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9.64,11.22,11.26,24.44,24.81,25.04,29.71,33.32,33.93,34.69,34.95,35.25,37.3,39.55,40.88,41.8,41.96,42.53,74.63,123.24,130.05,130.37,138.52,157.59,158.77,169.86,178.73,197.93,198.37
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cheryl_w: ½ð±Ò+8, ¡ïÓаïÖú 2015-05-30 09:05:56
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1 .     (24R)-24-ethylcholesta-4,22-dien-3-one
    ÏàËÆ¶È:68.9%
China Journal of Chinese Materia Medica          2008          33          405-408
Studies on phenolic compounds from Stellera chamaejasme
FENG Bao, GONG Xiaojie, SHI Liying, JIAN Ge, PEI Yue-hu, WANG Yong-qi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     stigmast-4,2 2-dien-3-one
    ÏàËÆ¶È:68.9%
Chinese Traditional and Herbal Drugs          2002          33          205-206
Studies on chemical constituents of Uvaria tonkinensis var. subglabra
LIU An; TIAN Jing kui; ZOU Zhong mei; XU Li zhen; MU Hong mei; YANG Shi lin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     compound 8
C29H46O     ÏàËÆ¶È:68.9%
European Journal of Organic Chemistry          2002          2002          1500-1504
Structure and Synthesis of a Progesterone Homologue from the Skin of the Dorid Nudibranch Aldisa smaragdina
Margherita Gavagnin, Nicon Ungur, Ernesto Mollo, Jos¨¦ Templado and Guido Cimino
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     stigmasta-4,22-dien-3-one
    ÏàËÆ¶È:68.9%
Journal of the Indian Chemical Society          1999          76          509-510
Steroidal constituents of Ailanthus excelsa Roxb.(Simarubaceae)
S.Mandal,P.C.Das,P.C.Joshi,S.R.Das,B.Mallick and A.Chatterjee
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     (24R)-24-ethylecholesta-4,22-dien-3-one
    ÏàËÆ¶È:68.9%
China Journal of Chinese Materia Medica          2012          37          1973-1976
Sesquiterpenes and monoterpene from Aquilaria sinensis
YANG Lin; QIAO Lirui; XIE Dan; DAI Jungui; GUO Shunxing
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     (24R)-24-¶¹çÞ-4,22-¶þÏ©-3-ͪ
    ÏàËÆ¶È:68.9%
China Journal of Chinese Materia Medica          2012          37          2092-2099
Non-anthraquinones constituents from the roots of Knoxia valerianoides
ZHAO Feng; WANG Sujuan; WU Xiuli; YU Yang; YUE Zhenggang; LIU Bo; LIN Sheng; ZHU Chenggen; YANG Yongchun; SHI Jiangong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     stigmast-4,22-dien-3-one
    ÏàËÆ¶È:68.9%
Research Journal of Phytochemistry          2014          8          52−56
Cytotoxic steroids from the stem barks of Pandanus tectorius
N. T. Hoa, P. H. Dien and D. N. Quang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     pachysamine H
    ÏàËÆ¶È:66.6%
Steroids          2010          75          818-824
Pregnane alkaloids from Pachysandra axillaris
Yun Sun, Yu-Xin Yan, Jian-Chao Chen, Lu Lu, Xian-Min Zhang, Yan Li, Ming-Hua Qiu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     methyl 3-oxocholesta-1,4-dien-26-oate
C28H42O3     ÏàËÆ¶È:65.5%
Journal of Natural Products          2005          68          1111-1115
Steroids from the Antarctic Octocoral Anthomastus bathyproctus
Gonzalo G. Mellado, Eva Zuba, Mara J. Ortega, and Pablo J. Lpez-Gonzlez
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     (22E,24S)-stigmasta-1,4,22-trien-3-one
C29H44O     ÏàËÆ¶È:65.5%
Planta Medica          2003          69          757-764
Anti-Platelet Aggregation and Chemical Constituents from the Rhizome of Gynura japonica
Wei-Yu Lin,Yueh-Hsiung Kuo,Ya-Ling Chang, Che-Ming Teng,Eng-Chi Wang, Tsutomu Ishikawa,Ih-Sheng Chen
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     Stigmasta-4,22-dien-3-one
C29H46O     ÏàËÆ¶È:65.5%
Steroids          2002          67          291-304
The synthesis of spermine analogs of the shark aminosterol squalamine
Youheng Shu, Stephen R. Jones, William A. Kinney, Barry S. Selinsky
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     5-Cholesten-3¦Â-yl formate (3¦Â-cholesterylformate
C28H46O2     ÏàËÆ¶È:65.5%
Steroids          2006          71          632-638
A simple, convenient and chemoselective formylation of sterols by Vilsmeier reagent
Vandana Srivastava, Arvind Singh Negi, J.K. Kumar, M.M. Gupta
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     6'-chloro-5¦Á-cholest[3,2-b]pyridine
C30H46NCl     ÏàËÆ¶È:65.5%
Steroids          2008          73          1137-1142
Convenient preparation of A-ring fused pyridines from steroidal enamides
Madan G. Barthakur, Moyurima Borthakur, Romesh C. Boruah
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     3-keto,16¦Á-hydroxyl,24-noroleanolic acid
    ÏàËÆ¶È:65.5%
Phytochemistry          1998          48          529-536
Triterpenoid saponins and sapogenins from Vaccaria segetalis
Zhonghua Jia, Kazuo Koike, Momoe Kudo, Hongyu Li, Tamotsu Nikaido
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     stigmasta-4,22-dien-3-one
    ÏàËÆ¶È:65.5%
China Journal of Chinese Materia Medica          2011          Vol 36,Issue 7          891-895
