| ²é¿´: 440 | »Ø¸´: 1 | |||
Ò©»¯Àí¹¤ÄÐгæ (СÓÐÃûÆø)
|
[ÇóÖú]
άÆÕÇóÖú ¼±¼±£¡£¡£¡ ÒÑÓÐ1È˲ÎÓë
|
|
JGX-ST CÆ×Êý¾Ý£º12.26,12.45,19.20,19.60,21.29,21.43,24.57,25.61,29.12,31.85,32.11,36.73,37.48,39.90,40.69,42.43,42.50,50.38,51.45,56.18,57.08,72.00,121.91,129.50,138.52,140.97 |
» ²ÂÄãϲ»¶
²ÄÁϸ´ÊÔÇóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸0703»¯Ñ§ÕÐ61×îÖÕÅÅÃû62»¯Ñ§Çóµ÷¼Á
ÒѾÓÐ17È˻ظ´
¿¼Ñе÷¼Á
ÒѾÓÐ5È˻ظ´
085600²ÄÁÏÓ뻯¹¤301·ÖÇóµ÷¼ÁԺУ
ÒѾÓÐ33È˻ظ´
284Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
269Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
283Çóµ÷¼Á
ÒѾÓÐ17È˻ظ´
292Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
070300»¯Ñ§ Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
¼±¼±¼±¼±¼±¼±£¬µµ°¸ÎÊÌ⣬ÇóÖú£¡£¡£¡£¡
ÒѾÓÐ22È˻ظ´
άÆÕÇóÖú£¬Ð»Ð»à¸£¡
ÒѾÓÐ3È˻ظ´
Journal of Chemical and Pharmaceutical Research£¬2015ÄêÊÇei¼ìË÷µÄÆÚ¿¯Ã´
ÒѾÓÐ5È˻ظ´
HETEROCYCLESͶ¸åÇóÖú
ÒѾÓÐ9È˻ظ´
άÆÕÇóÖú no-3 ¼±£¡
ÒѾÓÐ4È˻ظ´
άÆÕÇóÖú--www
ÒѾÓÐ4È˻ظ´
άÆÕÇóÖú£¡Ð»Ð»~
ÒѾÓÐ3È˻ظ´
Science of Synthesis Êý¾Ý¿âÊÔÓÃ
ÒѾÓÐ6È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏάÆÕÊý¾Ý
ÒѾÓÐ3È˻ظ´
ÇóÖúάÆÕÊý¾Ý½âÎö»¯ºÏÎï½á¹¹
ÒѾÓÐ8È˻ظ´
άÆÕÊý¾ÝÇóÖúX
ÒѾÓÐ3È˻ظ´
Á½¸öÆ×£¬¸÷ÐèÒªÏàËÆ¶Èǰ10µÄ£¬Ð»Ð»¡£
ÒѾÓÐ3È˻ظ´
άÆÕÇóÖú£¡£¡£¡
ÒѾÓÐ3È˻ظ´
ÌìȻҩÎﻯѧ°æ¿ì³ÉΪ¡°Î¬ÆÕ¡±ÇóÖú°æÁË£¬¿ª±Ù¸ö¡°Î¬ÆÕ¡±Êý¾ÝÇóÖú×Ó°æÈçºÎ£¿
ÒѾÓÐ19È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú ¼±¼±¼±£¡£¡£¡
ÒѾÓÐ4È˻ظ´
ÇóÖú3¸ö΢ÆÕÊý¾Ý
ÒѾÓÐ5È˻ظ´
½ô¼±ÇóÖú£¡£¡£¡Endnote X4µ¼ÈëPDFÎÞ·¨Ê¶±ðÁË
ÒѾÓÐ27È˻ظ´
sydong
Ìú¸Ëľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 403 (˶ʿ)
- ½ð±Ò: 7797.1
- ºì»¨: 22
- Ìû×Ó: 1800
- ÔÚÏß: 632.4Сʱ
- ³æºÅ: 1255872
- ×¢²á: 2011-04-05
- ÐÔ±ð: GG
- רҵ: ÓлúºÏ³É
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ò©»¯Àí¹¤ÄÐ: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-05-13 20:16:04
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ò©»¯Àí¹¤ÄÐ: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-05-13 20:16:04
|
²éѯ½á¹û£º¹²²éµ½1990¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Stigmasterol C29H48O ÏàËÆ¶È:100% Journal of China Pharmaceutical University 2004 35 404-405 Chemical Constituents from Xanthium sibiricum ZHANG Xia-Qi; QI Jin; YE Wen-Cai; ZHAO Shou-Xun Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (3S,9S,10S,13R,17R)-17-((2R,5S,E)-5-ethyl-6-methylhept-3-en-2-yl)-9,10,13-trimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol C30H50O ÏàËÆ¶È:100% Molecules 2014 19 756-766 Antimalarial Evaluation of the Chemical Constituents of Hairy Root Culture of Bixa orellana L. Bo Zhai, Julie Clark, Taotao Ling, Michele Connelly, Fabricio Medina-Bolivar and Fatima Rivas Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . stigmasterol C29 H48O ÏàËÆ¶È:100% Journal of Yunnan University 2007 29 613-616 Terpenes and sterols from Galinsoga parviflora PAN Zheng-hong, ZHAO Lei, HUANG Rong, MA Guo-yi, LI Zu-qiang Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . stigmasterol C29H48O ÏàËÆ¶È:96.2% Modern Chinese Medicine 2007 9(7) 13-14 Studies on the Constituents of Senecio laetus Edgew. Jin Jun, Zhang Chaofeng, ZhangMian Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . stigmasterol ÏàËÆ¶È:96.2% Journal of Guangdong Phamaceutical University 2007 23 1-2 Chemical constituents