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15.8,21.9,32.2,32.8,37.2,38.7,48.7,48.8,51.3,56.1,64.3,70.4,73.6,73.9,80.1,111.9,116.0,121.4,132.4,141.4,147.9 (CD3OD)
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1 .     ptilosteroid C
C21H34O7S     ÏàËÆ¶È:52.3%
Journal of Natural Products          2009          72          760-763
Sulfated Steroids: Ptilosteroids A-C and Ptilosaponosides A and B from the Solomon Islands Marine Sponge Ptilocaulis spiculifer
Marion Gabant, Isabelle Schmitz-Afonso, Jean-Franc¸ois Gallard,Jean-Louis Menou, Dominique Laurent,Cecile Debitus,and Ali Al-Mourabit
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     (3E)-hydroxyimino-17¦Á-methylandrost-1,4-dien-15¦Á,17¦Â-diol
C20H29NO3     ÏàËÆ¶È:52.3%
Steroids          2014          85          65-72
Biotransformation of dianabol with the filamentous fungi and ¦Â-glucuronidase inhibitory activity of resulting metabolites
Naik T. Khan, Salman Zafar, Shagufta Noreen, Abdullah M. Al Majid, Zeid A. Al Othman, Saud Ibrahim Al-Resayes, Atta-ur-Rahman, M. Iqbal Choudhary
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     3¦Â-Hydroxy-7¦Á-methoxy-pregn¦Á-5,16(17)-dien-20-one
C22H32O3     ÏàËÆ¶È:50%
Steroids          2011          76          43-47
Microbial transformation of 3-acetoxypregn¦Á-5,16-diene-20-one by Penicillium citrinum
Jin-Ming Gao, Jian-Wei Shen, Jing-Yi Wang, Zhen Yang, An-Ling Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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5Â¥: Originally posted by sydong at 2014-06-23 12:14:09
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1 .     ptilosteroid C
C21H34O7S     ÏàËÆ¶È:52.3%
Journal of Natural Products          2009          72          760-763
Sulfated Steroids: Ptiloste ...

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1 .     Hemiacetaljavanicin Z
C22H34O7     ÏàËÆ¶È:54.5%
Phytochemistry          1995          40          233-238
Picrasane quassinoids from Picrasma javanica
Kazuo Koike, Mika Yokoh, Mika Furukawa, Satoko Ishii, Taichi Ohmoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     1 7a-Ethyl-3¦Â-methoxy-17a-aza-D-homoandrost-5-en-17-one
C22H35NO2     ÏàËÆ¶È:54.5%
Steroids          1993          58          181-184
Synthesis of 17a-alkyl- and 17a-aryl-3¦Â-acetoxy- and 3¦Â-methoxy-17a-aza-d-homoandrost-5-en-17-one
Gustavo A. Revelli, Eduardo G. Gros
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     steroidal dicyanoalkene
C24H30N2O2     ÏàËÆ¶È:54.1%
Steroids          2013          78          494-499
Facile synthesis of novel D-ring modified steroidal dienamides via rearrangement of 2H-pyrans
Bin Yu, En Zhang, Xiao-Nan Sun, Jing-Li Ren, Yuan Fang, Bao-Le Zhang, De-Quan Yu, Hong-Min Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     ptilosteroid C
C21H34O7S     ÏàËÆ¶È:52.3%
Journal of Natural Products          2009          72          760-763
Sulfated Steroids: Ptilosteroids A-C and Ptilosaponosides A and B from the Solomon Islands Marine Sponge Ptilocaulis spiculifer
Marion Gabant, Isabelle Schmitz-Afonso, Jean-Franc¸ois Gallard,Jean-Louis Menou, Dominique Laurent,Cecile Debitus,and Ali Al-Mourabit
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     przewalskin E
C20H26O3     ÏàËÆ¶È:52.3%
Helvetica Chimica Acta          2009          92          409-413
Three New Diterpenoids from Salvia przewalskii Maxim
Gang Xu, Li-Yan Peng, Lin Tu, Xiao-Li Li, Yu Zhao, Peng-Tao Zhang, Qin-Shi Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     3¦Â-Hydroxy-17-iodo-13¦Á-androsta-5,16-diene
C19H27OI     ÏàËÆ¶È:52.3%
Steroids          2009          74          419-423
The synthesis of 13¦Á-androsta-5,16-diene derivatives with carboxylic acid, ester and carboxamido functionalities at position-17 via palladium-catalyzed carbonylation
P¨¦ter ¨¢cs, Attila Tak¨¢cs, Antal Szil¨¢gyi, J¨¢nos Wölfling, Gyula Schneider, L¨¢szl¨® Koll¨¢r
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     1-oxomanoyloxide
