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 13C谱（100MHz,CD3OD)16.6,18.2,20.1,20.4,21.3,28.3,2 9.5,31.5,34.3,35.2,38.5,39.9,41.3,44.3,47.4,51.6,84.7,121.5,126.7,133.7,134.9,136.8,158.6,189.8,201.6 |
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sydong
铁杆木虫 (著名写手)
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bixiaobin: 金币+5 2014-06-10 14:07:11
感谢参与，应助指数 +1
bixiaobin: 金币+5 2014-06-10 14:07:11
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查询结果：共查到106个化合物(查询结果仅供参考) 1 . 9α,11α-dihydroxyergosta-4,6,8(14),22-tetraen-3-one C28H40O3 相似度:60.7% Journal of Natural Products 2011 74 1281-1283 A Highly Conjugated Dihydroxylated C28 Steroid from a Myxobacterium Dnyaneshwar Gawas, Ronald Garcia, Volker Huch, and Rolf Müller Structure 13C NMR 碳谱模拟图 2 . ent-15β-angeloyloxy-9α-hydroxy-kaur-16-en-19-oic acid 相似度:60% Phytochemistry 2003 391-396 Studies of ent-kaurane diterpenes from Oyedaea verbesinoides for their inhibitory activity on vascular smooth muscle contraction Stefan Müller, Carlos R. Tirapelli, Ana M. de Oliveira, Renato Murillo,Victor Castro, Irmgard Merfort Structure 13C NMR 碳谱模拟图 3 . camaldulenic acid C30H46O4 相似度:58.6% Journal of Natural Products 1997 60 20-23 Triterpenoids from the Leaves of Eucalyptus camaldulensis var. obtusa Sabira Begum, Farhat, and Bina S. Siddiqui Structure 13C NMR 碳谱模拟图 4 . (23E)-27-Nor-25-oxo-5α-cholest-23-ene-3β,6α,8,14,15α-pentaol 15-O-sulfate,sodium salt C26H41O9SNa 相似度:57.6% Steroids 2010 75 897-904 Highly hydroxylated steroids of the starfish Archaster typicus from the Vietnamese waters Natalia V. Ivanchina, Alla A. Kicha, Trinh T.T. Huong, Anatoly I. Kalinovsky, Pavel S. Dmitrenok, Irina G. Agafonova, Pham Q. Long, Valentin A. Stonik Structure 13C NMR 碳谱模拟图 5 . pittosporatobiraside B C26H38O5 相似度:57.6% Phytochemistry 1989 28 3085-3091 Sesquiterpene glycosides and other terpene constituents from the flowers of Pittosporum tobira Kazuhito Ogihara,Kiyotaka Munesada,Takayuki Suga Structure 13C NMR 碳谱模拟图 6 . 24R-and 24S-methyl-3β,6 α,11-trihydroxy-9,11-seco-5 α-cholest-7,22E-diene-9-one 相似度:57.1% Steroids 1998 63 575-578 New 9,11-secosterols from gorgonia Subergorgia suberosa of the Indian Ocean M. Aknin, V. Costantino, A. Mangoni, E. Fattorusso, E. M. Gaydou Structure 13C NMR 碳谱模拟图 7 . 24,25,26,27-tetranor-apotirucall-6α,22-dihydroxy-7α-acetoxy-1,14,20(21)-trien-3-one-21,23-olide C28H36O7 相似度:57.1% Journal of Natural Products 2014 77 596-602 Bioactive Limonoids from the Leaves of Azaridachta indica (Neem) Maria J. Gualtieri, Nicola Malafronte, Antonio Vassallo, Alessandra Braca, Roberta Cotugno, Michele Vasaturo, Nunziatina De Tommasi, and Fabrizio Dal Piaz Structure 13C NMR 碳谱模拟图 8 . 22E-ergosta-4,6,8(14),22-tetraen-3-one C28H40O 相似度:57.1% Journal of Shenyang Pharmaceutical University 2012 29 678-684 A new disecosteroid from an endolichenic fungal stain Sporormiella irregularis(No.71-11-4-1) LI Yan-jun; LI Xiao-xia; CHEN Guo-dong; GAO Hao; GUO Liang-dong; YAO Xin-sheng Structure 13C NMR 碳谱模拟图 9 . camaldulenic acid methyl ester 相似度:56.6% Journal of Natural Products 1997 60 20-23 Triterpenoids from the Leaves of Eucalyptus camaldulensis var. obtusa Sabira Begum, Farhat, and Bina S. Siddiqui Structure 13C NMR 碳谱模拟图 10 . deacetyl-WF11605 C30H48O5 相似度:56.6% The Journal of Antibiotics 1992 45 704-708 WF11605, AN ANTAGONIST OF LEUKOTRIENE B4 PRODUCED BY A FUNGUSII. STRUCTURE DETERMINATION NOBUHARU SHIGEMATSU, EISAKU TSUJII, NATSUKO KAYAKIRI, SHIGEHIRO TAKASE, HIROKAZU TANAKA, TOSHIJI TADA Structure 13C NMR 碳谱模拟图 11 . compound 8 C22H34O4 相似度:56% Tetrahedron Letters 2002 43 9043-9046 Stypolactone, an interesting diterpenoid from the brown alga Stypopodium zonale Enrique Dorta, Mercedes Cueto, Ana R. Dı́az-Marrero, José Darias Structure 13C NMR 碳谱模拟图 12 . 2,3-dihydroxy-9(11)-fernen-23-oic acid 相似度:56% Natural Product Research and Development 2010 22 940-944 Chemical Constituents from Melastoma dodecandrum YANG Dan;MA Qing-yun; LIU Yu-qing; DING Zhong-tao; ZHOU Jun; ZHAO You-xing; Structure 13C NMR 碳谱模拟图 13 . Cholesta-8(14)-en-3β,5α,6α,25-tetrol C27H50O4N 相似度:55.5% Steroids 2005 70 954-959 Novel polyhydroxysterols from the Red Sea marine sponge Lamellodysidea herbacea Pierre Sauleau, Marie-Lise Bourguet-Kondracki Structure 13C NMR 碳谱模拟图 14 . (20R,22S,25S)-veratra-5,13-dien-3β-ol 相似度:55.5% China Journal of Chinese Materia Medica 2009 34 3039-3042 Steroidal alkaloids of from Veratrum dahuricum ZHAO Lang, OU Zhiqiang, WANG Kan, FU Hongzheng Structure 13C NMR 碳谱模拟图 15 . (2S,3R,5S,9R,10R,13R,14R,17R)-17-(2-((2R)-5-ethyl-5-methyl-tetrahydrofuran-2-yl)propan-2-yl)-2,3,5,14-tetrahydroxy-10,13,17-trimethyl-1,2,3,4,5,10,11,12,13,15,16,17-dodecahydro-9H-cyclopenta[a]phenanthren-6(14H)-one C30H48O6 相似度:55.5% Steroids 2011 76 1419-1424 Ecdysteroids from Polypodium vulgare L. András Simon, Attila Ványolós, Zoltán Béni, Miklós Dékány, Gábor Tóth, Mária Báthori Structure 13C NMR 碳谱模拟图 16 . ajugasterone D C27H42O7 相似度:55.5% Chinese Traditional and Herbal Drugs 2014 45 906-912 Chemical constituents from roots tubers of Serratula chinensis TANG Hai-jiao, FAN Chun-lin, WANG Gui-yang, WEI Wei, WANG Ying, YE Wen-cai Structure 13C NMR 碳谱模拟图 17 . 24-Methylene-shidasterone C28H42O6 相似度:53.5% Steroids 2007 72 751-755 Three new steroids from the roots of Serratula wolffii András Simon, Gábor Tóth, Erika Liktor-Busa, Zoltán Kele, Mária Takács, András Gergely, Mária Báthori Structure 13C NMR 碳谱模拟图 18 . (20S,22S)-3β,22-dihydroxycucurbita-5(10),24-diene-26,29-dioic acid δ-lactone C30H44O5 相似度:53.5% Natural Product Research 2002 16 261-266 New Triterpenoids from the Leaves of Abrus Precatorius Nam-Cheol Kim; Darrick Kim; A. Douglas Kinghorn Structure 13C NMR 碳谱模拟图 19 . Clionamine A C28H45NO3 相似度:53.5% Organic Letters 2008 Vol.10,No.14 2959-2962 Autophagy-Modulating Aminosteroids Isolated from the Sponge Cliona celata Robert A. Keyzers, Julie Daoust, Michael T. Davies-Coleman,Rob Van Soest,Aruna Balgi,Elizabeth Donohue, Michel Roberge, and Raymond J. Andersen Structure 13C NMR 碳谱模拟图 20 . 5α,6α-Epoxyergosta-8,22-diene-3β,7β-diol 相似度:53.5% Archives of Pharmacal Research 2008 31 579-586 Cytotoxic constituents of Amanita subjunquillea Ki Hyun Kim, Sang Un Choi, Ki Moon Park, Soon Ja Seok and Kang Ro Lee Structure 13C NMR 碳谱模拟图 21 . 22E,24R-ergosta-7,22-diene-3β,5α,6β,9α-tetraol C28H46O4 相似度:53.5% Chinese Journal of Medicinal Chemistry 2008 18 279-283 Chemical constituents from endophytic fungus S26 of Cephalotaxus hainanensis CHEN Ping, WU Jiao, DAI Hao-fu, XIE Xiu-chao, MEI Wen-li Structure 13C NMR 碳谱模拟图 22 . (22E,24R)-ergosta-7,22-diene-3β,5α,6α,9α-tetraol C32H52O4 相似度:53.5% 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 碳谱模拟图 23 . fomentarol B C28H46O 相似度:53.5% Phytochemistry 2013 92 137-145 Fomentarols A–D, sterols from the polypore macrofungus Fomes fomentarius Yi Zang, Juan Xiong, Wen-Zhu Zhai, Lei Cao, Sheng-Ping Zhang, Yu Tang, Ji Wang, Jing-Jing Su, Guo-Xun Yang, Yun Zhao, Hui Fan, Gang Xia, Chuan-Gui Wang, Jin-Feng Hu Structure 13C NMR 碳谱模拟图 24 . 15α-hydroxy-3,11-dione-oleana-12-en-30-oic ac 相似度:53.3% Journal of Asian Natural Products Research 2008 10 463-466 One new triterpenoid from biotransformation product of glycyrrhizic acid Li-Ping Kang, Jie Zhang, He-Shui Yua,4 Hong-Zhi Huang, Yong-Ze Wanga and Bai-Ping Ma Structure 13C NMR 碳谱模拟图 25 . cucurbita-5,23(E)-diene-3β,7β,25,29-tetraol C30H50O4 相似度:53.3% 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 Cátia Ramalhete, Joseph Molnár, Silva Mulhovo, Virgílio E. Rosário, Maria-José U. Ferreira Structure 13C NMR 碳谱模拟图 26 . 2α-hydroxyl-betulinic acid C30H48O4 相似度:53.3% Lishizhen Medicine and Materia Medica Research 2009 20 122-123 Studies on the Chemical Constituents of Potentilla discolor Bge LIU Pu; LI Jun-bo; LI Li-ying; YU Hua-ning; QIN Lin-lin; YIN Wei-ping Structure 13C NMR 碳谱模拟图 27 . 2α,3β-Dihydroxyolean-11-en-28,13β-olide C30H46O4 相似度:53.3% Phytochemistry 2013 94 229-237 Biotransformation of oleanolic and maslinic acids by Rhizomucor miehei Antonio Martinez, Francisco Rivas, Alberto Perojil, Andres Parra, Andres Garcia-Granados, Antonia Fernandez-Vivas Structure 13C NMR 碳谱模拟图 28 . 12α-bromo-2α,3β-dihydroxyolean-28,13β-olide C30H47BrO4 相似度:53.3% Phytochemistry 2013 94 229-237 Biotransformation of oleanolic and maslinic acids by Rhizomucor miehei Antonio Martinez, Francisco Rivas, Alberto Perojil, Andres Parra, Andres Garcia-Granados, Antonia Fernandez-Vivas Structure 13C NMR 碳谱模拟图 29 . 23-Hydroxybetulin 相似度:53.3% Natural Product Sciences 2013 19 269-274 Chemical Constituents from the Aerial Parts of Aster yomena Qinglong Jin, Hae Ju Ko, Young-Su Chang, and Eun-Rhan Woo* Structure 13C NMR 碳谱模拟图 30 . 1-hydroxy-20,22-didehydrotaxisterone C27H42O6 相似度:52% Journal of Natural Products 2007 70 884-886 Ecdysteroids from Serratula wolffii Roots Erika Liktor-Busa,András Simon, Gábor Tóth, Gábor Fekete, Zoltán Kele, and Mária Báthori Structure 13C NMR 碳谱模拟图 31 . compound 19 相似度:52% 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 碳谱模拟图 32 . 10-Acetoxy-18-hydroxy-2,7-dolabelladiene 相似度:52% Natural Product Sciences 2004 10 253-261 Bioactive Metabolites from the Brittle Star Ophioplocus japonicus Wang, Wei-Hong; Hong, Jong-Ki; Lee, Chong-Ok; Cho, Hee-Young; Shin, Sook; Jung, Jee-H. Structure 13C NMR 碳谱模拟图 33 . 3R,4S,5S,17R,20R-3,17,20-trihydroxy-4-methylpregn-8-en-7-one C22H34O4 相似度:52% Journal of Natural Products 2010 73 1294-1300 Homo- and Heptanor-sterols and Tremulane Sesquiterpenes from Cultures of Phellinus igniarius Xiuli Wu, Sheng Lin, Chenggen Zhu, Zhenggang Yue, Yang Yu, Feng Zhao, Bo Liu, Jungui Dai and Jiangong Shi Structure 13C NMR 碳谱模拟图 34 . compound 8 相似度:52% Journal of the Chemical Society, Perkin Transactions 1 1981 1773-1778 Cardenolide analogues. Part 12. 13C N.m.r. of semi-synthetic glycosides and side-chain modified genins H. T. Andrew Cheung, Lindsay Brown, John Boutagy and Richard Thomas Structure 13C NMR 碳谱模拟图 35 . petrosaspongiolide L C24H35O2N 相似度:52% Tetrahedron 1997 53 10451-10458 New cytotoxic sesterterpenes from the New Caledonian marine sponge Petrosaspongia nigra (Bergquist) Luigi Gomez Paloma, Antonio Randazzo, Luigi Minale, Cécile Debitus, Christos Roussakis Structure 13C NMR 碳谱模拟图 36 . compound 9a C25H35N3O4 相似度:52% The Journal of Organic Chemistry 2007 72 7190-7198 Spongolactams, Farnesyl Transferase Inhibitors from a Marine Sponge: Isolation through an LC/MS-Guided Assay, Structures, and Semisyntheses Daisuke Mori, Yuko Kimura, Shigeyuki Kitamura, Youji Sakagami, Yukio Yoshioka, Tomoaki Shintani, Tetsuji Okamoto, and Makoto Ojika Structure 13C NMR 碳谱模拟图 37 . 16-acetylkirenol C22H36O5 相似度:52% Chinese Journal of Natural Medicines 2012 10 13-15 A new carbamate with cytotoxic activity from the aerial parts of Siegesbeckia pubecens Jia LIU, Rong CHEN, Yu NIE, Lin FENG, Hai-Dao LI, Jing-Yu LIANG Structure 13C NMR 碳谱模拟图 38 . Neosymbioimine C21H27NO5S 相似度:52% Bioorganic & Medicinal Chemistry 2005 13 5253-5258 Symbioimine and neosymbioimine, amphoteric iminium metabolites from the symbiotic marine dinoflagellate Symbiodinium sp. Masaki Kita, Nao Ohishi, Kazuto Washida, Mikiko Kondo, Tomoyuki Koyama, Kaoru Yamada, Daisuke Uemura Structure 13C NMR 碳谱模拟图 39 . 3β-hydroxy-9(11)-fernen-23-oic acid C30H48O3 相似度:52% Chinese Traditional and Herbal Drugs 2011 42 1061-1065 Chemical constituents from Osbeckia chinensis CHEN, Chao, HU, Yu, SUN, Jia-xiang, PI, Hui-fang, ZHANG, Peng, RUAN, Han-li Structure 13C NMR 碳谱模拟图 40 . topsentisterol A3 C27H40O3 相似度:51.8% Journal of Natural Products 2006 69 1760-1768 26,27-Cyclosterols and Other Polyoxygenated Sterols from a Marine Sponge Topsentia sp. Xuan Luo, Famei Li, Pramod B. Shinde, Jongki Hong, Chong-O. Lee, Kwang Sik Im, and Jee H. Jung Structure 13C NMR 碳谱模拟图 41 . comnostin C C27H38O5 相似度:51.8% Journal of Natural Products 2000 63 339-343 Novel Extracellular Diterpenoids with Biological Activity from the Cyanobacterium Nostoc commune B. Jaki, J. Orjala, J. Heilmann, A. Linden, B. Vogler, and O. Sticher Structure 13C NMR 碳谱模拟图 42 . noscomin 相似度:51.8% Journal of Natural Products 1999 62 502-503 A Novel Extracellular Diterpenoid with Antibacterial Activity from the Cyanobacterium Nostoc commune Birgit Jaki, Jimmy Orjala, and Otto Sticher Structure 13C NMR 碳谱模拟图 43 . compound 18 相似度:51.8% 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 碳谱模拟图 44 . integristerone A 相似度:51.8% Helvetica Chimica Acta 2009 92 753-761 Ecdysteroids from Silene viridiflora András Simon, Noémi Tóth, Gábor Tóth, Zoltán Kele, Judit Groska, Mária Báthori Structure 13C NMR 碳谱模拟图 45 . integristerone A 相似度:51.8% Steroids 2004 69 389-394 A new ecdysteroid with unique 9β-OH and four other ecdysteroids from Silene italica ssp. nemoralis András Simon, Zita Pongrácz, Gábor Tóth, Marianna Mák, Imre Máthé, Mária Báthori Structure 13C NMR 碳谱模拟图 46 . moniloside C 相似度:51.8% Journal of Natural Products 1993 Vol 56 99 Brominated Indole Alkaloids from the Marine Tunicate Pseudodistoma arborescens Mohammed Chbani, Mary Païs, Jean-Marc Delauneux, Cécile Debitus Structure 13C NMR 碳谱模拟图 47 . β-ecdysterone 相似度:51.8% China Journal of Chinese Materia Medica 2010 35 2994-2998 Flavone and steroid chemical constituents from rhizome of Paris axialis HUANG Xianxiao; GAO Wenyuan; ZHAO Wanshun; ZHANG Tiejun; XU Jun Structure 13C NMR 碳谱模拟图 48 . 3β,6α,11-trihydroxy-9,11-seco-5α-cholest-7-ene-9-one C28H46O4 相似度:51.8% Steroids 1998 63 575-578 New 9,11-secosterols from gorgonia Subergorgia suberosa of the Indian Ocean M. Aknin, V. Costantino, A. Mangoni, E. Fattorusso, E. M. Gaydou Structure 13C NMR 碳谱模拟图 49 . 3β,5α,6α-trihydroxy-9,11-secocholest-7-en-9-one C27H44O4 相似度:51.8% 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 碳谱模拟图 50 . compound 10 C27H42O4 相似度:51.8% 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 碳谱模拟图 51 . 