產品櫥窗
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Acetosyringone
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產品型號：101-2478-38-8 商品規格： |
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3',5'-Dimethoxy-4'-hydroxyacetophenone. Synonym: 4′-Hydroxy-3′,5′-dimethoxyacetophenone, Acetosyringone
HOC6H2(OCH3)2COCH3
M.W.: 196.2.
Purity (HPLC): 98%
Melting Point: 125-126℃
Solubility: Soluble in Chloroform and DMSO
White Shining Powder
Acetosyringone is a phenolic natural product, and is a chemical compound related to acetophenone and 2,6-dimethoxyphenol. It was first described in relation to lignan/phenylpropanoid-type phytochemicals, with isolation from a variety of plant sources, in particular, in relation to wounding and other physiologic changes.
Historically, this substance has been best known for its involvement in plant-pathogen recognition, especially its role as a signal attracting and transforming unique, oncogenic bacteria in genus Agrobacterium. The virA gene on the Ti plasmid of Agrobacterium tumefaciens and the Ri plasmid of Agrobacterium rhizogenes is used by these soil bacteria to infect plants, via its encoding for a receptor for acetosyringone and other phenolic phytochemicals exuded by plant wounds. This compound also allows higher transformation efficiency in plants, in A. tumefaciens-mediated transformation procedures, and so is of importance in plant biotechnology.
Acetosyringone can also be found in Posidonia oceanica and a wide variety of other plants. It is secreted at wounded site of dicotyledons. This compound enhances the Agrobacterium-mediated gene transformation in dicot. Monocotyledons lack this wound response and it is considered as the limiting factor in Agrobacterium-mediated gene transformation in monocots.
Beil. 8,IV,2735
FT-IR 2 (2), 2429:D / FT-IR 1 (2), 46:C / FT-NMR 1 (2), 866:A / IR-Spectra (3), 875:B / IR-Spectra (2), 765:G / NMR-Reference 2 (2), 43:A / RegBook 1 (2), 1653:D / Structure Index 1, 260:B:7
M.W.: 196.2.
Purity (HPLC): 98%
Melting Point: 125-126℃
Solubility: Soluble in Chloroform and DMSO
White Shining Powder
Acetosyringone is a phenolic natural product, and is a chemical compound related to acetophenone and 2,6-dimethoxyphenol. It was first described in relation to lignan/phenylpropanoid-type phytochemicals, with isolation from a variety of plant sources, in particular, in relation to wounding and other physiologic changes.
Historically, this substance has been best known for its involvement in plant-pathogen recognition, especially its role as a signal attracting and transforming unique, oncogenic bacteria in genus Agrobacterium. The virA gene on the Ti plasmid of Agrobacterium tumefaciens and the Ri plasmid of Agrobacterium rhizogenes is used by these soil bacteria to infect plants, via its encoding for a receptor for acetosyringone and other phenolic phytochemicals exuded by plant wounds. This compound also allows higher transformation efficiency in plants, in A. tumefaciens-mediated transformation procedures, and so is of importance in plant biotechnology.
Acetosyringone can also be found in Posidonia oceanica and a wide variety of other plants. It is secreted at wounded site of dicotyledons. This compound enhances the Agrobacterium-mediated gene transformation in dicot. Monocotyledons lack this wound response and it is considered as the limiting factor in Agrobacterium-mediated gene transformation in monocots.
Beil. 8,IV,2735
FT-IR 2 (2), 2429:D / FT-IR 1 (2), 46:C / FT-NMR 1 (2), 866:A / IR-Spectra (3), 875:B / IR-Spectra (2), 765:G / NMR-Reference 2 (2), 43:A / RegBook 1 (2), 1653:D / Structure Index 1, 260:B:7
Store at 4℃
Irritant
Irritant