Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C17H16N2O |
| Molecular Weight | 264.3217 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)C1=C(C(=O)C2=CC=CN=C2)C3=C(N1)C=CC=C3
InChI
InChIKey=SOOXXPIIPHUERK-UHFFFAOYSA-N
InChI=1S/C17H16N2O/c1-11(2)16-15(13-7-3-4-8-14(13)19-16)17(20)12-6-5-9-18-10-12/h3-11,19H,1-2H3
| Molecular Formula | C17H16N2O |
| Molecular Weight | 264.3217 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/652049
Cats: forty minutes after intravenous administration of nictindole (2 mg/kg) the formation of platelet depostis was reduced by half. Three hours after i.v. administration of nictindole at a dose of 20 mg/kg the remaining anti-platelet activity was 18% for nictindole as compared to its antithrombotic action, which was recorded 40 min after their administration.
Route of Administration:
Intravenous
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/7126994
ATP and adenosine (10(-5) and 10(-4) M) caused a moderate contraction of the guinea-pig trachea under resting tone. This effect was antagonized by nictindole (10(-7) M).
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 06:54:08 GMT 2025
by
admin
on
Wed Apr 02 06:54:08 GMT 2025
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| Record UNII |
EDK3Z2X1IV
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| Record Status |
Validated (UNII)
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| Record Version |
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NCI_THESAURUS |
C257
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C002092
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253-070-1
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3259
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C76805
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CHEMBL2105174
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36504-64-0
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EDK3Z2X1IV
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