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wangali526

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²éѯ½á¹û£º¹²²éµ½1053¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     wanpeinine A
    ÏàËÆ¶È:66.6%
Chinese Chemical Letters          1992          3          979-980
SIECHUANSINE,A NEW STEROIDAL ALKALOID FROM FRITILLARIA SIECHUANICA X.S.CHEN
FENG PENG WANG,RONG ZHANG,XIN YUE TANG AND JIAN ZHONG WANG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     compound 6
    ÏàËÆ¶È:66.6%
Phytochemistry          1988          27          1665-1668
Three ecdysteroid glycosides from Pfaffia iresinoides
Nobushige Nishimoto,Yoshinori Shiobara,Shun-suke Inoue,Masumi Fujino,Tsunematsu Takemoto,Cheow Lin Yeoh,Fernando de Oliveira,Gokithi Akisue,Maria Kubota Akisue,Goro Hashimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     tuboanosigenin p-Bromobenzoate
    ÏàËÆ¶È:65.6%
Chemical & Pharmaceutical Bulletin          2008          56(7)          1038-1040
New C28 Steroidal Glycosides from Tubocapsicum anomalum
Naoko KIYOTA,Kazushi SHINGU,Koki YAMAGUCHI,Yasuyuki YOSHITAKE,Kazunobu HARANO,Hitoshi YOSHIMITSU,Hiroyuki MIYASHITA,Tsuyoshi IKEDA,Chie TAGAWA,and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     spinogenin D3
    ÏàËÆ¶È:63.3%
Phytochemistry          1993          33          891-895
3-epi-Oleanene type triterpene glycosyl esters from leaves of Acanthopanax spinosus
Masazumi Miyakoshi, Yoshiteru Ida, Susumu Isoda, Junzo Shoji
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     3-O-[¦Á-L-rhamnopyranosyl(1¡ú2)-¦Â-D-glucopyranosyl(1¡ú4)-¦Â-D-glucuronopyranosyl]-soyasapogenol B
    ÏàËÆ¶È:63.3%
Acta Chimica Sinica          1987          45          145-149
Studies on the Chemical Components of Oxtropis ochrocephala Bunge II. The Structures of Two Triterpenoid Saponins
Sun Rong-Qi Cheng Dong-Liang Jia Zhong-JianZhu Zi-Qing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     etioline
    ÏàËÆ¶È:62.9%
Phytochemistry          1996          43          705-707
Steroidal alkaloids from roots of Solanum spirale
Helmut Ripperger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     verticine
    ÏàËÆ¶È:62.9%
Acta Pharmaceutica Sinica          1988          Vol 23          34-37
CHEMICAL STUDIES OF EPIMEDIUM WUSHANENSE T. S. YING
HR Liang; WM Yan; JS Li and CS Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     verticinone
C27H43N3O     ÏàËÆ¶È:62.9%
Acta Pharmaceutica Sinica          1988          Vol 23          415-421
ISOLATION AND IDENTIFICATION OF ALKALOIDS FROM FRITILLARIA NINGGUOENSIS S.C.CHEN ET S. F. YIN
QH Li; ZH Wu; LL Zhang and L Shao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     Solafloridine
C27H43NO     ÏàËÆ¶È:62.9%
Phytochemistry          1996          41          1629-1631
22, 26-epiminocholestane alkaloids with unusual (20R)-configurations from Solanum species
Helmut Ripperger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     ent-15¦Â-Senecioyloxy-16-en-kaur-19-oic acid
    ÏàËÆ¶È:62.9%
Phytochemistry          1993          32          1611-1613
An ent-kaurenolide from Stevia lucida
J.Manuel Amaro-Luis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     peiminine
    ÏàËÆ¶È:62.9%
Phytochemistry          1986          25          2008-2009
Two steroidal alkaloids from fritillaria harelinii
Min Zhi-da, Qian Jing-fang, Munekazu Iinuma, Toshiyuki Tanaka, Mizuo Mizuno
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     (22E)-5 ¦Á-cholest-22-ene-3¦Â,6¦Á,8,15¦Á,24-pentol
C27H46O5     ÏàËÆ¶È:62.9%
Russian Chemical Bulletin          1997          46          186-191
New polyhydroxysteroids and steroid glycosides from the far east starfishCeramaster patagonicus
A. A. Kicha, A. I. Kalinovsky and V. A. Stonik
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²éѯ½á¹û£º¹²²éµ½4294¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     wanpeinine A
    ÏàËÆ¶È:66.6%
Chinese Chemical Letters          1992          3          979-980
SIECHUANSINE,A NEW STEROIDAL ALKALOID FROM FRITILLARIA SIECHUANICA X.S.CHEN
FENG PENG WANG,RONG ZHANG,XIN YUE TANG AND JIAN ZHONG WANG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     compound 6
    ÏàËÆ¶È:66.6%
Phytochemistry          1988          27          1665-1668
Three ecdysteroid glycosides from Pfaffia iresinoides
Nobushige Nishimoto,Yoshinori Shiobara,Shun-suke Inoue,Masumi Fujino,Tsunematsu Takemoto,Cheow Lin Yeoh,Fernando de Oliveira,Gokithi Akisue,Maria Kubota Akisue,Goro Hashimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     podecdysone B
    ÏàËÆ¶È:66.6%
Russian Journal of Organic Chemistry          2003          39          952-956
Transformation of 20-Hydroxyecdysone Acetonides into Podecdysone B
V. N. Odinokov, I. V. Galyautdinov, D. V. Nedopekin, N. A. Ves'kina and L. M. Khalilov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     tuboanosigenin p-Bromobenzoate
    ÏàËÆ¶È:65.6%
Chemical & Pharmaceutical Bulletin          2008          56(7)          1038-1040
New C28 Steroidal Glycosides from Tubocapsicum anomalum
Naoko KIYOTA,Kazushi SHINGU,Koki YAMAGUCHI,Yasuyuki YOSHITAKE,Kazunobu HARANO,Hitoshi YOSHIMITSU,Hiroyuki MIYASHITA,Tsuyoshi IKEDA,Chie TAGAWA,and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (3¦Â,5¦Á)-20-hydroxy-6-oxocevan-3-yl acetate
C29H45NO4     ÏàËÆ¶È:65.5%
Chemistry & Biodiversity          2008          Vol. 5          259
Cytotoxic Alkaloids from the Bulbs of Fritillaria hupehensis
Yong-Hui Zhang, Xi-Liang Yang, Peng Zhang, Xue-Feng Zhou, Han-Li Ruan, Hui-Fang Pi, Ji-Zhou Wu, and Han-Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (2¦Â,3¦Â,4¦Á,5¦Á,8¦Â,11¦Â)-4-methylergosta-22,24(28)-diene- 2,3,8,11-tetrol
    ÏàËÆ¶È:65.5%
Helvetica Chimica Acta          2006          Vol. 89          1330
Two New Polyhydroxylated Steroids from the Hainan Soft Coral Sinularia sp.
Rui Jia, Yue-Wei Guo, Ernesto Mollo, Margherita Gavagnin, and Guido Cimino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     hyrtiosterol
C29H48O4     ÏàËÆ¶È:65.5%
Journal of Natural Products          2004          67          1736-1739
Hyrtiosenolides A and B, Two New Sesquiterpene ¦Ã-Methoxybutenolidesand a New Sterol from a Red Sea Sponge Hyrtios Species
Diaa T. A. Youssef, Abdel Nasser B. Singab, Rob W. M. van Soest, and Nobuhiro Fusetani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     Philadelphicalactone C
C28H40O8     ÏàËÆ¶È:64.2%
Steroids          2011          76          724-728
Philadelphicalactones C and D and other cytotoxic compounds from Physalis philadelphica
Emma Maldonado, Ana L. P¨¦rez-Castorena, Consuelo Garc¨¦s, Mahinda Mart¨ªnez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (24S)-24-ethyl-4¦Â-methyl-5¦Á-cholestan-3¦Â-ol
C30H52O     ÏàËÆ¶È:64.2%
Marine Drugs          2012          10          2448-2466
Preliminary Structure-Activity Relationship on Theonellasterol, a New Chemotype of FXR Antagonist, from the Marine Sponge Theonella swinhoei
Valentina Sepe, Raffaella Ummarino, Maria Valeria D'Auria, Orazio Taglialatela-Scafati, Simona De Marino, Claudio D'Amore, Barbara Renga, Maria Giovanna Chini, Giuseppe Bifulco, Yoichi Nakao, Nobuhiro Fusetani, Stefano Fiorucci and Angela Zampella
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     1¦Â,3¦Â-dihydroxyurs-12-en-27-oic acid
C30H48O4     ÏàËÆ¶È:63.3%
Journal of Natural Products          2003          66          1628-1631
A Novel Antibacterial Iridoid and Triterpene from Caiophora coronata
Smriti Khera,Girma M. Woldemichael, Maya P. Singh,Enrique Suarez, and Barbara N. Timmermann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     spinogenin D3
    ÏàËÆ¶È:63.3%
Phytochemistry          1993          33          891-895
3-epi-Oleanene type triterpene glycosyl esters from leaves of Acanthopanax spinosus
Masazumi Miyakoshi, Yoshiteru Ida, Susumu Isoda, Junzo Shoji
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     maytenfolic acid
C30H48O4     ÏàËÆ¶È:63.3%
Phytochemistry          1986          25          479-485
Antitumour triterpenes of Maytenus diversifolia
Hiroshi Nozaki, Hideyo Suzuki, Teruhisa Hirayama, Ryoji Kasai, Rong-Yang Wu, Kuo-Hsiung Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     3-O-[¦Á-L-rhamnopyranosyl(1¡ú2)-¦Â-D-glucopyranosyl(1¡ú4)-¦Â-D-glucuronopyranosyl]-soyasapogenol B
    ÏàËÆ¶È:63.3%
Acta Chimica Sinica          1987          45          145-149
Studies on the Chemical Components of Oxtropis ochrocephala Bunge II. The Structures of Two Triterpenoid Saponins
Sun Rong-Qi Cheng Dong-Liang Jia Zhong-JianZhu Zi-Qing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     9¦Á,11-Epoxy-5¦Á-ergosta-7,22-dien-3¦Â-yl acetate
C30H46O3     ÏàËÆ¶È:63.3%
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
15 .     ebeiedine
    ÏàËÆ¶È:62.9%
Chemical & Pharmaceutical Bulletin          2002          50(8)          1013-1016
New Steroidal Alkaloids from Fritillaria imperialis and Their Cholinesterase Inhibiting Activities
ATTA-UR-RAHMAN,Muhammad Nadeem AKHTAR, Muhammad Iqbal CHOUDHARY, Yoshisuke TSUDA,Bilge SENER,Assad KHALID, and Masood PARVEZ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     certonardoside G
C27H46O4     ÏàËÆ¶È:62.9%
Journal of Natural Products          2003          66          384-391
Bioactive Sterols from the Starfish Certonardoa semiregularis
Weihong Wang, Famei Li, Yujin Park, Jongki Hong, Chong-Ok Lee, Jae Yang Kong, Sook Shin, Kwang Sik Im, and Jee H. Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     ebeiedine
    ÏàËÆ¶È:62.9%
Chemical & Pharmaceutical Bulletin          1988          36          4316-4329
The Structural Elucidation of Fritillaria Alkaloids from Fritillaria ebeiensis var. purpurea. I. : The Structures of Ebeienine, Ebeiedine and Ebeiedinone
PING LEE,YUKIE KITAMURA,KOH KANEKO,MOTOO SHIRO,GUO-JUN XU,YUH-PAN CHEN and HONG-YEN HSU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     peimine
    ÏàËÆ¶È:62.9%
Acta Pharmaceutica Sinica          1991          26          829-835
STUDIES ON CHEMICAL CONSTITUENTS OF FRITILLARIA IN HUBEI. ¢ü¢ñ ISOLATION AND STRUCTURE ELUCIDATION OF HUPEHEMONOSIDE
JZ Wu; M Tang and R Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     wanpemine
    ÏàËÆ¶È:62.9%
Acta Pharmaceutica Sinica          1991          26          829-835
STUDIES ON CHEMICAL CONSTITUENTS OF FRITILLARIA IN HUBEI. ¢ü¢ñ ISOLATION AND STRUCTURE ELUCIDATION OF HUPEHEMONOSIDE
JZ Wu; M Tang and R Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     etioline
    ÏàËÆ¶È:62.9%
Phytochemistry          1996          43          705-707
Steroidal alkaloids from roots of Solanum spirale
Helmut Ripperger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     cholest-5-ene-3¦Â,7¦Â,19-triol
C27H46O3     ÏàËÆ¶È:62.9%
Journal of Natural Products          1992          Vol 55          321
Four New Bioactive Polyhydroxylated Sterols from the Black Coral Antipathes subpinnata
Anna Aiello, Ernesto Fattorusso, Marialuisa Menna
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     verticine
    ÏàËÆ¶È:62.9%
Acta Pharmaceutica Sinica          1988          Vol 23          34-37
CHEMICAL STUDIES OF EPIMEDIUM WUSHANENSE T. S. YING
HR Liang; WM Yan; JS Li and CS Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     verticinone
C27H43N3O     ÏàËÆ¶È:62.9%
Acta Pharmaceutica Sinica          1988          Vol 23          415-421
ISOLATION AND IDENTIFICATION OF ALKALOIDS FROM FRITILLARIA NINGGUOENSIS S.C.CHEN ET S. F. YIN
QH Li; ZH Wu; LL Zhang and L Shao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     Solafloridine
C27H43NO     ÏàËÆ¶È:62.9%
Phytochemistry          1996          41          1629-1631
22, 26-epiminocholestane alkaloids with unusual (20R)-configurations from Solanum species
Helmut Ripperger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     ent-15¦Â-Senecioyloxy-16-en-kaur-19-oic acid
    ÏàËÆ¶È:62.9%
Phytochemistry          1993          32          1611-1613
An ent-kaurenolide from Stevia lucida
J.Manuel Amaro-Luis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     16,17-epoxy-15-[(2-methyl-1-oxo-2-butenyl)oxy]-4¦Á,15¦Â(E),kauran-18-oic acid
    ÏàËÆ¶È:62.9%
Planta Medica          2010          76          1870-1873
Antimalarial Activity of Aspilia pruliseta, a Medicinal Plant from Uganda
Sebisubi, Fred Musoke; Odyek, Olwa; Anokbonggo, William Wilberforce; Ogwal-Okeng, Jasper; Carcache-Blanco, Esperanza J.; Ma, Cuiying; Orjala, Jimmy; Tan, Ghee T.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     15¦Á-hydroxy-kaur-16-en-19-oic acid
C20H30O3     ÏàËÆ¶È:62.9%
Phytochemistry          1979          18          1681-1685
New diterpenes from Porella perrottetiana
Yoshinori Asakawa, Masao Toyota, Tsunematsu Takemoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     peiminine
    ÏàËÆ¶È:62.9%
Phytochemistry          1986          25          2008-2009
Two steroidal alkaloids from fritillaria harelinii
Min Zhi-da, Qian Jing-fang, Munekazu Iinuma, Toshiyuki Tanaka, Mizuo Mizuno
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     peimine
    ÏàËÆ¶È:62.9%
Chinese Traditional and Herbal Drugs          2009          40          15-17
Alkaloid constituents of Fritillaria cirrhosa
CAO Xin-wei; ZHANG Meng; LI Jun; XIAO Pei-gen; CHEN Si-bao; CHEN Shi-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     verticine
    ÏàËÆ¶È:62.9%
Chinese Traditional and Herbal Drugs          1994          25          344-346+390
Studies on the Chemical Constituents of the Stems and Leaves of Thunberg Fritillary (Fritillaria thunbergii)
Yan Mingming; Jin Xiangqun; Xu Dongming(Jilin provincial Institute of Trad itional Chinese Medicine and Materia Medica; Changchun);
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     lepidiumterpeniod
C27H48O2     ÏàËÆ¶È:62.9%
Pharmazie          1999          54          851-853
Three new phytoconstituents from Lepidium sativum
S.D. Pande - M. Ali - M. Iqbal - S.D. Pande
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     verticine
    ÏàËÆ¶È:62.9%
Tetrahedron letters          1979          20          3737-3740
13C-NMR studies on the cevanine alkaloids : the application of 13C-NMR spectrum for structure elucidation of new alkaloids, baimonidine and isoverticine
Kô Kaneko, Mikako Tanaka, Kimiaki Haruki, Nobuaki Naruse, Hiroshi Mitsuhashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     (22E,24S)-2¦Á,3¦Á-dihydroxy-5¦Á-stigmast-22-en-6-one
C29H48O3     ÏàËÆ¶È:62.9%
Steroids          2012          77          91-99
Brassinosteroids and analogs as neuroprotectors: Synthesis and structure¨Cactivity relationships
Jihane Ismaili, Martin Boisvert, Fanny Longpr¨¦, Julie Carange, C¨¦line Le Gall, Maria-Grazia Martinoli, Benoit Daoust
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     (24S)-3¦Â-hydroxy-5¦Á-stigmastan-6-one
C29H50O2     ÏàËÆ¶È:62.9%
Steroids          2012          77          91-99
Brassinosteroids and analogs as neuroprotectors: Synthesis and structure¨Cactivity relationships
Jihane Ismaili, Martin Boisvert, Fanny Longpr¨¦, Julie Carange, C¨¦line Le Gall, Maria-Grazia Martinoli, Benoit Daoust
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     (22E)-5 ¦Á-cholest-22-ene-3¦Â,6¦Á,8,15¦Á,24-pentol
C27H46O5     ÏàËÆ¶È:62.9%
Russian Chemical Bulletin          1997          46          186-191
New polyhydroxysteroids and steroid glycosides from the far east starfishCeramaster patagonicus
A. A. Kicha, A. I. Kalinovsky and V. A. Stonik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     (20R,24S)-5¦Á-cholestane-3¦Â,6¦Â,15¦Â,24-tetraol
C27H48O4     ÏàËÆ¶È:62.9%
Russian Chemical Bulletin          2002          51          2295-2298
Steroid polyols from the Far-Eastern starfish Henricia sanguinolenta
E. V. Levina, A. I. Kalinovskii, P. V. Andriyashchenko, V. A. Stonik and P. S. Dmitrenok
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     Iwayoside A
C26H42O8     ÏàËÆ¶È:62.9%
Bulletin of the Korean Chemical Society          2010          31          2422-2423
Iwayoside A, a New Diterpene Glycoside from Artemisia iwayomogi Kitamura that Enhances IL-2 Secretion
Yan Ding, Chun Liang, Seo Young Yang, Jun Ho Kim, Young Mi Lee, Young Ho Kim*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     compound 2
    ÏàËÆ¶È:62.9%
Phytotherapy Research          1995          9          460-462
Active constituents of the bulbs of Fritillaria ebeiensis and their antitumour activity in mice
Li Ping, Xu Guojun, Xu Luoshan and Wang Yixian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     ebeiedine
    ÏàËÆ¶È:62.9%
Phytotherapy Research          1995          9          460-462
Active constituents of the bulbs of Fritillaria ebeiensis and their antitumour activity in mice
Li Ping, Xu Guojun, Xu Luoshan and Wang Yixian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     cholesta-5-en-3,7,19-triol
    ÏàËÆ¶È:62.9%
Academic Journal of Second Military Medical University          2010          31          421-424
Studies on chemical constituents of Anthogorgia sp.
XU Yuan-yuan, LI Ling, YI Yang-hua, ZHANG Wen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     23R,24S)-5¦Á-cholestane-3¦Â,6¦Â,12¦Á,16¦Â,23,24-hexol
C27H48O6     ÏàËÆ¶È:62.9%
Journal of Natural Medicines          2013          67          590-598
New cholestane glycosides and sterols from the underground parts of Chamaelirium luteum and their cytotoxic activity
Akihito Yokosuka, Kenichi Takagi, Yoshihiro Mimaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     cholesta-7,22-diene-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:62.9%
Journal of Chinese Medicinal Materials          2006          29          555-557
Chemical Constituents from the South China Sea Gorgonian Coral Subergorgia reticulata
YANG Jin, QI Shu-hua, ZHANG Si, LI Qing-xin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     Lupa-1,12,20(29)-trien-3-oxo-28-oic acid
C30H44O3     ÏàËÆ¶È:62.5%
Natural Products and Bioprospecting          2012          2          210-216
Exploring of drug leads from diversity-oriented Michael-acceptor library derived from natural products
Xu DENG, Ling-Mei KONG,Yu ZHAO, Juan HE, Li-Yan PENG, Yan LI, and Qin-Shi ZHAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     22,23-Dihydrospinasterol
    ÏàËÆ¶È:62.0%
Acta Botanica Yunnanica          1995          17(1)          103-108
CHEMICAL CONSTITUENTS FROM CLERODENDRUM JAPONICUM
TIAN Jun, SUN Han-Dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     poriferastane-3¦Â,6¦Á-diol
C29H52O2     ÏàËÆ¶È:62.0%
Chemical & Pharmaceutical Bulletin          1995          43          1813-1817
Structures of Five Hydroxylated Sterols from the Seeds of Trichosanthes kirilowii MAXIM.
