Palmitic-acid-9-hydroxy-stearic-acid

• Description:

  palmitic-acid-9-hydroxy-stearic-acid_x000D_ Catalog number: B2017917_x000D_ Lot number: Batch Dependent_x000D_ Expiration Date: Batch dependent_x000D_ Amount: 100 mg_x000D_ Molecular Weight or Concentration: 538.89_x000D_ Supplied as: Powder_x000D_ Applications: a molecular tool for various biochemical applications_x000D_ Storage: 2-8℃_x000D_ Keywords: 9-PAHSA_x000D_ Grade: 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_ References:_x000D_ 1: Yore MM, Syed I, Moraes-Vieira PM, Zhang T, Herman MA, Homan EA, Patel RT, Lee J, Chen S, Peroni OD, Dhaneshwar AS, Hammarstedt A, Smith U, McGraw TE, Saghatelian A, Kahn BB. Discovery of a class of endogenous mammalian lipids with anti-diabetic and anti-inflammatory effects Cell. 2014 Oct 9;159(2):318-32._x000D_ 2: Nelson AT, Kolar MJ, Chu Q, Syed I, Kahn BB, Saghatelian A, Siegel D. Stereochemistry of Endogenous Palmitic Acid Ester of 9-Hydroxystearic Acid and Relevance of Absolute Configuration to Regulation J Am Chem Soc. 2017 Apr 5;139(13):4943-4947._x000D_ 3: Brejchova K, Balas L, Paluchova V, Brezinova M, Durand T, Kuda O. Understanding FAHFAs: From structure to metabolic regulation Prog Lipid Res. 2020 Jul;79:101053._x000D_ 4: Kuda O, Brezinova M, Silhavy J, Landa V, Zidek V, Dodia C, Kreuchwig F, Vrbacky M, Balas L, Durand T, Hübner N, Fisher AB, Kopecky J, Pravenec M. Nrf2-Mediated Antioxidant Defense and Peroxiredoxin 6 Are Linked to Biosynthesis of Palmitic Acid Ester of 9-Hydroxystearic Acid Diabetes. 2018 Jun;67(6):1190-1199._x000D_ 5: Rychtrmoc D, Staňková P, Kučera O, Červinková Z. Comparison of two anti-diabetic monoestolides regarding effects on intact murine liver tissue Arch Physiol Biochem. 2022 Aug;128(4):985-992._x000D_ 6: Xu X, Kang C, Sun R, Zuo YY. Biophysical properties of tear film lipid layer II. Polymorphism of FAHFA Biophys J. 2022 Feb 1;121(3):451-458._x000D_ 7: Aryal P, Syed I, Lee J, Patel R, Nelson AT, Siegel D, Saghatelian A, Kahn BB. Distinct biological activities of isomers from several families of branched fatty acid esters of hydroxy fatty acids (FAHFAs) J Lipid Res. 2021;62:100108._x000D_ 8: Sokolowska P, Jastrzebska E, Dobrzyn A, Brzozka Z. Investigation of the Therapeutic Potential of New Antidiabetic Compounds Using Islet-on-a-Chip Microfluidic Model Biosensors (Basel). 2022 May 5;12(5):302._x000D_ 9: Wang JT, Wang XR, Ren JQ, Lin JH, Yu ZY, Huang SS, Hu Y, Fu JY, Wang M, Zhang YL, Wang XC, Guo JC, Xiao JC, Zhou HG. S-9-PAHSA's neuroprotective effect mediated by CAIII suppresses apoptosis and oxidative stress in a mouse model of type 2 diabetes CNS Neurosci Ther. 2024 Feb;30(2):e14594._x000D_ 10: Syed I, Lee J, Moraes-Vieira PM, Donaldson CJ, Sontheimer A, Aryal P, Wellenstein K, Kolar MJ, Nelson AT, Siegel D, Mokrosinski J, Farooqi IS, Zhao JJ, Yore MM, Peroni OD, Saghatelian A, Kahn BB. Palmitic Acid Hydroxystearic Acids Activate GPR40, Which Is Involved in Their Beneficial Effects on Glucose Homeostasis Cell Metab. 2018 Feb 6;27(2):419-427.e4. _x000D_ _x000D_ Products Related to palmitic-acid-9-hydroxy-stearic-acid can be found at Chemicals

• Short Description:

  Catalog Number: B2017917 (100 mg)

• Weight:

  0.15

• Length:

  2

• Width:

  0.5

• Height:

  0.5

• Height :

  0.5