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compound1:
14.3,15.9,16.1,22.7,22.8,25.8,26.6,27.9,28.3,29.7,32.1,32.8,38.7,39.8,40.0,124.1,124.3,135.1,135.3
compound2:
10.3,10.4,17.7,18.3,26.5,27.7,29.1,29.8,33.2,33.6,37.2,37.8,38.2,43.7,46.1,66.3,69.3,72.8,73.3,176.6,177.5,177.6,180.5,206.9,211.4
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1 .     3¦Â-(Benzoyloxy)-8,12¦Á,14,17,20-pentahydroxy-5¦Á,14¦Â,17¦Á-pregnane
C26H40O7     ÏàËÆ¶È:56%
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
2 .     (22R,25R)-17¦Â-Methyl-18-norcholest-5,13-dien-3¦Â,22,26-triol
C27H44O3     ÏàËÆ¶È:55.5%
Natural Product Communications          2007          2          47-50
Synthesis of Polyhydroxylated ¦¤13-17,17-dialkyl-18-norsteroidsby BF3¡¤Et2O/Ac2O-promoted Wagner-MeerweinRearrangement of Furostanols
Mart¨ªn A. Iglesias-Arteaga, Jos¨¦. M. Mendez-Stivalet and Nury P¨¦rez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     sodium taurodeoxycholate
    ÏàËÆ¶È:53.8%
Acta Pharmaceutica Sinica          1992          27          674-678
STUDIES ON CHEMICAL CONSTITUENTS OF THE GALL OF PYTHON MOLURUS BIVITTATUS SCHLEGEL
YJ You; JG Lin; LF Ji
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     quadrangularic acid L
C30H50O6     ÏàËÆ¶È:53.3%
Journal of Natural Products          2000          63          57-64
Thirteen Novel Cycloartane-Type Triterpenes from Combretum quadrangulare
Arjun H. Banskota,Yasuhiro Tezuka, Kim Qui Tran, Ken Tanaka, Ikuo Saiki,and Shigetoshi Kadota
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     compound 181
    ÏàËÆ¶È:53.3%
Phytochemistry          1994          37          1517-1575
13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features
Shashi B. Mahato, Asish P. Kundu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     methyl (1S,4aS,8aR)-octahydro-1,2-dihydroxy-2,7,7-trimethyl-1-{(Z)-2-[(1aR,7aS,7bS)-octahydro-1a,4,4,7a-tetramethylnaphtho[1,2-b]oxiren-7b(1aH)-yl]ethenyl}naph-thalene-4a(2H)-carboxylate
C31H50O5     ÏàËÆ¶È:53.3%
Chemistry & Biodiversity          2010          7          421-439
Bioactive Compounds with Added Value Prepared from Terpenes Contained in Solid Wastes from the Olive Oil Industry
Andres Parra, Pilar E. Lopez and Andres Garcia-Granados
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     3¦Â,23,29-trihydroxyolean-12-en-28-oic acid
C30H48O5     ÏàËÆ¶È:53.3%
Natural Product Communications          2008          3          903-910
Triterpene Bisdesmosides from the Stems of Akebia quinata
Yoshihiro Mimaki and Saya Doi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     wrightiamine B
C21H35NO     ÏàËÆ¶È:52%
Chemical & Pharmaceutical Bulletin          2003          51(6)          737-739
Wrightiamines A and B, Two New Cytotoxic Pregnane Alkaloids from Wrightia javanica
Souichi KAWAMOTO,Takashi KOYANO,Thaworn KOWITHAYAKORN, Haruhiro FUJIMOTO,Emi OKUYAMA, Masahiko HAYASHI,Kanki KOMIYAMA, and Masami ISHIBASHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     6¦Á,13-dihydroxystemaran-19-oic acid
    ÏàËÆ¶È:52%
Phytochemistry          2006          67          1088-1093
Bioconversion of Stemodia maritima diterpenes and derivatives by Cunninghamella echinulata var. elegans and Phanerochaete chrysosporium
Andrew S. Lamm, William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     (+)-buxamine F
C26H44N2     ÏàËÆ¶È:52%
Journal of Natural Products          1999          62          665-669
New Steroidal Alkaloids from the Roots of Buxus sempervirens
Atta-ur-Rahman, Athar Ata, Samina Naz, M. Iqbal Choudhary, Bilge Sener, and Songul Turkoz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     lactones 2 and 3
C13H24O2/C13H24O2     ÏàËÆ¶È:52%
Journal of Natural Products          1999          62          358-360
Sphaeric Acid, a New Succinic Acid Derivative from a Sphaeropsis sp.
Royce A. Wilkinson, Gary Strobel, and Andrea Stierle
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     tenacigenin B
C21H32O5     ÏàËÆ¶È:52%
Chinese Chemical Letters          2005          16          487-490
Two New C21 Steroids from Marsdenia tenacissima
Jun DENG, Zhi Xin LIAO, Dao Feng CHEN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     yosgadensolide A
C25H38O5     ÏàËÆ¶È:52%
Phytochemistry          1996          42          1089-1092
Sesterterpenes and other constituents of Salvia yosgadensis
G¨¹laçti Topcu, Ayhan Ulubelen, Timothy C. -M. Tam, Chun Tao-Che
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     3¦Á,12¦Á-dihydroxy-5¦Â-cholan-24-ol sulfate
C24H41SO6     ÏàËÆ¶È:52%
Steroids          2011          76          291-300
Synthesis and olfactory activity of unnatural, sulfated 5-bile acid derivatives in the sea lamprey (Petromyzon marinus)
Aaron C. Burns, Peter W. Sorensen, Thomas R. Hoye
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     Sodium 3-keto-5¦Â-petromyzonol sulfate
C24H39SO7     ÏàËÆ¶È:52%
Steroids          2011          76          291-300
Synthesis and olfactory activity of unnatural, sulfated 5-bile acid derivatives in the sea lamprey (Petromyzon marinus)
Aaron C. Burns, Peter W. Sorensen, Thomas R. Hoye
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     Deoxycholic Acid
C24H40O4     ÏàËÆ¶È:52%
Chemistry & Biodiversity          2012          9          418-427
Studies on the Secondary Metabolites of a Pseudoalteromonas sp. Isolated from Sediments Collected at the Northeastern Coast of Brazil
Isabelle D. B. Arthaud, Felipe A. R. Rodrigues, Paula C. Jimenez,Raquel C. Montenegro, Alysson L. Angelim, Vania M. M. Maciel,Edilberto R. Silveira,Hozana P. S. Freitas, Thiciana S. Sousa, Ot lia D. L. Pessoa, Tito M. C. Lotufo,and Let cia V. Costa-Lotufo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     3¦Á,11¦Â,17¦Á-trihydroxy-21-sulfooxy-5¦Â-pregnan-20-one sodium salt
C21H33O8SNa     ÏàËÆ¶È:52%
Chemical & Pharmaceutical Bulletin          2010          58          344-353
Potential Corticoid Metabolites: Chemical Synthesis of 3- and 21-Monosulfates and Their Double-Conjugates of Tetrahydrocorticosteroids in the 5¦Á- and 5¦Â-Series
Rika Okihara, Kuniko Mitamura, Maki Hasegawa, Megumi Mori, Akina Muto, Genta Kakiyama, Shoujiro Ogawa, Takashi Iida, Miki Shimada, Nariyasu Mano and Shigeo Ikegawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     7¦Â,18-dihydroxy-ent-beyer-15-en-18-O-succinate methyl ester
C25H38O5     ÏàËÆ¶È:52%
Phytochemistry          1989          28          517-526
Sesquiterpene lactones and other constituents from Australian Helipterum species
C. Zdero,F. Bohlmann,R.M. King,H. Robinson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     Deoxycholic acid
    ÏàËÆ¶È:52%
Journal of Natural Medicines          2008          62          83-86
Bioproduction of bile acids and the glycine conjugates by Penicillium fungus
Kazuyoshi Ohashi, Yoshitaka Miyagawa, Yuhki Nakamura and Hirotaka Shibuya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     7¦Á-Hyd roxy-3-oxo-5¦Â-cholanoic acid
    ÏàËÆ¶È:52%
Steroids          1993          58          79-86
Bile acid transformations by Alcaligenes recti
Ipsita Mazumder, Shashi B. Mahato
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     16¦Á,1 7-Epoxy-16¦Â-methyl-5¦Á-pregn-9(11)-ene-3,20-dione
    ÏàËÆ¶È:52%
Steroids          1993          58          396-399
Synthesis and 1H and 13C nuclear magnetic resonance of 16-methylene-17¦Á-hydroxypregna-1,4,9(11)-triene-3,20-dione
Cirilo Garc¨ªa-Mart¨ªnez, Jorge Reyes-L¨®pez, Pedro Joseph-Nathan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     7¦Á,12¦Á-Dihydroxy-3-oxo-5¦Â-cholan-24-oic acid
    ÏàËÆ¶È:52%
Steroids          1993          58          484-490
Transformation of cholic acid by Arthrobacter simplex
Emele Mukherjee, Sukdeb Banerjee, Shashi B. Mahato
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     12¦Á-Hydroxy-3-ketocholanic acid
C24H37O4     ÏàËÆ¶È:52%
Archives of Pharmacal Research          2009          32          857-862
Bile acid derivatives from a sponge-associated bacterium Psychrobacter sp.
Huayue Li, Pramod B. Shinde, Hye Ja Lee, Eun Sook Yoo and Chong-O. Lee, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     3 ¦Á,12¦Á-Dihydroxycholanic acid
    ÏàËÆ¶È:52%
Archives of Pharmacal Research          2009          32          857-862
Bile acid derivatives from a sponge-associated bacterium Psychrobacter sp.
Huayue Li, Pramod B. Shinde, Hye Ja Lee, Eun Sook Yoo and Chong-O. Lee, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     (2R) 2-{[trans-2-(Octanoylamino)cyclopropyl]methoxy}-propionyl-L-alanyl-D-isoglutamine
C23H40N4O7     ÏàËÆ¶È:52%
Zeitschrift f¨¹r Naturforschung B          2003          58          1247-1254
Synthesis of Spacered Cyclopropanoid Muramyldipeptide Analogues as Potential Immunostimulants
R. Csuk and G. Göthe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     methyl (dimethylthexylsilyl 4-O-levulinoyl-2,3-di-O-pivaloyl-¦Â-D-glucopyranoside)uronate
C30H52O11Si     ÏàËÆ¶È:52%
European Journal of Organic Chemistry          2010                   2138-2147
Polymer-Supported Synthesis of Oligosaccharides Using a Diisopropylsiloxane Linker and Trichloroacetimidate Donors
M. Mar Kayser, Jos¨¦ L. de Paz and Pedro M. Nieto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     methyl [O-(tert-butyldimethylsilyl)-5-hydroxypentyl 4-O-levulinoyl-2,3-di-O-pivaloyl-¦Â-D-glucopyranoside]uronate
C33H58O12Si     ÏàËÆ¶È:52%
European Journal of Organic Chemistry          2010                   2138-2147
Polymer-Supported Synthesis of Oligosaccharides Using a Diisopropylsiloxane Linker and Trichloroacetimidate Donors
M. Mar Kayser, Jos¨¦ L. de Paz and Pedro M. Nieto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     compound 28
    ÏàËÆ¶È:52%
Organic Magnetic Resonance          1983          21          305-309
Carbon-13 NMR spectra of hydroxylated bile acid stereoisomers
Takashi Iida, Toshitake Tamura, Taro Matsumoto and Frederic C. Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     digoxigenone
    ÏàËÆ¶È:52%
Journal of the Brazilian Chemical Society          2005          16          614-619
Biotransformation of Digitoxigenin by Fusarium Ciliatum
Rodrigo M. P¨¢dua, Ala¨ªde B. Oliveira, Jos¨¦ D. Souza Filho, G¨¦ssy J. Vieira, Jacqueline A. Takahashi and Fernão C. Braga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     germine
    ÏàËÆ¶È:51.8%
Helvetica Chimica Acta          2007          Vol. 90          769
Four New Germine Esters from Veratrum dahuricum
Jian Tang, Hui-Liang Li, Yun-Heng Shen, Hui-Zi Jin, Shi-Kai Yan, Run-Hui Liu, and Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     norquadrangularic acid A
C27H42O6     ÏàËÆ¶È:51.8%
Journal of Natural Products          2000          63          57-64
Thirteen Novel Cycloartane-Type Triterpenes from Combretum quadrangulare
Arjun H. Banskota,Yasuhiro Tezuka, Kim Qui Tran, Ken Tanaka, Ikuo Saiki,and Shigetoshi Kadota
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     N-(3-Hydroxypropyl)3¦Á,7¦Á,12¦Á-trihydroxy-5¦Â-cholan-24-amide
C27H47NO5     ÏàËÆ¶È:51.8%
Steroids          2008          73          1228-1241
Syntheses and structural study of bile acid amidoalcohols
Arto Valkonen, Manu Lahtinen, Erkki Kolehmainen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     veramarine
    ÏàËÆ¶È:51.8%
Acta Pharmaceutica Sinica          1988          Vol 23          34-37
CHEMICAL STUDIES OF EPIMEDIUM WUSHANENSE T. S. YING
HR Liang; WM Yan; JS Li and CS Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     pingpeimine B
C27H45O6N     ÏàËÆ¶È:51.8%
Acta Pharmaceutica Sinica          1988          Vol 23          34-37
CHEMICAL STUDIES OF EPIMEDIUM WUSHANENSE T. S. YING
HR Liang; WM Yan; JS Li and CS Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     germine
    ÏàËÆ¶È:51.8%
Chinese Pharmaceutical Journal          2008          43          971-973
Studies on Chemical Constituents of Acetyl Acetate Extracted Fraction from Veratrum dahuricum
NIE Li-yue TANG Jian~LI Hui-liang JIN Hui-zi ZHANG Wei-dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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1 .     furanolipid
C21H34O     ÏàËÆ¶È:76.1%
Journal of Natural Products          2007          70          1824-1826
Cytotoxic Metabolites from an Indonesian Sponge Lendenfeldia sp.
Jingqiu Dai,Yang Liu,Yu-Dong Zhou, and Dale G. Nagle
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     2, 2'-Tetrahydrosqualene
C30H54     ÏàËÆ¶È:73.6%
Acta Botanica Yunnanica          2007          29(5)          586-590
Chemical Investigation of Sulcaria virens (Alectoriaceae)
ZHOU Zhong-Yu, WANGLi-Song,WANG Fei, LIU Ji-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (2E,6E,11S,12R)-3,7,11,15-tetramethylhexadeca-2,6,14-triene-1,12-diol
C20H36O2     ÏàËÆ¶È:70%
Journal of Natural Products          2007          70          830-834
Cytotoxic Germacranolides and Acyclic Diterpenoides from the Seeds of Carpesium triste
Xue Gao, Chang-Jun Lin, and Zhong-Jian Jia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     compound 1
C20H32O2     ÏàËÆ¶È:70%
Phytochemistry          1991          30          1801-1803
An insecticidal diterpene from Croton linearis
Ivor C. Alexander, Keith O. Pascoe, Percy Manchard, Lawrence A.D. Williams
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (+)-isobicyclogermacrene
    ÏàËÆ¶È:68.4%
Journal of the Chemical Society, Perkin Transactions 1          1984                   203-214
Structures and conformations of (¨C)-isobicyclogermacrenal and (¨C)-lepidozenal, two key sesquiterpenoids of the cis- and trans-10,3-bicyclic ring systems, from the liverwort Lepidozia vitrea : X-ray crystal structure analysis of the hydroxy derivative of (
Akihiko Matsuo, Hir¨­shi Nozaki, Naoji Kubota, Seiryo Uto and Mitsuru Nakayama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (5 E,9 E)-5,6-epoxy-6,10,14-trimethylpentadeca-9,13-dien-2-one
C18H30O2     ÏàËÆ¶È:68.4%
Australian Journal of Chemistry          1988          41          49-56
Terpenoids From the Brown Alga Cystophora moniliformis
IA Vanaltena
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     2,6,10,14-tetramethyl-7-(3-methylpent-4-enyl)pentadec-5,9-diene
    ÏàËÆ¶È:65.2%
Phytochemistry          1999          51          69-73
Highly branched C25 isoprenoids in axenic cultures of Haslea ostrearia
Emma J. Wraige, Lesley Johns, Simon T. Belt, Guillaume Masse, Jean-Michel Robert, Steven Rowland
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (1S,3S,4R)-cembra-7(E),11(E)-dien-3,4-diol
C20H36O2     ÏàËÆ¶È:65%
Chemistry of Natural Compounds          2007          43          143-148
SYNTHESIS OF N-METHYL UROCANATES OF HYDROXYDERIVATIVES OF ISOCEMBROL
F. A. Valeev,1 Sh. M. Salikhov,O. Yu. Krasnoslobodtseva,B. T. Sharipov L. V. Spirikhin, and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     compund 6a
C20H36O4     ÏàËÆ¶È:65%
Phytochemistry          1988          27          3897-3901
An acyclic diterpene and sesquiterpene lactones from Tithonia pedunculata
Ana-Lidia Perez,Alfredo Ortega,Alfonso Romo De Vivar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     All-carbon AFC
    ÏàËÆ¶È:65%
Bioorganic & Medicinal Chemistry Letters          2005          15          5080-5083
Synthesis of desthio prenylcysteine analogs: Sulfur is important for biological activity
Brian S. Henriksen, Jessica L. Anderson, Christine A. Hrycyna, Richard A. Gibbs
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     (6R,7S)-hydroxy-3,10-prenylbisaboladien-2-one
    ÏàËÆ¶È:65%
Tetrahedron          2002          58          7691-7700
Syntheses of a prenylbisabolane diterpene, a natural insecticide from Croton linearis, and of the bisabolane sesquiterpenes (−-delobanone and (−-epi-delobanone
Olof Smitt, Hans-Erik Högberg
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     Methyl 9,13-Dimethyl-8-tetradecenoate
    ÏàËÆ¶È:63.6%
Journal of Natural Products          2000          63          666-669
Identification and Total Synthesis of a Novel Dimethylated Fatty Acid from the Caribbean Sponge Calyx podatypa
N¨¦stor M. Carballeira and Mayra Pag¨¢n
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     (1E,6E)-3-[(E)-acetoxymethylidene]-7-methyl-9-(2,6,6-trimethylcyclohex-2-enyl)nona-1,6-dienyl acetate
C24H36O4     ÏàËÆ¶È:63.6%
Australian Journal of Chemistry          2000          53          67-71
Monocyclic Diterpenes from the Marine Alga Caulerpa trifaria (Chlorophyta)
Jackie T. Handley and Adrian J. Blackman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     2,3-dihydroxy-2,3-dihydrosqualene
    ÏàËÆ¶È:63.1%
Chemistry of Natural Compounds          1987          23          51-54
STRUCTURE OF THE COUMARIN GLYCOSIDE REOSELIN FROM THE ROOTS OF Ferula kirialovii
T. V. Bukreeva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     Squalene
    ÏàËÆ¶È:63.1%
Guihaia          2006          26          687-689
Extraction and structure identification of Siraitia grosvenorii squalene
CHEN Quan-bin; CHENG Zhong-quan; YANG Jian-xiang; YI Xiang-hui; DONG Chao-min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     ambliofuran
C22H32O4     ÏàËÆ¶È:63.1%
Journal of Natural Products          1988          Vol 51          1014
Chemistry of Sponges, V. Dictyodendrillolide, a New Prenylated Butenolide from a Sponge
R. C. Cambie, Patricia R. Bergquist, P. Karuso
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     2,3,22,23-tetrahydroxy-2,6,10,15,19,23-hexamethyl-6,10,14,18-tetracosatetraene
C30H54O4     ÏàËÆ¶È:63.1%
Phytochemistry          1996          42          803-807
Acyclic triterpenoids from Ekebergia capensis
Yumi Nishiyama, Masataka Moriyasu, Momoyo Ichimaru, Yoko Tachibana, Atsushi Kato, Simon G. Mathenge, Joseph N. Nganga, Francis D. Juma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     6E-geranylgeraniol-19-oic acid 6Z isomer
    ÏàËÆ¶È:63.1%
Chemical Research in Chinese Universities          2003          19          294-296
Synthesis of 6E-Geranylgeraniol-19-oic Acid
LI Shu-hua, PENG Li-Zeng, LI Wei-dong and LI Yu-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     conocandin
C18H30O3     ÏàËÆ¶È:63.1%
Helvetica Chimica Acta          1976          59          2506-2514
Stoffwechselprodukte von Mikroorganismen. 160. Mitteilung. Conocandin, ein fungistatisches Antibiotikum aus Hormococcus conorum (SACC. et ROUM.) ROBACK
Johannes M. M¨¹ller, Hermann Fuhrer, Johannes Gruner and Walter Voser
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     16-hydroxygeranylgeraniol
    ÏàËÆ¶È:63.1%
Phytochemistry          1990          29          1485-1489
Antifungal diterpenic esters from the mushroom Boletinus cavipes
Masao Toyota,Kurt Hostettmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     germacrenin B
    ÏàËÆ¶È:63.1%
China Journal of Chinese Materia Medica          2010          35          315-322
Terpenoids of Heteroplexis micocephala and their bioactivities
FAN Xiaona; LIN Sheng; ZHU Chenggen; HU Jinfeng; LIU Yang; CHEN Xiaoguang; CHEN Naihong; WANG Wenjie; SHI Jiangong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     Compound 13
    ÏàËÆ¶È:63.1%
Bioorganic & Medicinal Chemistry Letters          2006          16          3555-3558
Function of the alkyl side chains of ¦¤lac-acetogenins in the inhibitory effect on mitochondrial complex I (NADH-ubiquinone oxidoreductase)
