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1 .     compound 9A
    ÏàËÆ¶È:82.1%
Steroids          1989          54          1-10
Carbon-13 nuclear magnetic resonance spectra of D-homoannulated 17-hydroxypregnan-20-ones
Richard W. Draper, Mohindar S. Puar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

2 .     ( 11 ¦Â,16¦Á)-21-A cetylo xy-9-fluoro-11,16,17-trihydroxypregna-1,4-diene-3,20-dione
    ÏàËÆ¶È:71.4%
Steroids          1994          59          196-204
A reinvestigation of the D-homoannular rearrangement and subsequent degradation pathways of(11¦Â,16¦Á)-9-Fluoro-11,15,17,21-tetrahydroxypregna-1,4-diene-3,20-dione(triamcinolone)
Edward J. Delaney, Ronald G. Sherrill, Venkatapuram Palaniswamy, Thomas C. Sedergran, Stephan P. Taylor
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

3 .     compound 18
C25H32O6NF     ÏàËÆ¶È:67.8%
Journal of Medicinal Chemistry          1982          25          1492-1495
Synthesis and topical antiinflammatory activity of some steroidal [16.alpha.,17.alpha.-d]-isoxazolidines
Michael J. Green, Robert L. Tiberi, Richard Friary, Barry N. Lutsky, Joseph Berkenkoph, Xiomara Fernandez, Margaret Monahan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

4 .     21-Methylthio-9¦Á-fluoro-11¦Â,17¦Á-dihydroxy-16¦Á-methyl-1,4-pregnadiene-3,20-dione
C23H31FO4S     ÏàËÆ¶È:64.2%
Steroids          2008          73          69-76
Expeditious synthesis of steroids containing a 2-methylsulfanyl-acetyl side chain as potential glucocorticoid receptor imaging agents
Frank Wuest, Kathryn E. Carlson, John A. Katzenellenbogen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

5 .     (11¦Â)-9-Fluoro-11-hydroxy-17,21-[1-methylethylidenebis( oxy) ]pregna-1,4-diene-3,20-dione
C21H27O6F     ÏàËÆ¶È:64.2%
Steroids          1994          59          196-204
A reinvestigation of the D-homoannular rearrangement and subsequent degradation pathways of(11¦Â,16¦Á)-9-Fluoro-11,15,17,21-tetrahydroxypregna-1,4-diene-3,20-dione(triamcinolone)
Edward J. Delaney, Ronald G. Sherrill, Venkatapuram Palaniswamy, Thomas C. Sedergran, Stephan P. Taylor
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

6 .     21-acetoxy-9¦Á-bromo-11¦Â-formyl-17¦Á-hydroxy-16¦Á-methyl-1,4-dien-3-one(6,7,9,10,13,14)
    ÏàËÆ¶È:64.2%
Magnetic Resonance in Chemistry          1994          32          547-549
13C NMR spectroscopy of some 20-ketopregnanes
Jos¨¦ Alberto Ruiz Garcia, Fernando A. Verdecia Navarro and Herm¨¢N T. V¨¦lez Castro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

7 .     Chabrolosteroid G
C28H42O4     ÏàËÆ¶È:62.0%
Bulletin of the Chemical Society of Japan          2007          80          2208-2212
New Steroids from the Soft Coral Nephthea chabrolii
Jui-Hsin Su, Fang-Yee Lin, Chang-Feng Dai, Yang-Chang Wu, Chi-Hsin Hsu, Jyh-Horng Sheu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

8 .     21-(S)-Benzoylthio-11¦Â,17¦Á-dihydroxy-1,4-pregnadiene-3,20-dione
C28H32O5S     ÏàËÆ¶È:60.7%
Steroids          2008          73          69-76
Expeditious synthesis of steroids containing a 2-methylsulfanyl-acetyl side chain as potential glucocorticoid receptor imaging agents
Frank Wuest, Kathryn E. Carlson, John A. Katzenellenbogen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

9 .     compound 9
C28H38O9     ÏàËÆ¶È:60.7%
Journal of Asian Natural Products Research          2006          8          545-554
An attempt to enlarge the B ring of maoecrystal B,an ent-kaurane-type diterpene
L. XU and F.-P. WANG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

10 .     (11¦Â,16¦Á,17¦Á)-17-[(Acetyloxy) methyl]-9-fluoro-11-hydroxy-16,17-[1-methylethylidene-bis(oxy) ]-D-homoandrosta-1,4-diene-3,17a-dione
C26H33O7F     ÏàËÆ¶È:60.7%
Steroids          1994          59          196-204
A reinvestigation of the D-homoannular rearrangement and subsequent degradation pathways of(11¦Â,16¦Á)-9-Fluoro-11,15,17,21-tetrahydroxypregna-1,4-diene-3,20-dione(triamcinolone)
Edward J. Delaney, Ronald G. Sherrill, Venkatapuram Palaniswamy, Thomas C. Sedergran, Stephan P. Taylor
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

11 .     16¦Á,21-diacetoxy-9¦Á-fluoro-11¦Â,l7¦Á-dihydroxypregna-1,4-diene-3,20-dione
    ÏàËÆ¶È:60.7%
Steroids          1989          53          513-531
Recognition of d-homoannulation by proton and carbon NMR spectra
Leland L. Smith, Edward L. Ezell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

12 .     compound 3a
    ÏàËÆ¶È:58.6%
Phytochemistry          2002          59          379-384
nor-Oleanene type triterpene glycosides from the leaves of Acanthopanax japonicus
Sang-Yong Park, Seung-Yeup Chang, O-Jin Oh,Chang-Soo Yook, Toshihiro Nohara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

13 .     triamcinolone acetonide-glutaric acid linker
    ÏàËÆ¶È:58.6%
Journal of Medicinal Chemistry          2002          45          1122-1127
Synthesis, Pharmacokinetics, Efficacy, and Rat Retinal Toxicity of a Novel Mitomycin C-Triamcinolone Acetonide Conjugate
Tamer A. Macky, Carsten Oelkers, Uwe Rix, Martin L. Heredia, Eva K¨¹nzel, Mark Wimberly, Baerbel Rohrer, Craig E. Crosson, and J¨¹rgen Rohr
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

14 .     (18R)-18-O-acetyl-nephthoacetal
C29H42O4     ÏàËÆ¶È:58.6%
Bioorganic & Medicinal Chemistry Letters          2013          23          1079-1082
Pentacyclic hemiacetal sterol with antifouling and cytotoxic activities from the soft coral Nephthea sp.
Jun Zhang, Liang-Chun Li, Kai-Ling Wang, Xiao-Jian Liao, Zhou Deng, Shi-Hai Xu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

15 .     acetyl leucolactone
C34H52O6     ÏàËÆ¶È:58.0%
Phytochemistry          1990          29          1693-1695
A triterpenoid lactone from Leucas aspera
Bhim Prasad Pradhan,Dilip Kumar Chakraborty,Gyan Chandra Subba
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

16 .     Methyl 11¦Â,17¦Á ,20¦Á-trihydroxy-9¦Á-fluoro-3-oxo-1,4-pregnadien-21-oate 17,20-carbonate
C23H27FO7     ÏàËÆ¶È:57.1%
Steroids          2002          67          353-359
Effect of chirality at C-20 of methyl 11¦Â,17¦Á,20-trihydroxy-3-oxo-1,4-pregnadien-21-oate derivatives on antiinflammatory activity
Zhengqing You, Ann S. Heiman, Charles E. Hudson, Henry Joung Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

17 .     Loteprednol etabonate
    ÏàËÆ¶È:57.1%
Steroids          2004          69          23-34
Isolation and structure elucidation of the major photodegradation products of loteprednol etabonate
Yoshihisa Shirasaki, Katsuhiro Inada, Jun Inoue, Masayuki Nakamura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

18 .     Stoloniferone K
C28H46O4     ÏàËÆ¶È:57.1%
Steroids          2007          72          573-579
New cytotoxic steroids from the soft coral Clavularia viridis
Chang-Yih Duh, I-Wen Lo, Shang-Kwei Wang, Chang-Feng Dai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

19 .     5¦Á-cholest-7,24-diene-3¦Â ,6¦Á-diol
C27H46O2     ÏàËÆ¶È:57.1%
Journal of Natural Products          1986          Vol 49          779
New Dihydroxylated Sterols from the Marine Sponge Spongionella gracilis
Vincenzo Piccialli, Donato Sica
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

