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13C NMR (400 MHz, MeOD) ¦Ä 8.8, 16.1, 27.3, 29.6, 30.6, 34.9, 37.2, 37.6, 40.1, 43.3, 51.3, 52.2, 66.7, 74.1, 80.1, 116.7, 119.0, 140.0, 140.6, 140.7
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wuyuehua(¶¹¸ç´ú·¢): ½ð±Ò+5, лл 2013-09-21 11:20:45
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1 .     3¦Á,7¦Á,11¦Â,15¦Â-tetrahydroxy-ent-kaur-16-ene
C20H32O4     ÏàËÆ¶È:60%
Journal of Natural Products          1996          59          952-957
The Biotransformation of Two 3, 15-Oxygenate ent-Kaurane Derivatives by Gibberella fujikuroi
Braulio M. Fraga, Melchor G. Hern¨¢ndez, and Ricardo Guillermo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     dihydrorabdokunmin C
    ÏàËÆ¶È:60%
Acta Botanica Sinica          1998          40          461-465
The Chemical Constituents of Rabdosia coetsa
LI Wen-Wu, LI Bo-Gang, DING Li-Sheng, CHEN Yao-Zu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     dihydrorabdokunmin C
    ÏàËÆ¶È:60%
Phytochemistry          1989          28          3405-3409
Diterpenoids from Rabdosia kunmingensis
Zhang Hongjie,Sun Handong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     Kaur-16-en-11,15-dioxo-18-oic acid
C20H26O4     ÏàËÆ¶È:60%
Natural Products and Bioprospecting          2012          2          210-216
Exploring of drug leads from diversity-oriented Michael-acceptor library derived from natural products
Xu DENG, Ling-Mei KONG,Yu ZHAO, Juan HE, Li-Yan PENG, Yan LI, and Qin-Shi ZHAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     15¦Â-ailyl-1,3,5(10)-estratrien-3,17¦Â-diol
C21H28O2     ÏàËÆ¶È:57.1%
Steroids          1997          62          674-681
D-ring allyl derivatives of 17¦Â- and 17¦Á-estradiols: Chemical synthesis and 13C NMR data
Patricia Dionne, B¨¦atrice Tch¨¦dam Ngatcha, Donald Poirier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     phyllostacin F
C20H28O6     ÏàËÆ¶È:55%
Helvetica Chimica Acta          2008          Vol. 91          1130
ent-Kaurane Diterpenoids from Isodon phyllostachys
Xian Li, Zhi-Ying Weng, Yong Li, Jian-Xin Pu, Sheng-Xiong Huang, Wei-Lie Xiao, and Han-Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     ent-14 ,16-epoxy-8-pimarene-3 ,15¦Á-diol
C20H32O3     ÏàËÆ¶È:55%
Journal of Natural Products          2009          72          2005-2008
ent-Pimarane Diterpenoids from Siegesbeckia orientalis and Structure Revision of a Related Compound
Fei Wang, Xue-Lian Cheng, Ya-Ju Li, Song Shi, and Ji-Kai Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     13,14-dihydroanisotom-12E-ene-1,14-diol
C20H32O     ÏàËÆ¶È:55%
Phytochemistry          2002          59          293-304
Chemosystematic investigations of irregular diterpenes in Anisotome and related New Zealand Apiaceae
Christian Zidorn, Sonja Sturm, John W. Dawson, John W. van Klink,Hermann Stuppner, Nigel B. Perry
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     xerophilusin IV
C20H28O6     ÏàËÆ¶È:55%
Journal of Natural Products          2007          70          1295-1301