Yumiro KIMURA,Toshihiko AKIHISA,Ken YASUKAWA,Michio TAKIDO and Toshitake TAMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     (24R)-3¦Â-chloro-5,7¦Á-Dibromo-5¦Á -stigmastan-6-one
    ÏàËÆ¶È:62.0%
Chemistry of Natural Compounds          2002          38          257-263
SYNTHESIS AND DEHYDROHALOGENATION OF 3b-CHLORO-5a,7a-DIBROMO-6-KETOSTEROIDS OF THE STIGMASTANE AND CHOLESTANE SERIES
N. V. Kovganko and V. L. Survilo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     (22R,23R)-3¦Â-Bromo-5¦Á,22,23-trihydroxystigmastan-6-one
C31H52O3Br     ÏàËÆ¶È:62.0%
Steroids          2000          65          329-337
Synthesis and bioactivity evaluation of brassinosteroid analogs
Javier A. Ram¨ªrez, Osvaldo M. Teme Centuri¨®n, Eduardo G. Gros, Lydia R. Galagovsky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     Stigmastane-3¦Â,6¦Á-diol
    ÏàËÆ¶È:62.0%
Steroids          2006          71          700-705
Steryl esters and phenylethanol esters from Syringa komarowii
Yinggang Luo, Yan Liu, Huayi Qi, Zhijun Wu, Guolin Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     compound 28
    ÏàËÆ¶È:62.0%
Steroids          2006          71          700-705
Steryl esters and phenylethanol esters from Syringa komarowii
Yinggang Luo, Yan Liu, Huayi Qi, Zhijun Wu, Guolin Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     compound 29
    ÏàËÆ¶È:62.0%
Steroids          2006          71          700-705
Steryl esters and phenylethanol esters from Syringa komarowii
Yinggang Luo, Yan Liu, Huayi Qi, Zhijun Wu, Guolin Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
51 .     spinogenin C6
C29H46O5     ÏàËÆ¶È:62.0%
Phytochemistry          1997          46          1255-1259
3¦Á-hydroxy-oleanene type triterpene glycosyl esters from leaves of Acanthopanax spinosus
Masazumi Miyakoshi, Susumu Isoda, Hirotoshi Sato, Yasuaki Hirai, Junzo Shoji, Yoshiteru Ida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
52 .     24R-ethyl-5¦Á-cholestane-3¦Â,6¦Á-3-O-¦Â-D-glucoside
    ÏàËÆ¶È:62.0%
Journal of Natural Products          1987          Vol 50          881
Sterols and Steryl Glycosides from Urtica dioica
Neera Chaurasia, Max Wichtl
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
53 .     (22R,23R)-3¦Â,22,23-trihydroxy-5¦Á,6¦Á-oxidostigmastane
C29H52O4     ÏàËÆ¶È:62.0%
Bioorganic & Medicinal Chemistry          2008          16          1460-1473
Synthesis and cytotoxicity evaluation of 22,23-oxygenated stigmastane derivatives
Alexander Yu. Misharin, Arif R. Mehtiev, Galina E. Morozevich, Yaroslav V. Tkachev, Vladimir P. Timofeev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
54 .     ( 22S,23S)-2¦Â,3¦Â,22,23-tetrahydroxy-5¦Á-stigmastan-6-one
C22H35O4     ÏàËÆ¶È:62.0%
Steroids          1994          59          463-467
Synthesis of new brassinosteroids with potential activity as antiecdysteroids
Carme Brosa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
55 .     stigmasterol
    ÏàËÆ¶È:62.0%
Chinese Traditional and Herbal Drugs          2010          41          36-39
É¡»¨Ä¾»¯Ñ§³É·ÖÑо¿
ºÎéó; ÕÔÃ÷; ×ÚÓñÓ¢; ²ÌÈýЭ; ³µÕòÌÎ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
56 .     5¦Á-stigmastane-3¦Â,6¦Á-diol
C29H52O2     ÏàËÆ¶È:62.0%
Chinese Traditional and Herbal Drugs          2007          38          340-342
Chemical constituents from stems of Clematis armandii (¢ñ)
YAN Li-hua; XU Li-zhen; ZOU Zhong-mei; YANG Shi-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
57 .     5¦Á-¶¹çÞÍé-3¦Â,6¦Á-¶þ´¼
    ÏàËÆ¶È:62.0%
Chinese Pharmaceutical Journal          2004          39          173-175
Studies on the chemical constituents of Caragana rosea
CUI Yi-ling, MU Qing, HU Chang-qi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
58 .     22-dihydrochondrillasterol
    ÏàËÆ¶È:62.0%
Journal of the Chemical Society, Perkin Transactions 1          1989                   1969-1974
Biosynthesis of 24¦Â-ethylsterols in cultured cells of Trichosanthes kirilowii(cucurbitaceae) fed with [1,2-13C2]- and [2-13C2H3]-acetate: reinvestigation of the stereochemistry at C-25
Shujiro Seo, Atsuku Uomori, Yohko Yoshimura, Ken'ichi Takeda, Haruo Seto, Yutaka Ebizuka, Hiroshi Noguchi and Ushio Sankawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
59 .     stigmastane-3¦Â,6¦Á-diol
    ÏàËÆ¶È:62.0%
Natural Product Research and Development          2000          12(5)          14-16
STEROID CONSTITUENTS FROM EUONYMUS MUPINENSIS
Mao Shilong; Sang Shengmin; Lao Aina and Chen Zhongliang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
60 .     stigmasterol
    ÏàËÆ¶È:62.0%
Journal of Chinese Medicinal Materials          2012          35          404-406
Study on the Chemical Constituent from the Dichloromethane Extract.
