BMY 45778

Discontinued Product

1442 has been discontinued.

View all Prostanoid Receptors products.
说明: Non-prostanoid prostacyclin IP receptor partial agonist
化学名: [3-(4,5-Diphenyl[2,4'-bioxazol]-5'-yl)phenoxy]acetic acid
纯度: ≥99% (HPLC)
说明书
引用文献
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生物活性 for BMY 45778

BMY 45778 is a non-prostanoid prostacyclin mimetic that acts as a partial agonist at IP1 prostacyclin receptors. Potently inhibits platelet aggregation in vitro (IC50 = 27-35 nM).

许可信息

Sold with the permission of Bristol-Myers Squibb Company

技术数据 for BMY 45778

分子量 438.44
公式 C26H18N2O5
储存 Store at +4°C
纯度 ≥99% (HPLC)
CAS Number 152575-66-1
PubChem ID 127861
InChI Key DSRSEEYZGWTODH-UHFFFAOYSA-N
Smiles OC(=O)COC1=CC(=CC=C1)C1=C(N=CO1)C1=NC(=C(O1)C1=CC=CC=C1)C1=CC=CC=C1

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

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关键词: BMY 45778, BMY 45778 supplier, Non-prostanoid, prostacyclin, IP1, receptor, partial, agonist, Receptors, Prostanoid, PGI, prostaglandins, prostacyclins, eicosanoids, BMY45778, 1442, Tocris Bioscience

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