| CAS: | 74772-77-3 | ||||
| 分子式: | C18H23NO3S | ||||
| 分子量: | 333.4451 | ||||
| 沸点: | 504.5 °C at 760 mmHg | ||||
| 熔点: | 130-131 °C | ||||
| 英文名称: |
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| 货号 | 品牌 | 产品名称 | 规格 | 包装、参考价格 | |||||||||||||||||||||||||||||||||||||||
| C907382 | MACKLIN | 酪里达唑 | 95% | 4080元/25mg; | 咨询 | ||||||||||||||||||||||||||||||||||||||
储存:2-8°C | |||||||||||||||||||||||||||||||||||||||||||
| R11066 | Alfa Aesar | Ciglitazone Standard solution | 100ppm | 1048元/1ml; | 咨询 | ||||||||||||||||||||||||||||||||||||||
| 230950 | Sigma-Aldrich | Ciglitazone-CAS 74772-77-3-Calbiochem | A potent thiazolinedione (TDZ) type anti-hyperglycemic agent and a selective PPARγ agonist (EC₅₀ = 3 µM). | 2035.53元/5 MG; | 咨询 | ||||||||||||||||||||||||||||||||||||||
产品说明 一般描述 A potent thiazolinedione (TDZ) type anti-hyperglycemic agent and a selective PPARγ agonist (EC50 = 3 µM). 包装 5 mg in Plastic ampoule 生化/生理作用 Primary Target 警告 Toxicity: Harmful (C) 重悬 Stock solutions are stable for up to 3 months at -20°C. 其他说明 Jha, R.J. 1999. Clin. Exp. Hypertens. 21, 157. 法律信息 CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany 基本信息
产品性质
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| C3974 | Sigma-Aldrich | Ciglitizone | ≥98% (HPLC) | 4334.02元/5 MG; | 咨询 | ||||||||||||||||||||||||||||||||||||||
产品说明 应用 Ciglitizone has been used as a proliferator-activated receptor γ (PPARγ) agonist:
It also may be used to study its effects on cell cycle and apoptosis in monocytic cells. 包装 5 mg in glass insert 生化/生理作用 Ciglitizone belongs to the class of thiazolidinediones and is a peroxisome proliferator-activated receptor γ (PPARγ) agonist. It exhibits anti-diabetic activity. Ciglitizone has the potential to treat tumor necrosis factor α (TNFα)-related apoptosis-inducing ligand (TRAIL)-refractory high-grade urothelial cancers. 特点和优势 This compound was developed by Takeda. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here. 基本信息
产品性质
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| M01534 | Fluorochem | Ciglitazone | >98% | 4928元/5mg; | 咨询 | ||||||||||||||||||||||||||||||||||||||
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