Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H12FN3 |
| Molecular Weight | 193.2208 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC=C(F)C=C1NC2=NCCN2
InChI
InChIKey=UYIZEUBMWCOJFF-UHFFFAOYSA-N
InChI=1S/C10H12FN3/c1-7-2-3-8(11)6-9(7)14-10-12-4-5-13-10/h2-3,6H,4-5H2,1H3,(H2,12,13,14)
| Molecular Formula | C10H12FN3 |
| Molecular Weight | 193.2208 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Effect of flutonidine on ouabain-induced arrhythmias and lethality in guinea-pig. | 1993-05-01 |
|
| Diuretic effects of flutonidine, a newer clonidine analog. | 1987-01 |
|
| [Long-term treatment with a new antihypertensive drug: flutonidin]. | 1983-05-19 |
|
| alpha-Adrenoceptor activity of flutonidine (ST 600) in rat anococcygeus muscle and rabbit jejunum. | 1982-04 |
|
| A comparative trial of timolol and flutonidin as antihypertensive agents. | 1982-02 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:08:46 GMT 2025
by
admin
on
Mon Mar 31 18:08:46 GMT 2025
|
| Record UNII |
ZCC19F3X8K
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C29709
Created by
admin on Mon Mar 31 18:08:46 GMT 2025 , Edited by admin on Mon Mar 31 18:08:46 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
ZCC19F3X8K
Created by
admin on Mon Mar 31 18:08:46 GMT 2025 , Edited by admin on Mon Mar 31 18:08:46 GMT 2025
|
PRIMARY | |||
|
CHEMBL2106760
Created by
admin on Mon Mar 31 18:08:46 GMT 2025 , Edited by admin on Mon Mar 31 18:08:46 GMT 2025
|
PRIMARY | |||
|
DTXSID90182405
Created by
admin on Mon Mar 31 18:08:46 GMT 2025 , Edited by admin on Mon Mar 31 18:08:46 GMT 2025
|
PRIMARY | |||
|
65761
Created by
admin on Mon Mar 31 18:08:46 GMT 2025 , Edited by admin on Mon Mar 31 18:08:46 GMT 2025
|
PRIMARY | |||
|
SUB07763MIG
Created by
admin on Mon Mar 31 18:08:46 GMT 2025 , Edited by admin on Mon Mar 31 18:08:46 GMT 2025
|
PRIMARY | |||
|
100000080405
Created by
admin on Mon Mar 31 18:08:46 GMT 2025 , Edited by admin on Mon Mar 31 18:08:46 GMT 2025
|
PRIMARY | |||
|
C010227
Created by
admin on Mon Mar 31 18:08:46 GMT 2025 , Edited by admin on Mon Mar 31 18:08:46 GMT 2025
|
PRIMARY | |||
|
C65741
Created by
admin on Mon Mar 31 18:08:46 GMT 2025 , Edited by admin on Mon Mar 31 18:08:46 GMT 2025
|
PRIMARY | |||
|
28125-87-3
Created by
admin on Mon Mar 31 18:08:46 GMT 2025 , Edited by admin on Mon Mar 31 18:08:46 GMT 2025
|
PRIMARY | |||
|
3590
Created by
admin on Mon Mar 31 18:08:46 GMT 2025 , Edited by admin on Mon Mar 31 18:08:46 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |