中文名稱
N-(4-丁基-2-甲基苯基)-N'-羥基甲基亞氨基酰胺; N-羥基-N'-(4-正丁基-2-甲基苯基)甲idine; HET0016
英文名字
N-(4-butyl-2-methylphenyl)-N’-hydroxy-methanimidamide; N-hydroxy-N’-(4-n-butyl-2-methylphenyl)Formamidine; HET0016
供應(yīng)商
開(kāi)曼生物
產(chǎn)品貨號(hào)
75780-5
產(chǎn)品報(bào)價(jià)
¥877.8/5mg
產(chǎn)品說(shuō)明書(shū)
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購(gòu)買(mǎi)方式
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產(chǎn)品新聞
背景資料
20-HETE is a major biologically active cytochrome P450 (CYP450) metabolite of arachidonic acid in the kidney and liver. It regulates renal vascular and tubular functions as well as vascular tone in the cerebral circulation. HET0016 is an inhibitor of 20-HETE formation in human renal microsomes with an IC50 of 8.9 nM, selectively inhibiting CYP4A and 4F isoforms. HET0016 inhibits CYP2C9, CYP2D6, and CYP3A4, enzymes important in drug metabolism, significantly less effectively with IC50s in the uM range. The IC50 values for inhibition of cyclooxygenase and epoxyeicosatrienoic acids (EETs) formation are 2.3 and 2.8 uM, respectively.
產(chǎn)品描述
20-HETE is a major biologically active CYP450 metabolite of arachidonic acid in the kidney and liver. It regulates renal vascular and tubular functions as well as vascular tone in the cerebral circulation.{12466,12470,12468,12467,9023} HET0016 is an inhibitor of 20-HETE formation in human renal microsomes with an IC50 of 8.9 nM, selectively inhibiting CYP4A and 4F isoforms.{8946,12469} HET0016 inhibits CYP2C9, CYP2D6, and CYP3A4, enzymes important in drug metabolism, significantly less effectively with IC50 values in the uM range. The IC50 values for inhibition of COX and epoxyeicosatrienoic acids (EETs) formation are 2.3 and 2.8 uM, respectively.{8946}
保存建議
建議您在收到開(kāi)曼生物品牌的HET0016 (5 mg)產(chǎn)品后置于-20度保存,產(chǎn)品有效期為730天.
其他
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