Log in

Relevant bibliographies by topics / Acridinique

Contents

Journal articles
Dissertations / Theses
Books
Book chapters
Conference papers

Academic literature on the topic 'Acridinique'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Acridinique.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Acridinique"

1

Maas, Gerhard, and Berndt Singer. "Dikationether, 6 [1] Spektroskopische Vergleiche von 9,9′-Oxy-bis(acridinium)- und 9,9′-Thio-bis(acridinium)-Salzen mit anderen 9-substituierten Acridinium-Ionen / Dication Ethers, 6 [1] Spectroscopic Comparisons of 9,9′-Oxy-bis(acridinium)- and 9,9′-Thio-bis(acridinium) Salts with Other 9-Substituted Acridinium Ions." Zeitschrift für Naturforschung B 40, no. 1 (January 1, 1985): 90–99. http://dx.doi.org/10.1515/znb-1985-0118.

Full text

Abstract:

9,9′-Oxy-bis(acridinium) salts 2a and 2b as well as the 9,9′-thio-bis(acridinium) salt 2c have been compared with other 9-substituted acridinium salts by 1H NMR, 13C NMR, and UV/VIS spectra. The data show that the bond state of the acridine rings in 2a-c is quite similar to that in 9-(pseudo)halide-substituted acridinium ions, i.e., the aromatic conjugation throughout the heterocyclic system is not disturbed

APA, Harvard, Vancouver, ISO, and other styles

2

Natrajan, Anand, and David Wen. "A comparison of chemiluminescent acridinium dimethylphenyl ester labels with different conjugation sites." Organic & Biomolecular Chemistry 13, no. 9 (2015): 2622–33. http://dx.doi.org/10.1039/c4ob02528h.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Katoh, Makoto, Susumu Chishima, Nobukazu Kiuchi, Tomihiro Ikeo, and yasuhiko Sasaki. "A New Method for the Assay of Exposed Platelet Fibrinogen Receptor Using a Chemiluminescent Label." Thrombosis and Haemostasis 74, no. 06 (1995): 1546–50. http://dx.doi.org/10.1055/s-0038-1649980.

Full text

Abstract:

SummaryAssay of the platelet fibrinogen-binding receptor glycoprotein (GP) IIb/IIIa is widely performed using 125I-labeled fibrinogen (125I-fibrinogen). We successfully devised a receptor binding assay system with high selectivity and sensitivity using a stable chemiluminescent acridinium derivative I-labeled fibrinogen (acridinium-fibrinogen).Human fibrinogen in saline was labeled with equimolar acridinium dissolved in dimethylformamide, and allowed to react with gel-filtered human platelets in the presence of ADP. Acridinium-fibrinogen binding to GPIIb/IIIa was assayed by measuring chemiluminescence emitted on addition of 0.1 N NaOH containing 0.06% H202 in a luminometer. Non-specific binding was measured in the presence of 10 mM EDTA. Acridinium-fibrinogen binding to human platelets was rapid and reversible, specific and saturable, and dependent on ADP concentrations. Scatchard plot analysis revealed one class of binding sites with a Kd of 326 nM and Bmax of 7.8 pmol/108 platelets. These values were comparable to the data obtained by using 125I-fibrinogen. Unlabeled fibrinogen, RGDS, and HHLGGAKQAGDV (fibrinogen γ-chain 400-411) displaced acridinium-fibrinogen from its binding site with Ki values of 322 nM, 9.2 μM and 31.3μM, respectively. Thus, this binding assay system may be useful in measuring the binding between platelet GPIIb/IIIa and fibrinogen without using a radioisotop.

APA, Harvard, Vancouver, ISO, and other styles

4

Shaameri, Zurina, Ning Shan, and William Jones. "Acridinium isophthalate." Acta Crystallographica Section E Structure Reports Online 57, no. 10 (September 20, 2001): o945—o946. http://dx.doi.org/10.1107/s1600536801013927.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

White, Alexander, Leifeng Wang, and David Nicewicz. "Synthesis and Characterization of Acridinium Dyes for Photoredox Catalysis." Synlett 30, no. 07 (March 12, 2019): 827–32. http://dx.doi.org/10.1055/s-0037-1611744.

Full text

Abstract:

Photoredox catalysis is a rapidly evolving platform for synthetic methods development. The prominent use of acridinium salts as a sustainable option for photoredox catalysts has driven the development of more robust and synthetically useful versions based on this scaffold. However, more complicated syntheses, increased cost, and limited commercial availability have hindered the adoption of these catalysts by the greater synthetic community. By utilizing the direct conversion of a xanthylium salt into the corresponding acridinium as the key transformation, we present an efficient and scalable preparation of the most synthetically useful acridinium reported to date. This divergent strategy also enabled the preparation of a suite of novel acridinium dyes, allowing for a systematic investigation of substitution effects on their photophysical properties.

APA, Harvard, Vancouver, ISO, and other styles

6

Eshtiagh-Hosseini, Hossein, Azam Hassanpoor, Masoud Mirzaei, and Ali R. Salimi. "Acridinium 2-hydroxybenzoate." Acta Crystallographica Section E Structure Reports Online 66, no. 11 (October 31, 2010): o2996. http://dx.doi.org/10.1107/s160053681004345x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Zilate, Bouthayna, Christian Fischer, Lukas Schneider, and Christof Sparr. "Scalable Synthesis of Acridinium Catalysts for Photoredox Deuterations." Synthesis 51, no. 23 (October 21, 2019): 4359–65. http://dx.doi.org/10.1055/s-0039-1690694.

Full text

Abstract:

The continuous development of photocatalytic methods incentivizes the design of organic catalysts to complement the frequently used and precious polypyridyl transition metal systems. Herein, a scalable synthesis of suitable acridinium dyes and their application in photoredox deuterations are described. The acridinium catalysts, prepared on multi-gram scale, allowed the deuteration of a pharmaceutically relevant scaffold in high yield and selectivity under mild conditions.

APA, Harvard, Vancouver, ISO, and other styles

8

Derikvand, Zohreh, Hossein Aghabozorg, and Jafar Attar Gharamaleki. "Acridinium 3,5-dicarboxybenzoate monohydrate." Acta Crystallographica Section E Structure Reports Online 65, no. 5 (April 30, 2009): o1173. http://dx.doi.org/10.1107/s1600536809015529.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Zadykowicz, Beata, Damian Trzybiński, Artur Sikorski, and Jerzy Błażejowski. "9-(Methylsulfanyl)acridinium trifluoromethanesulfonate." Acta Crystallographica Section E Structure Reports Online 65, no. 3 (February 21, 2009): o566—o567. http://dx.doi.org/10.1107/s1600536809004978.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Natrajan, Anand, David Wen, and David Sharpe. "Synthesis and properties of chemiluminescent acridinium ester labels with fluorous tags." Org. Biomol. Chem. 12, no. 23 (2014): 3887–901. http://dx.doi.org/10.1039/c4ob00456f.

Full text

APA, Harvard, Vancouver, ISO, and other styles

More sources

Dissertations / Theses on the topic "Acridinique"

1

MANNANI, REZA. "Synthese et biologie de nouveaux amino-3 acridiniques : preparation de monomeres et de dimeres mono- et bi-pontes ; activites antiparasitaires, proprietes intercalantes et cytotoxicite." Aix-Marseille 2, 1990. http://www.theses.fr/1990AIX22986.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

GIOVANNANGELI, GEORGER GENEVIEVE. "Synthese d'oxo-9 et de thio-9 mono-tetrahydro-1,2,3,4 acridines, et de bis-tetrahydro-1,2,3,4 thioacridiniques : etude comparee de leur activite sur trypanosoma cruzi et sur leishmania donovani." Aix-Marseille 2, 1989. http://www.theses.fr/1989AIX22965.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Johnson, Comlan Ansah. "Thio-benzazoles et thio-pyridiniques : synthese et etude biologique de monomeres, dimeres et hetero-dimeres benzazolo- et/ou pyridino-acridiniques." Aix-Marseille 2, 1993. http://www.theses.fr/1993AIX22960.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

BSIRI, NADIA. "Synthese de derives 9 - thioarylacridiniques : criblage de leurs proprietes antiparasitaires et anticancereuses ; etude conformationnelle et evaluation de leur interaction dans l'acide desoxyribonucleique." Aix-Marseille 2, 1993. http://www.theses.fr/1993AIX22959.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Robin, Maxime. "Synthèse et études biologiques de tétracycles acridiniques et tétrahyro acridiniques." Aix-Marseille 3, 2000. http://www.theses.fr/2000AIX30071.

Full text

Abstract:

On a développé la synthèse de nouvelles acridines et tétrahydroacridines comportant un quatrième cycle de type thiazole, oxazole, dioxole, dioxane et benzimidazole. Pour cela, nous avons synthétisé de nouveaux intermédiaires de types benzothiazoles et benzoxazoles. De plus, l'étape limitante de la synthèse, l'obtention des acides N-anthraniliques, a été optimisée en développant une nouvelle méthode utilisant les ultrasons. Nous avons isolé et caractérisé neuf nouvelles séries de tétracyles acridiniques et quatre nouvelles séries de tétracycles tétrahydroacridiniques. Tous ces nouveaux composés ont été, ou sont en cours d'évaluation dans différents domaines d'activités. Certains résultats sont encourageants, en particulier en tant que colorants cellulaires. Des valeurs extrêmement importantes de mutagénicité ont été mises en évidence et reliées aux structures
We have developed the synthesis of new acridine and tetrahydroacridine derivatives bearing a supplementary ring System like thiazole, oxazole, dioxole, dioxane, and benzimidazole. In this pathway we have synthesized new benzothiazole and benzoxazole intermediates. The restrictive stage of the synthesis, obtention of N-anthranilic acid, was increase using ultrasonic irradiation's. We have synthesized and determined nine new tetracycle acridine collection's and four tetracyle tetrahydroacridine skeleton. All these new compounds were or will be tested in different scopes. First results show that they have potent pharmacological properties. Some interesting results was shown as cellular dye. Important mutagenic values were determined and structure activity relationship were done

APA, Harvard, Vancouver, ISO, and other styles

6

Rasolofoarimanana, Roland Michel. "Synthèse et étude physicochimique d'éthers couronnes 2,4-acridiniques." Aix-Marseille 3, 1992. http://www.theses.fr/1992AIX30031.

Full text

Abstract:

Par acylation de molecules ambidentes telles la 2-hydroxy, 9-acridinone et la 2-hydroxy, 9-thioacridinone, nous avons pu obtenir des derives acridiniques monoacyles en position 2. A partir de la 2,4-dihydroxy, 9-chloroacridine et de la 10-methyl, 2,4-dihydroxy, 9-acridinone, nous avons pu preparer des ethers couronnes acridiniques. A partir des composes chlores, on a pu obtenir des macrocycles portant un groupement amino ou une chaine dialkyl amino alkyl. Certaines molecules montrent des aptitudes a la complexation et une selectivite vis-a-vis des cations metalliques. La structure et la conformation de ces molecules ont ete determinees par rmn du #1h, et du #1#3c, et par rmn bidimensionnelle (correlation heteronucleaire #1#3c-#1h). Les proprietes ionophores ont ete evaluees par la methode d'extraction liquide-liquide. Les macrocycles, comme les autres composes acridiniques prepares, sont susceptibles d'etre des intercalants de l'adn et d'intervenir dans les processus biologiques adn-dependants

APA, Harvard, Vancouver, ISO, and other styles

7

Roubaud, Gabriel. "Synthèse de monomères acridiniques polymérisables à activité fluorescence." Aix-Marseille 3, 2002. http://www.theses.fr/2002AIX30067.

Full text

Abstract:

Nous présentons la synthèse de monomères acridiniques comportant : -Un motif acridinique utilisé comme sonde fluorescent. -Une double ou une triple liaison pour l’introduction du monomère sur du styrène par polymérisation radicalaire. -Une fonction spécifique pour permettre au polymère de fixer des protéines. Une étude spectroscopique a été réalisée sur les produits les plus intéressants au travers de mesures de fluorescence UV. Nous présentons également les premiers résultats concernant les polymères obtenus
We are presenting the synthesis of acridinic monomers including : -A acridinic pattern used as fluorescent probe. -A double or and triple bond to link monomer to the styrene by radical polymerization. -Specific function to allow the polymer to catch proteins. An ultraviolet spectroscopic study has been carried out for the most interesting products. We are also presenting the first results concerning the produced polymers

APA, Harvard, Vancouver, ISO, and other styles

8

Vichet, Alain. "Synthèses et propriétés physicochimiques d'éthers couronnes 2,7-acridiniques." Aix-Marseille 3, 1990. http://www.theses.fr/1990AIX30069.

Full text

Abstract:

Par alkylation de molecules ambidentes telles que la 4-hydroxy 9-acridinone et la 4-hydroxy 9-thioacridinone nous avons pu obtenir des derives diacridiniques pontes en 4,4 et 9,9. A partir de la 2,7-dihydroxy 9-chloroacridine et de la 10-methyl 2,7-dihydroxy 9-acridinone nous avons pu preparer des ethers couronnes, dont certains ont montre des aptitudes a la complexation et une forte selectivite vis-a-vis des cations metalliques. La structure et la conformation de ces molecules ont ete determinees par r. M. N. Du #1h et du #1#3c, par r. M. N. Bidimensionnelle (correlation heteronucleaire #1#3c-#1h) et par diffraction des rayons x. Les proprietes ionophores ont ete evaluees par la methode d'extraction liquide-liquide. Tous les composes diacridiniques ou macrocycliques synthetises sont susceptibles d'etre de bons intercalants de l'a. D. N. Et par la meme d'intervenir dans les processus biologiques a. D. N. Dependants

APA, Harvard, Vancouver, ISO, and other styles

9

Shimi, Kamal. "Synthèse de nouveaux dérivés acridiniques à potentialités biologiques." Aix-Marseille 3, 2004. http://www.theses.fr/2004AIX30006.

Full text

Abstract:

La préparation de nouveaux monomères et dimères acridiniques a été développée ainsi que la synthèse par N-arylation d'amines hétérocycliques au moyen de complexes bismuthés ou borés. L'obtention de ces composés passe par la mise au point de la préparation de deux intermédiaires clés : l'amino-4-acridine et l'acétamido-3-amino-6-acridine. Nous avons isolé et caractérisé cinq nouvelles séries de monomères acridiniques hétérocycliques, deux nouvelles séries de dimères acridiniques hétérocycliques, et une série de composés biacridiniques. Tous ces nouveaux composés sont en cours d'évaluation biologique
We have developed the synthesis of new acridinic monomers and dimers. Moreover, the N-arylation of heterocyclic amines using organometalic reagents wearing boron or bismuth has been also developped to yield different acridinic polycycles. This work needs the synthesis of two key intermediates: the 3-acetamido-6-aminoacridine and the 4-aminoacridine. Thus, we obtained five new series of heterocyclic acridinic monomers, two new series of acridinic dimers and one range of biacridines. All these new compounds are currently in biological testing

APA, Harvard, Vancouver, ISO, and other styles

10

Issmaili, Saadia. "Synthèse et études physico-chimiques de composés diacridinoniques et acridiniques 4,5-disubstitués." Aix-Marseille 3, 1997. http://www.theses.fr/1997AIX30010.

Full text

Abstract:

Le but de ce travail a ete d'elaborer de nouvelles molecules ayant comme cible l'adn. Notre objectif a donc ete de synthetiser des composes acridiniques a propriete intercalante. On a mis au point la preparation de la 4-amino-5-hydroxy-9(10h)-acridinone et de son homologue acridinique. L'acylation de ces composes s'est effectuee uniquement sur le groupement amino en positions 4,4'. A partir de ces derives diacridiniques monopontes, nous avons prepare des composes acridiniques bipontes par acylation sur les groupements hydroxy en positions 5,5'. A partir de la 4-amino-5-hydroxyacridine nous avons synthetise un ether couronne acridinique: la 4,5-(10-aza-1,4,7-trioxadecyl)-acridine. La structure des differents composes a ete determinee sans ambiguite par rmn #1h, #1#3c et rmn bidimensionnelle. Ces composes macrocycliques sont susceptibles d'etre des intercalants ou des bis-intercalants de l'adn

APA, Harvard, Vancouver, ISO, and other styles

More sources

Books on the topic "Acridinique"

1

Mason, Jacqueline Margaret. A rate and equilibrium study of the addition of carbon nucleophiles to acridinium and phenanthridinium cations. Ottawa: National Library of Canada, 1994.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

Book chapters on the topic "Acridinique"

1

Selby, I. A. "Acridinium Salts and Reduced Acridines." In Chemistry of Heterocyclic Compounds: A Series Of Monographs, 433–517. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186596.ch6.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Prager, R. H., and C. M. Williams. "Acridinium Salts." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-01713.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Fodran, Peter, Leticia Monjas, and Carl-Johan Wallentin. "Nitrogen Heterocycles: Acridinium Salts." In Photoorganocatalysis in Organic Synthesis, 359–421. WORLD SCIENTIFIC (EUROPE), 2019. http://dx.doi.org/10.1142/9781786346056_0009.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Weeks, Ian, Maria Sturgess, Richard C. Brown, and J. Stuart Woodhead. "[31] Immunoassays using acridinium esters." In Methods in Enzymology, 366–87. Elsevier, 1986. http://dx.doi.org/10.1016/0076-6879(86)33080-5.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Nelson, Norman C., Mark A. Reynolds, and Lyle J. Arnold. "Detection of Acridinium Esters by Chemiluminescence." In Nonisotopic DNA Probe Techniques, 275–310. Elsevier, 1992. http://dx.doi.org/10.1016/b978-0-12-426296-6.50016-2.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Prager, R. H., and C. M. Williams. "Oxidation of Acridines and Acridinium Salts." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-01747.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Nelson, Norman C., Mark A. Reynolds, and Lyle J. Arnold. "Detection of Acridinium Esters by Chemiluminescence." In Nonisotopic Probing, Blotting, and Sequencing, 391–428. Elsevier, 1995. http://dx.doi.org/10.1016/b978-012426291-1/50019-4.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

"12 Acridinium Dyes and Quinones in Photocatalysis." In Photocatalysis in Organic Synthesis, edited by König. Stuttgart: Georg Thieme Verlag, 2019. http://dx.doi.org/10.1055/sos-sd-229-00224.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

O'Brien, John F., George G. Klee, and C. L. Shellum. "THE MAGIC LITE SYSTEM AND ACRIDINIUM ESTER-BASED IMMUNOASSAYS." In Immunoassay Automation, 221–44. Elsevier, 1992. http://dx.doi.org/10.1016/b978-0-12-167632-2.50022-8.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Lambert, Tristan H. "Synthesis and Reactions of Alkenes." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0032.

Full text

Abstract:

Christine L. Willis and Varinder K. Aggarwal at the University of Bristol have developed (Angew. Chem. Int. Ed. 2012, 51, 12444) a procedure for the diastereodivergent synthesis of trisubstituted alkenes via the protodeboronation of allylic boronates, such as in the conversion of 1 to either 2 or 3. An alternative approach to the stereoselective synthesis of trisubstituted alkenes involving the reduction of the allylic C–O bond of cyclic allylic ethers (e.g., 4 to 5) was reported (Chem. Commun. 2012, 48, 7844) by Jon T. Njardarson at the University of Arizona. A novel synthesis of allylamines was developed (J. Am. Chem. Soc. 2012, 134, 20613) by Hanmin Huang at the Chinese Academy of Sciences with the Pd(II)-catalyzed vinylation of styrenes with aminals (e.g. 6 + 7 to 8). Eun Jin Cho at Hanyang University showed (J. Org. Chem. 2012, 77, 11383) that alkenes such as 9 could be trifluoromethylated with iodotrifluoromethane under visible light photoredox catalysis. David A. Nicewicz at the University of North Carolina at Chapel Hill developed (J. Am. Chem. Soc. 2012, 134, 18577) a photoredox procedure for the anti-Markovnikov hydroetherification of alkenols such as 11, using the acridinium salt 12 in the presence of phenylmalononitrile (13). A unique example of “catalysis through temporary intramolecularity” was reported (J. Am. Chem. Soc. 2012, 134, 16571) by André M. Beauchemin at the University of Ottawa with the formaldehyde-catalyzed Cope-type hydroamination of allyl amine 15 to produce the diamine 16. A free radical hydrofluorination of unactivated alkenes, including those bearing complex functionality such as 17, was developed (J. Am. Chem. Soc. 2012, 134, 13588) by Dale L. Boger at Scripps, La Jolla. Jennifer M. Schomaker at the University of Wisconsin at Madison reported (J. Am. Chem. Soc. 2012, 134, 16131) the copper-catalyzed conversion of bromostyrene 19 to 20 in what was termed an activating group recycling strategy. A rhodium complex 23 that incorporates a new chiral cyclopentadienyl ligand was developed (Science 2012, 338, 504) by Nicolai Cramer at the Swiss Federal Institute of Technology in Lausanne and was shown to promote the enantioselective merger of hydroxamic acid derivative 21 and styrene 22 to produce 24.

APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Acridinique"

1

SHAH, DINESH O., and VINCE A. SALBILLA. "AN ALTERNATIVE TO CHEMILUMINESCENT DETECTION: A FLUOROMETRIC METHOD TO QUANTITATE ACRIDINIUM IN ACRIDINIUM LABELED PROTEINS." In Proceedings of the 11th International Symposium. WORLD SCIENTIFIC, 2001. http://dx.doi.org/10.1142/9789812811158_0058.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

ADAMCZYK, MACIEJ, PHILLIP G. MATTINGLY, YON-YIH CHEN, and JAMES R. FINO. "MICROWAVE-ASSISTED SYNTHESIS OF CHEMILUMINESCENT ACRIDINIUM SALTS." In Proceedings of the 11th International Symposium. WORLD SCIENTIFIC, 2001. http://dx.doi.org/10.1142/9789812811158_0051.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

ADAMCZYK, MACIEJ, JONATHAN GROTE, PHILLIP G. MATTINGLY, JEFFREY A. MOORE, and YOU PAN. "CARBONYL-REACTIVE CHEMILUMINESCENT LABELS: ACRIDINIUM HYDROXYLAMINES (AHA)." In Proceedings of the 11th International Symposium. WORLD SCIENTIFIC, 2001. http://dx.doi.org/10.1142/9789812811158_0081.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

ADAMCZYK, MACIEJ, PHILLIP G. MATTINGLY, JEFFREY A. MOORE, and SUSHIL D. REGE. "THIOL-SPECIFIC ACRIDINIUM REAGENTS FOR LABELING PROTEINS AND NUCLEIC ACIDS." In Proceedings of the 11th International Symposium. WORLD SCIENTIFIC, 2001. http://dx.doi.org/10.1142/9789812811158_0082.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

GEBLER, JOHN C., MACIEJ ADAMCZYK, KEVIN SHREDER, and JIANG WU. "QUANTITATION OF FREE CHEMILUMINESCENT ACRIDINIUM-9-CARBOXAMIDE SALTS IN BIOCONJUGATES." In Proceedings of the 11th International Symposium. WORLD SCIENTIFIC, 2001. http://dx.doi.org/10.1142/9789812811158_0083.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

YIN, D. G., Y. F. HE, Y. B. LIU, D. C. SHEN, S. Q. HAN, Z. F. LUO, C. J. XIE, L. ZHANG, B. H. LIU, and M. H. WU. "A NOVEL CHEMILUMINESCENT IMMUNOASSAY OF TOTAL THYROXINE USING THE ACRIDINIUM ESTER 2',6'-DIMETHYL-4'-(N-SUCCINIMIDYLOXYCARBONYL) PHENYL-10-METHYL-ACRIDINIUM-9-CARBOXYLATE METHOSULFATE AS LABEL." In Proceedings of the 15th International Symposium. WORLD SCIENTIFIC, 2008. http://dx.doi.org/10.1142/9789812839589_0063.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Nguyen, T. H., Y. C. Lin, C. T. Chen, F. Surre, T. Venugopalan, T. Sun, and K. T. V. Grattan. "Fibre optic chloride sensor based on fluorescence quenching of an acridinium dye." In 20th International Conference on Optical Fibre Sensors, edited by Julian D. C. Jones. SPIE, 2009. http://dx.doi.org/10.1117/12.835607.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

GEBLER, JOHN C., MACIEJ ADAMCZYK, KEVIN SHREDER, and JIANG WU. "CHARACTERIZATION OF ACRIDINIUM-9-CARBOXAMIDE—MONOCLONAL ANTIBODY BIOCONJUGATES BY ELECTROSPRAY IONIZATION MASS SPECTROMETRY." In Proceedings of the 11th International Symposium. WORLD SCIENTIFIC, 2001. http://dx.doi.org/10.1142/9789812811158_0084.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

ADAMCZYK, MACIEJ, YON-YIH CHEN, JEFFREY R. FISHPAUGH, PHILLIP G. MATTINGLY, JEFFREY A. MOORE, YOU PAN, KEVIN SHREDER, and ZHIGUANG YU. "TOO MUCH OF A GOOD THING? MODULATING THE SIGNAL OF ACRIDINIUM-9-CARBOXAMIDE SALTS." In Proceedings of the 11th International Symposium. WORLD SCIENTIFIC, 2001. http://dx.doi.org/10.1142/9789812811158_0052.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

CHANG, C. D., K. Y. CHANG, L. JIANG, V. A. SABLILLA, and D. O. SHAH. "CONJUGATES OF (ACRIDINIUM)x-BSA ANTI-HCV CORE TO ENHANCE THE DETECTION OF HCV CORE ANTIGEN." In Proceedings of the 15th International Symposium. WORLD SCIENTIFIC, 2008. http://dx.doi.org/10.1142/9789812839589_0040.

Full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!