created by
admin on Mon Mar 31 18:55:55 GMT 2025 , Edited by admin on Mon Mar 31 18:55:55 GMT 2025
|
PRIMARY | |||
|
L9C364S02D
Created by
admin on Mon Mar 31 18:55:55 GMT 2025 , Edited by admin on Mon Mar 31 18:55:55 GMT 2025
|
PRIMARY | |||
|
CHEMBL2110969
Created by
admin on Mon Mar 31 18:55:55 GMT 2025 , Edited by admin on Mon Mar 31 18:55:55 GMT 2025
|
PRIMARY | |||
|
20055541
Created by
admin on Mon Mar 31 18:55:55 GMT 2025 , Edited by admin on Mon Mar 31 18:55:55 GMT 2025
|
PRIMARY | |||
|
C175843
Created by
admin on Mon Mar 31 18:55:55 GMT 2025 , Edited by admin on Mon Mar 31 18:55:55 GMT 2025
|
PRIMARY | |||
|
4991-68-8
Created by
admin on Mon Mar 31 18:55:55 GMT 2025 , Edited by admin on Mon Mar 31 18:55:55 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
PARENT -> SALT/SOLVATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |