Boc-Gly-OH (Highly Pure)
<strong>Boc-Gly-OH (Highly Pure)</strong>_x000D_ <strong>Catalog number:</strong> B2015524_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 1 g_x000D_ <strong>Molecular Weight or Concentration:</strong> 175.18_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> a molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> RT, Dry_x000D_ <strong>Keywords:</strong> N-(tert-Butoxycarbonyl)glycine, Boc-glycine_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: Vezenkov LT, Georgieva MG, Danalev DL, Ivanov TB, Ivanova GI. Synthesis and characterization of new galanthamine derivatives comprising peptide moiety Protein Pept Lett. 2009;16(9):1024-8._x000D_ 2: Sureshbabu VV, Naik SA, Hemantha HP, Narendra N, Das U, Guru Row TN. N-urethane-protected amino alkyl isothiocyanates: synthesis, isolation, characterization, and application to the synthesis of thioureidopeptides J Org Chem. 2009 Aug 7;74(15):5260-6._x000D_ 3: Ten Kortenaar PB, Wilkerson WW, Boggs NT 3rd, Madar DA, Koehler KA, Hiskey RG. Bovine prothrombin fragment 1, segment 1-10. Synthesis and immunological investigation Int J Pept Protein Res. 1980 Nov;16(5):440-9._x000D_ 4: Oo Y, Nealiga JQL, Suwanborirux K, Chamni S, Ecoy GAU, Pongrakhananon V, Chanvorachote P, Chaotham C. 22-O-(N-Boc-L-glycine) ester of renieramycin M inhibits migratory activity and suppresses epithelial-mesenchymal transition in human lung cancer cells J Nat Med. 2021 Sep;75(4):949-966._x000D_ 5: Arcoria PJ, Etzkorn FA. A fluoro-alkene mimic of Gly-trans-Pro produces a stable collagen triple helix Org Biomol Chem. 2023 May 17;21(19):4039-4051._x000D_ 6: Lelj F, Tamburro AM, Villani V, Grimaldi P, Guantieri V. Molecular dynamics study of the conformational behavior of a representative elastin building block: Boc-Gly-Val-Gly-Gly-Leu-OMe Biopolymers. 1992 Feb;32(2):161-72._x000D_ 7: Villani V, Tamburro AM. Conformational modeling of elastin tetrapeptide Boc-Gly-Leu-Gly-Gly-NMe by molecular dynamics simulations with improvements to the thermalization procedure J Biomol Struct Dyn. 1995 Jun;12(6):1173-202._x000D_ 8: Stiefel C, Schwack W. Reactivity of cosmetic UV filters towards skin proteins: model studies with Boc-lysine, Boc-Gly-Phe-Gly-Lys-OH, BSA and gelatin Int J Cosmet Sci. 2014 Dec;36(6):561-70._x000D_ 9: Pozdnyakova AN, Cheremnykh EG, Sokolov OY, Kost NV, Shevchenko KV, Shevchenko VP, Nagaev IY, Andreeva LA, Myasoedov NF. Assessment of the Cytotoxicity of Peptide Modifications of Doxorubicin on Tetrahymena pyriformis Dokl Biochem Biophys. 2021 Mar;497(1):104-107._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/36066113">10: Wu Z, Shen Y, Zhang X. TAG-TMTpro, a Hyperplexing Quantitative Approach for High-Throughput Proteomic Studies Anal Chem. 2022 Sep 20;94(37):12565-12569. </a>_x000D_ _x000D_ <strong>Products Related to Boc-Gly-OH (Highly Pure) can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>
Product Specifications
Short Description
Catalog Number: B2015524 (1 g)
Weight
0.8
Length
2
Width
0.9
Height
0.9
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