𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis and Cytotoxic Activity of Certain New Arylazothiazole Containing Compounds.

✍ Scribed by Salwa El-Meligie; Raafat A. El-Awady

Publisher
John Wiley and Sons
Year
2003
Weight
180 KB
Volume
34
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Synthesis and cytotoxic activity of cert
Synthesis and cytotoxic activity of certain new arylazothiazole containing compounds
✍ Salwa El-Meligie; Raafat A. El-Awady πŸ“‚ Article πŸ“… 2002 πŸ› Journal of Heterocyclic Chemistry 🌐 English βš– 57 KB

## Abstract 2‐Amino‐5‐arylazo‐4‐(2‐chlorophenyl)thiazoles (**2a‐e**) were prepared by the coupling of aryldiazonium chlorides with 2‐amino‐4‐(2‐chlorophenyl) thiazole (**1**). The thioureas **3a‐e** were obtained by condensing the arylazothiazoles **2a‐c** with the appropriate isothiocyanates. Reac

Synthesis and antimicrobial activities o
Synthesis and antimicrobial activities of certain cannabichromene and cannabigerol related compounds
✍ Hala N. Eisohly; Carlton E. Turner; Alice M. Clark; Mahmoud A. Eisohly πŸ“‚ Article πŸ“… 1982 πŸ› John Wiley and Sons 🌐 English βš– 594 KB

Cannabichromene homologs, analogs, and isomers as well as the CI-homolog and isomer of cannabigerol were prepared and tested for their antimicrobial and antifungal properties. Spectral data of all compounds synthesized are presented. Keyphrases 0 Cannabichromene-analogs, synthesis and antimicrobial

Design and synthesis of some new pyranox
Design and synthesis of some new pyranoxanthenones with cytotoxic activity
✍ Konstantinos Ghirtis; Nicole Pouli; Panagiotis Marakos; Alexios-Leandros Skaltso πŸ“‚ Article πŸ“… 2001 πŸ› Journal of Heterocyclic Chemistry 🌐 English βš– 79 KB

## Abstract As part of a research program directed towards the design and synthesis of pyranoxanthones structurally related to acronycine, we present here the synthesis and cytotoxic activity of the pyranoxanthones **3** and **4** (X= H, Br; R= H, OMe; R'= H, Ac). Some of these compounds inhibit L1