A more reliable synthesis of a Gemini vitamin D analog, a potentially effective chemotherapeutic agent for the treatment of colorectal carcinomas
Author:
Affiliation:
1. Departamento de Química Orgánica
2. Facultad de Química and Instituto de Investigación Sanitaria Galicia Sur (IISGS)
3. University of Vigo
4. 36310 Vigo
5. Spain
Abstract
After a serendipitous synthesis of a potentially effective chemotherapeutic agent for the treatment of colorectal carcinomas, a more reliable synthetic method is now described using our building blocks containing stereodefined stereochemistry at C-20.
Funder
Consellería de Cultura, Educación e Ordenación Universitaria, Xunta de Galicia
Universidade de Vigo
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2018/QO/C8QO00338F
Reference13 articles.
1. Formal Desymmetrization of the Diastereotopic Chains in Gemini Calcitriol Derivatives with Two Different Side Chains at C-20
2. Gene expression profiling changes induced by a novel Gemini Vitamin D derivative during the progression of breast cancer
3. Calcitriol derivatives with two different side chains at C-20
4. Gemini Vitamin D Analogues Inhibit Estrogen Receptor–Positive and Estrogen Receptor–Negative Mammary Tumorigenesis without Hypercalcemic Toxicity
5. Calcitriol Derivatives with Two Different Side Chains at C-20. V. Potent Inhibitors of Mammary Carcinogenesis and Inducers of Leukemia Differentiation
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1. Design, Synthesis, and Biological Evaluation of New Type of Gemini Analogues with a Cyclopropane Moiety in Their Side Chain;Journal of Medicinal Chemistry;2024-06-10
2. Design and synthesis of vitamin D analogs;Feldman and Pike' s Vitamin D;2024
3. Development of novel Gemini-cholesterol analogues for retinoid-related orphan receptors;Organic Chemistry Frontiers;2022
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