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LGD-6972

Catalog No.GC31343

LGD-6972 est un antagoniste sélectif et actif par voie orale des récepteurs du glucagon.

Products are for research use only. Not for human use. We do not sell to patients.

LGD-6972 Chemical Structure

Cas No.: 1207989-09-0

Taille Prix Stock Qté
10mM (in 1mL DMSO)
358,00 $US
En stock
1mg
99,00 $US
En stock
5mg
261,00 $US
En stock
10mg
423,00 $US
En stock
50mg
1 225,00 $US
En stock
100mg
1 821,00 $US
En stock

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

LGD-6972 is a glucagon receptor antagonist.

LGD-6972 has linear plasma pharmacokinetics consistent with once daily dosing that is comparable in healthy and T2DM subjects. Dose-dependent decreases in fasting plasma glucose are observed in all groups with a maximum of 3.15 mM (56.8 mg/dL) on day 14 in T2DM subjects. LGD-6972 also reduces plasma glucose in the postprandial state. Dose-dependent increases in fasting plasma glucagon are observed, but glucagon levels decrease and insulin levels increase after an oral glucose load in T2DM subjects. LGD-6972 is well tolerated at the doses tested without dose-related or clinically meaningful changes in clinical laboratory parameters. No subject experiences hypoglycaemia[1].

[1]. Vajda EG, et al. Pharmacokinetics and pharmacodynamics of single and multiple doses of the glucagon receptor antagonist LGD-6972 in healthy subjects and subjects with type 2 diabetes mellitus. Diabetes Obes Metab. 2017 Jan;19(1):24-32.

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