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Volumn 27, Issue 11, 2004, Pages 1109-1113

Pentacyclic triterpenoids fromMallotus apelta

Author keywords

Euphorbiaceae; Malloapelta A; Mallotus apelta; Triterpene

Indexed keywords

PLANT EXTRACT; POLYCYCLIC HYDROCARBON; TRITERPENE;

EID: 16644396786     PISSN: 02536269     EISSN: 19763786     Source Type: Journal    
DOI: 10.1007/BF02975113     Document Type: Article
Times cited : (59)

References (15)
  • 1
    • 0028920629 scopus 로고
    • NMR spectra of triterpenoids. III. Oleanenes and migrated oleanenes
    • COI: 1:CAS:528:DyaK2MXksVSht7c%3D
    • Ageta, H., Arai, Y., Suzuki, H., Kiyotani, T., and Kitabayashi, M., NMR spectra of triterpenoids. III. Oleanenes and migrated oleanenes.Chem. Pharm. Bull., 43, 198–203 (1995).
    • (1995) Chem. Pharm. Bull. , vol.43 , pp. 198-203
    • Ageta, H.1    Arai, Y.2    Suzuki, H.3    Kiyotani, T.4    Kitabayashi, M.5
  • 2
    • 0035858552 scopus 로고    scopus 로고
    • Benzopyran derivatives fromMallotus apelta
    • PID: 11382244, COI: 1:CAS:528:DC%2BD3MXjtFCnu7w%3D
    • An, T. Y., Hu, L. H., Cheng, X. F., and Chen, Z. L., Benzopyran derivatives fromMallotus apelta.Phytochemistry, 57, 273–278 (2001). DOI: 10.1016/S0031-9422(00)00512-4
    • (2001) Phytochemistry , vol.57 , pp. 273-278
    • An, T.Y.1    Hu, L.H.2    Cheng, X.F.3    Chen, Z.L.4
  • 3
    • 0000949791 scopus 로고
    • Three triterpenes and other terpenoids fromCatha cassinoides
    • COI: 1:CAS:528:DyaL3MXhtl2qur4%3D
    • Betancor, C., Freire, R., Gonzalez, A. G., Salazar, J. A., Pascard, C., and Prange, T., Three triterpenes and other terpenoids fromCatha cassinoides.Phytochemistry, 19, 1989–1991 (1980). DOI: 10.1016/0031-9422(80)83019-6
    • (1980) Phytochemistry , vol.19 , pp. 1989-1991
    • Betancor, C.1    Freire, R.2    Gonzalez, A.G.3    Salazar, J.A.4    Pascard, C.5    Prange, T.6
  • 4
    • 0031672408 scopus 로고    scopus 로고
    • A pyridine-type alkaloid fromMallotus apelta
    • COI: 1:CAS:528:DyaK1MXhvFGksw%3D%3D
    • Cheng, X. F., Meng, Z. M., and Chen, Z. L., A pyridine-type alkaloid fromMallotus apelta.Phytochemistry, 49, 2193–2194 (1998). DOI: 10.1016/S0031-9422(98)00395-1
    • (1998) Phytochemistry , vol.49 , pp. 2193-2194
    • Cheng, X.F.1    Meng, Z.M.2    Chen, Z.L.3
  • 5
    • 0033304101 scopus 로고    scopus 로고
    • Two new diterpenoids fromMallotus apelta Muell. Arg
    • COI: 1:CAS:528:DyaK1MXjtVGmtLw%3D
    • Cheng, X. F., Chen, Z. L., and Meng, Z. M., Two new diterpenoids fromMallotus apelta Muell. Arg.J. of Asian Nat. Prod. Res., 1, 163–168 (1999a). DOI: 10.1080/10286029908039860
    • (1999) J. of Asian Nat. Prod. Res. , vol.1 , pp. 163-168
    • Cheng, X.F.1    Chen, Z.L.2    Meng, Z.M.3
  • 6
    • 0033304206 scopus 로고    scopus 로고
    • Three new diterpenoids fromMallotus apelta Muell
    • COI: 1:CAS:528:DyaK1MXmtlCgs78%3D
    • Cheng, X. F. and Chen, Z. L., Three new diterpenoids fromMallotus apelta Muell.Arg. J. of Asian Nat. Prod. Res., 1, 319–325 (1999b). DOI: 10.1080/10286029908039881
    • (1999) Arg. J. of Asian Nat. Prod. Res. , vol.1 , pp. 319-325
