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Glymidine

Glymidine structure

Glymidine 

structure
  • CAS No:

    339-44-6

  • Formula:

    C13H15N3O4S

  • Chemical Name:

    Glymidine

  • Synonyms:

    Benzenesulfonamide,N-[5-(2-methoxyethoxy)-2-pyrimidinyl]-;N-[5-(2-Methoxyethoxy)-2-pyrimidinyl]benzenesulfonamide;2-Benzenesulfonamido-5-(2-methoxyethoxy)pyrimidine;Glymidine;Glidiazine

Description

Solid


Solid


Glymidine is a sulfonamide that is N-(pyrimidin-2-yl)benzenesulfonamide which is substituted at position 5 of the pyrimidine ring by a 2-methoxyethoxy group. It is a hypoglycemic drug used for the treatment of diabetes mellitus. It has a role as a hypoglycemic agent. It is a member of pyrimidines, a sulfonamide and a diether. It is a conjugate acid of a glymidine(1-).|Glycodiazine is used with diet to lower blood glucose by increasing the secretion of insulin from pancreas and increasing the sensitivity of peripheral tissues to insulin. The mechanism of action of glycodiazine in lowering blood glucose appears to be dependent on stimulating the release of insulin from functioning pancreatic beta cells, and increasing sensitivity of peripheral tissues to insulin. Glycodiazine likely binds to ATP-sensitive potassium channel receptors on the pancreatic cell surface, reducing potassium conductance and causing depolarization of the membrane. Membrane depolarization stimulates calcium ion influx through voltage-sensitive calcium channels. This increase in intracellular calcium ion concentration induces the secretion of insulin. It is used for the concomitant use with insulin for the treatment of noninsulin-dependent (type 2) diabetes mellitus.|Glymidine is a sulfapyrimidine derivative,also known as glycodiazine, with antihyperglycemic activity. Like sulfonylureas, glymidine is able to lower blood glucose levels by increasing the release of insulin from pancreatic beta cells and increasing the sensitivity of peripheral tissues to insulin.

Glymidine Basic Attributes

309.34100

309.34

222-399-2

4C5I4BQZ8F

DTXSID1023108

C72805

A - Alimentary tract and metabolism

2935009090

Characteristics

98.79000

2.45640

Solid

1.354g/cm3

153 °C

515.1ºC at 760mmHg

265.4ºC

1.588

1.24e-01 g/L

Toxicity

Severe hypoglycemic reactions with coma, seizure, or other neurological impairment.

90% bound to plasma proteins.

Drug Information

Glycodiazine is used concomitantly with insulin for the treatment of noninsulin-dependent (type 2) diabetes mellitus.

Glycodiazine is used with diet to lower blood glucose by increasing the secretion of insulin from pancreas and increasing the sensitivity of peripheral tissues to insulin.

Rapidly and completely absorbed following oral administration.

4 hours.

The mechanism of action of glycodiazine in lowering blood glucose appears to be dependent on stimulating the release of insulin from functioning pancreatic beta cells, and increasing sensitivity of peripheral tissues to insulin. Glycodiazine likely binds to ATP-sensitive potassium channel receptors on the pancreatic cell surface, reducing potassium conductance and causing depolarization of the membrane. Membrane depolarization stimulates calcium ion influx through voltage-sensitive calcium channels. The rise in intracellular calcium leads to increased fusion of insulin granulae with the cell membrane, and therefore increased secretion of (pro)insulin.

glidiazine

Computed Properties

Molecular Weight:309.34
XLogP3:0.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:7
Exact Mass:309.07832714
Monoisotopic Mass:309.07832714
Topological Polar Surface Area:98.8
Heavy Atom Count:21
Complexity:385
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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