Literature DB >> 14642335

Synthesis and antineoplastic activity of 2-alkylaminoethyl derivatives of various steroidal oximes.

Dharam Paul Jindal1, Raja Chattopadhaya, Sheetal Guleria, Ranju Gupta.   

Abstract

Various steroidal oxime ether derivatives in androstene and estrane series have been synthesized and evaluated for the antineoplastic activity at National Cancer Institute, Bethesda, Maryland, USA. O-alkylation of the oximes by various alkylaminoethyl halides gave the oxime ether derivatives. The 17alpha-ethynylandrostene derivatives 29 (DPJ-684), 30 (DPJ-685), 31 (DPJ-686) and estrane derivatives 35 (DPJ-531) and 36 (DPJ-532) were among the small percentage of compounds, which have been screened by NCI for in vivo hollow fiber assay by virtue of their activity against one or more human tumour cell lines in 60 cell line in vitro prescreen. The preliminary in vivo reports of hollow fiber assays have been referred to the Biological Evaluation Committee for Cancer Drugs for considering these compounds for further detailed in vivo testing.

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Year:  2003        PMID: 14642335     DOI: 10.1016/j.ejmech.2003.09.002

Source DB:  PubMed          Journal:  Eur J Med Chem        ISSN: 0223-5234            Impact factor:   6.514


  7 in total

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4.  Novel alkylaminoethyl derivatives of androstane 3-oximes as anticancer candidates: synthesis and evaluation of cytotoxic effects.

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Journal:  RSC Adv       Date:  2021-11-22       Impact factor: 3.361

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6.  Eco-friendly synthesis, physicochemical studies, biological assay and molecular docking of steroidal oxime-ethers.

Authors:  Mahboob Alam; Dong-Ung Lee
Journal:  EXCLI J       Date:  2015-03-02       Impact factor: 4.068

7.  Synthesis, reactivity and biological activity of novel bisbenzofuran-2-yl-methanone derivatives.

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  7 in total

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