²é¿´: 1051  |  »Ø¸´: 3

yjl2007

½ð³æ (ÕýʽдÊÖ)

[ÇóÖú] ÇóÖúÒ»»¯ºÏÎï΢Æ×Êý¾Ý½á¹¹

»¯ºÏÎïÊý¾Ý£º12.0, 17.3, 18.9, 19.0, 19.8, 21.2, 23.1, 26.1, 26.3, 28.6, 29.2, 31.2, 34.0, 36.1, 36.4, 38.3, 38.7, 41.8, 43.1, 45.4, 45.8, 49.9, 50.0, 54.7, 70.5, 126.1, 165.0, 202.3
ÈܼÁ£ºCDCl3
лл
»Ø¸´´ËÂ¥

» ²ÂÄãϲ»¶

» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:

ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

Æ·Æ·

ľ³æ (СÓÐÃûÆø)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
xiaoxiao270: ½ð±Ò+2, 3Q 2012-06-12 18:11:56
yjl2007: ½ð±Ò+10 2012-06-12 20:46:49
1 .     7-ketositosterol
C29H48O2     ÏàËÆ¶È:100%
Steroids          2005          70          886-895
Gram-scale chromatographic purification of ¦Â-sitosterol: Synthesis and characterization of ¦Â-sitosterol oxides
Xin Zhang, Philippe Geoffroy, Michel Miesch, Diane Julien-David, Francis Raul, Dalal Aoud¨¦-Werner, Eric Marchioni
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




2 .     3¦Â-hydroxystigmast-5-en-7-one
    ÏàËÆ¶È:96.5%
China Journal of Chinese Materia Medica          2009          34          1809-1811
Steroids from Monascus purpureus metabolite
SHANG Xiaoya, WANG Ruolan, YI N Suqin, LI Jinjie, JIN Zonglian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




3 .     3¦Â-hydroxy-stigmast-5-en-7-one
    ÏàËÆ¶È:96.5%
China Journal of Chinese Materia Medica          2006          31          131-133
Chemical constituents from roots of Ficus hirta
LI Chun, BU Pengbin, YUE Dangkun, SUN Youfu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




4 .     3¦Â-hydroxystigmast-5-en-7-one
C29H48O2     ÏàËÆ¶È:96.5%
China Journal of Chinese Materia Medica          2001          26          762-764
Studies on the Chemical Constitutents of Asarum longerhizomatosum C. F. Liang et C. S. Yang
ZHANG Shuxing, CAI Shaoqing, ZHAO Yuying
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




5 .     7-Keto-¦Â-sitosterol
    ÏàËÆ¶È:96.5%
Natural Product Sciences          2007          13          332-336
Norsesquiterpene and Steroid Constituents of Humulus japonicus
Yu, Byung-Chul; Yang, Min-Cheol; Lee, Kyu-Ha; Kim, Ki-Hyun; Lee, Kang-Ro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




6 .     7-Oxo-¦Â-sitosterol
    ÏàËÆ¶È:96.5%
Korean Journal of Pharmacognosy          2008          39(3)          186-193
Phytochemical Studies on Astragalus Root (3);Triterpenoids and Sterols
Jung, Hye-Sil; Lee, Eun-Ju; Lee, Je-Hyun; Kim, Ju-Sun; Kang, Sam-Sik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




7 .     stigmasta-5-en-3¦Â-ol-7-one
    ÏàËÆ¶È:96.5%
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   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




8 .     stigmast-5-en-7-oxo-3¦Â-ol
    ÏàËÆ¶È:96.5%
Chinese Traditional and Herbal Drugs          2010          41          195-197
ºÚÀÏ»¢¸ù»¯Ñ§³É·ÖµÄÑо¿
Íõéª;ÀîÕ¼ÁÖ;»ª»áÃ÷
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




9 .     3¦Â-hydroxy-stigmast-5-en-7-one
    ÏàËÆ¶È:96.5%
Chinese Traditional and Herbal Drugs          2007          38          14-17
Chemical constituents of whole herb of Dicliptera chinensis
GAO Yu-tao; YANG Xiu-wei; AI Tie-min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




10 .     stigmast-5-ene-3¦Â-ol-7-one
    ÏàËÆ¶È:96.5%
Pharmazie          2002          57          209-211
Two new steroids from Adenophora stenanthina subsp. xifengensis
Zhen-Fu Hou - Yong-Qiang Tu - Yu Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




