²é¿´: 301  |  »Ø¸´: 1

Ò©Îﻯѧli

гæ (СÓÐÃûÆø)

[ÇóÖú] лл ÒÑÓÐ1È˲ÎÓë

CÆ×Êý¾Ý  12.04,12.17,12.23,12.45,18.96,19.17,19.21,19.59,20.01,21.26,21.41,23.23,24.49,24.55,25.61,26.22,28.44,29.12,29.31,31.77,32.08,33.89,34.11,36.34,36.69,37.43,39.86,39.95,40.71,42.39,42.42,42.50,46.00,50.30,50.92,51.43,56.12,56.23,56.94,57.04,71.95,121.90,129.44,138.52,140.94,
»Ø¸´´ËÂ¥
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

seuseasoar

ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ò©Îﻯѧli: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2015-04-23 15:16:34
1 .     stigmasteryl-3¦Â-arachidate
C49H86O2     ÏàËÆ¶È:80%
Asian Journal of Chemistry          2014          26          3018-3020
Stigmasteryl Arachidate Constituent from the Straw of Oryza sativa
ILL-MIN CHUNG, JAE-YEON YOON, SEUNG-HYUN KIM and ATEEQUE AHMAD
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     compound A
    ÏàËÆ¶È:78.2%
Yakugaku Zasshi          1983          103          43-48
The Principles of Tetragonia tetragonoides Having an Antiulcerogenic Activity. I. Isolation and Identification of Sterylglucoside Mixture (Compound A)
EMI OKUYAMA, MIKIO YAMAZAKI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     aglycone-II
    ÏàËÆ¶È:73.3%
Yakugaku Zasshi          1983          103          43-48
The Principles of Tetragonia tetragonoides Having an Antiulcerogenic Activity. I. Isolation and Identification of Sterylglucoside Mixture (Compound A)
EMI OKUYAMA, MIKIO YAMAZAKI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     stigmast-5-en-3¦Â-ol-3-O-¦Â-D-(2'-n-triacontanoyl) glucopyranoside
C65H118O7     ÏàËÆ¶È:71.1%
Journal of Asian Natural Products Research          2012          14          301-307
New steroidal glycoside ester and aliphatic acid from the fruits of Lycium chinense
Woo-Suk Jung,Ill-Min Chung,Mohd Ali and Ateeque Ahmad
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     ¦Â-sitosterol-3-O-¦Â-D-glucoside-6'-O-eicosanate
    ÏàËÆ¶È:71.1%
Chinese Traditional and Herbal Drugs          2002          33          6-8
New steroid glycoside derivatives from Stelmatocrypton khasianum
New steroid glycoside derivatives from Stelmatocrypton khasianum
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     (6R,E)-6-((3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-3-(palmitoyloxy)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-3-ethyl-2-methylhept-4-enoic acid
C45H78O4     ÏàËÆ¶È:71.1%
