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̼Æ×Êý¾Ý169.73  155.7   153.73    131.21     130.90     124.87      123.33     116.52    116.01      90.62     73.61     72.66     68.18      66.85    64.42    63.41    61.67     55.94      50.53    48.48    44.57   43.69     42.92     41.95     41.89    40.41   40.0     39.0     38.43      36.62     29.12     24.94     22.24      19.98        19.22    18.66     17.92    17.72    17.48     ¿ÉÄÜ»áÓÐÔÓÖʷ壬ʵÔÚÌ«¶àÁË£¬¼±ÇóÖú
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1 .     urs-12-ene-3¦Â,6¦Â,16¦Â,21¦Â-tetraol-3-O-¦Â-glucopyranoside
C36H60O9     ÏàËÆ¶È:58.9%
Phytochemistry          2008          69          961-972
Triterpene saponins from Silphium radula
Lalita M. Calabria, Sonia Piacente, Ireneusz Kapusta,Suranganie F. Dharmawardhane, Frances M. Segarra, Peter J. Pessiki f, Tom J. Mabry
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     2¦Á,24-Dihydroxy-3¦Â-(trans-p-cowoyloxy)-urs-12-en-28-oic acid
    ÏàËÆ¶È:58.9%
Phytochemistry          1994          35          377-380
Triterpenoids from callus tissue of Actinidia polygama
Yutaka Sashida, Kazunori Ogawa, Tsuyoshi Yamanouchi, Hiroyuki Tanaka, Yukihiro Shoyama, Itsuo Nishioka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (E)-2¦Á-ôÇ»ùÎÚËÕËá-3-O-¶ÔÏã¶¹Ëáõ¥
    ÏàËÆ¶È:58.9%
Chinese Pharmaceutical Journal          2010          45          825-828
Isolation and Identification of 3-O-p-Coumaroyloxyl Pentacyclic Triterpenoids from Lysimachia clethroides Duby
XU Qiong-ming, TANG Li-hua, LI Xia, HAO Li-li, LI Xiao-ran*, YANG Shi-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     haliclotriol A
C38H56O5     ÏàËÆ¶È:58.9%
Tetrahedron          2000          56          9039-9046
New Triterpene-Ketides (Merotriterpenes), Haliclotriol A and B, from an Indo-Pacific Haliclona Sponge
Phillip Crews, Blaine Harrison
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     spirocarcolitone G
C42H52O10     ÏàËÆ¶È:57.5%
Journal of Natural Products          2007          70          1228-1232
Spirocaracolitone Triterpenoids from the Bark of Ruptiliocarpon caracolito
Muhammad Asim, Helmi Hussien,John Thor Arnason, Luis Poveda, and Tony Durst
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     guajanoic acid
C40H56O6     ÏàËÆ¶È:57.5%
Natural Product Research          2004          18          135-140
Chemical constituents from the leaves of Psidium guajava
Sabira Begum; Syed Imran Hassan; Syed Nawazish Ali; Bina S. Siddiqui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     1¦Á,23-dihydroxy-12-oleanen-29-oic acid-3¦Â-O-2,4 diacetyl-L-rhamnopyranoside
C40H62O11     ÏàËÆ¶È:57.5%
Journal of Ethnopharmacology          2007          110          56-60
Antimicrobial and anti-inflammatory activity of four known and one new triterpenoid from Combretum imberbe (Combretaceae)
J.E. Angeh, X. Huang, I. Sattler, G.E. Swan, H. Dahse, A. Härtl, J.N. Eloff
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     Isoracemosol A
C37H60O8     ÏàËÆ¶È:56.4%
Journal of Natural Products          2009          72          791-795
Oleanane-Type Isomeric Triterpenoids from Barringtonia racemosa
P. Mangala Gowri, S. V. S. Radhakrishnan, S. Jeelani Basha, A. V. S. Sarma, and J. Madhusudana Rao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     1¦Á,3¦Â-hydroxyimberbic acid 23-O-¦Á-L-4-acetylrhamnopyranoside
C38H60O10     ÏàËÆ¶È:56.4%
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
10 .     3¦Á-trans-feruloyloxy-2¦Á-hydroxyurs-12-en-28-oic acid
C40H56O7     ÏàËÆ¶È:56.4%
Journal of Natural Products          2001          64          737-740
Megastigmane Glycosides and an Acylated Triterpenoid from Eriobotrya japonica
Hideyuki Ito,Eri Kobayashi, Shu-Hua Li, Tsutomu Hatano, Daigo Sugita, Naoki Kubo, Susumu Shimura, Yoshio Itoh, and Takashi Yoshida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     3¦Â-O-trans-pcoumaroylalphitolic acid
    ÏàËÆ¶È:56.4%
Planta Medica          1997          63          47-50
Isolation and Structural Elucidation of Acylated Pentacyclic Triterpenoids from the Leaves of Eucalyptus camaldulensis var. obtusa
Bina S. Siddiqui, Farhat, Sabira Begum, and Salimuzzaman Siddiqui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     2¦Á-hydroxy-3¦Â-(trans-p-coumaroyloxy)-urs-12-en-28-oic acid
C39H54O6     ÏàËÆ¶È:56.4%
Acta Botanica Yunnanica          2008          30(1)          121-124
Triterpenoids from Saurauia napaulensis (Saurauiaceae)
WANGQiong,JU Peng,WANG Yi-Fen,LUO Shi-De
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     dammar-24-en-3¦Â,11¦Á,20(S)-triol 3-O-¦Â-D-2-O-acetyl-glucopyranoside
C38H64O9     ÏàËÆ¶È:56.4%
Chemical & Pharmaceutical Bulletin          1995          43          1937-1942
Chemical Evaluation of Betula Species in Japan. I.Constituents of Betula ermanii
Hiroyuki FUCHINO,Tetsuya SATOH and Nobutoshi TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     jacoumaic acid
    ÏàËÆ¶È:56.4%
Chemical & Pharmaceutical Bulletin          1989          37          648-651
Cytotoxic Triterpenes from a Chinese Medicine, Goreishi
Atsushi NUMATA,Peiming YANG,Chika TAKAHASHI,Ryoko FUJIKI,Michiko NABAE and Eiichi FUJITA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     coumarobtusane
C39H58O5     ÏàËÆ¶È:56.4%
Journal of Natural Products          1990          Vol 53          1332
Three Pentacyclic Triterpenoids from the Leaves of Plumeria obtusa
Salimuzzaman Siddiqui, Bina Shaheen Siddiqui, Akhtar Naeed, Sabira Begum
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     23-trans-p-coumaroyloxy-2¦Á,3¦Á-dihydroxy-olean-12-en-28-oic acid
C39H54O7     ÏàËÆ¶È:56.4%
Bioorganic & Medicinal Chemistry Letters          2010          20          1944-1947
Bioactivity-guided isolation of cytotoxic triterpenoids from the trunk of Berberis koreana
Ki Hyun Kim, Sang Un Choi, Kang Ro Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     Complanatumol D
C39H58O8     ÏàËÆ¶È:56.4%
Planta Medica          2010          76          353-357
Cytotoxic Serratane Triterpenes from Diphasiastrum complanatum with a Hydroxy Group at C-27
Yan, Jian; Sun, Lirong; Li, Wei; Zhou, Lin; Li, Zhongrong; Zhang, Xianmin; Yang, Ling; Qiu, Minghua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     23-hydroxyimberbic acid-23-O-¦Á-L-4-acetyl-rhamnopyranoside
    ÏàËÆ¶È:56.4%
Chinese Traditional and Herbal Drugs          2008          39          512-514
é­Ðη糵×ÓÒ¶ÖÐÝÆÀ໯ºÏÎïµÄÑо¿
ÎâÏþÅô;³Â¹âÓ¢;½¯²ÅÎä;Öì¹úÔª;·½ºêÑ«
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     (E)-ήÁê²ËËá-3-O-¶ÔÏã¶¹Ëáõ¥
    ÏàËÆ¶È:56.4%
Chinese Pharmaceutical Journal          2010          45          825-828
Isolation and Identification of 3-O-p-Coumaroyloxyl Pentacyclic Triterpenoids from Lysimachia clethroides Duby
XU Qiong-ming, TANG Li-hua, LI Xia, HAO Li-li, LI Xiao-ran*, YANG Shi-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     compound 4
C37H54O3     ÏàËÆ¶È:56.4%
Journal of Natural Products          2012          75          1451-1458
Halicloic Acids A and B Isolated from the Marine Sponge Haliclona sp. Collected in the Philippines Inhibit Indoleamine 2,3-Dioxygenase
David E. Williams, Anne Steinø, Nicole J. de Voogd, A. Grant Mauk, and Raymond J. Andersen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     2¦Á‑O-trans-p-coumaroyl-3¦Â,19¦Á-dihydroxy-urs-12-en-28-oic acid
C39H54O7     ÏàËÆ¶È:56.4%
Planta Medica          2013          79          365-368
Cytotoxic Pentacyclic Triterpenoids from Prinsepia utilis
Guan, Bin; Peng, Cheng-Cheng; Zeng, Qi; Cheng, Xiang-Rong; Yan, Shi-Kai; Jin, Hui-Zi; Zhang, Wei-Dong:
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     lotoideside D
C40H68O12     ÏàËÆ¶È:55%
Phytochemistry          2005          66          621-626
Hopane-type saponins from Glinus lotoides Linn
Tanusree Biswas, Moumita Gupta, Basudeb Achari, Bikas C. Pal
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     2¦Â,16¦Á,17-trihydroxy-ent-kauran-19-oic acid
C20H32O5     ÏàËÆ¶È:55%
Phytochemistry          2004          65          885-890
ent-Kaurenoic acids from Mikania hirsutissima (Compositae)
Emika Ohkoshi, Satoshi Kamo, Mitsuko Makino, Yasuo Fujimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     pittoviridagenin
C40H62O8     ÏàËÆ¶È:55%
Journal of Natural Products          2002          65          65-68
A New Triterpene Saponin from Pittosporum viridiflorum from the Madagascar Rainforest1
Youngwan Seo,John M. Berger, Jeannine Hoch, Kim M. Neddermann, Isia Bursuker,Steven W. Mamber, and David G. I. Kingston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     acodontasteroside A
    ÏàËÆ¶È:55%
Journal of Natural Products          1997          60          959-966
Isolation, Structure Elucidation, and Biological Activity of the Steroid Oligoglycosides and Polyhydroxysteroids from the Antarctic Starfish Acodontaster conspicuus
Simona De Marino, Maria Iorizzi, Franco Zollo, Luigi Minale, Charles D. Amsler, Bill J. Baker, and James B. McClintock
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     ent-16¦Â-hydroxykauran-17-yl ent-kaur-15-en-17-oate
C40H62O3     ÏàËÆ¶È:55%
Chemical & Pharmaceutical Bulletin          1982          30          3922-3931
Studies on the Constituents of the Crude Drug "Fritillariae Bulbus." IV. On the Diterpenoid Constituents of the Crude Drug "Fritillariae Bulbus"
JUNICHI KITAJIMA,NAOKI NODA,YOSHITERU IDA,TETSUYA KOMORI and TOSHIO KAWASAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     caraganoside B
C40H64O10     ÏàËÆ¶È:55%
Journal of Chinese Pharmaceutical Sciences          1998          7          1-6
Two NewTriter penoids from the Roots of Caragana intermedia K.
Wen-HanLin, Hong-Zheng Fu and Li-He Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     28-O-¦Á-L-rhamnopyranosyl (l¡ú2)-¦Â-D-glucopyranoside tormentic acidester
C42H68O14     ÏàËÆ¶È:54.7%
Chemistry of Natural Compounds          2009          45          197-199
A NEW TRITERPENE GLYCOSIDEFROM Premna microphylla
Zha-Jun Zhan, Lan Tang, and Wei-Guang Shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     compound 4
    ÏàËÆ¶È:54.7%
Journal of Natural Products          1990          Vol 53          1193
Saponins from Zygophyllum propinquum
Viqar Uddin Ahmad, Ghazala, Shafi Uddin, Shaheen Bano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     quinovic acid 38-O-¦Â-D-fucopyranosyl-(27¡ú1)-¦Â-D-ghtcopyranosylester
    ÏàËÆ¶È:54.7%
Phytochemistry          1991          30          1635-1637
Quinovic acid glycosides from Uncaria guianensis
Ana M.P. Y¨¦pez, Olga Lock de Ugaz, Carmen M.P. Alvarez, Vincenzo De Feo, Rita Aquino, Francesco De Simone, Cosimo Pizza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     azukisaponin V
    ÏàËÆ¶È:54.7%
Chemical & Pharmaceutical Bulletin          2008          56          1138-1142
Studies on the Constituents of Gueldenstaedtia multiflora
Yuki Tsunoda, Masafumi Okawa, Junei Kinjo, Tsuyoshi Ikeda and Toshihiro Nohara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     urs-12-ene-3-¦Á-L-rhamnopyraosyl(28¡ú1)-¦Â-D-glucopyranosylester
C42H68O12     ÏàËÆ¶È:54.7%
Indian Journal of Chemistry Section B          1997          36B          901-904
Novel triterpenoid glycosides and triterpenoid acid from the root extract of Acanthus montanus(Acanthace)
Edet M Anam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     compound IB
C42H66O12     ÏàËÆ¶È:54.7%
Journal of Tropical and Subtropical Botany          1998          6          357-361
ÂíÀ´²æÖù»¨Ò¶ÖеÄÒ»¸öÐÂÌðζ߰µÄ½á¹¹
ÅËÎĶ·, ƱԭÁ¼Ö¦, ³àÓðÕÉÃ÷, ´ó¹ÈÔ£Ö®, ÈÕ¹üÑÇÎ÷
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     haliclotriol A triacetate
    ÏàËÆ¶È:54.5%
Tetrahedron          2000          56          9039-9046
New Triterpene-Ketides (Merotriterpenes), Haliclotriol A and B, from an Indo-Pacific Haliclona Sponge
Phillip Crews, Blaine Harrison
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     11,21-dioxo- 3¦Â,15¦Á,24-trihydroxyurs-12-ene-24-O-¦Â-D-glucopyranoside
C36H56O10     ÏàËÆ¶È:53.8%
Journal of Natural Products          2009          72          1563-1567
Triterpenoids and Flavonoids from Celery (Apium graWeolens)
Kailan Zhou, Feng Zhao, Zhihui Liu, Yulei Zhuang, Lixia Chen,and Feng Qiu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     2-O-trans-p-coumaroyl maslinic acid
C39H54O6     ÏàËÆ¶È:53.8%
Chemical & Pharmaceutical Bulletin          2007          55(1)          15-18
Triterpenoids from Hippophae rhamnoides L. and Their Nitric Oxide Production-Inhibitory and DPPH Radical-Scavenging Activities
Zhi-Gang YANG,He-Ran LI,Li-Yan WANG,Yong-Hai LI,Shun-Guang LU,Xiu-Feng WEN,Jue WANG,Akihiro DAIKONYA,and Susumu KITANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     olean-12-ene-3¦Â,6¦Â,16¦Â,21¦Â-tetraol-3-O-¦Â-glucopyranoside
C36H60O9     ÏàËÆ¶È:53.8%
Phytochemistry          2008          69          961-972
Triterpene saponins from Silphium radula
Lalita M. Calabria, Sonia Piacente, Ireneusz Kapusta,Suranganie F. Dharmawardhane, Frances M. Segarra, Peter J. Pessiki f, Tom J. Mabry
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     3¦Â,16¦Â,23-trihydroxy-13,28-epoxyurs-11-ene-3-O-¦Â-D-glucopyranoside
C36H58O9     ÏàËÆ¶È:53.8%
Journal of Natural Products          2007          70          1889-1894
Triterpene, Antioxidant, and Antimicrobial Compounds from Melissa officinalis
Teresa Mencherini,Patrizia Picerno, Carla Scesa, and Rita Aquino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     certonardoside F
C39H67NaO17S     ÏàËÆ¶È:53.8%
Journal of Natural Products          2002          65          1649-1656
