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- CAS号:
869490-23-3
- 规格:
1mg/5mg/10mg/25mg/50mg
| 规格: | 1mg | 产品价格: | ¥848.0 |
|---|---|---|---|
| 规格: | 5mg | 产品价格: | ¥2120.0 |
| 规格: | 10mg | 产品价格: | ¥3176.0 |
| 规格: | 25mg | 产品价格: | ¥5104.0 |
| 规格: | 50mg | 产品价格: | ¥6872.0 |
Product Introduction
Bioactivity
| 名称 | Gosogliptin |
| 描述 | Gosogliptin is a potent, orally active, highly selective and competitive inhibitor of DPP-4 (dipeptidyl peptidase 4), increasing the levels of intestinal glucagon peptide (GLP-1) and glucose-dependent proinsulinotropic polypeptide (GIP), thereby enhancing insulin secretion and lowering blood glucose levels. In animal studies, Gosogliptin rapidly, orally and reversibly inhibits plasma DPP-4 activity. |
| 体外活性 | Gosogliptin (PF-00734200) 是一种强效、口服、选择性和竞争性的 DPP-IV 抑制剂,戈索列汀口服给大鼠、狗和猴子时,可快速且可逆地抑制血浆 DPP-4 活性。[2] |
| 体内活性 | 方法:Gosogliptin (PF-00734200)(口服)给完整的 SD 大鼠(5 mg/kg)、比格犬(5 mg/kg)和人类(20 mg),研究Dawley (SD) 大鼠、比格犬和人类中的代谢、药代动力学和排泄。 结果:Gosogliptin在给药后 168 小时内,在尿液、粪便和笼洗液中回收了平均 97.1% 的给药放射性。在粪便中回收的平均累积剂量为 66.0%。尿液中的平均累积排泄量为 30.8%。大约 95% 的排泄放射性恢复发生在前 48 小时内。[2] |
| 存储条件 | Store at low temperature Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
| 溶解度 | DMSO : 80 mg/mL (218.33 mM), Sonication is recommended. 10% DMSO+40% PEG300+5% Tween 80+45% Saline : 5 mg/mL (13.65 mM), Sonication is recommended. |
| 关键字 | PF 734200 | PF 00734200 | Gosogliptin | DPP-IV |
| 相关产品 | Teneligliptin hydrobromide | Sitagliptin phosphate | 10-Undecenoic acid | Sitagliptin | Anagliptin | Alloxan monohydrate | 10-Undecenoic acid zinc salt | Sitagliptin phosphate monohydrate | 4'-Hydroxychalcone | Vildagliptin | Aprotinin | Tripterin |
| 相关库 | Inhibitor Library | Bioactive Compound Library | Bioactive Compounds Library Max | ReFRAME Related Library | Fluorochemical Library | FDA-Approved & Pharmacopeia Drug Library | Approved Drug Library | Drug Repurposing Compound Library |
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戈格列汀【869490-23-3】
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