135531-86-1
135531-86-1
Chemical Structure
Camalexin
- CAS No.: 135531-86-1
- Formula:C11H8N2S
- Molecular Weight:200.26
IUPAC Name: 2-(1H-indol-3-yl)thiazole
InChIKey: IYODIJVWGPRBGQ-UHFFFAOYSA-N
SMILES: C12=C(C=CC=C2)NC=C1C3=NC=CS3
Biological Activity: Camalexin is a phytoalexin isolated from Camelina sativa (Cruciferae) with antibacterial, antifungal, antiproliferative and anticancer activities. Camalexin can induce reactive oxygen species (ROS) production[1][2][3].
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Camalexin | 99.70% | Camalexin is a phytoalexin isolated from Camelina sativa (Cruciferae) with antibacterial, antifungal, antiproliferative and anticancer activities. Camalexin can induce reactive oxygen species (ROS) production. | ||||||||||||||||||||
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Camalexin (Standard) | ≥98% | Camalexin (Standard) is the analytical standard of Camalexin. This product is intended for research and analytical applications. Camalexin is a phytoalexin isolated from Camelina sativa (Cruciferae) with antibacterial, antifungal, antiproliferative and anticancer activities. Camalexin can induce reactive oxygen species (ROS) production. | ||||||||||||||||||||
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References
- [1]. William A.Ayer, et al. Synthesis of camalexin and related phytoalexins. Tetrahedron. Volume 48, Issue 14, 1992, Pages 2919-2924.
- [2]. Glawischnig E. Camalexin. Phytochemistry. 2007 Feb;68(4):401-6. [Content Brief]
- [3]. Mezencev R, et al. Antiproliferative and cancer chemopreventive activity of phytoalexins: focus on indole phytoalexins from crucifers. Neoplasma. 2003;50(4):239-45. [Content Brief]
Keywords
