том 35 издание 19 страницы 3567-3572

5,5-Disubstituted hydantoins: syntheses and anti-HIV activity

Тип публикацииJournal Article
Дата публикации1992-09-01
SCImago Q1
Tоп 10% SCImago
WOS Q1
БС1
SJR1.726
CiteScore11.1
Impact factor7.3
ISSN00222623, 15204804
Drug Discovery
Molecular Medicine
Краткое описание
A series of 5,5-disubstituted hydantoin derivatives was synthesized by alkylating 5,5-bis(mercaptomethyl)-2,4-imidazolidinedione (3) with various halomethylaromatic or halomethylheteroaromatic precursors, or by using the Buchener-Berg procedure on the required ketone. When evaluated for their ability to inhibit HIV-induced cell killing and virus production in CEM or MT-2 cells only compounds 2, 4n, 4o, and 4i demonstrated modest activity, the latter with an IC50 = 53 microM.
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ГОСТ |
Цитировать
Comber R. N. et al. 5,5-Disubstituted hydantoins: syntheses and anti-HIV activity // Journal of Medicinal Chemistry. 1992. Vol. 35. No. 19. pp. 3567-3572.
ГОСТ со всеми авторами (до 50) Скопировать
Comber R. N. 5,5-Disubstituted hydantoins: syntheses and anti-HIV activity // Journal of Medicinal Chemistry. 1992. Vol. 35. No. 19. pp. 3567-3572.
RIS |
Цитировать
TY - JOUR
DO - 10.1021/jm00097a014
UR - https://doi.org/10.1021/jm00097a014
TI - 5,5-Disubstituted hydantoins: syntheses and anti-HIV activity
T2 - Journal of Medicinal Chemistry
AU - Comber, Robert N.
PY - 1992
DA - 1992/09/01
PB - American Chemical Society (ACS)
SP - 3567-3572
IS - 19
VL - 35
PMID - 1404236
SN - 0022-2623
SN - 1520-4804
ER -
BibTex |
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BibTex (до 50 авторов) Скопировать
@article{1992_Comber,
author = {Robert N. Comber},
title = {5,5-Disubstituted hydantoins: syntheses and anti-HIV activity},
journal = {Journal of Medicinal Chemistry},
year = {1992},
volume = {35},
publisher = {American Chemical Society (ACS)},
month = {sep},
url = {https://doi.org/10.1021/jm00097a014},
number = {19},
pages = {3567--3572},
doi = {10.1021/jm00097a014}
}
MLA
Цитировать
Comber, Robert N., et al. “5,5-Disubstituted hydantoins: syntheses and anti-HIV activity.” Journal of Medicinal Chemistry, vol. 35, no. 19, Sep. 1992, pp. 3567-3572. https://doi.org/10.1021/jm00097a014.
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