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BMS-986020

    
≥99%

BMS-986020

源葉(MedMol)
S82609 一鍵復制產品信息
1257213-50-5
C29H26N2O5
482.5271
1-{4'-[3-methyl-4-((R)-1-phenyl-ethoxycarbonylamino)-isoxazol-5-yl]-biphenyl-4-yl}-cyclopropanecarboxylic acid; (R)-1-(4'-(3-methyl-4-((1-phenylethoxy)carbonylamino)isoxazol-5-yl)biphenyl-4-yl)cyclopr
貨號 規格 價格 上海 北京 武漢 南京 購買數量
S82609-5mg
≥99% ¥336.00 10 - - -
S82609-10mg
≥99% ¥593.00 10 - - -
S82609-25mg
≥99% ¥1261.00 7 - - -
S82609-50mg
≥99% ¥2144.00 5 - - -
S82609-100mg
≥99% ¥3645.00 3 - - -
產品介紹 參考文獻 質檢證書(COA) 摩爾濃度計算器 相關產品

產品介紹

BMS-986020 (AM152, AP-3152 free acid) 是一種有效的 lysophosphatidic acid receptor 1 (LPA1) 的選擇性拮抗劑。BMS-986020 可抑制膽汁酸和磷脂轉運蛋白,對于BSEP、MRP4和MDR3的IC50值分別為4.8 μM、6.2 μM和7.5 μM。BMS-986020 具有治療特發性肺纖維化 idiopathic pulmonary fibrosis (IPF) 的潛力

產品描述: BMS-986020 (AM152, AP-3152 free acid) 是一種有效的 lysophosphatidic acid receptor 1 (LPA1) 的選擇性拮抗劑。BMS-986020 可抑制膽汁酸和磷脂轉運蛋白,對于BSEP、MRP4和MDR3的IC50值分別為4.8 μM、6.2 μM和7.5 μM。BMS-986020 具有治療特發性肺纖維化 idiopathic pulmonary fibrosis (IPF) 的潛力
靶點: LPA1; BSEP(Cell-free assay): 4.8 μM; MRP4(Cell-free assay):6.2 μM; MDR3(Cell-free assay):7.5 μM;LPAReceptor;?LPLReceptor
體外研究: BMS-986020, a selective and potent lysophosphatidic acid receptor 1 (LPA1) inhibitor, inhibits LPA1-induced fibrogenesis in the Scar-in-a-Jar in vitro model
細胞實驗: Cell lines: Human lung fibroblasts Concentrations: 12 days Incubation Time: 0.01, 0.05, 0.1, 0.5, 1, or 5 μM Method: Human lung fibroblasts were cultured in 48-well plates in Dulbecco’s Modified Eagle Medium (DMEM)?+?GlutaMax with 0.4% fetal bovine serum, 37.5 mg/mL Ficoll 70, 25 mg/mL Ficoll 400, and 1% ascorbic acid. Cells were stimulated with 1 ng/mL transforming growth factor beta 1 (TGF-β1) or 20 μM LPA with or without BMS-986020 (0.01, 0.05, 0.1, 0.5, 1, or 5 μM) diluted in dimethyl sulfoxide (DMSO), or vehicle (0.05% DMSO) in four replicates. Cells were cultured at 37 °C with 95% O2 and 5% CO2 for 12 days, and medium was changed at Day 4 and 8. Supernatants were stored at ???20 °C until biomarker measurements. alamarBlue was used to quantify cellular metabolism at Day 0 (prior to drug treatment) and Day 12. Release of lactate dehydrogenase (LDH) was quantified at Day 4, 8, and 12.
參考文獻: 1. Glenn Rosen, et al. LPA1 antagonists BMS-986020 and BMS-986234 for idiopathic pulmonary fibrosis: Preclinical evaluation of hepatobiliary homeostasis. European Respiratory Journal 2017 50: PA1038; vol. 50 no. suppl 61. 2. Decato BE, et al. LPA1 antagonist BMS-986020 changes collagen dynamics and exerts antifibrotic effects in vitro and in patients with idiopathic pulmonary fibrosis. Respir Res. 2022 Mar 18;23(1):61.
溶解性: Soluble  in  DMSO、Ethanol
保存條件: -20°C
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 2.072 ml 10.362 ml 20.724 ml
5 mM 0.414 ml 2.072 ml 4.145 ml
10 mM 0.207 ml 1.036 ml 2.072 ml
50 mM 0.041 ml 0.207 ml 0.414 ml
注意: 部分產品我司僅能提供部分信息,我司不保證所提供信息的權威性,僅供客戶參考交流研究之用。

參考文獻

質檢證書(COA)

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請輸入貨號和一個與之匹配的批號。
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批號:JS298415 貨號:S20001-25g
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摩爾濃度計算器

質量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)

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