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1 .     stigmast-4-ene-3,6-dione
    ÏàËÆ¶È:100%
Journal of Natural Products          2002          65          1857-1862
Antimicrobial Activities of Naphthazarins from Arnebia euchroma
Chien-Chang Shen,Wan-Jr Syu,Shyh-Yuan Li, Chia-Hung Lin, Gum-Hee Lee, and Chang-Ming Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     (24R)-24-ethylcholest-4-en-3,6-dione
    ÏàËÆ¶È:100%
Chemistry of Natural Compounds          2001          37          351-355
13C NMR SPECTRA OF 6-HYDROXIMINOSTEROIDS OF THE STIGMASTANE SERIES
N. V. Kovganko and Yu. G. Chernov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     compound 8
    ÏàËÆ¶È:100%
Chemistry of Natural Compounds          1999          35          646-649
13C NMR SPECTRA OF II-SITOSTEROL DERIVATIVES WITH OXIDIZED RINGS A AND B
N. V. Kovganko, Zh. N. Kashkan,E. V. Borisov, and E. V. Batura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     compound
    ÏàËÆ¶È:100%
Biochemical Systematics and Ecology          2000          28          911-913
Stigmast-4-ene-3,6-dione an unusual phytotoxic sterone from the roots of Echium vulgare L.
Fernando Pardo, Fernando Perich, Ren¨¦ Torres, Franco Delle Monache
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     stigmasta-4-ene-3,6-dione
    ÏàËÆ¶È:100%
China Journal of Chinese Materia Medica          2005          30          124-126
Studies on the chemical constituents in herb of Ranunculus sceleratus
GAO Xiaozhong, ZHOU Changxin, ZHANG Shuili, YAO Wei, ZHAO YU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     ¶¹çÞ-4-Ï©-3,6-¶þͪ
    ÏàËÆ¶È:100%
China Journal of Chinese Materia Medica          2003          28          278-279
¼Ô¹ûÞ§¹áÖÚ»¯Ñ§³É·ÖµÄÑо¿
Ñî á°, ÕÔÓñÓ¢, ÍÀßÏßÏ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     stigmastan-4-en-3,6-dione
    ÏàËÆ¶È:100%
Journal of Natural Products          1990          Vol 53          1430
Stigmasterols from Typha latifolia
Marina Della Greca, Pietro Monaco, Lucio Previtera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound 3
    ÏàËÆ¶È:100%
Acta Pharmaceutica Sinica          1999          Vol 34          682-685
STUDIES ON THE CHEMICAL CONSTITUENTS FROM DESMOS DUMOSUS (ROXB.) SAFF
Wu Jiuhong (Wu JH); Liao Shixuan (Liao SX); Mao Shilong (Mao SL); Yi Yanghua (Yi YH); Takeya K; Su Zhongwu (Su ZW) and Lan Chuanqing (Lan CQ)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (24R)-stigmast-4-ene-3,6-dione
C29H48O2     ÏàËÆ¶È:100%
Phytochemistry          1993          34          523-527
Steroidal constituents from mature wheat straw
Elvira M.M. Gaspar, Higuinaldo J.C. das Neves
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     22-dihydro-stigmast-4-en-3,6-dione
    ÏàËÆ¶È:100%
Korean Journal of Pharmacognosy          1996          27(1)          75-79
Phytochemical Constituents from Aconitum pseudolaeve Var. erectum
Kim, Dae-Keun; Kwak, Jong-Hwan; Song, Ki-Won; Kwon, Hack-Cheol; Zee, Ok-Pyo; Lee, Kang-Ro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     Stigmast-4-ene-3,6-dione
    ÏàËÆ¶È:100%
Magnetic Resonance in Chemistry          2004          42          355-359
Complete 1H and 13C NMR assignments of two phytosterols from roots of Piper nigrum
Kun Wei, Wei Li, Kazuo Koike, Yuping Pei, Yingjie Chen and Tamotsu Nikaido
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     ¶¹çÞ-4-Ï©-3,6-¶þͪ
C29H48O2     ÏàËÆ¶È:100%
Chinese Traditional and Herbal Drugs          2008          39          671-672
ºúÍÇ×ÓÒ¶»¯Ñ§³É·ÖÑо¿
¸¶Òå³É;ÍõÏþ¾²;¼ÖÏ×»Û;Àî¿¡æ¼
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     ¶¹çÞ-4-Ï©-3,6-¶þͪ
    ÏàËÆ¶È:100%
Chinese Traditional and Herbal Drugs          2006          37          1780-1781
Á¬Ç®²ÝÖÐÈýÝÆÀ໯ѧ³É·Ö
ÕÅǰ¾ü;ÑîСÉú;Ö캣Ñà;Ò¦ÔÆ;ºÂС½­;Ëα¦°²
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     stigmast-4-en-3,6-dione
    ÏàËÆ¶È:100%
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   Ì¼Æ×Ä£Äâͼ
15 .     stigmast-4-ene-3,6-dione
    ÏàËÆ¶È:100%
Chinese Pharmaceutical Journal          2009          44          576-580
Studies on Antitumor Steroids and Flavonoids from Tamarix chinensis Lour.
WANG Bin, REN Shu-wen, LI Guo-qiang, GUAN Hua-shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     stigmast-4-ene-3,6-dione
    ÏàËÆ¶È:100%
Chinese Journal of Medicinal Chemistry          2003          13          211-214
Studies on the chemical constituents of Fructus Ailanthi altissimae
ZHAO Chun-chao, WANG Jin-hui, LI Wen, SHA Yi, LI Xian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     stigmast-4-en-3,6-dione
    ÏàËÆ¶È:100%
Journal of Shenyang Pharmaceutical University          2009          26          874-877
Isolation and identification of steroids from the leaves of theMagnolia sieboldii K. Koch
WANG Ru-ping, WU Di, GAO Hui-yuan, SUN Bo-hang, HUANG Jian, WU Li-jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     stigmast-4-en-3,6-dione
    ÏàËÆ¶È:100%
Journal of Shenyang Pharmaceutical University          2009          26          357-360
Isolation and identification of chemical constituents from testa of Castanea mollissima Blume
LU Chuan, WU Zhao-hua, GAO Hui-yuan, SUN Bo-hang, HUANG Jian, WU Li-jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     stigmast-4-ene-3,6-dione
    ÏàËÆ¶È:100%
Natural Product Research and Development          2009          21          960-962
Study on the Chemical constituents of Callipteris esculenta(Athyriaceae)
WANG Zi-juan;ZHAO Qin-shi; PENG Li-yan; CHENG Xiao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     stigma-4-en-3,6-dione
C29H46O2     ÏàËÆ¶È:100%
Natural Product Research and Development          2004          16          210-212
STUDY ON THE CHEMICAL CONSTITUENTS OF OSTODES PANICULATA
QI Shu-hua; GUO Jian-wei; WU Da-gang; LUO Xiao-dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     enedione
    ÏàËÆ¶È:100%
Natural Product Research and Development          2000          12(5)          14-16
STEROID CONSTITUENTS FROM EUONYMUS MUPINENSIS
Mao Shilong; Sang Shengmin; Lao Aina and Chen Zhongliang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     stigma-4-en-3,6-dione
    ÏàËÆ¶È:100%
Zeitschrift f¨¹r Naturforschung C          2003          58          521-526
Cytotoxic Benzophenanthridine and Benzylisoquinoline Alkaloids from Argemone mexicana
Y.-C. Chang, F.-R. Chang, A. T. Khalil, P.-W. Hsieh, and Y.-C. Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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