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Details

Stereochemistry ACHIRAL
Molecular Formula C16H22N4O
Molecular Weight 286.3721
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 2
Charge 0

SHOW SMILES / InChI
Structure of LINOGLIRIDE

SMILES

CN1CCC\C1=N/C(=N/C2=CC=CC=C2)N3CCOCC3

InChI

InChIKey=OPPLDIXFHYTSSR-YQFKSOGVSA-N
InChI=1S/C16H22N4O/c1-19-9-5-8-15(19)18-16(20-10-12-21-13-11-20)17-14-6-3-2-4-7-14/h2-4,6-7H,5,8-13H2,1H3/b17-16-,18-15+

HIDE SMILES / InChI

Molecular Formula C16H22N4O
Molecular Weight 286.3721
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 2
Optical Activity NONE

Linogliride is a substituted guanidine structurally unrelated to the sulphonylureas but with a similar mechanism of action. Linogliride potentiates insulin release in isolated islets and in the perfused pancreas. In islets, linogliride is reported to stimulate insulin secretion in the presence of glucose but not in its absence. Linogliride and the sulphonylureas act via closely related mechanisms. Possible extrapancreatic effects of the agent have also been suggested. Linogliride produces hypoglycaemic effects in various non-diabetic and diabetic animals. In normal rats and dogs, it improves glucose tolerance and in fasted rats or mice, linogliride lowers blood glucose. Linogliride showed modest effects in the db/db mice but significantly lowered fasting blood glucose in neonatal streptozotocin-treated rats. Clinical studies with non-insulin-dependent diabetes patients have shown linogliride to be effective at lowering fasting and postprandial plasma glucose levels in non-insulin-dependent diabetes patients. linogliride leads to a decrease in the activity of ATP-sensitive K+ channels.

Approval Year

PubMed

PubMed

TitleDatePubMed
Determination of linogliride in biological fluids by high-performance liquid chromatography.
1984 Nov 28
Influence of the oral hypoglycemic agent linogliride (McN-3935) on insulin secretion from isolated rat islets of Langerhans.
1987 Mar
Linogliride fumarate, representing a new class of oral hypoglycemic agent for diabetes.
1987 Nov
Postreceptor regulation of insulin action in primary cultures of rat hepatocytes by oral hypoglycemic agents: effects of linogliride and chlorpropamide.
1989 Nov
Inhibition of ATP-sensitive K+ channels in pancreatic beta-cells by nonsulfonylurea drug linogliride.
1991 Jul
Effect of linogliride on hormone release from perfused rat pancreas. Fuel dependence and desensitization by tolbutamide.
1991 Jul
A novel series of N-(1-aminoalkylidene)carboximidamides as potential hypoglycemic agents.
1993 May 28
Inhibition of ATP-sensitive potassium channels causes reversible cell-cycle arrest of human breast cancer cells in tissue culture.
1995 Feb
Biotransformation of linogliride, a hypoglycemic agent in laboratory animals and humans.
1995 Jun
Mechanisms of hypoxic vasodilation in ferret pulmonary arteries.
1995 Sep
An ATP-sensitive K(+) current that regulates progression through early G1 phase of the cell cycle in MCF-7 human breast cancer cells.
1999 Sep 1
The preparation and evaluation of salt forms of linogliride with reduced solubilities as candidates for extended release.
2017 Mar

Sample Use Guides

Single dose - 100 mg per subject
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:30:10 UTC 2023
Edited
by admin
on Fri Dec 15 16:30:10 UTC 2023
Record UNII
7E521JYJ4X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LINOGLIRIDE
INN   USAN  
USAN   INN  
Official Name English
MCN 3935
Code English
linogliride [INN]
Common Name English
N-(1-METHYL-2-PYRROLIDINYLIDENE)-N'-PHENYL-4-MORPHOLINECARBOXAMIDINE
Systematic Name English
4-MORPHOLINECARBOXIMIDAMIDE, N-(1-METHYL-2-PYRROLIDINYLIDENE)-N'-PHENYL-
Systematic Name English
LINOGLIRIDE [USAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29711
Created by admin on Fri Dec 15 16:30:10 UTC 2023 , Edited by admin on Fri Dec 15 16:30:10 UTC 2023
Code System Code Type Description
FDA UNII
7E521JYJ4X
Created by admin on Fri Dec 15 16:30:10 UTC 2023 , Edited by admin on Fri Dec 15 16:30:10 UTC 2023
PRIMARY
EPA CompTox
DTXSID201024552
Created by admin on Fri Dec 15 16:30:10 UTC 2023 , Edited by admin on Fri Dec 15 16:30:10 UTC 2023
PRIMARY
SMS_ID
100000082317
Created by admin on Fri Dec 15 16:30:10 UTC 2023 , Edited by admin on Fri Dec 15 16:30:10 UTC 2023
PRIMARY
NCI_THESAURUS
C66015
Created by admin on Fri Dec 15 16:30:10 UTC 2023 , Edited by admin on Fri Dec 15 16:30:10 UTC 2023
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CAS
75358-37-1
Created by admin on Fri Dec 15 16:30:10 UTC 2023 , Edited by admin on Fri Dec 15 16:30:10 UTC 2023
PRIMARY
EVMPD
SUB08521MIG
Created by admin on Fri Dec 15 16:30:10 UTC 2023 , Edited by admin on Fri Dec 15 16:30:10 UTC 2023
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ChEMBL
CHEMBL40356
Created by admin on Fri Dec 15 16:30:10 UTC 2023 , Edited by admin on Fri Dec 15 16:30:10 UTC 2023
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MESH
C044425
Created by admin on Fri Dec 15 16:30:10 UTC 2023 , Edited by admin on Fri Dec 15 16:30:10 UTC 2023
PRIMARY
USAN
X-13
Created by admin on Fri Dec 15 16:30:10 UTC 2023 , Edited by admin on Fri Dec 15 16:30:10 UTC 2023
PRIMARY
INN
5262
Created by admin on Fri Dec 15 16:30:10 UTC 2023 , Edited by admin on Fri Dec 15 16:30:10 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY