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Coumarin-Quinone Conjugate

<strong>Coumarin-Quinone Conjugate</strong>_x000D_ <strong>Catalog number:</strong> B2012810_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 500 ug_x000D_ <strong>Molecular Weight or Concentration:</strong> 423.5 g/mol_x000D_ <strong>Supplied as:</strong> Lyophilized Powder_x000D_ <strong>Applications:</strong> molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> -20°C_x000D_ <strong>Keywords:</strong> A fluorescent substrate for NADH:ubiquinone oxidoreductases_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: Tanabe K, Hirata N, Harada H, Hiraoka M, Nishimoto S. Emission under hypoxia: one-electron reduction and fluorescence characteristics of an indolequinone-coumarin conjugate Chembiochem. 2008 Feb 15;9(3):426-32._x000D_ 2: Oprych D, Strehmel B. Mediated Generation of Conjugate Acid by UV and Blue Sensitizers with Upconversion Nanoparticles at 980 nm Chemistry. 2021 Mar 1;27(13):4297-4301._x000D_ 3: Wefers H, Sies H. Hepatic low-level chemiluminescence during redox cycling of menadione and the menadione-glutathione conjugate: relation to glutathione and NAD(P)H:quinone reductase (DT-diaphorase) activity Arch Biochem Biophys. 1983 Jul 15;224(2):568-78._x000D_ 4: Qiu ZW, Xu XT, Pan HP, Jia ZS, Ma AJ, Peng JB, Du JY, Feng N, Li BQ, Zhang XZ. Brønsted Acid-Catalyzed Formal (3+3)-Annulation of Propargylic (Aza)-para-Quinone Methides with 4-Hydroxycoumarins and 1,3-Dicarbonyl Compounds J Org Chem. 2021 May 7;86(9):6075-6089._x000D_ 5: Stoffman EJ, Clive DL. The coumarin--&gt;indole transformation--a method for preparing 4-halo-5-hydroxyindoles from coumarins Org Biomol Chem. 2009 Dec 7;7(23):4862-70._x000D_ 6: Yao C, Li Y, Wang Z, Song C, Hu X, Liu S. Cytosolic NQO1 Enzyme-Activated Near-Infrared Fluorescence Imaging and Photodynamic Therapy with Polymeric Vesicles ACS Nano. 2020 Feb 25;14(2):1919-1935._x000D_ 7: Talalay P. Mechanisms of induction of enzymes that protect against chemical carcinogenesis Adv Enzyme Regul. 1989;28:237-50._x000D_ 8: Hueso-Falcón I, Amesty Á, Anaissi-Afonso L, Lorenzo-Castrillejo I, Machín F, Estévez-Braun A. Synthesis and biological evaluation of naphthoquinone-coumarin conjugates as topoisomerase II inhibitors Bioorg Med Chem Lett. 2017 Feb 1;27(3):484-489._x000D_ 9: Aristizábal D, Gil J, Quiñones W, Durango D. Screening of Indanoyl-Type Compounds as Elicitors of Isoflavonoid Phytoalexins in Colombian Common Bean Cultivars Molecules. 2022 May 30;27(11):3500._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/8747698">10: Israels LG, Israels ED. Observations on vitamin K deficiency in the fetus and newborn: has nature made a mistake? Semin Thromb Hemost. 1995;21(4):357-63. </a>_x000D_ _x000D_ <strong>Products Related to Coumarin-Quinone Conjugate can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>

Product Specifications

Short Description

Catalog Number: B2012810 (500 ug)

Weight

0.15

Length

2

Width

0.5

Height

0.5

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