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D731798-1g6,9-diazaspiro[4.5]decan-10-one.
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D731798-2.5g6,9-diazaspiro[4.5]decan-10-one.
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5343350001A cell-permeable, spiral ketone derivative that acts as a highly potent inhibitor of acetyl-CoA carboxylase (ACC IC 50 = 27 and 33 nM for human ACC1 and ACC2, respectively). The inhibition appears to be uncompetitive with respect to ATP and
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C1017-25MGCitrinin is a mycotoxin from  Penicillium citrinin that comprises a quinone methide component. Application Citrinin has been used as: a standard for calibration curve preparation for citrinin quantification Monascus purpureus ATCC 36928 an
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C1017-5MGCitrinin is a mycotoxin from  Penicillium citrinin that comprises a quinone methide component. Application Citrinin has been used as: a standard for calibration curve preparation for citrinin quantification Monascus purpureus ATCC 36928 an
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35410-1MLCitrinin is a hepato-nephrotoxic mycotoxin. It can be produced by several filamentous fungi genera of Monauscus , Aspergillus , and Penicillium , which is commonly found as a contaminant in stored grains, foods, feedstuffs and also in biological
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C608577-100mgCJ-13,610 is an orally active and nonredox-type inhibitor of 5-lipoxygenase (5-LOX). CJ-13,610 inhibits the biosynthesis of leukotriene B4 and regulates the expression of IL-6 mRNA in macrophages.Application:CJ-13610 may be used to study
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C608577-10mgCJ-13,610 is an orally active and nonredox-type inhibitor of 5-lipoxygenase (5-LOX). CJ-13,610 inhibits the biosynthesis of leukotriene B4 and regulates the expression of IL-6 mRNA in macrophages.Application:CJ-13610 may be used to study
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C608577-1mgCJ-13,610 is an orally active and nonredox-type inhibitor of 5-lipoxygenase (5-LOX). CJ-13,610 inhibits the biosynthesis of leukotriene B4 and regulates the expression of IL-6 mRNA in macrophages.Application:CJ-13610 may be used to study