참고문헌
- Kim, J. S., Yean, M. H., Lee, J.-H., and Kang, S. S. (2009) Phytochemical Studies on Lonicera Caulis (1) - Sterols and Triterpenoids. Kor. J. Pharmacogn. 40, 319-325
- Wang, Z. and Clifford, M. N. (2008) Comparison of the profiles of chlorogenic acids and their derivatives from three Chinese traditional herbs by LC-MS. Acta Pharm. Sin. 43, 185-190
- Son, K. H., Park, J. O., Chung, K. C., Chang, H. W., Kim, H. P., Kim, J. S., and Kang, S. S. (1992) Flavonoids from the aerial parts of Lonicera japonica. Arch. Pharm. Res. 15, 365-370 https://doi.org/10.1007/BF02974114
- Son, K. H., Kim, J. S., Kang, S. S., Kim, H. P., and Chang, H. W. (1994) Isolation of flavonoids from Lonicera japonica. Kor. J. Pharmacogn. 25, 24-27
- Kumar, N., Singh, B., Bhandari, P., Gupta, A. P., Uniyal, S. K., and Kaul, V. K. (2005) Biflavonoids from Lonicera japonica. Phytochemistry 66, 2740-2744 https://doi.org/10.1016/j.phytochem.2005.10.002
- Qian, Z.-M., Li, H.-J., Li, P., Chen, J., and Tang, D. (2007) Simultaneous quantification of seven bioactive components in Caulis Lonicerae Japonicae by high performance liquid chromatography. Biomed. Chromatogr. 21, 649-654 https://doi.org/10.1002/bmc.803
- Kim, J. S., Kang, S. S., Son, K. H., Chang, H. W., Kim, H. P., and Bae, K.-H. (2002) Constituents from the roots of Hemerocallis fulva. Kor. J. Pharmacogn. 33, 105-109
- Kim, J. S., Kim, Y. J., Lee, J. Y., and Kang, S. S. (2008) Phytochemical studies on Paeoniae Radix (2) - Phenolic and related compounds. Kor. J. Pharmacogn. 39, 28-36
- Falsone, G., Cateni, F., Vrech, E., Birkofer, L., Lucchini, V., Wagner, H., Seligmann, O., and Lokar, L. C. (1994) Triacylglycerols, fucosterol, diacylglyceroglycolipids and fucoxanthin from Fucus virsoides J. AG. Z. Naturforsch. 49B, 1297-1304
- Sy, L.-K. and Brown, G. D. (1999) Coniferaldehyde derivatives from tissue culture of Artemisia annua and Tanacetum parthenium. Phytochemistry 50, 781-785 https://doi.org/10.1016/S0031-9422(98)00607-4
- Herath, H. M. T. B., Dassanayake, R. S., Priyadarshani, A. M. A., Susila De Silva, Wannigama, G. P., and Joanne Jamie (1998) Isoflavonoids and a pterocarpan from Gliricidia sepium. Phytochemistry 47, 117-119 https://doi.org/10.1016/S0031-9422(97)00517-7
- Kang, S. S. and Kim, C. M. (1987) Studies on the Korean indigenous plants. Isolation of 1-eicosanoyl cafferate from Echinosophora koreensis. Arch. Pharm. Res. 10, 67-68 https://doi.org/10.1007/BF02855623
- Gibbonsa, S., Mathewb, K. T., and Gray, A. I. (1999) A caffeic acid ester from Halocnemum strobilaceum. Phytochemistry 51, 465-467 https://doi.org/10.1016/S0031-9422(99)00007-2
- Eglinton, G., Hunneman, D. H., and McCormick, A. (1968) Gas chromatographic-mass spectrometric studies of long chain hydroxy acids.-III. The mass spectra of the methyl esters trimethylsilyl ethers of aliphatic hydroxy acids. A facile method of double bond location. Org. Mass Spectrom. 1, 593-611 https://doi.org/10.1002/oms.1210010413
- Oueslati, M. H., Ben Jannet, H., Mighri, Z., Chriaa, J., and Abreu, P. M. (2006) Phytochemical constituents from Salsola tetrandra. J. Nat. Prod. 69, 1366-1369 https://doi.org/10.1021/np060222w
