Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C17H23N5O2 |
| Molecular Weight | 329.3968 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC2=C(C=C1OC)C(N)=NC(=N2)N3CCN(CC=C)CC3
InChI
InChIKey=HSIPLPKNLDWHSE-UHFFFAOYSA-N
InChI=1S/C17H23N5O2/c1-4-5-21-6-8-22(9-7-21)17-19-13-11-15(24-3)14(23-2)10-12(13)16(18)20-17/h4,10-11H,1,5-9H2,2-3H3,(H2,18,19,20)
| Molecular Formula | C17H23N5O2 |
| Molecular Weight | 329.3968 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Quinazosin is a diaminoquinazoline derivative patented by Pfizer, Chas., and Co., Inc. as a hypotensive agent. Quinazosin acts as adrenoreceptor antagonist and in preclinical studies lowered systolic blood pressure in conscious hypertensive dogs, without having any significant effect on their heart rate. Quinazosin lowered blood pressure and reduced total peripheral vascular resistance, while the duration of these effects was dose-dependent. In cats, Quinazosin reduced or reversed the pressor effects of epinephrine, but did not alter those of angiotensin amide.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:38:02 GMT 2025
by
admin
on
Mon Mar 31 21:38:02 GMT 2025
|
| Record UNII |
436XK6QFMR
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C29713
Created by
admin on Mon Mar 31 21:38:02 GMT 2025 , Edited by admin on Mon Mar 31 21:38:02 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
27486
Created by
admin on Mon Mar 31 21:38:02 GMT 2025 , Edited by admin on Mon Mar 31 21:38:02 GMT 2025
|
PRIMARY | |||
|
C72924
Created by
admin on Mon Mar 31 21:38:02 GMT 2025 , Edited by admin on Mon Mar 31 21:38:02 GMT 2025
|
PRIMARY | |||
|
100000081107
Created by
admin on Mon Mar 31 21:38:02 GMT 2025 , Edited by admin on Mon Mar 31 21:38:02 GMT 2025
|
PRIMARY | |||
|
2321
Created by
admin on Mon Mar 31 21:38:02 GMT 2025 , Edited by admin on Mon Mar 31 21:38:02 GMT 2025
|
PRIMARY | |||
|
436XK6QFMR
Created by
admin on Mon Mar 31 21:38:02 GMT 2025 , Edited by admin on Mon Mar 31 21:38:02 GMT 2025
|
PRIMARY | |||
|
Quinazosin
Created by
admin on Mon Mar 31 21:38:02 GMT 2025 , Edited by admin on Mon Mar 31 21:38:02 GMT 2025
|
PRIMARY | |||
|
CHEMBL2111007
Created by
admin on Mon Mar 31 21:38:02 GMT 2025 , Edited by admin on Mon Mar 31 21:38:02 GMT 2025
|
PRIMARY | |||
|
DTXSID40166331
Created by
admin on Mon Mar 31 21:38:02 GMT 2025 , Edited by admin on Mon Mar 31 21:38:02 GMT 2025
|
PRIMARY | |||
|
15793-38-1
Created by
admin on Mon Mar 31 21:38:02 GMT 2025 , Edited by admin on Mon Mar 31 21:38:02 GMT 2025
|
PRIMARY | |||
|
SUB10203MIG
Created by
admin on Mon Mar 31 21:38:02 GMT 2025 , Edited by admin on Mon Mar 31 21:38:02 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |