Velagliflozin proline hydrate

Modify Date: 2024-09-21 13:56:21

Velagliflozin proline hydrate Structure
Velagliflozin proline hydrate structure
Common Name Velagliflozin proline hydrate
CAS Number 1661838-94-3 Molecular Weight 528.59
Density N/A Boiling Point N/A
Molecular Formula C28H36N2O8 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Velagliflozin proline hydrate


Velagliflozin proline hydrate is the clinical form of Velagliflozin (HY-109018). Velagliflozin is an oral sodium-glucose cotransporter 2 (SGLT2) inhibitor with antidiabetic activity. Velagliflozin reduces renal glucose reabsorption and stimulates glycosuria, which lowers blood sugar and insulin concentrations[1].

 Names

Name Velagliflozin proline hydrate

 Velagliflozin proline hydrate Biological Activity

Description Velagliflozin proline hydrate is the clinical form of Velagliflozin (HY-109018). Velagliflozin is an oral sodium-glucose cotransporter 2 (SGLT2) inhibitor with antidiabetic activity. Velagliflozin reduces renal glucose reabsorption and stimulates glycosuria, which lowers blood sugar and insulin concentrations[1].
Related Catalog
Target

SGLT2

In Vitro Velagliflozin proline hydrate 是一种钠-葡萄糖共转运蛋白 2 (SGLT2) 抑制剂,具有抗糖尿病活性[1]。
In Vivo Velagliflozin proline hydrate (1 mg/kg, 口服, 单剂量) 增加胆固醇、白蛋白、β -羟基丁酸 (BHB)、非酯化脂肪酸 (NEFA) 和尿葡萄糖排泄,并降低猫的呼吸交换比率[1]。 Velagliflozin proline hydrate (0.3 mg/kg; 口服; 每天 1 次, 共 18 天) 耐受性良好,可通过降低饮食非结构性碳水化合物 (NSC) 的高胰岛素反应来治疗小马的胰岛素失调和预防椎板炎[2]。
References

[1]. Hoenig M, et al. Effects of the sodium-glucose cotransporter 2 (SGLT2) inhibitor velagliflozin, a new drug with therapeutic potential to treat diabetes in cats. J Vet Pharmacol Ther. 2018 Apr;41(2):266-273.  

[2]. Meier A, et al. The sodium-glucose co-transporter 2 inhibitor velagliflozin reduces hyperinsulinemia and prevents laminitis in insulin-dysregulated ponies. PLoS One. 2018 Sep 13;13(9):e0203655.  

 Chemical & Physical Properties

Molecular Formula C28H36N2O8
Molecular Weight 528.59
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