- Takasugi, M., Anetai, M., and Masamune, T. (1974) 9,10,13-Trihydroxy-11,15-octadecadienoic acid and related fatty acids in the roots of kidney bean (Phaseolus vulgaris L., 'Beni-Kintoki'). Chem. Lett. 3, 947-950
-
Rossi, R., Caprita, A., Quirici, M. G., and Alberto Veracini, C. (1982) Insect pheromone components. Use of
$^{13}C$ NMR spectroscopy for assigning the configuration of C=C double bonds of monoenic or dienic pheromone components and for quantitative determination of Z/E mixtures. Tetrahedron 38, 639-644 https://doi.org/10.1016/0040-4020(82)80205-6 -
Herz, W. and Kulanthaivel, P. (1985) Trihydroxy-
$C_{18}$ -acids and a labdane from Rudbeckia fulgida. Phytochemistry 24, 89-91 https://doi.org/10.1016/S0031-9422(00)80813-4 - Cardellina, II, J. H. and Moore, R. E. (1980) Malyngic acid, a new fatty acid from Lyngbya majuscula. Tetrahedron 36, 993-996 https://doi.org/10.1016/0040-4020(80)80051-2
- Nagai, T., Kiyohara, H., Munakata, K., Shirahata, T., Sunazuka, T., Harigaya, Y., and Yamada, H. (2002) Pinellic acid from the tuber of Pinellia ternata Breitenbach as an effective oral adjuvant for nasal influenza vaccine. Int. Immunopharmacol. 2, 1183-1193 https://doi.org/10.1016/S1567-5769(02)00086-3
-
Kobayashi, M., Tawara, T., Tsuchida, T., and Mitsuhashi, H. (1990) Studies on the constituents of Umbelliferae plants. XVIII. Minor constituents of Bupleuri Radix: Occurrence of saikogenins, polyhydroxysterols, a trihydroxy
$C_{18}$ fatty acid, a lignan and a new chromone. Chem. Pharm. Bull. 38, 3169-3171 https://doi.org/10.1248/cpb.38.3169 -
Shirahata, T., Sunazuka, T., Yoshita, K., Yamamoto, D., Harigaya, Y., Nagai, T., Kiyohara, H., Yamada, H., Kuwajima, I., and
$\tilde{o}$ mura, S. (2003) Total synthesis and adjuvant activity of all stereoisomers of pinellic acid. Bioorg. Med. Chem. Lett. 13, 937-941 https://doi.org/10.1016/S0960-894X(02)01069-7 -
Sunazuka, T., Shirahata, T., Yoshita, K., Yamamoto, D., Harigaya, Y., Nagai, T., Kiyohara, H., Yamada, H., Kuwajima, I., and
$\tilde{o}$ mura, S. (2002) Total synthesis of pinellic acid, a potent oral adjuvant for nasal influenza vaccine. Determination of the relative and absolute configuration. Tetrahedron Lett. 43, 1265-1268 https://doi.org/10.1016/S0040-4039(01)02348-6 - Sabitha, G., Bhikshapathi, M., Reddy, E. V., and Yadav, J. (2009) Synthesis of (−)−pinellic acid and its (9R,12S,13S)-diastereoisomer. Helv. Chim. Acta 92, 2052-2057 https://doi.org/10.1002/hlca.200900095
- Steeves, V., Forster, H., Pommer, U., and Savidge, R. (2001) Coniferyl alcohol metabolism in conifers- I. Glucosidic turnover of cinnamyl aldehydes by UDPG: coniferyl alcohol glucosyltransferase from pine cambium. Phytochemistry 57, 1085-1093 https://doi.org/10.1016/S0031-9422(01)00107-8
- Sugiyama, M., Nagayama, E., and Kikuchi., M. (1993) Lignan and phenylpropanoid glycosides from Osmanthus asiaticus. Phytochemistry 33, 1215-1219 https://doi.org/10.1016/0031-9422(93)85052-S
- Della Greca, M., Ferara, M., Fiorentino, A., Monaco, P., and Previtera, L. (1998) Antialgal compounds from Zantedeschia aethiopica. Phytochemistry 49, 1299-1304 https://doi.org/10.1016/S0031-9422(98)00092-2
- Quintin, J. and Lewin, G. (2004) Semisynthesis of linarin, acacetin, and 6-iodoapigenin derivatives from diosmin. J. Nat. Prod. 67, 1624-1627 https://doi.org/10.1021/np040079b