Studies on RA derivatives. V. Synthesis and antitumor activity of Ala2- modified RA-VII derivatives

DOI: 10.1248/cpb.41.1402

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 1402 - 1410 (1993)

Update date:2022-09-26

Topics:

Authors:

Itokawa Itokawa

Kondo Kondo

Hitotsuyanagi

Isomura Isomura

Takeya Takeya

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Article abstract of DOI:10.1248/cpb.41.1402

A number of RA-VII derivatives having various amino acids including proline (6), pipecolic acid (11), norvaline (12), ornithine (14), aspartic acid (15) and methionine (20) in place of Ala² have been synthesized from RA-X methyl ester (3) and evaluated for cytotoxicity to P388 leukemia and KB cells in vitro. Comparison of the cytotoxicity of these compounds suggests that the polarity and the length of the 2nd amino acid residue affect the activity. An NMR study revealed that, in solution, 6 and 11 are locked in one conformational state, corresponding to conformer A of RA-VII.

Full text of DOI:10.1248/cpb.41.1402

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