Life Sciences          2013          92          202-210
Antiulcer and antioxidant activities of a new steroid from Morus alba
Aftab Ahmad, Gaurav Gupta, Muhammad Afzal, Imran Kazmi, Firoz Anwar
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     lanoscopariol
C46H80O3     ÏàËÆ¶È:69.5%
Journal of Natural Products          1996          59          181-184
New 9¦Â-Lanostane-Type Triterpenic and 13, 14-seco-Steroidal Esters from the Roots of Artemisia scoparia
Surendra Kumar Sharma and Mohammad Ali
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     artemisterol B
C44H72O4     ÏàËÆ¶È:68.8%
Journal of Natural Products          1996          59          181-184
New 9¦Â-Lanostane-Type Triterpenic and 13, 14-seco-Steroidal Esters from the Roots of Artemisia scoparia
Surendra Kumar Sharma and Mohammad Ali
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     ¦Â-sitosterol ¦Â-D-glucopyranoside tetraacetate
    ÏàËÆ¶È:68.8%
Planta Medica          1993          59          369-372
A New Oleanolic Acid Derivative from Securinega tinctoria
LuisM. Carvalho and J. Seita
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     stigmast-5-en-3-O-¦Â-D-glucopyranoside tetraacetate
C43H68O10     ÏàËÆ¶È:68.8%
Natural Product Sciences          1999          5          124-126
Sterols and Sterol Glycosides from Cuscuta Reflexa
Anis, E.; Mustafa, G.; Ahmed, S.; Nisarullah, Nisarullah; Malik, A.; Afza, N.; Badar, Y.
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     3-O-[6'-O-stearyl-¦Â-D-glucosyl]-clerosterol
    ÏàËÆ¶È:68.8%
Phytochemistry          1994          36          167-170
Acylglucosylsterols from two Aegiphila species
Suzana G. Leitão, Maria Auxiliadora C. Kaplan, Franco Delle Monache
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     sitosteryl-¦Â-D-glucopyranoside tetraacetate
    ÏàËÆ¶È:68.8%
Phytochemistry          1991          30          3383-3387
Steroids and triterpenoids from Rosa laevigata
Jim-Min Fang, Kuang-Chaun Wang, Yu-Shia Cheng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     compound 3a
    ÏàËÆ¶È:68.8%
Phytochemistry          1990          29          2351-2355
Sterol glucosides from Prunella vulgaris
Hisashi Kojima,Noriko Sato,Akiko Hatano,Haruo Ogura
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
ÄáºÕ
2Â¥2015-04-22 22:12:55
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ Ò©Îﻯѧli µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[ÕÒ¹¤×÷] ÊÛSCIÒ»ÇøT0PÎÄÕ£¬ÎÒ:8.O.55.1.O.54,¿ÆÄ¿ÆëÈ«,¿É+¼± +4 6F5UbRU2I5hL 2026-09-14 5/250 2026-09-16 05:11 by LH5NkK5Ud4bh
[¿¼ÑÐ] ÊÛSCIÎÄÕ£¬ÎÒ:8O5.5.1.O.54,¿ÆÄ¿ÆëÈ«,¿É+¼± +5 6F5UbRU2I5hL 2026-09-14 5/250 2026-09-16 05:03 by LH5NkK5Ud4bh
[ÕÒ¹¤×÷] ÊÛSCIÒ»ÇøT0PÎÄÕ£¬ÎÒ:8.O.55.1.O54,¿ÆÄ¿È«,¿ÉÙ¤¼± +4 s3fFTmArrBt6 2026-09-13 4/200 2026-09-16 03:38 by DgNGHc3h5tPl
[¹«Åɳö¹ú] ÊÛSCIÎÄÕ£¬ÎÒ:8O.5.5.1O.54,¿ÆÄ¿È«,¿ÉÊ®¼± +4 s3fFTmArrBt6 2026-09-13 6/300 2026-09-16 03:35 by DgNGHc3h5tPl
[ÕÒ¹¤×÷] ÊÛSCIÒ»ÇøT0PÎÄÕ£¬ÎÒ:8.O.55.1.O.54,¿ÆÄ¿ÆëÈ«,¿É+¼± +4 LwdutQ8HoqWP 2026-09-13 4/200 2026-09-16 03:23 by DgNGHc3h5tPl
[¿¼²©] ÊÛSCIÒ»ÇøT0PÎÄÕ£¬ÎÒ:8.O55.1.O.54,¿ÆÄ¿È«,¿ÉÊ®¼± +3 Aj1rhIDL5ixY 2026-09-14 3/150 2026-09-15 20:47 by zNcEhTcH7ihq
[¿¼²©] ÉϺ£¹¤³Ì¼¼Êõ´óѧ¼¤¹âÖÇÄÜÖÆÔì¿ÎÌâ×éÕÐÊÕ²©Ê¿Ñо¿Éú +6 Á½ÈýËêss 2026-09-14 6/300 2026-09-15 20:17 by Ö»³ÔÈâÆÏÌÑ
[¿¼ÑÐ] ÊÛSCIÒ»ÇøT0PÎÄÕ£¬ÎÒ:8.O55.1.O.54,¿ÆÄ¿È«,¿ÉÊ®¼± +3 Aj1rhIDL5ixY 2026-09-14 3/150 2026-09-15 20:14 by zNcEhTcH7ihq
[˶²©¼ÒÔ°] ÊÛSCIÒ»ÇøT0PÎÄÕ£¬ÎÒ:8.O55.1.O.54,¿ÆÄ¿È«,¿ÉÊ®¼± +5 s3fFTmArrBt6 2026-09-14 5/250 2026-09-15 16:35 by CgyNCDVNhGVg
[¿¼²©] ÊÛSCIÒ»ÇøÎÄÕ£¬ÎÒ:8O5.5.1.O5.4,¿ÆÄ¿È«,¿ÉÙ¤¼± +7 s3fFTmArrBt6 2026-09-14 7/350 2026-09-15 16:23 by CgyNCDVNhGVg
[˶²©¼ÒÔ°] ÊÛSCI-T0PÎÄÕ£¬ÎÒ:8O.5.5.1.O.54,¿ÆÄ¿ÆëÈ«,¿É+¼± +4 3n8v2C8RimXI 2026-09-13 4/200 2026-09-15 14:34 by VMDqgnlKimtZ
[²©ºóÖ®¼Ò] ÊÛSCIÒ»ÇøT0PÎÄÕ£¬ÎÒ:8O.55.1.O.54,¿ÆÄ¿È«,¿ÉÙ¤¼± +6 QUjhNVAcOSff 2026-09-13 7/350 2026-09-15 14:13 by VMDqgnlKimtZ
[¹«Åɳö¹ú] ÊÛSCIÎÄÕ£¬ÎÒ:8O5.5.1.O.54,¿ÆÄ¿ÆëÈ«,¿É+¼± +3 6F5UbRU2I5hL 2026-09-14 3/150 2026-09-15 08:58 by C79jjtjAKjEn
[½Ìʦ֮¼Ò] ÊÛSCIÒ»ÇøÎÄÕ£¬ÎÒ:8.O.551.O.5.4,¿ÆÄ¿È«,¿ÉÙ¤¼± +4 s3fFTmArrBt6 2026-09-13 4/200 2026-09-15 07:02 by 5BDX0d0WFp7t
[½Ìʦ֮¼Ò] ÊÛSCIÒ»ÇøT0PÎÄÕ£¬ÎÒ:8.O.55.1.O.54,¿ÆÄ¿ÆëÈ«,¿É+¼± +6 3n8v2C8RimXI 2026-09-13 6/300 2026-09-15 05:38 by 5BDX0d0WFp7t
[¹«Åɳö¹ú] ÊÛSCI-T0PÎÄÕ£¬ÎÒ:8O.5.5.1.O.54,¿ÆÄ¿ÆëÈ«,¿É+¼± +3 LwdutQ8HoqWP 2026-09-13 6/300 2026-09-14 22:37 by vZfe6xYu34yj
[²©ºóÖ®¼Ò] ÊÛSCIÒ»ÇøT0PÎÄÕ£¬ÎÒ:8.O.55.1.O.5.4,¿ÆÄ¿È«,¿É+¼± +4 QUjhNVAcOSff 2026-09-13 4/200 2026-09-14 21:37 by vZfe6xYu34yj
[»ù½ðÉêÇë] Çó½Ì¸÷λ´óÉñ£º2026½ÌÓý²¿ÈËÎÄÉç¿ÆÇàÄê»ù½ðÏîÄ¿ºÎʱ¹«Ê¾Ñ½£¿ +5 ÔÆÑçɽÈË 2026-09-10 7/350 2026-09-14 12:11 by ecnu2013
[¿¼²©] Î÷±±¹¤Òµ´óѧ²ÄÁÏѧԺµç»¯Ñ§´«¸ÐÓë´ß»¯¿ÎÌâ×éÕÐÊÕ2027ÄêÍÆÃâÑо¿Éú¡¢²©Ê¿Éú¡¢²©Ê¿ºó +3 Âí·½Ô° 2026-09-10 4/200 2026-09-14 09:29 by ChemÕÅzz
[¿¼²©] 27Çï¼¾²ÄÁϲ©Ê¿ÉêÇëÇóÖú 10+3 Cahal1 2026-09-11 4/200 2026-09-14 08:50 by ±±¾©À³Òð±à¼­
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û