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1 .     3-[2-'Hydroxy-4'-phenyl]-5-phenyl-1,2 Benzisoxazole 2-oxide
C25H17NO3     ÏàËÆ¶È:69.2%
Heterocycles          2011          83          1077-1091
Xanthones in Heterocyclic Synthesis. An Efficient Route for the Synthesis of C-3 o-Hydroxyaryl Substituted 1,2-Benzisoxazoles and Their N-Oxides, Potential Scaffolds for Angiotensin(II) Antagonist Hybrid Peptides
Yiannis Gardikis, Petros G. Tsoungas,* Constantinos Potamitis, Maria Zervou, and Paul Cordopatis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     salvianol acid C
    ÏàËÆ¶È:69.2%
China Journal of Chinese Materia Medica          2013          38          1556-1559
Chemical constituents of Salvia chinensis
GAO Jun-feng, DING Ling, ZHANG Peng, LIU Jian-xun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     salvianolic acid C
    ÏàËÆ¶È:65.3%
Journal of China Pharmaceutical University          1999          30          411-416
Studies on Isolation and Identification of Water Soluble Constituents of Salvia Miltiorrhiza
Zhou Changxin; Luo Houwei; Niwa Masatake
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     ningalin D
C40H27NO12     ÏàËÆ¶È:65.3%
The Journal of Organic Chemistry          1997          62          3254-3262
Ningalins A−D:  Novel Aromatic Alkaloids from a Western Australian Ascidian of the Genus Didemnum
Heonjoong Kang and William Fenical
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     salvianolic acid C
    ÏàËÆ¶È:65.3%
Journal of the Chinese Chemical Society          2003          50          1079-1083
Benzolignanoid and Polyphenols from Origanum vulgare
Yun-Lian Lin*, Chuen-Neu Wang, Young-Ji Shiao, Tzu-Ying Liu and Wan-Yi Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     Sebestenoid A
C27H22O10     ÏàËÆ¶È:62.9%
Phytochemistry          2010          71          2168-2173
Sebestenoids A¨CD, BACE1 inhibitors from Cordia sebestena
Jingqiu Dai, Analia Sorribas, Wesley Y. Yoshida, Philip G. Williams
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     methyl salvianol acid C
    ÏàËÆ¶È:62.9%
China Journal of Chinese Materia Medica          2013          38          1556-1559
Chemical constituents of Salvia chinensis
GAO Jun-feng, DING Ling, ZHANG Peng, LIU Jian-xun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     compound 1
C25H16O9     ÏàËÆ¶È:61.5%
Journal of Natural Products          2007          70          1790-1792
Vanillic Acid Derivatives from the Green Algae Cladophora socialis As Potent Protein Tyrosine Phosphatase 1B Inhibitors
Yunjiang Feng, Anthony R. Carroll, Rama Addepalli, Gregory A. Fechner, Vicky M. Avery, and Ronald J. Quinn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     3,3'-[Oxybis[(3,1)-(4',1')phenylenenitrilo]]bis[1,3-dihydro]-2H-indol-2-one
    ÏàËÆ¶È:61.5%
Molecules          2006          11          59-63
Synthesis of Some New bis-Schiff Bases of Isatin and 5-Fluoroisatin in a Water Suspension Medium
A. A. Jarrahpour and D. Khalili
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     salvianolic acid N
C26H20O10     ÏàËÆ¶È:61.5%
Journal of Asian Natural Products Research          2008          10          252-255
A potent anti-HIV polyphenol from Salvia yunnanensis
