메뉴 건너뛰기




Volumn 44, Issue 1, 2009, Pages 63-70

Two novel ceramides with a phytosphingolipid and a tertiary amide structure from Zephyranthes candida

Author keywords

Amaryllidaceae; Antimicrobial; Candidamide A; Candidamide B; Ceramides; Phytosphingolipid; Tertiary amide; Zephyranthes candida

Indexed keywords

3',7 DIHYDROXY 4' METHOXYFLAVAN; 4' HYDROXY 7 METHOXYFLAVAN; 4',7 DIHYDROXYFLAVAN; 7 HYDROXY 3', 4' METHYLENEDIOXYFLAVAN; AMBRETTOLIDE; BETA DAUCOSTEROL; CANDIDAMIDE A; CANDIDAMIDE B; CERAMIDE; DAUCOSTEROL; FLAVAN DERIVATIVE; HAEMANTHAMINE; HAEMANTHIDINE; LYCORINE; PANCRATISTATIN; PLANT EXTRACT; RUTOSIDE; SITOSTEROL; SPHINGOLIPID; UNCLASSIFIED DRUG;

EID: 57849148481     PISSN: 00244201     EISSN: 15589307     Source Type: Journal    
DOI: 10.1007/s11745-008-3246-6     Document Type: Article
Times cited : (28)

References (38)
  • 1
    • 0031545591 scopus 로고    scopus 로고
    • Meiotic behaviour and pollen fertility in three species of Zephyranthes (Amaryllidaceae)
    • DT Thoibi PK Borua 1997 Meiotic behaviour and pollen fertility in three species of Zephyranthes (Amaryllidaceae) Biol Plant 39 355 360
    • (1997) Biol Plant , vol.39 , pp. 355-360
    • Thoibi, D.T.1    Borua, P.K.2
  • 2
    • 0021734173 scopus 로고
    • Antineoplastic agents, 105. Zephyranthes grandiflora
    • GR Pettit V Gaddamidi GM Cragg 1984 Antineoplastic agents, 105. Zephyranthes grandiflora J Nat Prod 47 1018 1020
    • (1984) J Nat Prod , vol.47 , pp. 1018-1020
    • Pettit, G.R.1    Gaddamidi, V.2    Cragg, G.M.3
  • 5
    • 0001357850 scopus 로고
    • Chemical constituents of Amaryllidaceae. Part 25. Phosphatidylpyrrolophenanthridine alkaloids from Zephyranthes flava
    • S Ghosal SK Singh G Unnikrishnan 1987 Chemical constituents of Amaryllidaceae. Part 25. Phosphatidylpyrrolophenanthridine alkaloids from Zephyranthes flava Phytochemistry 26 823 828
    • (1987) Phytochemistry , vol.26 , pp. 823-828
    • Ghosal, S.1    Singh, S.K.2    Unnikrishnan, G.3
  • 7
    • 0024954772 scopus 로고
    • Determination of the presence of lactams in the plant Zephyranthes tubispatha Herb, Amaryllidaceae
    • 1-2
    • SS Iraida TA Zaida 1989 Determination of the presence of lactams in the plant Zephyranthes tubispatha Herb, Amaryllidaceae Revista Cubana de Farmacia 23 1-2 151 154
    • (1989) Revista Cubana de Farmacia , vol.23 , pp. 151-154
    • Iraida, S.S.1    Zaida, T.A.2
  • 9
    • 0034827579 scopus 로고    scopus 로고
    • Cytotoxic activities of alkaloids from Zephyranthes carinata
    • M Mutsuga K Kojima M Nose M Inoue Y Ogihara 2001 Cytotoxic activities of alkaloids from Zephyranthes carinata Nat Med 55 201 204
    • (2001) Nat Med , vol.55 , pp. 201-204
    • Mutsuga, M.1    Kojima, K.2    Nose, M.3    Inoue, M.4    Ogihara, Y.5
  • 11
    • 0017848773 scopus 로고
    • Isolation of kaempferol-3-O-rhamnoglucoside, a flavonoid glycoside from Zephyranthes candida
    • N Mitsuru H Tokunaru T Masao M Mitsuo H Shuichi 1978 Isolation of kaempferol-3-O-rhamnoglucoside, a flavonoid glycoside from Zephyranthes candida J Biosci 33C 587 588
    • (1978) J Biosci , vol.33 , pp. 587-588
    • Mitsuru, N.1    Tokunaru, H.2    Masao, T.3    Mitsuo, M.4    Shuichi, H.5
  • 12
    • 57849159462 scopus 로고
    • Alkaloids of Zephyranthes candida. I. Isolation of bases
    • S Ozeki 1964 Alkaloids of Zephyranthes candida. I. Isolation of bases Yakugaku Zasshi 84 1194 1197
    • (1964) Yakugaku Zasshi , vol.84 , pp. 1194-1197
    • Ozeki, S.1
  • 14
    • 35448939314 scopus 로고    scopus 로고
    • New sphingolipids from the root of Isatis indigotica and their cytotoxic activity
    • X Li DD Sun JW Chen LW He HQ Zhang HQ Xu 2007 New sphingolipids from the root of Isatis indigotica and their cytotoxic activity Fitoterapia 78 490 495
    • (2007) Fitoterapia , vol.78 , pp. 490-495
    • Li, X.1    Sun, D.D.2    Chen, J.W.3    He, L.W.4    Zhang, H.Q.5    Xu, H.Q.6
  • 15
    • 0028817726 scopus 로고
    • Halicylindrosides, antifungal and cytotoxic cerebrosides from the marine sponge Halichondria cylindroata
    • HY Li S Matsunaga N Fusetani 1995 Halicylindrosides, antifungal and cytotoxic cerebrosides from the marine sponge Halichondria cylindroata Tetrahedron 51 2273 2280
    • (1995) Tetrahedron , vol.51 , pp. 2273-2280
    • Li, H.Y.1    Matsunaga, S.2    Fusetani, N.3
  • 16
    • 34548203159 scopus 로고    scopus 로고
    • 20-sphingosine moiety from a marine algous endophytic fungus Aspergillus niger EN-13
    • 20-sphingosine moiety from a marine algous endophytic fungus Aspergillus niger EN-13 Lipids 42 759 764
