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1 .     Compound 1
C21H43N2O5PS     ÏàËÆ¶È:57.6%
Bioorganic & Medicinal Chemistry Letters          2005          15          2141-2144
Synthesis of sphingomyelin sulfur analogue and its behavior toward sphingomyelinase
Toshikazu Hakogi, Shinobu Fujii, Michio Morita, Kiyoshi Ikeda, Shigeo Katsumura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     compound 9
C23H30ClNO5     ÏàËÆ¶È:56.5%
Journal of the Chemical Society, Perkin Transactions 1          1998                   3585-3599
Absolute stereostructures of novel cytotoxic metabolites, gymnastatins A¨CE, from a Gymnascella species separated from a Halichondria sponge
Taro Amagata, Mitsunobu Doi, Takatoshi Ohta, Katsuhiko Minoura and Atsushi Numata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     aranochlor B
C23H32ClNO5     ÏàËÆ¶È:56.5%
The Journal of Antibiotics          1998          51          439-441
Aranochlor A and Aranochlor B, Two New Metabolites from Pseudoarachniotus roseus: Production, Isolation, Structure Elucidation and Biological Properties
TRIPTIKUMAR MUKHOPADHYAY, R. G. BHAT, KIRITY ROY, E. K. S. VIJAYAKUMAR, B. N. GANGULI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     callicarpic acid
C20H28O4     ÏàËÆ¶È:56.5%
Journal of Asian Natural Products Research          2013          15          30-34
Two new ent-3,4-seco-labdane diterpenoids from Callicarpa nudiflora
Lin Dong, Xiao-Po Zhang, Ming-Sheng Liu, Yan-Mei Li, Jin-Hui Wang & Yi Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     capsaicin 4-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:54.1%
Phytochemistry          2007          68          1391-1396
Glycosylation of capsaicin and 8-nordihydrocapsaicin by cultured cells of Catharanthus roseus
Kei Shimoda, Soonil Kwon, Akiko Utsuki, Shingo Ohiwa, Hisashi Katsuragi,Naoko Yonemoto, Hatsuyuki Hamada, Hiroki Hamada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     gymnastatins H
C24H35NO4     ÏàËÆ¶È:52.1%
Journal of Natural Products          2006          69          1384-1388
Gymnastatins F−H, Cytostatic Metabolites from the Sponge-Derived Fungus Gymnascella dankaliensis
Taro Amagata, Katsuhiko Minoura, and Atsushi Numata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     kopsiloscine B
C23H28N2O6     ÏàËÆ¶È:52.1%
Journal of Natural Products          2007          70          1783-1789
Biologically Active Aspidofractinine, Rhazinilam, Akuammiline, and Vincorine Alkaloids from Kopsia
G. Subramaniam, Osamu Hiraku,Masahiko Hayashi, Takashi Koyano, Kanki Komiyama, and Toh-Seok Kam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     16,17-seco-3-Benzyloxy-13¦Á-estra-1,3,5(10),16-tetraen-17-al
C26H30O2     ÏàËÆ¶È:52.1%
Steroids          2003          68          277-288
Synthesis and receptor-binding examinations of the normal and 13-epi-D-homoestrones and their 3-methyl ethers
J¨¢nos Wölfling, Erzs¨¦bet Merny¨¢k, ¨¦va Frank, George Falkay, ¨¢rp¨¢d M¨¢rki, Ren¨¢ta Minorics, Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     3-Hydroxy-1,3,5(10)-estratriene-17 ¦Â-O,17¦Á -pentanolactone
C23H30O3     ÏàËÆ¶È:52.1%
Steroids          2004          69          325-342
Inhibition of type 2 17¦Â-hydroxysteroid dehydrogenase by estradiol derivatives bearing a lactone on the D-ring: structure¨Cactivity relationships
Patrick Bydal, Serge Auger, Donald Poirier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     N(1)-methyl-14,15-didehydro-12-methoxyaspidofractinine
C21H26N2O     ÏàËÆ¶È:52.1%
