pyrophosphate and pyrene

pyrophosphate has been researched along with pyrene* in 3 studies

Other Studies

3 other study(ies) available for pyrophosphate and pyrene

ArticleYear
P(V) Reagents for the Scalable Synthesis of Natural and Modified Nucleoside Triphosphates.
    Journal of the American Chemical Society, 2019, 08-28, Volume: 141, Issue:34

    Natural and modified nucleoside triphosphates impact nearly every major aspect of healthcare research from DNA sequencing to drug discovery. However, a scalable synthetic route to these molecules has long been hindered by the need for purification by high performance liquid chromatography (HPLC). Here, we describe a fundamentally different approach that uses a novel P(V) pyrene pyrophosphate reagent to generate derivatives that are purified by silica gel chromatography and converted to the desired compounds on scales vastly exceeding those achievable by HPLC. The power of this approach is demonstrated through the synthesis of a broad range of natural and unnatural nucleoside triphosphates (dNTPs and xNTPs) using protocols that are efficient, inexpensive, and operationally straightforward.

    Topics: Chemistry Techniques, Synthetic; Chromatography, High Pressure Liquid; Diphosphates; Indicators and Reagents; Nucleotides; Pyrenes

2019
A Pyrene-functionalized Polynorbornene for Ratiometric Fluorescence Sensing of Pyrophosphate.
    Chemistry, an Asian journal, 2016, Mar-04, Volume: 11, Issue:5

    A novel pyrene-functionalized polynorbornene (P1) bearing sulfonamide NH and triazolium donors has been synthesized for ratiometric fluorescence sensing of PPi in aqueous solution. In addition, P1 is also used to monitor intracellular PPi and to detect PPi released during polymerase chain reaction.

    Topics: Diphosphates; Fluorescent Dyes; HeLa Cells; Humans; Microscopy, Confocal; Optical Imaging; Plastics; Pyrenes; Spectrometry, Fluorescence

2016
Zinc-cyclen coordination to UTP, TTP or pyrophosphate induces pyrene excimer emission.
    Dalton transactions (Cambridge, England : 2003), 2010, Aug-21, Volume: 39, Issue:31

    Pyrene labelled Zn(2+)-cyclen 1 and bis-Zn(2+)-bis-cyclen 2 complexes were synthesized. The reversible coordination at physiological pH of Zn(2+)-cyclens to phosphate anions and to imide moieties, as present in thymine and uracil nucleotides, is well known. In the presence of analytes bearing a phosphate and an imide or two phosphate groups the formation of a ternary complex consisting of two pyrene-labelled metal complexes and the analyte molecule, is observed. The close proximity of the pyrene labels in the complex induces pyrene excimer emission, which is observable by the unarmed eye. By this, the presence of UMP, UDP, UTP and TTP in buffered aqueous solution is signalled, while other nucleotides are not able to induce excimer emission. In the same way, Zn(2+)-cyclen-pyrene acts as luminescent chemosensor for PP(i) and fructose-1,6-bisphosphate in aqueous buffer.

    Topics: Coordination Complexes; Cyclams; Diphosphates; Heterocyclic Compounds; Pyrenes; Spectrometry, Fluorescence; Thymine Nucleotides; Uridine Triphosphate; Zinc

2010