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NHS-palmitic acid
Nombre químico: N-(palmitoyloxy)-succinimide // Sinónimos: 2,5-dioxopyrrolidin-1-yl palmitate, Palmitic acid N-hydroxysuccinimide ester, Hexadecanoic acid N-hydroxysuccinimide ester, N-Hydroxysuccinimide palmitate, Palmitic acid NHSester, Palmitic acid succ inimide ester, Succinimidyl hexadecanoate, Palm-NH
- Nº Artículo:RL-3810
- Nº CAS:14464-31-4
- Fórmula:C20H35NO4
- Storage temperature:-20°C
- Masa molecular:353,50 g/mol
- Pureza:min. 98%
from 190,00 €
description
Fatty acids are key components and abundant constituents of all biological systems and are subject of many clinical, nutritional, and metabolic studies as they play a crucial role for normal functioning at all levels of an organism. Protein lipidation/fatty acylation, a common co- and post-translational modification of proteins plays important roles in human physiology. Palmitoylation represents one of the major post translational modifications responsible for protein activity control.
Keep dry and store at -20 °C.
references
Controls on Polymer Molecular Weight May Be Used To Control the Size of Palmitoyl Glycol Chitosan Polymeric Vesicles; W. Wang, A. M. McConaghy, L. Tetley, I. F. Uchegbu; Langmuir 2001; 17(3): 631-636. https://doi.org/10.1021/la001078w.
Incorporation of fatty acid into food protein: palmitoyl soybean glycinin; Z. Haque, T. Matoba, M. Kito; J. Agric. Food Chem. 1982; 30(3): 481-486. https://doi.org/10.1021/jf00111a018.
Palmitoyl derivatives of interferon alpha: Potential for cutaneous delivery; M. Foldvari, S. Attah-Poku, J. Hu, Q. Li, H. Hughes, A. Babiuk Lorne, S. Kruger; J. Pharm. Sci. 1998; 87(10): 1203-1208. https://doi.org/10.1021/js980146k.
Palmitate-derivatized antibodies can function as surrogate receptors for mediating specific cell-cell interactions; A. S. Colsky, J. S. Peacock; J. Immunol. Methods 1989; 124(2): 179-187. https://doi.org/10.1016/0022-1759(89)90351-7.
Synthesis of fatty acyl CoA and other thiol esters using N-hydroxysuccinimide esters of fatty acids; A. Al-Arif, M. Blecher; J. Lipid Res. 1969, 10(3): 344-345. https://doi.org/10.1016/S0022-2275(20)43095-0.
Water-soluble fatty acid derivatives as acylating agents for reversible lipidization of polypeptides; H. M. Ekrami, A. R. Kennedy; W.-C. Shen; FEBS Letters 1995; 371(3): 283-286. https://doi.org/10.1016/0014-5793(95)00910-2.
Synthesis of palmitoyl derivatives of insulin and their biological activities; M. Hashimoto, . Takada, Y. Kiso, S. Muranishi; Pharm. Research 1989; 6: 171-176. https://doi.org/10.1023/A:1015992828666.
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All information contained in our webshop is compiled to the best of our knowledge.
Prices and product availability are subject to change and require reconfirmation. Please contact us for further information.
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