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²éѯ½á¹û£º¹²²éµ½114¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . sachalinoside B C16H28O7 ÏàËÆ¶È:81.2% Chemical & Pharmaceutical Bulletin 2001 49(4) 396-401 Prolyl Endopeptidase Inhibitors from the Underground Part of Rhodiola sachalinensis Wenzhe FAN,Yasuhiro TEZUKA,Khin May NI,and Shigetoshi KADOTA Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . trans-Linalool-3,6-oxide-¦Â-D-glucopyranoside C16H28O7 ÏàËÆ¶È:75% Planta Medica 2012 78 1574-1578 New Monoterpenes, Diterpenes, and Lignans from Abies recurvata Li, Yong-Li; Zhang, Ji-Gang; Yu, Ping; Ke, Bei-Lei; Ye, Ji; Yang, Xian-Wen; Jin, Hui-Zi; Zhang, Wei-Dong: Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Neroplofurol C15H28O4 ÏàËÆ¶È:60% Journal of Natural Products 2010 73 563-567 Sesquiterpenes from Oplopanax horridus Taichi Inui, Yuehong Wang, Dejan Nikolic, David C. Smith, Scott G. Franzblau and Guido F. Pauli Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . rel-(3S,6S,7R,10R)-7,10-epoxy-3,7,11-trimethyldodec-1-ene-3,6,11-triol ÏàËÆ¶È:60% Mycosystema 2011 30 268-274 Purification,identification and antitumor activities of secondary metabolites from marine fungus Eutypella scoparia FS26 SUN Li; LI Dong-Li CHEN Yu-Chan TAO Mei-Hua ZHANG Wei-Min DAN Fei-Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . rehmaionoside A ÏàËÆ¶È:57.8% Phytochemistry 1991 30 1639-1644 Norcarotenoid glycosides of Rehmannia glutinosa var. Purpurea Hiroshi Sasaki, Hiroaki Nishimura, Takashi Morota, Takao Katsuhara, Masao Chin (Chen Zhengxiong), Hiroshi Mitsuhashi Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . dihydroxy-¦Â-ionone ÏàËÆ¶È:57.8% Pharmazie 2003 58 593-595 Phytochemical studies of Rehmannia glutinosa rhizomes Anh, N. T. H. - Sung, T. V. - Franke, K. - Wessjohann, L. A. Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . sibirinine ÏàËÆ¶È:57.1% Chemistry of Natural Compounds 1987 23 569-573 ALKALOIDS OF Nitraria sibirica. STRUCTURE AND ABSOLUTE CONFIGURATION OF SIBIRININE A. A. Ibragimov, N. D. Abdullaev, Z. Osmanov, and S. Yu. Yunusov Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 5 C14H20O4 ÏàËÆ¶È:57.1% Organic Letters 2004 Vol. 6, No. 9 1501-1504 Synthesis of the CDE/FG Ring Models of Prymnesins: Reassignment of the Relative Configuration of the E/F Ring Juncture Makoto Sasaki, Makoto Ebine, Hiroyuki Takagi, Hiroyuki Takakura,Takeshi Shida, Masayuki Satake, Yasukatsu Oshima, Tomoji Igarashi, and Takeshi Yasumoto Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 5-O-Tosylate-1,2-O-isopropylidene-¦Á-D-xylofuranose ÏàËÆ¶È:57.1% Marine drugs 2012 10 881-889 First Total Synthesis of a Naturally Occurring Iodinated 5'-Deoxyxylofuranosyl Marine Nucleoside Jianyun Sun, Yanhui Dou, Haixin Ding, Ruchun Yang, Qi Sun and Qiang Xiao Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 2,3,4,-tri-O-benzyl-1-C-butyl-D-glucopyranose C31H38O6 ÏàËÆ¶È:57.1% Heterocycles 2010 82 531-542 A Synthetic Approach to Anhydroketopyranoses Having a 6,8-Dioxabicyclo[3.2.1]octane Structure from Ketopyranoses Takashi Yamanoi, Kazuhide Matsumura, Sho Matsuda, and Yoshiki Oda Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (-)-oleuropeic acid 8-O-¦Â-D-glucopyranoside [=(4S)-4-(1-¦Â-D-glucopyranosyloxy-1-methyl)ethyl-1-cyclohexene-1-carboxylic acid] C16H26O8 ÏàËÆ¶È:56.2% Chemical & Pharmaceutical Bulletin 2005 53(7) 783-787 A Monoterpene Glucoside and Three Megastigmane Glycosides from Juniperus communis var. depressa Tsutomu NAKANISHI,Naoki IIDA,Yuka INATOMI,Hiroko MURATA,Akira INADA,Jin MURATA,Frank A. LANG,Munekazu IINUMA,Toshiyuki TANAKA,and Yoshikazu SAKAGAMI Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 7 ÏàËÆ¶È:56.2% Journal of Natural Products 2000 63 749-752 Galloylglucosides from Berries of Pimenta dioica Hiroe Kikuzaki, Akemi Sato, Yoko Mayahara, and Nobuji Nakatani Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (4S)-p-menth-1-ene-7,8-diol 8-O-¦Â-D-glucopyranoside ÏàËÆ¶È:56.2% Chemical & Pharmaceutical Bulletin 1998 46 1595-1598 Monoterpenoid Glycosides of Glehnia littoralis Root and Rhizoma Junichi KITAJIMA,Chieko OKAMURA,Toru ISHIKAWA and Yasuko TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (-)-cis-chrysanthenol-O-¦Â-D-glucopyranoside ÏàËÆ¶È:56.2% China Journal of Chinese Materia Medica 2009 34 1520-1522 Chemical constituents from Centipeda minima PU Shoucheng, GUO Yuanqiang, GAO Wenyuan Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 6,7-dihydroxy-dihydrolinalool 7-O-¦Â-glucopyranoside C16H30O8 ÏàËÆ¶È:56.2% Phytochemistry 2000 53 937-940 Monoterpene and pregnane glucosides from Solenostemma argel M.S. Kamel, K. Ohtani, H.A. Hasanain, M.H. Mohamed, R. Kasai, K. Yamasaki Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (-)-¦Á-terpineol-8-O-¦Â-D-glucopyranoside C16H28O6 ÏàËÆ¶È:56.2% Chinese Traditional and Herbal Drugs 2010 41 533-536 Â黯¸ùµÄ»¯Ñ§³É·ÖÑо¿ ÌÕ»ªÃ÷;ÍõÁ¥Êé;´ÞÕ¼³¼;ÕÔ´óÇì;ÁõÓÀºê Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (+)-¦Á-terpineol-8-O-¦Â-D-glucopyranoside C16H28O6 ÏàËÆ¶È:56.2% Chinese Traditional and Herbal Drugs 2010 41 533-536 Â黯¸ùµÄ»¯Ñ§³É·ÖÑо¿ ÌÕ»ªÃ÷;ÍõÁ¥Êé;´ÞÕ¼³¼;ÕÔ´óÇì;ÁõÓÀºê Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . Betulabuside B ÏàËÆ¶È:56.2% Archives of Pharmacal Research 2010 33 75-80 A new norlupane triterpene from the leaves of Acanthopanax koreanum increases the differentiation of osteoblastic MC3T3-e1 cells Sang Hyouk Park, Nguyen Xuan Nhiem, Phan Van Kiem, Eun Mi Choi and Jeong Ah Kim, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 10¦Â,11bepoxyguaiane-1¦Á,4¦Á,7¦Á- triol C15H26O4 ÏàËÆ¶È:53.3% Phytochemistry 2008 69 2088-2094 Three types of sesquiterpenes from rhizomes of Atractylodes lancea He-Xiang Wang, Chun-Mei Liu, Quan Liu, Kun Gao Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . macrophyllilactone D ÏàËÆ¶È:53.3% Phytochemistry 2001 58 1121-1128 A bis-sesquiterpene and sesquiterpenolides from Inula macrophylla Bo Fu, Bao-Ning Su, Yoshihisa Takaishi, Gisho Honda, Michiho Ito,Yoshio Takeda, Olimjon K. Kodzhimatov, Ozodbek Ashurmetov Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . ainigmaptilone B ÏàËÆ¶È:53.3% Journal of Natural Products 2003 66 888-890 Ainigmaptilones, Sesquiterpenes from the Antarctic Gorgonian Coral Ainigmaptilon antarcticus Katrin B. Iken and Bill J. Baker Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 4 (15)-cadinene-6,10-diol C23H24O11 ÏàËÆ¶È:53.3% Journal of Asian Natural Products Research 2004 6 199-204 CHEMICAL CONSTITUENTS FROM ALPINIA TONKINENSIS JIAN ZHANG and LING-YI KONG Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . (1S,3S,4S,7S,10S)-3,4-dihydroxy-bisabolol oxide B C15H28O4 ÏàËÆ¶È:53.3% Phytochemistry 1995 39 1077-1080 Biotransformation of (− -¦Á-bisabolol by plant pathogenic fungus, Glomerella cingulataMitsuo Miyazawa, Hirokazu Nankai, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . (3aR*,7sR*)-2-(2,3-O-isopropyliden-¦Â-D-ribofuranosyl)perhydro-1,2-benzisoazole C15H25NO5 ÏàËÆ¶È:53.3% Helvetica Chimica Acta 1977 60 1273-1295 Stereoselektivitt und Reaktivitt bei der 1,3-dipolaren Cycloaddition chiraler N-(Alkoxyalkyl)nitrone Andrea Vasella Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 6-O-acetyl-2,3,4,-tri-O-benzyl-1-C-butyl-D-glucopyranose C33H40O7 ÏàËÆ¶È:53.3% Heterocycles 2010 82 531-542 A Synthetic Approach to Anhydroketopyranoses Having a 6,8-Dioxabicyclo[3.2.1]octane Structure from Ketopyranoses Takashi Yamanoi, Kazuhide Matsumura, Sho Matsuda, and Yoshiki Oda Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . 2,10-dibromo-3-chloro-7,8:9,10-diepoxychamigrane C15H21Br2ClO2 ÏàËÆ¶È:53.3% Bulletin of the Chemical Society of Japan 1999 72 289-292 Fourteen Chamigrane Derivatives from a Red Alga, Laurencia nidifica Junji Kimura, Noboru Kamada, Yoshikazu Tsujimoto Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . compound 37a C15H26O6 ÏàËÆ¶È:53.3% Bioorganic & Medicinal Chemistry 2010 18 2501-2514 Conjugates of plumbagin and phenyl-2-amino-1-thioglucoside inhibit MshB, a deacetylase involved in the biosynthesis of mycothiol David W. Gammon, Daniel J. Steenkamp, Vuyo Mavumengwana, Mohlopheni J. Marakalala, Theophilus T. Mudzunga, Roger Hunter, Muganza Munyololo Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . compound 37b C15H26O6 ÏàËÆ¶È:53.3% Bioorganic & Medicinal Chemistry 2010 18 2501-2514 Conjugates of plumbagin and phenyl-2-amino-1-thioglucoside inhibit MshB, a deacetylase involved in the biosynthesis of mycothiol David W. Gammon, Daniel J. Steenkamp, Vuyo Mavumengwana, Mohlopheni J. Marakalala, Theophilus T. Mudzunga, Roger Hunter, Muganza Munyololo Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . sinularone F C15H24O3 ÏàËÆ¶È:53.3% Marine Drugs 2012 10 1331-1344 Sinularones A¨CI, New Cyclopentenone and Butenolide Derivatives from a Marine Soft Coral Sinularia sp. and Their Antifouling Activity Haiyan Shi, Shanjiang Yu, Dong Liu, Leen van Ofwegen, Peter Proksch and Wenhan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . compound 34 C17H26O6S ÏàËÆ¶È:53.3% Heterocycles 2012 86 535-553 Synthesis of 15,28-Dideoxy-15,28-didehydrothyrsenol Mary A. Smart and Frank E. McDonald Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . (+)-pinocarveol 3-O-¦Â-D-glucopyranoside C16H26O6 ÏàËÆ¶È:53.3% Natural Product Communications 2013 8 847-849 Regioselective Hydroxylation and Glucosylation of ¦Á- and ¦Â-Pinenes with Cultured Cells of Eucalyptus perriniana Kei Shimoda, Naoji Kubota, Manabu Hamada, Ken Suwada, Hatsuyuki Hamada and Hiroki Hamada Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . (-)-pinocarveol 3-O-¦Â-D-glucopyranoside C16H26O6 ÏàËÆ¶È:53.3% Natural Product Communications 2013 8 847-849 Regioselective Hydroxylation and Glucosylation of ¦Á- and ¦Â-Pinenes with Cultured Cells of Eucalyptus perriniana Kei Shimoda, Naoji Kubota, Manabu Hamada, Ken Suwada, Hatsuyuki Hamada and Hiroki Hamada Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . (1S,6R,7S,10S)-7-isopropyl-10-methyl-4-methylenedecahydronaphthalene-6,10-diol C15H26O2 ÏàËÆ¶È:53.3% Acta Crystallographica Section E 2007 63 o3579 6¦Â,10¦Â-Cadinene-6,10-diol: a sesquiterpenoid from the rhizome of Acorus calamus L. Wei-Wei Dong, Kai-Bei Yu, Jian-Min Yue and Run-Hua Lu Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . rehmaionoside A C19H34O8 ÏàËÆ¶È:52.6% Chemical & Pharmaceutical Bulletin 1996 44 41-47 Chemical Studies on Crude Drug Processing IX. On the Constituents of Rehmanniae Radix. (3). Absolute Stereostructures of Rehmaionosides A, B, and C, and Rehmapicroside, Biologically Active Ionone Glucosides and a Monoterpene Glucoside Isolated from Chines Masayuki YOSHIKAWA,Youichi FUKUDA,Toshio TANIYAMA and Isao KITAGAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . rehmaionoside B C19H34O8 ÏàËÆ¶È:52.6% Chemical & Pharmaceutical Bulletin 1996 44 41-47 Chemical Studies on Crude Drug Processing IX. On the Constituents of Rehmanniae Radix. (4). Absolute Stereostructures of Rehmaionosides A, B, and C, and Rehmapicroside, Biologically Active Ionone Glucosides and a Monoterpene Glucoside Isolated from Chines Masayuki YOSHIKAWA,Youichi FUKUDA,Toshio TANIYAMA and Isao KITAGAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . 2-methoxyl derivative C20H36O8 ÏàËÆ¶È:52.6% Chemical & Pharmaceutical Bulletin 1996 44 41-47 Chemical Studies on Crude Drug Processing IX. On the Constituents of Rehmanniae Radix. (7). Absolute Stereostructures of Rehmaionosides A, B, and C, and Rehmapicroside, Biologically Active Ionone Glucosides and a Monoterpene Glucoside Isolated from Chines Masayuki YOSHIKAWA,Youichi FUKUDA,Toshio TANIYAMA and Isao KITAGAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . (1R,2R)-p-menth-3-ene-1,2-diol 1-O-¦Â-Dglucopyranoside C16H28O7 ÏàËÆ¶È:50% Phytochemistry 2004 65 3279-3287 Monoterpenoids and their glycosides from the leaf of thyme Junichi Kitajima, Toru Ishikawa, Atushi Urabe, Mitsuru Satoh Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . betulalbuside A C16H28O7 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2004 52(9) 1086-1090 Terpenic and Phenolic Glycosides from Leaves of Breynia officinalis HEMSL. Hiroyuki MORIKAWA,Ryoji KASAI, Hideaki OTSUKA,Eiji HIRATA,Takakazu SHINZATO,Mitsunori ARAMOTO,and Yoshio TAKEDA Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . 3,7-dimethyloct-l-ene-3,6,7-triol C15H30O8 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2000 48(7) 1090-1097 Conduritol F Glucosides and Terpenoid Glucosides from Cynanchum liukiuense and Distribution of Conduritol F Glucosides in Several Asclepiadaceous Plants Fumiko ABE and Tatsuo YAMAUCHI ,Keiichi HONDA,and Nanao HAYASHI Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . (1R,4R,6R)-4,6-dihydroxy-1,8-cineole-4-O-¦Â-D-glucopyranoside C16H28O8 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1996 44 337-342 Five New Monoterpene Glycosides and Other Compounds form Foeniculi Fructus (Fruit of Foeniculum vulgare MILLER) Masateru ONO,Yasuyuki ITO,Thoru ISHIKAWA,Junichi KITAJIMA,Yasuko TANAKA,Yujiro NIIHO and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . 1-cyclohexenylmethyl ¦Â-D-glucopyranoside ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1995 43 920-926 Inhibitory Effect of Perillosides A and C, and Related Monoterpene Glucosides on Aldose Reductase and Their Structure-Activity Relationships Tomoyuki FUJITA,Kumiko OHIRA,Kazutaka MIYATAKE,Yoshihisa NAKANO and Mitsuru NAKAYAMA Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . nardosinone ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1993 41 1183-1184 Cytotoxic Sesquiterpenes from Nardostachys chinensis Hideji ITOKAWA,Koichi MASUYAMA,Hiroshi MORITA and Koichi TAKEYA Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . compound 4 ÏàËÆ¶È:50% Chemistry of Natural Compounds 1985 21 197-202 STRUCTURE OF PSOLUSOSIDE A - THE MAIN TRITERPENE GLYCOSIDE FROM THE HOLOTHURIAN Vsolus fahricii V. I. Kalinin, A. I. Kalinovskii, and V. A. Stonik Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . angelitriol B C15H18O6 ÏàËÆ¶È:50% Chinese Chemical Letters 1993 4 885-886 TWO NEW COUMARINS FROM ANGELCIA PUBESCENS F.BISERRTA JIANG HUA LIU,YING JIE GUO,SUI XU XU,XIN SHENG YAO Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . compound 6 ÏàËÆ¶È:50% Chinese Chemical Letters 2006 17 1563-1565 Synthesis of New Thiazine and Thiosemicarbazone Derivatives from D-Xylose Xiao Ming JI, He Ping SUN, Hai Wei XU, Hong Min LIU Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . crenulatin C11H20O6 ÏàËÆ¶È:50% Acta Pharmaceutica Sinica 1992 27 117-120 STUDIES ON THE CHEMICAL COMPONENTS OF RHODIOLA CRENULATA S Wang; FP Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . foeniculoside VII ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1998 46 1738-1742 Water-Soluble Constituents of Fennel. VI. 1, 8-Cineole Type Glycosides Toru ISHIKAWA,Junichi KITAJIMA,Yasuko TANAKA,Masateru ONO,Yasuyuki ITO and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . 10-hydroxy-trans-linalyl oxide 7-O-¦Â-D-glucopyranoside C16H28O8 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1998 46 1748-1751 Water-Soluble Constituents of Fennel. VII. Acyclic Monoterpenoid Glycosides Toru ISHIKAWA,Yasuko TANAKA and Junichi KITAJIMA Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . betulalbuside A ÏàËÆ¶È:50% China Journal of Chinese Materia Medica 2009 34 2895-2897 Water-soluble chemical constituents from fruits of Phellodendron chinense var. glabriusculum YAN Chen, WANG Ye, HAO Xiaojiang Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . 3,7-dimethyloct-1-ene-3,6,7-triol 3-O-¦Â-D-glucopyranoside C16H30O8 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1999 47 639-642 Monoterpenoid Glucosides of Cnidium monnieri Fruit Junichi KITAJIMA,Yoshie AOKI,Toru ISHIKAWA and Yasuko TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ |
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-¦Á-bisabolol by plant pathogenic fungus, Glomerella cingulata