| ²é¿´: 312 | »Ø¸´: 1 | |||
lyy5563Òø³æ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
|
CD3OD 137.5,129.2,79.9,79.3,72.2,70.4,53.6,42.9,41.7,41.1,40.4,37.7,37.5,32.8,28.3,27.7,26.9,25.9,25.7,25.3,23.5,21.0,18.0,16.4,15.2,11.5 [ Last edited by ׿Խ_ÏÈ·æ on 2015-5-5 at 18:23 ] |
» ²ÂÄãϲ»¶
²ÄÁÏרҵ344Çóµ÷¼Á
ÒѾÓÐ19È˻ظ´
085404 298·ÖÇóµ÷¼Á
ÒѾÓÐ11È˻ظ´
296Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
³õÊÔ261
ÒѾÓÐ6È˻ظ´
284Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
²ÄÁÏ085601µ÷¼Á
ÒѾÓÐ25È˻ظ´
272·Ö²ÄÁÏ×ÓÇóµ÷¼Á
ÒѾÓÐ23È˻ظ´
22408µ÷¼ÁÇóÖú
ÒѾÓÐ7È˻ظ´
µ÷¼Á
ÒѾÓÐ17È˻ظ´
²ÄÁÏÀà284µ÷¼Á
ÒѾÓÐ43È˻ظ´
Ц¶à»á»³ÔÐ
Ìú¸Ëľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1216 (½²Ê¦)
- ½ð±Ò: 9788.1
- É¢½ð: 610
- ºì»¨: 40
- ɳ·¢: 3
- Ìû×Ó: 2723
- ÔÚÏß: 1284.6Сʱ
- ³æºÅ: 2010893
- ×¢²á: 2012-09-18
- ÐÔ±ð: GG
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
Ê×Ò³ ¹«Ë¾¼ò½é ¾«È·²éѯ Ä£ºý²éѯ Éî¶È²éѯ »ùÍŲéѯ ²»¾«È·¿â ʹÓÃÖ¸ÄÏ ÍøÕ¾¹«¸æ ÁôÑÔ°å ÎĵµÏÂÔØ ²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ̼Æ×¿â£º Nat Syn ²éѯ½á¹û£º¹²²éµ½144¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 1¦Â,2¦Á,3¦Á-trihydroxyurs-12-en-28-oic acid (1¦Â-hydroxyeuscaphic acid) C30H48O6 ÏàËÆ¶È:76.6% Natural Product Sciences 2009 15 76-82 NMR Assignment and Antimicrobial/Antioxidant Activities of 1¦Â-Hydroxyeuscaphic acid from the Seeds of Butyrospermum parkii Nyaa, Laurentine Bouquet Tankeu; Tapondjou, Leon Azefack; Barboni, Luciano; Tamokou, Jean De Dieu; Kuiate, Jules Roger; Tane, Pierre; Park, Hee-Juhn Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . methylbarbinervate ÏàËÆ¶È:76.6% Phytochemistry 1994 37 1517-1575 13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features Shashi B. Mahato, Asish P. Kundu Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . barbinervic acid methylate ÏàËÆ¶È:74.1% Chemical & Pharmaceutical Bulletin 1978 26 2689-2693 Studies on the Constituents of the Medicinal Plants. XXI. Constituents of the leaves of Clethra barbinervis SIEB. et ZUCC. (2) and the 13C-Nuclear Magnetic Resonance Spectra of 19¦Á-Hydroxyurs-12-en-28-oic Acid Type of Triterpenoids KOTARO TAKAHASHI and MASAKO TAKANI Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 6 ÏàËÆ¶È:70% Phytochemistry 1990 29 1326-1329 An A-ring contracted triterpenoid from Hyptis suaveolens K.V. Raja Rao,L.J.M. Rao,N.S. Prakasa Rao Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . euscaphic acid ÏàËÆ¶È:70% Pharmazie 2008 63 765-767 Euscaphic acid, a new hypoglycemic natural product from Folium Eriobotryae Jian Chen, Wei-Lin Li, Ju-Lan Wu, Bing-Ru Ren and Han-Qing Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . euscaphic acid ÏàËÆ¶È:70% Zeitschrift f¨¹r Naturforschung C 2009 64 201-209 Hepatoprotective Triterpenes from Hairy Root Cultures of Ocimum basilicum L. A. M. Marzouk Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . ¨¢cido eusc¨¢fco ÏàËÆ¶È:70% Qu¨ªmica Nova 2011 34 39-42 Chemical constituents of Hyptidendron canum (Pohl ex Benth.) R. Harley (Lamiaceae) Lemes, Geralda de F¨¢tima; Ferri, Pedro Henrique; Lopes, M¨¢rcia Nasser Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 3-O-acetyl pomolic acid ÏàËÆ¶È:70% Natural Product Research 2013 22 2219-2223 Triterpenoids from Fragaria ananassa calyx and their inhibitory effects on melanogenesis in B16-F10 mouse melanoma cells Na-Young Song, Jin-Gyeong Cho, Dongmoon Im, Dae-Young Lee, Qian Wu, Woo-Duck Seo, Hee Cheol Kang, Youn-Hyung Lee & Nam-In Baek Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . methyl euscaphate C31H50O5 ÏàËÆ¶È:67.7% Phytochemistry 1992 31 4285-4288 Musangicic acid, a triterpenoid constituent of Musanga cecropioides David Lontsi, Beibam-Lucas Sondengam, Marie-Therese Martin, Bernard Bodo Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Euscapic acid methylester ÏàËÆ¶È:67.7% Archives of Pharmacal Research 1991 14 225-230 Triterpenoids from the roots ofRubus parvifolius Yoon Soo Choi, Kun Ho Son and Jae Chul Do Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 19¦Á-hydroxy-3-acetyl-ursolic acid ÏàËÆ¶È:67.7% Journal of Shenyang Pharmaceutical University 1995 12 25-28 Å®Õê×Ó»¯Ñ§³É·ÖµÄÑо¿(¢ò) ÍõËØÏÍ, ÒüË«, ÎâÁ¢¾ü, Àîϳ, ÕÔÏéÃô, Ñî¾§, Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-05-05 17:00:09













»Ø¸´´ËÂ¥