H-ASCLYGQLPK-OH

Ref. 3D-PP42775

Produktinformation

• Name: H-ASCLYGQLPK-OH
• Synonyme: NH2-Ala-Ser-Cys-Leu-Tyr-Gly-Gln-Leu-Pro-Lys-OH

Beschreibung

Peptide H-ASCLYGQLPK-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-ASCLYGQLPK-OH include the following: CDDO-imidazolide targets multiple amino acid residues on the Nrf2 adaptor, Keap1 X Meng , JC Waddington, A Tailor , A Lister - Journal of Medicinal , 2020 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.jmedchem.0c01088 Abacavir forms novel cross-linking abacavir protein adducts in patients X Meng , AS Lawrenson , NG Berry - Chemical research in , 2014 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/tx400406p Detection of drug bioactivation in vivo: mechanism of nevirapine-albumin conjugate formation in patients X Meng , A Howarth, CJ Earnshaw - Chemical Research , 2013 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/tx4000107 Covalent protein modification: An unignorable factor for bisphenol A-induced hepatotoxicity X Hu, JL Wu , W Miao, F Long, H Pan - Environmental , 2022 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.est.2c01307 Mass spectrometric characterization of circulating covalent protein adducts derived from epoxide metabolites of carbamazepine in patients VLM Yip, X Meng , JL Maggs, RE Jenkins - Chemical Research , 2017 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.chemrestox.7b00063 Proteomic and Mass Spectroscopic Quantitation of Protein S-Nitrosation Differentiates NO-Donors V Sinha, GT Wijewickrama - ACS chemical , 2010 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/cb100054m Quinone-induced activation of Keap1/Nrf2 signaling by aspirin prodrugs masquerading as nitric oxide T Dunlap, SC Piyankarage - Chemical research in , 2012 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/tx3003609 alpha-Methylene-beta-Lactone Scaffold for Developing Chemical Probes at the Two Ends of the Selectivity Spectrum L Wang, LP Riel, B Bajrami , B Deng, AR Howell - , 2021 - Wiley Online Libraryhttps://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/cbic.202000605 No Evidence for Drug-Specific Activation of Circulating T Cells from Patients with HLA-DRB1*07:01-Restricted Lapatinib-Induced Liver Injury L Faulkner, X Meng , DJ Naisbitt - Chemical Research , 2016 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.chemrestox.6b00400 Isobaric tagging-based selection and quantitation of cerebrospinal fluid tryptic peptides with reporter calibration curves L Dayon , N Turck, S Kienle, P Schulz-Knappe - Analytical , 2010 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/ac901854k Mass Spectrometric Characterization of Protein Adducts of Multiple P450-Dependent Reactive Intermediates of Diclofenac to Human Glutathione-S-transferase P1-1 JS Boerma, S Dragovic, NPE Vermeulen - Chemical research in , 2012 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/tx300334w Application of CYP102A1M11H as a tool for the generation of protein adducts of reactive drug metabolites JS Boerma, NPE Vermeulen - Chemical research in , 2011 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/tx2001515 Mechanistic studies of inactivation of glutathione S-transferase Pi isozyme by a haloenol lactone derivative J Zheng, G Liu, B Tozkoparan, D Wen - Medicinal Chemistry, 2005 - ingentaconnect.comhttps://www.ingentaconnect.com/content/ben/mc/2005/00000001/00000002/art00010 Multiple adduction reactions of nitroso sulfamethoxazole with cysteinyl residues of peptides and proteins: implications for hapten formation HE Callan, RE Jenkins, JL Maggs - Chemical research in , 2009 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/tx900034r Glutathione S-transferase pi trapping method for generation and characterization of drug-protein adducts in human liver microsomes using liquid chromatography H Yukinaga, H Iwabuchi, O Okazaki, T Izumi - Journal of pharmaceutical , 2012 - Elsevierhttps://www.sciencedirect.com/science/article/pii/S0731708512002324 Characterizing protein modifications by reactive metabolites using magnetic bead bioreactors and LC-MS/MS D Li , YJ Fu, JF Rusling - Chemical communications, 2015 - pubs.rsc.orghttps://pubs.rsc.org/en/content/articlehtml/2015/cc/c5cc00420a Organ-specific screening for protein damage using magnetic bead bioreactors and LC-MS/MS D Jiang , M Shen , B Ahiadu , JF Rusling - Analytical chemistry, 2020 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.analchem.9b05871 A Mechanistic Investigation into the Irreversible Protein Binding and Antigenicity of p-Phenylenediamine C Jenkinson, RE Jenkins, JL Maggs - Chemical research in , 2009 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/tx900095r Definition of haptens derived from sulfamethoxazole: in vitro and in vivo A Tailor , JC Waddington, J Hamlett - Chemical research in , 2019 - ACS Publicationshttps://pubs.acs.org/doi/abs/10.1021/acs.chemrestox.9b00282

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 1,079.27 g/mol
• Formel: C₄₈H₇₆N₁₂O₁₃S