135158-54-2
Chemical Structure
Acibenzolar-S-methyl
Synonym(s): ASM
- CAS No.: 135158-54-2
- Formula:C8H6N2OS2
- Molecular Weight:210.28
IUPAC Name: S-methyl benzo[d][1,2,3]thiadiazole-7-carbothioate
InChIKey: UELITFHSCLAHKR-UHFFFAOYSA-N
SMILES: O=C(SC)C1=C2SN=NC2=CC=C1
Biological Activity: Acibenzolar-S-methyl (ASM) is a synthetic analog of Salicylic acid (HY-B0167) and a plant activator. Acibenzolar‑S‑methyl induces increased activities of defense-related enzymes such as peroxidase and chitinase, activates stomatal defense responses and PR defense gene expression, induces the production of ROS, triggers local and systemic acquired resistance, and inhibits the proliferation of bacterial and fungal pathogens in plants. Acibenzolar‑S‑methyl can be used in studies related to plant infection[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Acibenzolar-S-methyl | 99.77% | Acibenzolar-S-methyl (ASM) is a synthetic analog of Salicylic acid (HY-B0167) and a plant activator. Acibenzolar‑S‑methyl induces increased activities of defense-related enzymes such as peroxidase and chitinase, activates stomatal defense responses and PR defense gene expression, induces the production of ROS, triggers local and systemic acquired resistance, and inhibits the proliferation of bacterial and fungal pathogens in plants. Acibenzolar‑S‑methyl can be used in studies related to plant infection. | ||||||||||||||||||||
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Acibenzolar-S-methyl (Standard) | ≥98% | Acibenzolar-S-methyl (Standard) (ASM (Standard)) is the analytical standard of Acibenzolar-S-methyl (HY-116541). This product is intended for research and analytical applications. Acibenzolar-S-methyl (ASM) is a synthetic analog of Salicylic acid (HY-B0167) and a plant activator. Acibenzolar‑S‑methyl induces increased activities of defense-related enzymes such as peroxidase and chitinase, activates stomatal defense responses and PR defense gene expression, induces the production of ROS, triggers local and systemic acquired resistance, and inhibits the proliferation of bacterial and fungal pathogens in plants. Acibenzolar‑S‑methyl can be used in studies related to plant infection. | ||||||||||||||||||||
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- [1]. Sakata N, et al. Acibenzolar-S-Methyl Activates Stomatal-Based Defense Systemically in Japanese Radish. Frontiers in plant science. 2020;11:565745.
- [2]. Cole D L. The efficacy of acibenzolar‑S‑methyl, an inducer of systemic acquired resistance, against bacterial and fungal diseases of tobacco. Crop Protection, 1999,18(4):267‑273.
- [3]. Baysal Ö, et al. Induction of defence‑related enzymes and resistance by the plant activator acibenzolar‑S‑methyl in tomato seedlings against bacterial canker caused by Clavibacter michiganensis ssp. michiganensis. Plant Pathology, 2003,52(6):747‑753.
