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135531-86-1

135531-86-1 structure
135531-86-1 structure
  • Name: Camalexin
  • Chemical Name: camalexin
  • CAS Number: 135531-86-1
  • Molecular Formula: C11H8N2S
  • Molecular Weight: 200.26000
  • Catalog: Signaling Pathways Anti-infection Bacterial
  • Create Date: 2018-03-11 23:52:58
  • Modify Date: 2025-08-20 15:59:02
  • Camalexin is a phytoalexin isolated from Camelina sativa and Arabidopsis (Cruciferae) with antibacterial, antifungal, antiproliferative and anticancer activities. Camalexin can induce reactive oxygen species (ROS) production[1][2][3].

Name camalexin
Synonyms 2-(1H-indol-3-yl)thiazole
3-Thiazol-2-yl-1H-indole
Camalexin
Description Camalexin is a phytoalexin isolated from Camelina sativa and Arabidopsis (Cruciferae) with antibacterial, antifungal, antiproliferative and anticancer activities. Camalexin can induce reactive oxygen species (ROS) production[1][2][3].
Related Catalog
Target

Reactive oxygen species (ROS)[1][2]

In Vitro Camalexin shows antiproliferative activity against a human breast cancer cell line[2]. For the oomycetes Phytophthora and Pythium Nep1-like proteins (necrosis and ethylene-inducing peptide 1-like proteins) are the initial triggers of Camalexin synthesis and formation of reactive oxygen species (ROS). ROS appear to be of general relevance for Camalexin formation. Chemical induction of ROS, such as by application of acifluorfen, coincided with Camalexin synthesis. In a screen for enhanced susceptibility to Alternaria brassicicola the esa1 mutant is identified, which shows delayed Camalexin induction. Particularly in response to ROS inducing agents reduced Camalexin levels are synthesized. This crucial role for ESA1 is confirmed by the inability of esa1 mutants to synthesize Camalexin in response to Leptosphaeria maculans. An additional mutant that exhibits greatly reduced Camalexin accumulation is ups1, which is isolated on the basis of diminished expression of a tryptophan biosynthetic enzyme[2].
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.

[3]. Mezencev R, et al. Antiproliferative and cancer chemopreventive activity of phytoalexins: focus on indole phytoalexins from crucifers. Neoplasma. 2003;50(4):239-45.

Molecular Formula C11H8N2S
Molecular Weight 200.26000
Exact Mass 200.04100
PSA 56.92000
LogP 3.29140
Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H302-H315-H319-H335
Precautionary Statements P261-P305 + P351 + P338
Hazard Codes Xi
RIDADR NONH for all modes of transport
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