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chenjjun1982

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12.9, 15.2, 19.6, 21.7, 25.8, 31.2, 32.4, 38.4, 43.9, 46.3, 46.5, 49.4, 54.9, 59.3, 62.2, 70.0, 73.4, 75.9, 77.7, 99.1, 100.5, 116.5, 137.9, 148.1, 148.4, 188.1, 192.7, 198.8

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15.7, 16.0, 16.9, 19.4, 23.7, 26.2, 27.9, 28.9, 30.0, 33.7, 34.7, 43.6, 50.9, 209.6
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1 .     picrasinoside B
    ÏàËÆ¶È:85.7%
Journal of Natural Products          1991          Vol 54          844
Picrasinoside H, a New Quassinoid Glucoside, and Related Compounds from the Stem Wood of Picrasma ailanthoides
Takayuki Matsuzaki, Narihiko Fukamiya, Masayoshi Okano, Tomoyuki Fujita, Kiyoshi Tagahara, Kuo-Hsiung Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     picrasinoside-C
C22H34O6     ÏàËÆ¶È:64.2%
Bulletin of the Chemical Society of Japan          1985          58          1793-1800
New Quassinoid Glucosides, Picrasinoside-A, -B, -C, -D, -E, -F, and -G and New Hemiacetals, Picrasinol-A and -B, from the Stem Bark of Picrasma ailanthoides PLANCHON
Masayoshi Okano, Tomoyuki Fujita, Narihiko Fukamiya, Takaaki Aratani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     javanicinoside C
C27H38O11     ÏàËÆ¶È:60.7%
Phytochemistry          1990          29          2617-2621
Quassinoids from Picrasma javanica
Kazuo Koike,Taichi Ohmoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     javanicinoside J
C29H44O13     ÏàËÆ¶È:58.6%
Journal of Natural Products          1992          Vol 55          482
New Quassinoid Glucosides, Javanicinosides I, J, K, and L, from Picrasma javanica
Kazuo Koike, Taichi Ohmoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     picrasinoside C
    ÏàËÆ¶È:57.1%
Journal of Natural Products          1991          Vol 54          844
Picrasinoside H, a New Quassinoid Glucoside, and Related Compounds from the Stem Wood of Picrasma ailanthoides
Takayuki Matsuzaki, Narihiko Fukamiya, Masayoshi Okano, Tomoyuki Fujita, Kiyoshi Tagahara, Kuo-Hsiung Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     javanicinoside L
C27H42O12     ÏàËÆ¶È:57.1%
Journal of Natural Products          1992          Vol 55          482
New Quassinoid Glucosides, Javanicinosides I, J, K, and L, from Picrasma javanica
Kazuo Koike, Taichi Ohmoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     picrasinoside H
C30H44O13     ÏàËÆ¶È:56.6%
Journal of Natural Products          1991          Vol 54          844
Picrasinoside H, a New Quassinoid Glucoside, and Related Compounds from the Stem Wood of Picrasma ailanthoides
Takayuki Matsuzaki, Narihiko Fukamiya, Masayoshi Okano, Tomoyuki Fujita, Kiyoshi Tagahara, Kuo-Hsiung Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     11-¦Á-O-(B-glucopyranosyl)-16-¦Á-O-Methylneoquassin
    ÏàËÆ¶È:55.1%
Phytochemistry          1993          32          1007-1013
Quassinoids from Quassia amara
P. Barbetti, G. Grandolini, G. Fardella, I. Chiappini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     baimantuoluoline B
C28H42O7     ÏàËÆ¶È:53.5%
Helvetica Chimica Acta          2007          Vol. 90          1522
Withanolide Compounds from the Flower of Datura metel L.
Bingyou Yang, Qiuhong Wang, Yonggang Xia, Weisheng Feng, and Haixue Kuang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     tomatidine
    ÏàËÆ¶È:53.5%
Chemical & Pharmaceutical Bulletin          1990          38          827-829
STRUCTURES OF THREE NEW STEROIDAL ALKALOID GLYCOSIDES, SOLAVERINES I, II AND III FROM SOLANUM TOXICARIUM AND S. VERBASCIFOLIUM
Tomoyuki YAMASHITA,Nobuyo FUJIMURA,Shoji YAHARA,Toshihiro NOHARA,Syuji KAWANOBU and Kunimitsu FUJIEDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     soladunalinidine
C27H46N2O     ÏàËÆ¶È:53.5%
Phytochemistry          1996          43          913-915
3-Aminospirosolane alkaloids from Solanum arboreum
Anderson Maxwell, Ramish Pingal, William F. Reynolds, Stewart McLean
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     picrasinoside G
    ÏàËÆ¶È:53.5%
Journal of Natural Products          1991          Vol 54          844
Picrasinoside H, a New Quassinoid Glucoside, and Related Compounds from the Stem Wood of Picrasma ailanthoides
Takayuki Matsuzaki, Narihiko Fukamiya, Masayoshi Okano, Tomoyuki Fujita, Kiyoshi Tagahara, Kuo-Hsiung Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




13 .     16-¦Á-O-methylneoquassin
    ÏàËÆ¶È:53.5%
Phytochemistry          1993          32          1007-1013
Quassinoids from Quassia amara
P. Barbetti, G. Grandolini, G. Fardella, I. Chiappini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     scutalpin C
C27H38O9     ÏàËÆ¶È:53.5%
Phytochemistry          1993          34          1589-1594
Neo-clerodane diterpenoids from Scutellaria alpina subsp. javalambrensis
Maria C. de la Torre, Benjam¨ªn Rodr¨ªguez, Maurizio Bruno, Peter Y. Malakov, Georgi Y. Papanov, Franco Piozzi, Giuseppe Savona
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     tomatidine
    ÏàËÆ¶È:53.5%
Phytochemistry          1980          19          299-302
Structure of solanaviol, a new steroidal alkaloid from Solanum aviculare
Ko Kaneko, Kasuaki Niitsu, Naotoshi Yoshida, Hiroshi Mitsuhashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     compound 2a
    ÏàËÆ¶È:53.5%
Australian Journal of Chemistry          1977          30          917-921
Carbon-13 nuclear magnetic resonance spectroscopy of naturally occurring substances. LI. Solanum glycoalkaloids
RJ Weston, HE Gottlieb, EW Hagaman and E Wenkert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     N(3)-isopropylidenesoladunalinidine
    ÏàËÆ¶È:53.5%
Australian Journal of Chemistry          1979          32          611-617
Soladunalinidine, a New Dibasic Analogue of Tomatidine Extracted From Solanum dunalianum
GJ Bird, DJ Collins, FW Eastwood and JM Swan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     scutalpin B
C29H40O10     ÏàËÆ¶È:51.7%
Phytochemistry          1993          34          1589-1594
Neo-clerodane diterpenoids from Scutellaria alpina subsp. javalambrensis
Maria C. de la Torre, Benjam¨ªn Rodr¨ªguez, Maurizio Bruno, Peter Y. Malakov, Georgi Y. Papanov, Franco Piozzi, Giuseppe Savona
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




19 .     stigmastanol glucoside
    ÏàËÆ¶È:51.6%
Fitoterapia          2000          71          722-724
New constituents from Gliricidia sepium
H.M.T.B. Herath, Susila deSilva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     picraqualide B
C25H34O9     ÏàËÆ¶È:50%
Helvetica Chimica Acta          2004          Vol. 87          1591
Five New Quassinoids from the Bark of Picrasma quassioides
Sheng-Ping Yang, and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     2,3-dihydro-3¦Â-methoxyixocarpalactone B
C29H42O9     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          2003          51(5)          530-539
Minor Withanolides from Physalis philadelphica: Structures, Quinone Reductase Induction Activities, and Liquid Chromatography (LC)-MS-MS Investigation as Artifacts
Jian-Qiao GU, Wenkui LI, Young-Hwa KANG, Bao-Ning SU, Harry H. S. FONG,Richard B. VAN BREEMEN, John M. PEZZUTO, and A. Douglas KINGHORN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     tubocapsanolide A
