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19.59,25.68,27.28,28.88,29.18,36.58,39.66,41.06,44.22,52.19,56.80,63.21,125.26,
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karl2100: ½ð±Ò+1, 3Q 2013-09-14 00:28:16
wawlgch: ½ð±Ò+10, ¡ïÓаïÖú 2013-09-14 14:54:27
wawlgch(¶¹¸ç´ú·¢): ½ð±Ò+5, лл 2013-09-21 11:26:11
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1 .     sophocarpine
    ÏàËÆ¶È:86.6%
China Journal of Chinese Materia Medica          2006          31          557-560
Constituents in the alkaloid fraction of Kushen decoction
LIU Bin, SHI Rengbing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     (-)-sophocarpine
    ÏàËÆ¶È:86.6%
Phytochemistry          1999          50          189-193
Lupin alkaloids from seeds of Sophora viciifolia
Ping Xiao,Hajime Kubo,Hideaki Komiy¦Á, Kimio Higashiyam¦Á, Yu-ning Yan,Jia-shi Li , Shigeru Ohmiya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (-)-sophocarpine
C15H22N2O     ÏàËÆ¶È:86.6%
Bioorganic & Medicinal Chemistry Letters          2006          16          1231-1235
(+)-12¦Á-Hydroxysophocarpine, a new quinolizidine alkaloid and related anti-HBV alkaloids from Sophora flavescens
Pei-Lan Ding, Zhi-Xin Liao, Hai Huang, Pei Zhou, Dao-Feng Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     sophocarpine
    ÏàËÆ¶È:80%
China Journal of Chinese Materia Medica          1997          22          741-743
Alkaloids in Sophora alopecuroides Seed and Relevant Tests for Activity
Zhang Lanzhen and Li, P J Houghton and S Jackson, P R Twentyman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     9¦Á-hydroxysophocarpine
C15H22N2O2     ÏàËÆ¶È:80%
Phytochemistry          1999          50          189-193
Lupin alkaloids from seeds of Sophora viciifolia
Ping Xiao,Hajime Kubo,Hideaki Komiy¦Á, Kimio Higashiyam¦Á, Yu-ning Yan,Jia-shi Li , Shigeru Ohmiya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     9¦Á-hydroxysophocarpine
C15H22N2O2     ÏàËÆ¶È:80%
Phytochemistry          1999          50          189-193
Lupin alkaloids from seeds of Sophora viciifolia
Ping Xiao,Hajime Kubo,Hideaki Komiy¦Á, Kimio Higashiyam¦Á, Yu-ning Yan,Jia-shi Li , Shigeru Ohmiya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     compound 13
    ÏàËÆ¶È:80%
Journal of Natural Products          1984          Vol 47          658-662
New Sesquiterpene Lactone Type from Dugaldia hoopesii
F. Bohlmann, L. N. Misra, J. Jakupovic, H. Robinson, R. M. King
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (-)-sophocarpine
    ÏàËÆ¶È:80%
Natural Product Sciences          2001          7          5-8
Minor Constituents from the Roots of Sophora flavescens
Kim, Ju-Sun; Han, Sang-Jun; Byun, Ji-Hye; Xu, Yong-Nan; Yoo, Sang-Woo; Kang, Sam-Sik; Son, Kun-Ho; Chang, Hyeun-Wook; Kim, Hyun-Pyo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     silphinen
    ÏàËÆ¶È:80%
Phytochemistry          1980          19          259-265
Neue Sesquiterpen-Kohlenwasserstoffe mit anomalen Kohlenstoffger¨¹st aus Silphium-arten
Ferdinand Bohlmann, Jasmin Jakupovic
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     (-)-sophocarpine
    ÏàËÆ¶È:80%
Chinese Pharmaceutical Journal          2010          45          1451-1454
Studies on Chemical Constituents from Flowers of Sophora viciifolia Hance
WEN Min, MA Yun-bao, MAO Xiao-jian, ZHANG Xue-mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     (4Z,8¦Á,11S)-caryophyll-4(5)-ene-8,14-diol
C15H26O2     ÏàËÆ¶È:73.3%
Journal of Natural Products          2000          63          44-47
Biotransformation of (4E,8R)-Caryophyll-4(5)-en-8-ol by Botrytis cinerea
Rosa Dur¨¢n-Patr¨®n, Josefina Aleu, Rosario Hern¨¢ndez-Gal¨¢n, and Isidro G. Collado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     (-)-14¦Â-hydroxymatrine
C15H24N2O2     ÏàËÆ¶È:73.3%
Chemical & Pharmaceutical Bulletin          1996          44          1951-1953
(-)-14¦Â-Hydroxymatrine, a New Lupine Alkaloid from the Roots of Sophora tonkinensis
Ping XIAO,Jiashi LI,Hajime KUBO,Kazuki SAITO,Isamu MURAKOSHI and Shigeru OHMIYA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     sophorcarpine
C15H22N2O     ÏàËÆ¶È:73.3%
Chemistry of Natural Compounds          1996          32          737-858
ALKALOIDS. PLANTS, STRUCTURES, PROPERTIES" Chapter 2, continued
R. Shakirov, M. V. Telezhenetskaya, I. A. Bessonova,S. F. Aripova, I. A. Israilov, M. N. Sultankhodzhaev,V. I. Vinogradova, V. I. Akhmedzhanova, T. S. Tulyaganov,B. T. Salimov, and V. A. Tel'nov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     humula-4,9-dien-8-ol
    ÏàËÆ¶È:73.3%
Chemistry of Natural Compounds          1988          24          606-611
NEW SESQUITERPENOIDS FROM THE OLEORESIN OF Abies alba
V.A.Khan,A.V.tkachev,and V.A.pentegova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     (-)-14¦Â-hydroxymatrine
    ÏàËÆ¶È:73.3%
Chemical & Pharmaceutical Bulletin          1999          47          448-450
(-)-14¦Â-Acetoxymatrine and (+)-14¦Á-Acetoxymatrine, Two New Matrine-Type Lupin Alkaloids from the Leaves of Sophora tonkinensis
Ping XIAO,Hajime KUBO,Hideaki KOMIYA,Kimio HIGASHIYAMA,Yuning YAN,Jia-shi LI and Shigeru OHMIYA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     (1R,2S,3R,5S,8S,9R)-2,3,5,9-tetramethyltricyclo[6.3.0.0]undecan-3-ol
C15H16O     ÏàËÆ¶È:73.3%
Journal of Natural Products          1990          Vol 53          845
Tropical Marine Algae, VII. The Chemical Composition of Marine Algae from North Queensland Waters
Anthony D. Wright, John C. Coll, Ian R. Price
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     compound 36
C16H26O2     ÏàËÆ¶È:73.3%
Canadian Journal of Chemistry          2006          84          1456-1469
Intramolecular [4 + 3] cycloadditions -Stereochemical issues in the cycloaddition reactions of cyclopentenyl cations - A synthesis of (+)-dactylol1
Michael Harmata, Paitoon Rashatasakhon, and Charles L. Barnes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     (+)-Dactylol
C15H26O     ÏàËÆ¶È:73.3%
Canadian Journal of Chemistry          2006          84          1456-1469
Intramolecular [4 + 3] cycloadditions -Stereochemical issues in the cycloaddition reactions of cyclopentenyl cations - A synthesis of (+)-dactylol1
Michael Harmata, Paitoon Rashatasakhon, and Charles L. Barnes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     9-epi-¦Â-caryophyllen
    ÏàËÆ¶È:73.3%
Phytochemistry          1978          17          1135-1153
Neue furanoeremophilane und andere sesquiterpene aus vertretern der gattung Euryops
Ferdinand Bohlmann, Christa Zdero
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     9¦ÂH-caryophyllene
    ÏàËÆ¶È:73.3%
Phytochemistry          1985          24          2893-2898
Foliage sesquiterpenes of Dacrydium cupressinum: identification, variation and biosynthesis
Katherine M. Berry, Nigel B. Perry, Rex T. Weavers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     12-hydroxy-4(5),11(13)-eudesmadien-15-al
    ÏàËÆ¶È:73.3%
Phytochemistry          2010          71          804-809
Sesquiterpenes and diterpenes from Ambrosia arborescens
Marinella De Leo, Mariela Beatriz Vera Saltos, Blanca Fabiola Naranjo Puente, Nunziatina De Tommasi, Alessandra Braca
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     (-) 9¦Á-hydroxysophocarpine
    ÏàËÆ¶È:73.3%
Chinese Pharmaceutical Journal          2010          45          1451-1454
Studies on Chemical Constituents from Flowers of Sophora viciifolia Hance
WEN Min, MA Yun-bao, MAO Xiao-jian, ZHANG Xue-mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     compound 3
    ÏàËÆ¶È:73.3%
Tetrahedron          2012          68          2650-2656
Enantiospecific first total synthesis of (6S,7R)-silphiperfolan-6-ol
A. Srikrishna, Gopalasetty Nagaraju, Vishal M. Sheth
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     compound 3
    ÏàËÆ¶È:73.3%
Tetrahedron          2012          68          2650-2656
Enantiospecific first total synthesis of (6S,7R)-silphiperfolan-6-ol
A. Srikrishna, Gopalasetty Nagaraju, Vishal M. Sheth
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     11,12,14-trihydroxydrimene
C15H26O3     ÏàËÆ¶È:73.3%
Canadian Journal of Chemistry          1889          67          1371-1380
Metabolites of the fairy ring fungus, Marasmiusoreades. Part 2. Norsesquiterpenes, further sesquiterpenes, and agrocybin
William A. Ayer, Peter Craw
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     (-)-(3R)-3-hydroxy-isolongifolol
C15H26O2     ÏàËÆ¶È:73.3%
Journal of Oleo Science          2010          59          243-246
Microbial Transformation of (-)-Isolongifolol by Plant Pathogenic Fungus Glomerella cingulata
Mitsuo Miyazawa, Kazuki Sakata, Masashi Ueda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     caryophyllene oxide
C15H24     ÏàËÆ¶È:73.3%
Indian Journal of Chemistry          2004          43B          2452-2455
Constituents of high altitude Himalayan herb Angelica glauca
K S Khetwal*, S K Pathak, K Sajwan,Bharat Pandey & Alexey V Tkachev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     7-epi-cameroonanol
    ÏàËÆ¶È:73.3%
European Journal of Organic Chemistry          1998          1998          1205-1212
Cameroonane, Prenopsane and Nopsane, Three New Tricyclic Sesquiterpene Skeletons
Peter Weyerstahl, Helga Marschall, Ingo Seelmann and Jasmin Jakupovic
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     (5E,9E,13R)-13,14-Epoxy-6,10,14-trimethylpentadeca-5,9-dien-2-one
    ÏàËÆ¶È:70.5%
Australian Journal of Chemistry          1982          35          171-182
C18 terpenoid metabolites of the brown alga Cystophora moniliformis
BN Ravi, PT Murphy, RO Lidgard, RG Warren and RJ Wells
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     (5 E,9 E)-13,14-epoxy-6,10,14-trimethylpentadeca-5,9-dien-2-one
C18H30O2     ÏàËÆ¶È:70.5%
Australian Journal of Chemistry          1988          41          49-56
Terpenoids From the Brown Alga Cystophora moniliformis
IA Vanaltena
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-09-14 00:23:11
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