Cytotoxic ent-Kauranoids from the Medicinal Plant Isodon xerophilus
Li-Mei Li,Zhi-Ying Weng,Sheng-Xiong Huang, Jian-Xin Pu,Sheng-Hong Li,Hao Huang,Bing-Bing Yang,Yu Han,Wei-Lie Xiao, Ma-Lin Li, Quan-Bin Han,and Han-Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     3¦Á,7¦Á,11¦Â,15¦Â-tetrahydroxy-ent-kaur-16-ene tetraacetate
C26H38O7     ÏàËÆ¶È:55%
Journal of Natural Products          1996          59          952-957
The Biotransformation of Two 3, 15-Oxygenate ent-Kaurane Derivatives by Gibberella fujikuroi
Braulio M. Fraga, Melchor G. Hern¨¢ndez, and Ricardo Guillermo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     Baiyecrystal E
C20H28O6     ÏàËÆ¶È:55%
Journal of Asian Natural Products Research          2004          6          145-150
CYTOTOXIC ENT-KAURANOIDS FROM ISODON LEUCOPHYLLUS
AI-HUA ZHAO, WEI XIANG, ZHI NA, ZONG-YU WANG, ZHONG-WEN LIN and HAN-DONG SUN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     8¦Á,13R-epoxylabd-14-ene-1¦Á,5¦Á-diol
C20H34O3     ÏàËÆ¶È:55%
Phytochemistry          1994          36          735-738
Rearranged isopimarenes and other diterpenoids from Satureja gilliesii
Cecilia Labb¨¦, Mariano Castillo, Francesca Fainia, Josep Coll, Joseph D. Connolly
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     3¦Â,7¦Á,19-trihydroxy-isopimara-8(14),15-diene
C20H32O3     ÏàËÆ¶È:55%
Planta Medica          2011          77          1623-1630
Compounds from Platycladus orientalis and Their Inhibitory Effects on Nitric Oxide and TNF-¦Á Production
Si-Yang Fan, Yue-Hu Pei, Hua-Wu Zeng, Shou-De Zhang, Yong-Li Li, Li Li, Ji Ye, Yue-Xin Pan, Hong-Lin Li, Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     4¦Â-carboxy-17-hydroxy-19-nor-totarol
C20H29O4     ÏàËÆ¶È:55%
Heterocycles          2004          63          347-357
New Cytotoxic Norditerpene Dilactones from Leaves of Podocarpus macrophyllus var. maki
Hyun-Sun Park, Noriyuki Kai, Haruhiko Fukaya, Yutaka Aoyagi, and Koichi Takeya*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     17¦Á-Methyl-5¦Â-androstane-3¦Á,12¦Â,17¦Â-triol
C20H34O3     ÏàËÆ¶È:55%
Steroids          1983          41          493-500
Metabolism of 17¦Á-methyl-5¦Â-dihydrotestosterone in the rabbit
John F. Templeton, Chung-Ja Choi Jackson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     2¦Â-(pyrrolidinyl)-5¦Á-androstane-3¦Á,17¦Â-diol
C23H39NO2     ÏàËÆ¶È:55%
Bioorganic & Medicinal Chemistry          2008          16          5062-5077
Chemical synthesis of 2¦Â-amino-5¦Á-androstane-3¦Á,17¦Â-diol N-derivatives and their antiproliferative effect on HL-60 human leukemia cells
Dominic Thibeault, Jenny Roy, Patrick DeRoy, Donald Poirier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     19-nor-5¦Â,17¦Á-pregnane-3¦Á,17¦Â-diol
C20H34O2     ÏàËÆ¶È:55%
Australian Journal of Chemistry          2003          56          829-838
Equine Metabolites of Norethandrolone: Synthesis of a Series of 19-Nor-17¦Á-pregnanediols and 19-Nor-17¦Á-pregnanetriols
Andrew R. McKinney, Damon D. Ridley and Peter Turner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     {2-[3,3-bis(ethoxymethyl)cyclobutylidene]ethylidene}cyclohexane
C18H30O2     ÏàËÆ¶È:55%
Tetrahedron          2013          69          3961-3970
Synthesis of small ring-containing conjugated dienes via the coupling reaction of cyclopropyl- and cyclobutylmagnesium carbenoids with ¦Á-sulfonylallyllithiums
Tsutomu Kimura, Mio Inumaru, Takuma Migimatsu, Masashi Ishigaki, Tsuyoshi Satoh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     compound 21
    ÏàËÆ¶È:55%
Organic Magnetic Resonance          1984          22          736-738
Carbon-13 nuclear magnetic resonance spectra of some heterocyclic D-homoandrostanes
Deanna Marcano, Jeannette De M¨¦ndez, Ana C. Ortiz and Mirna Salinas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     Xerophilusin XIV
C20H34O4     ÏàËÆ¶È:55%
Archives of Pharmacal Research          2011          34          875-879
ent-Abietane Diterpenoids from Isodon xerophilus
Li Mei Li, Jian Xin Pu, Wei Lie Xiao, and Han Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     compound 9
C20H32O5     ÏàËÆ¶È:55%
Phytochemistry          2012          75          90-98
Oxygenated compounds from the bioconversion of isostevic acid and their inhibition of TNF-¦Á and COX-2 expressions in LPS-stimulated RAW 264.7 cells
Li-Ming Yang, Shwu-Fen Chang, Wen-Kuang Lin, Bo-Hon Chou, Li-Hsuan Wang, Pan-Chun Liu, Shwu-Jiuan Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     19-hydroxykovalic acid
C22H36O5     ÏàËÆ¶È:54.5%
Phytochemistry          1992          31          1703-1711
Clerodane and labdane derivatives from Olearia teretifolia
C. Zdero, F. Bohlmann, R.M. King
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     3¦Â,14¦Á-Dihydroxy-14,15-seco-5¦Â-card-20(22)-enolide-15-nitrile
C23H33NO4     ÏàËÆ¶È:54.5%
Steroids          1996          61          572-582
Digitalis-like compounds: Synthesis and biological evaluation of seco-D and D-homo derivatives
Mauro Gobbini, Alessandra Benicchio, Giuseppe Marazzi, Gloria Padoani, Marco Torri, Piero Melloni
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     2¦Â-(homopiperidinyl)-5¦Á-androstane-3¦Á,17¦Â-diol
C25H43NO2     ÏàËÆ¶È:54.5%
Bioorganic & Medicinal Chemistry          2008          16          5062-5077
Chemical synthesis of 2¦Â-amino-5¦Á-androstane-3¦Á,17¦Â-diol N-derivatives and their antiproliferative effect on HL-60 human leukemia cells
Dominic Thibeault, Jenny Roy, Patrick DeRoy, Donald Poirier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     picriside B
C21H30O8     ÏàËÆ¶È:52.3%
Chemical & Pharmaceutical Bulletin          1986          34          2518-2521
Sesquiterpene Lactones from Picris hieracioides L. var. japonica REGEL. I
KEIICHI NISHIMURA,TOSHIO MIYASE,AKIRA UENO,TADATAKA NORO,MASANORI KUROYANAGI and SEIGO FUKUSHIMA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     picriside B
    ÏàËÆ¶È:52.3%
Chemical & Pharmaceutical Bulletin          1987          35          2869-2874
Studies on Sesquiterpene Glycosides from Sonchus oleraceus L.
