Pharmacokinetics of B-Ring Unsubstituted Flavones

被引:19
|
作者
Ancuceanu, Robert [1 ]
Dinu, Mihaela [1 ]
Dinu-Pirvu, Cristina [2 ]
Anuta, Valentina [2 ]
Negulescu, Vlad [3 ]
机构
[1] Carol Davila Univ Med & Pharm, Fac Pharm, Dept Pharmaceut Bot & Cell Biol, Bucharest, Romania
[2] Carol Davila Univ Med & Pharm, Fac Pharm, Dept Phys Chem & Colloidal Chem, Bucharest 020956, Romania
[3] Carol Davila Univ Med & Pharm, Fac Med, Dept Toxicol Clin Pharmacol & Psychopharmacol, Bucharest 050474, Romania
关键词
B-ring unsubstituted flavones; chrysin; baicalein; wogonin; oroxylin A; pharmacokinetics; PERFORMANCE LIQUID-CHROMATOGRAPHY; MAJOR BIOACTIVE COMPONENTS; RADIX-SCUTELLARIAE EXTRACT; TANDEM MASS-SPECTROMETRY; NANOSTRUCTURED LIPID CARRIERS; LC-MS/MS METHOD; JIE-DU-TANG; INTESTINAL 1ST-PASS METABOLISM; TRADITIONAL CHINESE MEDICINE; OXYPHYLLAE-FRUCTUS EXTRACT;
D O I
10.3390/pharmaceutics11080370
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
B-ring unsubstituted flavones (of which the most widely known are chrysin, baicalein, wogonin, and oroxylin A) are 2-phenylchromen-4-one molecules of which the B-ring is devoid of any hydroxy, methoxy, or other substituent. They may be found naturally in a number of herbal products used for therapeutic purposes, and several have been designed by researchers and obtained in the laboratory. They have generated interest in the scientific community for their potential use in a variety of pathologies, and understanding their pharmacokinetics is important for a grasp of their optimal use. Based on a comprehensive survey of the relevant literature, this paper examines their absorption (with deglycosylation as a preliminary step) and their fate in the body, from metabolism to excretion. Differences among species (inter-individual) and within the same species (intra-individual) variability have been examined based on the available data, and finally, knowledge gaps and directions of future research are discussed.
引用
收藏
页数:38
相关论文
共 50 条
  • [21] STEROID B-RING LACTONES - REINVESTIGATION
    AHMAD, MS
    MOINUDDIN, G
    KHAN, IA
    JOURNAL OF ORGANIC CHEMISTRY, 1978, 43 (01): : 163 - 165
  • [22] ON THE RADIAL STRUCTURE OF SATURNS B-RING
    SHAN, LH
    GOERTZ, CK
    ASTROPHYSICAL JOURNAL, 1991, 367 (01): : 350 - 360
  • [23] SYNTHESIS OF THE A-RING AND B-RING SYSTEM OF HEMIBREVETOXIN-B
    FENG, F
    MURAI, A
    CHEMISTRY LETTERS, 1995, (01) : 23 - 24
  • [24] SYNTHESIS OF A-RING AND B-RING ANALOG OF COLEON-B
    MATSUMOTO, T
    IYO, K
    MIUCHI, S
    BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1982, 55 (12) : 3831 - 3835
  • [25] Formation of the unexpected 3-alkylated flavonoids in the alkylation of B-ring substituted 5,7-dihydroxy flavones
    Wang, CL
    Zheng, X
    Meng, WD
    Li, HQ
    Qing, FL
    TETRAHEDRON LETTERS, 2005, 46 (32) : 5399 - 5402
  • [26] PREPARATION OF B-RING BROMINATED DERIVATIVES OF ESTRADIOL
    LEON, AA
    METTLER, FA
    HYLARIDES, MD
    STEROIDS, 1986, 48 (5-6) : 395 - 400
  • [27] Recent efforts to construct the B-ring of bryostatins
    Gao, Lu
    Lu, Ji
    Song, Zhenlei
    CHEMICAL COMMUNICATIONS, 2013, 49 (87) : 10211 - 10220
  • [28] DETECTION OF HIDDEN RESONANCES IN SATURNS B-RING
    THIESSENHUSEN, KU
    ESPOSITO, LW
    KURTHS, J
    SPAHN, F
    ICARUS, 1995, 113 (01) : 206 - 212
  • [29] HYDROBORATION OF B-RING UNSATURATED BILE ACIDS
    MATKOVICS, B
    TEGYEY, Z
    GONDOS, G
    STEROIDS, 1965, 5 (01) : 117 - +
  • [30] An effective approach to B-ring aromatization of equilin
    Cao, ZS
    Liehr, JG
    SYNTHETIC COMMUNICATIONS, 1997, 27 (01) : 145 - 155