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²éѯ½á¹û£º¹²²éµ½13¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 3¦Á-hydroxysulphonyloxy-5¦Á,6¦Á-epoxy-megastigmen-9-one C13H20O6S ÏàËÆ¶È:92.3% Journal of Asian Natural Products Research 2008 10 319-321 A new sulphated nor-sesquiterpene from mangrove Laguncularia racemosa (L.) Gaertn. F. Duo-Qing Xue, Ji-Dong Wang and Yue-Wei Guo Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (3S,5R,6S,7E)-3,5,6-trihydroxy-7-megastigmen-9-one C13H19O4 ÏàËÆ¶È:69.2% Natural Product Research and Development 2013 25 1658-1661 Chemical Constituents from Croton caudatus var. tomentosus ZHONG Jin-dong, LI Yan-ping, LI Hong-mei, LI Hai-zhou, LI Rong-tao* Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (3S,5R,6S,7E)-3,5,6-trihydroxy-7-megastigmen-9-one ÏàËÆ¶È:69.2% Archives of Pharmacal Research 2011 34 533-542 Isolation of megastigmane sesquiterpenes from the silkworm (Bombyx mori L.) droppings and their promotion activity on HO-1 and SIRT1 Ji-Hae Park, Do-Gyeong Lee, Seung-Woo Yeon, Hyuk-Sang Kwon and Jong-Hee Ko, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3¦Â-hydroxy-5¦Á,6¦Á-epoxy-7-megastigmen-9-one ÏàËÆ¶È:61.5% China Journal of Chinese Materia Medica 2013 38 839-843 Chemical constituents from leaves of Rhododendron rubiginosum var. rubiginosum YANG Yong-xun, YAN Yong-ming, TAO Ming, LUO Qian, DONG Xiao-ping Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3-Hydroxy-5¦Á,6¦Á-epoxy-¦Â-ionone C13H20O3 ÏàËÆ¶È:53.8% Archives of Pharmacal Research 2004 27 600-603 Norisoprenoids and hepatoprotective flavone glycosides from the aerial parts of Beta vulgaris var. cicla Inkyum Kim, Young-Won Chin, Song Won Lim, Young Choong Kim and Jinwoong Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (+)-(3S,6R,7R)-tremulene-6,11,12-triol C15H26O3 ÏàËÆ¶È:53.3% 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 ̼Æ×Ä£Äâͼ 7 . (4R)-4-hydroxy-1,10-seco-muurol-5-ene-1,10-dione C15H24O3 ÏàËÆ¶È:53.3% Magnetic Resonance in Chemistry 2014 52 51-56 Muurolane-type sesquiterpenes from marine sponge Dysidea cinerea Phan Van Kiem, Chau Van Minh, Nguyen Xuan Nhiem, Nguyen Thi Cuc, Ngo Van Quang, Hoang Le Tuan Anh, Bui Huu Tai, Pham Hai Yen, Nguyen Thi Hoai, Kim Young Ho, Nanyoung Kim, SeonJu Park and Seung Hyun Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 8-hydroxy-3,7-dimethyl-l,6-octadiene ÏàËÆ¶È:50% Journal of Natural Products 1987 Vol 50 1048 Phytochemical Investigations on Penstemon hirsutus Birgit Gering, Max Wichtl Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . linalool C10H18O ÏàËÆ¶È:50% Phytochemistry 1994 36 709-716 Monoterpenoid and phenylethanoid glycosides from Ligustrum pedunculare Zheng-Dan He, Shinichi Ueda, Masako Akaji, Tetsuro Fujita, Kenichiro Inoue, Chong-Ren Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 2-(butylamino)-2-methylcyclohexanone C11H21NO ÏàËÆ¶È:50% Molecules 2012 17 6784-6807 Improved Methods for Thermal Rearrangement of Alicyclic ¦Á-Hydroxyimines to ¦Á-Aminoketones: Synthesis of Ketamine Analogues as Antisepsis Candidates Hagit Elhawi, Hadar Eini, Amos Douvdevani and Gerardo Byk Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . linalool ÏàËÆ¶È:50% Chemistry & Biodiversity 2013 10 96-128 Chemical Constituents and Biological Activities of Plants from the Genus Ligustrum Bei-Bei Gao, Gai-Mei She and Dong-Mei She Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 4¦Á,10¦Â-dimethyl-decahydronaphthalene-1¦Â,3¦Â,5¦Á,8¦Á-tetraol C12H22O4 ÏàËÆ¶È:50% Phytochemistry Letters 2013 6 110-112 Two new sesquiterpene derivatives from soil actinomycete Streptomyces albospinus 15-4-2 Lei Yu, Hao-fu Dai, You-xing Zhao, Wen-jian Zuo, Wen-hua Dong, Wen-li Mei, Hui-cai Zeng Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . rel-3a,6,7,7a-tetrahydro-7-hydroxy-2,2-dimethyl-[3a¦Á-(3a¦Á,7¦Á,7a¦Á)]-1,3-benzodioxole-5-carboxylic acid ÏàËÆ¶È:50% Journal of Agricultural and Food Chemistry 2002 50 3143-3146 Acylated and Non-Acylated Flavonol Monoglycosides from the Indian Minor Spice Nagkesar (Mammea longifolia) Lingamallu Jagan Mohan Rao, Hiroshi Yada, Hiroshi Ono, and Mitsuru Yoshida Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2014-06-27 11:47:29
guoquan5001
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3Â¥2014-06-27 11:49:19
guoquan5001
½ð³æ (СÓÐÃûÆø)
- Ó¦Öú: 48 (СѧÉú)
- ½ð±Ò: 809
- É¢½ð: 63
- ºì»¨: 2
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renhui1: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2014-07-01 14:58:16
renhui1: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2014-07-01 14:58:16
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Õý½â£º ²éѯ½á¹û£º¹²²éµ½17¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ixerin H C21H32O8 ÏàËÆ¶È:57.1% Chemical & Pharmaceutical Bulletin 1984 32 3403-3409 Sesquiterpene Lactones from Ixeris tamagawaensis KITAM. III HIDEHISA ASADA,TOSHIO MIYASE and SEIGO FUKUSHIMA Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . picrionoside A ÏàËÆ¶È:55.5% Phytochemistry 1990 29 2947-2951 Terpenoid glycosides from Picris hieracioides Taketo Uchiyama,Keiichi Nishimura,Toshio Miyase,Akira Ueno Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . kankanoside A C16H26O8 ÏàËÆ¶È:52.9% Chemical & Pharmaceutical Bulletin 2006 54(5) 669-675 Monoterpene Constituents from Cistanche tubulosa¡ªChemical Structures of Kankanosides A¡ªE and Kankanol¡ª Haihui XIE,Toshio MORIKAWA,Hisashi MATSUDA,Seikou NAKAMURA,Osamu MURAOKA,andMasayuki YOSHIKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . rehmapicroside C16H26O8 ÏàËÆ¶È:52.9% Chemical & Pharmaceutical Bulletin 1996 44 41-47 Chemical Studies on Crude Drug Processing IX. On the Constituents of Rehmanniae Radix. 12). 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 5 . (1S,3R,4R)-8,10-dihydroxyfenchone 10-O-¦Â-D-glucopyranoside C16H26O8 ÏàËÆ¶È:52.9% Chemical & Pharmaceutical Bulletin 1998 46 1599-1602 Water-Soluble Constituents of Fennel. III. Fenchane-Type monoterpenoid Glycosides Toru ISHIKAWA,Junichi KITAJIMA and Yasuko TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . laevigatanoside A ÏàËÆ¶È:52.9% China Journal of Chinese Materia Medica 1997 22 298-299 A Study on Chemical Componen tsfrom Rosa laeviga ta M ichx. L i Xiangri, Wei Luxue Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (1R,4R,7R)-8-hydroxybornan-2-one 8-O-¦Â-D-glucopyranoside ÏàËÆ¶È:52.9% Phytochemistry 1994 35 941-945 Biotransformation of (+)-camphor by cultured cells of Eucalyptus perriniana Yutaka Orihara, Takahiro Noguchi and Tsuomu Furuya Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 2-(4-oxo-2,2,3-trimethylcyclopenty)-thyl-¦Â-D-glucopyranoside ÏàËÆ¶È:52.9% Phytochemistry 1994 35 941-945 Biotransformation of (+)-camphor by cultured cells of Eucalyptus perriniana Yutaka Orihara, Takahiro Noguchi and Tsuomu Furuya Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . picrionoside B ÏàËÆ¶È:52.6% Phytochemistry 1990 29 2947-2951 Terpenoid glycosides from Picris hieracioides Taketo Uchiyama,Keiichi Nishimura,Toshio Miyase,Akira Ueno Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Oleanolic acid 3-O-¦Â-D-glucuronopyranosyl-28-3-O-¦Â-D-glucopyranoside C42H66O14 ÏàËÆ¶È:52.6% Natural Product Research and Development 2012 24 465-468 Chemical Constituents of Deutzia setchuenensis LI Chang-song; YU Hong-wei; CHEN Xiao-zhen; WU Xiao-qing; FANG Dong-mei; LI Guo-you Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . icariside C1 ÏàËÆ¶È:52.3% Chemical & Pharmaceutical Bulletin 2007 55(4) 551-556 Two New Steroid Glycosides and a New Sesquiterpenoid Glycoside from the Underground Parts of Trillium kamtschaticum Masateru ONO,Chika TAKAMURA,Fumie SUGITA,Chikako MASUOKA,Hitoshi YOSHIMITSU,Tsuyoshi IKEDA,and Toshihiro NOHARAc Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ixerin H ÏàËÆ¶È:52.3% Chemical & Pharmaceutical Bulletin 1986 34 4170-4176 Sesquiterpene Lactones from Ixeris dentata NAKAI MAMORU SETO,TOSHIO MIYASE and SEIGO FUKUSHIMA Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . icariside C1 C21H38O8 ÏàËÆ¶È:52.3% Chemical & Pharmaceutical Bulletin 1987 35 1109-1117 Studies on the Glycosides of Epimedium grandiflorum MORR. Var. thunbergianum (MIQ.) NAKAI. I TOSHIO MIYASE,AKIRA UENO,NOBUO TAKIZAWA,HIROMI KOBAYASHI and HIROKO KARASAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Henrylactone E C21H33O10Cl ÏàËÆ¶È:52.3% Planta Medica 2010 76 152-158 Henrylactones A¨CE and Anti-HBV Constituents from Illicium henryi Liu, Ji-Feng; Jiang, Zhi-Yong; Zhang, Quan; Shi, Yao; Ma, Yun-Bao; Xie, Ming-Jin; Zhang, Xue-Mei; Chen, Ji-Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . patrinoside-aglycone-11-O-2'-deoxy-¦Â-D-glucopyranoside C21H34O10 ÏàËÆ¶È:50% Journal of Natural Products 2009 72 1798-1803 Iridoid Glycosides from the Leaves of Sambucus ebulus Valerio Pieri, Stefan Schwaiger, Ernst P. Ellmerer, and Hermann Stuppner Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . Rakanmakilactone C C20H26O7S ÏàËÆ¶È:50% Tetrahedron 2004 60 171-177 Rakanmakilactones A¨CF, new cytotoxic sulfur-containing norditerpene dilactones from leaves of Podocarpus macrophyllus var. maki Hyun-Sun Park, Naoki Yoda, Haruhiko Fukaya, Yutaka Aoyagi, Koichi Takeya Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . Patrinoside-aglycone-11-O-2'-deoxy-¦Â-glucopyranoside C21H34O10 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2011 59 803-833 Naturally Occurring Iridoids and Secoiridoids. An Updated Review, Part 4 Biswanath DINDA, Sudhan DEBNATH, and Rajarshi BANIK Structure 13C NMR ̼Æ×Ä£Äâͼ |
4Â¥2014-06-27 11:51:39














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