Physicochemical and biological properties of luteolin-7-O-β-d- glucoside (cynaroside) isolated from Anthriscus sylvestris (L.) Hoffm.

Monatshefte fur Chemie

Volumn 145, Issue 8, 2014, Pages 1307-1318

  Žemlička, Lukáš ^a   Fodran, Peter ^b   Lukeš, Vladimír ^a   Vagánek, Adam ^a   Slováková, Mariana ^a   Staško, Andrej ^a   Dubaj, Tibor ^a   Liptaj, Tibor ^a   Karabín, Michal ^a   Birošová, Lucia ^a   Rapta, Peter ^a  

^a SLOVAK UNIVERSITY OF TECHNOLOGY   (Slovakia)

^b FLOP Inc   (Slovakia)

Author keywords

Biological activity; Cynaroside; DFT calculations; NMR and EPR spectroscopy; Spectroelectrochemistry

Indexed keywords

EID: 84904254273     PISSN: 00269247     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00706-014-1228-3     Document Type: Article

References (47)

1. Lopez-Lazaro M (2009) Mini Rev Med Chem 9:31
2. Brown JE, Rice-Evans CA (1998) Free Radic Res 29:247
3. Bouaziz M, Sayadi S (2005) Eur J Lip Sci Technol 107:497
4. Chiruvella KK, Mohammed A, Dampuri G, Ghanta RG, Raghavan SC (2007) Int J Biomed Sci 3:269
5. Odontuya G, Hoult JRS, Houghton PJ (2005) Phytother Res 19:782
6. Baskar AA, Ignacimuthu S, Michael GP, Al Numair KS (2011) Nutr Cancer 63:130
7. Gnanamanichan SS, Mansfield JW (1981) Phytochemistry 20:997
8. Miski M, Ulubelen O, Jobanson C, Mabry TJ (1983) J Nat Prod 46:874
9. Schinor EC, Salvador MJ, Ito IY, Dias DA (2007) Braz J Microbiol 38:145
10. Bírošová L, Mikulášová M, Vaverková Š (2007) J Agric Food Chem 55:10183
11. Raveendran R, Wattal C, Sharma A, Oberoi JK, Prasad KJ, Datta S (2008) Indian J Med Microbiol 26:50
12. Sandasi M, Leonard CM, Viljoen AM (2010) Lett Appl Microbiol 50:30
13. Bavington C, Page C (2005) Respiration 72:335
14. Lemanska K, Szymusiak H, Tyrakowska B, Zielinski R, Soffers EMF, Rietjens IMCM (2001) Free Radic Biol Med 31:869
15. Brett AMO, Ghica M-E (2003) Electroanalysis 15:1745
16. Marković Z, Milenković D, Orović J, Marković JMD, Stepanić V, Lučić B, Amić D (2012) Food Chem 134:1754
17. Amić A, Marković Z, Marković JMD, Stepanić V, Lučić B, Amić D (2014) Food Chem 152:578
18. Sauerwald N, Schwenk M, Polster J, Bengsch E (1998) Z Naturforsch B Chem 53:315
19. Dangles O, Saito N, Brouillard R (1993) J Am Chem Soc 115:3125
20. Tungjai M, Poompimon W, Loetchutinat C, Kothan S, Dechsupa N, Mankhetkorn S (2008) Open Drug Deliv J 2:10
21. Tosun F, Akyüz Kizilay Ç (2003) J Fac Pharm Ankara Univ 32:121
22. Yadava RN, Raj M (2012) Indian J Chem B 51:635
23. Harborne JB (1994) The flavonoids: advances in research since 1986. Chapman and Hall, London
24. Mulkens A, Kapetanidis I (1987) Pharm Acta Helv 62:19
25. Kuruüzüm-Uz A, Güvenali Z, Ströch K, Demirezer LÖ, Zeeck A (2008) J Pharm Sci 33:11
26. Taj S, Nagarajan B (1996) Mutat Res 369:97
27. Samejima K, Kanazawa K, Ashida H, Danno G (1995) J Agric Food Chem 43:410
28. Kumar CG, Anand SK (1998) Int J Food Microbiol 42:9
29. Cerca N, Martins S, Pier GB, Oliveira R, Azeredo J (2005) Res Microbiol 156:650
30. Hrabárová E, Valachová K, Rapta P, Šoltés L (2010) Chem Biodivers 7:2191
31. Brezová V, Šlebodová A, Staško A (2009) Food Chem 114:859
32. Gerson F, Huber W (2003) Electron spin resonance spectroscopy of organic radicals. Wiley-VCH, Weinheim
33. Rapta P, Mišík V, Staško A, Vrábel I (1995) Free Radic Biol Med 18:901
34. Bosma WB, Schnupf U, Willett JL, Momany FA (2009) J Mol Struct THEOCHEM 905:56
35. Namazian M, Kalantary-Fotooh F, Noorbala MR, Searles DJ, Coote ML (2006) J Mol Struct THEOCHEM 758:275
36. Kocevar N, Glavac I, Injac R, Kreft S (2008) J Pharm Biomed Anal 46:609
37. Parekh J, Nair R, Chanda S (2005) Indian J Pharmacol 37:408
38. Maron D, Ames B (1983) Mutat Res 113:173
39. Beenken KE, Blevins JS, Smeltzer MS (2003) Infect Immun 71:4206
40. Re R, Pellegrini N, Proteggente A, Pannala A, Rice-Evans C (1999) Free Radic Biol Med 26:1231
41. Frisch MJ, Trucks GW, Schlegel HB, Scuseria GE, Robb MA, Cheeseman JR, Montgomery JA Jr., Vreven T, Kudin KN, Burant JC, Millam JM, Iyengar SS, Tomasi J, Barone V, Mennucci B, Cossi M, Scalmani G, Rega N, Petersson GA, Nakatsuji H, Hada M, Ehara M, Toyota K, Fukuda R, Hasegava J, Ishida M, Nakajima T, Honda Y, Kitao O, Nakai H, Klene M, Li X, Knox JE, Hratchian HP, Cross JB, Adamo C, Jaramillo J, Gomperts R, Stratmann RE, Yazyev O, Austin AJ, Cammi R, Pomelli C, Ochterski JW, Ayala PY, Morokuma K, Voth GA, Salvador P, Dannenberg JJ, Zakrzewski VG, Dapprich S, Daniels AD, Strain M-C, Farkas O, Malick DK, Rabuck AD, Raghavachari K, Foresman JB, Ortiz JV, Cui Q, Baboul AG, Clifford S, Cioslowski J, Stefanov BB, Liu G, Liashenko A, Piskorz P, Komaromi I, Martin RL, Fox DJ, Keith T, Al-Laham MA, Peng CY, Nakaryakkara A, Chalacombe M, Gill PMW, Johnson B, Chen W, Wong MW, Gonzales C, Pople JA (2003) GAUSSIAN 03, Revision A.1. Gaussian Inc., Pittsburgh
42. Becke AD (1993) J Chem Phys 98:5648
43. Furche F, Ahlrichs R (2002) J Chem Phys 117:7433
44. Ditchfield R (1974) Mol Phys 27:789
45. Cancès E, Mennucci B (1998) J Math Chem 23:309
46. Binkley JS, Pople JA, Hehre WJ (1980) J Am Chem Soc 102:939
47. Kutzelnigg W, Fleischer U, Schindler M (1990) The IGLO-method: ab-initio calculation and interpretation of NMR chemical shifts and magnetic susceptibilities. In: Seelig J (ed) NMR basic principles and progress, vol 23. Springer, Berlin, p 165