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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1650 |
Chlorzoxazone
Paraflex,Chlorzoxazon,氯唑沙宗 |
P450; Potassium Channel | Membrane transporter/Ion channel; Metabolism |
Chlorzoxazone (Chlorzoxazon) 是作用于中枢的肌肉松弛剂, 可用于肌肉痉挛的研究。 | |||
T37306 |
6-hydroxy Chlorzoxazone
6-hydroxy Chlorzoxazone,NSC 24955 |
Others | Others |
6-hydroxy Chlorzoxazone is a metabolite of chlorzoxazone. [1] It is formed by metabolism of chlorzoxazone by the cytochrome P450 (CYP) isoform CYP2E1 in human hepatic microsomes. | |||
T37852 |
Chlorzoxazone N-Glucuronide
|
Others | Others |
Chlorzoxazone N-glucuronide is a phase II metabolite of the skeletal muscle relaxant chlorzoxazone . Chlorzoxazone N-glucuronide is formed via glucuronidation of chlorzoxazone by the UDP-glucuronosyltransferase (UGT) isoform UGT1A9. | |||
T71882 |
Pifexole
|
Others | Others |
Pifexole is the 1,2,4-oxadiazole derivative. It has a similar profile of muscle-relaxant activity in animals to that of chlorzoxazone. In rats, pifexole is reported to be seven times more potent than chlorzoxazone in inhibition of strychnine-induced convulsions. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3696 |
polygalaxanthone III
|
Others; P450 | Metabolism; Others |
Polygalaxanthone III 提取自远志polygala tenuifolia wild,可抑制CYP450酶。它能够抑制由 CYP2E1 催化的氯唑沙宗 6-羟基化(IC50:50.56μM)。 | |||
T2S2211 |
Tenuifoliside C
|
Dehydrogenase | Metabolism |
Tenuifoliside C 是从野生的 polygala tenuifolia 中分离得到的。它对 CYP2E1 催化氯唑酮 6-羟基化反应具有抑制作用。 |