Naoya Ichimaru, Masato Abe, Masatoshi Murai, Mai Senoh, Takaaki Nishioka, Hideto Miyoshi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     4-oxo-4((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl-oxy)butanoic acid
C19H30O4     ÏàËÆ¶È:63.1%
Bioorganic & Medicinal Chemistry          2010          18          543-556
Towards the synthesis of bisubstrate inhibitors of protein farnesyltransferase: Synthesis and biological evaluation of new farnesylpyrophosphate analogues
St¨¦phanie Duez, Laëtitia Coudray, Elisabeth Mouray, Philippe Grellier, Joëlle Dubois
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     (2R/S,6R,7S)-7-hydroxy-3,10-prenyl-bisaboladien-2-ol
    ÏàËÆ¶È:63.1%
Tetrahedron          2002          58          7691-7700
Syntheses of a prenylbisabolane diterpene, a natural insecticide from Croton linearis, and of the bisabolane sesquiterpenes (−-delobanone and (−-epi-delobanone
Olof Smitt, Hans-Erik Högberg
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     (E,E,E,E)-1-isopropyl-4,8,12-trimethylcyclotetradeca-1,3,7,ll-tetraene
    ÏàËÆ¶È:63.1%
Australian Journal of Chemistry          1978          31          2707-2712
Studies of Australian soft corals. X. The isolation of epoxyisoneocembrene-A from Sinularia grayi and isoneocembrene-A from Sarcophyton ehrenbergi
BF Bowden, JC Coll, W Hicks, R Kazlauskas and SJ Mitchell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     (18S)-5,18-epoxyserrulatane-8,18-diyl diacetate
C24H34O5     ÏàËÆ¶È:63.1%
Australian Journal of Chemistry          1985          38          1837-1845
The Structure of a Stable Serrulatane Diterpenoid Acetal From Eremophila-Rotundifolia
AD Abell, E Horn, GP Jones, MR Snow, RA Massywestropp and R Riccio
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     compound 7
C29H47F3O     ÏàËÆ¶È:62.5%
Tetrahedron Letters          2000          41          6367-6370
Trifluoromethyl ketones derived from squalene: inhibition of the cholesterol biosynthesis in HepG2 cells
Farid Benayoud, Ahmed Abouabdellah, Cyrille Richard, Dani¨¨le Bonnet-Delpon, Jean-Pierre B¨¦gu¨¦, Danielle Levasseur, Olivier Boutaud, Francis Schuber
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     (2S,2'R,3R,4E,8E)-N-2'-Hydroxyhexadecanoyl-2-amino-9-methyl-4,8-octadecadiene-1,3-diol
C35H67NO4     ÏàËÆ¶È:60.8%
Chemical & Pharmaceutical Bulletin          2002          50(5)          681-684
Ceramide Constituents from Five Mushrooms
Yasunori YAOITA, Rie KOHATA, Rie KAKUDA, Koichi MACHIDA, and Masao KIKUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     compound 10
C30H50O     ÏàËÆ¶È:60.8%
Tetrahedron          1986          42          3789-3792
Isolation of (10R,11R)-(+)-squalene-10,11-epoxide from the red alga laurencia okamurai and its enantioselective synthesis
Hideo Kigoshi, Makoto Ojika, Yoshikazu Shizuri, Haruki Niwa, Kiyoyuki Yamada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     (1R,3E,7E,11S,12R)-dolabella-3,7- dien-18-ol
    ÏàËÆ¶È:60%
Helvetica Chimica Acta          2005          Vol. 88          2938
Dolabellane Diterpenoids from the Higher Plant Aglaia odorata
Xiang-Hai Cai, Xiao-Dong Luo, Jun Zhou, and Xiao-Jiang Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     (1R,3E,7E,11R,12Z)-(+)-verticilla-3,7,12-triene
    ÏàËÆ¶È:60%
Journal of Natural Products          2005          68          1598-1602
Verticillane Derivatives from Bursera suntui and Bursera kerberi
Juan D. Hernndez-Hernndez, Luisa U. Romn-Marn, Carlos M. Cerda-Garca-Rojas, and Pedro Joseph-Nathan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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