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Alagebrium chloride

Cat. No. M10648

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Alagebrium chloride Structure
Synonym:

ALT711

Size Price Availability Quantity
200mg USD 48  USD48 In stock
500mg USD 80  USD80 In stock
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Quality Control & Documentation
Biological Activity

Alagebrium Chloride, also known as ALT711, is an advanced glycation end product (AGE) inhibitor. Endothelial cell (EC) proliferation is increased for all groups receiving Alagebrium (ALT-711), particularly when seeded on matrix from the AAo of obese (ZO) and diabetic (ZD) rats. Treatment with Alagebrium in diabetic RAGE apoE double-KO mice is associated with a further reduction in glomerular collagen IV levels, approaching levels observed in control mice. Alagebrium increases blood flow (BF) in ZO rats but reduces distal vascular resistance in ZD rats. A decrease in neointimal hyperplasia (NH) intrastrut thickness as a function of local radius is found in all groups with Alagebrium treatment. A significant increase in TGF-β expression is also found in the AAo of ZL rats treated with Alagebrium. It was the first drug candidate to be clinically tested for the purpose of breaking the crosslinks caused by advanced glycation endproducts (AGEs), thereby reversing one of the main mechanisms of aging. Through this effect Alagebrium is designed to reverse the stiffening of blood vessel walls that contributes to hypertension and cardiovascular disease, as well as many other forms of degradation associated with protein crosslinking. Alagebrium has proven effective in reducing systolic blood pressure and providing therapeutic benefit for patients with diastolic.

Chemical Information
Molecular Weight 267.77
Formula C13H14ClNOS
CAS Number 341028-37-3
Solubility (25°C) Water ≥ 30 mg/mL
DMSO ≥ 20 mg/mL
Storage 2-8°C, dry, sealed
References

[1] Cigdem Toprak, et al. Eurasian J Med . Functional Effects of Alagebrium (ALT-711)-Isolated Rat Carotid Artery

[2] Hongfeng Wang, et al. Am J Physiol Heart Circ Physiol . Alagebrium inhibits neointimal hyperplasia and restores distributions of wall shear stress by reducing downstream vascular resistance in obese and diabetic rats

[3] Anna M D Watson, et al. Diabetes . Alagebrium reduces glomerular fibrogenesis and inflammation beyond preventing RAGE activation in diabetic apolipoprotein E knockout mice

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Keywords: Alagebrium chloride, ALT711 supplier, Metabolite/Endogenous Metabolite, inhibitors, activators

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