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²éѯ½á¹û£º¹²²éµ½342¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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·, ƱÔÁ¼Ö¦, ³àÓðÕÉÃ÷, ´ó¹ÈÔ£Ö®, ÈÕ¹üÑÇÎ÷ Structure 13C NMR ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

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