25-hydroxydacryhainansterone C27H42O7 相似度:51.8% Journal of China Pharmaceutical University 2006 37 487-490 Chemical constituents from Asparagus filicinus WU Jia-jun; WANG Hao; YE Wen-cai; ZUO Xiao-feng; ZHAO Shou-xun Structure 13C NMR 碳谱模拟图 52 . 20β-hydroxy-ecdysone-2-O-β-D-glucopyranoside 相似度:51.8% Natural Product Research and Development 2005 17 125-127 Chemical Constituents of Tinospora craveniana LI Hong-bo; HU Jun; CHEN Jian-chao; QIU Ming-hua Structure 13C NMR 碳谱模拟图 53 . 1α,20R-hydroxyecdysone 相似度:51.8% Natural Product Research and Development 2002 14(1) 9-12 STUDY ON THE CHEMICAL CONSTITUENTS OF LYCHNIS CORONARIA DAI Hao-fu; LIU Yu-qing; DENG Shi-ming; TAN Ning-hua; ZHOU Jun Structure 13C NMR 碳谱模拟图 54 . polypodingB 相似度:51.8% Natural Product Research and Development 2002 14(1) 9-12 STUDY ON THE CHEMICAL CONSTITUENTS OF LYCHNIS CORONARIA DAI Hao-fu; LIU Yu-qing; DENG Shi-ming; TAN Ning-hua; ZHOU Jun Structure 13C NMR 碳谱模拟图 55 . betulinic acid 相似度:51.8% Journal of Guangdong Phamaceutical University 2012 28 142-144 Studies on chemical constituents from Rubus alceaefolius Poir. XU Dan-dan, ZHOU Hong-bo, FANG Zhi-jian Structure 13C NMR 碳谱模拟图 56 . polypodine B C27H44O8 相似度:51.8% Chinese Traditional and Herbal Drugs 2014 45 906-912 Chemical constituents from roots tubers of Serratula chinensis TANG Hai-jiao, FAN Chun-lin, WANG Gui-yang, WEI Wei, WANG Ying, YE Wen-cai Structure 13C NMR 碳谱模拟图 57 . 25-hydroxydacryhainansterone 相似度:51.8% Chinese Traditional and Herbal Drugs 2012 43 1716-1720 Steroids from tubers of Asparagus filicinus TAO Hua-ming; WANG Li-shu; ZHAO Da-qing; ZHU Quan-hong; YIN Yong-guan; LIU Yong-hong Structure 13C NMR 碳谱模拟图 58 . 20-Hydroxyecdysone C27H44O7 相似度:51.8% Monatshefte für Chemie 2000 131 195-204 Three Saponins, a Steroid, and a Flavanol Glycoside from Achyrantes aspera Olaf Kunert, Ernst Haslinger, Martin G. Schmid, Josef Reiner, Franz Bucar, Efrem Mulatu, Dawit Abebe, and Asfaw Debella Structure 13C NMR 碳谱模拟图 59 . 水龙骨甾酮B C27H44O8 相似度:51.8% Journal of Tropical and Subtropical Botany 2013 21 57-62 Chemical Constituents from Roots of Achyranthes bidentata TANG Xin, PEI Gang, ZHOU Zhong-yu, TAN Jian-wen Structure 13C NMR 碳谱模拟图 60 . compound 4 相似度:51.8% The Journal of Organic Chemistry 1991 56 1146-1153 Novel marine polyhydroxylated steroids from the starfish Myxoderma platyacanthum Ester Finamore, Luigi Minale, Raffaele Riccio, Gaetano Rinaldo, Franco Zollo Structure 13C NMR 碳谱模拟图 61 . songarosaponin A C54H88O21 相似度:51.7% Phytochemistry 1991 30 3395-3400 Triterpene saponins from Verbascum songaricum Karlheiz Seifert, Alfred Preiss, Siegfried Johne, Jürgen Schmidt, Nguyen T. Lien, Catherine Lavaud, Georges Massiot Structure 13C NMR 碳谱模拟图 62 . crustulinol C30H50O6 相似度:51.7% Tetrahedron letters 1983 24 1635-1638 Fungal metabolites XIII: New cytotoxic triterpene from Hebeloma species (basidiomycetes) M. De Bernardi, G. Fronza, M.P. Gianotti, G. Mellerio, G. Vidari, P. Vita-Finzi Structure 13C NMR 碳谱模拟图 63 . 5α-stigmasta-7,9(11),24(28)Z-triene-3β,26,29-triol C29H46O3 相似度:51.7% Phytochemistry 2013 96 288-298 Steroids with anti-inflammatory activity from Vernonia nigritiana Oliv. & Hiern. Antonio Vassallo, Nunziatina De Tommasi, Irmgard Merfort, Rokia Sanogo, Lorella Severino, Marco Pelin, Roberto Della Loggia, Aurelia Tubaro, Silvio Sosa Structure 13C NMR 碳谱模拟图 64 . sarcsteroid C 相似度:51.7% Steroids 2013 78 1353-1358 Bioactive polyhydroxylated sterols from the marine sponge Haliclona crassiloba Zhong-Bin Cheng, Han Xiao, Cheng-Qi Fan, Ya-Nan Lu, Ge Zhang, Sheng Yin Structure 13C NMR 碳谱模拟图 65 . Rubrajaleelic acid C29H46O4 相似度:51.7% Phytochemistry Letters 2013 6 291-298 Isolation and characterization of the chemical constituents from Plumeria rubra Nasim Akhtar, Muhammad Saleem, Naheed Riaz, M. Shaiq Ali, Asma Yaqoob, Faiz-ul-Hassan Nasim, Abdul Jabbar Structure 13C NMR 碳谱模拟图 66 . 3β-Hydroxy-4,4-dimethylcholesta-8,24-dien-23-one 3-β-D-Xyloside 相似度:51.7% The Journal of Organic Chemistry 1988 53 5941-5947 Sarasinoside A1: a saponin containing amino sugars isolated from a sponge Francis J. Schmitz, Mohamad B. Ksebati, Sarath P. Gunasekera, Santosh Agarwal Structure 13C NMR 碳谱模拟图 67 . serrulatin E C30H50O6 相似度:50% Helvetica Chimica Acta 2008 Vol. 91 665 Triterpenoids from the Edible Leaves of Photinia serrulata Ya-Ling Song, Yue-Hu Wang, Qing Lu, Hui-Jun Qiao, and Yong-Xian Cheng Structure 13C NMR 碳谱模拟图 68 . cylindrictone C C28H46O4 相似度:50% Helvetica Chimica Acta 2008 Vol. 91 1578 Six New Dammarane Triterpenoids from Viburnum cylindricum Lin Tu, Yu Zhao, Zu-Yin Yu, Yu-Wen Cong, Gang Xu, Li-Yan Peng, Peng-Tao Zhang, Xiao Cheng, and Qin-Shi Zhao Structure 13C NMR 碳谱模拟图 69 . topsentisterol B4 C28H44O3 相似度:50% Journal of Natural Products 2006 69 1760-1768 26,27-Cyclosterols and Other Polyoxygenated Sterols from a Marine Sponge Topsentia sp. Xuan Luo, Famei Li, Pramod B. Shinde, Jongki Hong, Chong-O. Lee, Kwang Sik Im, and Jee H. Jung Structure 13C NMR 碳谱模拟图 70 . topsentisterol B5 C28H44O3 相似度:50% Journal of Natural Products 2006 69 1760-1768 26,27-Cyclosterols and Other Polyoxygenated Sterols from a Marine Sponge Topsentia sp. Xuan Luo, Famei Li, Pramod B. Shinde, Jongki Hong, Chong-O. Lee, Kwang Sik Im, and Jee H. Jung Structure 13C NMR 碳谱模拟图 71 . topsentisterol D3 C28H42O2 相似度:50% Journal of Natural Products 2006 69 1760-1768 26,27-Cyclosterols and Other Polyoxygenated Sterols from a Marine Sponge Topsentia sp. Xuan Luo, Famei Li, Pramod B. Shinde, Jongki Hong, Chong-O. Lee, Kwang Sik Im, and Jee H. Jung Structure 13C NMR 碳谱模拟图 72 . mahureone D 32H48O6 相似度:50% Journal of Natural Products 2005 68 979-984 Acylphloroglucinol Derivatives from Mahurea palustris Georges Massiot, Christophe Long, Bruno David, Marie-Jeanne Serrano, Florence Daubi, Frdric Alby, Frdric Ausseil, Martine Knibiehler, Christian Moretti, Jean-Sbastien Hoffmann, Christophe Cazaux, and Catherine Lavaud Structure 13C NMR 碳谱模拟图 73 . plakinamine J C30H50N2 相似度:50% Journal of Natural Products 2003 66 1536-1539 New Cytotoxic Steroidal Alkaloids from the Philippine Sponge Corticium niger Christian P. Ridley and D. John Faulkner Structure 13C NMR 碳谱模拟图 74 . 20,22-didehydrotaxisterone C27H42O5 相似度:50% Journal of Natural Products 2007 70 884-886 Ecdysteroids from Serratula wolffii Roots Erika Liktor-Busa,András Simon, Gábor Tóth, Gábor Fekete, Zoltán Kele, and Mária Báthori Structure 13C NMR 碳谱模拟图 75 . (22E)-2α-Fluoro-5α-stigmasta-22-en-3,6-dione C29H45O2F 相似度:50% Steroids 2009 74 435-440 Synthesis and biological activity of brassinosteroids fluorinated at C-2 Sofía L. Acebedo, Javier A. Ramírez, Lydia R. Galagovsky Structure 13C NMR 碳谱模拟图 76 . 22E,4R-ergosta-7,22-diene-3β,5α,6β,9α,14α-pentol C28H46O5 相似度:50% Natural Product Research 2008 22 1137-1142 Sterols and triterpenoids from the spores of Ganoderma lucidum Chuan-Rui Zhang; Sheng-Ping Yang; Jian-Min Yue Structure 13C NMR 碳谱模拟图 77 . 