of the Pine Needles of Cedrus deodara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
61 .     compound 7(24S)
    ÏàËÆ¶È:62.0%
Shoyakugaku Zasshi          1992          46          302-309
Chemical Components of a Commercial Crude Drug "Byakken" (Ampelopsis Radix)
KATO TAKESHI, SUYAMA TETSUO, YAMANE FUJITOSHI, MORITA YUTAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
62 .     (22R,23R)-3¦Â-Hydroxy-22,23-isopropylidenedioxy-5¦Á-ergost-8(14)-en-15-one
    ÏàËÆ¶È:61.2%
Steroids          2007          72          305-312
Novel side chain modified ¦¤8(14)-15-ketosterols
Alexander Yu. Misharin, Vitali S. Ivanov, Arif R. Mehtiev, Galina E. Morozevich, Yaroslav V. Tkachev, Vladimir P. Timofeev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
63 .     25-methoxycucurbita-5,23(E)-diene-3¦Â,7¦Â,29-triol
C31H52O4     ÏàËÆ¶È:61.2%
Bioorganic & Medicinal Chemistry          2009          17          6942-6951
New potent P-glycoprotein modulators with the cucurbitane scaffold and their synergistic interaction with doxorubicin on resistant cancer cells
C¨¢tia Ramalhete, Joseph Moln¨¢r, Silva Mulhovo, Virg¨ªlio E. Ros¨¢rio, Maria-Jos¨¦ U. Ferreira
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
64 .     ergosta-5,8(14),22-trien-3¦Â-ol
C28H44O     ÏàËÆ¶È:60.7%
Journal of Natural Products          1998          61          1491-1496
Phycomysterols and Other Sterols from the Fungus Phycomyces blakesleeanus
Alejandro F. Barrero, J. Enrique Oltra, Juan A. Poyatos, David Jim¨¦nez, and Eulalia Oliver
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
65 .     (23R,25S)-3¦Â-Acetoxy-16¦Â,23:23,26-diepoxy-5¦Á-cholestan-22-one
    ÏàËÆ¶È:60.7%
Steroids          2004          69          395-400
Rearrangement of 23-oxospirostanes to the 22-oxo-23-spiroketal isomers promoted by Lewis acids¡ªX-ray crystal structure of (23R,25S)-3¦Â-acetoxy-16¦Â,23:23,26-diepoxy-5¦Â-cholestan-22-one
Micha¨ª K. Cyra¨½ski, Jadwiga Frelek, Izabella Jastrzębska, Jacek W. Morzycki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
66 .     Stylisterol B
C28H46O4     ÏàËÆ¶È:60.7%
Steroids          2005          70          63-70
New polyhydroxylated sterols stylisterols A¨CC and a novel 5,19-cyclosterol hatomasterol from the Okinawan marine sponge Stylissa sp.
Hidemichi Mitome, Nao Shirato, Ayako Hoshino, Hiroaki Miyaoka, Yasuji Yamada, Rob W.M. Van Soest
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
67 .     (22R,23R)-5¦Á-ergost-8(14)-en-15-on-3¦Â,22,23-triol
    ÏàËÆ¶È:60.7%
Steroids          2007          72          305-312
Novel side chain modified ¦¤8(14)-15-ketosterols
Alexander Yu. Misharin, Vitali S. Ivanov, Arif R. Mehtiev, Galina E. Morozevich, Yaroslav V. Tkachev, Vladimir P. Timofeev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
68 .     Primulagenin A
    ÏàËÆ¶È:60.7%
Journal of Natural Products          1991          Vol 54          1044
Triterpenoid Saponins of Eleutherococcus senticosus Roots
Ewa Segiet-Kujawa, Macki Kaloga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
69 .     16¦Â-hydroxy-17-acetoxykauran-18-oic acid 18-O-¦Â-D-glucopyranoside
C28H44O10     ÏàËÆ¶È:60.7%
Journal of Natural Products          1993          Vol 56          1917
New Kaurane Diterpenoids from Aster tongolensis
R. X. Tan, Y. H. Hu, Z. L. Liu, X. Pan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
70 .     16¦Â-hydroxy-17-acetoxy-(-)-kauran-19-oic acid-¦Â-D-glucopyranosyl ester
C28H44O10     ÏàËÆ¶È:60.7%
Phytochemistry          1993          33          1181-1183
Kaurane diterpenoids from Aster ageratoides
Cheng Dong-Liang, Cao Xiao-Ping, Wei Han-Xun, He Lan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
71 .     (22R,23R)-19-Norstigmasta-1,3,5(10)-triene-3,22,23-triol
C28H44O3     ÏàËÆ¶È:60.7%
Tetrahedron          2012          68          3685-3691
Synthesis of aromatic stigmastanes: application to the synthesis of aromatic analogs of brassinosteroids
Sof¨ªa L. Acebedo, Fernando Alonso, Javier A. Ram¨ªrez, Lydia R. Galagovsky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
72 .     (22E,24R)-ergosta-7,22-diene-3¦Â,5¦Á,6¦Á,9¦Á-tetraol
C32H52O4     ÏàËÆ¶È:60.7%
Natural Product Research and Development          2007          19          436-438
Chemical Constituents of Basidiomycetes Russula subnigricans
GONG Qing-fang; ZHANG Yu-mei; TAN Ning-hua; CHEN Zuo-hong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
73 .     1(10¡ú6)abeo-ergosta-5,7,9,22-tetraen-11¦Â-methoxy-3¦Á-ol
C29H44O2     ÏàËÆ¶È:60.7%
Tetrahedron          2000          56          2595-2602
Three New Metabolites of Hybrid Strain KO 0231, Derived from Penicillium citreo-viride IFO 6200 and 4692