11 .     3¦Â-hydroxystigmast-5-en-7-one
    ÏàËÆ¶È:96.5%
Archives of Pharmacal Research          2005          28          1147-1151
Antimicrobial constituents from fruits of Ailanthus altissima SWINGLE
Chun-Chao Zhao, Jian-Hua Shao, Xian Li, Jing Xu and Peng Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




12 .     7-oxo-3¦Â-stigmasterol
    ÏàËÆ¶È:96.5%
Chinese Pharmaceutical Journal          2008          43          897-899
Study on Steroids from the Stem of Croton caudatus Geisel.var.tomentosus Hook
WANG Yuan, ZOU Zhong-mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




13 .     3-hydroxy-stigmast-5-en-7-one
    ÏàËÆ¶È:96.5%
Chinese Journal of Medicinal Chemistry          2007          17          170-172
Chemical constituents of Tribulus terrestris L.
LÜ A-li, ZHANG Nan, MA Hong-yu, WANG Ding, DANG Quan, PEI Yue-hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




14 .     3¦Â-hydroxy-Stigmasta-5-en-7-one
C29H48O2     ÏàËÆ¶È:96.5%
Acta Scientiarum Naturalium Universitatis Sunyatseni          2001          40(2)          54-57
Steroids from the Marine Sponge Stelletta tenuis Lindgren
YAN Su-jun, SU Jing-yu, ZHANG Guang-wen, WANG Yan-hong, LI Hong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




15 .     7-Oxo-¦Â-sitosterol
C29H48O2     ÏàËÆ¶È:96.4%
Journal of Natural Products          2000          63          72-78
Isolation and Structures of Schleicherastatins 1-7 and Schleicheols 1 and 2 from the Teak Forest Medicinal Tree Schleichera oleosa1
George R. Pettit,Atsushi Numata, Gordon M. Cragg, Delbert L. Herald, Tamie Takada,Chika Iwamoto,Roland Riesen, Jean M. Schmidt, Dennis L. Doubek, and Animesh Goswami
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




16 .     7-oxo-¦Â-sitosterol
    ÏàËÆ¶È:96.4%
Natural Product Research and Development          2009          21          593-599
Chemical Constituents of Osmanthus yunnanensis
MA Xiao-li;LIN Wen-bing; ZHANG Guo-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




17 .     compound 9
    ÏàËÆ¶È:93.1%
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

--------------------------------------------------------------------------------




18 .     7-Oxositosterol (3¦Â-hydroxystigmast-5-en-7-one)
    ÏàËÆ¶È:93.1%
Pharmazie          2004          59          885-888
Terpenoids and steroids from Lappula anocarpa
Yuan-Peng Jin, and Yan-Ping Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




19 .     stigmast-5-en-3¦Â-ol-7-one
    ÏàËÆ¶È:93.1%
Pharmazie          2005          60          464-467
Steroids from Saussurea ussuriensis
Jia-Tao Feng and Yan-Ping Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




20 .     ¶¹çÞ-5-Ï©-3¦Â-´¼-7-ͪ
    ÏàËÆ¶È:93.1%
Journal of Shenyang Pharmaceutical University          2005          22          422-424
Studies on the chemical constituents of Malt
LING Jun-hong, WANG Jin-hui, WANG Nan, LI Wen, SHA Yi, LI Xian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




21 .     3¦Â-hydroxystigmast-5-en-7-one
    ÏàËÆ¶È:93.1%
Journal of the Chinese Chemical Society          2004          51          437-441
New Prenylated Flavones from the Roots of Ficus beecheyana
Ching-kuo Lee*, Chung-kuang Lu, Yuen-Hsiung Kuo,Jian-Zhi Chen and Guang-Zhong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




22 .     7¦Â-hydroxystigmast-4-en-3-one
C29H48O2     ÏàËÆ¶È:86.2%
Natural Product Research          2006          20          327-334
Potential cancer chemopreventive agents from Arbutus unedo
Esperanza J. Carcache-Blanco; Muriel Cuendet; Eun Jung Park; Bao-Ning Su; J. Fausto Rivero-Cruz; Norman R. Farnsworth; John M. Pezzuto; A. Douglas Kinghorn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




23 .     7-oxositosterol
    ÏàËÆ¶È:86.2%
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

--------------------------------------------------------------------------------




24 .     gelliusterol C
C27H40O2     ÏàËÆ¶È:85.7%
Journal of Natural Products          2001          64          741-744
Gelliusterols A-D, New Acetylenic Sterols from a Sponge, Gellius Species
Winklet A. Gallimore, Michelle Kelly, and Paul J. Scheuer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




