Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C19H28N4O2S |
Molecular Weight | 376.516 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12CC3=CNC4=CC=CC(=C34)[C@@]1([H])C[C@@H](CN2C)NS(=O)(=O)N(CC)CC
InChI
InChIKey=YHEIHLVIKSTGJE-YXJHDRRASA-N
InChI=1S/C19H28N4O2S/c1-4-23(5-2)26(24,25)21-14-10-16-15-7-6-8-17-19(15)13(11-20-17)9-18(16)22(3)12-14/h6-8,11,14,16,18,20-21H,4-5,9-10,12H2,1-3H3/t14-,16+,18+/m0/s1
Molecular Formula | C19H28N4O2S |
Molecular Weight | 376.516 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
CNS Activity
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Neurochemical effects of some ergot derivatives: a basis for their antiparkinson actions. | 1981 |
|
Treatment of Parkinson's disease with the ergoline derivatives CQ 32-084 and CU 32-085. | 1983 |
|
The selectivity of some ergot derivatives for alpha 1 and alpha 2-adrenoceptors of rat cerebral cortex. | 1983 Aug 5 |
|
Selectivity of some ergot derivatives for 5-HT1 and 5-HT2 receptors of rat cerebral cortex. | 1986 |
|
Effects of the dopamine D2 agonists lisuride and CQ 32-084 on rat feeding behaviour. | 1992 Apr |
|
Behavioural profile in the chicken of CQ 32-084 and CQP 201-403, two dopamine agonists. | 1993 May |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:20:14 GMT 2023
by
admin
on
Fri Dec 15 16:20:14 GMT 2023
|
Record UNII |
28N73Q6O7Y
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C66884
Created by
admin on Fri Dec 15 16:20:14 GMT 2023 , Edited by admin on Fri Dec 15 16:20:14 GMT 2023
|
||
|
NCI_THESAURUS |
C221
Created by
admin on Fri Dec 15 16:20:14 GMT 2023 , Edited by admin on Fri Dec 15 16:20:14 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
C031648
Created by
admin on Fri Dec 15 16:20:14 GMT 2023 , Edited by admin on Fri Dec 15 16:20:14 GMT 2023
|
PRIMARY | |||
|
CHEMBL38992
Created by
admin on Fri Dec 15 16:20:14 GMT 2023 , Edited by admin on Fri Dec 15 16:20:14 GMT 2023
|
PRIMARY | |||
|
100000082080
Created by
admin on Fri Dec 15 16:20:14 GMT 2023 , Edited by admin on Fri Dec 15 16:20:14 GMT 2023
|
PRIMARY | |||
|
28N73Q6O7Y
Created by
admin on Fri Dec 15 16:20:14 GMT 2023 , Edited by admin on Fri Dec 15 16:20:14 GMT 2023
|
PRIMARY | |||
|
68847
Created by
admin on Fri Dec 15 16:20:14 GMT 2023 , Edited by admin on Fri Dec 15 16:20:14 GMT 2023
|
PRIMARY | |||
|
C65582
Created by
admin on Fri Dec 15 16:20:14 GMT 2023 , Edited by admin on Fri Dec 15 16:20:14 GMT 2023
|
PRIMARY | |||
|
SUB07312MIG
Created by
admin on Fri Dec 15 16:20:14 GMT 2023 , Edited by admin on Fri Dec 15 16:20:14 GMT 2023
|
PRIMARY | |||
|
5160
Created by
admin on Fri Dec 15 16:20:14 GMT 2023 , Edited by admin on Fri Dec 15 16:20:14 GMT 2023
|
PRIMARY | |||
|
64795-23-9
Created by
admin on Fri Dec 15 16:20:14 GMT 2023 , Edited by admin on Fri Dec 15 16:20:14 GMT 2023
|
PRIMARY | |||
|
DTXSID101024323
Created by
admin on Fri Dec 15 16:20:14 GMT 2023 , Edited by admin on Fri Dec 15 16:20:14 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |