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1 .     sodium 1¦Â,2¦Â,3¦Â,4¦Â,5¦Â-tetrahydroxy-(25R)-5¦Â-spirostan-4¦Â-yl sulfate
C27H43O10S     ÏàËÆ¶È:62.9%
Chemical & Pharmaceutical Bulletin          1994          42          926-931
Steroidal Constituents from the Underground Parts of Reineckea carnea and Their Inhibitory Activity on cAMP Phosphodiesterase
Toshihiro KANMOTO,Yoshihiro MIMAKI,Yutaka SASHIDA,Tamotsu NIKAIDO,Kazuo KOIKE and Taichi OHMOTO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     sodium 1¦Â,2¦Â,3¦Â,4¦Â,5¦Â-tetrahydroxy-(25R)-5¦Â-spirostan-4¦Â-yl sulfate
C27H43O10S     ÏàËÆ¶È:62.9%
Chemical & Pharmaceutical Bulletin          1994          42          926-931
Steroidal Constituents from the Underground Parts of Reineckea carnea and Their Inhibitory Activity on cAMP Phosphodiesterase
Toshihiro KANMOTO,Yoshihiro MIMAKI,Yutaka SASHIDA,Tamotsu NIKAIDO,Kazuo KOIKE and Taichi OHMOTO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     ajugamarin F2
C27H40O8     ÏàËÆ¶È:62.9%
Chemical & Pharmaceutical Bulletin          1989          37          988-992
Neo-clerodane Diterpenes from Ajuga ciliata var. villosior
Hiroko SHIMOMURA,Yutaka SASHIDA and Kazunori OGAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     anzurogenin A
    ÏàËÆ¶È:62.9%
Chemistry of Natural Compounds          1989          25          431-435
STEROIDS OF THE SPIROSTAN AND FUROSTAN SERIES FROM PLANTS OF THE GENUS Allium.XXVI. STRUCTURE OF ANZUROGENIN AND ANZUROSIDE FROM THE COLLECTIVE FRUITS OF Allium suvorovii AND Allium stipitatum
Yu. S. Vollerner, S. D. Kravets,A. S. Shashkov, M. B. Gorovits,and N. K. Abubakirov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     Anzurogenin A
    ÏàËÆ¶È:62.9%
Chemistry of Natural Compounds          1988          24          58-62
STEROIDS OF THE SPIROSTAN AND FUROSTAN SERIES FROM PLANTS OF THE GENUS Allium. STRUCTURE OF ANZUROGENIN A FROM Allium suvorovii AND A. stipitatum
Yu. S. Vollerner, S. D. Kravits, A. S. Shashkov,M. B. Gorovits, and N. K. Abubakirov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (25R)-5¦Á-spirostan-2¦Á,3¦Â,5¦Á,6¦Á-tetraol 2-O-¦Â-D-glucopyranoside aglycone
C27H44O6     ÏàËÆ¶È:62.9%
Phytochemistry          1991          30          3063-3067
Steroidal saponins from Allium giganteum and A. aflatunense
Kazuhiro Kawashima, Yoshihiro Mimaki, Yutaka Sashida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     polygalasterol A
C27H48O7S     ÏàËÆ¶È:62.9%
Natural Product Communications          2012          7          1165-1168
A Novel Sterol Sulfate and New Oligosaccharide Polyester from the Aerial Parts of Polygala sibirica
Yue Lin Song, Si Xiang Zhou, He Lin Wei, Yong Jiang and Peng Fei Tu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     ajugamarin F1
C25H38O7     ÏàËÆ¶È:61.5%
Chemical & Pharmaceutical Bulletin          1989          37          988-992
Neo-clerodane Diterpenes from Ajuga ciliata var. villosior
Hiroko SHIMOMURA,Yutaka SASHIDA and Kazunori OGAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (3RS,5RS,8RS)-4-[ (2H3)Methyl]-4,5,8-trimethyl-1-oxaspiro[2.5]octane
    ÏàËÆ¶È:61.5%
Helvetica Chimica Acta          2009          92          1782-1799
Synthesis of Deuterium-Labeled Perfume Ingredients as Internal Standards for Their GC/MS Quantification
Christian Chapuis, Carole Cantatore, Peter Fankhauser, Ren¨¦ Challand, Jean-Jacques Riedhauser
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     compound 11
    ÏàËÆ¶È:61.5%
Biochemical Systematics and Ecology          2013          51          171-174
Chemical constituents from Chonemorpha griffithii
Jun-Qi Bai, Kun Jiang, Jun-Jie Tan, Xiao-Hui Qiu, Chang-Heng Tan, Jun Chang, Da-Yuan Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     17¦Â-(2',5'-Dihydro-5'-oxo-3'-furyl)-5¦Á-androstane-3¦Â,5,6¦Â,17-tetrol 6-acetate
C26H36O7     ÏàËÆ¶È:61.5%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     1¦Á,2¦Á,3¦Â-trihydroxyl-olean-12- en-28-oic acid
C30H48O5     ÏàËÆ¶È:60%
Chinese Chemical Letters          2002          13          345-348
Two New Pentacyclic Triterpenes from Sabia parviflora
Jin CHEN, Bin CHEN, Jun TIAN, Feng E WU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     (25R)-3¦Â -(t-Butyldimethylsilyloxy)-5¦Á-spirostane-5,6¦Â -diol
C33H58SiO5     ÏàËÆ¶È:60%
Steroids          2006          71          2010-1-11
Novel 5¦Â-hydroxyspirostan-6-ones ecdysteroid antagonists: Synthesis and biological testing
Daniel G. Rivera, Fredy Le¨®n, Francisco Coll, Gema P. Davison
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     (25¦Á)-5¦Á-spirostane-2¦Á,3¦Â,6¦Á-triol
    ÏàËÆ¶È:59.2%
Journal of Natural Products          1999          62          194-197
Steroidal Glycosides from the Bulbs of Allium jesdianum
Yoshihiro Mimaki, Minpei Kuroda, Tetsuichi Fukasawa, and Yutaka Sashida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     agigenin
    ÏàËÆ¶È:59.2%
Journal of Natural Products          1997          60          1003-1007
Porrigenins A and B, Novel Cytotoxic and Antiproliferative Sapogenins Isolated from Allium porrum
Alfonso Carotenuto, Ernesto Fattorusso, Virginia Lanzotti, Silvana Magno, Vincenzo De Feo, Rosa Carnuccio, and Fulvio D¡¯Acquisto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     2¦Â,12¦Â-dihydroxy-(25R)-spirosta-4,7-dien-3-one
C27H38O5     ÏàËÆ¶È:59.2%
Journal of Natural Products          1997          60          1017-1022
Antiprotozoal Compounds from Asparagus africanus
H. A. Oketch-Rabah and S. F. Dossaji
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     ajugamarin F3
    ÏàËÆ¶È:59.2%
Chemical & Pharmaceutical Bulletin          1989          37          988-992
Neo-clerodane Diterpenes from Ajuga ciliata var. villosior
Hiroko SHIMOMURA,Yutaka SASHIDA and Kazunori OGAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     compound I'
    ÏàËÆ¶È:59.2%
Acta Botanica Sinica          1999          41          1249-1251
Steroidal saponins from Speirantha gardenii
Chen Meng-jing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     Ajugamarin F3
    ÏàËÆ¶È:59.2%
Phytochemical Analysis          2002          13          372-380
NMR shift data of neo-clerodane diterpenes from the genus Ajuga
Josep Coll
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     wattigenin B
C27H44O9     ÏàËÆ¶È:59.2%
Acta Botanica Sinica          2003          45          626-629
Polyhydroxylated Steroidal Sapogenins from Tupistra wattii
SHEN Ping, WANG San-Long, YANG Chong-Ren, CAI Bing, YAO Xin-Sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     kitigenin
    ÏàËÆ¶È:59.2%
Acta Botanica Sinica          2003          45          626-629
Polyhydroxylated Steroidal Sapogenins from Tupistra wattii
SHEN Ping, WANG San-Long, YANG Chong-Ren, CAI Bing, YAO Xin-Sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     Ophiogenin
C27H42O7S     ÏàËÆ¶È:59.2%
Fitoterapia          2013          85          57-63
Chemical constituents from the fibrous root of Ophiopogon japonicus, and their effect on tube formation in human myocardial microvascular endothelial cells
Shen Lan, Feng Yi, Lian Shuang, Wang ChenJie, Xiang-Wei Zheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     compound 31
    ÏàËÆ¶È:59.2%
Magnetic Resonance in Chemistry          1995          33          923-953
NMR spectroscopy of steroidal sapogenins and steroidal saponins: An update
Pawan K. Agrawal, Dharam C. Jain and Ashish K. Pathak
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     21,23-dihydro-23-hydroxy-21-oxodeacetylnomilin
C26H32O10     ÏàËÆ¶È:57.6%