20 .     9¦Á-fluoro-11¦Â,16¦Á,l7¦Á,21-tetrahydroxypregna-1,4-diene-3,20-dione
    ÏàËÆ¶È:57.1%
Steroids          1989          53          513-531
Recognition of d-homoannulation by proton and carbon NMR spectra
Leland L. Smith, Edward L. Ezell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

21 .     compound 9C
    ÏàËÆ¶È:57.1%
Steroids          1989          54          1-10
Carbon-13 nuclear magnetic resonance spectra of D-homoannulated 17-hydroxypregnan-20-ones
Richard W. Draper, Mohindar S. Puar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

22 .     compound 9D
    ÏàËÆ¶È:57.1%
Steroids          1989          54          1-10
Carbon-13 nuclear magnetic resonance spectra of D-homoannulated 17-hydroxypregnan-20-ones
Richard W. Draper, Mohindar S. Puar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

23 .     Chabrolosteroid B
C28H42O3     ÏàËÆ¶È:57.1%
Tetrahedron          2007          63          703-707
Novel steroids from the soft coral Nephthea chabrolii
Jui-Hsin Su, Fang-Yee Lin, Ho-Cheng Huang, Chang-Feng Dai, Yang-Chang Wu, Wan-Ping Hu, Chi-Hsin Hsu, Jyh-Horng Sheu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

24 .     5,6-de-epoxy-5-en-7-one-17-hydroxy withaferin A
C28H36O7     ÏàËÆ¶È:57.1%
Natural Product Research          2014          28          392-398
5,6-De-epoxy-5-en-7-one-17-hydroxy withaferin A, a new cytotoxic steroid from Withania somnifera L. Dunal leaves
Amreen A. Siddique, Pallavi Joshi, Laxminarain Misra, Neelam S. Sangwan & Mahendra P. Darokar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

25 .     21-(1,4-Dithiapent-1-yl)progesterone
C24H36O2S2     ÏàËÆ¶È:57.1%
Bioorganic & Medicinal Chemistry          1999          7          1827-1835
Synthesis of novel progestin¨Crhenium conjugates as potential ligands for the progesterone receptor
F. W¨¹st, M.B. Skaddan, P. Leibnitz, H. Spies, J.A. Katzenellenbogen, B. Johannsen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

26 .     17¦Á,21-Dihydroxy-9¦Â,11¦Â-epoxy-16¦Á-methylpregna-1,4-diene-3,20-dione 21-acetate
C24H30O6     ÏàËÆ¶È:57.1%
Steroids          2013          78          1281-1287
Expedient synthesis of 17¦Á,21-dihydroxy-9¦Â,11¦Â-epoxy-16¦Á-methylpregna-1,4-diene-3,20-dione 21-acetate from prednisolone utilising a novel Mattox rearrangement
David G. Hulcoop, Peter D.P. Shapland
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

27 .     5¦Á,6¦Á,20¦Â-trihydroxy-1-oxowitha-2,24-dienolide
C28H40O6     ÏàËÆ¶È:57.1%
Steroids          2014          79          19-27
Epoxide group relationship with cytotoxicity in withanolide derivatives from Withania somnifera
Pallavi Joshi, Laxminarain Misra, Amreen A. Siddique, Monica Srivastava, Shiv Kumar, Mahendra P. Darokar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

28 .     21-acetoxy-17¦Á-hydroxy-16¦Á-methyl-1,4,9(11)-trien(6,7,9-12)
    ÏàËÆ¶È:57.1%
Magnetic Resonance in Chemistry          1994          32          547-549
13C NMR spectroscopy of some 20-ketopregnanes
Jos¨¦ Alberto Ruiz Garcia, Fernando A. Verdecia Navarro and Herm¨¢N T. V¨¦lez Castro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

29 .     betamethasone-17-valerate
    ÏàËÆ¶È:57.1%
Magnetic Resonance in Chemistry          1995          33          501-505
Carbon-13 NMR investigations of three fluorinated steroids
Steven A. Carss, Robin K. Harris and Richard A. Fletton
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

30 .     champalinol
C30H50O2     ÏàËÆ¶È:56.6%
Phytochemistry          2004          65          2077-2084
Chemical constituents of leaves and stem bark of Plumeria obtusa
Bina S. Siddiqui, Firdous Ilyas, Munawwer Rasheed, Sabira Begum
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

