Cavidine MedChemExpress (MCE)

Product Name	(6S,6aR)-8,9-dimethoxy-6-methyl-6,11,12,14-tetrahydro-6aH-[1,3]dioxolo[4,5-h]isoquino[2,1-b]isoquinoline
Synonyms	Cavidine (+)-cavidine (6S,6aR)-8,9-dimethoxy-6-methyl-6,11,12,14-tetrahydro-6aH-[1,3]dioxolo[4,5-h]isoquino[2,1-b]isoquinoline (6R,6aS)-8,9-dimethoxy-6-methyl-6,11,12,14-tetrahydro-6aH-[1,3]dioxolo[4,5-h]isoquino[2,1-b]isoquinoline Synonyms Cavidine (+)-cavidine (6S,6aR)-8,9-dimethoxy-6-methyl-6,11,12,14-tetrahydro-6aH-[1,3]dioxolo[4,5-h]isoquino[2,1-b]isoquinoline (6R,6aS)-8,9-dimethoxy-6-methyl-6,11,12,14-tetrahydro-6aH-[1,3]dioxolo[4,5-h]isoquino[2,1-b]isoquinoline 12H-benzo[a]-1,3-benzodioxolo[4,5-g]quinolizine, 6,6a,11,14-tetrahydro-8,9-dimethoxy-6-methyl-, (6S,6aR)- 12H-Benzo[a]-1,3-benzodioxolo[4,5-g]quinolizine, 6,6a,11,14-tetrahydro-8,9-dimethoxy-6-methyl-, (6S,6aR)- 12H-benzo[a]-1,3-benzodioxolo[4,5-g]quinolizine, 6,6a,11,14-tetrahydro-8,9-dimethoxy-6-methyl-, (6R,6aS)-
CAS	32728-75-9
EINECS
Chemical Formula	C21H23NO4
Molecular Weight	353.416
inchi	InChI=1/C21H23NO4/c1-12-14-4-5-17-21(26-11-25-17)16(14)10-22-7-6-13-8-18(23-2)19(24-3)9-15(13)20(12)22/h4-5,8-9,12,20H,6-7,10-11H2,1-3H3/t12-,20+/m0/s1
Package	5 mg
Price	Email to quote
Descriptions	Cavidine Cavidine MedChemExpress (MCE) HY-101546A 32728-75-9 (+)-Cavidine Please store the product under the recommended conditions in the Certificate of Analysis. Room temperature in continental US Descriptions Cavidine Cavidine MedChemExpress (MCE) HY-101546A 32728-75-9 (+)-Cavidine Please store the product under the recommended conditions in the Certificate of Analysis. Room temperature in continental US may vary elsewhere. Cavidine ((+)-Cavidine) is a selective COX-2 inhibitor which possesses anti-inflammatory activity. Cavidine can be used for the research of skin injuries, hepatitis, cholecystitis, and scabies. Cavidine ameliorates LPS (HY-D1056)-induced acute lung injury via NF-κB signaling pathway. \| \| \| \| \| \| \| \| \| \| [1]. Niu X, et, al. Anti-inflammatory effects of cavidine in vitro and in vivo, a selective COX-2 inhibitor in LPS-induced peritoneal macrophages of mouse. Inflammation. 2015 Apr 38(2):923-33. [Content Brief] [2]. Niu X, et, al. Cavidine Ameliorates Lipopolysaccharide-Induced Acute Lung Injury via NF-κB Signaling Pathway in vivo and in vitro. Inflammation. 2017 Aug 40(4):1111-1122. [Content Brief] [3]. Niu X, et, al. Protective effect of cavidine on acetic acid-induced murine colitis via regulating antioxidant, cytokine profile and NF-κB signal transduction pathways. Chem Biol Interact. 2015 Sep 5:239:34-45. [Content Brief]
Supplier Website	https://www.medchemexpress.com/cavidine.html
Last Update	2025-04-01 14:45:47

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