25 .     24-methylene-27-methylcholest-5-en-3¦Â-ol-7-one
    ÏàËÆ¶È:82.7%
Journal of Natural Products          2007          70          1114-1117
Stellettins L and M, Cytotoxic Isomalabaricane-Type Triterpenes, and Sterols from the Marine Sponge Stelletta tenuis
Hou-wen Lin,Zeng-lei Wang,Jiu-hong Wu, Ning Shi, Hong-jun Zhang,Wan-sheng Chen,Susan L. Morris-Natschke, and An-Shen Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




26 .     7-oxopetrosterol
C29H46O2     ÏàËÆ¶È:82.7%
Journal of Natural Products          2000          63          1540-1542
Two New 26,27-Cyclosterols from the Marine Sponge Strongylophora corticata
Akemi Umeyama, Seiichi Ito, Ayuko Yoshigaki, and Shigenobu Arihara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




27 .     (24R)-3¦Â -chlorostigmast-5-en-7-one
    ÏàËÆ¶È:82.7%
Chemistry of Natural Compounds          2000          36          595-598
13C NMR SPECTRA OF FUNCTIONALLY SUBSTITUTED 3 ¦Â-CHLORODERIVATIVES OF CHOLESTEROL AND ¦Â -SITOSTEROL
N. V. Kovganko, Zh. N. Kashkan, and E. V. Borisov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




28 .     3¦Â-Acetoxysitost-5-en-7-one
C31H50O3     ÏàËÆ¶È:82.7%
Steroids          2005          70          886-895
Gram-scale chromatographic purification of ¦Â-sitosterol: Synthesis and characterization of ¦Â-sitosterol oxides
Xin Zhang, Philippe Geoffroy, Michel Miesch, Diane Julien-David, Francis Raul, Dalal Aoud¨¦-Werner, Eric Marchioni
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




29 .     decortinone
C29H46O2     ÏàËÆ¶È:82.7%
Phytochemistry          1993          33          1189-1192
Sterols from marine green alga Codium decorticatum
Viqar Uddin Ahmad, Rahman Aliya, Shaista Perveen, Mustafa Shameel
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




30 .     3¦Â-hydroxycholesta-5-en-7-one
    ÏàËÆ¶È:82.1%
Natural Product Research          2010          24          1518-1522
Isolation and identification of two steroid compounds from Oviductus Ranae
Yongsheng Wang; Lili Wang; Yan Hu; Lantong Zhang; Zhihan Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2012-06-12 15:18:13
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

1301050218

Ìú¸Ëľ³æ (ÖøÃûдÊÖ)

¹¤±ø

ÒýÓûØÌû:
2Â¥: Originally posted by Æ·Æ· at 2012-06-12 15:18:13
1 .     7-ketositosterol
C29H48O2     ÏàËÆ¶È:100%
Steroids          2005          70          886-895
Gram-scale chromatographic purification of ¦Â-sitosterol: Synthesis and characterization of ...

Â¥ÉÏÊÇÔÚÄǸöÊý¾Ý¿â±È¶ÔµÄ°¡£¿
ллָ½Ì°¡
¿ªÐÄÃæ¶ÔÿһÌ죬ÿÌì¶¼»á³äÂúÑô¹Ø
3Â¥2012-06-12 17:33:18
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

Æ·Æ·

ľ³æ (СÓÐÃûÆø)

ÒýÓûØÌû:
3Â¥: Originally posted by 1301050218 at 2012-06-12 17:33:18
Â¥ÉÏÊÇÔÚÄǸöÊý¾Ý¿â±È¶ÔµÄ°¡£¿
ллָ½Ì°¡...

΢Æ×Êý¾Ý-ºË´Å¹²Õñ̼Æ×Êý¾Ý¿â£¨13C-NMR¿â£©£¬ÄãÎʵÄÊÇÕâ¸öÒâ˼°É
4Â¥2012-06-13 09:26:41
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ yjl2007 µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[ÂÛÎÄͶ¸å] ÉêÇë»Ø¸åÑÓÆÚÒ»¸öÔ£¬±à¼­Í¬ÒâÁË¡£µ«ÏµÍ³ÉϵÄʱ¼äû±ä£¬¸ø±à¼­ÓÖдÓʼþÁË£¬Ã»»Ø¸´ 10+3 wangf9518 2026-03-17 4/200 2026-03-19 23:55 by babero
[¿¼ÑÐ] Ò»Ö¾Ô¸Öйúº£Ñó´óѧ£¬ÉúÎïѧ£¬301·Ö£¬Çóµ÷¼Á +5 1ËïÎò¿Õ 2026-03-17 6/300 2026-03-19 23:46 by zcl123
[¿¼²©] ¶«»ªÀí¹¤´óѧ»¯²Äרҵ26½ì˶ʿ²©Ê¿ÉêÇë +8 zlingli 2026-03-13 8/400 2026-03-19 16:32 by ÇáËɲ»ÉÙËæ
[¿¼ÑÐ] 271²ÄÁϹ¤³ÌÇóµ÷¼Á +6 .6lL 2026-03-18 6/300 2026-03-19 15:41 by haoshis
[¿¼ÑÐ] 085601²ÄÁϹ¤³Ìר˶Çóµ÷¼Á +10 Ľº®mio 2026-03-16 10/500 2026-03-19 15:26 by ¶¡¶¡*
[¿¼ÑÐ] ±¾ÈË¿¼085602 »¯Ñ§¹¤³Ì ר˶ +17 ²»ÖªµÀ½Ðʲô£¡ 2026-03-15 19/950 2026-03-19 15:06 by ¾¡Ë´Ò¢1
[¿¼ÑÐ] Çóµ÷¼Á£¬Ò»Ö¾Ô¸:ÄϾ©º½¿Õº½Ìì´óѧ´óѧ £¬080500²ÄÁÏ¿ÆÑ§Ó빤³Ìѧ˶£¬×Ü·Ö289·Ö +3 @taotao 2026-03-19 3/150 2026-03-19 14:07 by peike
[¿¼ÑÐ] Ò»Ö¾Ô¸Ìì´ó²ÄÁÏÓ뻯¹¤£¨085600£©×Ü·Ö338 +5 ²Ì´óÃÀÅ® 2026-03-13 5/250 2026-03-19 10:44 by ÊÇСÁõѽ¡«
[¿¼ÑÐ] Ò»Ö¾Ô¸985£¬±¾¿Æ211£¬0817»¯Ñ§¹¤³ÌÓë¼¼Êõ319Çóµ÷¼Á +10 Liwangman 2026-03-15 10/500 2026-03-19 10:25 by Î޼ʵIJÝÔ­
[¿¼ÑÐ] 331Çóµ÷¼Á£¨0703Óлú»¯Ñ§ +7 ZY-05 2026-03-13 8/400 2026-03-18 14:13 by 007_lilei
[¿¼ÑÐ] 0854£¬¼ÆËã»úÀàÕÐÊÕµ÷¼Á +3 ºúÀ±ÌÀ·ÅÌÇ 2026-03-15 6/300 2026-03-18 12:09 by Éϰ¶Éϰ¶¡­¡­..
[¿¼ÑÐ] 334Çóµ÷¼Á +3 Ö¾´æ¸ßÔ¶ÒâÔÚ»úÐ 2026-03-16 3/150 2026-03-18 08:34 by lm4875102
[¿¼ÑÐ] 326Çóµ÷¼Á +5 Éϰ¶µÄСÆÏ 2026-03-15 6/300 2026-03-17 17:26 by ruiyingmiao
[¿¼²©] 26É격 +4 °Ë6°Ë68 2026-03-16 4/200 2026-03-17 13:00 by ÇáËɲ»ÉÙËæ
[¿¼ÑÐ] ²ÄÁϹ¤³Ìר˶274Ò»Ö¾Ô¸211Çóµ÷¼Á +6 Ñ¦ÔÆÅô 2026-03-15 6/300 2026-03-17 11:05 by ѧԱh26Tkc
[¿¼ÑÐ] 275Çóµ÷¼Á +4 Ì«Ñô»¨ÌìÌ쿪ÐÄ 2026-03-16 4/200 2026-03-17 10:53 by ¹¦·ò·è¿ñ
[¿¼ÑÐ] 304Çóµ÷¼Á +4 ahbd 2026-03-14 4/200 2026-03-16 16:48 by ÎҵĴ¬Îҵĺ£
[¿¼ÑÐ] 0703 ÎïÀí»¯Ñ§µ÷¼Á +3 ÎÒ¿ÉÒÔÉϰ¶µÄ¶Ô 2026-03-13 5/250 2026-03-16 10:50 by ÎÒ¿ÉÒÔÉϰ¶µÄ¶ÔÂ
[¿¼ÑÐ] ÇóÀÏʦÊÕÁôµ÷¼Á +4 jiang½ª66 2026-03-14 5/250 2026-03-15 20:11 by Winj1e
[¿¼ÑÐ] 080500£¬²ÄÁÏѧ˶302·ÖÇóµ÷¼ÁѧУ +4 ³õʶ¿ÉÀÖ 2026-03-14 5/250 2026-03-14 21:08 by peike
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û