Molecular recognition of deoxycholic acids by pyrene-appended γ- cyclodextrin connected with a rigid azacrown spacer

Chemical and Pharmaceutical Bulletin

Volumn 47, Issue 2, 1999, Pages 151-155

  Suzuki, Iwao ^a   Ito, Maki ^a   Osa, Tetsuo ^a   Anzai, Jun ichi ^a  

^a TOHOKU UNIVERSITY   (Japan)

Author keywords

Azacrown ether; Fluorescent chemosensor; Photo induced electron transfer; Pyrene; 7 cyclodextrin

Indexed keywords

CHENODEOXYCHOLIC ACID; DEOXYCHOLIC ACID DERIVATIVE; DIMER; GAMMA CYCLODEXTRIN DERIVATIVE; HYDROXYL GROUP; HYODEOXYCHOLIC ACID; MONOMER; N (1 PYRENECARBONYL) N' [(6 DEOXY GAMMA CYCLODEXTRON) 6 YL] 4,13 DIAZA 18 CROWN 6 ETHER; PYRENE; UNCLASSIFIED DRUG; URSODEOXYCHOLIC ACID;

ARTICLE; DRUG STRUCTURE; ELECTRON TRANSPORT; FLUORESCENCE; MOLECULAR RECOGNITION; SYNTHESIS;

EID: 0032956237     PISSN: 00092363     EISSN: None     Source Type: Journal    
DOI: 10.1248/cpb.47.151     Document Type: Article

References (23)

1. Bender M. L., Komiyama M., "Cyclodextrin Chemistry," Springer-Verlag, New York, 1978.
2. Szejtli J., "Cyclodextrin Technology," Kluwar Academic Publishers, Dordrecht, 1988.
3. Saenger W., Angew. Chem., Int. Ed. Engl., 19, 344-362 (1980).
4. Osa T., Suzuki I., "Comprehensive Supramolecular Chemistry, Vol. 3, Cyclodextrins," ed. by Szejtli J., Osa T., Pergamon, Oxford, 1996, pp. 367-400.
5. Uekama K., Irie T., "Comprehensive Supramolecular Chemistry, Vol. 3, Cyclodextrins," ed. by Szejtli J., Osa T., Pergamon, Oxford, 1996, pp. 451-482.
6. Ueno A., Supramol. Sci., 3, 31 (1996).
7. Osa T., Suzuki I., Yukagaku (J. Jpn. Oil. Chem. Soc.), 43, 857-867 (1994).
8. Bissell R. A., de Silva A. P., Gunaratne H. Q. N., Lynch P. L. M., Maguire G. E. M., Sandanayake K. R. A. S., Chem. Soc. Rev., 1992, 187-195.
9. Fabbrizzi L., Poggi A., Chem. Soc. Rev., 1995, 197-202.
10. de Silva A. P., Gunaratne H. Q. N., McCoy C. P., Nature (London), 364, 42-44 (1993).
11. Turro N. J., "Modern Molecular Photochemistry," Chapter 10, Benjamin/Cummings, Menlo Park, 1978.
12. Ueno A., Suzuki I., and Osa T., Anal. Chem., 62, 2461-2466 (1990).
13. Suzuki I., Ueno A., Osa T., Chem. Lett., 1989, 2013-2016.
14. Gatto V. J., Arnold K. A., Viscariello A. M., Miller S. R., Morgan C. R., Gokel G. W., J. Org. Chem., 51, 5373-5384 (1986).
15. Escabi-Perez J. R., Fendler J. H., J. Am. Chem. Soc., 100, 2234-2236 (1978).
16. Ueno A., Suzuki I., Osa T., J Am. Chem. Soc., 111, 6391-6397 (1989).
17. Suzuki I., Chen Q., Ueno A., Osa T., Bull. Chem. Soc. Jpn., 66, 1472-1481 (1993).
18. Hamasaki K., Ueno A., Toda F., Suzuki I., Osa T., Bull. Chem. Soc. Jpn., 67, 516-523 (1994).
19. Suzuki I., Kato Y., Osa T., J. Chem. Soc., Perkin Trans. 2, 1997, 1061-1063.
20. Izatt R. M., Terry R. E., Nelson D. P., Chan Y., Eatough D. J., Bradshaw J. S., Hansen L. D., Christensen J. J., J. Am. Chem. Soc., 98, 7626-7630 (1976).
21. Cox G. S., Turro N. J., Yang N. C., Chen M., J. Am. Chem. Soc., 106, 422-424 (1984).
22. For example; Cromwell W. C., Byström K., Eftink M. R., J. Phys. Chem., 89, 326-332 (1985)
23. Mucci A., Schenetti, L., Vandelli M. A., Forni F., Ventura P., Salvioli G., J. Chem. Soc., Perkin Trans. 2, 1996, 2347-2349.