Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Indigofera spicata

Occurs In legume species Indigofera spicata and Indigofera linnaei... [Pg.35]

Indospicine (= I-2-Amino- Indigofera spicata, I. spp. (Fabaceae) cNOS, iNOS (Arginase)... [Pg.279]

Glucose esters of 3-N. (endecaphyllins) are responsible for the toxicity of Indigofera endecaphylla for grazing animals. 3-N. functions as suicide substrate of succinate dehydrogenase where the formed 3-nitro-acrylic acid adds to the active thiol group of the enzyme. The compound is formed biosynthetically in Penicillium atrovenetum from L-aspartic acid which is oxidized to the a-nitrosuccinate and then decarboxy-lated to furnish the aci-nitro form of 3-N.. Malonate and N-hydroxymalonamate appear to be intermediates in Indigofera spicata. [Pg.436]

Indospicine [L-2-amino-6-(amidino)hexanoic acid] (83) (Fig. 13.16) has been isolated from Indigofera spicata, a legume that is widely cultivated as a forage crop. The amino acid is quite toxic and causes abortion and hepatotoxicity. Nothing is known of the biosynthetic origin of indospicine (Hegarty, 1970, 1978). [Pg.227]


See other pages where Indigofera spicata is mentioned: [Pg.125]    [Pg.578]    [Pg.787]    [Pg.30]    [Pg.125]    [Pg.578]    [Pg.787]    [Pg.30]    [Pg.123]    [Pg.71]    [Pg.828]   
See also in sourсe #XX -- [ Pg.71 ]

See also in sourсe #XX -- [ Pg.227 , Pg.232 ]




SEARCH



Indigofera

© 2024 chempedia.info