Lignans: Chemical, Biological and Clinical PropertiesLignans are widely occurring plant compounds and are closely related to lignin, which forms the woody component of trees and other plants. The lignans are characterized by their dimeric composition from cinnamic acids, and they are attracting increasing attention as a result of their pharmacological properties. The volume surveys the chemical, biological and clinical properties of lignans as well as providing information on their isolation, purification, identification and chemical synthesis. |
Contents
III | 1 |
IV | 4 |
V | 8 |
VI | 9 |
VII | 10 |
VIII | 12 |
X | 14 |
XI | 15 |
XC | 199 |
XCI | 202 |
XCII | 203 |
XCIII | 206 |
XCIV | 208 |
XCV | 213 |
XCVI | 216 |
XCVII | 219 |
XIII | 16 |
XV | 17 |
XVI | 85 |
XVII | 87 |
XVIII | 90 |
XX | 93 |
XXI | 94 |
XXII | 95 |
XXIV | 97 |
XXV | 98 |
XXVII | 99 |
XXVIII | 100 |
XXIX | 102 |
XXX | 103 |
XXXI | 105 |
XXXII | 106 |
XXXIII | 113 |
XXXIV | 114 |
XXXV | 116 |
XXXVI | 117 |
XXXVII | 118 |
XXXIX | 122 |
XLI | 125 |
XLII | 127 |
XLIII | 128 |
XLIV | 129 |
XLV | 130 |
XLVII | 132 |
XLVIII | 138 |
L | 140 |
LII | 141 |
LIII | 142 |
LIV | 144 |
LV | 145 |
LVII | 146 |
LVIII | 148 |
LX | 149 |
LXII | 151 |
LXIII | 153 |
LXIV | 155 |
LXV | 156 |
LXVII | 157 |
LXVIII | 159 |
LXIX | 166 |
LXXI | 170 |
LXXIV | 171 |
LXXVII | 175 |
LXXVIII | 177 |
LXXIX | 180 |
LXXX | 183 |
LXXXI | 185 |
LXXXII | 186 |
LXXXIII | 190 |
LXXXIV | 191 |
LXXXV | 192 |
LXXXVI | 195 |
LXXXIX | 197 |
XCVIII | 220 |
XCIX | 221 |
C | 228 |
CI | 230 |
CII | 235 |
CIII | 237 |
CIV | 242 |
CV | 246 |
CVI | 247 |
CVIII | 249 |
CXI | 253 |
CXII | 256 |
| 257 | |
CXIV | 269 |
CXVI | 273 |
CXVII | 274 |
CXVIII | 275 |
CXX | 278 |
CXXI | 279 |
CXXII | 280 |
CXXIII | 287 |
CXXVI | 291 |
CXXVII | 295 |
CXXVIII | 296 |
CXXIX | 298 |
CXXX | 303 |
CXXXII | 306 |
CXXXIII | 310 |
CXXXIV | 313 |
CXXXV | 315 |
CXXXVI | 318 |
CXXXVII | 322 |
CXXXVIII | 325 |
CXXXIX | 330 |
CXLI | 333 |
CXLII | 334 |
CXLIII | 337 |
CXLIV | 338 |
CXLV | 339 |
CXLVI | 340 |
CXLVII | 341 |
CXLVIII | 342 |
CXLIX | 344 |
CL | 345 |
CLI | 346 |
CLII | 350 |
CLIII | 354 |
CLVI | 355 |
CLVIII | 356 |
CLIX | 357 |
CLX | 362 |
CLXI | 368 |
CLXII | 370 |
| 373 | |
| 385 | |
| 388 | |
Other editions - View all
Lignans: Chemical, Biological and Clinical Properties David C. Ayres,John D. Loike No preview available - 2008 |
Lignans: Chemical, Biological and Clinical Properties David C.. Ayres,David C. Ayres,John D. Loike No preview available - 1990 |
Lignans: Chemical, Biological and Clinical Properties David C. Ayres,John D. Loike No preview available - 1990 |
Common terms and phrases
absolute configuration acetate acid activity alcohol Ar₁ arctigenin aromatic aryl aryltetralin Ayres benzyl Bull cells CH2OH characterised Chem chemical shifts chromatography cleavage CO₂H CO₂Me compounds conjugated coupling cyclisation cytotoxic derivatives Dewick diphyllin drug ester ether Etoposide Etoposide and Teniposide furan furofurans glucoside gmelinol gomisin H H H H MeO H OH hydrogen hydroxyl hydroxyl group Ikeya inhibition isol isomers J.Chem justicidin lactone lignans matairesinol MeO MeO MeO MeO MeO OMe MeO OMe MeO MeO OMe OMe methyl methylenedioxy microtubule molecules neolignans Nishibe obtained OH H OH OH OH OMe OMe H OMe MeO OMe OMe OH oxidation peak Pelter Pharm phenolic Phytochem Phytochemistry pinoresinol plant podophyllotoxin Podophyllum precursor protons R₁ reaction ring Scheme Schizandra Schizandra chinensis secoisolariciresinol sesamin shown spectrum steganacin steganone structure studies substituents synth synthesis Teniposide Tetrahedron Lett tetralin tion topoisomerase topoisomerase II tubulin Virola Virola sebifera vitro yield