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1 .     Neosarcodonin O
    ÏàËÆ¶È:58.3%
Bioscience, Biotechnology, and Biochemistry          2004          68          1362-1365
Anti-inflammatory Cyathane Diterpenoids from Sarcodon scabrosus
Tsunashi KAMO, Yuki IMURA, Tomomi HAGIO, Hidefumi MAKABE, Hisao SHIBATA and Mitsuru HIROTA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     chrodrimanin F
C25H34O6     ÏàËÆ¶È:56%
Bioscience, Biotechnology, and Biochemistry          2012          76          1765-1768
New Chrodrimanin Congeners, Chrodrimanins D¨CH, from YO-2 of Talaromyces sp.
Hideo HAYASHI, Yuki OKA, Kenji KAI, Kohki AKIYAMA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     lobophynin A
C22H34O3     ÏàËÆ¶È:54.1%
Journal of Natural Products          1997          60          798-801
Bioactive Terpenoids from Octocorallia. 4. Three New Cembrane-Type Diterpenoids from the Soft Coral Lobophytum schoedei
Koji Yamada, Kenjiro Ryu, Tomofumi Miyamoto, and Ryuichi Higuchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     De-A,B-24,25-dihydroxy-cholestan-8-benzyloxymethylether
C18H33O2     ÏàËÆ¶È:54.1%
Steroids          2000          65          252-265
Synthesis and biological activities of the two C(23) epimers of 1¦Á,23,25-trihydroxy-24-oxo-19-nor-vitamin D3: novel analogs of 1¦Á,23(S),25-trihydroxy-24-oxo-vitamin D3, a natural metabolite of 1¦Á,25-dihydroxyvitamin D3
Nancy E. Lee, Paul G. Williard, Alex J. Brown, Moray J. Campbell, H. Phillip Koeffler, Sara Peleg, D. Sunita Rao, G. Satyanarayana Reddy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     bis-(3-hydroxyestra-1,3,5(10)-triene-17-oximinyl)1,12-dodecanedioate
C48H64N2O     ÏàËÆ¶È:54.1%
Steroids          2010          75          825-833
Synthesis and functional analysis of novel bivalent estrogens
Alison E. Wendlandt, Sharon M. Yelton, Dingyuan Lou, David S. Watt, Daniel J. Noonan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     3-¦Â-hydroxyartemisinic acid ¦Â-D-glucopyranosyl ester
    ÏàËÆ¶È:54.1%
Phytochemistry          1998          48          1329-1333
Biotransformation of artemisinic acid by cultured cells of Artemisia annua
Hiroshi Kawamoto, Yoshihisa Asada, Hiroshi Sekine, Tsutomu Furuya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     melissoidesin C
C24H36O8     ÏàËÆ¶È:54.1%
Phytochemistry          1998          47          1089-1092
diterpenoids from isodon melissoides
Qin-Shi Zhao, Jun Tian, Jian-Min Yue, Shao-Nong Chen, Zhong-Wen Lin, Han-Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     ent-3¦Á,15,16-trihydroxypimar-8(14)-en-15,16-acetonide
C23H38O3     ÏàËÆ¶È:54.1%
Journal of Natural Products          2010          73          17-21
ent-Kaurane and ent-Pimarane Diterpenoids from Siegesbeckia pubescens
Rui Wang, Wen-Hao Chen and Yan-Ping Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     1¦Â,11¦Â-diacetate-dihydroxy-erythroxydiol X
C24H38O6     ÏàËÆ¶È:54.1%
Phytochemistry          1993          32          937-943
Diterpenes from the timber of Erythroxylum australe
Steven M. Ansell, Karl H. Pegel, David A.H. Taylor
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     oryzalexin E
C20H32O2     ÏàËÆ¶È:54.1%
Phytochemistry          1993          33          79-81
Oryzalexin E, A diterpene phytoalexin from UV-irradiated rice leaves
Hideki Kato, Osamu Kodama, Tadami Akatsuka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     compound 19
C26H37NO6S     ÏàËÆ¶È:54.1%
Organic Letters          2004          Vol. 6, No. 7          1123-1126
Total Synthesis of (¡À)-Kalihinol C
Ryan D. White, Gregg F. Keaney, Corin D. Slown, and John L. Wood
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     compound
C22H28O4     ÏàËÆ¶È:54.1%
Heterocycles          2009          77          1185-1208
Synthesis of Marine Oxylipin Agardhilactone and its Analogues: A Structural Revision
Hiromi Miyaoka, Yoshinori Hara, Ikuo Shinohara, Takao Kurokawa, Etsuko Kawashima, and Yasuji Yamada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     3¦Â-Hydroxy-28-noroleana-12,17-dien-16-one
C29H44O2     ÏàËÆ¶È:54.1%
Phytochemistry          1981          20          2539-2542
Two triterpenes from the flowers of Camellia japonica
Hideji Itokawa, Hiroyuki Nakajima, Akira Ikuta, Yoichi Iitaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     Erinacol
C20H32O     ÏàËÆ¶È:54.1%
Bioscience, Biotechnology, and Biochemistry          2004          68          1786-1789
Erinacol (Cyatha-3,12-dien-14¦Â-ol) and 11-O-Acetylcyathin A3, New Cyathane Metabolites from an Erinacine Q-Producing Hericium erinaceum
Hiromichi KENMOKU, Kazumi TANAKA, Katsuhide OKADA, Nobuo KATO and Takeshi SASSA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     compound 4
C22H32O2     ÏàËÆ¶È:54.1%
Bulletin of the Chemical Society of Japan          1986          59          661-662
Amijitrienol and 14-Deoxyisoamijiol, Two New Diterpenoids from the Brown Seaweed Dictyota linearis
Masamitsu Ochi, Kazuhiko Asao, Hiyoshizo Kotsuki, Iwao Miura, Kozo Shibata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     Cyanthiwigin V
C20H30O3     ÏàËÆ¶È:54.1%
Tetrahedron          2002          58          7809-7819
The new bioactive diterpenes cyanthiwigins E¨CAA from the Jamaican sponge Myrmekioderma styx
Jiangnan Peng, Kelly Walsh, Valarie Weedman, Jennifer D Bergthold, John Lynch, Kuo L Lieu, Irwin A Braude, Michelle Kelly, Mark T Hamann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     paxdaphnidine A
C23H35NO2     ÏàËÆ¶È:54.1%
The Journal of Organic Chemistry          2004          69          1726-1729
Paxdaphnidines A and B, Novel Penta-and Tetracyclic Alkaloids from Daphniphyllum paxianum
Zha-Jun Zhan, Sheng-Ping Yang, and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     (3S,6R,7R,8R)-3,14-dihydroxy-8-(2'-methylbutyroyloxy)-helianga-1(10),4,11(13)-trien-6,12-olide
C22H30O7     ÏàËÆ¶È:54.1%
Bioorganic & Medicinal Chemistry          2009          17          3189-3197
Inhibitory effects of sesquiterpene lactones isolated from Eupatorium chinense L. on IgE-mediated degranulation in rat basophilic leukemia RBL-2H3 cells and passive cutaneous anaphylaxis reaction in mice
Tomohiro Itoh, Masayoshi Oyama, Norihiko Takimoto, Chihiro Kato, Yoshinori Nozawa, Yukihiro Akao, Munekazu Iinuma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     boscarterol E
C20H32O2     ÏàËÆ¶È:54.1%
Journal of Natural Products          2013          76          2074-2079
Hepatoprotective Prenylaromadendrane-Type Diterpenes from the Gum Resin of Boswellia carterii
Yan-gai Wang, Jin Ren, Ai-guo Wang, Jian-bo Yang, Teng-fei Ji, Qin-Ge Ma, Jin Tian, and Ya-lun Su
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     compound 42
    ÏàËÆ¶È:54.1%
Natural Product Communications          2008          3          399-412
Structural Elucidation of Pimarane and IsopimaraneDiterpenoids: The 13C NMR Contribution
Ana M. L. Seca, Diana C. G. A. Pinto and Artur M. S. Silva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     cleroserroside B
C26H44O8     ÏàËÆ¶È:53.8%
Chinese Chemical Letters          1999          10          1023-1026
Two New Diterpenoid Glucosides from Clerodendrum serratum
Hui YANG , Jia WANG, Ai Jun HOU, Zhong Wen LIN and Han Dong SUN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     3,16S,20S,24-Tetrahydroxy-24-cholestan- ¡÷1,3,5(10)-estratriene
C29H44O3     ÏàËÆ¶È:53.8%
Steroids          2010          75          432-444
Further study on synthesis and evaluation of 3,16,20-polyoxygenated steroids of marine origin and their analogs as potent cytotoxic agents
Potjamarn Bunyathaworn, Suthinee Boonananwong, Boonsong Kongkathip, Ngampong Kongkathip
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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