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Volumn 28, Issue 19, 2014, Pages 1583-1590

Urgineaglyceride A: A new monoacylglycerol from the Egyptian Drimia maritima bulbs

Author keywords

Drimia maritima; in vitro growth inhibitory activity; monoacylglycerol; urgineaglyceride A

Indexed keywords

2 HYDROXYNARINGENIN 4' O BETA DEXTRO GLUCOPYRANOSIDE; 3,5,7,3',5' PENTAHYDROXYDIHYDROFLAVONOL; 5BETA FUROSTANE 3BETA 22ALPHA 26 TRIOL; ANTINEOPLASTIC AGENT; MONOACYLGLYCEROL; QUERCETIN 3' O BETA DEXTRO GLUCOPYRANOSIDE; SCILLARIDIN A; SQUILL; STIGMASTEROL; UNCLASSIFIED DRUG; URGINEAGLYCERIDE A; MONOSACCHARIDE; QUERCETIN; QUERCETIN-3'-O-BETA-D-GLUCOPYRANOSIDE;

EID: 84908468854     PISSN: 14786419     EISSN: 14786427     Source Type: Journal    
DOI: 10.1080/14786419.2014.927468     Document Type: Article
Times cited : (14)

References (32)
  • 1
    • 84887465104 scopus 로고    scopus 로고
    • Lupeol-3-o-decanoate, a new triterpene ester from cadaba farinosa forssk growing in saudi arabia
    • Al-Musayeib NM, Mohamed GA, Ibrahim SRM, Ross SA. 2013. Lupeol-3-O-decanoate, a new triterpene ester from Cadaba farinosa Forssk. growing in Saudi Arabia. Med Chem Res. 22:5297-5302
    • (2013) Med Chem Res , vol.22 , pp. 5297-5302
    • Al-Musayeib, N.M.1    Mohamed, G.A.2    Ibrahim, S.R.M.3    Ross, S.A.4
  • 3
    • 84908472493 scopus 로고    scopus 로고
    • Cairo: Al Hadara Publishing;
    • Boulos L. 2002. Flora of Egypt. Vol. 2. Cairo: Al Hadara Publishing; p. 359-360
    • (2002) Flora of Egypt , vol.2 , pp. 359-360
    • Boulos, L.1
  • 5
    • 83155181784 scopus 로고    scopus 로고
    • Urginea maritima l) baker (liliaceae) extract induces more cytotoxicity than standard chemotherapeutics in the a549 non-small cell lung cancer (nsclc) cell line
    • Bozcuk H, Ö zdoʇan M, Aykurt O, Topçuoʇlu F, Ö ztürk H, Ekinci D, Karadeniz A, Mutlu A, Burgucu D. 2011. Urginea maritima (L.) Baker (Liliaceae) extract induces more cytotoxicity than standard chemotherapeutics in the A549 non-small cell lung cancer (NSCLC) cell line. Turk J Med Sci. 41:101-108
    • (2011) Turk J Med Sci , vol.41 , pp. 101-108
    • Bozcuk, H.1    Özdoʇan, M.2    Aykurt, O.3    Topçuoʇlu, F.4    Öztürk, H.5    Ekinci, D.6    Karadeniz, A.7    Mutlu, A.8    Burgucu, D.9
  • 6
    • 0022425355 scopus 로고
    • Synthesis and polymorphism of 3-acyl-sn-glycerols
    • Dharma RK, Trevor GR, Donald MS. 1985. Synthesis and polymorphism of 3-acyl-sn-glycerols. Biochemistry. 24:519-525
    • (1985) Biochemistry , vol.24 , pp. 519-525
    • Dharma, R.K.1    Trevor, G.R.2    Donald, M.S.3
  • 7
    • 0003511577 scopus 로고
    • Algonac (MI): Reference Publications, Inc., ISBN 0-917256;
    • Duke JA, Ayensu ES. 1985. Medicinal plants of China. Algonac (MI): Reference Publications, Inc., ISBN 0-917256; p. 20-24
    • (1985) Medicinal Plants of China , pp. 20-24
    • Duke, J.A.1    Ayensu, E.S.2
  • 8
    • 84872898819 scopus 로고    scopus 로고
    • The traditional medical uses and cytotoxic activities of sixty-one Egyptian plants: Discovery of an active cardiac glycoside from Urginea maritima
    • El-Seedia HR, Burmana R, Mansour A, Turki Z, Boulos L, Gullbo J, Göransson U. 2013. The traditional medical uses and cytotoxic activities of sixty-one Egyptian plants: discovery of an active cardiac glycoside from Urginea maritima. J Ethnopharmacol. 145:746-757
