𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis and study of a new adenine–acridine tandem, inhibitor of exonuclease III

✍ Scribed by Philippe Belmont; Martine Demeunynck; Jean-François Constant; Jean Lhomme


Publisher
Elsevier Science
Year
2000
Tongue
English
Weight
168 KB
Volume
10
Category
Article
ISSN
0960-894X

No coin nor oath required. For personal study only.

✦ Synopsis


A new heterodimer adenine-chain-acridine containing a mixed amido-guanidinium linker chain was synthesized. To achieve the synthesis a new method of introduction of aminoalkyl chain at position 9 of adenine was designed. The heterodimer interacts specifically with the abasic sites in DNA and inhibits the major base excision repair enzyme in Escherichia coli, Exonuclease III.


📜 SIMILAR VOLUMES


ChemInform Abstract: Synthesis and Study
✍ Philippe Belmont; Martine Demeunynck; Jean-Francois Constant; Jean Lhomme 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

Improved syntheses of acridines. Part V.
✍ Albert, Adrien ;Willis, John Bryan 📂 Article 📅 1946 🏛 Wiley (John Wiley & Sons) ⚖ 365 KB

## Abstract B‐Chloroacridine (II) was converted to acridine in 80% yiold by hydrogenation in the presence of potassium hydroxide and ranoy‐nicked catalyst at atmospheric picture followed by oxidation of the resulting acridnn (III) with chromic acid. The scope of the now reaction for the preparation

A new synthesis ofL-talose and preparati
✍ Leon M. Lerner; Gary Mennitt 📂 Article 📅 1994 🏛 Elsevier Science 🌐 English ⚖ 783 KB

Methyl 2,3-0-isopropylidene-S,6-di-D-methylsulfonyl-l3-n-allofuranoside, prepared by a route starting from n-glucose and its conversion to 1,2: S,6-di-O-isopropylidene-a-D-allofuranose and n-allose, has been used as the starting material for a new synthesis of L-talose. The configuration at e-S was