VI. Synthesis, conformation, and ion-binding of two bicyclic nonapeptides *
โ Scribed by ZANOTTI, G.C. ;CAMPBELL, B.E. ;EASWARAN, K.R.K. ;BLOUT, E.R.
- Book ID
- 115098847
- Publisher
- Wiley (Blackwell Publishing)
- Year
- 2009
- Tongue
- English
- Weight
- 610 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0367-8377
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
The ion binding characteristics of two bicyclic peptides, cyclo(Lys-Pro-Gly-Pro-Gly-Glu-Pro-Gly-Pro-G1y)-cyclo(1c + 6 y ) Gly (BCP7) and cyclo(Lys-Pro-Gly-Pro-Gly-Glu-Pro-Gly-Pro-G1y)qclo(lr + 6 y ) Gly-Gly (BCP8) in a lipophilic solvent, acetonitrile, have been studied using CD and nmr spectroscopy
A bicyclic undecapeptide of sequence cyclo-(Ala(1)-Pro(2)-Asp(3)-Glu(4)-Lys(5)-Ala(6)-Pro(7)-Asp(8)-Ser(9) -Glu(10))-cyclo-(10gamma --> 5varepsilon)-Gly(11), designed to mimic the calcium coordination site I of Calmodulin, has been synthesized and its conformation and calcium binding properties have
It is reported the synthesis of ligands 6 and $ combining one calix[4]arene unit in the 1,3-alternate conformation and crown ether and aza crown ether elements. Preliminary comp|exations are given.