A novel and efficient synthetic route was developed for the preparation of protoberberine derivatives. A methodology, designed primarily to control the substitution patterns on the terminal rings, was used to access a small array of these compounds. An initial biological profiling suggested an anticancer potential of the synthesised derivatives, while structure-based target fishing identified their potential targets and established a rational basis for further structural modifications. Although the activities need further improvement, the study demonstrated that the described approach may be useful in the discovery of novel lead compounds.
Source:
Journal of the Serbian Chemical Society, 2016, 81, 2, 103-123
TY - JOUR
AU - Simić, Milena
AU - Damjanović, Ana B.
AU - Kalinić, Marko
AU - Tasić, Gordana
AU - Erić, Slavica
AU - Antić-Stanković, Jelena
AU - Savić, Vladimir
PY - 2016
UR - http://farfar.pharmacy.bg.ac.rs/handle/123456789/2606
AB - A novel and efficient synthetic route was developed for the preparation of protoberberine derivatives. A methodology, designed primarily to control the substitution patterns on the terminal rings, was used to access a small array of these compounds. An initial biological profiling suggested an anticancer potential of the synthesised derivatives, while structure-based target fishing identified their potential targets and established a rational basis for further structural modifications. Although the activities need further improvement, the study demonstrated that the described approach may be useful in the discovery of novel lead compounds.
PB - Srpsko hemijsko društvo, Beograd
T2 - Journal of the Serbian Chemical Society
T1 - Synthesis, cytotoxicity and computational study of novel protoberberine derivatives
VL - 81
IS - 2
SP - 103
EP - 123
DO - 10.2298/JSC150525090S
ER -
@article{
author = "Simić, Milena and Damjanović, Ana B. and Kalinić, Marko and Tasić, Gordana and Erić, Slavica and Antić-Stanković, Jelena and Savić, Vladimir",
year = "2016",
url = "http://farfar.pharmacy.bg.ac.rs/handle/123456789/2606",
abstract = "A novel and efficient synthetic route was developed for the preparation of protoberberine derivatives. A methodology, designed primarily to control the substitution patterns on the terminal rings, was used to access a small array of these compounds. An initial biological profiling suggested an anticancer potential of the synthesised derivatives, while structure-based target fishing identified their potential targets and established a rational basis for further structural modifications. Although the activities need further improvement, the study demonstrated that the described approach may be useful in the discovery of novel lead compounds.",
publisher = "Srpsko hemijsko društvo, Beograd",
journal = "Journal of the Serbian Chemical Society",
title = "Synthesis, cytotoxicity and computational study of novel protoberberine derivatives",
volume = "81",
number = "2",
pages = "103-123",
doi = "10.2298/JSC150525090S"
}
Simić, M., Damjanović, A. B., Kalinić, M., Tasić, G., Erić, S., Antić-Stanković, J.,& Savić, V. (2016). Synthesis, cytotoxicity and computational study of novel protoberberine derivatives.
Journal of the Serbian Chemical Society
Srpsko hemijsko društvo, Beograd., 81(2), 103-123.
https://doi.org/10.2298/JSC150525090S
Simić M, Damjanović AB, Kalinić M, Tasić G, Erić S, Antić-Stanković J, Savić V. Synthesis, cytotoxicity and computational study of novel protoberberine derivatives. Journal of the Serbian Chemical Society. 2016;81(2):103-123
Simić Milena, Damjanović Ana B., Kalinić Marko, Tasić Gordana, Erić Slavica, Antić-Stanković Jelena, Savić Vladimir, "Synthesis, cytotoxicity and computational study of novel protoberberine derivatives" Journal of the Serbian Chemical Society, 81, no. 2 (2016):103-123,
https://doi.org/10.2298/JSC150525090S .
