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1 Ergebnisse
1
Manipulating Diastereomeric Bicyclononynes to Sensitively D..:
Chien-Hui Huang
;
Sin-Yu Hou
;
Scott Severance
...
doi:10.1021/acsomega.3c07083.s001. , 2023
Link:
https://doi.org/10.1021/acsomega.3c07083.s001
RT Journal T1
Manipulating Diastereomeric Bicyclononynes to Sensitively Determine Enzyme Activity and Facilitate Macromolecule Conjugations
UL https://suche.suub.uni-bremen.de/peid=base-ftdeakinunifig:oai:figshare.com:article_24590483&Exemplar=1&LAN=DE A1 Chien-Hui Huang A1 Sin-Yu Hou A1 Scott Severance A1 Chi-Ching Hwang A1 Bo-Kai Fang A1 Ming-Mao Gong A1 Siao-Lei Yu A1 Yung-Chieh Weng A1 Li-Fang Wang A1 Chia-Yen Dai A1 Su-Hung Wang A1 Hsing-Tao Kuo A1 Jeh-Jeng Wang A1 Tzu-Pin Wang YR 2023 K1 Biophysics K1 Biochemistry K1 Microbiology K1 Neuroscience K1 Pharmacology K1 Biotechnology K1 Infectious Diseases K1 Plant Biology K1 Virology K1 Chemical Sciences not elsewhere classified K1 two serum biomarkers K1 tricyclic fused rings K1 successfully conjugate bsa K1 steric structural differences K1 manipulating diastereomeric bicyclononynes K1 fam derivative compound K1 different steric structures K1 commonly used cycloalkynes K1 6 )- fam K1 6 )- carboxyfluorescein K1 0 ] nonyne K1 spaac reaction products K1 corresponding spaac products K1 new fluorescence turn K1 spaac products synthesized K1 >- bcn derivatives K1 >- bcn compounds K1 >- bcn K1 spaac ) K1 also synthesized K1 fluorescence quenching K1 fluorescence always K1 bcn diastereomers K1 previously studied K1 potential significance K1 likely due K1 first demonstrated K1 exo </ K1 endo </ K1 constitutional isomer K1 chemical probe K1 bis </ K1 based product JF doi:10.1021/acsomega.3c07083.s001 LK http://dx.doi.org/https://doi.org/10.1021/acsomega.3c07083.s001 DO https://doi.org/10.1021/acsomega.3c07083.s001 SF ELIB - SuUB Bremen
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