    • (2013) J Ethnopharmacol , vol.145 , pp. 746-757
    • El-Seedia, H.R.1    Burmana, R.2    Mansour, A.3    Turki, Z.4    Boulos, L.5    Gullbo, J.6    Göransson, U.7
  • 12
    • 78751539203 scopus 로고    scopus 로고
    • Two new guaianolides from Amberboa ramosa
    • Ibrahim M, Khan R, Malik A. 2010. Two new guaianolides from Amberboa ramosa. Nat Prod Commun. 5:1865-1868
    • (2010) Nat Prod Commun , vol.5 , pp. 1865-1868
    • Ibrahim, M.1    Khan, R.2    Malik, A.3
  • 13
    • 84894492939 scopus 로고    scopus 로고
    • New chromone and triglyceride from Cucumis melo Seeds
    • Ibrahim SRM. 2014. New chromone and triglyceride from Cucumis melo Seeds. Nat Prod Commun. 9:205-208
    • (2014) Nat Prod Commun , vol.9 , pp. 205-208
    • Ibrahim, S.R.M.1
  • 14
    • 84905383874 scopus 로고    scopus 로고
    • Proceraside A, a new cardiac glycoside from the root barks of Calotropis procera with in vitro anticancer effects
    • Ibrahim SRM, Mohamed GA, Shaala LA, Banuls LMY, Kiss R, Youssef DTA. 2014. Proceraside A, a new cardiac glycoside from the root barks of Calotropis procera with in vitro anticancer effects. Nat Prod Res. http://dx.doi. org/10.1080/14786419.2014.901323
    • (2014) Nat Prod Res
    • Ibrahim, S.R.M.1    Mohamed, G.A.2    Shaala, L.A.3    Banuls, L.M.Y.4    Kiss, R.5    Youssef, D.T.A.6
  • 16
    • 0035081908 scopus 로고    scopus 로고
    • Bufadienolides and a new lignan from the bulbs of Urginea maritima
    • Iizuka M, Warashina T, Noro T. 2001. Bufadienolides and a new lignan from the bulbs of Urginea maritima. Chem Pharm Bull. 49:282-286
    • (2001) Chem Pharm Bull , vol.49 , pp. 282-286
    • Iizuka, M.1    Warashina, T.2    Noro, T.3
  • 17
    • 14344253060 scopus 로고    scopus 로고
    • Four new steroid constituents from the waste residue of fibre separation from Agave americana Leaves
    • Jin JM, Zhang YJ, Yang CR. 2004. Four new steroid constituents from the waste residue of fibre separation from Agave americana Leaves. Chem Pharm Bull. 52:654-658
    • (2004) Chem Pharm Bull , vol.52 , pp. 654-658
    • Jin, J.M.1    Zhang, Y.J.2    Yang, C.R.3
  • 18
    • 0033840038 scopus 로고    scopus 로고
    • Flavanone glycoside from the fruits of Chaenomeles sinensis
    • Kim HK, Jeon WK, Ko BS. 2000. Flavanone glycoside from the fruits of Chaenomeles sinensis. Nat Prod Sci. 6:79-81
    • (2000) Nat Prod Sci , vol.6 , pp. 79-81
    • Kim, H.K.1    Jeon, W.K.2    Ko, B.S.3
  • 22
    • 0034177368 scopus 로고    scopus 로고
    • New bufadienolides from Urginea maritima sensu strictu
    • Krenn L, Jelovina M, Kopp B. 2000. New bufadienolides from Urginea maritima sensu strictu. Fitoterapia. 71:126-129
    • (2000) Fitoterapia , vol.71 , pp. 126-129
    • Krenn, L.1    Jelovina, M.2    Kopp, B.3
  • 23
    • 0036924734 scopus 로고    scopus 로고
    • Phenolic compounds of plants of the scutellaria l genus distribution, structure, and properties
    • Malikov VM, Yuldashev MP. 2002. Phenolic compounds of plants of the Scutellaria L. genus. Distribution, structure, and properties. Chem Nat Compd. 38:358-406
    • (2002) Chem Nat Compd , vol.38 , pp. 358-406
    • Malikov, V.M.1    Yuldashev, M.P.2
  • 24
    • 79958773646 scopus 로고    scopus 로고
    • Effects of the high doses of urginea maritima (l)
