H-GIVE-OH
Rif. 3D-PP48415
1mg | 172,00 € | ||
10mg | 196,00 € | ||
100mg | 303,00 € |
Informazioni sul prodotto
Peptide H-GIVE-OH 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 H-GIVE-OH include the following: Hemoglobin as a source of endogenous bioactive peptides: The concept of tissue-specific peptide pool VT Ivanov, AA Karelin, MM Philippova - Peptide , 1997 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/(SICI)1097-0282(1997)43:2%3C171::AID-BIP10%3E3.0.CO;2-O Synthesis of peptide-oligonucleotide conjugates with single and multiple peptides attached to 2 '-aldehydes through thiazolidine, oxime, and hydrazine linkages TS Zatsepin, DA Stetsenko, AA Arzumanov - Bioconjugate , 2002 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/bc020016+ Supramolecular design by covalent capture. Design of a peptide cylinder via hydrogen-bond-promoted intermolecular olefin metathesis TD Clark, MR Ghadiri - Journal of the American Chemical Society, 1995 - ACS Publicationshttps://pubs.acs.org/doi/pdf/10.1021/ja00154a051 Cylindrical beta-sheet peptide assemblies TD Clark, JM Buriak , K Kobayashi - Journal of the , 1998 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ja981485i Why are B ions stable species in peptide spectra? T Yalcin , C Khouw, IG Csizmadia - Journal of the , 1995 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1016/1044-0305(95)00569-2 γ-Glutamyl and d- or l-peptide linkages in mycobacillin, a cyclic peptide antibiotic S Sengupta, AB Banerjee, SK Bose - Biochemical Journal, 1971 - portlandpress.comhttps://portlandpress.com/biochemj/article-abstract/121/5/839/17191 Synthesis and anti-cancer activity of covalent conjugates of artemisinin and a transferrin-receptor targeting peptide S Oh, BJ Kim, NP Singh , H Lai, T Sasaki - Cancer letters, 2009 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S030438350800668X Rapid peptide synthesis in liquid phase. Preparation of angiotensin II and delta-sleep-inducing peptide by the" Hold-in-solution" method. S Nozaki, I Muramatsu - Bulletin of the Chemical Society of Japan, 1982 - jlc.jst.go.jphttp://jlc.jst.go.jp/DN/JALC/00194132242?from=Google Peptide-mediated targeted drug delivery S Majumdar, TJ Siahaan - Medicinal research reviews, 2012 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/med.20225 Synthesis of peptide analogues using the multipin peptide synthesis method RM Valerio, M Benstead, AM Bray, RA Campbell - Analytical , 1991 - Elsevierhttps://www.sciencedirect.com/science/article/pii/0003269791903743 Multipin peptide synthesis at the micromole scale using 2-hydroxyethyl methacryiate grafted polyethylene supports RM Valerio, AM BRAY, RA CAMPBELL - Journal of Peptide , 1993 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1111/j.1399-3011.1993.tb00341.x Aspartimide formation in peptide chemistry: occurrence, prevention strategies and the role of N-hydroxylamines R Subiros-Funosas, A El-Faham , F Albericio - Tetrahedron, 2011 - Elsevierhttps://www.sciencedirect.com/science/article/abs/pii/S0040402011012488 Advances in Fmoc solid-phase peptide synthesis R Behrendt, P White, J Offer - Journal of Peptide Science, 2016 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/psc.2836 Preparation and use of benzhydrylamine polymers in peptide synthesis. II. Synthesis of thyrotropin releasing hormone, thyrocalcitonin 26-32, and eledoisin PG Pietta, PF Cavallo, K Takahashi - The Journal of Organic , 1974 - ACS Publicationshttps://pubs.acs.org/doi/pdf/10.1021/jo00915a008 Cyclic peptides from linear unprotected peptide precursors through thiazolidine formation P Botti, TD Pallin, JP Tam - Journal of the American Chemical , 1996 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ja954278g alpha-Oxo aldehyde or glyoxylyl group chemistry in peptide bioconjugation O El-Mahdi, O Melnyk - Bioconjugate chemistry, 2013 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/bc300516f Efficient Building Blocks for Solid-Phase Peptide Synthesis of Spin Labeled Peptides for Electron Paramagnetic Resonance and Dynamic Nuclear Polarization M Brodrecht, K Herr, S Bothe, M de Oliveira Jr - , 2019 - Wiley Online Libraryhttps://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/cphc.201900211 Chemical modifications designed to improve peptide stability: incorporation of non-natural amino acids, pseudo-peptide bonds, and cyclization L Gentilucci , R De