Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C17H25N5O2.2ClH |
| Molecular Weight | 404.335 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.Cl.CC(C)(C)NCC(O)COC1=CC=CC=C1C2=NN=C(NN)C=C2
InChI
InChIKey=JXYMAOJZCNBDTB-UHFFFAOYSA-N
InChI=1S/C17H25N5O2.2ClH/c1-17(2,3)19-10-12(23)11-24-15-7-5-4-6-13(15)14-8-9-16(20-18)22-21-14;;/h4-9,12,19,23H,10-11,18H2,1-3H3,(H,20,22);2*1H
| 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 |
| Molecular Formula | C17H25N5O2 |
| Molecular Weight | 331.4127 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Prizidilol (also known as SKF 92657) is arylpyridazinylhydrazine derivative patented by Smith Kline and French Laboratories Ltd. as an antihypertensive agent. In clinical trials, Supine and standing blood pressure measured 24--27 h after drug intake was reduced Slight but significant decreases in heart rate were seen after moderate doses of prizidilol. A more pronounced blood pressure reduction was noticed 2--7 h after drug administration. Prizidilol was well tolerated, although dizziness and tiredness were reported by four patients and edema by two.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Clinical pharmacology and pharmacokinetics of prizidilol in hypertensive patients. | 1983-11-01 |
|
| Studies on the autonomic nervous system with SK&F 92657, a new antihypertensive agent causing direct arterial vasodilatation and beta-adrenoceptor blockade. | 1981-03-01 |
|
| Hemodynamic profile of a new antihypertensive agent D,L-3-[2-(3-t-butylamino-2-hydroxypropoxy)phenyl]-6-hydrazinopyridazine (SK&F 92657). | 1981-03-01 |
|
| SK&F 92657, a novel antihypertensive acting by precapillary vasodilatation and beta-adrenoreceptor blockade. | 1979-12 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6196556
600 mg
Route of Administration:
Oral
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:58:50 GMT 2025
by
admin
on
Mon Mar 31 17:58:50 GMT 2025
|
| Record UNII |
U6QG1RWA7B
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C29576
Created by
admin on Mon Mar 31 17:58:50 GMT 2025 , Edited by admin on Mon Mar 31 17:58:50 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
DTXSID60979869
Created by
admin on Mon Mar 31 17:58:50 GMT 2025 , Edited by admin on Mon Mar 31 17:58:50 GMT 2025
|
PRIMARY | |||
|
73793-66-5
Created by
admin on Mon Mar 31 17:58:50 GMT 2025 , Edited by admin on Mon Mar 31 17:58:50 GMT 2025
|
PRIMARY | |||
|
C76558
Created by
admin on Mon Mar 31 17:58:50 GMT 2025 , Edited by admin on Mon Mar 31 17:58:50 GMT 2025
|
PRIMARY | |||
|
U6QG1RWA7B
Created by
admin on Mon Mar 31 17:58:50 GMT 2025 , Edited by admin on Mon Mar 31 17:58:50 GMT 2025
|
PRIMARY | |||
|
71951
Created by
admin on Mon Mar 31 17:58:50 GMT 2025 , Edited by admin on Mon Mar 31 17:58:50 GMT 2025
|
PRIMARY | |||
|
63642-19-3
Created by
admin on Mon Mar 31 17:58:50 GMT 2025 , Edited by admin on Mon Mar 31 17:58:50 GMT 2025
|
SUPERSEDED | |||
|
300000055017
Created by
admin on Mon Mar 31 17:58:50 GMT 2025 , Edited by admin on Mon Mar 31 17:58:50 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
SOLVATE->ANHYDROUS | |||
|
|
PARENT -> SALT/SOLVATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |