About: Antitumour activity of N-6-substituted PMEDAP derivatives against T-cell lymphoma     Goto   Sponge   NotDistinct   Permalink

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  • The antitumour activity of four N-6-substituted PMEDAP derivatives, Me2NEt-PMEDAP, allyl-PMEDAP, Me-2-PMEDAP and cypr-PMEDAP, selected on the basis of their in vitro cytostatic activity, was studied in an in vivo model of haematological malignancy of inbred Sprague-Dawley rats. These compounds are believed to serve as the prodrugs of another (phosphonomethoxy) ethyl derivative, PMEG (9-[2-phosphonomethoxy) ethyl] guanine. We compared their toxicity and ability to inhibit tumour development in two different dosage regimes with those of their parent compound PMEDAP, as well with PMEG. The study confirmed the anticancer efficacy of the parental compound PMEDAP. Unlike PMEDAP, its N-6-mono- and disubstituted congeners Me2NEt-PMEDAP, allyl-PMEDAP and Me-2-PMEDAP were less potent or exhibited the same antineoplastic effect as PMEDAP. cypr-PMEDAP significantly decreased the survival of lymphoma-bearing rats due to high toxicity, which was approximately the same as that of PMEG, Therefore, these acyclic nucle
  • The antitumour activity of four N-6-substituted PMEDAP derivatives, Me2NEt-PMEDAP, allyl-PMEDAP, Me-2-PMEDAP and cypr-PMEDAP, selected on the basis of their in vitro cytostatic activity, was studied in an in vivo model of haematological malignancy of inbred Sprague-Dawley rats. These compounds are believed to serve as the prodrugs of another (phosphonomethoxy) ethyl derivative, PMEG (9-[2-phosphonomethoxy) ethyl] guanine. We compared their toxicity and ability to inhibit tumour development in two different dosage regimes with those of their parent compound PMEDAP, as well with PMEG. The study confirmed the anticancer efficacy of the parental compound PMEDAP. Unlike PMEDAP, its N-6-mono- and disubstituted congeners Me2NEt-PMEDAP, allyl-PMEDAP and Me-2-PMEDAP were less potent or exhibited the same antineoplastic effect as PMEDAP. cypr-PMEDAP significantly decreased the survival of lymphoma-bearing rats due to high toxicity, which was approximately the same as that of PMEG, Therefore, these acyclic nucle (en)
Title
  • Antitumour activity of N-6-substituted PMEDAP derivatives against T-cell lymphoma
  • Antitumour activity of N-6-substituted PMEDAP derivatives against T-cell lymphoma (en)
skos:prefLabel
  • Antitumour activity of N-6-substituted PMEDAP derivatives against T-cell lymphoma
  • Antitumour activity of N-6-substituted PMEDAP derivatives against T-cell lymphoma (en)
skos:notation
  • RIV/00216208:11120/01:00003665!RIV12-MSM-11120___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(GV203/96/K128), P(NL5423), Z(AV0Z4055905), Z(AV0Z5039906), Z(MSM 111200002)
http://linked.open...iv/cisloPeriodika
  • 3B
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
  • 673535
http://linked.open...ai/riv/idVysledku
  • RIV/00216208:11120/01:00003665
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • rat; spontaneous lymphoma; PMEDAP derivatives (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GR - Řecká republika
http://linked.open...ontrolniKodProRIV
  • [2938ACEC1014]
http://linked.open...i/riv/nazevZdroje
  • Anticancer Research
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
  • 21
http://linked.open...iv/tvurceVysledku
  • Mandys, Václav
  • Valeriánová, M.
http://linked.open...ain/vavai/riv/wos
  • 000170276600054
http://linked.open...n/vavai/riv/zamer
issn
  • 0250-7005
number of pages
http://localhost/t...ganizacniJednotka
  • 11120
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