31 .     12¦Â,20R-dihydroxydammaran-3-one
C30H52O3     ÏàËÆ¶È:56.6%
Journal of Natural Products          1997          60          1236-1241
Microbial Transformation of Protopanaxadiol and Protopanaxatriol Derivatives with Mycobacterium sp. (NRRL B-3805)
K. C. Wang, Perng-Haur Wang, and Shoei-Sheng Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

32 .     1¦Á,11¦Á,22-trihydroxyhopane
    ÏàËÆ¶È:56.6%
Chemical & Pharmaceutical Bulletin          1990          38          2130-2132
Fern Constituents : Triterpenoids Isolated from the Leaves of Cheiropleuria bicuspis
Rumiko KAMAYA,Yoshiko TANAKA,Rie HIYAMA and Hiroyuki AGETA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

33 .     compound 8
    ÏàËÆ¶È:56.6%
Chemical & Pharmaceutical Bulletin          1985          33          127-134
Studies on the Constituents of Xanthoceras sorbifolia BUNGE. III. Minor Prosapogenins from the Fruits of Xanthoceras sorbifolia BUNGE
YINGJIE CHEN,TADAHIRO TAKEDA and YUKIO OGIHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

34 .     protoaescigenin
    ÏàËÆ¶È:56.6%
Chemical & Pharmaceutical Bulletin          1985          33          1043-1048
Studies on the Constituents of Xanthoceras sorbifolia BUNGE. IV. Structures of the Minor Prosapogenins
YINGJIE CHEN,TADAHIRO TAKEDA and YUKIO OGIHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

35 .     protoaescigenin
    ÏàËÆ¶È:56.6%
Chemical & Pharmaceutical Bulletin          1985          33          1387-1394
Studies on the Constituents of Xanthoceras sorbifolia BUNGE. V. Major Saponins from the Fruits of Xanthoceras sorbifolia BUNGE
YINGJIE CHEN,TADAHIRO TAKEDA and YUKIO OGIHARA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

36 .     Protoaescigenin
    ÏàËÆ¶È:56.6%
Chemistry of Natural Compounds          1992          28          1-23
13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES
A. I. Kalinovskii
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

37 .     compound 17
    ÏàËÆ¶È:56.6%
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
--------------------------------------------------------------------------------

38 .     compound 53
    ÏàËÆ¶È:56.6%
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
--------------------------------------------------------------------------------

39 .     compound 344
    ÏàËÆ¶È:56.6%
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
--------------------------------------------------------------------------------

40 .     3¦Â-O-sulfate gypsogenin
C30H46O7S     ÏàËÆ¶È:56.6%
Journal of Asian Natural Products Research          2011          Vol.13,No.6          529-533
Three new sulfated triterpenoids from the roots of Gypsophila pacifica
Jian-Guang Luo, Wei Nie and Ling-Yi Kong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

41 .     1¦Á,11¦Á,22,25-tetrahydroxyhopane
C30H52O4     ÏàËÆ¶È:56.6%
Chemical & Pharmaceutical Bulletin          1987          35          4016-4021
Chemical and Chemotaxonomical Studies of Filices. LXXI. Chemical Studies on the Constituents of Cheiropleuria bicuspis (BL.) PR.
NOBUTOSHI TANAKA,HIROSHI WADA,MASAAKI KOJIMA,TAKAO MURAKAMI,YASUHISA SAIKI,CHIU-MING CHEN and YOICHI IITAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

42 .     (23R,25S)-3¦Â,23¦Á,26-triacetoxy-16¦Â,23-cyclo-5¦Â-cholest-17-en-22-one
C33H48O7     ÏàËÆ¶È:56.2%
Steroids          2012          77          534-541
Regioselective cleavage of 22-oxo-23-spiroketals. Novel cholestanic frameworks with pyranone and cyclopentenone E rings on the side chain
Yliana L¨®pez ,Le¨®n Rodr¨ªguez,Rosa E. del R¨ªo,Norberto Farf¨¢n,Jacek W. Morzycki,Rosa Santillan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

43 .     17¦Â-hydroxy-3,16-dioxo-28-norolean-12-ene
C29H44O3     ÏàËÆ¶È:55.1%
Planta Medica          2003          69          258-264
New Dihydrobenzofurans and Triterpenoids from Roots of Microglossa pyrifolia
homas J.Schmidt,Meike R.Hildebrand,G¨¹nter Willuhn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

