1H-NMR studies on substance P hexapeptide analogs
β Scribed by Anthony Ribeiro; Oleg Jardetzky; Chaim Gilon; Dina Teitelbaum; Michael Chorev
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1983
- Tongue
- English
- Weight
- 323 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0006-3525
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β¦ Synopsis
Synopsis
'H-nmr studies of [pG1u6]SPs~1, [gpG1u6,mPhe7]SP6 11, and [pGlu6,N-CH3Phe7]SPg~~ in DMSO-ds reveal characteristic chemical shifts, 3 5 ~~ a ~~, temperature dependence, as well as deuterium exchange half-times. Marked similarities are revealed for the two first analogs, whereas the N-methylated analog is clearly different. Possible conformations are considered.
π SIMILAR VOLUMES
The conformational properties of spantide [ (D-Arg', D-Trp7.', Leu") substance PI have been studied by fluorescence, CD, and nmr techniques. The fluorescence, CD, and nmr parameters in different solvents and in a micellar environment (SDS) are compared with the data collected for bombesin. A prelimi
Proton nrnr parameters are reported for DMSO-d, solutions of two receptor-selective substance P analogues: Ac[Arg6,Pr$lSP,,,, which is selective for the NK-1 (SP-P) receptor and [pGlu6, N-MePhe8]SP,11, which selectively activates the NK-3 (SP-N) receptor. Full peak assignments of both analogues were
## Abstract A study is presented on the configuration and conformation of 2βmethylchromoneβdimer, as well as on khellinβdimer, based on ^1^H NMR spectroscopy.
Conformational studies on poly(oxyethy1ene)-bound homo-, oligo-, guest-host, and sequential peptides synthesized according to the liquid-phase method were carried out by means of 'H-nmr spectroscopy. The solubilizing effect of the C-terminal polymeric support allowed a thorough investigation of the