of the root of Mirabilis jalapa KUANG Jia-le, ZHANG De-zhi Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . stigmasterol C29H48O ÏàËÆ¶È:96.2% Journal of Tropical and Subtropical Botany 2014 22 413-418 Phenolic Derivatives and Steroids from Eupatorium adenophorum Spreng REN Hui, ZHANG Mei, ZHOU Zhong-yu, TAN Jian-wen, WAN Fang-hao Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . stigmasterol ÏàËÆ¶È:96.2% Journal of Shenyang Pharmaceutical University 2012 29 348-358 Isolation and identification of chemical constituents from the marine organism Artemia cysts YU Jian-ting; LIN Jun-ming; ZOU Xiao-nan; GUO Hai-yan; LI Yu-shan Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . ¶¹çÞ´¼ ÏàËÆ¶È:96.2% China Journal of Chinese Materia Medica 2012 37 1788-1792 Chemical constituents contained in Desmodium caudatum WU Yao; LUO Qiang; SUN Cuiling; WANG Guanghui; CHEN Quancheng; GUO Zhijian; ZOU Xiuhong; CHEN Haifeng Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . ¶¹çÞ´¼ ÏàËÆ¶È:96.2% Journal of Chinese Medicinal Materials 2007 30 1259-1261 н®ºÚÖÖ²Ý×ӵĻ¯Ñ§³É·ÖÑо¿ °¬ÄáÍÞ¶û¡¤°¬¿Ëľ, ÈÈÄÈ¡¤¿¨Ë¹Ä¾ Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . stigmasta-5,22(E)-dien-3-beta-ol C29H48O ÏàËÆ¶È:96.1% Acta Botanica Boreali-Occidentalia Sinica 2006 26 1001-1006 Active AntimicrobiaLingredients in Mikania micrantha Stems and Leaves YU Xin-ping, FENG Jun-tao, LIU Xiao-ming, ZHUANG Shi-hong, ZHANG Xing Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ¦Â-sitosterol ÏàËÆ¶È:96.1% Acta Botanica Boreali-Occidentalia Sinica 2009 29 1893-1897 Isolation and identif ication of Acaricidal Composition of Thymus mongolicus FENG Gang, ZHANG Jing, BAI Jun, PENG Zheng-qiang Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ¶¹çÞ´¼ ÏàËÆ¶È:96.1% Chinese Traditional and Herbal Drugs 2009 40 701-704 À«°ú¾ÕµÄ»¯Ñ§³É·ÖÑо¿ ÇñÔÌç²;ÆáÊ绪;ÕÅ‚Æ;ÀîÇìÐÀ Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . stigmasterol ÏàËÆ¶È:96.1% Natural Product Research and Development 1997 9(2) 4-6 NON-ALKALOIDAL CONSTITUENTS FROM MECONOPSIS PUNICEA MAXIM Zhang Guolin; Li Bogang; Zhou Zhengzhi Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Stigmasterol ÏàËÆ¶È:96.1% Guihaia 2014 34 155-159 Study on the chemical constituents of Peristrophe roxburghiana GE Li, LAN Liu-Feng, BAO Hui-Bin, YANG Ke-Di Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . stigmasterol C29H48O ÏàËÆ¶È:96.1% Chinese Traditional and Herbal Drugs 2012 43 38-42 Chemical constituents from Dysoxylum lenticellatum TANG Ting; NA Zhi; XU You-kai Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . stigmasterol ÏàËÆ¶È:96.1% Chinese Joumal of Experimental Traditional Medical Fomulae 2014 20 46-48 Chemical Constituents of Amydrium hainanense HUANG Yan, LI Xing-yu, LIU Yuan, LIU Bu-ming, SONG Zhi-zhao, LIN Xiao, WEN Zhi-yun Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . stigmasterol ÏàËÆ¶È:96.1% Chinese Joumal of Experimental Traditional Medical Fomulae 2010 16 40-42 ³£É½»¯Ñ§³É·ÖÑо¿ ÕÅÑÅ, Àî´º, À×¹úÁ« Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . stigmasterol ÏàËÆ¶È:92.8% Planta Medica 1986 52 499-500 Antihepatotoxic Principles of Wedelia chinensis Herbs Ling-Ling Yang, Kun-Ying