44 .     villosagenin I
C29H44O3     ÏàËÆ¶È:55.1%
Natural Product Research          1994          4          297-301
Villosagenin I and II Two Novel Pentacyclic 28-Nortriterpenes from Silene villosa (Forssk.)
M. Hani; A. Elgamal; Hesham S. M. Soliman; Mohamed S. Karawya; Helmut Duddeck
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

45 .     11-acetoxy-3¦Â,6¦Á-dihydroxy-9,11-seco-5¦Á-cholest-7-en-9-one
C29H48O5     ÏàËÆ¶È:55.1%
Bioorganic & Medicinal Chemistry          2009          17          4537-4541
9,11-Secosterols with antiproliferative activity from the gorgonian Eunicella cavolini
Efstathia Ioannou, Ayman F. Abdel-Razik, Xanthippi Alexi, Constantinos Vagias, Michael N. Alexis, Vassilios Roussis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

46 .     20-isopropyl-5,9-dimethyl-5-methoxycarbonyl-17-oxopentacyclo[10.6.2(1,10).0(4,9).0(13,18)]-icos-19-ene-14-yl acetate
C29H42O5     ÏàËÆ¶È:55.1%
Russian Journal of Organic Chemistry          2008          44          1598-1605
Synthesis, structure, and acylation of dihydroquinopimaric acid hydroxy derivatives
I. E. Smirnova, E. V. Tret¡¯yakova, O. B. Flekhter, L. V. Spirikhin and F. Z. Galin, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

47 .     sentulic acid
C30H46O4     ÏàËÆ¶È:55.1%
Bioorganic & Medicinal Chemistry Letters          2012          22          4242-4245
Sentulic acid: A cytotoxic ring A-seco triterpenoid from Sandoricum koetjape Merr
Mai Efdi, Masayuki Ninomiya, Erma Suryani, Kaori Tanaka, Sanusi Ibrahim, Kunitomo Watanabe, Mamoru Koketsu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

48 .     7¦Á,9¦Á,11¦Á-trihydroxy-5¦Á-cholest-8(14)-en-3¦Â-yl acetate
    ÏàËÆ¶È:55.1%
European Journal of Organic Chemistry          2001          2001          3731-3739
Reactivity of Steroidal Dienes towards the Methyltrioxorhenium/H2O2−Urea Oxidation System: Isolation and Characterization of New Oxygenated Steroids
Donato Sica, Domenica Musumeci, Franco Zollo and Simona De Marino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

49 .     3¦Â,16¦Á,17-trihydroxy-olean-12-ene
C29H48O3     ÏàËÆ¶È:55.1%
Phytochemistry          2014          103          99-106
Oleanane triterpenes as protein tyrosine phosphatase 1B (PTP1B) inhibitors from Camellia japonica
Mohammad Nasir Uddin, Govinda Sharma, Jun-Li Yang, Hong Seok Choi, Seong-IL Lim, Keon Wook Kang, Won Keun Oh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

50 .     Minabeolide-5
C29H40O5     ÏàËÆ¶È:55.1%
The Journal of Organic Chemistry          1988          53          3926-3929
Minabeolides: a group of withanolides from a soft coral, Minabea sp
Mohamad B. Ksebati, Francis J. Schmitz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

51 .     cordianol I
C31H52O6     ÏàËÆ¶È:54.8%
Journal of Natural Products          2003          66          1307-1312
Dammarane-Type Triterpenes from the Brazilian Medicinal Plant Cordia multispicata
Masanori Kuroyanagi, Nobuo Kawahara, Setsuko Sekita,Motoyoshi Satake,Tatsuo Hayashi,Yoichi Takase,and Kazuo Masuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

52 .     12¦Â-O-2-methylbutyryltenacigenin A
    ÏàËÆ¶È:53.5%
Phytochemistry          2005          66          1040-1051
Marsdenosides A¨CH, polyoxypregnane glycosides from Marsdenia tenacissima
Jun Deng, Zhixin Liao, Daofeng Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

53 .     suberiphenol
C27H38O3     ÏàËÆ¶È:53.5%
Journal of Natural Products          2004          67          672-674
New Sesterterpenes from the Antarctic Sponge Suberites sp.
Hyi-Seung Lee, Jong-Woong Ahn, Youn-Ho Lee, Jung-Rae Rho, and Jongheon Shin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

