β-Benzyloxyaspartate derivatives with photosensitive groups
AssigneeSuntory Holdings Limited
InventorsKeiko Shimamoto, Kiyo Takaoka
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AssigneeSuntory Holdings Limited
InventorsKeiko Shimamoto, Kiyo Takaoka
Estimating the term…
The present invention relates to photosensitive derivatives of optically active L-threo-β-benzyloxyaspartate or its benzene ring-substituted analogs, represented by the following formula (1) or (2): (1) (2) wherein R1 represents hydrogen atom, amino group, straight or branched lower aliphatic acylamino group optionally substituted at the acyl group portion, alicyclic acylamino group or aromatic acylamino group optionally having a substituent on the aromatic ring, R2 represents hydrogen atom or one or more straight or branched optionally substituted lower aliphatic alkyloxy groups on the benzene ring, R3 represents hydrogen atom, methyl group or carboxyl group, and R4 and R5 each represent hydrogen atom, hydroxyl group, straight or branched lower alkyloxy group optionally substituted at the alkyl portion, amino group, straight or branched lower alkyl-substituted amino group, or a halogen atom, which upon photoirradiation can produce compounds exhibiting a function of suppressing the glutamate uptake activity of L-glutamate transporters.
A compound having a substituted coumarylmethyl group connected to the nitrogen atom of the α-amino group of an L-threo-β-benzyloxylasparate or its benzene ring-substituted analog through a carbamate bond, represented by the following formula (2):
Dependencies are inferred from the claim text.