Z-gly-Pro-OH
CAS: 1160-54-9
Ref. 3D-FG40278
1g | A consultar | ||
2g | A consultar | ||
5g | A consultar | ||
10g | A consultar | ||
500mg | A consultar |
Informação sobre produto
- (Benzyloxycarbonyl)glycyl-<span class="text-smallcaps">L</span>-proline
- <span class="text-smallcaps">L</span>-Proline, 1-[N-[(phenylmethoxy)carbonyl]glycyl]-
- <span class="text-smallcaps">L</span>-Proline, N-[(phenylmethoxy)carbonyl]glycyl-
- Carbobenzoxyglycyl-<span class="text-smallcaps">L</span>-proline
- Cbz-gly-pro-oh
- N-Carbobenzoxyglycyl-L-proline
- N-[(Phenylmethoxy)carbonyl]glycyl-<span class="text-smallcaps">L</span>-proline
- NSC 89634
- Proline, 1-(N-carboxyglycyl)-, N-benzyl ester, <span class="text-smallcaps">L</span>-
- Z-Gly-Pro-Oh
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Z-gly-Pro-OH is a synthetic peptide substrate that has been used to study the activity of serine proteases, specifically histidine-specific proteases. It has been shown to be hydrolyzed by human liver and intestinal enzymes, including serine proteases, in vitro. This peptide also reacts with epirubicin, a drug that is used in chemotherapy for treating cancer. The reaction between the two compounds results in an increased potency of epirubicin and a decreased potency of z-gly-pro-OH. Z-gly-Pro-OH can be synthesized from L-histidine and glycylproline using the method of intramolecular hydrogenation to form an amide bond between the amino acid and the proline residue. The synthesis can be completed using a chromatographic method or titration method. This synthetic peptide is also used as a substrate for studying histidine specific peptidases, which are responsible for cle
Propriedades químicas
Consulta técnica sobre: 3D-FG40278 Z-gly-Pro-OH
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