Takashi Nakada, Shosuke Yamamura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
74 .     9¦Á,11-Epoxy-5¦Á-ergosta-7,22-dien-3¦Â-ol
C28H44O2     ÏàËÆ¶È:60.7%
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
75 .     tuboanosigenin
    ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          2008          56(7)          1038-1040
New C28 Steroidal Glycosides from Tubocapsicum anomalum
Naoko KIYOTA,Kazushi SHINGU,Koki YAMAGUCHI,Yasuyuki YOSHITAKE,Kazunobu HARANO,Hitoshi YOSHIMITSU,Hiroyuki MIYASHITA,Tsuyoshi IKEDA,Chie TAGAWA,and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
76 .     isotubocaposigenin
C30H44O6     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          2007          55(1)          34-36
New C28 Steroidal Glycosides from Tubocapsicum anomalum
Naoko KIYOTA,Kazushi SHINGU,Koki YAMAGUCHI,Yasuyuki YOSHITAKE,Kazunobu HARANO,Hitoshi YOSHIMITSU,Tsuyoshi IKEDA,and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
77 .     Acanjapogenin D
C30H46O6     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          2005          53(9)          1147-1151
New Oleanene Glycosides from the Leaves of Acanthopanax japonicus
Sang-Yong PARK,Chang-Soo YOOK,and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
78 .     Acanjapogenin I
C30H44O6     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          2005          53(9)          1147-1151
New Oleanene Glycosides from the Leaves of Acanthopanax japonicus
Sang-Yong PARK,Chang-Soo YOOK,and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
79 .     3-oxo-25-hydroxylup-20(29)-en-28-oic acid
C30H46O4     ÏàËÆ¶È:60%
Phytochemistry          2007          68          834-839
Biotransformation of betulinic and betulonic acids by fungi
Denise Z.L. Bastos,Ida C. Pimentel, Daniel A. de Jesus,Br¨¢s H. de Oliveira
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
80 .     ¦¤1-lupenone
C30H46O     ÏàËÆ¶È:60%
Phytochemistry          2005          66          2388-2392
Unusual naphthoquinones, catechin and triterpene from Byrsonima microphylla
Rosane M. Aguiar, Juceni P. David, Jorge M. David
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
81 .     1¦Á,3¦Â-dihydroxyolean-12-en-29-oic acid
C30H48O4     ÏàËÆ¶È:60%
Phytochemistry          2003                   81-88
Antimicrobial activity of pentacyclic triterpenes isolated from African Combretaceae
David R. Katerere, Alexander I. Gray, Robert J. Nash, Roger D. Waigh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
82 .     3¦Â,22¦Á-dihydroxyolean-12-en-30-oic acid
C30H48O4     ÏàËÆ¶È:60%
Journal of Natural Products          2008          71(5)          789-792
Oleanane-Type Triterpenes from the Flowers and Roots of Saussurea muliensis
Chun-Mei Liu, He-Xiang Wang, Shi-Lei Wei, and Kun Gao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
83 .     microfokienoxane A
C30H48O3     ÏàËÆ¶È:60%
Journal of Natural Products          2006          69          1543-1546
Cytotoxic Triterpenoids from the Leaves of Microtropis fokienensis
I-Hsiao Chen, Fang-Rong Chang, Chin-Chung Wu, Shu-Li Chen,Pei-Wen Hsieh, Hsin-Fu Yen, Ying-Chi Du, and Yang-Chang Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
84 .     galphimine B
C30H46O7     ÏàËÆ¶È:60%
Journal of Natural Products          2004          67          644-649
Isolation of Nor-secofriedelanes from the Sedative Extracts of Galphimia glauca
Alexandre T. Cardoso Taketa, Jorge Lozada-Lechuga, Mabel Fragoso-Serrano, Mara Luisa Villarreal, and Rogelio Pereda-Miranda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
85 .     polasterol B
C30H50O     ÏàËÆ¶È:60%
Journal of Natural Products          2000          63          1175-1177
New 24-Isopropylcholesterol and 24-Isopropenylcholesterol Sulfate from the Marine Sponge Epipolasis Species
Akemi Umeyama, Kanako Adachi, Seiichi Ito, and Shigenobu Arihara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
86 .     29- or 30-hydroxylated hederagenin
    ÏàËÆ¶È:60%
Journal of Natural Products          1999          62          445-448
Triterpenoid Saponins of Acanthopanax nipponicus Leaves
Masazumi Miyakoshi, Katsuya Shirasuna, Yasuaki Hirai, Kazushi Shingu, Susumu Isoda, Junzo Shoji, Yoshiteru Ida, and Torao Shimizu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
87 .     sterol ether
C30H52O2     ÏàËÆ¶È:60%
Journal of Natural Products          1996          59          161-162
A New Cytotoxic Sterol Methoxymethyl Ether from a Deep Water Marine Sponge Scleritoderma sp. cf. paccardi
Sarath P. Gunasekera, Michelle Kelly-Borges, and Ross E. Longley
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
