These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

133 related articles for article (PubMed ID: 36100868)

  • 1. Preparation of a novel group of chemiluminescent N-substituted acridinium esters.
    Smith K; Mu X; Li Z; Woodhead JS; El-Hiti GA
    Luminescence; 2022 Nov; 37(11):1982-1990. PubMed ID: 36100868
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Synthesis, structure elucidation, and chemiluminescent activity of new 9-substituted 10-(ω-(succinimidyloxycarbonyl)alkyl)acridinium esters.
    Smith K; Mu X; Li Z; Holland AM; Woodhead JS; El-Hiti GA
    Luminescence; 2023 Apr; 38(4):487-496. PubMed ID: 36882939
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Synthesis and chemiluminescent characteristics of two new acridinium esters.
    Smith K; Mu X; Li Z; Woodhead JS; El-Hiti GA
    Luminescence; 2023 Nov; 38(11):1857-1863. PubMed ID: 37555552
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Synthesis and properties of chemiluminescent acridinium ester labels with fluorous tags.
    Natrajan A; Wen D; Sharpe D
    Org Biomol Chem; 2014 Jun; 12(23):3887-901. PubMed ID: 24788381
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Chemiluminescence from alkoxy-substituted acridinium dimethylphenyl ester labels.
    Natrajan A; Sharpe D; Wen D
    Org Biomol Chem; 2012 May; 10(17):3432-47. PubMed ID: 22441905
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Synthesis and properties of differently charged chemiluminescent acridinium ester labels.
    Natrajan A; Sharpe D
    Org Biomol Chem; 2013 Feb; 11(6):1026-39. PubMed ID: 23296263
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Syntheses of Hindered-Polymethylacridinium Esters with Potential for Biological Probe Nanoarchitectonics.
    Smith K; Ahmed Z; Woodhead JS; El-Hiti GA
    J Oleo Sci; 2023 Mar; 72(4):447-460. PubMed ID: 36908180
    [TBL] [Abstract][Full Text] [Related]  

  • 8. What Other Than Acridinium Esters? Computational Search for New Acridinium-Based Chemiluminogens.
    Pieńkos M; Zadykowicz B
    Int J Mol Sci; 2023 May; 24(11):. PubMed ID: 37298422
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A comparison of chemiluminescent acridinium dimethylphenyl ester labels with different conjugation sites.
    Natrajan A; Wen D
    Org Biomol Chem; 2015 Mar; 13(9):2622-33. PubMed ID: 25581208
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Synthesis of 9-(substituted phenoxycarbonyl)-10-methylacridinium trifluoromethanesulfonates: Effects of the leaving group on chemiluminescent properties.
    Smith K; Holland AM; Woodhead JS; El-Hiti GA
    Luminescence; 2024 Jun; 39(6):e4794. PubMed ID: 38887175
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Solvent Effect on the Chemiluminescence of Acridinium Thioester: A Computational Study.
    Pieńkos M; Zadykowicz B
    Chemphyschem; 2022 Aug; 23(15):e202200166. PubMed ID: 35607880
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Acridinium Ester Chemiluminescence: Methyl Substitution on the Acridine Moiety.
    Nakazono M; Nanbu S; Akita T; Hamase K
    J Oleo Sci; 2021; 70(11):1677-1684. PubMed ID: 34732638
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Enhancement effect on the chemiluminescence of acridinium esters under neutral conditions.
    Nakazono M; Nanbu S
    Luminescence; 2018 Mar; 33(2):345-348. PubMed ID: 29115007
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Computational Insights on the Mechanism of the Chemiluminescence Reaction of New Group of Chemiluminogens-10-Methyl-9-thiophenoxycarbonylacridinium Cations.
    Pieńkos M; Zadykowicz B
    Int J Mol Sci; 2020 Jun; 21(12):. PubMed ID: 32575922
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Enhanced immunoassay sensitivity using chemiluminescent acridinium esters with increased light output.
    Natrajan A; Sharpe D; Costello J; Jiang Q
    Anal Biochem; 2010 Nov; 406(2):204-13. PubMed ID: 20670613
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel poly-substituted aryl acridinium esters and their use in immunoassay.
    Law SJ; Miller T; Piran U; Klukas C; Chang S; Unger J
    J Biolumin Chemilumin; 1989 Jul; 4(1):88-98. PubMed ID: 2801251
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A rainbow of acridinium chemiluminescence.
    Best QA; Haack RA; Swift KM; Bax BM; Tetin SY; Hershberger SJ
    Luminescence; 2021 Jun; 36(4):1097-1106. PubMed ID: 33617125
    [TBL] [Abstract][Full Text] [Related]  

  • 18. On the use of acridinium indicators for the chemiluminescent determination of the total antioxidant capacity of dietary supplements.
    Krzymiński KK; Roshal AD; Rudnicki-Velasquez PB; Żamojć K
    Luminescence; 2019 Aug; 34(5):512-519. PubMed ID: 30972942
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Development and application of a novel acridinium ester for use as a chemiluminescent emitter in nucleic acid hybridisation assays using chemiluminescence quenching.
    Brown RC; Li Z; Rutter AJ; Mu X; Weeks OH; Smith K; Weeks I
    Org Biomol Chem; 2009 Jan; 7(2):386-94. PubMed ID: 19109686
    [TBL] [Abstract][Full Text] [Related]  

  • 20. High stability and high efficiency chemiluminescent acridinium compounds obtained from 9-acridine carboxylic esters of hydroxamic and sulphohydroxamic acids.
    Renotte R; Sarlet G; Thunus L; Lejeune R
    Luminescence; 2000; 15(5):311-20. PubMed ID: 11038489
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.