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Palmityl palmitate

<strong>Palmityl palmitate</strong>_x000D_ <strong>Catalog number:</strong> B2017938_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 50 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> 480.85 g/mol_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> a molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> 2-8°C_x000D_ <strong>Keywords:</strong> Cetyl palmitate, Hexadecyl hexadecanoate, Palmitic acid palmityl ester_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity &gt;18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: Molé PA, Oscai LB, Holloszy JO. Adaptation of muscle to exercise. Increase in levels of palmityl Coa synthetase, carnitine palmityltransferase, and palmityl Coa dehydrogenase, and in the capacity to oxidize fatty acids J Clin Invest. 1971 Nov;50(11):2323-30._x000D_ 2: Bremer J, Norum KR. Palmityl-CoA: carnitine O-palmityltransferase in the mitochondrial oxidation of palmityl-CoA Eur J Biochem. 1967 Jun;1(4):427-33._x000D_ 3: Coupland CE, Andrei SA, Ansell TB, Carrique L, Kumar P, Sefer L, Schwab RA, Byrne EFX, Pardon E, Steyaert J, Magee AI, Lanyon-Hogg T, Sansom MSP, Tate EW, Siebold C. Structure, mechanism, and inhibition of Hedgehog acyltransferase Mol Cell. 2021 Dec 16;81(24):5025-5038.e10._x000D_ 4: Wititsuwannakul D, Kim KH. Mechanism of palmityl coenzyme A inhibition of liver glycogen synthase J Biol Chem. 1977 Nov 10;252(21):7812-7._x000D_ 5: Bank WJ, DiMauro S, Bonilla E, Capuzzi DM, Rowland LP. A disorder of muscle lipid metabolism and myoglobinuria. Absence of carnitine palmityl transferase N Engl J Med. 1975 Feb 27;292(9):443-9._x000D_ 6: Lee C, Choi JS, Kim I, Byeon HJ, Kim TH, Oh KT, Lee ES, Lee KC, Youn YS. Decanoic acid-modified glycol chitosan hydrogels containing tightly adsorbed palmityl-acylated exendin-4 as a long-acting sustained-release anti-diabetic system Acta Biomater. 2014 Feb;10(2):812-20._x000D_ 7: SENIOR JR, ISSELBACHER KJ. Formation of higher glycerides from monopalmitin and palmityl-CoA by microsomes of rat intestinal mucosa Biochem Biophys Res Commun. 1961 Nov 29;6:274-8._x000D_ 8: Bremer J, Norum KR. The mechanism of substrate inhibition of palmityl coenzyme A:carnitine palmityltransferase by palmityl coenzyme A J Biol Chem. 1967 Apr 25;242(8):1744-8._x000D_ 9: Stults JT, Griffin PR, Lesikar DD, Naidu A, Moffat B, Benson BJ. Lung surfactant protein SP-C from human, bovine, and canine sources contains palmityl cysteine thioester linkages Am J Physiol. 1991 Aug;261(2 Pt 1):L118-25._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/1100391">10: Knobling A, Schiffmann D, Sickinger HD, Schweizer E. Malonyl and palmityl transferase-less mutants of the yeast fatty-acid-synthetase complex Eur J Biochem. 1975 Aug 15;56(2):359-67. </a>_x000D_ _x000D_ <strong>Products Related to Palmityl palmitate can be found at</strong> <a href="https://moleculardepot.com/product-category/Lipids/"> Lipids</a>

Product Specifications

Short Description

Catalog Number: B2017938 (50 mg)

Weight

0.15

Length

2

Width

0.5

Height

0.5

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