    ÏàËÆ¶È:52.3%
Phytochemistry          1993          34          865-867
Hydroxymanoyloxides from Kyllinga erecta
Yaya Mahmout, Jean-Marie Bessiere, Ren¨¦ Dolmazon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     Brussonol
C20H28O3     ÏàËÆ¶È:52.3%
Organic Letters          2007          Vol. 9, No. 14          2705-2708
Reconciling Icetexane Biosynthetic Connections with Their Chemical Synthesis: Total Synthesis of (¡À)-5,6-Dihydro-6r-hydroxysalviasperanol,(¡À)-Brussonol, and (¡À)-Abrotanone
Eric M. Simmons, Jennifer R. Yen, and Richmond Sarpong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     ¡÷5-pregnene-3¦Â,16¦Â,20(R)-triol
C21H34O3     ÏàËÆ¶È:52.3%
Phytochemistry          1988          27          1173-1179
Pregnane glycosides from an antitumour fraction of Periploca sepium
Hideji itokawa,Junping Xu,Koichi Takeya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     compound 6d
    ÏàËÆ¶È:52.3%
Phytochemistry          1982          21          715-720
Seven guaianolides from Eupatorium chinense
Kazuo Ito, Yoshihisa Sakakibara, Mitsumasa Haruna
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     15¦Â-Hydroxy-17-oxoandrost-5-en-3¦Â-yl acetate
C21H30O4     ÏàËÆ¶È:52.3%
Steroids          1996          61          58-64
Chemical synthesis of 15¦Â-hydroxytestosterone and its derivatives using a(4-methoxyphenyl)methyl protecting group
Ivan Černy, Jan Fajkoš, Vladim¨ªr Pouzar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     17a-Aza-3¦Â-methoxy-D-homoandrost-5-en-17-one
    ÏàËÆ¶È:52.3%
Steroids          1993          58          181-184
Synthesis of 17a-alkyl- and 17a-aryl-3¦Â-acetoxy- and 3¦Â-methoxy-17a-aza-d-homoandrost-5-en-17-one
Gustavo A. Revelli, Eduardo G. Gros
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     Ïª»Æ²ÝÒÒËØ
C20H30O6     ÏàËÆ¶È:52.3%
Journal of China Pharmaceutical University          1987          18          172-174
STRUCTURE OF RABDOSERRIN B,ISOLATED FROM RABDOSIA SERRA
Jin Renling; Cheng Peiyuan and Xu Guangyi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     iso-Drevogenin P
C21H32O5     ÏàËÆ¶È:52.3%
Tetrahedron          2003          59          8399-8403
Polyhydroxy pregnanes from Dregea volubilis
Nilendu Panda, Nirup B Mondal, Sukdeb Banerjee, Niranjan P Sahu, Kazuo Koike, Tamotsu Nikaido, Manuela Weber, Peter Luger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     przewalskin E
    ÏàËÆ¶È:52.3%
Tetrahedron Letters          2013          54          1356-1359
Obtusinones D and E, linear and angular fused dimeric icetexane diterpenoids from Premna obtusifolia roots
Abdul-wahab Salae, Nawong Boonnak
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     (-)-brussonol
    ÏàËÆ¶È:52.3%
Tetrahedron Letters          2013          54          1356-1359
Obtusinones D and E, linear and angular fused dimeric icetexane diterpenoids from Premna obtusifolia roots
Abdul-wahab Salae, Nawong Boonnak
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     ajugarin I
    ÏàËÆ¶È:52.3%
Organic Magnetic Resonance          1982          19          95-97
The assignment of 13C NMR shift data in clerodanes and related structures
J. M. Luteijn, A. Van Veldhuizen and A. De Groot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     Conessine
C24H40N2     ÏàËÆ¶È:52.3%
Natural Product Research          2012          26          987-992
Antimicrobial activity of the methanolic bark extract of Holarrhena pubescens (Buch. Ham), its fractions and the pure compound conessine
Bina S. Siddiqui, Syed Tahir Ali, Ghazala H. Rizwani, Sabira Begum, Saima Tauseef & Aqeel Ahmad
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     Brussonol
C20H28O3     ÏàËÆ¶È:52.3%
Journal of Agricultural and Food Chemistry          2005          53          5200-5206
Diterpenes from Salvia broussonetii Transformed Roots and Their Insecticidal Activity