    • Baker extract on chromosomes
    • Metin M, Bürün B. 2010. Effects of the high doses of Urginea maritima (L.) Baker extract on chromosomes. Caryologia. 63:367-375
    • (2010) Caryologia , vol.63 , pp. 367-375
    • Metin, M.1    Bürün, B.2
  • 25
    • 33644974357 scopus 로고    scopus 로고
    • The cardenolide UNBS1450 is able to deactivate NF-kB-mediated cytoprotective effects in human non-small-cell-lung cancer (NSCLC) cells
    • Mijatovic T, Op De Beeck A, Van Quaquebeke E, Dewelle J, Darro F, de Launoit Y, Kiss R. 2006. The cardenolide UNBS1450 is able to deactivate NF-kB-mediated cytoprotective effects in human non-small-cell-lung cancer (NSCLC) cells. Mol Cancer Ther. 5:1-9
    • (2006) Mol Cancer Ther , vol.5 , pp. 1-9
    • Mijatovic, T.1    Op De Beeck, A.2    Van Quaquebeke, E.3    Dewelle, J.4    Darro, F.5    De Launoit, Y.6    Kiss, R.7
  • 26
    • 36849045267 scopus 로고    scopus 로고
    • Eucalyptone G: A new phloroglucinol derivative and other constituents from Eucalyptus globulus Labill
    • Mohamed GA, Ibrahim SRM. 2007. Eucalyptone G: a new phloroglucinol derivative and other constituents from Eucalyptus globulus Labill. ARKIVOC. xv:281-291
    • (2007) ARKIVOC , vol.15 , pp. 281-291
    • Mohamed, G.A.1    Srm, I.2
  • 27
    • 0000125597 scopus 로고
    • Scilliroside and other scilla compounds in red squill
    • Patel J, Banigan TF, Schatz RA. 1986. Scilliroside and other scilla compounds in red squill. J Agric Food Chem. 34:973-979
    • (1986) J Agric Food Chem , vol.34 , pp. 973-979
    • Patel, J.1    Banigan, T.F.2    Schatz, R.A.3
  • 28
    • 79955475425 scopus 로고    scopus 로고
    • Stilbenes and flavonoids from Artocarpus nitidus subsp
    • Ti H, Wu P, Lin L, Wei X. 2011. Stilbenes and flavonoids from Artocarpus nitidus subsp. Lingnanensis. Fitoterapia. 82:662-665
    • (2011) Lingnanensis. Fitoterapia , vol.82 , pp. 662-665
    • Ti, H.1    Wu, P.2    Lin, L.3    Wei, X.4
  • 29
    • 0345232056 scopus 로고
    • Anthocyanins of red squill, Urginea maritima
    • Vega FA, Garcia JI, Fernandez M. 1972. Anthocyanins of red squill, Urginea maritima. Phytochemistry. 11:2896-2899
    • (1972) Phytochemistry , vol.11 , pp. 2896-2899
    • Vega, F.A.1    Garcia, J.I.2    Fernandez, M.3
  • 30
    • 0000906478 scopus 로고    scopus 로고
    • Application of NMR to the study of olive oils
    • Vlahov G. 1999. Application of NMR to the study of olive oils. Prog Nucl Magn Reson Spectrom. 35:341-357
    • (1999) Prog Nucl Magn Reson Spectrom , vol.35 , pp. 341-357
    • Vlahov, G.1
  • 31
    • 56349141011 scopus 로고    scopus 로고
    • A new phloroglucinol diglycoside derivative from Hypericum japonicum Thunb
    • Wang XW, Mao Y, Wang N, Yao XS. 2008. A new phloroglucinol diglycoside derivative from Hypericum japonicum Thunb. Molecules. 13:2796-2803
    • (2008) Molecules , vol.13 , pp. 2796-2803
    • Wang, X.W.1    Mao, Y.2    Wang, N.3    Yao, X.S.4
  • 32
    • 0742297438 scopus 로고    scopus 로고
    • Two new furostanol glycosides from Asparagus cochinensis
    • Yang CY, Huang SY, Shi JG. 2002. Two new furostanol glycosides from Asparagus cochinensis. Chin Chem Lett. 13:1185-1188
    • (2002) Chin Chem Lett , vol.13 , pp. 1185-1188
    • Yang, C.Y.1    Huang, S.Y.2    Shi, J.G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.