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1 .     (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:68.7%
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   Ì¼Æ×Ä£Äâͼ

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2 .     N-palmitoyl-D-erythro-(2S,3R)-17-methyl-octadecasphinga-4(E),8(E)-dienine
C35H67NO3     ÏàËÆ¶È:65.6%
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   Ì¼Æ×Ä£Äâͼ

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3 .     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   Ì¼Æ×Ä£Äâͼ

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4 .     5,13-Dimethyl-5-heptadecen-1-ol
    ÏàËÆ¶È:62.5%
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   Ì¼Æ×Ä£Äâͼ

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5 .     ingenol-20-myristinate
C34H54O6     ÏàËÆ¶È:61.7%
Chinese Traditional and Herbal Drugs          2005          36          1763-1767
Ingenane diterpene ester constituents from Tibetan medicine Euphorbia wallichii
LI Yu-lin; SUO You-rui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     (4E,8E)-2-N-(2 -Hydroxypalmitoyl)-1-O-(¦Â-D-glucopyranosyl)-9-methyl-4,8-sphingadienine
    ÏàËÆ¶È:59.3%
Helvetica Chimica Acta          2004          Vol. 87          1912
Vibratilicin: a Novel Compound from the Basidiomycete Cortinarius vibratilis
Fei Wang, Jian-Wen Tan, and Ji-Kai Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     haliclonacyclamine E
C32H55N2     ÏàËÆ¶È:59.3%
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   Ì¼Æ×Ä£Äâͼ

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8 .     compound 12
C37H67O4     ÏàËÆ¶È:59.3%
Journal of Natural Products          1997          60          1251-1260
New Acylated Sulfoglycolipids and Digalactolipids and Related Known Glycolipids from Cyanobacteria with a Potential To Inhibit the Reverse Transcriptase of HIV-1
Vered Reshef, Erez Mizrachi, Tal Maretzki, Colin Silberstein, Shoshana Loya, Amnon Hizi, and Shmuel Carmeli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     N-palmitoyl-octadecasphinga-4(E),8(E)-dienine
C34H65NO3     ÏàËÆ¶È:59.3%
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   Ì¼Æ×Ä£Äâͼ

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10 .     N-palmitoyl-D-erythro-(2S,3R)-octadecasphinga-4(E),8(E),10(E)-trienine
C34H63NO3     ÏàËÆ¶È:59.3%
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   Ì¼Æ×Ä£Äâͼ

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11 .     Chrysogeside E
C41H77NO9     ÏàËÆ¶È:59.3%
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   Ì¼Æ×Ä£Äâͼ

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12 .     (2S,3R,4E,8E)-[(2'R)-2'-hydroxyheptadecanoylamino]-4,8-octadecadiene-1,3-diol
C35H67NO4     ÏàËÆ¶È:57.5%
Chemical & Pharmaceutical Bulletin          2005          53(2)          168-171
New Sphingolipids and a Sterol from a Lobophytum Species of the Indian Ocean
Pendyala MURALIDHAR, Muthyala Muralikrishna KUMAR,Nallamothu KRISHNA,Chaganty Bheemasankara RAO, and Desaraju Venkata RAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     compound 4
    ÏàËÆ¶È:57.1%
Tetrahedron Letters          2002          43          9641-9644
Facile transformation of 2-azetidinones to unsaturated ketones: application to the formal synthesis of sphingosine and phytosphingosine
Hyeon Kyu Lee, Eun-Kyung Kim, Chwang Siek Pak
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     compound 7
    ÏàËÆ¶È:56.2%
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   Ì¼Æ×Ä£Äâͼ

