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L-2,4-Diaminobutanoic acid

A structure somewhat related to the acyl phosphonate analogue (VIII.83) has been briefly described [278] in a report on FPGS inhibitors. The preparation of this compound (VIII.86) was achieved from V -(4-amino-4-deoxy-V °-methylpteroyl)-L-lysine and 4-nitrophenyl phosphonoacetate. While (VIII.86) obviously contained too many CH2 groups to be considered a close analogue of (VIII.83), the shorter-chain compound (VIII.87), a derivative of V -(4-amino-4-deoxy-V °-methylpteroyl)-L-2,3-diaminobutanoic acid, would seem to be reasonable candidate for this role. [Pg.181]

Diaminobutanoic acid methyl ester, L Ornithine methyl ester, L Lysine methyl ester, L... [Pg.334]


See other pages where L-2,4-Diaminobutanoic acid is mentioned: [Pg.224]    [Pg.28]    [Pg.33]    [Pg.827]    [Pg.828]    [Pg.29]    [Pg.224]    [Pg.28]    [Pg.33]    [Pg.827]    [Pg.828]    [Pg.29]    [Pg.866]    [Pg.1135]    [Pg.806]    [Pg.228]    [Pg.222]    [Pg.1349]    [Pg.1295]    [Pg.1345]    [Pg.414]    [Pg.370]   
See also in sourсe #XX -- [ Pg.29 ]




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2,4-Diaminobutanoic acid

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