| ²é¿´: 406 | »Ø¸´: 1 | |||
wprsahanľ³æ (СÓÐÃûÆø)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý²éѯ
|
| »¯ºÏÎï2£º10.5, 13.5, 18.3, 19.6, 20.1, 21.0, 22.9, 25.9, 26.0, 26.9, 29.2, 34.5, 35.9, 36.1, 39.5, 40.1, 47.2, 49.7, 51.2, 58.5, 70.5, 119.0, 122.8, 128.8, 136.6, 138.1, 144.0, 144.9, 147.8, 217.84 (125 MHz, CDCL3) |
» ²ÂÄãϲ»¶
324Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
311Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
085404£¬285·ÖÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
275 Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
µ÷¼Á
ÒѾÓÐ3È˻ظ´
ÉúÎïÓëÒ½Ò©273Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
274Çóµ÷¼ÁÇóµ÷¼Á
ÒѾÓÐ12È˻ظ´
0703»¯Ñ§
ÒѾÓÐ26È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ
ÒѾÓÐ3È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ£¡¼±Çó£¡
ÒѾÓÐ6È˻ظ´
10½ð±ÒÇóÖú΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
mzp-0
ľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 138 (¸ßÖÐÉú)
- ½ð±Ò: 3037.8
- ºì»¨: 3
- Ìû×Ó: 425
- ÔÚÏß: 45.1Сʱ
- ³æºÅ: 1739290
- ×¢²á: 2012-04-06
- ÐÔ±ð: MM
- רҵ: ÖÐÒ©ÖÊÁ¿ÆÀ¼Û
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
wprsahan(¶¹¸ç´ú·¢): ½ð±Ò+20, лл 2013-05-29 15:45:23
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
wprsahan(¶¹¸ç´ú·¢): ½ð±Ò+20, лл 2013-05-29 15:45:23
|
1 . 23-hydroxy-8(14¡ú13)-abeo-17,13-fried-3-oxolanosta-8,14(15),24-triene-26,23-olide C30H42O4 ÏàËÆ¶È:73.3% Phytochemistry 2013 86 168-175 Lipase inhibitory and LDL anti-oxidative triterpenes from Abies sibirica Mizuho Handa, Toshihiro Murata, Kyoko Kobayashi, Erdenechimeg Selenge, Toshio Miyase, Javzan Batkhuu, Fumihiko Yoshizaki Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 5 ÏàËÆ¶È:70.9% Chemistry of Natural Compounds 1991 27 444-449 TRITERPENOIDS FROM Abies SPECIES XII. (24Z)- and (24E)-8(14¡ú13)-ABEO-17,13-FRIEDOLANOSTA- 8,14(30),24-TRIENE-3,23-DION-26-OIC ACIDS - NEW TRITERPENOIDS FROM THE NEEDLES OF THE SIBERIAN FIR V. A. Raldugin, M. M. Shakirov,T. V. Leibyuk, and S. A. Shevtsov Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . dyvariabilin H C30H46O2 ÏàËÆ¶È:66.6% Journal of Natural Products 2001 64 159-163 New Tirucallane-Type Triterpenes from Dysoxylum variabile Hongmei Liu, Jörg Heilmann, Topul Rali, and Otto Sticher Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . quadrangularic acid J C31H50O5 ÏàËÆ¶È:64.5% Journal of Natural Products 2000 63 57-64 Thirteen Novel Cycloartane-Type Triterpenes from Combretum quadrangulare Arjun H. Banskota,Yasuhiro Tezuka, Kim Qui Tran, Ken Tanaka, Ikuo Saiki,and Shigetoshi Kadota Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3-oxotirucalla-7,24Z-dien-26-oic acid C30H46O3 ÏàËÆ¶È:63.3% Planta Medica 2000 66 463-468 Bioactive Compounds from Celaenodendron mexicanum Maria del Rayo Camacho,Rachel Mata, Perla Castaneda,Geoffrey C.Kirby,David C.Warhurst,Simon L.Croft,J.David Phillipson Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 24,25-Epoxy-tirucall-7-ene-3,23-dione C30H46O3 ÏàËÆ¶È:63.3% Acta Botanica Sinica 2004 46 1256-1260 A New Triterpenoid froMamoora dasyclada WANG Huan, ZHANG Xiao-Feng, YANG Shu-Min, LUO Xiao-Dong Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . centaurione C30H44O3 ÏàËÆ¶È:63.3% Fitoterapia 2000 71 130-133 Two new triterpene lactones from Centaurium pulchellum Hafsa Bibi, Saeed Anwer, G.A. Miana,Saeed Ahmad, Atta-ur-Rahman Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . hispidol B ÏàËÆ¶È:63.3% Chinese Traditional and Herbal Drugs 2009 40 1201-1204 ºìÊ÷ÁÖÖ²Îïľ¹û鬻¯Ñ§³É·ÖµÄÑо¿ ÉòÁ¢Èã;¹ù¶°;Òü±¦Î°;ÕÅÇà;ÕÔÀ×;»ô³¤ºç;ÕÅ‹ Àö;Ê·ÇåÎÄ;ÍõÓÀÀû Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . theonellasterone C30H48O ÏàËÆ¶È:63.3% 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 ̼Æ×Ä£Äâͼ 10 . Lamesticumin D C30H46O3 ÏàËÆ¶È:63.3% Journal of Natural Products 2011 74 1042-1048 Onoceranoid-Type Triterpenoids from Lansium domesticum Shi-Hui Dong, Chuan-Rui Zhang, Lei Dong, Yan Wu, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 3-Oxo-20-hydroxy-30¦Á-methyl,17(29)¦Á-epoxy-28-norlupane C29H46O3 ÏàËÆ¶È:63.3% Chemical & Pharmaceutical Bulletin 2012 60 955-961 Cytotoxic Terpenes from the Stems of Dipterocarpus obtusifolius Collected in Cambodia Piseth Khiev, Ok-Kyoung Kwon, Hyuk-Hwan Song, Sei-Ryang Oh, Kyung-Seop Ahn, Hyeong-Kyu Lee, Young-Won Chin Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 25-methoxy-tirucall-7-23 (trans)-diene-3-one C31H50O2 ÏàËÆ¶È:61.2% Phytochemistry 1995 40 1485-1487 Tirucallane triterpenes from the stem bark of Aglaia leucophylla Abdelilah Benosman, Pascal Richomme, Thierry Sevenet, Guillaume Perromat, A. Hamid A. Hadi, Jean Bruneton Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 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 ̼Æ×Ä£Äâͼ 14 . cornusalterin A C31H52O2 ÏàËÆ¶È:61.2% Journal of Natural Products 2011 74 54-59 Tirucallane Triterpenoids from Cornus walteri Ki Hyun Kim, Sang Un Choi, Young Choong Kim, and Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . cornusalterin H C31H50O2 ÏàËÆ¶È:61.2% Journal of Natural Products 2011 74 54-59 Tirucallane Triterpenoids from Cornus walteri Ki Hyun Kim, Sang Un Choi, Young Choong Kim, and Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . Methyl (13Z,15E,17E,22E)-3¦Â-hydroxy-12-oxomalabarica-13,15,17,22,24-pentaen-28-oate C31H44O4 ÏàËÆ¶È:61.2% Australian Journal of Chemistry 1982 35 39-50 Malabaricane triterpenes from a Great Barrier Reef collection of the sponge Jaspis stellifera BN Ravi and RJ Wells Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . toosendanic acid A C30H48O4 ÏàËÆ¶È:60% Journal of Natural Products 2009 72 917-920 Protolimonoids from Melia toosendan Yi Shu Sang,Chun Yan Zhou, Ai Jun Lu, Xiao Jin Yin,Zhi Da Min,and Ren Xiang Tan Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . neoabieslactone A C30H46O4 ÏàËÆ¶È:60% Journal of Natural Products 2009 72 1065-1068 Terpenoid Constituents of Abies chensiensis with Potential Anti-inflammatory Activity Yong-Li Li, Xian-Wen Yang, Su-Mei Li, Yun-Heng Shen, Hua-Wu Zeng, Xiao-Hua Liu, Jian Tang,and Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . neoabieslactone E C30H42O4 ÏàËÆ¶È:60% Journal of Natural Products 2009 72 1065-1068 Terpenoid Constituents of Abies chensiensis with Potential Anti-inflammatory Activity Yong-Li Li, Xian-Wen Yang, Su-Mei Li, Yun-Heng Shen, Hua-Wu Zeng, Xiao-Hua Liu, Jian Tang,and Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . foliasalaci B2 C30H50O2 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2008 56(7) 915-920 Hnew Triterpene Constituents, Foliasalacins A1¡ªA4, B1¡ªB3, and C, from the Leaves of Salacia chinensis Masayuki YOSHIKAWA,Yi ZHANG, Tao WANG, Seikou NAKAMURA, and Hisashi MATSUDA Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . ganoderic acid ¦Å C30H44O7 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2000 48(7) 1026-1033 Triterpenes from the Spores of Ganoderma lucidum and Their Cytotoxicity against Meth-A and LLC Tumor Cells Byung-Sun MIN,Jiang-Jing GAO,Norio NAKAMURA and Masao HATTORI Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 3,22-dioxo-20-taraxastene C30H46O2 ÏàËÆ¶È:60% Phytochemistry 2005 66 495-501 Cytotoxic triterpenes from the aerial roots of Ficus microcarpa Yi-Ming Chiang, Jang-Yang Chang, Ching-Chuan Kuo,Chi-Yen Chang, Yueh-Hsiung Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . stellettin K C30H42O4 ÏàËÆ¶È:60% Journal of Natural Products 2006 69(3) 373-376 Bioactive Isomalabaricane Triterpenoids from Rhabdastrella globostellata that Stabilize the Binding of DNA Polymerase ¦Â to DNA Jason A. Clement, Mei Li, Sidney M. Hecht, and David G. I. Kingston Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 3-oxotirucalla-7,24-dien-21-oic acid ÏàËÆ¶È:60% Journal of Natural Products 2000 63 238-242 Inhibitory Effects on HIV-1 Protease of Constituents from the Wood of Xanthoceras sorbifolia Chao-mei Ma, Norio Nakamura,Masao Hattori, Hiroko Kakuda,Jun-chan Qiao, and Hai-lan Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . carnosiflogenin C ÏàËÆ¶È:60% Planta Medica 2005 71 983-986 Four New Cucurbitane Glycosides from Hemsleya jinfushanensis Jian-Chao Chen, Xue-Mei Niu , Zhong-Rong Li , Ming-Hua Qiu Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . cycloart-23-ene-3, 25-diol C30H50O2 ÏàËÆ¶È:60% Acta Botanica Yunnanica 1999 21(2) 260-264 The constituents of Ervatamia divaricata YU Yang,LIU Ji-Kai Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . alisol B ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1993 41 2109-2112 Crude Drugs from Aquatic Plants. II. On the Constituents of the Rhizome of Alisma orientale JUZEP. Originating from Japan, Taiwan, and China. Absolute Stereostructures of 11-Deoxyalisols B and B 23-Acetate Masayuki YOSHIKAWA,Shoko HATAKEYAMA,Nobumitsu TANAKA,Toshiro MATSUOKA,Johji YAMAHARA and Nobutoshi MURAKAMI Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . scandenogenin C C30H50O3 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1988 36 234-243 Glycosides from Chinese Medicinal Plant, Hemsleya panacis-scandens, and Structure-Taste Relationship of Cucurbitane Glycosides RYOJI KASAI,KAZUHIRO MATSUMOTO,RUI-LIN NIE,JUN ZHOU and OSAMU TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . compound 22 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1988 36 234-243 Glycosides from Chinese Medicinal Plant, Hemsleya panacis-scandens, and Structure-Taste Relationship of Cucurbitane Glycosides RYOJI KASAI,KAZUHIRO MATSUMOTO,RUI-LIN NIE,JUN ZHOU and OSAMU TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . 2-cyano-2,3-seco-19¦Â,28-epoxy-18¦Á-oleanan-3-al' C30H47NO2 ÏàËÆ¶È:60% Chemistry of Natural Compounds 2008 44 606-611 SYNTHESIS OF LUPANE AND 19¦Â,28-EPOXY-18¦Á-OLEANANE 2,3-seco-DERIVATIVES BASED ON BETULIN I. A. Tolmacheva, A. V. Nazarov, O. A. Maiorova, and V. V. Grishko Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . compound 17 ÏàËÆ¶È:60% Chemistry of Natural Compounds 1985 21 328-332 TRITERPENOIDS FROM THE LEAVES OF THE SIBERIAN SPECIES OF BIRCH Betula nana and B. exilis N. D. Pokhilo, G. V. Malinovskaya, V. V. Makhan'kov, V. A. Denisenko, and N. I. Uvarova Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . compound 11 ÏàËÆ¶È:60% Chemistry of Natural Compounds 1984 20 170-173 GLYCOSYLATION OF BETULIN AND ITS ACETATES IN THE PRESENCE OF CADMIUM CARBONATE L. E. Odinokova, G. I. Oshitok, V. A. Denisenko, V. F. Anufriev, A. M, Tolkach, and N. I. Uvarova Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . olean-3-oxo-12-en-28,29-diol acetate ÏàËÆ¶È:60% Acta Pharmaceutica Sinica 1993 28 684-689 STUDIDS ON THE CHEMICAL CONSTITUENTS OF EUONYMUS MUPINENSIS XL Yah; SX Liao; HQ Liang and P Zhou Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . ganoderic acid ¦Å C30H44O7 ÏàËÆ¶È:60% Journal of Asian Natural Products Research 2002 4 129-134 A NEW LANOSTANE-TYPE TRITERPENE FROM THE FRUITING BODIES OF GANODERMA LUCIDUM JUN LUO, YU-YING ZHAO and ZHI-BIN LIN Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . 7¦Â-hydroxystigmasterol ÏàËÆ¶È:60% China Journal of Chinese Materia Medica 2009 34 1809-1811 Steroids from Monascus purpureus metabolite SHANG Xiaoya, WANG Ruolan, YI N Suqin, LI Jinjie, JIN Zonglian Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . dymacrin K C30H48O3 ÏàËÆ¶È:60% Phytochemistry 1999 52 1461-1468 Tirucallane triterpenes from Dysoxylum macranthum Khalit Mohamad, Marie-Th¨¦r¨¦se Martin, Marc Litaudon, Christiane Gaspard, Thierry S¨¦venet, Mary Païs Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . compound 2 ÏàËÆ¶È:60% Journal of Natural Products 1986 Vol 49 148 3-Oxo-28,29-Dihydroxyolean-12-Ene from Orthosphenia mexicana Antonio G. Gonzalez, Carmen M. Gonzalez, Angel G. Ravelo, Xorge A. Dominguez, Braulio M. Fraga Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . penasterone C30H46O3 ÏàËÆ¶È:60% Journal of Natural Products 1992 Vol 55 1682 Potent Inhibitors of Histamine Release, Two Novel Triterpenoids from the Okinawan Marine Sponge Penares incrustans Noboru Shoji, Akemi Umeyama, Setsuko Motoki, Shigenobu Arihara, Toshimasa Ishida, Kyosuke Nomoto, Jun'ichi Kobayashi, Masao Takei Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . lupenone ÏàËÆ¶È:60% Natural Product Sciences 2002 8 62-65 Chemical Constituents from Sorbus commixta Na, Min-Kyun; An, Ren-Bo; Min, Byung-Sun; Lee, Sang-Myung; Kim, Young-Ho; Bae, Ki-Hwan Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . carnosiflogenin C ÏàËÆ¶È:60% Phytochemistry 1996 41 1169-1174 Cucurbitane glycosides from Hemsleya panacis-scandens rhizomes Hideo Kubo, Kazuhiro Ohtani, Ryoji Kasai, Kazuo Yamasaki, Rui-Lin Nie, Osamu Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . 13¦Á,14¦Â,17¦Á-1anosta-7,24diene-3¦Â,11¦Â,16¦Á-triol C30H50O3 ÏàËÆ¶È:60% Phytochemistry 1994 36 417-419 A tetracyclic triterpenoid from Garuga pinnata G. Venkatraman, P. S. Thombare, B. K. Sabata Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . Alisol B C30H48O4 ÏàËÆ¶È:60% Phytochemistry 1994 36 119-127 Terpenoids of Alisma orientale rhizome and the crude drug alismatis rhizoma Yoshijiro Nakajima, Yohko Satoh, Masumi Katsumata (nee Ohtsuka), Kazuko Tsujiyama (nee Mikoshiba), Yoshiteru Ida, Junzo Shoji Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . Alisol C C30H46O5 ÏàËÆ¶È:60% Phytochemistry 1994 36 119-127 Terpenoids of Alisma orientale rhizome and the crude drug alismatis rhizoma Yoshijiro Nakajima, Yohko Satoh, Masumi Katsumata (nee Ohtsuka), Kazuko Tsujiyama (nee Mikoshiba), Yoshiteru Ida, Junzo Shoji Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . 6¦Â-hydroxy-lup-20(30)-en-3-one ÏàËÆ¶È:60% Phytochemistry 1991 30 3490-3493 11,11-dimethyl-1,3,8,10-tetrahydroxy-9-methoxypeltogynan and three pentacyclic triterpenes from Cassine transvaalensis Siegfried E. Drewes, M. Jeffrey Mashimbye, John S. Field, Niyum Ramesar Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . (5R,20R)-23-hydroxyl-8(14¡ú13R)-abeo-17,13-friedo-3-oxolanosta-8,14(30),24-triene-26,23-olide C30H42O4 ÏàËÆ¶È:60% Phytochemistry 2011 72 2197-2204 Miscellaneous terpenoid constituents of Abies nephrolepis and their moderate cytotoxic activities Dan-Wei Ou-Yang, Liang Wu, Yong-Li Li, Pei-Ming Yang, De-Yun Kong, Xian-Wen Yang, Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . 3¦Â-hydroxy-5¦Á,6¦Á-epoxy-9-oxo-9,11-secogorgostan-11-ol C30H50O4 ÏàËÆ¶È:60% Tetrahedron Letters 2000 41 6035-6040 New antiproliferative epoxysecosterols from Pseudopterogorgia americana Samina Naz, Russell G. Kerr, Ramaswamy Narayanan Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . compound 9 C30H50O3 ÏàËÆ¶È:60% Phytochemistry 1987 26 1371-1376 Sweet and bitter cucurbitane glycosides from hemsleya carnosiflora Ryoji Kasai,Kazuhiro Matsumoto,Rui-Lin Nie,Toshinobu Morita,Akimi Awazu,Jun Zhou,Osamu Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . 3-oxoolean-12-ene-20¦Á-carboxylic acid C30H46O3 ÏàËÆ¶È:60% Phytochemistry 1990 29 3259-3261 Friedelane and oleanane triterpenoids from bark wood ofAustroplenckia populnea Jost R. De Sousa,Gracia D.F. Silva,Jose¡äL. Pedersoli,Ricardo J Alves Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . 3¦Â,5¦Á,6¦Á-trihydroxy-9,11-secocholest-7-en-9-one C27H44O4 ÏàËÆ¶È:60% Steroids 1995 60 666-673 New cytotoxic steroids from the marine sponge Dysidea fragilis coming from the lagoon of Venice Anna Aiello, Ernesto Fattorusso, Marialuisa Menna, Rosa Carnuccio, Teresa Iuvone Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . 16,23-oxidoalisol B C30H46O4 ÏàËÆ¶È:60% Chinese Traditional and Herbal Drugs 2008 39 1788-1790 Ôóк»¯Ñ§³É·ÖµÄÑо¿ ºúÑ©ÑÞ;³Âº£Ï¼;¸ßÎÄÔ¶;ÁõÐÂÇÅ Structure 13C NMR ̼Æ×Ä£Äâͼ 51 . piscidinol A ÏàËÆ¶È:60% Chinese Journal of Natural Medicines 2009 7 31-33 Triterpenes from the Fruits of Phellodendron chinense Schneid var. glabriusculum Schneid YAN Chen; WANG Ye; HAO Xiao-Jiang Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . stigmast-5,22-dien-3¦Â,7¦Â-diol ÏàËÆ¶È:60% Journal of Shenyang Pharmaceutical University 2011 28 120-123 Isolation and identification of chemical constituents from whole plant of Saussurea involucrata Kar. et kir. HOU Peng-yi, HUANG Jian, SUN Bo-hang, WU Li-jun, GAO Hui-yuan Structure 13C NMR ̼Æ×Ä£Äâͼ 53 . (22E,24S)-3¦Á,5-cyclo-stigmast-22-en-6-one ÏàËÆ¶È:60% 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 ̼Æ×Ä£Äâͼ 54 . dyvariabilin H C30H48O3 ÏàËÆ¶È:60% Organic & Biomolecular Chemistry 2011 9 7685-7696 Protolimonoids and norlimonoids from the stem bark of Toona ciliata var. pubescens Jian-Rong Wang, Hai-Li Liu, Tibor Kurt¨¢n, Attila M¨¢ndi, S¨¢ndor Antus, Jia Li, Hai-Yan Zhang and Yue-Wei Guo Structure 13C NMR ̼Æ×Ä£Äâͼ 55 . alisol C ÏàËÆ¶È:60% Natural Product Research and Development 2001 13(4) 1-4 TERPENOIDS OF ALISMA ORIENTALIS JUZEP. PENG Guo ping; LOU Feng chang Structure 13C NMR ̼Æ×Ä£Äâͼ 56 . sodwanone R C30H46O4 ÏàËÆ¶È:60% Tetrahedron 1999 55 5555-5566 Several new isoprenoids from two marine sponges of the family Axinellidae Amira Rudi, Tesfamariam Yosief, Michael Schleyer, Yoel Kashman Structure 13C NMR ̼Æ×Ä£Äâͼ 57 . alisol B ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry Letters 2012 22 4787-4792 Triterpenes from Alisma orientalis act as farnesoid X receptor agonists Hsiang-Ru Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 58 . (24S)-24-ethyl-4¦Â-methyl-5¦Á-cholestan-3-one C30H50O ÏàËÆ¶È:60% 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 ̼Æ×Ä£Äâͼ 59 . alisol B C30H48O4 ÏàËÆ¶È:60% Biological and Pharmaceutical Bulletin 2012 35 1581-1587 The Rhizomes of Alisma orientale and Alisol Derivatives Inhibit Allergic Response and Experimental Atopic Dermatitis Je Hyeong Lee, Oh Song Kwon, Hong-Guang Jin, Eun-Rhan Woo, Yeong Shik Kim, Hyun Pyo Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 60 . 11¦Á-Hydroxy-¦Â-boswellic acid C30H48O4 ÏàËÆ¶È:60% Natural Product Communications 2008 3 21-26 Boswellic Acids with Acetylcholinesterase InhibitoryProperties from Frankincense Masahiro Ota and Peter J. Houghton Structure 13C NMR ̼Æ×Ä£Äâͼ 61 . 17¦Á-Hydroxy-28-nor-18¦Á(H)-lupan-3-one C29H48O2 ÏàËÆ¶È:60% Natural Product Communications 2008 3 1569-1574 Oxidative Decarboxylation of Triterpene C-28 Acids ofLupane Series Nataliya G. §¬omissarova, Nataliya G. Belenkova, Olga V. Shitikova, Leonid V. Spirikhin andMarat S. Yunusov Structure 13C NMR ̼Æ×Ä£Äâͼ 62 . 3-Hydroxymogrol C30H52O4 ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry 2011 19 5776-5781 Potential AMPK activators of cucurbitane triterpenoids from Siraitia grosvenorii Swingle Xu-bing Chen, Jing-jing Zhuang, Jun-hua Liu, Min Lei, Lei Ma, Jing Chen, Xu Shen, Li-hong Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 63 . compound 2a ÏàËÆ¶È:60% Chemistry of Natural Compounds 2012 48 821-826 Preparation and nitration of allobetulin seco-derivatives A. V. Shernyukov , I. Ya. Mainagashev, D. V. Korchagina, Yu. V. Gatilov, N. F. Salakhutdinov, G. A. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ 64 . 2,2-dinitrobetulone ÏàËÆ¶È:60% Chemistry of Natural Compounds 2012 48 821-826 Preparation and nitration of allobetulin seco-derivatives A. V. Shernyukov , I. Ya. Mainagashev, D. V. Korchagina, Yu. V. Gatilov, N. F. Salakhutdinov, G. A. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ 65 . Alisol B ÏàËÆ¶È:60% Archives of Pharmacal Research 2012 35 1919-1926 A new triterpenoid from Alisma orientale and their antibacterial effect Hong-Guang Jin, Qinglong Jin, A. Ryun Kim, Hyemin Choi, Je Hyun Lee, Yeong Shik Kim, Dong Gun Lee, Eun-Rhan Woo Structure 13C NMR ̼Æ×Ä£Äâͼ 66 . alisol A ÏàËÆ¶È:60% Chinese Traditional and Herbal Drugs 2012 43 841-843 A new triterpene in rhizome of Alisma orientale XU Nan; ZHANG Hong-da; XIE Xue Structure 13C NMR ̼Æ×Ä£Äâͼ 67 . 25-methoxy-cyc loart-23E-en-3¦Â-ol ÏàËÆ¶È:60% Chinese Journal of Applied & Environmental Biology 2005 11 265-270 CHEMICAL STUDY OF STREPTOCAULON GRIFFITHII MA Chunhui; HUANG Tianfang; QI Huayi; LI Bogang; ZHANG Guolin Structure 13C NMR ̼Æ×Ä£Äâͼ 68 . 29-O-acetyl-3-oxotirucalla-7,24-dien-21-oic acid ÏàËÆ¶È:59.3% Journal of Natural Products 2000 63 238-242 Inhibitory Effects on HIV-1 Protease of Constituents from the Wood of Xanthoceras sorbifolia Chao-mei Ma, Norio Nakamura,Masao Hattori, Hiroko Kakuda,Jun-chan Qiao, and Hai-lan Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 69 . acetoxyketone ÏàËÆ¶È:59.3% Chemistry of Natural Compounds 2007 43 153-158 REACTION OF 3-ACETOXY-(2,3),(19b,28)-DIEPOXYOLEANANE WITH CYCLIC AND LINEAR AMINES I. A. Tolmacheva, L. N. Shelepen'kina, A. S. Shashkov,V. V. Grishko, V. A. Glushkov, and A. G. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ 70 . 23(E)-cycloart-23-en-25-ethoxy-3¦Â-ol C32H54O2 ÏàËÆ¶È:59.3% Journal of the Chinese Chemical Society 2007 54 1565-1572 Triterpenoids and Other Constituents from Euphorbia humifusa Ying-Ge Pei, Quan-Xiang Wu and Yan-Ping Shi* Structure 13C NMR ̼Æ×Ä£Äâͼ 71 . quadrangularate N C31H48O4 ÏàËÆ¶È:58.0% Chemical & Pharmaceutical Bulletin 2000 48(4) 496-504 Methyl Quadrangularates A-D and Related Triterpenes from Combretum quadrangulare Arjun Hari BANSKOTA,Yasuhiro TEZUKA,Kim Qui TRAN,Ken TANAKA, Ikuo SAIKI and Shigetoshi KADOTA Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-04-11 18:08:06














»Ø¸´´ËÂ¥