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Key Documents

BP368

Gliclazide

British Pharmacopoeia (BP) Reference Standard

Sinonimo/i:

1-(3-Azabicyclo[3.3.0]oct-3-yl)-3-p-tolylsulphonylurea

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About This Item

Formula empirica (notazione di Hill):
C15H21N3O3S
Numero CAS:
Peso molecolare:
323.41
Numero CE:
Numero MDL:
Codice UNSPSC:
12352125
NACRES:
NA.24

Grado

pharmaceutical primary standard

Famiglia di API

gliclazide

Forma fisica

crystalline powder

Durata

limited shelf life, expiry date on the label

Produttore/marchio commerciale

BP

Punto di fusione

163-169 °C (lit.)

applicazioni

pharmaceutical
pharmaceutical small molecule

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

Cc1ccc(cc1)S(=O)(=O)NC(=O)NN2CC3CCCC3C2

InChI

1S/C15H21N3O3S/c1-11-5-7-14(8-6-11)22(20,21)17-15(19)16-18-9-12-3-2-4-13(12)10-18/h5-8,12-13H,2-4,9-10H2,1H3,(H2,16,17,19)
BOVGTQGAOIONJV-UHFFFAOYSA-N

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Descrizione generale

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.

Applicazioni

Gliclazide BP Reference standard, intended for use in laboratory tests only as specifically prescribed in the British Pharmacopoeia.

Also used in monographs such as:
  • Gliclazide Tablets
  • Used in the treatment of non-insulin dependent diabetes mellitus (NIDDM).

    Azioni biochim/fisiol

    Oxidative modification of low-density lipoprotein (LDL) plays an important role in vascular dysfunction associated with diabetes mellitus. Gliclazide is a second-generation sulfonylurea with free-radical-scavenging activity. Incubation of human aortic smooth muscle cell (HASMC) with native human LDL (100 μg/mL) in the presence of increasing concentrations of gliclazide (1 to 10 μg/mL) resulted in a dose-dependent decrease in HASMC-mediated LDL oxidation. Exposure of HASMCs to gliclazide (1 to 10 μg/mL) and native LDL (100 μg/mL) also led to a dose-dependent decrease in oxidized LDL-induced human monocyte adhesion to HASMCs. In addition, incubation of HASMCs with gliclazide dramatically reduced the ability of oxidized LDL to stimulate the proliferation of these cells. Finally, treatment of HASMCs with gliclazide resulted in a marked decrease in oxidatively modified LDL-induced monocyte chemoattractant protein (MCP)-1 and human heat shock protein 70 (HSP 70) expression, both at the gene and protein levels. These results show that gliclazide, at concentrations in the therapeutic range (5 to 10 μg/mL), is effective in vitro in reducing vascular smooth muscle cell (VSMC) dysfunction induced by oxidatively modified LDL. Administration of gliclazide to type 2 diabetic patients could form part of the strategy for the prevention and management of diabetic cardiovascular diseases

    Confezionamento

    Unit quantity: 200 mg. Subject to change. The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity please visit British Pharmacopoeia

    Altre note

    Sales restrictions may apply.

    Pittogrammi

    Exclamation mark

    Avvertenze

    Warning

    Indicazioni di pericolo

    Consigli di prudenza

    Classi di pericolo

    Acute Tox. 4 Oral

    Codice della classe di stoccaggio

    11 - Combustible Solids

    Classe di pericolosità dell'acqua (WGK)

    WGK 2

    Punto d’infiammabilità (°F)

    Not applicable

    Punto d’infiammabilità (°C)

    Not applicable


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