
Glimepiride
CAS No. 93479-97-1
Glimepiride ( HOE 490 )
产品货号. M16685 CAS No. 93479-97-1
格列美脲是第一代磺酰脲,它是一种非常有效、作用持续时间长的磺酰脲。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
200MG | ¥267 | 有现货 |
![]() ![]() |
500MG | ¥437 | 有现货 |
![]() ![]() |
1G | ¥721 | 有现货 |
![]() ![]() |
生物学信息
-
产品名称Glimepiride
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述格列美脲是第一代磺酰脲,它是一种非常有效、作用持续时间长的磺酰脲。
-
产品描述Glimepiride is the first III generation sulphonyl urea it is a very potent sulphonyl urea with long duration of action. (In Vivo):Glimepiride (Glimperide) is a new sulfonylurea. After oral administration of Hoe 490 to rabbits, blood glucose was lowered 3.5 times more than after glibenclamide (HB 419) and after intravenous administration, 2.5 times more. Glimepiride (Glimperide) decreased extracellular Aβ40 and Aβ42 levels. glimepiride may serve as a promising drug for the treatment of AD associated with diabetes. Glimepiride (Glimperide) was generally associated with lower risk of hypoglycemia and less weight gain compared to other sulfonylureas. Glimepiride (Glimperide) use may be safer in patients with cardiovascular disease because of its lack of detrimental effects on ischemic preconditioning.
-
体外实验——
-
体内实验——
-
同义词HOE 490
-
通路Cell Cycle/DNA Damage
-
靶点Potassium Channel
-
受体SUR1| SUR2A| SUR2B
-
研究领域Metabolic Disease
-
适应症——
化学信息
-
CAS Number93479-97-1
-
分子量490.62
-
分子式C24H34N4O5S
-
纯度>98% (HPLC)
-
溶解度DMSO: 11 mg/mL (22.42 mM)
-
SMILESCCC1=C(CN(C1=O)C(=O)NCCC2=CC=C(C=C2)S(=O)(=O)NC(=O)NC3CCC(CC3)C)C
-
化学全称4-ethyl-3-methyl-N-[2-[4-[(4-methylcyclohexyl)carbamoylsulfamoyl]phenyl]ethyl]-5-oxo-2H-pyrrole-1-carboxamide
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1.Song DK, Ashcroft FM. Br J Pharmacol. 2001 May;133(1):193-9.
产品手册




关联产品
-
AVE-0118
AVE-0118 是一种有效的 I(to)/I(Kur) 阻滞剂、Kv1.5 通道抑制剂,IC50 为 5.6 uM。
-
Linopirdine dihydroc...
Linopirdine (DUP-996) 是一种有效的 Kv7 (KCNQ) 电压门控钾通道阻断剂;阻断 KV7.1+7.3 (KCNQ2+3) / M 电流 (IC50=4-7 uM) 和 KV7.1 (KCNQ1) 同聚通道 (IC50=8.9 uM)。
-
VU0134992 hydrochlor...
VU0134992 盐酸盐是第一个亚型偏好的、口服活性的、选择性的 Kir4.1 钾通道孔阻滞剂(IC50:0.97 μM)。