Marco - Current pharmaceutical , 2010 - ingentaconnect.comhttps://www.ingentaconnect.com/content/ben/cpd/2010/00000016/00000028/art00012 Synthesis and purification of aggregation-prone hydrophobic peptides by the incorporation of an Fmoc dipeptide with the peptide bond protected with a modified 2 K Wahlström, O Planstedt, A Unden - Tetrahedron letters, 2008 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0040403908007107 Peptide synthesis using unprotected peptides through orthogonal coupling methods. JP Tam , YIAN Lu, CFA Liu - Proceedings of the , 1995 - National Acad Scienceshttps://www.pnas.org/doi/abs/10.1073/pnas.92.26.12485 Self-assembling peptide nanotubes JD Hartgerink , JR Granja , RA Milligan - Journal of the , 1996 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ja953070s Synthesis of human GLP-1 (7-36) by chemoselective alpha-ketoacid-hydroxylamine peptide ligation of unprotected fragments J Wu, J Ruiz-Rodriguez, JM Comstock, JZ Dong - Chemical , 2011 - pubs.rsc.orghttps://pubs.rsc.org/en/content/articlehtml/2011/sc/c1sc00398d Amphipathic peptides and drug delivery J Fernandez-Carneado, MJ Kogan - Peptide Science , 2004 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/bip.10585 New segment-coupling method for peptide synthesis in aqueous solution: application to synthesis of human [Gly17]-beta-endorphin. J Blake, CHA Li - Proceedings of the National Academy of , 1981 - National Acad Scienceshttps://www.pnas.org/doi/abs/10.1073/pnas.78.7.4055 Basic principles of protease-catalyzed peptide bond formation HD Jakubke, P Kuhl, A Könnecke - Chemie International Edition , 1985 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/anie.198500851 The Mercaptomethyl Group Facilitates an Efficient One-Pot Ligation at Xaa-Ser/Thr for (Glyco) peptide Synthesis H Hojo, C Ozawa, H Katayama, A Ueki - Angewandte , 2010 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/ange.201000384 Three-dimensional orthogonal protection scheme for solid-phase peptide synthesis under mild conditions G Barany , F Albericio - Journal of the American Chemical Society, 1985 - ACS Publicationshttps://pubs.acs.org/doi/pdf/10.1021/ja00303a019 Multivalent Thioether-Peptide Conjugates: B Cell Tolerance of an Anti-Peptide Immune Response DS Jones, SM Coutts, CA Gamino - Bioconjugate , 1999 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/bc9801373 Glycylglycine rotaxanes-The hydrogen bond directed assembly of synthetic peptide rotaxanes DA Leigh , A Murphy, JP Smart - International Edition in , 1997 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/anie.199707281 Hydrolysis of a peptide bond in neutral water D Kahne, WC Still - Journal of the American Chemical Society, 1988 - ACS Publicationshttps://pubs.acs.org/doi/pdf/10.1021/ja00230a041 Chemical ligation approach to form a peptide bond between unprotected peptide segments. Concept and model study CF Liu , JP Tam - Journal of the American Chemical Society, 1994 - ACS Publicationshttps://pubs.acs.org/doi/pdf/10.1021/ja00089a001 Development of aspartic acid ligation for peptide cyclization derived from serine/threonine ligation C Xu , J Xu, H Liu , X Li - Chinese Chemical Letters, 2018 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S1001841718301153 Transport of peptidomimetic drugs by the intestinal di/tri-peptide transporter, PepT1 B Brodin , CU Nielsen , B Steffansen - Pharmacology & , 2002 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1034/j.1600-0773.2002.900601.x Peptide-based molecular shuttles AS Lane, DA Leigh , A Murphy - Journal of the American Chemical , 1997 - ACS Publicationshttps://pubs.acs.org/doi/full/10.1021/ja971224t Automated synthesis of peptide C-terminal aldehydes AM Murphy, R Dagnino Jr, PL Vallar - Journal of the , 1992 - ACS Publicationshttps://pubs.acs.org/doi/pdf/10.1021/ja00034a082 Exploiting enzymatic (reversed) hydrolysis in directed self-assembly of peptide nanostructures AK Das , R Collins , RV Ulijn - Small, 2008 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/smll.200700889 Antimicrobial activity and secondary structure of a novel peptide derived from ovalbumin A Tan, R Suzuki, C Yokoyama, S Yano - Journal of peptide , 2020 - Wiley Online Libraryhttps://onlinelibrary.wiley.com/doi/abs/10.1002/psc.3276
Proprietà chimiche
Richiesta tecnica su: 3D-PP48415 H-GIVE-OH
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