    • (2007) Lipids , vol.42 , pp. 759-764
    • Zhang, Y.1    Wang, S.2    Li, X.M.3    Cui, C.M.4    Feng, C.5    Wang, B.G.6
  • 17
    • 0142043455 scopus 로고    scopus 로고
    • Pinelloside, an antimicrobial cerebroside from Pinellia ternata
    • JH Chen GY Cui JY Liu RX Tan 2003 Pinelloside, an antimicrobial cerebroside from Pinellia ternata Phytochemistry 64 903 906
    • (2003) Phytochemistry , vol.64 , pp. 903-906
    • Chen, J.H.1    Cui, G.Y.2    Liu, J.Y.3    Tan, R.X.4
  • 18
    • 0344741283 scopus 로고    scopus 로고
    • New cerebrosides from Euphorbia peplis L.: Antimicrobial activity evaluation
    • F Cateni J Zilic G Falsone G Scialino E Banfi 2003 New cerebrosides from Euphorbia peplis L.: antimicrobial activity evaluation Bioorg Med Chem Lett 13 4345 4350
    • (2003) Bioorg Med Chem Lett , vol.13 , pp. 4345-4350
    • Cateni, F.1    Zilic, J.2    Falsone, G.3    Scialino, G.4    Banfi, E.5
  • 19
    • 24344480032 scopus 로고    scopus 로고
    • Glycolipids and other constituents from Desmodium gangeticum with antileishmanial and immunomodulatory activities
    • PK Mishra N Singh G Ahmad A Dube R Maurya 2005 Glycolipids and other constituents from Desmodium gangeticum with antileishmanial and immunomodulatory activities Bioorg Med Chem Lett 15 4543 4546
    • (2005) Bioorg Med Chem Lett , vol.15 , pp. 4543-4546
    • Mishra, P.K.1    Singh, N.2    Ahmad, G.3    Dube, A.4    Maurya, R.5
  • 20
    • 0141788086 scopus 로고    scopus 로고
    • Preliminary biological assay on cerebroside mixture from Euphorbia nicaeensis All. Isolation and structure determination of five glucocerebrosides
    • F Cateni J Zilic G Falsone F Hollan F Frausin V Scarcia 2003 Preliminary biological assay on cerebroside mixture from Euphorbia nicaeensis All. Isolation and structure determination of five glucocerebrosides IL Farmaco 58 809 817
    • (2003) IL Farmaco , vol.58 , pp. 809-817
    • Cateni, F.1    Zilic, J.2    Falsone, G.3    Hollan, F.4    Frausin, F.5    Scarcia, V.6
  • 21
    • 0028204397 scopus 로고
    • Agelasphins, novel antitumor and immunostimulatory cerebrosides from the marine sponge Agelas mauritianus
    • T Natori M Morita K Akimoto Y Koezuka 1994 Agelasphins, novel antitumor and immunostimulatory cerebrosides from the marine sponge Agelas mauritianus Tetrahedron 50 2771 2784
    • (1994) Tetrahedron , vol.50 , pp. 2771-2784
    • Natori, T.1    Morita, M.2    Akimoto, K.3    Koezuka, Y.4
  • 22
    • 0035209786 scopus 로고    scopus 로고
    • Armillaramide, a new sphingolipid from the fungus Armillaria mellea
    • JM Gao X Yang CY Wang JK Liu 2001 Armillaramide, a new sphingolipid from the fungus Armillaria mellea Fitoterapia 72 857 972
    • (2001) Fitoterapia , vol.72 , pp. 857-972
    • Gao, J.M.1    Yang, X.2    Wang, C.Y.3    Liu, J.K.4
  • 23
    • 84988141857 scopus 로고
    • Isolation and structure of cerebrosides from the sea cucumber Pentacta australis
    • R Higuchi M Inagaki K Togawa T Miyamoto T Komori 1994 Isolation and structure of cerebrosides from the sea cucumber Pentacta australis Liebigs Ann Chem 7 653 658
    • (1994) Liebigs Ann Chem , vol.7 , pp. 653-658
    • Higuchi, R.1    Inagaki, M.2    Togawa, K.3    Miyamoto, T.4    Komori, T.5
  • 24
    • 26044469153 scopus 로고    scopus 로고
    • A new cerebrosides, asperiamide A, from the marine fungus Asperillus sp
    • MA Ouyang R Liu YH Kuo 2005 A new cerebrosides, asperiamide A, from the marine fungus Asperillus sp J Asian Nat Prod Res 7 761 765
    • (2005) J Asian Nat Prod Res , vol.7 , pp. 761-765
    • Ouyang, M.A.1    Liu, R.2    Kuo, Y.H.3
  • 26
    • 0037029842 scopus 로고    scopus 로고
