Literature DB >> 641817

Synthesis and antitumor evaluation of 4-ethoxycarbonyl cyclophosphamide analogs.

E L Foster.   

Abstract

4-Ethoxycarbonyl analogs of cyclophosphamide and its five-membered ring homolog were synthesized utilizing the cyclization method previously described. N,N-Bis(2-chloroethyl)-4-ethoxycarbonyl-1,3,2-oxazaphospholidin-2-amine 2-oxide demonstrated activity against L-1210 lymphoid leukemia whereas N,N-bis(2-chloroethyl)-4-(ethoxycarbonyl)tetrahydro-2H-1,3,2-oxazaphosphorin-2-amine 2-oxide did not. The oxazaphosphorin-2-amine was evaluated against human epidermoid carcinoma of the nasopharynx (cell culture). The results again were negative: ED50 = 2.8 X 10.

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Year:  1978        PMID: 641817     DOI: 10.1002/jps.2600670539

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  1 in total

1.  Crystal structures of chiral 2-[bis-(2-chloro-eth-yl)amino]-1,3,2-oxaza-phospho-lidin-2-one derivatives for the absolute configuration at phospho-rus.

Authors:  Laurence N Rohde; Matthias Zeller; John A Jackson
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2018-08-24
  1 in total

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