54 .     ergosta-7-en-3¦Â-ol
    ÏàËÆ¶È:53.5%
Chemical & Pharmaceutical Bulletin          1991          39          1958-1961
New Toxic Metabolites from a Mushroom, Hebeloma vinosophyllum. III. Isolation and Structures of Three New Glycosides, Hebevinosides XII, XIII and XIV, and Productivity of the Hebevinosides at Three Growth Stages of the Mushroom
Haruhiro FUJIMOTO,Kaijiro MAEDA and Mikio YAMAZAKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

55 .     compound 15
C25H29FO7     ÏàËÆ¶È:53.5%
Steroids          2000          65          109-115
Novel steroid spiro enones: condensation of prednisolone derivatives with diethyl oxalate
Zhengqing You, Ann S. Heiman, Meiqin Chen, Henry Joung Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

56 .     Yonarasterol H
C28H45O3Cl     ÏàËÆ¶È:53.5%
Steroids          2001          66          25-32
Three new chlorinated marine steroids, yonarasterols G, H and I, isolated from the Okinawan soft coral, Clavularia viridis
Makoto Iwashima, Ken Nara, Yoshiyuki Nakamichi, Kazuo Iguchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

57 .     Cholest-4-eno[2,3-d]isoxazole
    ÏàËÆ¶È:53.5%
Steroids          2002          67          203-209
Synthesis of some A- and D-ring fused steroidal pyrazoles, isoxazoles and pyrimidines
Warjeet S. Laitonjam, Tombisana S. Rajkumar, Brajakishor S. Chingakham
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

58 .     Methyl 11 ¦Â,17¦Á,20¦Á-trihydroxy-9¦Á-fluoro-3-oxo-1,4-pregnadien-21-oate 17,20-acetonide
C25H33FO6     ÏàËÆ¶È:53.5%
Steroids          2002          67          353-359
Effect of chirality at C-20 of methyl 11¦Â,17¦Á,20-trihydroxy-3-oxo-1,4-pregnadien-21-oate derivatives on antiinflammatory activity
Zhengqing You, Ann S. Heiman, Charles E. Hudson, Henry Joung Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

59 .     Methyl 11¦Â ,17¦Á,20¦Â-trihydroxy-9¦Á-fluoro-3-oxo-1,4-pregnadien-21-oate 17,20-carbonate
C23H27FO7     ÏàËÆ¶È:53.5%
Steroids          2002          67          353-359
Effect of chirality at C-20 of methyl 11¦Â,17¦Á,20-trihydroxy-3-oxo-1,4-pregnadien-21-oate derivatives on antiinflammatory activity
Zhengqing You, Ann S. Heiman, Charles E. Hudson, Henry Joung Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

60 .     (22R,24R)-[26,27-2H6]6¦Â -methoxy-24-methyl-3¦Á ,5-cyclo-5¦Á-cholestan-22-ol
C29H44D6O2     ÏàËÆ¶È:53.5%
Steroids          2004          69          617-628
Synthesis of [26,27-2H6]brassinosteroids from 23,24-bisnorcholenic acid methyl ester
Andrey P. Antonchick, Bernd Schneider, Vladimir N. Zhabinskii, Vladimir A. Khripach
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

61 .     24(S)-Ergost-5-en-1¦Á,3¦Â,11¦Á ,18-tetrol
C28H48O4     ÏàËÆ¶È:53.5%
Steroids          2005          70          487-493
Polyhydroxylated steroids from the soft coral Sinularia dissecta
Pengfei Jin, Zhiwei Deng, Yuehu Pei, Hongzheng Fu, Jun Li, Leen Van Ofwegen, Peter Proksch, Wenhan Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

62 .     Stoloniferone I
C28H44O4     ÏàËÆ¶È:53.5%
Steroids          2007          72          573-579
New cytotoxic steroids from the soft coral Clavularia viridis
Chang-Yih Duh, I-Wen Lo, Shang-Kwei Wang, Chang-Feng Dai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

