Benzophenoxazine-based fluorescent dyes for labeling biomolecules

被引:207
作者
Jose, Jiney [1 ]
Burgess, Kevin [1 ]
机构
[1] Texas A&M Univ, Dept Chem, College Stn, TX 77841 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.tet.2006.08.056
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Some desirable attributes of Medola's Blue 1, Nile Red 2, and Nile Blue 3, contained as fluorescent probes, are analyzed. Phenoxazines without strongly electron withdrawing or donating substituents have unexceptional absorbance characteristics. Meloda's Blue has one dimethylamino substituent and the heterocyclic core is oxidized. Nile Red has a neutral oxidized phenoxazine system such as phenoxazinone. The 9-diethylamino substituent is able to donate electron density into the carbonyl group across the ring. The water-solubility of Nile-Red is extremely poor, but in other solvents its fluorescence maxima and intensity are good indicators of the dye's environment-polarity. The first synthesis of Nile red was a condensation reaction of a nitrosophenol. The original consequence of the difference in charges for Nile Red 2 and Blue 3 is that water-solubility of Nile Blue is significantly better.
引用
收藏
页码:11021 / 11037
页数:17
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共 50 条
[1]   Development of a disposable pyruvate biosensor to determine pungency in onions (Allium cepa L.) [J].
Abayomi, LA ;
Terry, LA ;
White, SF ;
Warner, PJ .
BIOSENSORS & BIOELECTRONICS, 2006, 21 (11) :2176-2179
[2]   New biarsenical Ligands and tetracysteine motifs for protein labeling in vitro and in vivo: Synthesis and biological applications [J].
Adams, SR ;
Campbell, RE ;
Gross, LA ;
Martin, BR ;
Walkup, GK ;
Yao, Y ;
Llopis, J ;
Tsien, RY .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (21) :6063-6076
[3]  
AFANASEVA GB, 1971, KHIM GETEROTSIKL, V7, P742
[4]   Design of organic molecules with large two-photon absorption cross sections [J].
Albota, M ;
Beljonne, D ;
Brédas, JL ;
Ehrlich, JE ;
Fu, JY ;
Heikal, AA ;
Hess, SE ;
Kogej, T ;
Levin, MD ;
Marder, SR ;
McCord-Maughon, D ;
Perry, JW ;
Röckel, H ;
Rumi, M ;
Subramaniam, C ;
Webb, WW ;
Wu, XL ;
Xu, C .
SCIENCE, 1998, 281 (5383) :1653-1656
[5]  
ALEKSEEV NN, 1984, Patent No. 1109393
[6]  
ALEKSEEVA VI, 1995, CHEM HETEROCYCL COMP, V31, P112
[7]  
[Anonymous], J CHEM SOC P1
[8]  
[Anonymous], 1997, RUSS J ORG CHEM
[9]   PHENOXAZONES - NEW CLASS OF LASER-DYES [J].
BASTING, D ;
OUW, D ;
SCHAFER, FP .
OPTICS COMMUNICATIONS, 1976, 18 (03) :260-262
[10]   THE PHOTOSENSITIZERS BENZOPHENOXAZINE AND BENZOTHIAZINE - COMPREHENSIVE INVESTIGATION OF PHOTOPHYSICAL AND PHOTOCHEMICAL PROPERTIES [J].
BECKER, RS ;
CHAKRAVORTI, S ;
DAS, S .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1990, 51 (05) :533-538