(+)-Allo-octopine is a naturally occurring compound classified as an amino acid derivative and is part of the opine family, which are compounds produced by certain plants and bacteria. It is characterized by its chiral nature, possessing a specific stereochemistry that contributes to its biological activity. The molecular structure of (+)-allo-octopine includes a hydroxyl group and an amine group, which are key functional groups that influence its reactivity and interactions in biological systems. This compound is primarily associated with the metabolism of certain plant pathogens, particularly in the context of plant-microbe interactions. Its role in the nitrogen metabolism of plants and its potential as a signaling molecule in plant defense mechanisms are areas of interest in biochemical research. Additionally, (+)-allo-octopine can be synthesized through various chemical pathways, making it a subject of study in organic synthesis and agricultural biotechnology. Its CAS number, 63358-47-4, is a unique identifier that facilitates its identification in chemical databases and literature.

(+)-allo-octopine

63358-47-4: (+)-Allo-octopine is a naturally occurring compound classified as an amino acid derivative and is part of the opine family, which are compounds produced by certain plants and bacteria. It is characterized by its chiral nature, possessing a specific stereochemistry that contributes to its biological activity. The molecular structure of (+)-allo-octopine includes a hydroxyl group and an amine group, which are key functional groups that influence its reactivity and interactions in biological systems. This compound is primarily associated with the metabolism of certain plant pathogens, particularly in the context of plant-microbe interactions. Its role in the nitrogen metabolism of plants and its potential as a signaling molecule in plant defense mechanisms are areas of interest in biochemical research. Additionally, (+)-allo-octopine can be synthesized through various chemical pathways, making it a subject of study in organic synthesis and agricultural biotechnology. Its CAS number, 63358-47-4, is a unique identifier that facilitates its identification in chemical databases and literature.

Stability Hygroscopic Applications A competitive inhibitor of Octopine (O239850). Inhibits callus proliferation in apple. References Sagisaka, S. et al.: Biosci. Biotech. Bioch. 58, 978 (1994); Biellmann, J. et al.: Bioorg. Chem. 6, 89 (1977)

L-Allooctopine

L-Allooctopine competitively inhibits D-octopine [1].

CAS 63358-47-4

(+)-allo-octopine

L-Allooctopine

Ref: TR-A546800

L-Allooctopine

Ref: TM-T81954