Betulinic Glycine Amide (Highly Pure)

<strong>Betulinic Glycine Amide (Highly Pure)</strong>_x000D_ <strong>Catalog number:</strong> B2017486_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 1 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> N/A_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> a molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> -20°C_x000D_ <strong>Keywords:</strong> N/A_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: Lombrea A, Semenescu AD, Magyari-Pavel IZ, Turks M, Lugiņina J, Peipiņš U, Muntean D, Dehelean CA, Dinu S, Danciu C. Comparison of In Vitro Antimelanoma and Antimicrobial Activity of 2,3-Indolo-betulinic Acid and Its Glycine Conjugates Plants (Basel). 2023 Mar 9;12(6):1253._x000D_ 2: Lombrea A, Watz CG, Bora L, Dehelean CA, Diaconeasa Z, Dinu S, Turks M, Lugiņina J, Peipiņš U, Danciu C. Enhanced Cytotoxicity and Antimelanoma Activity of Novel Semisynthetic Derivatives of Betulinic Acid with Indole Conjugation Plants (Basel). 2023 Dec 21;13(1):36._x000D_ 3: Zhao H, Holmes SS, Baker GA, Challa S, Bose HS, Song Z. Ionic derivatives of betulinic acid as novel HIV-1 protease inhibitors J Enzyme Inhib Med Chem. 2012 Oct;27(5):715-21._x000D_ 4: Takahashi H, Abo C, Suzuki H, Romsuk J, Oi T, Yanagawa A, Gorai T, Tomisaki Y, Jitsui M, Shimamura S, Mori H, Kaga A, Ishimoto M, Seki H, Muranaka T, Nakazono M. Triterpenoids in aerenchymatous phellem contribute to internal root aeration and waterlogging adaptability in soybeans New Phytol. 2023 Aug;239(3):936-948._x000D_ 5: Jin X, Zhou J, Zhang Z, Lv H. Doxorubicin combined with betulinic acid or lonidamine in RGD ligand-targeted pH-sensitive micellar system for ovarian cancer treatment Int J Pharm. 2019 Nov 25;571:118751._x000D_ 6: Shu Q, Wu J, Chen Q. Synthesis, Characterization of Liposomes Modified with Biosurfactant MEL-A Loading Betulinic Acid and Its Anticancer Effect in HepG2 Cell Molecules. 2019 Oct 31;24(21):3939._x000D_ 7: Rajemiarimiraho M, Banzouzi JT, Nicolau-Travers ML, Ramos S, Cheikh-Ali Z, Bories C, Rakotonandrasana OL, Rakotonandrasana S, Andrianary PA, Benoit-Vical F. Antiprotozoal activities of Millettia richardiana (Fabaceae) from Madagascar Molecules. 2014 Apr 3;19(4):4200-11._x000D_ 8: Khusnutdinova EF, Petrova AV, Thu HNT, Tu ALT, Thanh TN, Thi CB, Babkov DA, Kazakova OB. Structural modifications of 2,3-indolobetulinic acid: Design and synthesis of highly potent α-glucosidase inhibitors Bioorg Chem. 2019 Jul;88:102957._x000D_ 9: Pardo-Rodriguez D, Lasso P, Santamaría-Torres M, Cala MP, Puerta CJ, Méndez Arteaga JJ, Robles J, Cuervo C. Clethra fimbriata hexanic extract triggers alteration in the energy metabolism in epimastigotes of Trypanosoma cruzi Front Mol Biosci. 2023 Sep 25;10:1206074._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/26192809">10: Banzouzi JT, Soh PN, Ramos S, Toto P, Cavé A, Hemez J, Benoit-Vical F. Samvisterin, a new natural antiplasmodial betulin derivative from Uapaca paludosa (Euphorbiaceae) J Ethnopharmacol. 2015 Sep 15;173:100-4. </a>_x000D_ _x000D_ <strong>Products Related to Betulinic Glycine Amide (Highly Pure) can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>