Braulio M. Fraga, Carmen E. D¨ªaz, Ana Guadaño, and Azucena Gonz¨¢lez-Coloma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     Ethyl 2-(2-methoxyphenylamino)-6-p-tolyl-2-(trifluoromethyl)hexa-3,5-diynoate
C23H20F3NO3     ÏàËÆ¶È:52.3%
Tetrahedron          2012          68          7663-7669
Zinc-mediated enantioselective addition of terminal 1,3-diynes to N-arylimines of trifluoropyruvates
Fa-Guang Zhang, Hai Ma, Yan Zheng, Jun-An Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     capsaicin
    ÏàËÆ¶È:52.3%
Journal of Separation Science          2009          32          2967-2973
Preparative separation of capsaicin and dihydrocapsaicin from Capsicum frutescens by high-speed counter-current chromatography
Aihua Peng, Haoyu Ye, Xia Li and Lijuan Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     compound 56
C20H28O4     ÏàËÆ¶È:52.3%
Tetrahedron          2014          70          3030-3041
Efficient transformation of 7,14-dihydroxy-ent-kaurenes to novel ent-abietanes having cis-fused ¦Á-methylene ¦Ã-lactones under Mitsunobu reaction conditions and their cytotoxicities
Yutaka Aoyagi, Kei Ozawa, Tatsuya Kobayashi, Tomoyo Hasuda, Ming-Yu Gui, Yong-Ri Jin, Xu-Wen Li, Haruhiko Fukaya, Reiko Yano, Yukio Hitotsuyanagi, Koichi Takeya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     compound 14d
    ÏàËÆ¶È:52.1%
Phytochemistry          1994          36          491-499
Neolignans from bark and leaves of Ocotea porosa
Jorge M. David, Massayoshi Yoshida, Otto R. Gottlieb
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     17a-Allyl-3¦Â-methoxy-17a-aza-D-homoandrost-5-en-17-one
C23H35NO2     ÏàËÆ¶È:52.1%
Steroids          1993          58          181-184
Synthesis of 17a-alkyl- and 17a-aryl-3¦Â-acetoxy- and 3¦Â-methoxy-17a-aza-d-homoandrost-5-en-17-one
Gustavo A. Revelli, Eduardo G. Gros
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     compound 16
    ÏàËÆ¶È:52.1%
The Journal of Antibiotics          1979          32          1360-1364
SYNTHESES AND PROPERTIES OF THE 6'-C-ALKYL DERIVATIVES OF 3', 4'-DIDEOXYKANAMYCIN B
HAMAO UMEZAWA, DAISHIRO IKEDA, TSUYOSHI MIYASAKA, SHINICHI KONDO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     3¦Â,20S-dihydroxy-23-norchol-5-enoic acid
    ÏàËÆ¶È:52.1%
Magnetic Resonance in Chemistry          1986          24          239-242
13C NMR studies of epimeric 20(R,S)-hydroxy-23-norcholanoic acid derivatives
Alicia M. Seldes, Marta S. Maier and Eduardo G. Gros
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     junceellin B
C28H35O12Cl     ÏàËÆ¶È:52.1%
Acta Scientiarum Naturalium Universitatis Sunyatseni          1987          26(2)          15-20
Studies on the Chemical Constituents of the Chinese Gorgonia VI-Junceellin B, a New Chlorine-containing Diterpenoid from Junceella Squamata
Long Kanghou Lin Yongcheng Huang Weixong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     17¦Â-(2',5'-Dihydro-5'-oxo-3'-furyl)androst-5-en-3¦Â-ol
C23H32O3     ÏàËÆ¶È:52.1%
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
29 .     sucutinirane F
C22H32O4     ÏàËÆ¶È:50%
Journal of Natural Products          2009          72          976-979
Sucutiniranes C-F, Cassane-Type Diterpenes from Bowdichia nitida
Yosuke Matsuno, Jun Deguchi, Takahiro Hosoya, Yusuke Hirasawa,Chieko Hirobe, Motoo Shiro, and Hiroshi Morita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     ent-6a-acetoxy-18-hydroxy-13-epi-manoyl oxide
C22H36O4     ÏàËÆ¶È:50%
Phytochemistry          2006          67          2294-2302
Biotransformations of ent-18-acetoxy-6-ketomanoyl oxides epimers at C-13 with filamentous fungi
Hanae Ghoumari, Mohamed-Hassan Benajiba, Andr¨¦s Garc¨ªa-Granados,Antonia Fern¨¢ndez, Antonio Mart¨ªnez, Francisco Rivas, Jos¨¦ M. Arias
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     caesalpinins F
C23H30O7     ÏàËÆ¶È:50%
Journal of Natural Products          2005          68          706-710
Cassane- and Norcassane-Type Diterpenes from Caesalpinia crista of Indonesia and Their Antimalarial Activity against the Growth of Plasmodium falciparum
Thein Zaw Linn, Suresh Awale, Yasuhiro Tezuka, Arjun H. Banskota, Surya K. Kalauni, Faisal Attamimi, Jun-ya Ueda, Puji Budi Setia Asih, Din Syafruddin, Ken Tanaka, and Shigetoshi Kadota
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     ent-7¦Á-acetoxy-17-hydroxybeye¦Á-15-en-12-one
C22H32O4     ÏàËÆ¶È:50%
Journal of Natural Products          1997          60          86-92
Biotransformation of ent-Atisenes and ent-Beyerenes by Rhizopus nigricans and Fusarium moniliforme Cultures
Andr¨¦s Garc¨ªa-Granados, Andr¨¦s Parra, and Jos¨¦Mar¨ªa Arias
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     ent-7¦Á-acetoxy-12¦Á,17-dihydroxy-15¦Á,16¦Á-epoxybeyerane
C22H34O5     ÏàËÆ¶È:50%
Journal of Natural Products          1997          60          86-92
Biotransformation of ent-Atisenes and ent-Beyerenes by Rhizopus nigricans and Fusarium moniliforme Cultures
Andr¨¦s Garc¨ªa-Granados, Andr¨¦s Parra, and Jos¨¦Mar¨ªa Arias
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     3¦Â-O-acetyl-ent-atisane-16¦Á, 27-diol
C22H36O4     ÏàËÆ¶È:50%
Planta Medica          1991          57          569-571
New Diterpenoids from Euphorbia sieboldiana
Zhongjian Jia and Yili Ding
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     atisane-3¦Â-acetyl-16¦Á,17-diol
C20H36O4     ÏàËÆ¶È:50%
Chinese Chemical Letters          1990          1          13-16
FIVE NEW DITERPENES FROM EUPHORBIA SIEBOLDIANA
YI LI DING ZHONG JIAN JIA AND YU TING LIU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     3¦Â-Hydroxy-17-(N-tert-butylcarboxamido)-13¦Á-androsta-5,16-diene
C24H37O2N     ÏàËÆ¶È:50%
Steroids          2009          74          419-423
The synthesis of 13¦Á-androsta-5,16-diene derivatives with carboxylic acid, ester and carboxamido functionalities at position-17 via palladium-catalyzed carbonylation
P¨¦ter ¨¢cs, Attila Tak¨¢cs, Antal Szil¨¢gyi, J¨¢nos Wölfling, Gyula Schneider, L¨¢szl¨® Koll¨¢r
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     exsertifolin E
C24H32O7     ÏàËÆ¶È:50%
Phytochemistry          1996          41          1129-1141
Ent-kaurane-type diterpenoids from the liverwort Jungermannia exsertifolia ssp. Cordifolia
Fumihiro Nagashima, Hironao Tanaka, Shigeru Takaoka, Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     compound 12
C22H30O6     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2011          19          2450-2457
Synthesis of rabdokunmin C analogues and their inhibitory effect on NF-§ÜB activation
Yutaka Aoyagi,Yoshiyuki Adachi, Kei Ozawa ,Chihiro Yokomizo ,Ming-Yu Gui , Yong-Ri Jin,Xu-Wen Li, Naohito Ohno , Koichi Takeya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     Dictyocrenulol
C24H38O5     ÏàËÆ¶È:50%
Zeitschrift f¨¹r Naturforschung B          2003          58b          795-798
A New Diterpene from Dictyota crenulata
H. Soto, J. Rovirosa, and A. San-Mart¨ªn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     lancifolin D
C22H28O5     ÏàËÆ¶È:50%
Phytochemical Analysis          1998          9          71-74
Stereochemistry of diastereomeric neolignans from Piper hookeri by nuclear magnetic resonance spectroscopy
Padmanava Pradhan and Asoke Banerji
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     l 7¦Á-Cyano-3,3'-(ethylenedioxy)androst-5-en-17¦Â-ol
    ÏàËÆ¶È:50%
Steroids          1997          62          603-620
Synthesis and characterization by 1H and 13C nuclear magnetic resonance spectroscopy of 17¦Á-cyano, 17¦Á-aminomethyl, and 17¦Á-alkylamidomethyl derivatives of 5¦Á-dihydrotestosterone and testosterone
Elisabeth Mappus, Christophe Chambon, Marc Rolland de Ravel, Catherine Grenot, Claude Y. Cuilleron
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     lancifolin D
    ÏàËÆ¶È:50%
Acta Chemica Scandinavica          1995          49          68-71
Structure Determination of 6-Hydroxycyanidin- and 6-Hydroxydelphinidin-3-(6''-O-alpha-L-rhamnopyranosyl-beta-D-glucopyranosides) and Other Anthocyanins from Alstroemeria Cultivars.
