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Ìú¸Ëľ³æ (ÕýʽдÊÖ)
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chenyao1949: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-03-14 08:42:03
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chenyao1949: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-03-14 08:42:03
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1 . 1-O-(9Z,12Z,15Z-octadecatrienoyl)-2-O-hexadecanoyl-3-O-¦Á-(6-sulfoquinovopyranosyl)glycerol ÏàËÆ¶È:68.4% Phytochemistry Letters 2008 1 207-210 Glyceroglycolipids, a novel class of platelet-activating factor antagonists from Kalimeris indica Gao-jun Fan, Sanghee Kim, Byung Hoon Han, Yong Nam Han Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 2¦Á-N,N'-Dibutyl-1¦Á-25(OH)2 vitamin D3 C35H62NO3 ÏàËÆ¶È:63.1% Organic & Biomolecular Chemistry 2012 10 7826-7839 Synthesis of vitamin D3 derivatives with nitrogen-linked substituents at A-ring C-2 and evaluation of their vitamin D receptor-mediated transcriptional activity Junko Abe, Yu Nagai, Rui Higashikuni, Keisuke Iida, Takatsugu Hirokawa, Hazuki Nagai, Kaichiro Kominato, Toshio Tsuchida, Michiko Hirata, Masaki Inada, Chisato Miyaura and Kazuo Nagasawa Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . fanuxydol linoleate C35H54O3 ÏàËÆ¶È:60.5% Phytochemistry 1994 35 963-967 Linoleoylated polyacetylenes from the root of Panax ginseng Kazuhiro Hirakura, Makoto Morita, Kazuaki Niitsu, Yukinobu Ikeya, Masao Maruno Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 13-O-dodecanoylingenol ÏàËÆ¶È:60.5% Zeitschrift f¨¹r Naturforschung C 2008 63 59-65 Antinematodal Activities of Ingenane Diterpenes from Euphorbia kansui and their Derivatives against the Pine Wood Nematode (Bursaphelenchus xylophilus) J. Shi, Z. Li, T. Nitoda, M. Izumi, H. Kanzaki, N. Baba, K. Kawazu, and S. Nakajima Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . stigmast-7-en-3-ol-palmitate ÏàËÆ¶È:60% Journal of Shenyang Pharmaceutical University 2006 23 702-705 Chemistry study of Stellaria dichatoma L. var. lanceolata Bge. SUN Bo-hang, Yashikawa, CHEN Ying-jie, WU Li-jun Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Stigmastanol-3¦Â-p-butanoxydihydrocoumaroate C42H68O3 ÏàËÆ¶È:59.5% Phytochemical Analysis 2006 17 36-45 Chemical constituents of rice (Oryza sativa) hulls and their herbicidal activity against duckweed (Lemna paucicostata Hegelm 381) Ill Min Chung, Mohd Ali, Ateeque Ahmad, Jung Dae Lim, Chang Yeon Yu and Jin Seog Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Compound 2 C51H78O13 ÏàËÆ¶È:58.9% Bioorganic & Medicinal Chemistry Letters 2007 17 1003-1007 Synthesis of OSW saponin analogs with modified sugar residues and their antiproliferative activities Pingping Tang, Fatemah Mamdani, Xiaoyi Hu, Jun O. Liu, Biao Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Compound 3 C41H68O10 ÏàËÆ¶È:58.9% Bioorganic & Medicinal Chemistry Letters 2007 17 1003-1007 Synthesis of OSW saponin analogs with modified sugar residues and their antiproliferative activities Pingping Tang, Fatemah Mamdani, Xiaoyi Hu, Jun O. Liu, Biao Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . ergosta-7,22-dien-3¦Â-yl-palmitate ÏàËÆ¶È:58.9% Chinese Pharmaceutical Journal 2010 45 413-415 A New Sterol from the Fruiting Bodies of Ganoderma sinense Zhao, Xu et Zhang LIU Chao, CHEN Ruo-yun Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Stigmastanol-3¦Â-p-glyceroxydihydrocoumaroate C41H66O5 ÏàËÆ¶È:58.5% Phytochemical Analysis 2006 17 36-45 Chemical constituents of rice (Oryza sativa) hulls and their herbicidal activity against duckweed (Lemna paucicostata Hegelm 381) Ill Min Chung, Mohd Ali, Ateeque Ahmad, Jung Dae Lim, Chang Yeon Yu and Jin Seog Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Compound 5 C47H72O11 ÏàËÆ¶È:58.1% Bioorganic & Medicinal Chemistry Letters 2007 17 1003-1007 Synthesis of OSW saponin analogs with modified sugar residues and their antiproliferative activities Pingping Tang, Fatemah Mamdani, Xiaoyi Hu, Jun O. Liu, Biao Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . rouremin C45H87NO9 ÏàËÆ¶È:57.8% Phytochemistry 2006 67 1378-1384 Rourinoside and rouremin, antimalarial constituents from Rourea minor Zhen-Dan He, Cui-Ying Ma, Ghee Teng Tan, Kongmany Sydara, Pamela Tamez,Bounhoong Southavong, Somsanith Bouamanivong, D. Doel Soejarto,John M. Pezzuto, Harry H.S. Fong, Hong-Jie Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . oleoyl isocupressic acid ÏàËÆ¶È:57.8% Phytochemistry 2009 70 1262-1271 Terpenes with antimicrobial activity from Cretan propolis Milena P. Popova , Ioanna B. Chinou , Ilko N. Marekov , Vassya S. Bankova Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 3,7,11,15,19-Pentamethyl-9a,10a,11a,17a,18a-pentahydroxy-n-tetracosan-1-oxy-p-hydroxycaffeoate C18H32O2 ÏàËÆ¶È:57.8% Chemistry of Natural Compounds 2005 41 650-653 CHEMICAL CONSTITUENTS OF BROWN RICE GRAIN (Oryza sativa) I. M. Chung, Mohd Ali, A. Ahmad,C. Y. Yu,K. H. Ma, J. G. Gwag, and Y. J. Park Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . Pnnaxynol linoleute C35H54O2 ÏàËÆ¶È:57.8% Phytochemistry 1994 35 963-967 Linoleoylated polyacetylenes from the root of Panax ginseng Kazuhiro Hirakura, Makoto Morita, Kazuaki Niitsu, Yukinobu Ikeya, Masao Maruno Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . Compound 2b C35H60O5 ÏàËÆ¶È:57.8% Bioorganic & Medicinal Chemistry Letters 2002 12 3255-3258 Synthesis and testing of 2¦Á-Modified 1¦Á,25-Dihydroxyvitamin D3 analogues with a double side chain: marked cell differentiation activity Yoshitomo Suhara, Atsushi Kittaka, Seishi Kishimoto, Martin J. Calverley, Toshie Fujishima, Nozomi Saito, Takayuki Sugiura, Keizo Waku, Hiroaki Takayama Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 20-O-(2,3-dimethylbutanoy l)-13-O-dodecanoylingenol ÏàËÆ¶È:57.8% Chinese Traditional and Herbal Drugs 2010 41 877-881 ¸ÊË컯ѧ³É·ÖµÄÑо¿ ÎâÏþÀÚ;ÅËÇÚ Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 3-O-(2,3-dimethy lbutanoyl)-13-dodecanoylingenol ÏàËÆ¶È:57.8% Chinese Traditional and Herbal Drugs 2010 41 877-881 ¸ÊË컯ѧ³É·ÖµÄÑо¿ ÎâÏþÀÚ;ÅËÇÚ Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 1-O-(9 Z-octadecenoyl)-2-O-(8Z,11Z-octadecadienoyl)-sn-glycero-3-phosphorylcholine ÏàËÆ¶È:57.8% Archives of Pharmacal Research 2003 26 471-477 Phospholipids from Bombycis corpus and their neurotrophic effects Hak Cheol Kwon, I Yeon Jung, Se Yeon Cho, Ock Ryun Cho and Min Cheol Yang, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 3-O-(2'',3''-dimethylbutanoyl)-13-O-dodecanoylingenol C38H60O8 ÏàËÆ¶È:57.8% Zeitschrift f¨¹r Naturforschung C 2008 63 59-65 Antinematodal Activities of Ingenane Diterpenes from Euphorbia kansui and their Derivatives against the Pine Wood Nematode (Bursaphelenchus xylophilus) J. Shi, Z. Li, T. Nitoda, M. Izumi, H. Kanzaki, N. Baba, K. Kawazu, and S. Nakajima Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 5-O-(2,3-Dimethylbutanoyl)-13-O-dodecanoyl-20-O-deoxyingenol C38H60O7 ÏàËÆ¶È:57.8% Archives of Pharmacal Research 2012 35 1553-1558 Ingenane-type diterpenes with a modulatory effect on IFN-¦Ã production from the roots of Euphorbia kansui Piseth Khiev, Jae Wha Kim, Song Jae Sung, Hyuk-Hwan Song and Dong-Ho Choung, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 3-O-(2,3-Dimethylbutanoyl)-13-O-dodecanoyl-20-O-acetylingenol C40H61O9 ÏàËÆ¶È:57.5% Chemical & Pharmaceutical Bulletin 2003 51(8) 935-941 Diterpenes from the Roots of Euphorbia kansui and Their in Vitro Effects on the Cell Division of Xenopus(2) Li-Yan WANG,Nai-Li WANG,Xin-Sheng YAO,Syohei MIYATA,and Susumu KITANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . (3¦Â,22E)-stigmasta-5,9(11),22-trien-3-yl heptadecanoate C46H78O2 ÏàËÆ¶È:57.1% Chemistry & Biodiversity 2007 Vol. 4 1578 New Lipoxygenase-Inhibiting Constituents from Calligonum polygonoides Mirza Arfan Yawer, Ejaz Ahmed, Abdul Malik, Muhammad Ashraf, Muhammad Azam Rasool, and Nighat Afza Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . Compound 6 C50H76O11 ÏàËÆ¶È:57.1% Bioorganic & Medicinal Chemistry Letters 2007 17 1003-1007 Synthesis of OSW saponin analogs with modified sugar residues and their antiproliferative activities Pingping Tang, Fatemah Mamdani, Xiaoyi Hu, Jun O. Liu, Biao Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 17-benzoyloxy-3-O-(2,3-dimethylbutanoyl)-13-octanoyloxyingenol C41H56O10 ÏàËÆ¶È:56.4% Phytochemistry 2008 69 812-819 Ingenane diterpenoids from Euphorbia esula Zhi-Qiang Lu, Min Yang, Jin-Qiang Zhang, Guang-Tong Chen, Hui-Lian Huang,Shu-Hong Guan, Chao Ma, Xuan Liu, De-An Guo Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-03-13 19:17:45
chenyao1949
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3Â¥2013-03-14 08:40:57
chenyao1949
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4Â¥2013-03-14 08:41:15














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