메뉴 건너뛰기




Volumn 71, Issue 11, 2007, Pages 2751-2758

Parvitexins A-E, clerodane-type diterpenes isolated from the in Vitro-cultured liverwort, Scapania parvitexta

Author keywords

Clerodane type; Diterpene; Hepaticae; Parvitexin

Indexed keywords

CELL GROWTH; HYDROCARBONS; ISOMERS; PLANT CELL CULTURE;

EID: 36448990838     PISSN: 09168451     EISSN: 13476947     Source Type: Journal    
DOI: 10.1271/bbb.70360     Document Type: Article
Times cited : (10)

References (19)
  • 1
    • 0012012184 scopus 로고
    • Gymnocolin, A new cis-clerodane diterpenoid from the liverwort Gymnocolea inflata. Crystal structure analysis
    • Huneck, S., Asakawa, Y., Taira, Z., Cameron, A. F., Connolly, J. D., and Rycroft, D. S., Gymnocolin, A new cis-clerodane diterpenoid from the liverwort Gymnocolea inflata. Crystal structure analysis. Tetrahedron Lett., 24, 115-116 (1983).
    • (1983) Tetrahedron Lett , vol.24 , pp. 115-116
    • Huneck, S.1    Asakawa, Y.2    Taira, Z.3    Cameron, A.F.4    Connolly, J.D.5    Rycroft, D.S.6
  • 2
    • 0343229010 scopus 로고
    • Rearranged cuparane-type sesqui- and Clerodane-type diterpenoids from the liverwort Demotarisia linguifolia
    • Nagashima, F., and Asakawa, Y., Rearranged cuparane-type sesqui- and Clerodane-type diterpenoids from the liverwort Demotarisia linguifolia. Phytochemistry, 29, 3229-3231 (1990).
    • (1990) Phytochemistry , vol.29 , pp. 3229-3231
    • Nagashima, F.1    Asakawa, Y.2
  • 3
    • 36448986980 scopus 로고    scopus 로고
    • Rycroft, D. S., Some recent NMR studies of diterpenoids from Hepaticae. In Bryophytes: Their Chemistry and Chemical Taxonomy, eds. Zinsmeister, H. D., and Mues, R., Oxford University Press, Oxford, pp. 109-120 (1990).
    • Rycroft, D. S., Some recent NMR studies of diterpenoids from Hepaticae. In "Bryophytes: Their Chemistry and Chemical Taxonomy," eds. Zinsmeister, H. D., and Mues, R., Oxford University Press, Oxford, pp. 109-120 (1990).
  • 4
    • 0028112310 scopus 로고
    • A furanoditerpenoid from the liverwort Jamesoniella autumnalis
    • Tazaki, H., Blechschmidt, M., Huch, V., Veith, M., and Becker, H., A furanoditerpenoid from the liverwort Jamesoniella autumnalis. Phytochemistry, 37, 491-494 (1994).
    • (1994) Phytochemistry , vol.37 , pp. 491-494
    • Tazaki, H.1    Blechschmidt, M.2    Huch, V.3    Veith, M.4    Becker, H.5
  • 5
    • 0028813445 scopus 로고
    • Diterpenes from in vitro cultures of the liverwort Jamesoniella autumnalis
    • Tazaki, H., Zapp, J., and Becker, H., Diterpenes from in vitro cultures of the liverwort Jamesoniella autumnalis. Phytochemistry, 39, 859-868 (1995).
    • (1995) Phytochemistry , vol.39 , pp. 859-868
    • Tazaki, H.1    Zapp, J.2    Becker, H.3
  • 6
    • 0032103042 scopus 로고    scopus 로고
    • Clerodane-type diterpenoids from axenic cultures of the liverwort Jamesoniella autumnalis
    • Tazaki, H., Nabeta, K., and Becker, H., Clerodane-type diterpenoids from axenic cultures of the liverwort Jamesoniella autumnalis. Phytochemistry, 48, 681-685 (1998).
    • (1998) Phytochemistry , vol.48 , pp. 681-685
    • Tazaki, H.1    Nabeta, K.2    Becker, H.3
  • 7
    • 0033067470 scopus 로고    scopus 로고
    • Tazaki, H., Becker, H., and Nabeta, K., Seco-clerodane diterpenoids jamesoniellides H, I and J in axenic cultures of the liverwort Jamesoniella autumnalis. Phytochemistry, 51, 743-750 (1999).
    • Tazaki, H., Becker, H., and Nabeta, K., Seco-clerodane diterpenoids jamesoniellides H, I and J in axenic cultures of the liverwort Jamesoniella autumnalis. Phytochemistry, 51, 743-750 (1999).
  • 9
    • 36448979420 scopus 로고
    • Isolation of five sterols from the liverwort, Scapania parvitexta Steph
    • Matsuo, A., Nakayama, M., Hayashi, S., and Yasuda, S., Isolation of five sterols from the liverwort, Scapania parvitexta Steph. Biosci. Biotechnol. Biochem., 36, 2241-2242 (1972).
    • (1972) Biosci. Biotechnol. Biochem , vol.36 , pp. 2241-2242
    • Matsuo, A.1    Nakayama, M.2    Hayashi, S.3    Yasuda, S.4
  • 11
    • 0036483544 scopus 로고    scopus 로고
    • Subulatin, an antioxidic caffeic acid derivative isolated from the in vitro cultured liverwort, Jungermannia subulata, Lophocolea heterophylla, and Scapania parvitexta
    • Tazaki, H., Ito, M., Miyoshi, M., Kawabata, J., Fukushi, E., Fujita, T., Motouri, M., Furuki, T., and Nabeta, K., Subulatin, an antioxidic caffeic acid derivative isolated from the in vitro cultured liverwort, Jungermannia subulata, Lophocolea heterophylla, and Scapania parvitexta. Biosci. Biotechnol. Biochem., 66, 255-261 (2002).
    • (2002) Biosci. Biotechnol. Biochem , vol.66 , pp. 255-261
    • Tazaki, H.1    Ito, M.2    Miyoshi, M.3    Kawabata, J.4    Fukushi, E.5    Fujita, T.6    Motouri, M.7    Furuki, T.8    Nabeta, K.9
  • 12
    • 0001432137 scopus 로고
    • Growth and sesquiterpenoid production by Calypogeia granulata Inoue cells in suspension culture
    • Takeda, R., and Katoh, K., Growth and sesquiterpenoid production by Calypogeia granulata Inoue cells in suspension culture. Planta, 151, 525-530 (1981).
    • (1981) Planta , vol.151 , pp. 525-530
    • Takeda, R.1    Katoh, K.2
  • 13
    • 37049067806 scopus 로고
    • An efficient algorithm for searching low-energy conformers of cyclic and acyclic molecules
    • Goto, H., and Osawa, E., An efficient algorithm for searching low-energy conformers of cyclic and acyclic molecules. J. Chem. Soc., Perkin Trans. 2, 187-198 (1993).
    • (1993) J. Chem. Soc., Perkin Trans , vol.2 , pp. 187-198
    • Goto, H.1    Osawa, E.2
  • 14
    • 0024821263 scopus 로고
    • Molecular mechanics. The MM3 force field for hydrocarbons. 1
    • Allinger, N. L., Yuh, Y. H., and Lii, J. H., Molecular mechanics. The MM3 force field for hydrocarbons. 1. J. Am. Chem. Soc., 111, 8551-8566 (1989).
    • (1989) J. Am. Chem. Soc , vol.111 , pp. 8551-8566
    • Allinger, N.L.1    Yuh, Y.H.2    Lii, J.H.3
  • 15
    • 0024843595 scopus 로고
    • Molecular mechanics. The MM3 force field for hydrocarbons. 2. Vibrational frequencies and thermodynamics
    • Lii, J. H., and Allinger, N. L., Molecular mechanics. The MM3 force field for hydrocarbons. 2. Vibrational frequencies and thermodynamics. J. Am. Chem. Soc., 111, 8566-8575 (1989).
    • (1989) J. Am. Chem. Soc , vol.111 , pp. 8566-8575
    • Lii, J.H.1    Allinger, N.L.2
  • 16
    • 0024804228 scopus 로고
    • Molecular mechanics. The MM3 force field for hydrocarbons. 3. The van der Waals' potentials and crystal data for aliphatic and aromatic hydrocarbons
    • Lii, J. H., and Allinger, N. L., Molecular mechanics. The MM3 force field for hydrocarbons. 3. The van der Waals' potentials and crystal data for aliphatic and aromatic hydrocarbons. J. Am. Chem. Soc., 111, 8576-8582 (1989).
    • (1989) J. Am. Chem. Soc , vol.111 , pp. 8576-8582
    • Lii, J.H.1    Allinger, N.L.2
  • 17
    • 2142858450 scopus 로고
    • High-field FT NMR application of Mosher's method. The absolute configuration of marine terpenoids
    • Ohtani, I., Kusumi, T., Kashman, Y., and Kakisawa, H., High-field FT NMR application of Mosher's method. The absolute configuration of marine terpenoids. J. Am. Chem. Soc., 113, 4092-4096 (1991).
    • (1991) J. Am. Chem. Soc , vol.113 , pp. 4092-4096
    • Ohtani, I.1    Kusumi, T.2    Kashman, Y.3    Kakisawa, H.4
  • 18
    • 0001771128 scopus 로고
    • eds. Herz, W, Kirby, G. W, Moore, R. E, Steglich, W, and Tamm, C, Springer, Vienna, pp
    • Asakawa, Y., "Progress in the Chemistry of Organic Natural Products" Vol. 65, eds. Herz, W., Kirby, G. W., Moore, R. E., Steglich, W., and Tamm, C., Springer, Vienna, pp. 1-618 (1995).
    • (1995) Progress in the Chemistry of Organic Natural Products , vol.65 , pp. 1-618
    • Asakawa, Y.1
  • 19
    • 0026026289 scopus 로고    scopus 로고
    • de la Torre, M. C., Bruno, M., Piozzi, F., Savon, G., Omar, A. A., Perales, A., and Rodríguez, B., Two neo-clerodane diterpenoids containing an unusual 2,6-dioxabicyclo[2.2.1]heptane structural moiety. Tetrahedron, 47, 3463-3470 (1991).
    • de la Torre, M. C., Bruno, M., Piozzi, F., Savon, G., Omar, A. A., Perales, A., and Rodríguez, B., Two neo-clerodane diterpenoids containing an unusual 2,6-dioxabicyclo[2.2.1]heptane structural moiety. Tetrahedron, 47, 3463-3470 (1991).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.