References
- Andreas, C. and Thomas, H., Structural and sensory characterization of compounds contributing to the bitter off-taste of carrots (Daucus carota L.) and carrot puree. J. Agric. Food Chem., 51, 3865-3873 (2003) https://doi.org/10.1021/jf034085+
- Bernart, W. M., Cardellina, H. J., Balaschak, S. M., Alexander, R. M., Shoemaker, H. R., and Boyd, R. M., Cytotoxic falcarinol oxylipins from Dendropanax arboreus. J. Nat. Prod., 59, 748-753 (1996) https://doi.org/10.1021/np960224o
- Chang, F. R., Yang, P. Y., Lin, J. Y., Lee, K. H., and Wu, Y. C., Bioactive kaurane diterpenoids from Annona glabra. J. Nat. Prod., 61, 437-439 (1998) https://doi.org/10.1021/np970497z
- Emery, P., COX-1, COX-2: So what? Scand. J. Rheumatol., 28, 6-9 (1999) https://doi.org/10.1080/03009749950155715
- Han, B. H., Han, Y. N., Han, L. A., Park, M. H., and Lee, E. O., Studies on the anti-inflammatory activity of Aralia continentalis (I). Arch. Pharm. Res., 6, 17-23 (1983) https://doi.org/10.1007/BF02855697
- Hung, C. Y. and Yen, G. C., Extraction and identification of antioxidative components of Hsian-tsao (Mesona procumbens Hemsl.). Lebensm.-Wiss. u.-Technol., 34, 306-311 (2001) https://doi.org/10.1006/fstl.2001.0775
- Kim, J. S. and Kang, S. S., Saponins from the aerial parts of Aralia continentalis. Natural Products Sciences, 4, 45-50 (1998)
- Kwon, H. C. and Lee, K. R., Phytochemical constituents of Artemisia japonica ssp. littoricola. Arch. Pharm. Res., 24, 194-197 (2001) https://doi.org/10.1007/BF02978255
- Matsuo, A., Uto, S., Nakayama, M., Hayashi, S., Yamasaki, K., Kasai, R., and Tanaka, O., (-)-Thermarol. A new ent-pimaraneclass diterpene diol from Jungermannia thermerum (liverwort). Tetrahedron Letters, 28, 2451-2454 (1976) https://doi.org/10.1016/0040-4039(76)90017-4
- Mihashi, S., Yanagisawa, I., Tanaka, O., and Shibata, S., Further study on the diterpenes of Aralia spp. Tetrahedron Lett., 21, 1683-1686 (1969)
- Okuyama, E., Nishimura, S., and Yamazaki, M., Analgesic principles from Aralia cordata Thunb. Chem. Pharm. Bull., 39, 405-407 (1991) https://doi.org/10.1248/cpb.39.405
- Okuyama, E., Nishimura, S., Ohmori, S., Ozaki, Y., Satake, M., and Yamazaki, M., Analgesic components of Notopterygium incisum Ting. Chem. Pharm. Bull., 41, 926-929 (1993) https://doi.org/10.1248/cpb.41.926
- Park, S. Y. and Kim, J. W., Cytotoxic polyacetylenes from Aralia cordata. Yakhak Hoeji, 39, 681-688 (1995)
-
Rahman, A. and Ahmad, V. Q.,
$^{13}$ C-NMR of natural products. Plenum Press, 2, 258 (1992) - Sang, S. M., Kikuzaki, H., Lapsley, K., Rosen, R. T., Nakatani, N., and Ho, C. T., Sphingolipid and other constituents from almond nuts (Prunus amygdalucs Batsch). J. Agric. Food Chem., 50, 4709-4712 (2002) https://doi.org/10.1021/jf020262f
- Shibata, S., Mihashi, S., and Tanaka, O., The occurrence of (-) pimarane-type diterpene in Aralia cordata Thunb. Tetrahedron Lett., 51, 5241-5243 (1967) https://doi.org/10.1016/S0040-4039(01)89652-0
- Silva, E. A., Takashi, J. A., Boaventura, M. A. D., Oliveira, A. B., The biotransformation of ent-kaur-16-en-19-oic acid by Rhizopus stolonifer. Phytochemistry, 52, 397-400 (1999) https://doi.org/10.1016/S0031-9422(99)00219-8
- Tanaka, O., Mihashi, S., Yanagisawa, I., Niaido, T., and Shibata, S., Diterpenes of Aralia cordata: Oxidative transformation of 4-axial aldehyde of some diterpenes and a note to the naturally occurring 4-hydroxy-18 (or 19) norditerpenes. Tetrahedron, 28, 4523-4537 (1972) https://doi.org/10.1016/0040-4020(72)80034-6
- Yahara, S., Ishida, M., Yamazaki, K., Tanaka, O., and Mihashi, S., Minor diterpenes of Aralia cordata Thunb: 17-hydroxyent- kaur-15-en-19-oic acid and grandifloric acid. Chem. Pharm. Bull., 22, 1629-1631 (1974) https://doi.org/10.1248/cpb.22.1629
- Ylva, N., Therese, R., Premila, P., Helena, D., and Lars, B., Development of a Radiochemical Cyclooxygenase-1 and 2 in vitro assay for identification of natural products as inhibitor of prostaglandin biosynthesis. J. Nat. Prod., 61, 2-7 (1998) https://doi.org/10.1021/np970343j
- Zhang, Y. M., Yang, J. S., and Xu, X. D., A new kaurane derivative from Aralia fargesii. Chinese Chemical Letters, 10, 673-674 (1999)
- Zheng, G., Lu, W., and Cai, J., Stereoselective total synthesis of (3R, 8S)-falcarindiol, a common polyacetylene compound from Umbellifers. J. Nat. Prod., 62, 626-628 (1999) https://doi.org/10.1021/np980418z