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15 .     asimin
    ÏàËÆ¶È:56.2%
Journal of Natural Products          1999          62          1123-1127
Total Synthesis of the Cytotoxic Threo, Trans, Threo, Trans, Threo Annonaceous Acetogenin Asimin and Its C-10 Epimer: Unambiguous Confirmation of Absolute Stereochemistry
James A. Marshall and Hongjian Jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     farnesyl oleate
C33H58O2     ÏàËÆ¶È:56.2%
Phytochemistry          1994          36          1203-1207
Formation of farnesyl oleate and three other farnesyl fatty acid esters by cell-free extracts from Botryococcus braunii B race
Hitoshi Inoue, Tatsumi Korenaga, Hiroshi Sagami, Tanetoshi Koyama, Hiroshi Sugiyama, Kyozo Ogura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     farnesyl palmitate
C31H56O2     ÏàËÆ¶È:56.2%
Phytochemistry          1994          36          1203-1207
Formation of farnesyl oleate and three other farnesyl fatty acid esters by cell-free extracts from Botryococcus braunii B race
Hitoshi Inoue, Tatsumi Korenaga, Hiroshi Sagami, Tanetoshi Koyama, Hiroshi Sugiyama, Kyozo Ogura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     benzyloxybenzoic acid 2,3-bis-hexadecanoyloxypropyl esters(b)
    ÏàËÆ¶È:56.2%
Canadian Journal of Chemistry          2006          84          1411-1415
Synthesis and characterization of a series of novel phenol- and polyphenol-based glycerolipids1
Rolf Schmidt, Joseph G. Carrigan, and Christine E. DeWolf
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     2-nitro-3,4,4-trichloro-1-(octadecylthio)-1-[4-(diphenylmethyl)piperazin-1-yl]-1,3-butadiene
C39H56N3O2S1Cl3     ÏàËÆ¶È:56.2%
Indian Journal of Chemistry          2008          47B          1407-1413
The reactions of polyhalogenated-2-nitro-1,3-butadiene with alkylthio,thiomorpholine and piperazine derivatives
Ibis,Cemil; Deniz,N Gulsah
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     ceramide
    ÏàËÆ¶È:56.2%
Indian Journal of Chemistry          2007          46B          1868-1872
Antifungal and phytochemical studies of Eupatorium birmanicum DC.
Devi,L Reena; Singh,Th Shyamkeshor; Laitonjam,Warjeet S
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     4-benzyloxy-6-[2-(dimethylamino)ethoxy]-3-dodecyl-2-methylquinoline N,N'-dioxide
C33H48N2O4     ÏàËÆ¶È:56.2%
Heterocycles          2010          82          377-396
Synthesis of Novel 1-Hydroxyquinolones with High Anti-Toxoplasma Activity
Lutz F. Tietze and Ling Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     amphidinol 2
    ÏàËÆ¶È:56.2%
Bioorganic & Medicinal Chemistry Letters          2004          14          3117-3120
Lingshuiol, a novel polyhydroxyl compound with strongly cytotoxic activity from the marine dinoflagellate Amphidinium sp
Xiao-Chun Huang, Di Zhao, Yue-Wei Guo, Hou-Ming Wu, Li-Ping Lin, Zhong-Hua Wang, Jian Ding, Yong-Shui Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     compound (2S,3R,4E,6R)-2
56H104NO9     ÏàËÆ¶È:56.2%
Tetrahedron Letters          2003          44          9197-9200
Synthesis and stereochemistry of ceramide B, (2S,3R,4E,6R)-N-(30-hydroxytriacontanoyl)-6-hydroxy-4-sphingenine, a new ceramide in human epidermis
Kenji Mori, Yui Masuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     compound 3
C36H66O6     ÏàËÆ¶È:56.2%
Tetrahedron Letters          2005          46          5775-5779
Synthesis of non-THF analogs of acetogenin toward simplified mimics
Daisuke Fujita, Naoya Ichimaru, Masato Abe, Masatoshi Murai, Takeshi Hamada, Takaaki Nishioka, Hideto Miyoshi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     compound 4
C36H66O6     ÏàËÆ¶È:56.2%
Tetrahedron Letters          2005          46          5775-5779
Synthesis of non-THF analogs of acetogenin toward simplified mimics
Daisuke Fujita, Naoya Ichimaru, Masato Abe, Masatoshi Murai, Takeshi Hamada, Takaaki Nishioka, Hideto Miyoshi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     3,3'''-Didodecyl-5-methyl-2,2':5',2'':5'',2'''-quaterthiophene
C41H60S4     ÏàËÆ¶È:56.2%
Tetrahedron          2012          68          349-355
Quaterthiophene-based dimers containing an ethylene bridge: molecular design, synthesis, and optoelectronic properties
Maud Jenart, Claude Niebel, Jean-Yves Balandier, Julie Leroy, Alix Mignolet, Sara Stas, Antoine Van Vooren, J¨¦rôme Cornil, Yves Henri Geerts
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     compound 1a
    ÏàËÆ¶È:56.2%
Russian Chemical Bulletin          2001          50          1474-1477
Glycosphingolipid with a branched sphingosine base from soft corals from the Andaman Islands
A. S. Dmitrenok, V. Anjaneyulu, P. V. Subba Rao, P. Radhika and P. S. Dmitrenok, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     (4E,8E)-N-D-2'-hydroxydocosanoyl-1-O-¦Â-D-glycopyranosyl-9-methyl-4,8-sphingadienine
    ÏàËÆ¶È:56.2%
Natural Product Research and Development          2009          21          919-921
Chemical Ingredient Studies on the Soft Coral Sinularia robusta macfadyen
HE Xi-Xin;LV Yang; ZHENG Qi-Tai; ZENG Long-Mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     dideoxypetrosynol B
C30H42O2     ÏàËÆ¶È:56.2%
Tetrahedron          1998          54          3151-3158
New bioactive polyacetylenes from the marine sponge Petrosia sp.
Jung S. Kim, Kwang S. Im, Jee H. Jung, Young-L. Kim, Jinwoong Kim, Chung J. Shim, Chong-O. Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     dideoxypetrosynol C
C30H42O2     ÏàËÆ¶È:56.2%
Tetrahedron          1998          54          3151-3158
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