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cuitianzeng: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-04-19 10:42:56
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1 .     4-O-demethylmanassantin B
C40H46O11     ÏàËÆ¶È:60.6%
Journal of Natural Products          2004          67          767-771
Molecular-Targeted Antitumor Agents: The Saururus cernuus Dineolignans Manassantin B and 4-O-Demethylmanassantin B Are Potent Inhibitors of Hypoxia-Activated HIF-1
Tyler W. Hodges, Chowdhury Faiz Hossain, Yong-Pil Kim, Yu-Dong Zhou, and Dale G. Nagle
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     manassantin B
    ÏàËÆ¶È:60.6%
Korean Journal of Pharmacognosy          2007          38(2)          176-180
Hepatoprotective Constituents of Saururus chinensis Roots Against Tacrine-induced Cytotoxicity in Human Liver-derived Hep G2 Cells
Jeong, Gil-Saeng; Li, Bin; Lee, Dong-Sung; Kwon, Ji-Wung; Lee, Hye-Suk; Kwon, Tae-Oh; Kim, Youn-Chul
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     Compound 2c
    ÏàËÆ¶È:60.6%
Bioorganic & Medicinal Chemistry Letters          2005          15          385-388
Saucerneol B derivatives as human acyl-CoA: cholesterol acyltransferase inhibitors
Tae-Sook Jeong, Kyung Soon Kim, Hana Yu, Mi Jeong Kim, Kyung-Hyun Cho, Yang-Kyu Choi, Hyoung-Chin Kim, Ho-Yong Park, Woo Song Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     saucernetin-7
    ÏàËÆ¶È:60.6%
Chinese Traditional and Herbal Drugs          2001          32          9-11
Studies on chemical constituents of Saururus chinensis (¢ñ)
MA Min; RUAN Jin lan; Koppaka V RAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     Saucernetin 7
    ÏàËÆ¶È:60.6%
Chemistry of Natural Compounds          2010          46          450-451
Lignans from Saururus chinensis
Lishu Wang, Xuefeng Zhou, Tunhai Xu, Xianwen Yang and Yonghong Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     manassantin B
C41H48O11     ÏàËÆ¶È:60.6%
Phytotherapy Research          2009          23          1531-1536
Manassantin A and B from Saururus chinensis inhibiting cellular melanin production
Chang-Seob Seo, Won-Hee Lee, Hee-Wook Chung, Eun Ju Chang, Seung Ho Lee, Yurngdong Jahng, Bang Yeon Hwang, Jong-Keun Son, Sang-Bae Han and Youngsoo Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     saucerneol D
C31H36O8     ÏàËÆ¶È:57.5%
Phytochemistry          2003          64          765-771
Lignans from Saururus chinensis inhibiting the transcription factor NF-kB
Bang Yeon Hwang, Jeong-Hyung Lee, Jeong Bum Nam, Young-Soo Hong,Jung Joon Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     4-O-demethylmanassantin A
C41H50O11     ÏàËÆ¶È:57.5%
Fitoterapia          2006          77          487-488
A new dineolignan from Saururus chinensis root
Sang Hyun Sung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     saucerneol D
C31H36O8     ÏàËÆ¶È:54.5%
Acta Bot. Boreal. -Occident. Sin.          2005          25          781-785
Antibiotic Constituents in Chimonan thuspraecox Seeds
HU Hao-bin, ZHENG Xu-dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     cerberalignan M
C50H58O18     ÏàËÆ¶È:54.5%
Phytochemistry          1989          28          3473-3476
Cerberalignans J-N,oligolignans from Cerbera manghas
Fumiko Abe,Tatsuo Yamauchi,Alfred S.C. Want
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     Quiquesetinerviusin C
C36H36O11     ÏàËÆ¶È:52.7%
Journal of Natural Products          2010          73          1482-1488
Antioxidant and Anti-inflammatory Phenylpropanoid Derivatives from Calamus quiquesetinervius
Chao-Lin Chang, Li-Jie Zhang, Ru Yin Chen, Li-Ming Yang Kuo, Jhih-Ping Huang, Hui-Chi Huang, Kuo-Hsiung Lee, Yang-Chang Wu, and Yao-Haur Kuo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     ¡÷8',3,3',4-trymethoxy neolignan
    ÏàËÆ¶È:52.6%
Phytochemistry          1984          23          2025-2028
13C NMR spectral and conformational analysis of 8-O-4¡ä neolignans
Antonio C. Herrera Braga, Susana Zacchino, H¨¦ctor Badano, Manuel Gonz¨¢lez Sierra, Edmundo A. R¨²veda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     3'-hydroxyscutellarein 7-O-(6''-O-trans-feruloyl)-bglucopyranoside
    ÏàËÆ¶È:51.5%
Phytochemistry          2004          65          2379-2385
Acylated flavonoids and phenol glycosides from Veronica thymoides subsp. pseudocinerea
Iclal Saracoglu, Mehtap Varel, U. Sebnem Harput, Akito Nagatsu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     saucerneol E
C30H34O8     ÏàËÆ¶È:51.5%
Phytochemistry          2003          64          765-771
Lignans from Saururus chinensis inhibiting the transcription factor NF-kB
Bang Yeon Hwang, Jeong-Hyung Lee, Jeong Bum Nam, Young-Soo Hong,Jung Joon Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     4¦Â-[4-(6-Methoxy-1,3-benzothiazole-2-yl)anilino]-4-desoxypodophyllotoxin
    ÏàËÆ¶È:51.5%
Bioorganic & Medicinal Chemistry Letters          2011          21          350-353
An efficient one-pot synthesis of benzothiazolo-4¦Â-anilino-podophyllotoxin congeners: DNA topoisomerase-II inhibition and anticancer activity
Ahmed Kamal, B. Ashwini Kumar, Paidakula Suresh, Nagula Shankaraiah, M. Shiva Kumar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     4-O-Demethyl-4¦Â-[4-(6-methoxy-1,3-benzothiazole-2-yl)anilino]-4-desoxypodophyllotoxin
    ÏàËÆ¶È:51.5%
Bioorganic & Medicinal Chemistry Letters          2011          21          350-353
An efficient one-pot synthesis of benzothiazolo-4¦Â-anilino-podophyllotoxin congeners: DNA topoisomerase-II inhibition and anticancer activity
Ahmed Kamal, B. Ashwini Kumar, Paidakula Suresh, Nagula Shankaraiah, M. Shiva Kumar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     Clausenawalline E
C32H28N2O4     ÏàËÆ¶È:51.5%
Journal of Natural Products          2012          75          741-746
Bioactive Carbazole Alkaloids from Clausena wallichii Roots
Wisanu Maneerat, Thunwadee Ritthiwigrom, Sarot Cheenpracha, Trinop Promgool, Kulsiri Yossathera, Suwanna Deachathai, Wong Phakhodee, and Surat Laphookhieo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     cerberalignan F
C30H36O11     ÏàËÆ¶È:51.5%
Phytochemistry          1988          27          3627-3631
Sesqui-,sester-and trilignans from stems of Cerbera manghas and C. odollam
Fumiko Abe,Tatsuo Yamauchi,Alfred S.C. Wan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     cerberalignan G
C30H36O11     ÏàËÆ¶È:51.5%
Phytochemistry          1988          27          3627-3631
Sesqui-,sester-and trilignans from stems of Cerbera manghas and C. odollam
Fumiko Abe,Tatsuo Yamauchi,Alfred S.C. Wan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     cerberalignan J
C30H36O11     ÏàËÆ¶È:51.5%
Phytochemistry          1989          28          3473-3476
Cerberalignans J-N,oligolignans from Cerbera manghas
Fumiko Abe,Tatsuo Yamauchi,Alfred S.C. Want
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     4¦Â-(6''-chrycenylamino)-4-desoxypodophyllotoxin
C40H37NO7     ÏàËÆ¶È:51.5%
Bioorganic & Medicinal Chemistry          2010          18          8493-8500
Synthesis of 4¦Â-N-polyaromatic substituted podophyllotoxins: DNA topoisomerase inhibition, anticancer and apoptosis-inducing activities
Ahmed Kamal, B. Ashwini Kumar, Paidakula Suresh, Satyam Kumar Agrawal, Gousia Chashoo, Shashank K. Singh, A.K. Saxena
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     9-O-[3-(ferulic acid)propyl] berberine bromide
C32H28NO8Br     ÏàËÆ¶È:51.5%
Bioorganic & Medicinal Chemistry          2011          19          7228-7235
Benzenediol-berberine hybrids: Multifunctional agents for Alzheimer¡¯s disease
Huailei Jiang, Xu Wang, Ling Huang, Zonghua Luo, Tao Su, Ke Ding, Xingshu Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     7-O-ethylfangchinoline 2'-N-¦Â-oxide
C39H44N2O7     ÏàËÆ¶È:50%
Natural Medicines          1998          52          172-178
Studies on the Crude Drug Containing Angiotensin I Converting Enzyme Inhibitors (III) : On the Activity of the Principles in Stephania tetrandra S. MOORE and their Derivertives
OGINO Tatsunori,SATO Toshitsugu, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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