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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
Structure of NICTINDOLE

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

HIDE SMILES / InChI

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

Nictindole is a non-steroidal anti-inflammatory agent. It is a thromboxane synthetase inhibitor. Nictindole inhibits generation of TXA2 in human platelet rich plasma.

Approval Year

PubMed

PubMed

TitleDatePubMed
ATP-sensitive potassium channels and endogenous adenosine are involved in spinal antinociception produced by locus coeruleus stimulation.
2004 Aug

Sample Use Guides

In Vivo Use Guide
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
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 Sat Dec 16 15:54:30 GMT 2023
Edited
by admin
on Sat Dec 16 15:54:30 GMT 2023
Record UNII
EDK3Z2X1IV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NICTINDOLE
INN  
INN  
Official Name English
L-8027
Code English
nictindole [INN]
Common Name English
L 8027
Code English
2-ISOPROPYLINDOL-3-YL 3-PYRIDYL KETONE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C257
Created by admin on Sat Dec 16 15:54:30 GMT 2023 , Edited by admin on Sat Dec 16 15:54:30 GMT 2023
Code System Code Type Description
MESH
C002092
Created by admin on Sat Dec 16 15:54:30 GMT 2023 , Edited by admin on Sat Dec 16 15:54:30 GMT 2023
PRIMARY
ECHA (EC/EINECS)
253-070-1
Created by admin on Sat Dec 16 15:54:30 GMT 2023 , Edited by admin on Sat Dec 16 15:54:30 GMT 2023
PRIMARY
INN
3259
Created by admin on Sat Dec 16 15:54:30 GMT 2023 , Edited by admin on Sat Dec 16 15:54:30 GMT 2023
PRIMARY
NCI_THESAURUS
C76805
Created by admin on Sat Dec 16 15:54:30 GMT 2023 , Edited by admin on Sat Dec 16 15:54:30 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105174
Created by admin on Sat Dec 16 15:54:30 GMT 2023 , Edited by admin on Sat Dec 16 15:54:30 GMT 2023
PRIMARY
EVMPD
SUB09251MIG
Created by admin on Sat Dec 16 15:54:30 GMT 2023 , Edited by admin on Sat Dec 16 15:54:30 GMT 2023
PRIMARY
EPA CompTox
DTXSID30190004
Created by admin on Sat Dec 16 15:54:30 GMT 2023 , Edited by admin on Sat Dec 16 15:54:30 GMT 2023
PRIMARY
PUBCHEM
65796
Created by admin on Sat Dec 16 15:54:30 GMT 2023 , Edited by admin on Sat Dec 16 15:54:30 GMT 2023
PRIMARY
CAS
36504-64-0
Created by admin on Sat Dec 16 15:54:30 GMT 2023 , Edited by admin on Sat Dec 16 15:54:30 GMT 2023
PRIMARY
SMS_ID
100000084420
Created by admin on Sat Dec 16 15:54:30 GMT 2023 , Edited by admin on Sat Dec 16 15:54:30 GMT 2023
PRIMARY
FDA UNII
EDK3Z2X1IV
Created by admin on Sat Dec 16 15:54:30 GMT 2023 , Edited by admin on Sat Dec 16 15:54:30 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY