Back to Search
Start Over
Tentoxin as a Scaffold for Drug Discovery. Total Solid-Phase Synthesis of Tentoxin and a Library of Analogues
- Source :
- Organic Letters. 5:2115-2118
- Publication Year :
- 2003
- Publisher :
- American Chemical Society (ACS), 2003.
-
Abstract
- [reaction: see text] A solid-phase method for the synthesis of tentoxin has been developed. Two key steps-dehydration and N-alkylation-are carried out while the peptide is anchored to the resin. The method, which has been validated by the preparation of a library of tentoxin analogues, should be applicable to the generation of further libraries that have the tentoxin scaffold structure, as well as other structures containing N-alkylated didehydroamino acids.
- Subjects :
- chemistry.chemical_classification
Scaffold
Stereochemistry
Chemistry
Drug discovery
Organic Chemistry
Peptide
Mycotoxins
Peptides, Cyclic
Biochemistry
Combinatorial chemistry
Structure-Activity Relationship
chemistry.chemical_compound
Solid-phase synthesis
Tentoxin
Combinatorial Chemistry Techniques
Structure–activity relationship
Amino Acid Sequence
Physical and Theoretical Chemistry
Subjects
Details
- ISSN :
- 15237052 and 15237060
- Volume :
- 5
- Database :
- OpenAIRE
- Journal :
- Organic Letters
- Accession number :
- edsair.doi.dedup.....2c261b3e5b7a4a8bd46f405cb64747fd
- Full Text :
- https://doi.org/10.1021/ol0345273