Yen, Chohachi Konno, Yoshiteru Oshima,Yoshinobu Kiso and Hiroshi Hikino Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . Stigmasterol ÏàËÆ¶È:92.8% Archives of Pharmacal Research 2008 31 965-969 A new cytotoxic prenylated dihydrobenzofuran derivative and other chemical constituents from the rhizomes of Atractylodes lancea DC Jin-ao Duan, Liuying Wang, Shihui Qian, Shulan Su and Yuping Tang Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . stigmasterol ÏàËÆ¶È:92.8% Natural Product Research and Development 2012 24 892-896 Chemical Constituents from the Seed of Nigella glandulifera Freyn XIN Xue-lei; WANG Han-qing; AISA Haji Akber; Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . Stigmasterol ÏàËÆ¶È:92.5% Phytochemistry 1985 24 1505-1508 Isotachin A and isotachin B, two sulphur-containing acrylates from the liverwort isotachis japonica Yoshinori Asakawa, Masao Toyota, Leslie J. Harrison Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . stigmasterol ÏàËÆ¶È:92.5% Journal of Chinese Medicinal Materials 2012 35 64-66 Study on the Chemical Constituets in Ethyl Acetante Extraction from Semen Litchi HUANG Kai-wen, GUO Jie-wen, CHEN Jian-mei, Lin Li-jing, XU Feng Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . stigmasterol ÏàËÆ¶È:92.5% Journal of Medicinal Plants Research 2012 6 168-170 Five chemical constituents of the ethyl acetate fraction from ethanol extract of semen litchi Jie-wen Guo, Jian-mei Chen, Li-jing Lin and Feng Xu Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . stigmasterol ÏàËÆ¶È:92.5% Asian Journal of Chemistry 2014 26 1011-1014 Phytochemical Investigation on Eucalyptus globulus Labill M. IBRAHIM, S. AMBREEN, A. HUSSAIN, N. HUSSAIN, M. IMRAN, B. ALI, S.H. SUMRRA, M. YOUSUF and F.S. REHMANI Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . stigmasterol ÏàËÆ¶È:92.3% Chemical & Pharmaceutical Bulletin 1993 41 2007-2009 Constituents of Prunus zippeliana Leaves and Branches Junichi KITAJIMA and Yasuko TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . ergosta-5,22-dien-3-ol ÏàËÆ¶È:92.3% Natural Product Research 2013 27 76-79 Allelopathic activity studies of Mikania scandens K.G. Nelum P. Piyasena & H. Ranjith W. Dharmaratne Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . stigmasterol ÏàËÆ¶È:92.3% Journal of Wood Science 2013 59 155-159 Antibacterial compounds from shoot skins of moso bamboo (Phyllostachys pubescens) Akinobu Tanaka, Kuniyoshi Shimizu, Ryuichiro Kondo Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . Stigmasterol ÏàËÆ¶È:89.6% Chemistry of Natural Compounds 2004 40 457-459 A NEW HYDROQUINONE DIGLUCOSIDE FROM Lysimachia fordiana Xin-an Huang and Ren-Zhou Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . stigmasterol ÏàËÆ¶È:89.6% Acta Botanica Sinica 1999 41 107-110 Chemical constituents of the Anemone tomentosa Root Wang Jun-Ru, Peng Shu-Lin, Wang Ming-Kui, Feng Jun-Tao, Ding Li-Sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . stigmasterol ÏàËÆ¶È:89.6% Journal of Chinese Pharmaceutical Sciences 1999 8 237-240 Chemical Constituents of Stelmatocrypton khasianum Zhang Qingying; Zhao Yuying; Ma Libin; Cheng Tieming Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . tigmasterol