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Details

Stereochemistry ACHIRAL
Molecular Formula C15H11Cl2N2.Br
Molecular Weight 370.071
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NOLINIUM BROMIDE

SMILES

[Br-].ClC1=CC=C(NC2=CC=[N+]3C=CC=CC3=C2)C=C1Cl

InChI

InChIKey=CQJHTZPBHIZIPT-UHFFFAOYSA-N
InChI=1S/C15H10Cl2N2.BrH/c16-14-5-4-11(10-15(14)17)18-12-6-8-19-7-2-1-3-13(19)9-12;/h1-10H;1H

HIDE SMILES / InChI

Molecular Formula C15H10Cl2N2
Molecular Weight 289.159
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Molecular Formula BrH
Molecular Weight 80.912
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Nolinium bromide (NB) is a nonanticholinergic, gastric acid antisecretory agent and a gastrointestinal tract antispasmodic agent. The gastrointestinal antispasmodic action of NB has been demonstrated in a variety of test systems. The compound inhibited electrically induced contractions of rabbit ileum and nicotine-induced contractions of rat ileum in vitro, gastric emptying in fasted rats, and intestinal transport of a charcoal meal in mice. In the anesthetized dog, NB antagonized colonic contractions induced by acetylcholine, histamine, serotonin, and pelvic nerve stimulation, and duodenal contractions due to vagal stimulation and acetylcholine. In the unanesthetized dog, feeding induced colonic and duodenal motilities were inhibited by NB. The antisecretory action of NB may involve inhibition of enzymes of gastric acid secretion, specifically histamine-stimulated adenylate cyclase and potassium-stimulated ATPase. NB has no direct histamine-H2 receptor blocking properties. Nolinium bromide inhibits in a dose-dependent manner both the gastric H+, K+-ATPase activity and H+ uptake ability of the gastric microsomes. Increasing concentrations of K+ could reverse the nolinium bromide inhibition of both the H+, K+-ATPase activity and vesicular H+ transport. Nolinium bromide interferes primarily with the K+-dependent phosphatase step and thereby reduces the turnover of the enzyme. The drug acts as a K+ antagonist in the gastric H+ +K+-dependent ATPase reaction.

Approval Year

PubMed

PubMed

TitleDatePubMed
Inhibition of histamine-sensitive adenylate cyclase from the guinea pig gastric mucosa by nolinium bromide.
1979
Mechanism of gastric antisecretory effects of nolinium bromide.
1983 Oct
Effect of nolinium bromide on vascular smooth muscle.
1984 Sep

Sample Use Guides

In Vitro Use Guide
Nolinium bromide (50-200 uM) was a reversible, insurmountable inhibitor of contractions induced by Ca2+ (in 40 mM KC1 depolarizing medium) and norepinephrine, with IC50 values of 96 and 118 uM, respectively, for suppression of maximum contractile force. Contractions in response to Asn1Val5-angiotensin II in both 2.5 mM Ca2+ and 0 mM Ca2+ medium were also inhibited (IC50 value = 110 uM under both conditions).
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:14:23 GMT 2023
Edited
by admin
on Fri Dec 15 15:14:23 GMT 2023
Record UNII
N018S592LP
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NOLINIUM BROMIDE
INN   USAN  
INN   USAN  
Official Name English
QUINOLIZINIUM, 2-((3,4-DICHLOROPHENYL)AMINO)-, BROMIDE (1:1)
Systematic Name English
EU-2972
Code English
DICLONIUM BROMIDE
Common Name English
NSC-220927
Code English
nolinium bromide [INN]
Common Name English
2-(3,4-Dichloroanilino)quinolizinium bromide
Systematic Name English
QUINOLIZINIUM, 2-((3,4-DICHLOROPHENYL)AMINO)-, BROMIDE
Systematic Name English
NOLINIUM BROMIDE [USAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29701
Created by admin on Fri Dec 15 15:14:23 GMT 2023 , Edited by admin on Fri Dec 15 15:14:23 GMT 2023
Code System Code Type Description
SMS_ID
100000083566
Created by admin on Fri Dec 15 15:14:23 GMT 2023 , Edited by admin on Fri Dec 15 15:14:23 GMT 2023
PRIMARY
INN
4235
Created by admin on Fri Dec 15 15:14:23 GMT 2023 , Edited by admin on Fri Dec 15 15:14:23 GMT 2023
PRIMARY
PUBCHEM
38666
Created by admin on Fri Dec 15 15:14:23 GMT 2023 , Edited by admin on Fri Dec 15 15:14:23 GMT 2023
PRIMARY
EPA CompTox
DTXSID60961183
Created by admin on Fri Dec 15 15:14:23 GMT 2023 , Edited by admin on Fri Dec 15 15:14:23 GMT 2023
PRIMARY
CAS
40759-33-9
Created by admin on Fri Dec 15 15:14:23 GMT 2023 , Edited by admin on Fri Dec 15 15:14:23 GMT 2023
PRIMARY
NSC
220927
Created by admin on Fri Dec 15 15:14:23 GMT 2023 , Edited by admin on Fri Dec 15 15:14:23 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110689
Created by admin on Fri Dec 15 15:14:23 GMT 2023 , Edited by admin on Fri Dec 15 15:14:23 GMT 2023
PRIMARY
NCI_THESAURUS
C90777
Created by admin on Fri Dec 15 15:14:23 GMT 2023 , Edited by admin on Fri Dec 15 15:14:23 GMT 2023
PRIMARY
EVMPD
SUB09343MIG
Created by admin on Fri Dec 15 15:14:23 GMT 2023 , Edited by admin on Fri Dec 15 15:14:23 GMT 2023
PRIMARY
FDA UNII
N018S592LP
Created by admin on Fri Dec 15 15:14:23 GMT 2023 , Edited by admin on Fri Dec 15 15:14:23 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY