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Volumn 53, Issue 23, 2005, Pages 8987-8992

Chemistry and bioactivity of royal jelly from Greece

Author keywords

Antimicrobial activities; Decanoic and dodecanoic acid derivatives; Fatty acids; Royal jelly

Indexed keywords

ANTIINFECTIVE AGENT; FATTY ACID; ROYAL JELLY;

EID: 28444485394     PISSN: 00218561     EISSN: None     Source Type: Journal    
DOI: 10.1021/jf051550p     Document Type: Article
Times cited : (124)

References (25)
  • 1
    • 51249182679 scopus 로고
    • Components of royal jelly: I. Identification of the organic acids
    • Lercker, G.; Capella, P.; Conte, L. S.; Ruini, F.; Giordani, G. Components of royal jelly: I. Identification of the organic acids. Lipids 1981, 12, 912-919.
    • (1981) Lipids , vol.12 , pp. 912-919
    • Lercker, G.1    Capella, P.2    Conte, L.S.3    Ruini, F.4    Giordani, G.5
  • 2
    • 33846010755 scopus 로고
    • Activity of 10-hydroxydecenoic acid from royal jelly against experimental leukaemia and ascitic tumours
    • Townsend, G. F.; Morgan, J. F.; Hazlett, B. Activity of 10-hydroxydecenoic acid from royal jelly against experimental leukaemia and ascitic tumours. Nature 1959, 183, 1270-1271.
    • (1959) Nature , vol.183 , pp. 1270-1271
    • Townsend, G.F.1    Morgan, J.F.2    Hazlett, B.3
  • 3
    • 0001556214 scopus 로고
    • 10-Hydroxy-2Δ-decenoic acid, an antibiotic found in royal jelly
    • Blum, M. S.; Novak, A. F.; Taber, S. 10-Hydroxy-2Δ-decenoic acid, an antibiotic found in royal jelly. Science 1959, 130, 452-453.
    • (1959) Science , vol.130 , pp. 452-453
    • Blum, M.S.1    Novak, A.F.2    Taber, S.3
  • 4
    • 0142248297 scopus 로고    scopus 로고
    • Preparation and the functional properties of water extract and alkaline extract of royal jelly
    • Nagai, T.; Inoue, R. Preparation and the functional properties of water extract and alkaline extract of royal jelly. Food Chem. 2004, 84, 181-186.
    • (2004) Food Chem. , vol.84 , pp. 181-186
    • Nagai, T.1    Inoue, R.2
  • 5
    • 0029998979 scopus 로고    scopus 로고
    • Caste-selective pheromone biosynthesis in honeybees
    • Plettner, E.; Slessor, K. N.; Winston, M. L.; Oliver, J. E. Caste-selective pheromone biosynthesis in honeybees. Science 1996, 271, 1851-1853.
    • (1996) Science , vol.271 , pp. 1851-1853
    • Plettner, E.1    Slessor, K.N.2    Winston, M.L.3    Oliver, J.E.4
  • 6
    • 0031959023 scopus 로고    scopus 로고
    • Biosynthesis of mandibular acids in honeybees (Apis mellifera): De novo synthesis, route of fatty acid hydroxylation and caste selective β-oxidation
    • Plettner, E.; Slessor, K. N.; Winston, M. L. Biosynthesis of mandibular acids in honeybees (Apis mellifera): de novo synthesis, route of fatty acid hydroxylation and caste selective β-oxidation. Insect Biochem. Mol. Biol. 1998, 28, 31-42.
    • (1998) Insect Biochem. Mol. Biol. , vol.28 , pp. 31-42
    • Plettner, E.1    Slessor, K.N.2    Winston, M.L.3
  • 11
    • 0002231990 scopus 로고
    • La reaction de wittig-horner en milieu heterogene VI. Selectivite de la reaction sur des composes bifonctionnels
    • Villieras, J.; Rambaud, M.; Graff, M. La reaction de wittig-horner en milieu heterogene VI. Selectivite de la reaction sur des composes bifonctionnels. Tetrahedron Lett. 1985, 26, 53-56.
