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΢Æ×ÇóÖú£¬Ð»Ð»£¡ ÒÑÓÐ1È˲ÎÓë
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| 13C NMR (151 MHz, CDCl3) ¦Ä 14.11, 16.04, 22.71, 27.77, 28.24, 29.29, 29.43, 29.61, 29.70, 29.75, 29.83, 29.85, 29.90, 29.94, 31.96, 32.58, 32.72, 39.85, 40.82, 53.36, 72.99, 73.30, 76.04, 102.98, 123.25, 126.64, 128.61, 133.98, 134.33, 135.93, 174.68. |
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·çÐÅ×Ó0208: ½ð±Ò+10, ¡ïÓаïÖú 2015-06-26 17:07:38
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·çÐÅ×Ó0208: ½ð±Ò+10, ¡ïÓаïÖú 2015-06-26 17:07:38
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1 . (2S,2'R,3R,3'E,4E,8E)-1-O-¦Â-D-glucopyranosyl-2-N-(2'-hy-droxy-3'-octadecenoyl)-3-hydroxy-9-methyl-4,8-sphingadienine C43H79NO9 ÏàËÆ¶È:65.6% Lipids 2004 39 667-673 Antibacterial and xanthine oxidase inhibitory cerebrosides from Fusarium sp. IFB-121, and endophytic fungus in Quercus variabilis R. G. Shu, F. W. Wang, Y. M. Yang, Y. X. Liu and R. X. Tan Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Chrysogeside E C41H77NO9 ÏàËÆ¶È:65.6% Journal of Natural Products 2011 74 1298-1302 Cerebrosides and 2-Pyridone Alkaloids from the Halotolerant Fungus Penicillium chrysogenum Grown in a Hypersaline Medium Xiaoping Peng, Yi Wang, Kunlai Sun, Peipei Liu, Xia Yin, and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Chrysogeside D C43H79NO9 ÏàËÆ¶È:64.7% Journal of Natural Products 2011 74 1298-1302 Cerebrosides and 2-Pyridone Alkaloids from the Halotolerant Fungus Penicillium chrysogenum Grown in a Hypersaline Medium Xiaoping Peng, Yi Wang, Kunlai Sun, Peipei Liu, Xia Yin, and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . N-palmitoyl-D-erythro-(2S,3R)-17-methyl-octadecasphinga-4(E),8(E)-dienine C35H67NO3 ÏàËÆ¶È:64.5% Journal of Natural Products 1995 Vol 58 948-953 Isolation of New Ceramides from the Gorgonian Acabaria undulata Jongheon Shin, Youngwan Seo Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 2-dodecanyl-7-b isopranyl monoscodilone C28H42O4 ÏàËÆ¶È:64.5% Natural Product Research 2013 27 1848-1855 Five new secondary metabolites from Monascus purpureus-fermented Hordeum vulgare and Sorghum bicolor Md. Pravej Ansari, Alka Puri, M. Ali & Bibhu Prasad Panda Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . cerebroside B C41H77NO9 ÏàËÆ¶È:63.6% Chinese Traditional and Herbal Drugs 2004 35 493-495 È˹¤Ó¼³æ²Ý»¯Ñ§³É·ÖÑо¿ Íõ¸Õ,Âé±ø¼Ì,Áõ¼ª¿ª Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . arenosclerin A C32H55N2O ÏàËÆ¶È:62.5% Journal of Natural Products 2000 63 1098-1105 Arenosclerins A-C and Haliclonacyclamine E, New Tetracyclic Alkaloids from a Brazilian Endemic Haplosclerid Sponge Arenosclera brasiliensis Yohandra R. Torres, Roberto G. S. Berlinck, Alvicl¨¦r Magalhães, Alexandre B. Schefer, Antonio G. Ferreira, Eduardo Hajdu, and Guilherme Muricy Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Cerebroside C ÏàËÆ¶È:62.5% European Food Research and Technology 2014 239 365−376 A new glucitol from an endophytic fungus Fusarium equiseti Salicorn 8 Hui Wang, Tianxing Liu, Zhihong Xin Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . alternaroside B C42H77NO9 ÏàËÆ¶È:61.2% Journal of Natural Products 2009 72 1695-1698 Cerebrosides of the Halotolerant Fungus Alternaria raphani