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
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+
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.
Originator
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/8562609
Single dose - 100 mg per subject
Route of Administration:
Oral
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NCI_THESAURUS |
C29711
Created by
admin on Fri Dec 15 15:30:04 GMT 2023 , Edited by admin on Fri Dec 15 15:30:04 GMT 2023
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C044425
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78782-47-5
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T-15
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C87619
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66630041
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4326S15UIP
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CHEMBL40356
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ACTIVE MOIETY
PARENT (SALT/SOLVATE)
SUBSTANCE RECORD