    • Cheng, X.F.1    Chen, Z.L.2
  • 7
    • 0034212333 scopus 로고    scopus 로고
    • Coumarinolignoids ofMallotus apelta
    • PID: 10844178, COI: 1:CAS:528:DC%2BD3cXltlyhurk%3D
    • Cheng, X. F. and Chen, Z. L., Coumarinolignoids ofMallotus apelta.Fitoterapia, 71, 341–342 (2000). DOI: 10.1016/S0367-326X(99)00160-4
    • (2000) Fitoterapia , vol.71 , pp. 341-342
    • Cheng, X.F.1    Chen, Z.L.2
  • 8
    • 85164456259 scopus 로고    scopus 로고
    • Vietnamese Medical Plant Dictionary, Ha Noi Medicine Pub
    • Chi, V. V., (ed.), Vietnamese Medical Plant Dictionary, Ha Noi Medicine Pub., 1997.
    • (1997) (Ed.)
    • Chi, V.V.1
  • 9
    • 0034283729 scopus 로고    scopus 로고
    • Antitumor activity of epifriedelanol fromVitis trifolia
    • PID: 11449513, COI: 1:CAS:528:DC%2BD3cXlvFWgsrw%3D
    • Kundu, J. K., Rouf. A. S. S., Hossain, N., Hassan, C. M., and Rashid, M. A., Antitumor activity of epifriedelanol fromVitis trifolia.Fitoterapia, 71, 577–579 (2000). DOI: 10.1016/S0367-326X(00)00191-X
    • (2000) Fitoterapia , vol.71 , pp. 577-579
    • Kundu, J.K.1    Rouf, A.S.S.2    Hossain, N.3    Hassan, C.M.4    Rashid, M.A.5
  • 10
    • 85164510986 scopus 로고    scopus 로고
    • Glossary of Vietnamese Medical Plants, Hanoi S&T Pub
    • Loi D. T., (ed.), Glossary of Vietnamese Medical Plants, Hanoi S&T Pub., (2001).
    • (2001) (Ed.)
    • Loi, D.T.1
  • 12
    • 0001425457 scopus 로고
    • 3β-Methoxyhop-22(29)-ene fromChionochloa cheesemanii
    • COI: 1:CAS:528:DyaK38XhvFWjtb4%3D
    • Rowan, D. D. and Russell, B. G., 3β-Methoxyhop-22(29)-ene fromChionochloa cheesemanii.Phytochemistry, 31, 702–703 (1992). DOI: 10.1016/0031-9422(92)90066-Y
    • (1992) Phytochemistry , vol.31 , pp. 702-703
    • Rowan, D.D.1    Russell, B.G.2
  • 13
    • 46149131274 scopus 로고
    • Triterpenoids fromMyricia rubra
    • Sakurai, N., Yaguchi, Y., and Inoue, T., Triterpenoids fromMyricia rubra.Phytochemistry, 26, 217–219 (1987). DOI: 10.1016/S0031-9422(00)81515-0
    • (1987) Phytochemistry , vol.26 , pp. 217-219
    • Sakurai, N.1    Yaguchi, Y.2    Inoue, T.3
  • 14
    • 0011436471 scopus 로고
    • 5,5,3′,5′-Pentahydroxyflavan and 3α-methoxyfriedelan fromHumboldtia laurifolia
    • COI: 1:CAS:528:DyaL3sXlslarsrk%3D
    • Samaraweera, U., Sotheeswaran, S., and Sultanbawa, M. U. S., 5,5,3′,5′-Pentahydroxyflavan and 3α-methoxyfriedelan fromHumboldtia laurifolia.Phytochemistry, 22, 565–567 (1983). DOI: 10.1016/0031-9422(83)83047-7
    • (1983) Phytochemistry , vol.22 , pp. 565-567
    • Samaraweera, U.1    Sotheeswaran, S.2    Sultanbawa, M.U.S.3
  • 15
    • 0025271574 scopus 로고
    • Fern constituents: Two new triterpenoid hydrocarbons, hop-16-ene and isohop-22(29)-ene, isolated fromDavallia marriesii
    • COI: 1:CAS:528:DyaK3cXkslCktbk%3D
    • Shiojima, K. and Ageta, H., Fern constituents: Two new triterpenoid hydrocarbons, hop-16-ene and isohop-22(29)-ene, isolated fromDavallia marriesii.Chem. Pharm. Bull. 38, 347–349 (1990).
    • (1990) Chem. Pharm. Bull. , vol.38 , pp. 347-349
    • Shiojima, K.1    Ageta, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.