    • Structure determination and synthesis of a new cerebrosides isolation from the traditional Chinese medicine Typhonium giganteum Engl
    • XS Chen YL Wu DH Chen 2002 Structure determination and synthesis of a new cerebrosides isolation from the traditional Chinese medicine Typhonium giganteum Engl Tetrahedron Lett 43 3529 3532
    • (2002) Tetrahedron Lett , vol.43 , pp. 3529-3532
    • Chen, X.S.1    Wu, Y.L.2    Chen, D.H.3
  • 27
    • 33646118265 scopus 로고    scopus 로고
    • Lonijaposides, novel cerebrosides from Lonicer japonica
    • N Kumar B Singh AP Gupta VK Kaul 2006 Lonijaposides, novel cerebrosides from Lonicer japonica Tetrahedron 62 4317 4322
    • (2006) Tetrahedron , vol.62 , pp. 4317-4322
    • Kumar, N.1    Singh, B.2    Gupta, A.P.3    Kaul, V.K.4
  • 29
    • 0032853292 scopus 로고    scopus 로고
    • Morinins H-K, four novel phenylpropanol ester lipid metabolites from Morina chinensis
    • BN Su Y Takaishi 1999 Morinins H-K, four novel phenylpropanol ester lipid metabolites from Morina chinensis J Nat Prod 62 1325 1327
    • (1999) J Nat Prod , vol.62 , pp. 1325-1327
    • Su, B.N.1    Takaishi, Y.2
  • 30
    • 0025647272 scopus 로고
    • Sphingolipids and glycerolipids.I. Chemical structure and ionophoretic activities of soyacerebrosides I and II from soybean
    • H Shibuya K Kawashima M Sakagami H Kawanishi M Shimomura K Ohashi I Kitagawa 1990 Sphingolipids and glycerolipids.I. Chemical structure and ionophoretic activities of soyacerebrosides I and II from soybean Chem Pharm Bull 38 2933 2938
    • (1990) Chem Pharm Bull , vol.38 , pp. 2933-2938
    • Shibuya, H.1    Kawashima, K.2    Sakagami, M.3    Kawanishi, H.4    Shimomura, M.5    Ohashi, K.6    Kitagawa, I.7
  • 31
    • 28944438060 scopus 로고    scopus 로고
    • A new cerebroside from Uvaria tonkinensis var. subglabra
    • A Liu ZM Zou LZ Xu SL Yang 2005 A new cerebroside from Uvaria tonkinensis var. subglabra J Asian Nat Prod Res 7 861 865
    • (2005) J Asian Nat Prod Res , vol.7 , pp. 861-865
    • Liu, A.1    Zou, Z.M.2    Xu, L.Z.3    Yang, S.L.4
  • 33
    • 33644609183 scopus 로고    scopus 로고
    • Novel imine from Hemsleya macrocarpa var. clavata
    • YP Lin J Yan MH Qiu 2006 Novel imine from Hemsleya macrocarpa var. clavata Lipids 41 97 99
    • (2006) Lipids , vol.41 , pp. 97-99
    • Lin, Y.P.1    Yan, J.2    Qiu, M.H.3
  • 34
    • 0029109585 scopus 로고
    • Flavonoids of dragon's blood from Dracaena cinnabari
    • M Masaoud H Ripperger A Porzel 1995 Flavonoids of dragon's blood from Dracaena cinnabari Phytochemistry 38 745 749
    • (1995) Phytochemistry , vol.38 , pp. 745-749
    • Masaoud, M.1    Ripperger, H.2    Porzel, A.3
  • 35
    • 45549112609 scopus 로고
    • Flavonoid and other constituents of Bauhinia manca
    • H Achenbach M Stocker AC Manael 1988 Flavonoid and other constituents of Bauhinia manca Phytochemistry 27 1835 1842
    • (1988) Phytochemistry , vol.27 , pp. 1835-1842
    • Achenbach, H.1    Stocker, M.2    Manael, A.C.3
  • 36
    • 37049106350 scopus 로고
    • Synthesis of ambrettolide from phloionolic acid
    • V San E Seoan 1982 Synthesis of ambrettolide from phloionolic acid Perkin Trans I 7 1837 1838
    • (1982) Perkin Trans I , vol.7 , pp. 1837-1838
    • San, V.1    Seoan, E.2
  • 38
    • 0025775942 scopus 로고
    • Alkaloidal constituents of the flowers of Lycoris radiata Herb (Amaryllidaceae)
    • M Kihara K Konishi L Xu S Kobayashi 1991 Alkaloidal constituents of the flowers of Lycoris radiata Herb (Amaryllidaceae) Chem Pharm Bull 39 1849 1853
    • (1991) Chem Pharm Bull , vol.39 , pp. 1849-1853
    • Kihara, M.1    Konishi, K.2    Xu, L.3    Kobayashi, S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.