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Synthesis, acute toxicity and chemotherapeutic anti-cancer activities of a new tripeptidic mustard.

作者信息

De Barbieri A, Dall'Asta L, Comini A, Springolo V, Mosconi P, Coppi G

出版信息

Farmaco Sci. 1983 Apr;38(4):205-18.

PMID:6861998
Abstract

A new antitumor agent having the chemical composition of 3-(p-fluorophenyl)-Lalanyl-3-[m-bis-(2-chloroethyl)aminophenyl]-L- alanyl-L-methionine ethyl ester hydrochloride (PTT 119) was synthetized. It fundamental toxicological data in mice and rats were assessed; its antitumor activity was investigated by establishing in mice, inoculated with L 1210 leukemia or in AKR mice with spontaneous leukemia of viral origin, a significant increase in Mean Survival Time as well as a percent increase of Increased Life Span and of the number of survivors.

摘要

相似文献

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Synthesis, acute toxicity and chemotherapeutic anti-cancer activities of a new tripeptidic mustard.
Farmaco Sci. 1983 Apr;38(4):205-18.
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[Research on compounds with antiblastic activity. XLI. Synthesis of new nitrogen mustards correlated with N,N-bis-(beta-chlorethyl) aniline].
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引用本文的文献

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Cancer Chemother Pharmacol. 1986;16(2):129-32. doi: 10.1007/BF00256162.
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Phase I study of beta-alanyl-melphalan as a potent anticancer drug.β-丙氨酰-美法仑作为一种强效抗癌药物的I期研究。
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4
Phase II study of a new alkylating agent (PTT-119) in resistant-relapsed non-Hodgkin's lymphomas.新型烷化剂(PTT-119)用于难治性复发非霍奇金淋巴瘤的II期研究
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5
Evaluation of p-F-Phe-m-bis-(2-chloroethyl)amino-L-Phe-Met-ethoxy HCl against transplantable and spontaneous murine neoplasia.对盐酸对氟苯丙氨酸 - 间 - 双(2 - 氯乙基)氨基 - L - 苯丙氨酸 - 甲硫氨酸乙酯抗可移植性和自发性小鼠肿瘤的评估。
Cancer Chemother Pharmacol. 1990;26(3):215-20. doi: 10.1007/BF02897202.
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Blut. 1990 Mar;60(3):172-6. doi: 10.1007/BF01720271.
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Evidence for increased intracellular transport of m-sarcolysine (alkylating moiety) when combined with two amino acid analogs (PTT-119).当与两种氨基酸类似物(PTT-119)联合使用时,间氮芥(烷基化部分)细胞内转运增加的证据。
Blut. 1990 Nov;61(5):311-3. doi: 10.1007/BF01732884.