Isolated from a Sea Salt Field Wenliang Wang, Yi Wang, Hongwen Tao, Xiaoping Peng, Peipei Liu, and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (2S,3R,4E,8E,9'Z,12'Z)-N-9',12'-Octadecadienoyl-2-amino-9-methyl-4,8-octadecadiene-1,3-diol C37H67NO3 ÏàËÆ¶È:61.2% Chemical & Pharmaceutical Bulletin 2002 50(5) 681-684 Ceramide Constituents from Five Mushrooms Yasunori YAOITA, Rie KOHATA, Rie KAKUDA, Koichi MACHIDA, and Masao KIKUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . N-palmitoyl-octadecasphinga-4(E),8(E)-dienine C34H65NO3 ÏàËÆ¶È:61.2% Journal of Natural Products 1995 Vol 58 948-953 Isolation of New Ceramides from the Gorgonian Acabaria undulata Jongheon Shin, Youngwan Seo Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ceramide ÏàËÆ¶È:61.2% Indian Journal of Chemistry Section B 2007 46B 1868-1872 Antifungal and phytochemical studies of Eupatorium birmanicum DC. Devi,L Reena; Singh,Th Shyamkeshor; Laitonjam,Warjeet S Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 5,13-Dimethyl-5-heptadecen-1-ol ÏàËÆ¶È:61.2% Bioscience, Biotechnology, and Biochemistry 2009 73 1618-1622 Synthesis and Field Evaluation of Methyl-branched Ketones, Sex Pheromone Components Produced by Lithosiinae Female Moths in the Family of Arctiidae Nguyen Duc DO, Masakatsu KINJO, Tomonori TAGURI, Yasushi ADACHI, Rei YAMAKAWA and Tetsu ANDO Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . phytoceramide C36H71NO4 ÏàËÆ¶È:61.2% Molecules 2011 16 9090-9100 Phytoceramide Shows Neuroprotection and Ameliorates Scopolamine-Induced Memory Impairment Jae-Chul Jung, Yeonju Lee, Sohyeon Moon, Jong Hoon Ryu and Seikwan Oh Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . bullatenicin C37H66O5 ÏàËÆ¶È:61.2% Natural Toxins 1992 1 4-14 Bullatencin, 4-deoxyasimicin, and the uvariamicins: Additional bioactive annonaceous acetogenins from Annona bullata rich. (Annonaceae) Yu-Hua Hui, Karl V. Wood and Jerry L. McLaughlin Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 2-n-undecanyloxo-7-b-isoprenylankaflavin C29H48O5 ÏàËÆ¶È:61.2% Natural Product Research 2013 27 1848-1855 Five new secondary metabolites from Monascus purpureus-fermented Hordeum vulgare and Sorghum bicolor Md. Pravej Ansari, Alka Puri, M. Ali & Bibhu Prasad Panda Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 3b C55H80N4O3Se2 ÏàËÆ¶È:61.2% The Journal of Organic Chemistry 2012 77 10931-10937 Easily Reducible Materials from the Reactions of Diselenopheno[3,2-b:2¡ä,3¡ä-d]pyrrole and Dithieno[3,2-b:2¡ä,3¡ä-d]pyrrole with Tetracyanoethylene Yulia A. Getmanenko, Thomas A. Purcell, Do Kyung Hwang, Bernard Kippelen, and Seth R. Marder Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . urticifolene C31H52O4 ÏàËÆ¶È:61.2% Journal of Medicinal Plants Research 2011 5 4202-4211 Novel polyene from Vernonia urticifolia (Asteraceae) J. J. Kiplimo, C. A. Everia and N. A. Koorbanally Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . compound 4 C37H64O6 ÏàËÆ¶È:60.6% Journal of Natural Products 2007 70 300-303 Biogenetic Relationships between Annonaceous Acetogenins: Squamocin Is Not a Precursor of Chamuvarinin Based on a Semisynthetic Study S¨¦verine Derbr¨¦, Erwan Poupon, Christophe Gleye, and Reynald Hocquemiller Structure 13C NMR ̼Æ×Ä£Äâͼ |
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