5α-ergosta-7,22-diene-3β,5,6β-triol 相似度:50% Journal of Natural Products 1988 Vol 51 1098 Polar Steroids from the Marine Scallop Patinopecten yessoensis Maria Iorizzi, Luigi Minale, Raffaele Riccio, Jong-Soo Lee, Takeshi Yasumoto Structure 13C NMR 碳谱模拟图 78 . 6-oxotingenol C28H36O4 相似度:50% Journal of Natural Products 1994 Vol 57 1675 Cytotoxic Aromatic Triterpenes from Maytenus ilicifolia and Maytenus chuchuhuasca Osamu Shirota, Hiroshi Morita, Koichi Takeya, Hideji Itokawa, Yoichi Iitaka Structure 13C NMR 碳谱模拟图 79 . (22E,24R,25S)-24-methyl-5α-cholesta-22-en-3β,5,6β,15α,26-pentaol 26-sulfate 相似度:50% Journal of Natural Products 1995 Vol 58 653-671 Chemical and Biological Investigation of the Polar Constituents of the Starfish Luidia clathrata, Collected in the Gulf of Mexico Maria Iorizzi, Patrick Bryan, James McClintock, Luigi Minale, Elio Palagiano, Stefano Maurelli, Raffaele Riccio, Franco Zollo Structure 13C NMR 碳谱模拟图 80 . (22E,24R)-3β,5α,9α-trihydroxyergosta-7,22-dien-6-one 相似度:50% Chinese Journal of Marine Drugs 2009 28(5) 11-16 Cytotoxic metabolites from symbiotic fungus Penicilliom sp.HK13-8 with Rhizophora stylosa HAN Xiu-li, LIN Zhen-jian, TAO Hong-wen, LIU Pei-pei, WANG Yi, ZHU Wei-ming Structure 13C NMR 碳谱模拟图 81 . compound 1a 相似度:50% Zeitschrift für Naturforschung B 2011 66b 624-628 Dialiumoside, an Olean-18-ene Triterpenoid from Dialium excelsum Angelbert F. Awantu, Bruno N. Lenta, Tobias Bogner, Yanick F. Fongang,Silvère Ngouela, Jean D. Wansi, Etienne Tsamo, and Norbert Sewald Structure 13C NMR 碳谱模拟图 82 . 7α,21α-dihydroxyfriedelane-3-one C30H50O3 相似度:50% Zeitschrift für Naturforschung B 2010 65b 1284-1288 Study on Chemical Constituents and Cytotoxic Activities of Salacia chinensis Growing in Vietnam Tran Thi Minh, Nguyen Thi Hoang Anh, Vu Dao Thang, and Tran Van Sung Structure 13C NMR 碳谱模拟图 83 . 2α,3β-dihydroxylup-20(29)-en-28-oic acid C30H48O4 相似度:50% Phytochemistry Letters 2011 4 259-266 Seven new triterpene glycosides from the pericarps of Stryphnodendron fissuratum Akihito Yokosuka, Sachiko Kawakami, Mitsue Haraguchi, Yoshihiro Mimaki Structure 13C NMR 碳谱模拟图 84 . (24R)-24-Hydroxymethyl-24-bydroxycholesterol 相似度:50% Journal of Natural Products 1995 58 653-671 Chemical and Biological Investigation of the Polar Constituents of the Starfish Luidia clathrata, Collected in the Gulf of Mexico Maria Iorizzi, Patrick Bryan, James McClintock, Luigi Minale, Elio Palagiano, Stefano Maurelli, Raffaele Riccio, Franco Zollo Structure 13C NMR 碳谱模拟图 85 . compound 12 相似度:50% 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 碳谱模拟图 86 . betulinic acid 相似度:50% Chinese Traditional and Herbal Drugs 2009 40 1039-1042 山矾的化学成分研究 霍长虹;梁鸿;张庆英;王邠;赵玉英 Structure 13C NMR 碳谱模拟图 87 . 3β,11-dihydroxy-24-methyl-9,11-secocholest-5-en-9-one 相似度:50% Chinese Journal of Natural Medicines 2010 8 186-188 Cytotoxic 9,11-Secosterols from the Marine Soft Coral Sinularia robusta HE Xi-Xin; ZHANG Cui-Xian; ZENG Long-Mei; YANG Xiao-Ping Structure 13C NMR 碳谱模拟图 88 . 25-Epi-pseudolarolide Q C30H42O7 相似度:50% Planta Medica 2011 77 1924-1931 Antimicrobial, Cytotoxic Lignans and Terpenoids from the Twigs of Pseudolarix kaempferi He, Wen-Jun; Chu, Hong-Biao; Zhang, Yu-Mei; Han, Hong-Jin; Yan, He; Zeng, Guang-Zhi; Fu, Zhao-Hui; Olubanke, Ogunlana; Tan, Ning-Hua: Structure 13C NMR 碳谱模拟图 89 . balsaminol E C30H48O3 相似度:50% Bioorganic & Medicinal Chemistry 2010 18 5254-5260 New antimalarials with a triterpenic scaffold from Momordica balsamina Cátia Ramalhete, Dinora Lopes, Silva Mulhovo, Joseph Molnár, Virgílio E. Rosário, Maria-José U. Ferreira Structure 13C NMR 碳谱模拟图 90 . (22E,24R)-ergosta-7,22-diene-3β,5α,6β-triol C28H46O3 相似度:50% Natural Product Research and Development 2007 19 620-622 Chemical Constituents of Piper pedicellatum C. DC LI Jun-zhu; LIU Hai-yang; DONG Qiu; CHEN Chang-xiang Structure 13C NMR 碳谱模拟图 91 . betulinic acid 相似度:50% Natural Product Research and Development 2006 18 58-60 Chemical Constituents from Euphorbia latifolia ZHANG Lei-hong; ZHANG Xian-tao; YE Wen-cai; YIN Zhi-qi; ZHENG Dan; ZHAO Shou-xun Structure 13C NMR 碳谱模拟图 92 . simiarenol 相似度:50% Natural Product Research and Development 2004 16 131-132 STUDIES ON CHEMICAL CONSTITUENTS OF GENDARUSSA VENTRICOSA ZHANG Xiao-li;YU Zheng-wen;GUO Fang-qin; YANG Xiao-sheng *; HAO Xiao-jiang Structure 13C NMR 碳谱模拟图 93 . parathiosteroid B C26H39NO3S 相似度:50% The Journal of Organic Chemistry 2008 73 7978-7984 Isolation, Biological Significance, Synthesis, and Cytotoxic Evaluation of New Natural Parathiosteroids A−C and Analogues from the Soft Coral Paragorgia sp. Javier Jesus Poza, Rogelio Fernandez, Fernando Reyes, Jaime Rodriguez and Carlos Jimenez Structure 13C NMR 碳谱模拟图 94 . (20R,22R)-2β,3β,20,22,25-pentahydroxy-5β-cholest-8(14)-en-6-one 相似度:50% Russian Journal of Organic Chemistry 2010 46 1735-1740 Δ8(14)-14α-deoxy- and 14α-deoxy-14α-hydroperoxyecdysteroids A. Sh. Ibragimova, N. A. Ves’kina, I. V. Galyautdinov and V. N. Odinokov Structure 13C NMR 碳谱模拟图 95 . andrastin C 相似度:50% The Journal of Antibiotics 1996 49 1278-1280 Andrastin D, Novel Protein Farnesyltransferase Inhibitor Produced by Penidllium sp. FO-3929 RYUJI UCHIDA, KAZURO SHIOMI, JUNJI INOKOSHI, HARUO TANAKA, YUZURU IWAI, SATOSHI OMURA Structure 13C NMR 碳谱模拟图 96 . andrastin D C26H36O5 相似度:50% The Journal of Antibiotics 1996 49 1278-1280 Andrastin D, Novel Protein Farnesyltransferase Inhibitor Produced by Penidllium sp. FO-3929 RYUJI UCHIDA, KAZURO SHIOMI, JUNJI INOKOSHI, HARUO TANAKA, YUZURU IWAI, SATOSHI OMURA Structure 13C NMR 碳谱模拟图 97 . 12-O-β-D-glucopyranosyl-3,11,16-trihydroxyabieta-8,11,13-triene 相似度:50% Phytotherapy Research 2010 24 1720-1723 Anti-complement activity of isolated compounds from the roots of Clerodendrum bungei Steud. 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(22E,24R)-5α,8α,-epidioxyergosta-6,9,22-triene-3β-ol 相似度:50% Journal of Guangdong Phamaceutical University 2011 27 256-259 Chemical constituents of the mycelia of Guignardia mangiferae,an endophyte from Smilax glabra LIANG Fa-liang, LI Dong-li, TAO Mei-hua, ZHANG De-zhi, ZHANG Wei-min Structure 13C NMR 碳谱模拟图 102 . monacolin O acetone ketal C28H44O8 相似度:50% Journal of Asian Natural Products Research 2013 15 600-609 Cytotoxic monacolin analogs from Monascus purpureus-fermented rice Ming-Tao Liu, A-Li Wang, Zhen Sun, Jin-Jie Li, Xiu-Li Wu, Yan-Xia Liu & Xiao-Ya Shang Structure 13C NMR 碳谱模拟图 103 . fomentarol A C28H44O 相似度:50% Phytochemistry 2013 92 137-145 Fomentarols A–D, sterols from the polypore macrofungus Fomes fomentarius Yi Zang, Juan Xiong, Wen-Zhu Zhai, Lei Cao, Sheng-Ping Zhang, Yu Tang, Ji Wang, Jing-Jing Su, Guo-Xun Yang, Yun Zhao, Hui Fan, Gang Xia, Chuan-Gui Wang, Jin-Feng Hu Structure 13C NMR 碳谱模拟图 104 . 24,25,26,27-tetranor-apotirucall-6α-hydroxy-7α-acetoxy-14-en-3-one-21,24-anhydride C28H38O7 相似度:50% Journal of Natural Products 2014 77 596-602 Bioactive Limonoids from the Leaves of Azaridachta indica (Neem) Maria J. 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