Synthesis and properties of cyclic gomesin and analogues
✍ Scribed by Alessandra Machado; Marcos A. Fázio; Antonio Miranda; Sirlei Daffre; M. Teresa Machini
- Book ID
- 118285936
- Publisher
- John Wiley and Sons
- Year
- 2012
- Tongue
- English
- Weight
- 378 KB
- Volume
- 18
- Category
- Article
- ISSN
- 1075-2617
- DOI
- 10.1002/psc.2439
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📜 SIMILAR VOLUMES
Three oligomers of ethylene-bridged 3,6-fluorene were synthesized starting from phenanthrenequinone. McMurry reaction was applied to synthesize the cyclic compound. Horner-Emmons reaction was used to synthesize the linear compounds with all-trans configuration. The crystal structure of the cyclic c
## Abstract Gomesin (__Gm__) is a potent antimicrobial peptide isolated from the spider Acanthoscurria gomesiana. The two disulfide bridges Cys^2,15^ and Cys^6,11^ facilitate the folding of the molecule in a β‐hairpin structure, conferring on the peptide a high stability in human plasma. We report