TOSHIO MIYASE and SEIGO FUKUSHIMA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     neocynapanogenin F
    ÏàËÆ¶È:52.3%
Chinese Chemical Letters          2007          18          300-302
New C21 steroidal glycoside from Cynanchum paniculatum
Jing Dou, Ping Li , Zhi Ming Bi , Jian Liang Zhou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     methyl 15-hydroxy-1(10)-ent-halimen-18-oate
    ÏàËÆ¶È:52.3%
Phytochemistry          1997          44          1301-1307
Hydrohalimic acids from Halimium viscosum
Dina I. M. D. de Mendonça, Jesus M. L. Rodilla, Anna M. Lithgow, Isidro S. Marcos
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     Boucergenin
C21H34O4     ÏàËÆ¶È:52.3%
Phytochemistry Letters          2009          2          134-138
Steroidal glycosides from Caralluma umbellata
Olaf Kunert, Nebojsa Simic, Earla Ravinder, Belvotagi Venkatrao Adavi Rao, Bobbala Ravi Kumar, Robert Michael Alex, Doris Kuehnelt, Achanta Venkata Narasimha Appa Rao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     crovatin
C21H26O6     ÏàËÆ¶È:52.3%
Phytochemistry          1992          31          1421-1423
Crovatin, a furanoid diterpene from Croton levatii
Claude Moulis, Maryse Bon, Joel Jaud, Isabelle Fouraste
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     16¦Â-Amino-2¦Á,3¦Á,5,17¦Á-tetrahydroxy-5¦Á-pregna-6,20-dione
C21H33O6N     ÏàËÆ¶È:52.3%
Canadian Journal of Chemistry          2005          83          1084-1092
Synthesis and preliminary bioactivity evaluation of new pregnane brassinosteroid-like compounds
Daniel G. Rivera and Francisco Coll
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     methyl-14S,15-dihydroxy-1(10),13(16)-ent-halimadien-18-oate
    ÏàËÆ¶È:52.3%
Phytochemistry          1990          29          1247-1251
ent-Halimane diterpenes from Halimium viscosum
Julio G. Urones,Isidro S¨¢nchez Marcos,MJos¨¦ Sexmero Cuadrado,Pilar Basabe,Anna M. Lithgow Bertelloni
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     methyl-14R,15-dihydroxy-1(10),13(16)-ent-halimadien-18-oate
    ÏàËÆ¶È:52.3%
Phytochemistry          1990          29          1247-1251
ent-Halimane diterpenes from Halimium viscosum
Julio G. Urones,Isidro S¨¢nchez Marcos,MJos¨¦ Sexmero Cuadrado,Pilar Basabe,Anna M. Lithgow Bertelloni
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     15¦Á-allyl-1,3,5(10)-estratrien-3,17¦Á-diol
C21H28O2     ÏàËÆ¶È:52.3%
Steroids          1997          62          674-681
D-ring allyl derivatives of 17¦Â- and 17¦Á-estradiols: Chemical synthesis and 13C NMR data
Patricia Dionne, B¨¦atrice Tch¨¦dam Ngatcha, Donald Poirier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     neocynapanogenin F
C21H28O6     ÏàËÆ¶È:52.3%
Chinese Journal of Natural Medicines          2006          4          192-194
C_(21)Steroidal Compounds in Roots of Cynanchum paniculatum
DOU Jing; BI Zhi-Ming; ZHANG Yong-Qing; LI Ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     compound 21
C21H30O3     ÏàËÆ¶È:52.3%
Bioorganic & Medicinal Chemistry          2010          18          1724-1735
Synthesis and induction of apoptosis signaling pathway of ent-kaurane derivatives
Idaira Hueso-Falc¨®n, Natalia Gir¨®n, Pilar Velasco, Juan M. Amaro-Luis, Angel G. Ravelo, Beatriz de las Heras, Sonsoles Hortelano, Ana Estevez-Braun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     paxdaphnine B
C21H31NO3     ÏàËÆ¶È:52.3%
Tetrahedron          2007          63          115-119
Novel alkaloids, paxdaphnines A and B with unprecedented skeletons from the seeds of Daphniphyllum paxianum
Cheng-Qi Fan, Sheng Yin, Jun-Juan Xue, Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     Epoxychiromodine
    ÏàËÆ¶È:52.3%
Natural Product Communications          2006          1          319-336
Clerodane Diterpenes from Croton Species: Distribution anda Compilation of their 13C NMR Spectral Data
Sebastião F. Palmeira J¨²nior, Lucia M. Conserva and Jos¨¦ Maria Barbosa Filho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     Crovatin
    ÏàËÆ¶È:52.3%