New Saponins from the Starfish Certonardoa semiregularis
Weihong Wang,Famei Li,Naseer Alam, Yonghong Liu,Jongki Hong,Chong-Kyo Lee,Kwang Sik Im,and Jee H. Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     certonardoside A derivative
39H65O14     ÏàËÆ¶È:53.8%
Journal of Natural Products          2002          65          1649-1656
New Saponins from the Starfish Certonardoa semiregularis
Weihong Wang,Famei Li,Naseer Alam, Yonghong Liu,Jongki Hong,Chong-Kyo Lee,Kwang Sik Im,and Jee H. Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     halityloside I
    ÏàËÆ¶È:53.8%
Journal of Natural Products          1997          60          959-966
Isolation, Structure Elucidation, and Biological Activity of the Steroid Oligoglycosides and Polyhydroxysteroids from the Antarctic Starfish Acodontaster conspicuus
Simona De Marino, Maria Iorizzi, Franco Zollo, Luigi Minale, Charles D. Amsler, Bill J. Baker, and James B. McClintock
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     3¦Â-O-trans-caffeoyl-29-hydroxybetulin
C39H56O6     ÏàËÆ¶È:53.8%
Planta Medica          2006          72          180-183
Lupane Triterpenoids and a Diaryl-heptanoid from Clematoclethra actinidioides
Hui Guo, Bo-Gang Li , Zhi-Jun Wu , Guo-Lin Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     27-(4-hydroxy-3'-methoxybenzoyloxy)-betulinic acid
    ÏàËÆ¶È:53.8%
Planta Medica          1999          65          740-743
New Triterpenoids with Antibacterial Activity from Zizyphus joazeiro
Wolfgang Sch¨¹hly, Jörg Heilmann, Ihsan Çalis, and Otto Sticher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     dammar-24-ene-3¦Â,20(S),26-triol 3-O-caffeate
C39H58O5     ÏàËÆ¶È:53.8%
Chemical & Pharmaceutical Bulletin          1996          44          1748-1753
Chemical Evaluation of Betula Species in Japan. III. Constiutents of Betula maximowicziana
Hiroyuki FUCHINO,Tetsuya SATOH and Nobutoshi TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     dammar-24-ene-3¦Â,20(S),26-triol 3-O-p-coumarate
C39H58O5     ÏàËÆ¶È:53.8%
Chemical & Pharmaceutical Bulletin          1996          44          1748-1753
Chemical Evaluation of Betula Species in Japan. III. Constiutents of Betula maximowicziana
Hiroyuki FUCHINO,Tetsuya SATOH and Nobutoshi TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     presapogenin III
    ÏàËÆ¶È:53.8%
Chemical & Pharmaceutical Bulletin          1994          42          1422-1426
Hosenkosides F, G, H, I, J, and K, Novel Baccharane Glycosides from the Seeds of Impatiens balsamina
Noboru SHOJI,Akemi UMEYAMA,Nobuaki SAITOU,Kazuko YOSHIKAWA,Masahiro NAGAI and Shigenobu ARIHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     3-O-trans-p-coumaroyltormentic acid
    ÏàËÆ¶È:53.8%
Chemical & Pharmaceutical Bulletin          1989          37          648-651
Cytotoxic Triterpenes from a Chinese Medicine, Goreishi
Atsushi NUMATA,Peiming YANG,Chika TAKAHASHI,Ryoko FUJIKI,Michiko NABAE and Eiichi FUJITA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     3¦Â,6¦Á,20,26-tetrahydroxy-(20S)-dammar-24-ene
    ÏàËÆ¶È:53.8%
Chemical & Pharmaceutical Bulletin          1987          35          553-561
Studies on the Constituents of Actinostemma lobatum MAXIM. IStructures of Actinostemmosides A, B, C and D, Dammarane Triterpene Glycosides Isolated from the Herb
MASAYO IWAMOTO,TOSHIHIRO FUJIOKA,HIKARU OKABE,KUNIHIDE MIHASHI and TATSUO YAMAUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     compound 2
    ÏàËÆ¶È:53.8%
Chinese Chemical Letters          2006          17          211-214
A New Triterpenoid Spaonin Isolated from the Seeds of Aesculus assamica Griff
Hong Wei LIU, Xin Sheng YAO, Nai Li WANG, Guo Ping CAI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     jacoumaric acid
    ÏàËÆ¶È:53.8%
China Journal of Chinese Materia Medica          2009          34          3225-3228
Chemical constituents of Periploca forrestii
GAN Xiuhai, ZHOU Xin, CHEN Huaguo, GONG Xiaojian, ZHAO Chao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
51 .     jacoum-aric acid
    ÏàËÆ¶È:53.8%
China Journal of Chinese Materia Medica          2002          27          519-522
Studies on Chemical Constituents of the Rhizomae of Ligusticum chuangxiong
Xiao Yongqng, LI Li, YOU Xiaolin, MASAHIKO TANIGUCHI, KIMIYEBABA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
52 .     comoound 3
C35H56O     ÏàËÆ¶È:53.8%
Journal of Natural Products          2010          73          204-207
C35-Terpenes from Bacillus subtilis KSM 6-10
Hirofumi Takigawa, Mitsuru Sugiyama and Yusuke Shibuya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
53 .     coumarobtusanoic acid
C39H56O7     ÏàËÆ¶È:53.8%
Journal of Natural Products          1990          Vol 53          1332
Three Pentacyclic Triterpenoids from the Leaves of Plumeria obtusa
Salimuzzaman Siddiqui, Bina Shaheen Siddiqui, Akhtar Naeed, Sabira Begum
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
54 .     2¦Á,3-dihydroxy-3¦Â-(trans-p-coumaroyloxy)-urs-12-en-28-oic acid
    ÏàËÆ¶È:53.8%
Phytochemistry          1992          31          2801-2804
Triterpenoids from the fruit galls of Actinidia polygama
Yutaka Sashida, Kazunori Ogawa, Noriaki Mori, Tsuyoshi Yamanouchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
55 .     compound 24
C47H68O10Si2     ÏàËÆ¶È:53.8%
Canadian Journal of Chemistry          2005          83          728-740
Studies towards the total synthesis of ouabagenin1
Ling Chen and Pierre Deslongchamps
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
56 .     methyl 2¦Á,3¦Á,24-trihydroxyurs-12-en-28-oate triacetate
C57H56O8     ÏàËÆ¶È:53.8%
Phytochemistry          1987          26          1107-1111
Pentacyclic triterpenoids from Prunella vulgaris
Hisashi Kojima,Hideo Tominaga,Shigeki Sato,Haruo Ogura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
57 .     methyl 2¦Á,3¦Á,23-trihydroxyurs-12-en-28-oate triacetate
    ÏàËÆ¶È:53.8%
Phytochemistry          1989          28          1703-1710
Configurational studies on hydroxy groups at C-2,3 and 23 or 24 of oleanene and ursene-type triterpenes by NMR spectroscopy
Hisashi Kojima,Haruo Ogura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
58 .     Taraxasterol-3-O-¦Â-D-glucoside
    ÏàËÆ¶È:53.8%
Helvetica Chimica Acta          2010          93          414-421
Two New Sesquiterpene Lactones and a Triterpene Glycoside from Cichorium glandulosum
Hankui Wu, Zhen Su, Xuelei Xin and Haji Akber Aisa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
59 .     29-O-¦Â-D-Glucopyranosy-3¦Â,23-dihydroxyolean-12-en-28-oic
C48H70O16     ÏàËÆ¶È:53.8%
Pharmazie          2006          61          474-477
¦Ã-Pyranone derivatives and other constituents from Erigeron annuus
Xin Li, Jing Pan and Kun Gao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
60 .     3-O-trans-p-Coumaroyl actinidic acid
C39H52O7     ÏàËÆ¶È:53.8%
Archives of Pharmacal Research          2008          31          666-670
A new pancreatic lipase inhibitor isolated from the roots of Actinidia arguta
Dae Sik Jang, Ga Young Lee, Junghyun Kim, Yun Mi Lee and Jong Min Kim, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
61 .     (Z)-2¦Á-ôÇ»ùÎÚËÕËá-3-O-¶ÔÏã¶¹Ëáõ¥
    ÏàËÆ¶È:53.8%
Chinese Pharmaceutical Journal          2010          45          825-828
Isolation and Identification of 3-O-p-Coumaroyloxyl Pentacyclic Triterpenoids from Lysimachia clethroides Duby
XU Qiong-ming, TANG Li-hua, LI Xia, HAO Li-li, LI Xiao-ran*, YANG Shi-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
62 .     (20R)-20,25-epoxy-dammaran-3¦Â,6¦Á,12¦Â¦Â-triol-3-(3',3'-dimethyl) succinate
C36H60O7     ÏàËÆ¶È:53.8%
Bioorganic & Medicinal Chemistry          2009          17          3003-3010
Synthesis of dammarane-type triterpene derivatives and their ability to inhibit HIV and HCV proteases
Ying Wei, Chao-Mei Ma, Masao Hattori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
63 .     jacoumaric acid
    ÏàËÆ¶È:53.8%
Journal of the Chinese Chemical Society          2005          52          1275-1280
Triterpene Acids from the Leaves of Planchonella duclitan (Blanco) Bakhuizan
Tzong-Huei Lee*, Shin-Hun Juang Feng-Lin Hsu and Cheng-Yi Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
64 .     3¦Â-O-cis-p-coumaroyltormentic acid
C39H54O7     ÏàËÆ¶È:53.8%
Journal of Ethnopharmacology          2008          116          554-560
Antibacterial compounds from Planchonia careya leaf extracts
Jacqui M. McRae, Qi Yang, Russell J. Crawford, Enzo A. Palombo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
65 .     enfumafungin
C38H60O12     ÏàËÆ¶È:53.8%
Journal of the American Chemical Society          2000          122          4882-4886
Isolation and Structural Determination of Enfumafungin, a Triterpene Glycoside Antifungal Agent That Is a Specific Inhibitor of Glucan Synthesis
Robert E. Schwartz, Scott K. Smith, Janet C. Onishi, Maria Meinz, Myra Kurtz, Robert A. Giacobbe, Kenneth E. Wilson, Jerrold Liesch, Deborah Zink, Wendy Horn, Sandra Morris, Angeles Cabello, and Francisca Vicente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
66 .     compound 3
    ÏàËÆ¶È:53.8%
Journal of the American Chemical Society          2000          122          4882-4886
Isolation and Structural Determination of Enfumafungin, a Triterpene Glycoside Antifungal Agent That Is a Specific Inhibitor of Glucan Synthesis
Robert E. Schwartz, Scott K. Smith, Janet C. Onishi, Maria Meinz, Myra Kurtz, Robert A. Giacobbe, Kenneth E. Wilson, Jerrold Liesch, Deborah Zink, Wendy Horn, Sandra Morris, Angeles Cabello, and Francisca Vicente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
67 .     compound 4
C35H58O     ÏàËÆ¶È:53.8%
Journal of the American Chemical Society          2011          132          9734-9737
Sesquarterpenes (C35 Terpenes) Biosynthesized via the Cyclization of a Linear C35 Isoprenoid by a Tetraprenyl-¦Â-curcumene Synthase and a Tetraprenyl-¦Â-curcumene Cyclase: Identification of a New Terpene Cyclase
Tsutomu Sato, Satoru Yoshida, Hiroko Hoshino, Mizuki Tanno, Mami Nakajima, and Tsutomu Hoshino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
68 .     (20R)-12¦Â-O-(Boc-L-glycyl)-dammarane-3¦Â,20,25-triol
C37H65NO7     ÏàËÆ¶È:53.8%
Steroids          2013          78          203-209
Synthesis and anti-tumor evaluation of novel 25-hydroxyprotopanaxadiol analogs incorporating natural amino acids
Peng Wang, Xiu-Li Bi, Jing Xu, Hao-Nan Yuan, Hu-Ri Piao, Yu-Qing Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
69 .     3¦Â-(trans-p-coumaroyloxy)-2¦Á,23-dihydroxyurs-12,20(30)-dien-28-oic acid
    ÏàËÆ¶È:53.8%
China Journal of Chinese Materia Medica          2013          38          358-361
Triterpenes from aerial parts of Clematoclethra scandens subsp. actinidioides
XIAO Shi-ji, HE Da-hai, DING Li-sheng, ZHOU Yan, CHEN Fang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
70 .     Halicloic acid A
C38H56O5     ÏàËÆ¶È:53.8%
Journal of Natural Products          2012          75          1451-1458
Halicloic Acids A and B Isolated from the Marine Sponge Haliclona sp. Collected in the Philippines Inhibit Indoleamine 2,3-Dioxygenase
David E. Williams, Anne Steinø, Nicole J. de Voogd, A. Grant Mauk, and Raymond J. Andersen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
71 .     Halicloic acid B
C38H56O5     ÏàËÆ¶È:53.8%
Journal of Natural Products          2012          75          1451-1458
Halicloic Acids A and B Isolated from the Marine Sponge Haliclona sp. Collected in the Philippines Inhibit Indoleamine 2,3-Dioxygenase
David E. Williams, Anne Steinø, Nicole J. de Voogd, A. Grant Mauk, and Raymond J. Andersen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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