C28H36O6     ÏàËÆ¶È:50%
Journal of Natural Products          2007          70          747-753
Cytotoxic Withanolides from Tubocapsicum anomalum
Pei-Wen Hsieh,Zih-You Huang, Jyun-Hong Chen, Fang-Rong Chang, Ching-Chung Wu, Yu-Liang Yang,Michael Y. Chiang, Ming-Hon Yen, Shu-Li Chen,Hsin-Fu Yen, Tilo L¨¹bken,Wen-Chun Hung,and Yang-Chang Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     anomanolide A
C28H38O7     ÏàËÆ¶È:50%
Journal of Natural Products          2007          70          747-753
Cytotoxic Withanolides from Tubocapsicum anomalum
Pei-Wen Hsieh,Zih-You Huang, Jyun-Hong Chen, Fang-Rong Chang, Ching-Chung Wu, Yu-Liang Yang,Michael Y. Chiang, Ming-Hon Yen, Shu-Li Chen,Hsin-Fu Yen, Tilo L¨¹bken,Wen-Chun Hung,and Yang-Chang Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

»¯ºÏÎï2£º

1 .     ent-3¦Â-Hydroxyspathulenol
    ÏàËÆ¶È:93.3%
Phytochemistry          2000          53          845-849
Sesquiterpenoids and diterpenoids from the Chilean liverwort Lepicolea ochroleuca
Huei-Ju Liu, Chia-Li Wu, Hans Becker, Josef Zapp
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     japodic acid
C13H22O3     ÏàËÆ¶È:78.5%
Records of Natural Products          2008          2          100-106
Japodic acid, A Novel Aliphatic Acid from Jatropha podagrica Hook
Olapeju O. Aiyelaagbe and James B. Gloer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     4¦Â-dihydroeudesmol
    ÏàËÆ¶È:73.3%
Planta Medica          1982          46          20-22
Constituents of Local Plants XXV, Constitution of the Antispasmodic Principle of Cymbopogon proximus
H. D. Locksley, M. B. E. Fayez, A. S. Radwan, V. M. Chari, G. A. Cordell and H. Wagner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     1-epinitraramine
    ÏàËÆ¶È:71.4%
Natural Product Research          1995          6          119-125
Alkaloids from Nitraria billardieri
May Ying Shen; Jos¨¦ Angelo Zuanazzi; Christiane Kan; Jean-Charles Quirion; Henri-Philippe Husson; I. R. C. Bick
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     yielded (-)-apoaromadendrone
    ÏàËÆ¶È:71.4%
Natural Product Research          2000          14          447-452
(-)-Ledol from Calophyllum teysmanii: Structure and Stereochemistry
Shu-Geng Cao; Keng-Yeow Sim; S. H. Goh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     (1S,10S)-9¦Á-hydroxy-allo-aromadendrane
C15H26O     ÏàËÆ¶È:66.6%
Phytochemistry          2002          60          475-481
Aromadendrane transformations by Curvularia lunata ATCC 12017
Dwight O. Collins, William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     alpinolide
    ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1987          35          2849-2859
Novel Guaiane-and Secoguaiane-Type Sesquiterpenes from Alpinia japonica (THUNB.) MIQ.
HIDEJI ITOKAWA,HIROSHI MORITA,KENJI OSAWA,KINZO WATANABE and YOICHI IITAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     epoxycyperene
C15H24O     ÏàËÆ¶È:66.6%
Phytochemistry          1997          45          1435-1439
Sesquiterpenes from the essential oil of Cyperus alopecuroides
Mesmin Mekem Sonwa, Wilfried A. König, Karl-Heinz Kubeczka, Otakar Motl
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     dihydroeudesmol
    ÏàËÆ¶È:66.6%
Australian Journal of Chemistry          1978          31          2527-2538
The Constituents of Rubus rosifolius. The Structure of Rosifoliol, a Biogenetically Significant Sesquiterpenoid
I Southwell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     5,5-Dimethyl-9-oxodecansaure-methylester
C13H24O3     ÏàËÆ¶È:64.2%
Helvetica Chimica Acta          1980          63          1833-1855
Photochemische Reaktionen 111. Mitteilung [1] Zur Photochemie , -ungesättigter , -Epoxyester I: Singulett- versus Triplettreaktivität
Alex Peter Alder, Hans Richard Wolf, Oskar Jeger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     cyprotene
C14H24     ÏàËÆ¶È:64.2%
Phytochemistry          1997          45          1435-1439
