DuP 697

Discontinued Product

1430 has been discontinued.

View all Cyclooxygenases products.
说明: Cyclooxygenase-2 (COX-2) inhibitor
化学名: 5-Bromo-2-(4-fluorophenyl)-3-[4-(methylsulfonyl)phenyl]-thiophene
纯度: ≥99% (HPLC)
说明书
引用文献 (5)
评论
文献 (2)

生物活性 for DuP 697

DuP 697 is a potent and selective inhibitor of cyclooxygenase-2 (IC50 values are 10 and 800 nM for COX-2 and COX-1 respectively). Inhibits prostaglandin synthesis and is anti-inflammatory in vivo. Orally active.

化合物库 for DuP 697

DuP 697 is also offered as part of the Tocriscreen 2.0 Max and Tocriscreen Antiviral Library. 了解 Tocris 化合物库的更多信息。

技术数据 for DuP 697

分子量 411.3
公式 C17H12BrFO2S2
储存 Store at +4°C
纯度 ≥99% (HPLC)
CAS Number 88149-94-4
PubChem ID 3177
InChI Key AJFTZWGGHJXZOB-UHFFFAOYSA-N
Smiles CS(=O)(=O)C1=CC=C(C=C1)C1=C(SC(Br)=C1)C1=CC=C(F)C=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.

参考文献 for DuP 697

参考文献是支持产品生物活性的出版物。

Gans et al (1990) Anti-inflammatory and safety profile of DuP 697, a novel orally effective prostaglandin synthesis inhibitor. J.Pharmacol.Exp.Ther. 254 180 PMID: 2366180

Gierse et al (1995) Expression and selective inhibition of the constitutive and inducible forms of human cyclo-oxygenase. Biochem.J. 305 479 PMID: 7832763

Rossoni et al (2002) Inhibition of cyclo-oxygenase-2 exacerbates ischaemia-induced acute myocardial dysfunction in the rabbit. Br.J.Pharmacol. 135 1540 PMID: 11906968

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关键词: DuP 697, DuP 697 supplier, Cyclooxygenase-2, COX-2, inhibitors, inhibits, Cyclooxygenase, Oxygenases, Oxidases, DuP697, 1430, Tocris Bioscience

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