About: Substituted 2-hydroxy-N-(arylalkyl)benzamides induce apoptosis in cancer cell lines     Goto   Sponge   NotDistinct   Permalink

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  • Variously substituted 2-hydroxy-N-(arylallcyl)benzamides were prepared and screened for anti-proliferative and cytotoxic activity in cancer cell lines in vitro. Five compounds, out of 33 showed single-digit micromolar IC50 values against several human cancer cell lines. One of the most potent compounds N-((R)-1-(4-chlorophenylcarbamoyl)-2-phenylethyl)-5-chloro-2-hydroxybenzamide (6k) reduced proliferation and induced apoptosis in the melanoma cell line G361 in a dose-dependent manner, as shown by decrease in 5-bromo-2'-deoxyuridine incorporation and increase in several apoptotic markers, including subdiploid population increase, activation of caspases and site-specific poly-(ADP-ribose)polymerase (PARP) cleavage.
  • Variously substituted 2-hydroxy-N-(arylallcyl)benzamides were prepared and screened for anti-proliferative and cytotoxic activity in cancer cell lines in vitro. Five compounds, out of 33 showed single-digit micromolar IC50 values against several human cancer cell lines. One of the most potent compounds N-((R)-1-(4-chlorophenylcarbamoyl)-2-phenylethyl)-5-chloro-2-hydroxybenzamide (6k) reduced proliferation and induced apoptosis in the melanoma cell line G361 in a dose-dependent manner, as shown by decrease in 5-bromo-2'-deoxyuridine incorporation and increase in several apoptotic markers, including subdiploid population increase, activation of caspases and site-specific poly-(ADP-ribose)polymerase (PARP) cleavage. (en)
Title
  • Substituted 2-hydroxy-N-(arylalkyl)benzamides induce apoptosis in cancer cell lines
  • Substituted 2-hydroxy-N-(arylalkyl)benzamides induce apoptosis in cancer cell lines (en)
skos:prefLabel
  • Substituted 2-hydroxy-N-(arylalkyl)benzamides induce apoptosis in cancer cell lines
  • Substituted 2-hydroxy-N-(arylalkyl)benzamides induce apoptosis in cancer cell lines (en)
skos:notation
  • RIV/61389030:_____/13:00423094!RIV14-GA0-61389030
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(ED2.1.00/03.0101), P(GA301/08/1649), P(GAP305/12/0783), S, Z(AV0Z50380511)
http://linked.open...iv/cisloPeriodika
  • 2013
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 108907
http://linked.open...ai/riv/idVysledku
  • RIV/61389030:_____/13:00423094
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • Diamides; Apoptosis; Cytotoxicity (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • FR - Francouzská republika
http://linked.open...ontrolniKodProRIV
  • [477C1D723230]
http://linked.open...i/riv/nazevZdroje
  • European Journal of Medicinal Chemistry
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 68
http://linked.open...iv/tvurceVysledku
  • Dušek, J.
  • Jorda, Radek
  • Kryštof, Vladimír
  • Hanousek, J.
  • Řezníčková, Eva
  • Imramovský, A.
  • Pauk, K.
http://linked.open...ain/vavai/riv/wos
  • 000326902300027
http://linked.open...n/vavai/riv/zamer
issn
  • 0223-5234
number of pages
http://bibframe.org/vocab/doi
  • 10.1016/j.ejmech.2013.08.009
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