Zheng-Fu Zhang, Hong-Shan Chen, Zong-Gen Peng, Zhuo-Rong Li and Jian-Dong Jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     salvianolic acid A
    ÏàËÆ¶È:61.5%
Journal of Asian Natural Products Research          2008          10          391-396
Three new derivatives of anti-HIV-1 polyphenols isolated from Salvia yunnanensis
Zheng-Fu Zhang, Zong-Gen Peng, Lei Gao, Biao Dong, Jian-Rui Li, Zhuo-Yong Li and Hong-Shan Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     baculiferin N
C26H17NO10     ÏàËÆ¶È:61.5%
Bioorganic & Medicinal Chemistry          2010          18          5466-5474
Baculiferins A¨CO, O-sulfated pyrrole alkaloids with anti-HIV-1 activity, from the Chinese marine sponge Iotrochota baculifera
Guotao Fan, Zelin Li, Shi Shen, Yi Zeng, Yishu Yang, Minjuang Xu, Torsten Bruhn, Heike Bruhn, Joachim Morschhäuser, Gerhard Bringmann, Wenhan Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     6-hydroxy-E-3-(2,5-dimethoxybenzylidine)-2',5'-dimethoxyflavanone
C26H24O7     ÏàËÆ¶È:61.5%
Natural Product Communications          2009          4          59-62
Flavonoids from Tephrosia calophylla
Ramireddy V. Narahari Reddya, Shaik I. Khalivullaa, Bandi A.K. Reddya,Mopuru V. Bhaskar Reddya,b, Duvvuru Gunasekara,, Alexandre Devillec and Bernard Bodo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     µ¤·ÓËáA
C26H22O10     ÏàËÆ¶È:61.5%
Chinese Traditional and Herbal Drugs          2011          42          247-250
Isolation and identification of chemical constituents from thermal decomposition extract of salvianolic acid B
LIU Sheng-sheng, HAN Fei, XU Hui, LIU Ke,
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     butesuperin A
    ÏàËÆ¶È:61.5%
Chinese Pharmaceutical Journal          2011          46          1389-1393
Study on Chemical Constituents in Stems of Pueraria lobata
ZHANG, De-wu, DAI, Sheng-jun, YU, Qun-ying, LI, Gui-hai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     salvianolic acid A
    ÏàËÆ¶È:61.5%
China Journal of Chinese Materia Medica          2013          38          1556-1559
Chemical constituents of Salvia chinensis
GAO Jun-feng, DING Ling, ZHANG Peng, LIU Jian-xun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     litseaefoloside C
C30H30O14     ÏàËÆ¶È:60%
Journal of Natural Products          2005          68          1531-1535
Phenolic and Triterpene Glycosides from the Stems of Ilex litseaefolia
Ai-Lian Zhang, Qi Ye, Bo-Gang Li, Hua-Yi Qi, and Guo-Lin Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     crossbyanol B
C30H15Br7O12S2     ÏàËÆ¶È:60%
Journal of Natural Products          2010          73          517-522
Crossbyanols A−D, Toxic Brominated Polyphenyl Ethers from the Hawai¡¯ian Bloom-Forming Cyanobacterium Leptolyngbya crossbyana
Hyukjae Choi, Niclas Engene, Jennifer E. Smith, Linda B. Preskitt and William H. Gerwick
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     crossbyanol C
C30H15Br7O9S     ÏàËÆ¶È:60%
Journal of Natural Products          2010          73          517-522
Crossbyanols A−D, Toxic Brominated Polyphenyl Ethers from the Hawai¡¯ian Bloom-Forming Cyanobacterium Leptolyngbya crossbyana
Hyukjae Choi, Niclas Engene, Jennifer E. Smith, Linda B. Preskitt and William H. Gerwick
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     lamellarin Z
C27H22NO8     ÏàËÆ¶È:59.2%
Journal of Natural Products          1999          62          419-424
New Lamellarin Alkaloids from the Australian Ascidian, Didemnum chartaceum
Rohan A. Davis, Anthony R. Carroll, Gregory K. Pierens, and Ronald J. Quinn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-09-03 09:24:18
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1 .     luteolin 6-C-(4''-methyl-6''-O-trans-caffeoylglucoside
C31H28O15     ÏàËÆ¶È:56.2%
Phytochemistry          1997          46          521-524
Cytotoxic flavonoids from Vitex agnus-castus
Chieko Hirobe, Zhi-Sheng Qiao, Koichi Takeya, Hideji Itokawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     luteolin 6-C-(6''-O-trans-caffeoylglucoside
C30H26O15     ÏàËÆ¶È:56.2%
Phytochemistry          1997          46          521-524
Cytotoxic flavonoids from Vitex agnus-castus
Chieko Hirobe, Zhi-Sheng Qiao, Koichi Takeya, Hideji Itokawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     clinopodic acid H
C29H26O12     ÏàËÆ¶È:53.1%
Journal of Natural Products          2009          72          1379-1384
Matrix Metalloproteinase-2 Inhibitors from Clinopodium chinense var. parWiflorum
Toshihiro Murata,Kenroh Sasaki,Kumiko Sato, Fumihiko Yoshizaki, Haruna Yamada, Hiromichi Mutoh, Kaoru Umehara,Toshio Miyase,Tsutomu Warashina,Hiroaki Aoshima, Homare Tabata, and Kouichi Matsubara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     balanophotannin B
C29H22O16     ÏàËÆ¶È:53.1%
Chemical & Pharmaceutical Bulletin          2005          53(3)          339-341
Ellagitannins and Lignan Glycosides from Balanophora japonica (Balanophoraceae)
Zhi-Hong JIANG,Takashi TANAKA,Hiromi IWATA,Saori SAKAMOTO,Yoko HIROSE,and Isao KOUNO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     melitric acid A
C27H22O12     ÏàËÆ¶È:53.1%
Chemical & Pharmaceutical Bulletin          1993          41          1608-1611
Melitric Acids A and B, New Trimeric Caffeic Acid Derivatives from Melissa officinalis
Isao AGATA,Hijiri KUSAKABE,Tsutomu HATANO,Sansei NISHIBE and Takuo OKUDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     3,5,4',3'',5'',7'',3''',4'''-nonahydroxy-3',6''-biflavanone
    ÏàËÆ¶È:53.1%
Phytochemistry          1992          31          3233-3237
Hypnogenols and other dihydroflavonols from the moss Hypnum cupressiforme
Hartwig Sievers, Gunther Burkhardt, Hans Becker, Hans D. Zinsmeister
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     (2R,3R,4R)-3,3',4',7-tetrahydroxyflavan-(4¦Â¡ú8)-epicatechin
    ÏàËÆ¶È:53.1%
Phytochemistry          1989          28          2183-2186
Two proanthocyanidins from the bark of Dalbergia monet̊ari
Domingos S. Nunes,Armin Haag,Hans-J¨¹rgen Bestmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     Sedacin C
C32H30O15     ÏàËÆ¶È:53.1%
Heterocycles          2011          83          135-141
Two New Flavonol Glycosides from Sedum aizoon L.
Wei Lin Li,* Qiu Yan Luo, Li qiang Wu, and Lei Xiao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     Sedacin D
C33H32O15     ÏàËÆ¶È:53.1%
Heterocycles          2011          83          135-141
Two New Flavonol Glycosides from Sedum aizoon L.
