2-Methoxyestradiol and its analogs. Synthesis and structure—antiproliferative activity relationship

Verfasser / Beitragende:
[N. Zefirov, O. Zefirova]
Ort, Verlag, Jahr:
2015
Enthalten in:
Russian Journal of Organic Chemistry, 51/9(2015-09-01), 1207-1216
Format:
Artikel (online)
ID: 605529108
LEADER caa a22 4500
001 605529108
003 CHVBK
005 20210128100816.0
007 cr unu---uuuuu
008 210128e20150901xx s 000 0 eng
024 7 0 |a 10.1134/S1070428015090018  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1134/S1070428015090018 
245 0 0 |a 2-Methoxyestradiol and its analogs. Synthesis and structure—antiproliferative activity relationship  |h [Elektronische Daten]  |c [N. Zefirov, O. Zefirova] 
520 3 |a 2-Methoxyestradiol is an estradiol metabolite capable of binding to the colchicine domain of the cell protein tubulin. The review systematizes the results of structure—activity studies on 2-methoxyestradiol analogs with various modifications of the A, B, and D rings and describes some synthetic approaches to such analogs. Ways of synthesis of metabolically stable 2-methoxyestradiol via modification of the 3- and 17-hydroxy groups, as well as by introduction of bulky substituents into the 17-position, are discussed. The design of 2-methoxyestradiol analogs lacking steroid fragment is also described. 
540 |a Pleiades Publishing, Ltd., 2015 
700 1 |a Zefirov  |D N.  |u Faculty of Chemistry, Moscow State University, Leninskie gory 1, 119992, Moscow, Russia  |4 aut 
700 1 |a Zefirova  |D O.  |u Faculty of Chemistry, Moscow State University, Leninskie gory 1, 119992, Moscow, Russia  |4 aut 
773 0 |t Russian Journal of Organic Chemistry  |d Pleiades Publishing  |g 51/9(2015-09-01), 1207-1216  |x 1070-4280  |q 51:9<1207  |1 2015  |2 51  |o 11178 
856 4 0 |u https://doi.org/10.1134/S1070428015090018  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1134/S1070428015090018  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Zefirov  |D N.  |u Faculty of Chemistry, Moscow State University, Leninskie gory 1, 119992, Moscow, Russia  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Zefirova  |D O.  |u Faculty of Chemistry, Moscow State University, Leninskie gory 1, 119992, Moscow, Russia  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Russian Journal of Organic Chemistry  |d Pleiades Publishing  |g 51/9(2015-09-01), 1207-1216  |x 1070-4280  |q 51:9<1207  |1 2015  |2 51  |o 11178