    • (1985) Tetrahedron Lett. , vol.26 , pp. 53-56
    • Villieras, J.1    Rambaud, M.2    Graff, M.3
  • 12
    • 0037012833 scopus 로고    scopus 로고
    • Total synthesis of (S)-(+)-imperanene. Effective use of regio- and enantioselective intramolecular carbon-hydrogen insertion reactions catalyzed by chiral dirhodium(II) carboxamidates
    • Doyle, M.; Hu, W.; Valenzuela, M. V. Total synthesis of (S)-(+)-imperanene. Effective use of regio- and enantioselective intramolecular carbon-hydrogen insertion reactions catalyzed by chiral dirhodium(II) carboxamidates. J. Org. Chem. 2002, 67, 2954-2959.
    • (2002) J. Org. Chem. , vol.67 , pp. 2954-2959
    • Doyle, M.1    Hu, W.2    Valenzuela, M.V.3
  • 13
    • 0000556664 scopus 로고
    • Stereochemical differences in the anatomical distribution of C-24 alkylated sterols in Kalanchoe daigremoutiana
    • Kalinowska, M.; Nes, W. R.; CrumLey, F. G.; Nes, W. D. Stereochemical differences in the anatomical distribution of C-24 alkylated sterols in Kalanchoe daigremoutiana. Phytochemistry 1990, 11, 3427-3434.
    • (1990) Phytochemistry , vol.11 , pp. 3427-3434
    • Kalinowska, M.1    Nes, W.R.2    Crumley, F.G.3    Nes, W.D.4
  • 14
    • 85008068550 scopus 로고
    • Novel 19-oxygenated sterols from the Okinawan soft coral Litophyton viridis
    • Kazuo, I.; Shuichi, S.; Yasuzi, Y. Novel 19-oxygenated sterols from the Okinawan soft coral Litophyton viridis. Chem. Pharm. Bull. 1989, 9, 2553-2554.
    • (1989) Chem. Pharm. Bull. , vol.9 , pp. 2553-2554
    • Kazuo, I.1    Shuichi, S.2    Yasuzi, Y.3
  • 15
    • 3042836536 scopus 로고    scopus 로고
    • Chemical analysis and antimicrobial activity of Greek propolis
    • Melliou, E.; Chinou, I. Chemical analysis and antimicrobial activity of Greek propolis. Planta Med. 2004, 70, 515-519.
    • (2004) Planta Med. , vol.70 , pp. 515-519
    • Melliou, E.1    Chinou, I.2
  • 16
    • 28444442554 scopus 로고
    • Auftrennung der sauren anteile von extrakten aus bienenköniginnen (Apis mellifera L.); Isolierung des als königinnen-substanz bezeichneten pheromones
    • Barbier, M.; Lederer, E.; Reichstein, T.; Schindler, O. Auftrennung der sauren anteile von extrakten aus bienenköniginnen (Apis mellifera L.); Isolierung des als königinnen-substanz bezeichneten pheromones Helv. Chim. Acta 1960, 207, 1682-1689.
    • (1960) Helv. Chim. Acta , vol.207 , pp. 1682-1689
    • Barbier, M.1    Lederer, E.2    Reichstein, T.3    Schindler, O.4
  • 17
    • 0030845502 scopus 로고    scopus 로고
    • Mandibular gland volatiles and their ontogenetic patterns in queen honey bees, Apis mellifera carnica
    • Engels, W.; Rosenkranz, P.; Adler, A.; Taghizadeh, T.; Lubke, G.; Francke, W. Mandibular gland volatiles and their ontogenetic patterns in queen honey bees, Apis mellifera carnica. J. Insect Physiol. 1997, 43, 307-313.
    • (1997) J. Insect Physiol. , vol.43 , pp. 307-313
    • Engels, W.1    Rosenkranz, P.2    Adler, A.3    Taghizadeh, T.4    Lubke, G.5    Francke, W.6
  • 18
    • 51249191020 scopus 로고
    • Novel fatty acids from the royal jelly of honeybees (Apis mellifera, L.)
    • Weaver, N.; Johnston, N. C.; Benzamin, R.; Law, J. H. Novel fatty acids from the royal jelly of honeybees (Apis mellifera, L.). Lipids 1968, 6, 535-538.
