chlorzoxazone

Chlorzoxazone (Chlorzoxazon) is a Muscle Relaxant. The physiologic effect of chlorzoxazone is by means of Centrally-mediated Muscle Relaxation.

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.

Chlorzoxazone-D3 is the deuterated form of Chlorzoxazone (T1650) and can be used for isotope tracing.

Chlorzoxazone-N-glucuronide is a Phase II metabolite of the skeletal muscle relaxant chlorzoxazone. It is synthesized through glucuronidation of chlorzoxazone by UGT1A9.

6-Hydroxy Chlorzoxazone is the major metabolite of the muscle relaxant chlorzoxazone. 6-Hydroxy Chlorzoxazone is a chlorinated benzoxazolone generated by metabolism via the CYP2E1 enzyme in the liver. 6-Hydroxy Chlorzoxazone serves as a reliable marker for assessing CYP2E1 metabolic activity and is used as a reference standard in biochemical research.

Chlorzoxazone (Standard) is the standard substance of Chlorzoxazone, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Chlorzoxazone (Chlorzoxazon) is a Muscle Relaxant. The physiologic effect of chlorzoxazone is by means of Centrally-mediated Muscle Relaxation.

Chlorzoxazone-[13C6] (Standard) is a reference standard of Chlorzoxazone-[13C6] intended for quantitative analysis, quality control, and related biochemical research applications.

6-HydroxyChlorzoxazone-13C6 is a 13C-labeled compound of 6-HydroxyChlorzoxazone (T37306) and can be used for isotope tracing.

6-Hydroxychlorzoxazone-13C6 (Standard) is a reference standard of 6-Hydroxychlorzoxazone-13C6 intended for quantitative analysis, quality control, and related biochemical research applications. 6-HydroxyChlorzoxazone-13C6 is a 13C-labeled compound of 6-HydroxyChlorzoxazone and can be used for isotope tracing.

Tenuifoliside C, isolated from Polygala tenuifolia Willd, is a targeted lactate dehydrogenase inhibitor that significantly inhibits chlorzoxazone 6-hydroxylation catalyzed by CYP2E1[1].

Polygalaxanthone III can significantly inhibit chlorzoxazone 6-hydroxylation catalyzed by CYP2E1.

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.

polygalaxanthone III (Standard) is a reference standard for research and analysis in studies involving polygalaxanthone III. Polygalaxanthone III can significantly inhibit chlorzoxazone 6-hydroxylation catalyzed by CYP2E1.