810610 | 4-palmitamido-TEMPO
N-tempoyl palmitamide

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4-palmitamido-TEMPO
N-tempoyl palmitamide
This amphiphilic compound binds strongly to membranes by virture of its long hydrocarbon chain, but the polarity of the amide linkage is expected to localize the nitroxide function in the aqueous phase adjacent to the membrane surface. The location of the nitroxide function allows one to investigate electrostatic potentials and lipid-protein interactions at the membrane surface.
CAS Registry Number is a Registered Trademark of the American Chemical Society
2,2,6,6-Tetramethyl-4-[(1-oxohexadecyl)amino]-1-piperidinyloxy
2,2,6,6-tetramethyl-4-palmitamidopiperidinooxy
2,2,6,6-Tetramethylpalmitoylamidopiperidine-1-oxyl
4-(Palmitylimino)-2,2,6,6-tetramethyl-1-piperidinyloxy
Ben-Zichri S, Kolusheva S, Danilenko M, Ossikbayeva S, Stabbert WJ, Poggio JL, Stein DE, Orynbayeva Z, Jelinek R. Cardiolipin mediates curcumin interactions with mitochondrial membranes. Biochim Biophys Acta Biomembr. 2019 Jan;1861(1):75-82. doi: 10.1016/j.bbamem.2018.10.016. Epub 2018 Oct 31.
PubMed ID: 30389425Shin YK, Hubbell WL. Determination of electrostatic potentials at biological interfaces using electron-electron double resonance. Biophys J. 1992 Jun;61(6):1443-53. doi: 10.1016/S0006-3495(92)81950-1. PMID: 1319760; PMCID: PMC1260440.
PubMed ID: 1319760- Certificate of Analysis (Lot No. 810610P-1MG-A-016 and 5463PGA016)
- Certificate of Analysis (Lot No. 810610P-1MG-B-016 and 5463PGB016)
- Certificate of Analysis (Lot No. 810610P-1MG-C-016 and 5463PGC016)
- Certificate of Analysis (Lot No. 810610P-1MG-D-016 and 5463PGD016)