Wei Lin Li,* Qiu Yan Luo, Li qiang Wu, and Lei Xiao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     ningalin C
C32H23NO10     ÏàËÆ¶È:53.1%
The Journal of Organic Chemistry          1997          62          3254-3262
Ningalins A−D:  Novel Aromatic Alkaloids from a Western Australian Ascidian of the Genus Didemnum
Heonjoong Kang and William Fenical
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     Artocarmitin B
C30H28O8     ÏàËÆ¶È:53.1%
Journal of Natural Products          2012          75          1951-1955
Tyrosinase Inhibitors from the Wood of Artocarpus heterophyllus
Nhan Trung Nguyen, Mai Ha Khoa Nguyen, Hai Xuan Nguyen, Ngan Kim Nguyen Bui, and Mai Thanh Thi Nguyen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     balanophotannin C
C36H26O20     ÏàËÆ¶È:52.9%
Chemical & Pharmaceutical Bulletin          2005          53(3)          339-341
Ellagitannins and Lignan Glycosides from Balanophora japonica (Balanophoraceae)
Zhi-Hong JIANG,Takashi TANAKA,Hiromi IWATA,Saori SAKAMOTO,Yoko HIROSE,and Isao KOUNO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     olgensisinol C
C30H22O12     ÏàËÆ¶È:50%
Helvetica Chimica Acta          2005          Vol. 88          2892
Spiro-biflavonoids from Larix olgensis HENRY var. koreana NAKAI
Bao-Hua Yang, Wei-Dong Zhang, Run-Hui Liu, Chang-Heng Tan, Ting-Zhao Li, Chuan Zhang, Xi-Ke Xu, and Juan Su
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     clinopodic acid D
C28H24O12     ÏàËÆ¶È:50%
Journal of Natural Products          2009          72          1379-1384
Matrix Metalloproteinase-2 Inhibitors from Clinopodium chinense var. parWiflorum
Toshihiro Murata,Kenroh Sasaki,Kumiko Sato, Fumihiko Yoshizaki, Haruna Yamada, Hiromichi Mutoh, Kaoru Umehara,Toshio Miyase,Tsutomu Warashina,Hiroaki Aoshima, Homare Tabata, and Kouichi Matsubara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

15 .     clinopodic acid F
C28H24O12     ÏàËÆ¶È:50%
Journal of Natural Products          2009          72          1379-1384
Matrix Metalloproteinase-2 Inhibitors from Clinopodium chinense var. parWiflorum
Toshihiro Murata,Kenroh Sasaki,Kumiko Sato, Fumihiko Yoshizaki, Haruna Yamada, Hiromichi Mutoh, Kaoru Umehara,Toshio Miyase,Tsutomu Warashina,Hiroaki Aoshima, Homare Tabata, and Kouichi Matsubara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     eriodictyol 7-O-(6''-feruloyl)-¦Â-D-glucopyranoside
C31H30O14     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          2008          56(4)          592-594
Three New Flavonoid Glycosides Isolated from Elsholtzia bodinieri
Rong-Tao LI,Jin-Tong LI,Jing-Kun WANG,Quan-Bin HAN,Zhao-Yun ZHU,and Han-Dong SUN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     eriodictyol 7-O-[6''- (3''-hydroxy-4''-methoxy cinnamoyl)]-¦Â-D-glucopyranoside
C31H30O14     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          2008          56(4)          592-594
Three New Flavonoid Glycosides Isolated from Elsholtzia bodinieri
Rong-Tao LI,Jin-Tong LI,Jing-Kun WANG,Quan-Bin HAN,Zhao-Yun ZHU,and Han-Dong SUN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     compounds 18
C34H42O13     ÏàËÆ¶È:50%
Phytochemistry          2004          65          2003-2011
Constituents from the bark of Tabebuia impetiginosa
Tsutomu Warashina, Yoshimi Nagatani, Tadataka Noro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     4'''-Oacetylverbascoside
C31H38O16     ÏàËÆ¶È:50%
Phytochemistry          2002          59          565-570
Phenolic glycosides from Barnettia kerrii
Tripetch Kanchanapoom, Ryoji Kasai, Kazuo Yamasaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     balanophotannin D
C28H23O16     ÏàËÆ¶È:50%
Journal of Natural Products          2008          71(4)          719-723
Cytotoxic Hydrolyzable Tannins from Balanophora japonica
Zhi-Hong Jiang, Xiao-Yun Wen, Takashi Tanaka, Shao-Yu Wu,Zhongqiu Liu, Hiromi Iwata, Yoko Hirose, Shuguang Wu, and Isao Kouno
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3Â¥2013-09-03 09:25:09
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