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719660960

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化合物1:   17.54,18.46,20,20.06,28.13,29.16,34.1,34.98,36.02,40.32,40.88,54.74,62.79,63.09,69.28,71.56,71.62,75.73,77.66,77.93,78.26,79.03,90.88,106.93,107.74,118.34,134.61,135.26,136.48,143.12,149.25
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1 .     3,12-O-β-D-diglucopyranosyl-11,16-dihydroxyabieta-8,11,13-triene
C32H50O14     相似度:96.8%
Journal of Natural Products          2008          71(5)          755-759
Abietane Diterpenoids from Clerodendrum bungei
Shanshan Liu, Huilin Zhu, Shuwei Zhang, Xiaohui Zhang, Qiang Yu, and Lijiang Xuan
Structure      13C NMR   碳谱模拟图

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2 .     3,12-O-β-D-diglucopyranosyl-11,16-dihydroxyabieta-8,11,13-triene
    相似度:96.8%
Phytotherapy Research          2010          24          1720-1723
Anti-complement activity of isolated compounds from the roots of Clerodendrum bungei Steud.
Soo-Ki Kim, Sang-Buem Cho and Hyung-In Moon
Structure      13C NMR   碳谱模拟图

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3 .     12-O-β-D-glucopyranosyl-3,11,16-trihydroxyabieta-8,11,13-triene
C26H40O9     相似度:83.8%
Journal of Natural Products          2008          71(5)          755-759
Abietane Diterpenoids from Clerodendrum bungei
Shanshan Liu, Huilin Zhu, Shuwei Zhang, Xiaohui Zhang, Qiang Yu, and Lijiang Xuan
Structure      13C NMR   碳谱模拟图

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4 .     12-O-β-D-glucopyranosyl-3,11,16-trihydroxyabieta-8,11,13-triene
    相似度:83.8%
Phytotherapy Research          2010          24          1720-1723
Anti-complement activity of isolated compounds from the roots of Clerodendrum bungei Steud.
Soo-Ki Kim, Sang-Buem Cho and Hyung-In Moon
Structure      13C NMR   碳谱模拟图

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5 .     ajugaside A
C32H50O14     相似度:81.2%
Journal of Natural Products          1998          61          1105-1109
New Glycosides from Ajuga decumbens
Midori Takasaki, Isao Yamauchi, Mitsumasa Haruna, and Takao Konoshima
Structure      13C NMR   碳谱模拟图

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6 .     compound 6
    相似度:78.1%
Journal of Natural Products          2008          71(5)          755-759
Abietane Diterpenoids from Clerodendrum bungei
Shanshan Liu, Huilin Zhu, Shuwei Zhang, Xiaohui Zhang, Qiang Yu, and Lijiang Xuan
Structure      13C NMR   碳谱模拟图

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7 .     monoglucoside
C26H40O9     相似度:74.1%
Journal of Natural Products          1998          61          1105-1109
New Glycosides from Ajuga decumbens
Midori Takasaki, Isao Yamauchi, Mitsumasa Haruna, and Takao Konoshima
Structure      13C NMR   碳谱模拟图

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8 .     19-O-β-D-carboxyglucopyranosyl-12-O-β-D-glucopyranosyl-11,16-dihydroxyabieta-8,11,13-triene
C32H48O15     相似度:71.8%
Journal of Natural Products          2008          71(5)          755-759
Abietane Diterpenoids from Clerodendrum bungei
Shanshan Liu, Huilin Zhu, Shuwei Zhang, Xiaohui Zhang, Qiang Yu, and Lijiang Xuan
Structure      13C NMR   碳谱模拟图

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9 .     alpindenoside B
C32H48O13     相似度:59.3%
Journal of Natural Products          2009          72          1097-1101
Labdane Diterpenoid Glycosides from Alpinia densespicata and Their Nitric Oxide Inhibitory Activities in Macrophages
Yu-Jen Kuo, Ping-Chun Hsiao, Li-Jie Zhang, Ming-Der Wu, Yu-Han Liang, Hsiu-O Ho, and Yao-Haur Kuo
Structure      13C NMR   碳谱模拟图

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10 .     coronalactoside I
C32H48O13     相似度:59.3%
Chemical & Pharmaceutical Bulletin          2008          56(12)          1704-1709
Medicinal Flowers. XXIV.1) Chemical Structures and Hepatoprotective Effects of Constituents from Flowers of Hedychium coronarium
Seikou NAKAMURA,Yoshie OKAZAKI,Kiyofumi NINOMIYA,b Toshio MORIKAWA,Hisashi MATSUDA,and Masayuki YOSHIKAWA
Structure      13C NMR   碳谱模拟图

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11 .     phlomisoside-II
C32H50O12     相似度:59.3%
Chemical & Pharmaceutical Bulletin          1985          33          4275-4280
Sweet and Bitter Principles of the Chinese Plant Drug, Bai-Yun-Shen : Revision of the Assignment of the Source Plant and Isolation of Two New Diterpene Glycosides
TAKASHI TANAKA,OSAMU TANAKA,ZHONGWEN LIN and JUN ZHOU
Structure      13C NMR   碳谱模拟图

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12 .     phlomisoside II
    相似度:59.3%
Phytochemistry          1994          35          439-442
Diterpenoid glycosyl esters from Phlomis younghusbandii and P. medicinalis roots
Masako Katagiri, Kazuhiro Ohtani, Ryoji Kasai, Kazuo Yamasaki, Chong-Ren Yang, Osamu Tanaka
Structure      13C NMR   碳谱模拟图

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13 .     coronalactosides I
C32H48O13     相似度:59.3%
Chemical & Pharmaceutical Bulletin          2008          56          1704-1709
Medicinal Flowers. XXIV. Chemical Structures and Hepatoprotective Effects of Constituents from Flowers of Hedychium coronarium
Seikou Nakamura, Yoshie Okazaki, Kiyofumi Ninomiya, Toshio Morikawa, Hisashi Matsuda and Masayuki Yoshikawa
Structure      13C NMR   碳谱模拟图

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14 .     prosapogenin G'
C36H56O8     相似度:58.3%
Journal of the Chemical Society, Perkin Transactions 1          1981                   1923-1927
Three new saponins from the leaves of Hovenia dulcis(Rhamnaceae)
Yasuko Kimura, Yoshimasa Kobayashi, Tadahiro Takeda and Yukio Ogihara
Structure      13C NMR   碳谱模拟图

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15 .     sylvestriside B
C26H42O7     相似度:58.0%
Planta Medica          2009          75          1436-1441
Diterpenoids from Casearia sylvestris
WeiWang, Jianpin Zhao, Yan-hongWang, Troy A. Smillie, Xing-Cong Li, Ikhlas A. Khan
Structure      13C NMR   碳谱模拟图

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16 .     compound 3a
    相似度:58.0%
Journal of Natural Products          1990          Vol 53          1000
Starfish Saponins, Part 44. Steroidal Glycosides from the Starfish Pisaster giganteus
Franco Zollo, Ester Finamore, Caterina Martuccio, Luigi Minale
Structure      13C NMR   碳谱模拟图

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17 .     Vernonioside A2
    相似度:57.1%
Phytochemistry          1993          34          409-413
Steroid glucosides from vernonia amygdalina, a possible chimpanzee medicinal plant
Mitsuo Jisaka, Hajime Ohigashi, Kazunori Takegawa, Mitsuru Hirota, Ryozo Irie, Michael A. Huffman, Koichi Koshimįzu
Structure      13C NMR   碳谱模拟图

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18 .     vernonioside A2
C35H52O10     相似度:57.1%
Tetrahedron          1992          48          625-632
Bitter steroid glucosides, vernoniosides A1, A2, and A3, and related B1 from a possible medicinal plant, Vernonia amygdalina, used by wild chimpanzees.
Mitsuo Jisaka, Hajime Ohigashi, Teruyoshi Takagaki, Hiroshi Nozaki, Toshiji Tada, Mitsuru Hirota, Ryozo Irie, Michael A. Huffman, Toshida Nishida, Mikio Kaji, Koichi Koshimizu
Structure      13C NMR   碳谱模拟图

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19 .     alpindenoside A
C32H48O13     相似度:56.2%
Journal of Natural Products          2009          72          1097-1101
Labdane Diterpenoid Glycosides from Alpinia densespicata and Their Nitric Oxide Inhibitory Activities in Macrophages
Yu-Jen Kuo, Ping-Chun Hsiao, Li-Jie Zhang, Ming-Der Wu, Yu-Han Liang, Hsiu-O Ho, and Yao-Haur Kuo
Structure      13C NMR   碳谱模拟图

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20 .     3-O-β-D-glucopyranosyl-13-O-α-L-rhamnopyranosyl-3β-hydroxymanool
    相似度:56.2%
Chemical & Pharmaceutical Bulletin          1995          43          5-8
Fern Constituents : Four New Diterpenoid Glycosides from Fresh Leaflets of Gleichenia japonica
Kenji SHIOJIMA,Masayoshi SUZUKI,Hiroshi AOKI and Hiroyuki AGETA
Structure      13C NMR   碳谱模拟图

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21 .     paniculosideV
C32H50O13     相似度:56.2%
Chemical & Pharmaceutical Bulletin          1977          25          2895-2899
Application of 13C Nuclear Magnetic Resonance Spectroscopy to Chemistry of Glycosides : Structures of Paniculosides-I, -II, -III, -IV, and -V, Diterpene Glucosides of Stevia paniculata LAG.
KAZUO YAMASAKI,HIROSHI KOHDA,TOSHIKO KOBAYASHI,NORITO KANEDA,RYOJI KASAI,OSAMU TANAKA and KOZABURO NISHI
Structure      13C NMR   碳谱模拟图

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22 .     Tricalysioside Y
C32H54O14     相似度:56.2%
Chemical & Pharmaceutical Bulletin          2011          59(1)          72-77
Tricalysionoside A, a Megastigmane Gentiobioside, Sulfatricalysines A-F, and Tricalysiosides X-Z, ent-Kaurane Glucosides, from the Leaves of Tricalysia dubia
Junko SHITAMOTO, Sachiko SUGIMOTO, Katsuyoshi MATSUNAMI, Hideaki OTSUKA,Takakazu SHINZATO, and Yoshio TAKEDA
Structure      13C NMR   碳谱模拟图

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23 .     3β-O-glucopyranosyl-5,8-epidioxyergosta-6,22-diene
C34H54O8     相似度:55.8%
Phytochemistry          1991          30          4117-4120
Glycosides of ergosterol derivatives from Hericum erinacens
Yoshihisa Takaishi, Minoru Uda, Takashi Ohashi, Kimiko Nakano, Koutarou Murakami, Toshiaki Tomimatsu
Structure      13C NMR   碳谱模拟图

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24 .     Mogroside I E1
C36H62O9     相似度:55.8%
Chinese Journal of Natural Medicines          2010          8          21-24
Chemical Constituents from the Stems and Leaves of Elaeocarpus glabripetalus
ZHANG Sheng; TAO Zheng-Ming; ZHANG Yi; SHEN Zheng-Wu; QIN Guo-Wei
Structure      13C NMR   碳谱模拟图
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