U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C16H22N4O.C4H4O4
Molecular Weight 402.4442
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 3
Charge 0

SHOW SMILES / InChI
Structure of LINOGLIRIDE FUMARATE

SMILES

OC(=O)\C=C\C(O)=O.CN1CCCC1=NC(=NC2=CC=CC=C2)N3CCOCC3

InChI

InChIKey=ZSAMTXUUUFXIII-WLHGVMLRSA-N
InChI=1S/C16H22N4O.C4H4O4/c1-19-9-5-8-15(19)18-16(20-10-12-21-13-11-20)17-14-6-3-2-4-7-14;5-3(6)1-2-4(7)8/h2-4,6-7H,5,8-13H2,1H3;1-2H,(H,5,6)(H,7,8)/b;2-1+

HIDE SMILES / InChI

Molecular Formula C4H4O4
Molecular Weight 116.0722
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

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
The preparation and evaluation of salt forms of linogliride with reduced solubilities as candidates for extended release.
2017-03
An ATP-sensitive K(+) current that regulates progression through early G1 phase of the cell cycle in MCF-7 human breast cancer cells.
1999-09-01
Mechanisms of hypoxic vasodilation in ferret pulmonary arteries.
1995-09
Biotransformation of linogliride, a hypoglycemic agent in laboratory animals and humans.
1995-06
Inhibition of ATP-sensitive potassium channels causes reversible cell-cycle arrest of human breast cancer cells in tissue culture.
1995-02
A novel series of N-(1-aminoalkylidene)carboximidamides as potential hypoglycemic agents.
1993-05-28
Inhibition of ATP-sensitive K+ channels in pancreatic beta-cells by nonsulfonylurea drug linogliride.
1991-07
Effect of linogliride on hormone release from perfused rat pancreas. Fuel dependence and desensitization by tolbutamide.
1991-07
Postreceptor regulation of insulin action in primary cultures of rat hepatocytes by oral hypoglycemic agents: effects of linogliride and chlorpropamide.
1989-11
Linogliride fumarate, representing a new class of oral hypoglycemic agent for diabetes.
1987-11
Influence of the oral hypoglycemic agent linogliride (McN-3935) on insulin secretion from isolated rat islets of Langerhans.
1987-03
Determination of linogliride in biological fluids by high-performance liquid chromatography.
1984-11-28

Sample Use Guides

Single dose - 100 mg per subject
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:59:13 GMT 2025
Edited
by admin
on Mon Mar 31 17:59:13 GMT 2025
Record UNII
4326S15UIP
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MCN-3935
Preferred Name English
LINOGLIRIDE FUMARATE
USAN  
USAN  
Official Name English
LINOGLIRIDE FUMARATE [USAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29711
Created by admin on Mon Mar 31 17:59:13 GMT 2025 , Edited by admin on Mon Mar 31 17:59:13 GMT 2025
Code System Code Type Description
MESH
C044425
Created by admin on Mon Mar 31 17:59:13 GMT 2025 , Edited by admin on Mon Mar 31 17:59:13 GMT 2025
PRIMARY
CAS
78782-47-5
Created by admin on Mon Mar 31 17:59:13 GMT 2025 , Edited by admin on Mon Mar 31 17:59:13 GMT 2025
PRIMARY
USAN
T-15
Created by admin on Mon Mar 31 17:59:13 GMT 2025 , Edited by admin on Mon Mar 31 17:59:13 GMT 2025
PRIMARY
NCI_THESAURUS
C87619
Created by admin on Mon Mar 31 17:59:13 GMT 2025 , Edited by admin on Mon Mar 31 17:59:13 GMT 2025
PRIMARY
PUBCHEM
66630041
Created by admin on Mon Mar 31 17:59:13 GMT 2025 , Edited by admin on Mon Mar 31 17:59:13 GMT 2025
PRIMARY
FDA UNII
4326S15UIP
Created by admin on Mon Mar 31 17:59:13 GMT 2025 , Edited by admin on Mon Mar 31 17:59:13 GMT 2025
PRIMARY
SMS_ID
300000055213
Created by admin on Mon Mar 31 17:59:13 GMT 2025 , Edited by admin on Mon Mar 31 17:59:13 GMT 2025
PRIMARY
ChEMBL
CHEMBL40356
Created by admin on Mon Mar 31 17:59:13 GMT 2025 , Edited by admin on Mon Mar 31 17:59:13 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY