Pegloxenatide
Based on 1 Customer Validation
Pegloxenatide (Polyethylene glycol loxenatide) is a long-acting glucagon-like peptide-1 receptor (GLP-1RA) agonist. Pegloxenatide has various activities such as lowering blood glucose, lowering blood lipids, improving body weight, anti-inflammation, promoting wound healing, protecting the liver, and protecting the heart. Pegloxenatide can be used in the research of type 2 diabetes and its multiple complications.
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- 純度: 90.00%
- CAS 番号: 2420483-82-3
- 分子式: (C₂H₄O)n(C₂H₄O)nC₂₀₆H₃₁₇N₅₅O₆₇S
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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生物活性
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化学情報
- 純度とドキュメンテーション
- 参考文献
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Help & FAQs
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生物活性
Pegloxenatide (100-200 nM; 24 h) can activate the PI3K/AKT pathway in high glucose-treated HepG2 cells, while the PI3K inhibitor LY294002 (HY-10108) can inhibit its activation[1].
Pegloxenatide (250 nM; 24 h) can restore tube formation and migratory capacity, increase NO production, reduce mitochondrial ROS generation, improve mitochondrial membrane potential and respiratory function, and restore autophagic flux in human endothelial progenitor cells treated with high glucose and Palmitic acid (HY-N0830)[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:High glucose-treated HepG2 cells
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Concentration:100 and 200 nM
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Incubation Time:24 h
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Result:Significantly increased the levels of p-PI3K and p-AKT.
Pegloxenatide (0.03 mg/kg/week; intraperitoneal injection; 12 weeks) has activities of improving glucose metabolism, anti-inflammation and accelerating wound healing in db/db mice[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:C57BL/6-db/db male mice[1]
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Dosage:0.3 and 1 mg/kg
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Administration:Subcutaneous injection; once every 3 days; 4 weeks
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Result:Significantly reduced body weight and fasting glucose, mincreased glucose tolerance, improved serum and liver biochemical parameters, and attenuated hepatic steatosis and liver and pancreatic tissue damages in db/db mice.
Considerably inhibited oxidative stress, decreased pro-inflammatory factor (TNF-α, IL-6, and MCP-1) levels, increased anti-inflammatory factor IL-10 levels, upregulated Sirt1, p-AMPK, and p-ACC expressions in the Sirt1/AMPK/ACC pathway, promoted GLP-1R expression by inhibiting β-cell apoptosis, and activated the insulin PI3K/AKT pathway to exert hypoglycemic and hepatoprotective effects.
| NCT Number | Sponsor | Condition | Start Date |
Phase
|
|---|---|---|---|---|
| NCT01329991 | Plexxikon| | 2011-05 | PHASE1 |
化学情報
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CAS 番号 2420483-82-3
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性状 Liquid
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分子式 (C₂H₄O)n(C₂H₄O)nC₂₀₆H₃₁₇N₅₅O₆₇S
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Color Colorless to light yellow
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別名
Polyethylene glycol loxenatide; PEX 168
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配列
PEGn-His-{d-Ala}-Glu-Gly-Thr-Phe-Thr-Ser-Asp-Leu-Ser-Lys-Gln-{Nle}-Glu-Glu-Glu-Ala-Val-Arg-Leu-Phe-Ile-Glu-Trp-Leu-Lys-Gln-Gly-Gly-Pro-Ser-Ser-Gly-Ala-Pro-Pro-Pro-Cys-NH2
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シーケンスの短縮
PEGn-H-{d-Ala}-EGTFTSDLSKQ-{Nle}-EEEAVRLFIEWLKQGGPSSGAPPPC-NH2
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
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データシート (270 KB)
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SDS (252 KB)
- English - EN (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
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取扱説明書 (2659 KB)
参考文献
[1]. Zhang Y, et al. Protective Effects and Mechanisms of Polyethylene Glycol Loxenatide Against Hyperglycemia and Liver Injury in db/db diabetic Mice. Front Pharmacol. 2021 Dec 6;12:781856. [Content Brief]
[2]. Ding Z, et al. Polyethylene Glycol Loxenatide Accelerates Diabetic Wound Healing by Downregulating Systemic Inflammation and Improving Endothelial Progenitor Cell Functions. Int J Mol Sci. 2025 Mar 6;26(5):2367. [Content Brief]
[3]. Wang J, et al. Polyethylene glycol loxenatide (PEX168) in subjects with renal impairment: A pharmacokinetic study. Br J Clin Pharmacol. 2019 Dec;85(12):2714-2720. [Content Brief]
[4]. Li XY, et al. Effect of polyethylene Glycol Loxenatide (long-acting GLP-1RA) on lipid, glucose levels and weight in type 2 diabetes mellitus patients with obesity. Eur Rev Med Pharmacol Sci. 2022 Nov;26(21):7996-8003. [Content Brief]
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
Pegloxenatide 関連分類
HY-P3491 関連分類
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- Pegloxenatide
- 2420483-82-3
- Polyethylene glycol loxenatide
- PEX 168
- PEX168
- PEX 168
- PEX-168
- GCGR
- PI3K
- Akt
- Reactive Oxygen Species (ROS)
- Autophagy
- Interleukin Related
- Sirtuin
- AMPK
- Apoptosis
- polyethylene glycol loxenatide
- long-acting
- glucagon-like peptide-1 receptor
- type 2 diabetes mellitus (T2DM)
- db/db male mice
- Inhibitor
- inhibitor
- inhibit