Phytochemistry          1998          47          149-151
Indole alkaloids from aerial parts of Vinca sardoa
M. Nicoletti, M. Serafini, E. Federici, C. Galeffi, F. Poli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     isozonarol
C21H30O2     ÏàËÆ¶È:52.1%
Tetrahedron Letters          2000          41          5469-5473
Total synthesis of the marine sesquiterpene hydroquinones zonarol and isozonarol and the sesquiterpene quinones zonarone and isozonarone
Jörg Schröder, Christine Magg, Karlheinz Seifert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     compound 5a
C23H30Br2NO3     ÏàËÆ¶È:52.1%
Heterocycles          2010          81          897-907
Gymnastatins I-K, Cancer Cell Growth Inhibitors from a Sponge-Derived Gymnascella dankaliensis
Taro Amagata, Keiko Takigawa, Katsuhiko Minoura, and Atsushi Numata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     compound 8
    ÏàËÆ¶È:52.1%
Heterocycles          2010          81          897-907
Gymnastatins I-K, Cancer Cell Growth Inhibitors from a Sponge-Derived Gymnascella dankaliensis
Taro Amagata, Keiko Takigawa, Katsuhiko Minoura, and Atsushi Numata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     compound 10
C23H31Cl2NO5     ÏàËÆ¶È:52.1%
Journal of the Chemical Society, Perkin Transactions 1          1998                   3585-3599
Absolute stereostructures of novel cytotoxic metabolites, gymnastatins A¨CE, from a Gymnascella species separated from a Halichondria sponge
Taro Amagata, Mitsunobu Doi, Takatoshi Ohta, Katsuhiko Minoura and Atsushi Numata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     methylcallicarpate
C21H30O4     ÏàËÆ¶È:52.1%
Journal of Asian Natural Products Research          2013          15          30-34
Two new ent-3,4-seco-labdane diterpenoids from Callicarpa nudiflora
Lin Dong, Xiao-Po Zhang, Ming-Sheng Liu, Yan-Mei Li, Jin-Hui Wang & Yi Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     compound 17
C25H33Cl2NO6S     ÏàËÆ¶È:52%
Journal of the Chemical Society, Perkin Transactions 1          1998                   3585-3599
Absolute stereostructures of novel cytotoxic metabolites, gymnastatins A¨CE, from a Gymnascella species separated from a Halichondria sponge
Taro Amagata, Mitsunobu Doi, Takatoshi Ohta, Katsuhiko Minoura and Atsushi Numata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     dankastatin A
24H35Cl2NO5     ÏàËÆ¶È:50%
Journal of Natural Products          2008          71(3)          340-345
Gymnastatins and Dankastatins, Growth Inhibitory Metabolites of a Gymnascella Species from a Halichondria Sponge
Taro Amagata, Makoto Tanaka, Takeshi Yamada, Katsuhiko Minoura, and Atsushi Numata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     compound 12I
C26H30ClFN2O3     ÏàËÆ¶È:50%
Steroids          2006          71          558-564
Synthesis and stereochemical investigations of novel nitrogen-containing 13¦Á-estrone derivatives
Erzs¨¦bet Merny¨¢k, Gyula Schneider, Regine Herbst-Irmer, Melanie Kubas, J¨¢nos Wölfling
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     17-(N,N-3-oxapentan-1,5-diyl-carboxamido)-androst-5,16-diene-3-ethylene ketal
C26H37O4N     ÏàËÆ¶È:50%
Steroids          2011          76          280-290
Systematic investigation on the synthesis of androstane-based 3-, 11-and 17-carboxamides via palladium-catalyzed aminocarbonylation
P¨¦ter ¨¢cs, Attila Tak¨¢cs, Merc¨¦desz Kiss, No¨¦mi P¨¢link¨¢s, S¨¢ndor Mah¨®, L¨¢szl¨® Koll¨¢r
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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