ÏàËÆ¶È:89.6% Guihaia 2007 27 140-142 Chemical constituents from leaves of Livistona chinensis LIU Zhi-Ping; CUI Jian-Guo ; LIU Hong-Xing; HUANG Chu-Sheng; ZHONG Zhen-Guo Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . Stigmasterol ÏàËÆ¶È:89.6% Steroids 2004 69 43-50 Gradient enhanced selective experiments in the 1H NMR chemical shift assignment of the skeleton and side-chain resonances of stigmasterol, a phytosterol derivative Peter Forgo, Katalin E. Köv¨¦r Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . stigmasterol ÏàËÆ¶È:89.6% Natural Product Research 2006 20 485-491 Inophyllin A, a new pyranoxanthone from Calophyllum inophyllum (Guttiferae) G. C. L. Ee; A. S. M. Kua; C. K. Lim; V. Jong; H. L. Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . stigmasterol ÏàËÆ¶È:89.6% China Journal of Chinese Materia Medica 2009 34 705-707 Study on chemical constituents from Cicuta virosa var. latisecta L I Zhenlin1, Q I AN Shihui, PU Sheban Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . stigmasterol ÏàËÆ¶È:89.6% China Journal of Chinese Materia Medica 1997 22 295-296 Studies on the Chemical Constituents of Begonia evansiana Andr Zhang J iam in and Chen Yaozu, L iBogang andW angM ingkui Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . stigmasterol ÏàËÆ¶È:89.6% China Journal of Chinese Materia Medica 1996 21 483-484 A Study on the Chemical Contituents of Aster albscens Hand. -Mazz. He Lan and Cheng Dongliang, Pan Xuan Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . stigmasterol ÏàËÆ¶È:89.6% China Journal of Chinese Materia Medica 1994 19 611-612 Studies on the Chemical Constituents of Flower of David Lily Feng Shilan, He Lan, Wang Min and Jiao Kejie Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . stigmasterol ÏàËÆ¶È:89.6% Acta Pharmaceutica Sinica 2000 Vol 35 29-31 STRUCTURE IDENTIFICATION OF VULGARSAPONIN A Tian Jing; Xiao Zhiyan; Chen Yayan; Zhao Yuying and Wang Zhuju Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . Poriferasterol ÏàËÆ¶È:89.6% Zeitschrift f¨¹r Naturforschung B 2005 60b 1006-1011 Eupatoric Acid: A Novel Triterpene from Eupatorium odoratum L. (Asteraceae) Sajan Amatyaa and Sarbajna M. Tuladhar Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . stigmasterol ÏàËÆ¶È:89.6% Phytochemistry 1990 29 2351-2355 Sterol glucosides from Prunella vulgaris Hisashi Kojima,Noriko Sato,Akiko Hatano,Haruo Ogura Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . stigmasterol ÏàËÆ¶È:89.6% Phytochemistry 1990 29 2957-2959 Steroid glycosides from Asparagus adscendens Mamta Tandon,Yogendra N. Shukla,Raghunath S. Thakur Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . Stigmasterol ÏàËÆ¶È:89.6% Phytochemical Analysis 1992 3 38-41 Characterization of acylated steryl glycosides from Euryale ferox by nuclear magnetic resonance spectroscopy Zhao Haoru and Zhao Shoushun Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . stigmasterol ÏàËÆ¶È:89.6% Phytochemical Analysis 2004 15 125-129 Steroids and triterpenes from Eleocharis acutangula and E. sellowiana (cyperaceae) Maria do Carmo E. Amaral, Aparecida D. Faria, Aderbal F. Mag |

2Â¥2015-05-13 19:47:31













»Ø¸´´ËÂ¥