88 .     alstonic acid A
C30H48O3     ÏàËÆ¶È:60%
Phytochemistry          2009          70          650-654
Alstonic acids A and B, unusual 2,3-secofernane triterpenoids from Alstonia scholaris
Fei Wang, Fu-Cai Ren, Ji-Kai Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
89 .     wistariasapogenol B
    ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1995          43          636-640
Five New Triterpene Glycosides from Wisteria branchybotrys (Leguminosae)
Junei KINJO,Yoshie FUJISHIMA,Kazuyo SAINO,Rui-hua TIAN and Toshihiro NOHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
90 .     compound 9
C30H48O5     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1989          37          3251-3254
Saponins from Leaves of Kalopanax septemlobus (THUNB.) KOIDZ. : Structures of Kalopanax-saponins La, Lb and Lc
Chun-Jie SHAO,Ryoji KASAI,Kazuhiro OHTANI,Jing-Da XU and Osamu TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
91 .     compound6
C30H47NaO7S     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1988          36          4269-4274
Phytochemical Studies of Seeds of Medicinal Plants. I. : Two Sulfated Triterpenoid Glycosides, Sulfapatrinosides I and II, from Seeds of Patrinia scabiosaefolia FISCHER
AKIRA INADA,MASAAKI YAMADA,HIROKO MURATA,MARI KOBAYASHI,HARUMASA TOYA,YOSHIKO KATO and TSUTOMU NAKANISHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
92 .     2,3-seco-1-cyanolup-20(29)-en-3,28-dioic acid
C30H45NO4     ÏàËÆ¶È:60%
Chemistry of Natural Compounds          2009          45          673-676
SYNTHESIS AND ANTIVIRAL ACTIVITY OF2,3-seco-DERIVATIVES OF BETULONIC ACID
I. A. Tolmacheva, V. V. Grishko, E. I. BorekoO. V. Savinova, and N. I. Pavlova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
93 .     cycloorbigenin B
    ÏàËÆ¶È:60%
Chemistry of Natural Compounds          1998          34          477-479
TRITERPENE GLYCOSIDES OF Astragalus AND THEIR GENINS LVIII. THE STRUCTURE OF DIHYDROCYCLOORBIGENIN A
M. A. Agzamova and M. I. Isaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
94 .     cycloorbigenin B
    ÏàËÆ¶È:60%
Chemistry of Natural Compounds          1990          26          595-596
TRITERPENE GLYCOSIDES OF Astragalus AND THEIR GENINS XXXIII. CYCLOORBICOSIDE B FROM Astragalus orbiculatus
M. A. Agzamova, M. I. Isaev,and N. K. Abubakirov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
95 .     Soyasapogenol B
C30H50O3     ÏàËÆ¶È:60%
Journal of Asian Natural Products Research          2005          7          237-243
Three new isoprenylated flavonoids from the roots of Sophora flavescens
PEI-LAN DING, AI-JUN HOU and DAO-FENG CHEN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
96 .     cyclohopenol
C30H48O     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1998          46          730-732
FERN CONSTITUENTS : CYCLOHOPENOL AND CYCLOHOPANEDIOL, NOVEL SKELETAL TRITERPENOIDS FROM RHIZOMES OF PYRROSIA LINGUA
Hiroshi YAMASHITA,Kazuo MASUDA,Hiroyuki AGETA and Kenji SHIOJIMA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
97 .     dehydroprotochiisanogenin
    ÏàËÆ¶È:60%
Phytochemistry          1997          45          579-584
Lupane triterpenoid glycosyl esters from leaves of Acanthopanax divaricatus
Katsuya Shirasuna, Masazumi Miyakoshi, Sawako Mimoto, Susumu Isoda, Yohko Satoh, Yasuaki Hirai, Yoshiteru Ida, Junzo Shoji
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
98 .     soyasapogenol B
    ÏàËÆ¶È:60%
Journal of Natural Products          1990          Vol 53          298
Sapogenin Structure: Analysis of the 13C- and 1H-nmr Spectra of Soyasapogenol B
Robert L. Baxter, Keith R. Price, G. Roger Fenwick
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
99 .     dillenic acid A
C30H46O4     ÏàËÆ¶È:60%
Journal of Natural Products          1994          Vol 57          1245
Antibacterial Triterpenoid Acids from Dillenia papuana
Andr¨¦ Nick, Anthony D. Wright, Otto Sticher, Topul Rali
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
100 .     Soyasapogenol B
    ÏàËÆ¶È:60%
Phytochemistry          1996          41          1573-1577
Triterpenoids from Melilotus messanensis; soyasapogenol G, the first natural carbonate derivative
Francisco A. Mac¨ªas*, Ana M. Simonet, M. Dolores Esteban, Juan Carlos G. Galindo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
101 .     3¦Â,21¦Â,23-trihydroxyolean-12-en-28-oic acid
    ÏàËÆ¶È:60%
Korean Journal of Pharmacognosy          1987          18(3)          151-167
13C NMR Spectroscopy of Amyrins
Kang, Sam-Sik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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