Journal of Natural Products          2006          69          1177-1179
Chemical Constituents from the Peels of Citrus sudachi
Hiroyuki Nakagawa, Yoshihisa Takaishi, Naonobu Tanaka,Koichiro Tsuchiya, Hirofumi Shibata, and Tomihiko Higuti
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     lupulin B
C30H46O10     ÏàËÆ¶È:57.6%
Journal of Natural Products          1996          59          668-670
Antibacterial Neoclerodane Diterpenoids from Ajuga lupulina
Hao Chen, Ren Xiang Tan, Zhi Li Liu, and Yong Zhang, Li Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     4¦Â,5¦Â-Epoxy-17,21-dihydroxy-A-homo-4-oxapregnan-3,20-dione
C22H32O7     ÏàËÆ¶È:57.6%
Steroids          2006          71          116-119
Steroidal seven-membered A-ring epoxy lactones by oxidation of the corresponding ¦¤4-3-ketosteroids
Maria L. Di Gioia, Antonella Leggio, Adolfo Le Pera, Francesca Perri, Andrea F. Pitrelli, Angelo Liguori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     4¦Á,5¦Á-Epoxy-17,21-dihydroxy-A-homo-4-oxapregnan-3,20-dione
C22H32O7     ÏàËÆ¶È:57.6%
Steroids          2006          71          116-119
Steroidal seven-membered A-ring epoxy lactones by oxidation of the corresponding ¦¤4-3-ketosteroids
Maria L. Di Gioia, Antonella Leggio, Adolfo Le Pera, Francesca Perri, Andrea F. Pitrelli, Angelo Liguori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     compound 7
    ÏàËÆ¶È:57.6%
Journal of Natural Products          1990          Vol 53          830
Structure and In Vitro Antiviral Activity of Sesquiterpene Glycosides from Calendula arvensis
Nunziatina De Tommasi, Cosimo Pizza, Cinzia Conti, Nicola Orsi, Maria Luisa Stein
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     compound-3
    ÏàËÆ¶È:57.6%
Phytochemistry          1988          27          2205-2208
Sesquiterpene glycosides based on the alloaromaden-drane skeleton from Calendula arvensis
Cosimo Pizza,Nunziatina De Tommasi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     27-nor-5¦Á-cholestane-3¦Â,4¦Â,5,6¦Á,8,14,15¦Á,24¦Á-octaol
    ÏàËÆ¶È:57.6%
Journal of the Chemical Society, Perkin Transactions 1          1986                   665-670
Highly hydroxylated marine steroids from the starfish Archaster typicus
Raffaele Riccio, Olinda Squillace Greco, Luigi Minale, Dominique Laurent and Daniel Duhet
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     (3S,5S,8R,9S,10S,13S,14S,17S)-3-{[tert-butyl(dimethyl)silyl]oxy}-10,13-dimethyloctadecahydrospiro [cyclopenta[a]phenanthrene-17,2'-pyran]-6'(3'H)-one
    ÏàËÆ¶È:57.6%
Molecules          2013          18          914-933
Synthesis of 5¦Á-Androstane-17-spiro-¦Ä-lactones with a 3-Keto, 3-Hydroxy, 3-Spirocarbamate or 3-Spiromorpholinone as Inhibitors of 17¦Â-Hydroxysteroid Dehydrogenases
Guy Bertrand Djigou¨¦, B¨¦atrice Tch¨¦dam Ngatcha, Jenny Roy and Donald Poirier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     (25R)-3-oxa-6¦Â-acetoxy-5-hydroxy-4a-homo-5¦Á-spirostan-4-one
C29H44NaO7     ÏàËÆ¶È:57.1%
Steroids          2007          72          466-473
Studies on the regioselectivity of the Baeyer-Villiger reaction of 3-keto steroids: Conformational effects determine the migration aptitude
Daniel G. Rivera, Orlando Pando, Reynier Suardiaz, Francisco Coll
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     Compound 9a
    ÏàËÆ¶È:57.1%
Journal of Natural Products          1995          58          653-671
Chemical and Biological Investigation of the Polar Constituents of the Starfish Luidia clathrata, Collected in the Gulf of Mexico
Maria Iorizzi, Patrick Bryan, James McClintock, Luigi Minale, Elio Palagiano, Stefano Maurelli, Raffaele Riccio, Franco Zollo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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