Ac-CAY-NH2

Ref. 3D-PP45319

Informations sur le produit

• Nom: Ac-CAY-NH2
• Synonymes: Ac-Cys-Ala-Tyr-amide

Description

Peptide Ac-CAY-NH2 is a Research Peptide with significant interest within the field academic and medical research. This peptide is available for purchase at Cymit Quimica in multiple sizes and with a specification of your choice. Recent citations using Ac-CAY-NH2 include the following: N, S-double labeling of N-terminal cysteines via an alternative conjugation pathway with 2-cyanobenzothiazole W Wang , J Gao - The Journal of Organic Chemistry, 2019 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.joc.9b02959 Discobahamins A and B, new peptides from the Bahamian deep water marine sponge Discodermia sp. SP Gunasekera, SA Pomponi - Journal of natural , 1994 - ACS Publicationshttps://pubs.acs.org/doi/pdf/10.1021/np50103a011 CC16 Inhibits the Migration of Eosinophils Towards the Formyl Peptide fMLF but not Towards PGD2 S Johansson, K Andersson, G Wennergren - Inflammation, 2009 - Springerhttps://link.springer.com/article/10.1007/s10753-008-9103-1 Phosphorylation status of peptide monolayers modulates hydrogen bonding and orientations of nematic liquid crystals R Abbasi , C Wang , Y Bai, NL Abbott - Liquid Crystals, 2018 - Taylor & Francishttps://www.tandfonline.com/doi/abs/10.1080/02678292.2018.1509389 Role of the NH2-terminal Domain of Angiotensin I1 (ANG 11) and [SarllAngiotensin I1 on Conformation and Activity JM MatsoUkasi, J Hondrelisi, M Keramidai - Citeseerhttps://citeseerx.ist.psu.edu/document?repid=rep1&type=pdf&doi=774e927a38340f6cc970bc87377aea8c1067eead of angiotensin II (ANG II) and [Sar1] angiotensin II on conformation and activity. NMR evidence for aromatic ring clustering and peptide backbone folding compared JM Matsoukas, J Hondrelis, M Keramida - Journal of Biological , 1994 - ASBMBhttps://www.jbc.org/article/S0021-9258(17)37688-3/abstract Synthesis of w-conotoxin GVIA inspired small molecules in the search for relief of neuropathic pain JE Graham - 2009 - bridges.monash.eduhttps://bridges.monash.edu/articles/thesis/Synthesis_of_w-conotoxin_GVIA_inspired_small_molecules_in_the_search_for_relief_of_neuropathic_pain/4555594 A ratiometric expressible FRET sensor for phosphoinositides displays a signal change in highly dynamic membrane structures in fibroblasts G Cicchetti, M Biernacki, J Farquharson, PG Allen - Biochemistry, 2004 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/bi035480w Reaction pathway and free energy profile determined for specific recognition of oligosaccharide moiety of carboxypeptidase Y E Senkara-Barwijuk, T Kobiela, K Lebed - Biosensors and , 2012 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0956566312002308 Structure-function studies of peptides for cell adhesion inhibition: Identification of key residues by alanine mutation and peptide-truncation approach C Li, SD Satyanarayanajois - Peptides, 2007 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0196978107002276 Characterization of the carboxyl-terminal 10-kDa cyanogen bromide fragment of caldesmon as an actin-calmodulin-binding region. A Bartegi, A Fattoum, J Derancourt, R Kassab - Journal of Biological , 1990 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0021925818772463

• Marque: Biosynth