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F125720-100gProduct Description:Febuxostat(TEI 6720:TMX 67 ) is selective xanthine oxidase inhibitor with Ki of 0.6 nM.An inhibitor xanthine oxidase and xanthine dehydrogenase.Febuxostat is a potent, non-purine compound, which inhibits the expression of
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F125720-10gProduct Description:Febuxostat(TEI 6720:TMX 67 ) is selective xanthine oxidase inhibitor with Ki of 0.6 nM.An inhibitor xanthine oxidase and xanthine dehydrogenase.Febuxostat is a potent, non-purine compound, which inhibits the expression of
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F125720-1gProduct Description:Febuxostat(TEI 6720:TMX 67 ) is selective xanthine oxidase inhibitor with Ki of 0.6 nM.An inhibitor xanthine oxidase and xanthine dehydrogenase.Febuxostat is a potent, non-purine compound, which inhibits the expression of
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F125720-200mgProduct Description:Febuxostat(TEI 6720:TMX 67 ) is selective xanthine oxidase inhibitor with Ki of 0.6 nM.An inhibitor xanthine oxidase and xanthine dehydrogenase.Febuxostat is a potent, non-purine compound, which inhibits the expression of
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F125720-250mgProduct Description:Febuxostat(TEI 6720:TMX 67 ) is selective xanthine oxidase inhibitor with Ki of 0.6 nM.An inhibitor xanthine oxidase and xanthine dehydrogenase.Febuxostat is a potent, non-purine compound, which inhibits the expression of
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F125720-25gProduct Description:Febuxostat(TEI 6720:TMX 67 ) is selective xanthine oxidase inhibitor with Ki of 0.6 nM.An inhibitor xanthine oxidase and xanthine dehydrogenase.Febuxostat is a potent, non-purine compound, which inhibits the expression of
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F125720-5gProduct Description:Febuxostat(TEI 6720:TMX 67 ) is selective xanthine oxidase inhibitor with Ki of 0.6 nM.An inhibitor xanthine oxidase and xanthine dehydrogenase.Febuxostat is a potent, non-purine compound, which inhibits the expression of
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F648207-10mgFedovapagon (VA106483) is a selective and orally active Vasotocin V2 receptor (V2R) agonist with an EC 50 of 24 nM. Fedovapagon can be used in the research of nocturiaIn VivoFedovapagon (1 mg/kg, oral administration) inhibits urine output with 81%
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F648207-50mgFedovapagon (VA106483) is a selective and orally active Vasotocin V2 receptor (V2R) agonist with an EC 50 of 24 nM. Fedovapagon can be used in the research of nocturiaIn VivoFedovapagon (1 mg/kg, oral administration) inhibits urine output with 81%
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F648207-5mgFedovapagon (VA106483) is a selective and orally active Vasotocin V2 receptor (V2R) agonist with an EC 50 of 24 nM. Fedovapagon can be used in the research of nocturiaIn VivoFedovapagon (1 mg/kg, oral administration) inhibits urine output with 81%