Chemical constituents from petroleum ether portion of Abelmoschus esculentus
JIA Lu, GUO M ingm ing, LI Dong, JING Lin lin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     21-Hydroxy-3-oxocholest-4,20(22)-diene
C27H42O2     ÏàËÆ¶È:65.5%
Planta Medica          2011          77          945-950
Chemical Characterization of a Commercial Commiphora wightii Resin Sample and Chemical Profiling to Assess for Authenticity
Rida Ahmed, Zulfiqar Ali, Yunshan Wu, Swapnil Kulkarni, Mitchell A. Avery,Muhammed Iqbal Choudhary, Atta-ur-Rahman, Ikhlas A. Khan
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     stigmasta-4,22-dien-3-one
    ÏàËÆ¶È:65.5%
Chinese Journal of Marine Drugs          2008          27(1)          40-42
Studies on the chemical constituents of Nypa fruticans
NAN Hai-han, YIN Hao, ZHANG Si
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     stigmasta-4,22-dien-3-one
C29H46O     ÏàËÆ¶È:65.5%
Chinese Journal of Marine Drugs          2007          26(6)          5-9
Studies on chemical constituents in ethanol ic extract from A-ca nt hus ilici f olius as a pharmaceutic mangrove
ZHANG Liang-liang, WANG Zhan-chang, CHEN Jun-de, LIN Peng, YANG Zhi-wei, LIN Yi-ming
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     4-aza-A-Homocholest-3,6-dione-6-semicarbazone
    ÏàËÆ¶È:65.5%
Steroids          2011          76          1346-1350
Synthesis and antiproliferative activity of some steroidal lactams
Yanmin Huang, Jianguo Cui, Sijing Chen, Chunfang Gan, Aimin Zhou
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     Haloxysterol C
C29H46O2     ÏàËÆ¶È:65.5%
Bioorganic & Medicinal Chemistry Letters          2006          16          573-580
Isolation and cholinesterase-inhibition studies of sterols from Haloxylon recurvum
Ejaz Ahmed, Sarfraz A. Nawaz, Abdul Malik, M. Iqbal Choudhary
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
21 .     3-Keto,16¦Á-hydroxy,24-noroleanolic acid
    ÏàËÆ¶È:65.5%
Bioorganic & Medicinal Chemistry          2008          16          2912-2920
New triterpenoid saponins with strong ¦Á-glucosidase inhibitory activity from the roots of Gypsophila oldhamiana
Jian-Guang Luo, Li Ma, Ling-Yi Kong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
22 .     7¦Â-Hydroxycholest-4-en-3-one
C27H44O2     ÏàËÆ¶È:65.5%
Steroids          1995          60          290-294
A convenient synthesis of 7¦Á-hydroxycholest-4-en-3-one by the hydroxypropyl-¦Â-cyclodextrin-facilitated cholesterol oxidase oxidation of 3¦Â,7¦Á-cholest-5-ene-3,7-diol
David L. Alexander, Jed F. Fisher
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
23 .     stigmasta-4,22-dien-3-one
    ÏàËÆ¶È:65.5%
Chinese Traditional and Herbal Drugs          2005          36          328-332
Chemical constituents of Schefflera venulosa and their antitumor activities
LIU Rui; GU Qian-qun; CUI Cheng-bin; HAN Bing; CAI Bing; LIU Hong-bing
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
24 .     compound 10
    ÏàËÆ¶È:65.5%
Tetrahedron          1993          49          4447-4462
Autooxidation of simvastatin
George B. Smith, Lisa DiMichele, Lawrence F. Colwell Jr., George C. Dezeny, Alan W. Douglas, Robert A. Reamer, Thomas R. Verhoeven
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
25 .     [26-2H3](22R,23R,24S)-22,23-dihydroxy-24-methylcholest-4-en-3-one
    ÏàËÆ¶È:65.5%
Natural Product Communications          2013          8          771-774
Synthesis and Mass Spectral Fragmentation Patterns of Brassinolide Early Biosynthetic Precursors Labeled at C-26
Vladimir A. Khripach, Danuše Tarkowsk¨¢, Vladimir N. Zhabinskii, Olga V. Gulyakevich, Yurii V. Ermolovich, Pavel Drašar and Miroslav Strnad
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
26 .     (22E,24S)-Stigmasta-4,22,25-trien-3-one
C29H44O     ÏàËÆ¶È:65.5%
Natural Product Communications          2008          3          1787-1792
Secondary Metabolites from Clerodendrum chinense
Tanya H. Layne, William F. Reynolds, Stewart McLean and Winston F. Tinto
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
27 .     Paraminabeolide D
C28H40O4     ÏàËÆ¶È:65.5%
Journal of Natural Products          2011          74          1132-1141
Paraminabeolides A−F, Cytotoxic and Anti-inflammatory Marine Withanolides from the Soft Coral Paraminabea acronocephala
Chih-Hua Chao, Kuei-Ju Chou, Zhi-Hong Wen, Guey-Horng Wang, Yang-Chang Wu, Chang-Feng Dai, and Jyh-Horng Sheu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
28 .     Paraminabeolide D
C28H40O4     ÏàËÆ¶È:65.5%
Journal of Natural Products          2011          74          1132-1141
Paraminabeolides A−F, Cytotoxic and Anti-inflammatory Marine Withanolides from the Soft Coral Paraminabea acronocephala
Chih-Hua Chao, Kuei-Ju Chou, Zhi-Hong Wen, Guey-Horng Wang, Yang-Chang Wu, Chang-Feng Dai, and Jyh-Horng Sheu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
29 .     stigmasta-4,22-dien-3-one
C29H46O     ÏàËÆ¶È:65.5%
Journal of Tropical and Subtropical Botany          2014          22          413-418
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