HAN JUEI, WANG CHEN-KANG, CHI HSIU-CHAN, LI KUANG-TSUI, LIU KENG-T'AO, CHANG HUI-YUN, HO SHIH, FAN LI-LI AND LEI HAI-P'ENG, . STUDIES ON ANTITUMOR DRUGS VIII. THE ANTITUMOR EFFECT OF THE ETHYL ESTER OF N-FORMYL-SARCOLYSIN-PHENYLALANINE ON EXPERIMENTAL TUMORSJ. Acta Pharmaceutica Sinica, 1963, 10(8): 460-465.
Citation: HAN JUEI, WANG CHEN-KANG, CHI HSIU-CHAN, LI KUANG-TSUI, LIU KENG-T'AO, CHANG HUI-YUN, HO SHIH, FAN LI-LI AND LEI HAI-P'ENG, . STUDIES ON ANTITUMOR DRUGS VIII. THE ANTITUMOR EFFECT OF THE ETHYL ESTER OF N-FORMYL-SARCOLYSIN-PHENYLALANINE ON EXPERIMENTAL TUMORSJ. Acta Pharmaceutica Sinica, 1963, 10(8): 460-465.

STUDIES ON ANTITUMOR DRUGS VIII. THE ANTITUMOR EFFECT OF THE ETHYL ESTER OF N-FORMYL-SARCOLYSIN-PHENYLALANINE ON EXPERIMENTAL TUMORS

  • The ethyl ester of N-formyl-sarcolycine-phenylalanine (FSPA) was synthetized in this institute. At a daily dosage of 100-200 mg/kg FSPA markedly inhibited the growth of Yoshida ascites sarcoma. The intraperitoneal LD50 for mice was 4.5 gm/kg. When the drug was administered orally to normal monkeys at 100 mg/kg daily for 14 days, no change in blood picture or impairment of liver and kidney functions was noted. However, at 200 mg/kg FSPA showed definite inhibitory effect on the bone marrow. This compound has been recommended for clinical trial.
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