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T6646Rosiglitazone hydrochloridemellitus,hepatocellular,PPAR,antihyperglycemic,Inhibitor,cancer,senescenc
Rosiglitazone HCl is a blood glucose-lowering drugs, stimulating insulin secretion by binding to the PPAR receptors in fat cells.
价 格：￥电议型 号：T6646产 地：中国大陆
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T1622Rosiglitazone maleate马来酸罗格列酮；BRL 49653C；BRL 49653
Rosiglitazone Maleate is the maleate salt of rosiglitazone, an orally-active thiazolidinedione with antidiabetic properties and potential antineoplastic activity.
价 格：￥电议型 号：T1622产 地：中国大陆
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T0334Rosiglitazone罗格列酮；BRL49653
Rosiglitazone is an insulin sensitizing agent and thiazolidinedione that is indicated for the treatment of type 2 diabetes. Rosiglitazone has been linked to rare instances of acute liver injury.
价 格：￥电议型 号：T0334产 地：中国大陆
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T0334RosiglitazoneRosiglitazone,BRL49653,
Rosiglitazone is an insulin sensitizing agent and thiazolidinedione that is indicated for the treatment of type 2 diabetes. Rosiglitazone has been linked to rare instances of acute liver injury.
价 格：￥电议型 号：T0334产 地：美洲
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T1622Rosiglitazone maleateRosiglitazone maleate,BRL 49653C,BRL 49653
Rosiglitazone Maleate is the maleate salt of rosiglitazone, an orally-active thiazolidinedione with antidiabetic properties and potential antineoplastic activity.
价 格：￥电议型 号：T1622产 地：美洲
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T6646Rosiglitazone hydrochloride盐酸罗格列酮盐酸罗格列酮|||BRL-49653 HCl|||Rosiglitazone HCl
Rosiglitazone hydrochloride (BRL-49653 HCl) is a blood glucose-lowering drugs, stimulating insulin secretion by binding to the PPAR receptors in fat cells.
价 格：￥电议型 号：T6646产 地：中国大陆
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T61848Rosiglitazone potassium；化合物 Rosiglitazone potassiumRosiglitazone potassium
Rosiglitazone (BRL 49653) potassium is a potent and selective PPARγ agonist (EC 50: 60 nM, Kd: 40 nM), administered orally. It also serves as an activator of TRPC5 (EC 50: 30 μM) and an inhibitor of TRPM3. This compound, widely used in research, has shown promise in investigating obesity, diabetes, senescence, and ovarian cancer [1] [2] [4] [7].
价 格：￥电议型 号：T61848产 地：中国大陆
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T35717N-desmethyl Rosiglitazone；N-desmethyl RosiglitazoneN-desmethyl Rosiglitazone
N-desmethyl Rosiglitazone is a major metabolite of rosiglitazone , a potent and selective PPARγ ligand present in formulations that have been used to treat type 2 diabetes. Rosiglitazone is metabolized by the cytochrome P450 (CYP) isoform CYP2C8 to form N-desmethyl rosiglitazone.
价 格：￥电议型 号：T35717产 地：中国大陆
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T1622Rosiglitazone maleate；马来酸罗格列酮BRL 49653C|||BRL 49653；BRL 49653C|||BRL 49653|||马来酸罗格列酮
Rosiglitazone maleate (BRL 49653) is the maleate salt of rosiglitazone, an orally-active thiazolidinedione with antidiabetic properties and potential antineoplastic activity.
价 格：￥电议型 号：T1622产 地：中国大陆
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T0334Rosiglitazone；罗格列酮BRL49653；BRL49653|||罗格列酮
Rosiglitazone (BRL49653) is a PPARγ agonist, TRPC5 activator, and TRPM3 inhibitor with oral activity. Rosiglitazone is also a hypoglycemic agent and a thiazolidinedione insulin sensitizer.
价 格：￥电议型 号：T0334产 地：中国大陆