    • (1968) Lipids , vol.6 , pp. 535-538
    • Weaver, N.1    Johnston, N.C.2    Benzamin, R.3    Law, J.H.4
  • 19
    • 84987589081 scopus 로고
    • Comparative study of the essential oils from hops of various Humulus lupulus L. cultivars
    • Katsiotis, S. T.; Langezaal, C. R.; Sceffer, J. J. C.; Verpoorte, R.; Comparative study of the essential oils from hops of various Humulus lupulus L. cultivars. Flavour Fragrance J. 1989, 4, 187-191.
    • (1989) Flavour Fragrance J. , vol.4 , pp. 187-191
    • Katsiotis, S.T.1    Langezaal, C.R.2    Sceffer, J.J.C.3    Verpoorte, R.4
  • 20
    • 0000023711 scopus 로고
    • Extractives from New Zealand honeys. 5. Aliphatic dicarboxylic acids in New Zealand rewarewa (Knightea excelsa) honey
    • Wilkins, A. L.; Lu, Y.; Tan, S. T. Extractives from New Zealand honeys. 5. Aliphatic dicarboxylic acids in New Zealand rewarewa (Knightea excelsa) honey. J. Agric. Food Chem. 1995, 43, 3021-3025.
    • (1995) J. Agric. Food Chem. , vol.43 , pp. 3021-3025
    • Wilkins, A.L.1    Lu, Y.2    Tan, S.T.3
  • 21
    • 0000207195 scopus 로고
    • Molecular and crystal structure of hyptolide, a naturally occurring α,β-unsaturated δ-lactone
    • Achmad, S.; Høyer, T.; Kjær, A.; Makmur, L.; Norrestam, R. Molecular and crystal structure of hyptolide, a naturally occurring α,β-unsaturated δ-lactone. Acta Chem. Scand. 1987, 41, 599-609.
    • (1987) Acta Chem. Scand. , vol.41 , pp. 599-609
    • Achmad, S.1    Høyer, T.2    Kjær, A.3    Makmur, L.4    Norrestam, R.5
  • 22
    • 33751385689 scopus 로고
    • Diastereoselectivity (enantioselectivity) of aldol condensations catalyzed by rabbit muscle aldolase at c-2 of RCHOHCHO if R has an appropriately placed negatively charged group
    • Lees, W. J.; Whitesides, G. M. Diastereoselectivity (enantioselectivity) of aldol condensations catalyzed by rabbit muscle aldolase at c-2 of RCHOHCHO if R has an appropriately placed negatively charged group. J. Org. Chem. 1993, 58, 1887-1894.
    • (1993) J. Org. Chem. , vol.58 , pp. 1887-1894
    • Lees, W.J.1    Whitesides, G.M.2
  • 23
    • 0009148211 scopus 로고
    • New synthesis of royal jelly acid
    • Chiron, R. New synthesis of royal jelly acid. J. Chem. Ecol. 1982, 8, 709-713.
    • (1982) J. Chem. Ecol. , vol.8 , pp. 709-713
    • Chiron, R.1
  • 24
    • 0031839039 scopus 로고    scopus 로고
    • Reductive cleavage of 2,2,2-trichloroethyl esters with sodium telluride
    • Blay, G.; Gardona, L.; Garcia, B.; Garcia, C. L.; Pedro, J. R. Reductive cleavage of 2,2,2-trichloroethyl esters with sodium telluride. Synth. Commun. 1998, 28, 1405-1414.
    • (1998) Synth. Commun. , vol.28 , pp. 1405-1414
    • Blay, G.1    Gardona, L.2    Garcia, B.3    Garcia, C.L.4    Pedro, J.R.5
  • 25
    • 0028844797 scopus 로고
    • Insect pheromone synthesis using Mn-salen catalysed asymmetric epoxidation as a key step
    • Hamada, T.; Daikai, K.; Irie, R.; Katsuki, T. Insect pheromone synthesis using Mn-salen catalysed asymmetric epoxidation as a key step. Tetrahedron Asymm. 1995, 6, 2441-2451.
    • (1995) Tetrahedron Asymm. , vol.6 , pp. 2441-2451
    • Hamada, T.1    Daikai, K.2    Irie, R.3    Katsuki, T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.