Literature DB >> 978676

Potential antitumor agents. 19. Multiply substituted 4'-(9-acridinylamino)methanesulfonanilides.

B F Cain, G Atwell.   

Abstract

A series of 42 multiply substituted 4'-(9-acridinylamino)methanesulfonanilides has been prepared and evaluated in the L1210 system. In addition to biologic activity changes resulting from altered agent lipophilic-hydrophilic balance variants containing both acridine 4-CH3 and 3-NH2, NHCOCH3 or NO2 substituents have reduced activity. Variants 3,6-disubstituted, using functions of differing electronic character, have depressed activity, suggesting that there is limited site bulk tolerance. Asymmetric 3,5-disubstitution should then be the preferred pattern; the 3-ND-5CH-3'-OCH variant is the most dose potent (optimum dose qd 1-5, 1.25 mg/kg/day) of the high activity agents of this series so far prepared.

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Year:  1976        PMID: 978676     DOI: 10.1021/jm00231a008

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  2 in total

1.  The tissue localization of m-AMSA and its effect on thymidine incorporation in various tissues in vivo.

Authors:  B Hellman; B S Andersson; P Slanina; A Mohammed; I Brandt; M Beran
Journal:  Med Oncol Tumor Pharmacother       Date:  1986

Review 2.  Medicinal chemistry of acridine and its analogues.

Authors:  Parteek Prasher; Mousmee Sharma
Journal:  Medchemcomm       Date:  2018-08-14       Impact factor: 3.597

  2 in total

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