Informations sur le produit
- Z-L-Nva-OH
- (2S)-2-(Phenylmethoxycarbonylamino)pentanoic acid
- (Benzyloxycarbonyl)norvaline
- <span class="text-smallcaps">L</span>-(Carbobenzyloxy)norvaline
- <span class="text-smallcaps">L</span>-Norvaline, N-[(phenylmethoxy)carbonyl]-
- CBZ-L-norvaline
- Cbz-<span class="text-smallcaps">L</span>-norvaline
- Cbz-Norvaline
- N-(Benzyloxycarbonyl)-<span class="text-smallcaps">L</span>-norvaline
- N-(Benzyloxycarbonyl)norvaline
- Voir d'autres synonymes
- N-(Carbobenzoxy)norvaline
- N-Carbobenzyloxy-<span class="text-smallcaps">L</span>-norvaline
- N-[(Phenylmethoxy)carbonyl]-<span class="text-smallcaps">L</span>-norvaline
- N-[(benzyloxy)carbonyl]-L-norvaline
- Norvaline, N-carboxy-, N-benzyl ester, <span class="text-smallcaps">L</span>-
- Z-<span class="text-smallcaps">L</span>-Norvaline
Z-L-Norvaline is a homogeneous, undecapeptide that has been synthesized from the condensation of L-Valine with D-Lysine. Cyclosporin A is a cyclic peptide consisting of ten amino acids. The synthesis of Z-L-norvaline is achieved by the stepwise conversion of cyclosporin A to its subfragments, which are then condensed with L-Valine and D-Lysine to form Z-L-norvaline. This compound has been shown to be insoluble in water and can be purified by chromatography. It also has an optical purity of 99%. The yield was found to be 100% for this reaction. Z-L-norvaline is an analogue of cyclosporin A because it shares many structural similarities as well as biological activities such as inhibition of prostaglandin synthesis and immunosuppression.
Propriétés chimiques
Question d’ordre technique sur : 3D-FN47298 Z-L-norvaline
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