The synthesis and some biological properties of 4-hydroxymethyltetrahydro- and 4-hydroxymethylbenzopsoralen are reported. The two compounds exhibited activity in the dark and by UVA irradiation. The tetrahydrobenzo derivative was more effective than the corresponding aromatic compound. Benzopsoralens were more cytotoxic in malignant (HL60 and HeLa) cell lines than in normal ones (NCTC 2544). Their toxicity decreased in confluent cultures of NCTC 2544 cells.

4-Hydroxymethyltetrahydro- and 4-hydroxymethyl-benzopsoralen: synthesis and biological activity.

CONCONI, MARIA TERESA;GUIOTTO, ADRIANO;MANZINI, PAOLO;CHILIN, ADRIANA;PARNIGOTTO, PIER PAOLO;
1995

Abstract

The synthesis and some biological properties of 4-hydroxymethyltetrahydro- and 4-hydroxymethylbenzopsoralen are reported. The two compounds exhibited activity in the dark and by UVA irradiation. The tetrahydrobenzo derivative was more effective than the corresponding aromatic compound. Benzopsoralens were more cytotoxic in malignant (HL60 and HeLa) cell lines than in normal ones (NCTC 2544). Their toxicity decreased in confluent cultures of NCTC 2544 cells.
1995
STAMPA
Inglese
50
2
125
130
6
SOC CHIMICA ITALIANA, VIALE LIEGI 48, I-00198 ROME, ITALY
Internazionale
Sì, ma tipo non specificato
The Pharmacology/Toxicology category covers resources on all aspects of clinical pharmacology and toxicology including psycho-pharmacology, pharmacokinetics, pharmacotherapy, drug monitoring and drug safety, chemotherapy, clinical and hospital pharmacy, and clinical trials.
DNA, PHOTOCHEMOTHERAPY, PSORALENS, FUROCOUMARINS, DERIVATIVES, TOXICITY
ITALIA
none
Conconi, Maria Teresa; Guiotto, Adriano; Manzini, Paolo; Chilin, Adriana; Bassani, V; Parnigotto, Pier Paolo; Rodighiero, P.
01 CONTRIBUTO IN RIVISTA::01.01 - Articolo in rivista
info:eu-repo/semantics/article
7
262
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11577/2470835
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