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Yatakemycin: total synthesis, DNA alkylation, and biological properties
- Source :
- Nat. Prod. Rep.. 25:220-226
- Publication Year :
- 2008
- Publisher :
- Royal Society of Chemistry (RSC), 2008.
-
Abstract
- Covering: up to 2007 DNA-binding small molecules are an important source of anticancer therapeutics that display a diverse array of mechanisms of action. Synthetic studies on the new DNA-alkylating natural product yatakemycin, detailed in this Highlight, have served to reassign its structure, assign the absolute stereochemistry, and provide access to yatakemycin and a series of structural analogues for biological evaluation. Studies on the DNA alkylation properties of (+)- and ent-(−)-yatakemycin and related analogues have demonstrated the enhanced DNA alkylation properties of this class of agents and provided insight into their interaction with DNA.
- Subjects :
- Indoles
Natural product
Alkylation
Molecular Structure
Chemistry
Organic Chemistry
Molecular Conformation
Total synthesis
Stereoisomerism
DNA
Crystallography, X-Ray
Yatakemycin
Biochemistry
Combinatorial chemistry
Small molecule
Duocarmycins
DNA Alkylation
chemistry.chemical_compound
Biological property
Drug Discovery
Pyrroles
Biological evaluation
Subjects
Details
- ISSN :
- 14604752 and 02650568
- Volume :
- 25
- Database :
- OpenAIRE
- Journal :
- Nat. Prod. Rep.
- Accession number :
- edsair.doi.dedup.....8e2d7ee792133d7023cfc16ff12583f8
- Full Text :
- https://doi.org/10.1039/b705665f