Nygård, Anne-Mette; Aksnes, Dagfinn W.; Andersen, Øyvind M.; Bakken, Anne Kjersti
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     (1R,2R,4S,5S,9S,12S)-4-methoxycarbonyl-7,7-dimethyl-16-propyl-azapentacyclo[10,3,1,0(2,4),0(2,11),0(5,9)]-hexadec-10-en-14-one
C22H31NO3     ÏàËÆ¶È:50%
Acta Chemica Scandinavica          1998          52          1350-1352
Stereochemistry of 1,6-Germacradien-5-ol, a Constituent of the Needles of Scots Pine (Pinus sylvestris) and of the Defence Secretion from Larvae of the Pine Sawfly Neodiprion sertifer.
Nordin, Ove; Hedenström, Erik; Högberg, Hans-Erik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     5¦Á,14¦Â-diacetoxy-6b,10¦Â-dihydroxy-taxa-4(20),11(12)-diene
C24H36O6     ÏàËÆ¶È:50%
Tetrahedron          2008          64          8102-8116
Structural diversification of taxanes by whole-cell biotransformation
Jungui Dai, Runjiang Qu, Jian-hua Zou, Xiaoguang Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     5¦Á,14¦Â-diacetoxy-7¦Â,10¦Â-dihydroxy-taxa-4(20),11(12)-diene
C24H36O6     ÏàËÆ¶È:50%
Tetrahedron          2008          64          8102-8116
Structural diversification of taxanes by whole-cell biotransformation
Jungui Dai, Runjiang Qu, Jian-hua Zou, Xiaoguang Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     prostratin
C22H30O6     ÏàËÆ¶È:50%
Journal of Medicinal Chemistry          1992          35          1978-1986
A nonpromoting phorbol from the Samoan medicinal plant Homalanthus nutans inhibits cell killing by HIV-1
Kirk R. Gustafson, John H. Cardellina II, James B. McMahon, Robert J. Gulakowski, Junichi Ishitoya, Zoltan Szallasi, Nancy E. Lewin, Peter M. Blumberg, Owen S. Weislow,
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     seco-limonoid ichangin
    ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          2011          59          855-859
seco-Limonoids and Quinoline Alkaloids from Raputia heptaphylla and Their Antileishmanial Activity
Carlos Andres Coy Barrera, Ericsson David Coy Barrera, Diana Susana Granados Falla, Gabriela Delgado Murcia and Luis Enrique Cuca Suarez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     16¦Á-(Acetyloxymethyl)androst-5-ene-3¦Â,17¦Á-diol diacetate
C26H38O6     ÏàËÆ¶È:50%
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
49 .     N-(2-aminoethyl)-6¦Á,7¦Â-di-hydroxyvouacapan-17¦Â-amide
    ÏàËÆ¶È:50%
Journal of the Brazilian Chemical Society          1997          8          203-209
Synthesis of 6a,7b-Di-Hydroxyvouacapan-17b-Oic Acid Derivatives Part III : Synthesis, 1H- and 13C-NMR of Amide Derivatives.
C¨¦lia Regina A. Maltha, Guglielmo M. Stefani, Dorila Pilo-Veloso, and Dalton Luiz Ferreira Alves
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     prostratin
    ÏàËÆ¶È:50%
Journal of Chinese Medicinal Materials          2010          33          1406-1409
Study on the Chemical Constituents from Fresh Roots of Euphorbia fischeriana
WANG Jin-lan, WANG Yu-qi, LI Tao, WANG Huan, ZHAO Ming, ZHANG Shu-jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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