Antiproliferative activity of 2-[N,N-bis-2-chloroethyl}-amino]-4-[2-sulfonato-ethylthio]-tetrahydro-2H-1,3,2-oxazaphosphorine-2-oxide cyclohexamine (ASIA Z 7557, INN mafosfamide) against human and murine tumor cells in vitro

1984 ◽  
Vol 2 (2) ◽  
Author(s):  
JohnS. Kovach ◽  
PhyllisA. Svingen
1989 ◽  
Vol 68 (2) ◽  
pp. 186-191 ◽  
Author(s):  
Angela Dieckmann-Schuppert ◽  
Andreas Ruppel ◽  
Reinhard Burger ◽  
Werner Frank

Oncology ◽  
1984 ◽  
Vol 41 (1) ◽  
pp. 43-48 ◽  
Author(s):  
Kouji Okamoto ◽  
Yoshifumi Tomita ◽  
Hiroo Yonezawa ◽  
Tomio Hirohata ◽  
Ryohei Ogura ◽  
...  

1970 ◽  
Vol 48 (1) ◽  
pp. 75-78 ◽  
Author(s):  
G. A. LePage

The in vitro metabolism of 9-β-D-arabinofuranosyladenine (Ara-A) in TA3 ascites tumor cells was examined and compared with that of its metabolite 9-β-D-arabinofuranosylhypoxanthine (Ara-H). Some evidence for reamination of Ara-H to Ara-A was obtained. Such reamination may explain its activity as an antiviral agent. Unlike Ara-A, Ara-H was not phosphorylated and it did not inhibit DNA polymerase. Incorporation of radioactivity from Ara-A-14C or Ara-H-14C into RNA occurred, but was shown to have proceeded by a cleavage to free base and efficient reutilization of the labeled base.


1992 ◽  
Vol 65 (3) ◽  
pp. 209-213 ◽  
Author(s):  
Dennis S. Huang ◽  
Olalekan E. Odeleye ◽  
Ronald R. Watson

Molecules ◽  
2020 ◽  
Vol 25 (18) ◽  
pp. 4293
Author(s):  
Zhen-Wang Li ◽  
Chun-Yan Zhong ◽  
Xiao-Ran Wang ◽  
Shi-Nian Li ◽  
Chun-Yuan Pan ◽  
...  

Novel imidazole derivatives were designed, prepared, and evaluated in vitro for antitumor activity. The majority of the tested derivatives showed improved antiproliferative activity compared to the positive control drugs 5-FU and MTX. Among them, compound 4f exhibited outstanding antiproliferative activity against three cancer cell lines and was considerably more potent than both 5-FU and MTX. In particular, the selectivity index indicated that the tolerance of normal L-02 cells to 4f was 23–46-fold higher than that of tumor cells. This selectivity was significantly higher than that exhibited by the positive control drugs. Furthermore, compound 4f induced cell apoptosis by increasing the protein expression levels of Bax and decreasing those of Bcl-2 in a time-dependent manner. Therefore, 4f could be a potential candidate for the development of a novel antitumor agent.


Author(s):  
Alexandra Treister ◽  
Orit Sagi-Assif ◽  
Michal Meer ◽  
Nechama I. Smorodinsky ◽  
Romema Anavi ◽  
...  

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