63 .     (22R)-2¦Á,3¦Á,5¦Á-Trihydroxy-furostan-6-one
C27H43O5     ÏàËÆ¶È:53.5%
Steroids          2007          72          955-959
Synthesis and biological activity of furostanic analogues of brassinosteroids bearing the 5¦Á-hydroxy-6-oxo moiety
Margarita Romero-Avila, Guadalupe de Dios-Bravo, J¨®se M. Mendez-Stivalet, Rogelio Rodr¨ªguez-Sotres, Martin A. Iglesias-Arteaga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

64 .     Pregn-4-en-17¦Á,21-diol-3,20-dione-21-O-glucuronide
    ÏàËÆ¶È:53.5%
Steroids          2009          74          870-875
Corticosteroids 21-glucuronides: Synthesis and complete characterization by 1H and 13C NMR
Pierangela Ciuffreda, Silvana Casati, Maria De Mieri, Patrizia Ferraboschi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

65 .     (4S,20S,22R)-4,27-Dihydroxy-1-oxo-witha-2,5,16,24-tetraenolide
C28H36O5     ÏàËÆ¶È:53.5%
Steroids          2010          75          974-981
Withanolides from Withania aristata and their cytotoxic activity
Gabriel G. LLanos, Liliana M. Araujo, Ignacio A. Jim¨¦nez, Laila M. Moujir, Jes¨²s T. V¨¢zquez, Isabel L. Bazzocchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

66 .     (4S,22R)-4,16¦Â,27-Trihydroxy-1-oxo-witha-2,5,17(20),24-tetraenolide
C28H36O6     ÏàËÆ¶È:53.5%
Steroids          2010          75          974-981
Withanolides from Withania aristata and their cytotoxic activity
Gabriel G. LLanos, Liliana M. Araujo, Ignacio A. Jim¨¦nez, Laila M. Moujir, Jes¨²s T. V¨¢zquez, Isabel L. Bazzocchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

67 .     glabcensin W
C28H38O9     ÏàËÆ¶È:53.5%
Phytochemistry          1999          50          123-126
Glabcensin V-Y, four ent-kaurane diterpenoids from Isodon angustifolius var. Glabrescens
Qin-Shi Zhao, Zhong-Wen Lin, Bei Jiang, Jia Wang, Han-Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

68 .     fungisterol
C28H48O     ÏàËÆ¶È:53.5%
Natural Product Sciences          2008          14          1-11
Peroxynitrite scavengers from Phellinus linteus
Jeong, Da-Mi; Jung, Hyun-Ah; Kang, Hye-Sook; Choi, Jae-Sue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

69 .     2¦Á,3¦Á-dihydroxy-urs-12-ene-24-oic acid
C30H48O4     ÏàËÆ¶È:53.5%
Phytochemistry          1995          39          453-455
Two triterpenoids from Boswellia serrata gum resin
Babita Mahajan, S. C. Taneja, V. K. Sethi, K. L. Dhar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

70 .     triterpenoid X acetate
    ÏàËÆ¶È:53.5%
Phytochemistry          1992          31          2546-2547
A triterpenoid from the root-bark of Chiococca alba
Jnanabrata Bhattacharyya, Emidio V.L. Cunha
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

71 .     5-hydroxyecdysone
C27H44O7     ÏàËÆ¶È:53.5%
Steroids          2011          76          1419-1424
Ecdysteroids from Polypodium vulgare L.
Andr¨¢s Simon, Attila V¨¢nyol¨®s, Zolt¨¢n B¨¦ni, Mikl¨®s D¨¦k¨¢ny, G¨¢bor T¨®th, M¨¢ria B¨¢thori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

72 .     viteagnusin F
C23H38O7     ÏàËÆ¶È:53.5%
Chemical & Pharmaceutical Bulletin          2009          57          1132-1135
Three New Diterpenoids from the Fruit of Vitex agnus-castus
Masateru Ono, Yumiko Nagasawa, Tsuyoshi Ikeda, Ryota Tsuchihashi, Masafumi Okawa, Junei Kinjo, Hitoshi Yoshimitsu and Toshihiro Nohara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

73 .     6¦Á-methylprednisolone¨Ccarboranyl ester
    ÏàËÆ¶È:53.5%
Tetrahedron Letters          2000          41          1355-1358
The synthesis of corticosteroid¨Ccarborane esters for the treatment of rheumatoid arthritis via boron neutron capture synovectomy
John F. Valliant, Paul Schaffer, James F. Britten, Alan Davison, Alun G. Jones, Jacquelyn C. Yanch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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