Details
Stereochemistry | ACHIRAL |
Molecular Formula | C24H31N3O2 |
Molecular Weight | 393.5218 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@]12CC[C@]([H])(C[C@@H](C1)NC(=O)C3=CN(C4CCCCC4)C5=CC=CC=C5C3=O)N2C
InChI
InChIKey=RFXHBILZLMJCSN-GGPHIMKMSA-N
InChI=1S/C24H31N3O2/c1-26-18-11-12-19(26)14-16(13-18)25-24(29)21-15-27(17-7-3-2-4-8-17)22-10-6-5-9-20(22)23(21)28/h5-6,9-10,15-19H,2-4,7-8,11-14H2,1H3,(H,25,29)/t16-,18+,19-
Molecular Formula | C24H31N3O2 |
Molecular Weight | 393.5218 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Mirisetron (also known as WAY-100579) was developed as 5-HT3 receptor antagonist by Wyeth-Ayerst in the USA. This drug participated in clinical trials phase I for the treatment of anxiety disorders and for sleep disorders. In addition, in preclinical studies, the drug was used in cognition disorders. However, all these studies were discontinued.
Originator
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Comparison of the effects of the 5-HT3 receptor antagonists WAY-100579 and ondansetron on spatial learning in the water maze in rats with excitotoxic lesions of the forebrain cholinergic projection system. | 1996 May |
|
The effects of 5-HT3 receptor antagonists on cognitive performance in aged monkeys. | 1997 Jan-Feb |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:29:54 GMT 2023
by
admin
on
Fri Dec 15 18:29:54 GMT 2023
|
Record UNII |
9H3O05X8UL
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
135905-89-4
Created by
admin on Fri Dec 15 18:29:55 GMT 2023 , Edited by admin on Fri Dec 15 18:29:55 GMT 2023
|
PRIMARY | |||
|
SUB08992MIG
Created by
admin on Fri Dec 15 18:29:55 GMT 2023 , Edited by admin on Fri Dec 15 18:29:55 GMT 2023
|
PRIMARY | |||
|
C174577
Created by
admin on Fri Dec 15 18:29:55 GMT 2023 , Edited by admin on Fri Dec 15 18:29:55 GMT 2023
|
PRIMARY | |||
|
CHEMBL2110961
Created by
admin on Fri Dec 15 18:29:55 GMT 2023 , Edited by admin on Fri Dec 15 18:29:55 GMT 2023
|
PRIMARY | |||
|
60931
Created by
admin on Fri Dec 15 18:29:55 GMT 2023 , Edited by admin on Fri Dec 15 18:29:55 GMT 2023
|
PRIMARY | |||
|
C104926
Created by
admin on Fri Dec 15 18:29:55 GMT 2023 , Edited by admin on Fri Dec 15 18:29:55 GMT 2023
|
PRIMARY | |||
|
9H3O05X8UL
Created by
admin on Fri Dec 15 18:29:55 GMT 2023 , Edited by admin on Fri Dec 15 18:29:55 GMT 2023
|
PRIMARY | |||
|
100000080646
Created by
admin on Fri Dec 15 18:29:55 GMT 2023 , Edited by admin on Fri Dec 15 18:29:55 GMT 2023
|
PRIMARY | |||
|
7284
Created by
admin on Fri Dec 15 18:29:55 GMT 2023 , Edited by admin on Fri Dec 15 18:29:55 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
TARGET -> INHIBITOR |
|
||
|
SALT/SOLVATE -> PARENT |
|
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |
|