Tumorhemmende β-Aminoketone
✍ Scribed by Wolfgang Meindl; Reiner Laske; Miroslava Böhm
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 312 KB
- Volume
- 320
- Category
- Article
- ISSN
- 0365-6233
No coin nor oath required. For personal study only.
✦ Synopsis
Synthese der Verbindungen 1-9 und Testung auf Aktivitat an der P388D, Tumorzellinie werden beschrieben. Stark wirksam sind die P-Aminoketone 2-4, 7 und 9, die in der a-Stellung eine zusatzliche Aminomethylgruppierung besitzen.
Tumor Inhibiting P-Aminoketones
Synthesis of the compounds 1-9 and testing for activity against the P388Dl tumor celline are described. The p-aminoketones 2-4, 7 and 9, which bear an additional aminomethyl group in a-position. are strongly active.
📜 SIMILAR VOLUMES
Mannich bases were prepared from quinolinols, isoquinolinols, phenols, biphenols, and ketones in order to have their antimicrobial properties evaluated. HE USE OF 3-azabicyclo[3.2.2]nonane (I), Talso known as AZBN, in the Mannich reaction was reported by Blanton and Nobles in 1962 (I). In biological