Natural Product Communications          2006          1          319-336
Clerodane Diterpenes from Croton Species: Distribution anda Compilation of their 13C NMR Spectral Data
Sebastião F. Palmeira J¨²nior, Lucia M. Conserva and Jos¨¦ Maria Barbosa Filho
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     3¦Â,8,12¦Â,14,17-Pentahydroxy-14¦Â,17¦Á-pregn-5-en-20-one
C21H32O6     ÏàËÆ¶È:52.3%
Organic Magnetic Resonance          1977          9          439-464
13C N.m.r. Spectra of steroids¡ªA Survey and Commentary
J.W.Blunt and J.B.Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     uzarigenin-3-O-sulfate
C23H34O7S     ÏàËÆ¶È:52.1%
Phytochemistry          1999          52          1075-1084
Sulfates as novel steroid metabolites in higher plants
Guido F. Pauli, Uwe Matthiesen, Frank R. Fronczek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     Uzarigenin
    ÏàËÆ¶È:52.1%
Journal of the Chemical Society, Perkin Transactions 1          1981                   1773-1778
Cardenolide analogues. Part 12. 13C N.m.r. of semi-synthetic glycosides and side-chain modified genins
H. T. Andrew Cheung, Lindsay Brown, John Boutagy and Richard Thomas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     dendronobilin N
C15H24O4     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          2008          56(6)          854-857
Copacamphane, Picrotoxane and Cyclocopacamphane Sesquiterpenes from Dendrobium nobile
Xue ZHANG,Feng-Juan TU,Hai-Yang YU,Nai-Li WANG,Zhao WANG,and Xin-Sheng YAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     crotonkinensin A
C20H24O4     ÏàËÆ¶È:50%
Journal of Natural Products          2009          72          2040-2042
Crotonkinensins A and B, Diterpenoids from the Vietnamese Medicinal Plant Croton tonkinensis
Phuong-Thien Thuong,Trong-Tuan Dao, Thi-Hong-Minh Pham, Phi-Hung Nguyen, Thi-Van-Thu Le, Kwang-Youl Lee,and Won-Keun Oh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     ballodiolic acid
C20H34O4     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          2004          52(4)          441-443
Two New Diterpenoids from Ballota limbata
Viqar Uddin AHMAD,Umar FAROOQ, Javid HUSSAIN, Farman ULLAH, Sarfraz Ahmad NAWAZ, and Muhammad Iqbal CHOUDHARY
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     8,13,19-trihydroxystemarane
C20H34O3     ÏàËÆ¶È:50%
Phytochemistry          2005          66          1898-1902
Stemodane and stemarane diterpenoid hydroxylation by Mucor plumbeus and Whetzelinia sclerotiorum
Avril R.M. Chen, Peter L.D. Ruddock, Andrew S. Lamm,William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     13-hydroxy-cis-ent-cleroda-3,14-diene
C20H34O     ÏàËÆ¶È:50%
Phytochemistry          2004          65          127-137
ent-Clerodane diterpenes and other constituents from the liverwort Adelanthus lindenbergianus (Lehm.) Mitt.
Barbara Blä s, Josef Zapp, Hans Becker
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     8¦Â,17-epoxy-3¦Â,7¦Â-dihydroxy-12(E)-labden-16,15-olide
C20H30O5     ÏàËÆ¶È:50%
Phytochemistry          2002          60          197-200
Three labdane diterpenoids from Aframomum sceptrum (Zingiberaceae)
Christabel Tomla, Pierre Kamnaing, Godfred A. Ayimele, Eric A. Tanifum,Apollinaire Tsopmo, Pierre Tane, Johnson F. Ayafor, Joseph D. Connolly
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     3¦Â,7¦Â,8¦Â,12¦Æ,17-pentahydroxylabdan-16,15-olide
C20H34O7     ÏàËÆ¶È:50%
Phytochemistry          2002          60          197-200
Three labdane diterpenoids from Aframomum sceptrum (Zingiberaceae)
Christabel Tomla, Pierre Kamnaing, Godfred A. Ayimele, Eric A. Tanifum,Apollinaire Tsopmo, Pierre Tane, Johnson F. Ayafor, Joseph D. Connolly
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     13,16¦Â-dihydroxystemodan-2-one
    ÏàËÆ¶È:50%
Phytochemistry          2002          59          57-62
Biotransformation of terpenes from Stemodia maritima by Aspergillus niger ATCC 9142
Avril R.M. Chen, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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