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chenyao1949: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-03-14 08:42:03
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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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
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Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     3-O-(2,3-dimethy lbutanoyl)-13-dodecanoylingenol
    ÏàËÆ¶È:57.8%
Chinese Traditional and Herbal Drugs          2010          41          877-881
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Structure      13C NMR   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
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2Â¥2013-03-13 19:17:45
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chenyao1949

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3Â¥2013-03-14 08:40:57
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chenyao1949

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2Â¥: Originally posted by wq0616 at 2013-03-13 19:17:45
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
Glyceroglyco ...

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