Sesquiterpenes from the essential oil of Cyperus alopecuroides
Mesmin Mekem Sonwa, Wilfried A. König, Karl-Heinz Kubeczka, Otakar Motl
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     pathylactone A(synthetic)
    ÏàËÆ¶È:64.2%
Tetrahedron          2002          58          1647-1656
Studies on the synthesis of (¡À)-pathylactone A, a nor-sesquiterpene lactone isolated from marine sources
Fernando Coelho, Gaspar Diaz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     (¡À)-10-hydroxy-6,7-dimethyl-6-(2-oxopropyl)-1-oxaspiro[4,5]decane-2-one
C14H22O4     ÏàËÆ¶È:64.2%
Tetrahedron          2002          58          1647-1656
Studies on the synthesis of (¡À)-pathylactone A, a nor-sesquiterpene lactone isolated from marine sources
Fernando Coelho, Gaspar Diaz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     (-)-nor-aromadendr-10¦Â-ol
    ÏàËÆ¶È:64.2%
Zeitschrift f¨¹r Naturforschung C          2009          64          840-846
Structure-Activity Relationships of Aromadendranes in Uterus-Relaxant Activity
N. P¨¦rez-Hern¨¢ndez, H. Ponce-Monter, M. I. Ortiz, R. Cariño-Cort¨¦sa, and P. Joseph-Nathan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     (6¦Á,8¦Á)-6-hydroxyeremophil-7(11)-en-12,8-olide
C15H22O3     ÏàËÆ¶È:60%
Helvetica Chimica Acta          2006          Vol. 89          915
Terpenoids from the Roots of Ligularia muliensis
Qiu-Hong Wu, Chun-Mei Liu, Yan-Jun Chen, and Kun Gao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     pentadeca-(8Z,13Z)-dien-11-yn-2-one
C15H22O     ÏàËÆ¶È:60%
Phytochemistry          2006          67          1359-1364
Isolation and structure elucidation of cytotoxic polyacetylenes and polyenes from Echinacea pallida
Federica Pellati, Samuele Cal¨°, Stefania Benvenuti, Barbara Adinolfi, Paola Nieri, Michele Melegari
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     11-Hydroxy-4-oxo-tetradecanoic acid methyl ester
C15H28O4     ÏàËÆ¶È:60%
Journal of Natural Products          2005          68          487-492
Ipomoeassins A−E, Cytotoxic Macrocyclic Glycoresins from the Leaves of Ipomoea squamosa from the Suriname Rainforest
Shugeng Cao, Rebecca C. Guza, Jan H. Wisse, James S. Miller, Randy Evans, and David G. I. Kingston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     (9R)-9-hydroxypatchoulol
C15H26O2     ÏàËÆ¶È:60%
Journal of Natural Products          1999          62          437-440
Biotransformation of the Fungistatic Sesquiterpenoid Patchoulol by Botrytis cinerea
Josefina Aleu, James R. Hanson, Rosario Hern¨¢ndez Gal¨¢n, and Isidro G. Collado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     6¦Á-hydroxy-8¦ÂHeremophil-7(11)-en-12,8¦Á-olide
C15H22O3     ÏàËÆ¶È:60%
Chinese Chemical Letters          2006          17          215-217
Two New Eremophilenolides from Ligularia muliensis
Qiu Hong WU, He Xiang WANG, Kun GAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     curcarabranol A
C15H24O3     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1998          46          1186-1188
Absolute Stereostructures of Carabrane-Type Sesquiterpenes, Curcumenone, 4S-Dihydrocurcumenone, and Curcarabranols A and B : Vasorelaxant Activity of Zedoary Sesquiterpenes
Masayuki YOSHIKAWA,Toshiyuki MURAKAMI,Toshio MORIKAWA and Hisashi MATSUDA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     6¦Â-hydroxy-7(11)-eremophilen-12,8¦Á-olide
    ÏàËÆ¶È:60%
China Journal of Chinese Materia Medica          2001          26          835-837
Constituents of Liguliria vellerea (Franch.)Hand-Mazz.
LI Yunsen, LUO Shide, ZHANG Mian, CHEN Jijun, WANG Zhengtao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     1¦Á,10¦Â,11-trihydroxy-4¦Á,5¦Á,7¦Â-eremophilane
C15H28O3     ÏàËÆ¶È:60%
Phytochemistry          1999          52          1063-1067
The hydroxylation of the sesquiterpenoid valerianol by Mucor plumbeus
Simone Fontes Arantes, James R. Hanson, Peter B. Hitchcock
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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