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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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |
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