| ²é¿´: 272 | »Ø¸´: 1 | ||
º£ÑóÁÔÈËͳæ (ÕýʽдÊÖ)
|
[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
|
CDcl3 CÆ× 211.20, 170.99, 129.84, 82.38, 80.50, 72.36, 56.86, 55.45, 49.18, 45.18, 43.38, 39.94, 39.40, 39.04, 38.52, 38.32, 35.94, 34.04, 33.98, 33.60, 31.92, 31.88, 31.40, 31.31, 30.55, 29.78, 29.71, 29.62, 29.61, 29.56, 29.53, 29.48, 29.24, 28.21, 27.22, 25.54, 25.04, 23.84, 22.69, 22.57, 21.36, 20.52, 18.47, 17.56, 16.48, 16.06, 14.13 |
» ²ÂÄãϲ»¶
329Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
¸´ÊÔµ÷¼Á
ÒѾÓÐ4È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ10È˻ظ´
292Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
363Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
0703×Ü·Ö331Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
²ÄÁÏר˶(0856) 339·ÖÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´

lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
º£ÑóÁÔÈË: ½ð±Ò+10, ¶àл 2015-02-05 17:31:07
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
º£ÑóÁÔÈË: ½ð±Ò+10, ¶àл 2015-02-05 17:31:07
|
²éѯ½á¹û£º¹²²éµ½432¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (3¦Â)-olean-18-en-3-yl stearate ÏàËÆ¶È:75% Helvetica Chimica Acta 2007 Vol. 90 652 Triterpene Esters Isolated from Leaves of Maytenus salicifolia Reissek Roqueline Rodrigues Silva de Miranda, Gr¨¢cia Divina de F¨¢tima Silva, Lucienir Pains Duarte, and SidneyA ugusto Vieira Filho Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 3¦Â-palmitoyl-11-carboyl-urs-12-ene C46H78O3 ÏàËÆ¶È:74.4% Natural Product Research and Development 1997 9(3) 19-23 TRITERPENE ESTERS AND TRITERPENES FROM ILEX KUDINCHA Ouyang Mingan; Wang Hanqing Su Junhua Liu Yuqing; Yang Chongren Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 11 ,12 :13 ,28-diepoxyoleanan-3 -yl (9Z)-hexadec-9-enoate C46H76O4 ÏàËÆ¶È:72.3% Helvetica Chimica Acta 2004 Vol. 87 46 Palmitoleate (=(9Z)-Hexadeca-9-enoate) Esters of Oleanane Triterpenoids from the Golden Flowers of Tagetes erecta: Isolation and Autoxidation Products Shaheen Faizi and Aneela Naz Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . ursa-12-sene-3¦Â,11¦Â-diol 3-O-palmitate C46H80O3 ÏàËÆ¶È:72.3% Journal of Asian Natural Products Research 2011 13 105-110 Triterpenoids from Viburnum betulifolium Jiang Hu; Xuan-Qin Chen; Qin-Shi Zhao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . (3¦Â)-urs-12-en-3-yl stearate ÏàËÆ¶È:70.2% Helvetica Chimica Acta 2007 Vol. 90 652 Triterpene Esters Isolated from Leaves of Maytenus salicifolia Reissek Roqueline Rodrigues Silva de Miranda, Gr¨¢cia Divina de F¨¢tima Silva, Lucienir Pains Duarte, and SidneyA ugusto Vieira Filho Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (3¦Â)-lup-20(29)-en-3-yl stearate ÏàËÆ¶È:70.2% Helvetica Chimica Acta 2007 Vol. 90 652 Triterpene Esters Isolated from Leaves of Maytenus salicifolia Reissek Roqueline Rodrigues Silva de Miranda, Gr¨¢cia Divina de F¨¢tima Silva, Lucienir Pains Duarte, and SidneyA ugusto Vieira Filho Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 3b-linoleyloxyergost-7-ene ÏàËÆ¶È:70.2% Phytochemistry 2000 54 603-610 Constituents of various wood-rotting basidiomycetes Joachim Rösecke, Wilfried A. König Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 1-5 ÏàËÆ¶È:70.2% Bioscience, Biotechnology, and Biochemistry 2001 65 1198-1201 Lupeol Esters from the Twig Bark of Japanese Pear (Pyrus serotina Rehd.) cv. Shinko Hideyuki TOMOSAKA, Hiroyuki KOSHINO, Tatsuharu TAJIKA, Saburo OMATA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . lupenyl palmitate ÏàËÆ¶È:70.2% Natural Product Research and Development 2006 18 954-957 Studies on Chemical Constituents of Poacynum hendersonii ZHANG Yun-feng; WEI Dong; GUO Si-yuan; CHEN Feng; DU Nian-sheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 3¦Â-palmitoyl-¦Á-amyrin C46H80O2 ÏàËÆ¶È:70.2% Natural Product Research and Development 1997 9(3) 19-23 TRITERPENE ESTERS AND TRITERPENES FROM ILEX KUDINCHA Ouyang Mingan; Wang Hanqing Su Junhua Liu Yuqing; Yang Chongren Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . lupenylpalmitate ÏàËÆ¶È:70.2% Journal of Guangxi Traditional Chinese Medical University 2008 11 44-46 Studies on chemical constituents of Poacynum pictum Lv Hua-jun, Huang Jv-peng, Lu Jian, Zhang Yun-feng, Li Jian-bin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 12-ursadien-3¦Â-ol 3-O-palmitate C46H78O2 ÏàËÆ¶È:68.0% Chemical & Pharmaceutical Bulletin 2003 51(7) 885¡ª887 Studies on the Constituents of Gentiana Species. II. A New Triterpenoid, and (S)-(1)- and (R)-(2)-Gentiolactones from Gentiana lutea Rie KAKUDA, Koichi MACHIDA, Yasunori YAOITA, Masafumi KIKUCHI, and Masao KIKUCHI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 5,6¦Â-Epoxysitosteryl oleate C47H82O3 ÏàËÆ¶È:68.0% Steroids 2008 73 1098-1109 Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1] Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 7-Ketositosteryl-9,10-dihydroxystearate C47H82O5 ÏàËÆ¶È:68.0% Steroids 2008 73 1098-1109 Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1] Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 5,6¦Â-Epoxysitosteryl-9,10-dihydroxystearate C47H84O5 ÏàËÆ¶È:68.0% Steroids 2008 73 1098-1109 Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1] Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 1¦Â,11¦Á,28-Tyrihydroxy oleana-9(11),12-dien-3¦Â-palmitate C46H80O5 ÏàËÆ¶È:68.0% Archives of Pharmacal Research 2014 37 1515-1521 Cytotoxic triterpenoids from Saussurea phyllocephala Jiang Hu, Yan Song, Benshou Yang, Xiang Zuo, Xiao Mao, Xiaodong Shi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . ligustrin C ÏàËÆ¶È:67.3% Phytochemistry 1997 46 977-979 Acylated triterpenoids from Ligustrum ovalifolium Koichi Machida, Toshio Yamaguchi, Yoshiko Kamiya, Masao Kikuchi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . urs-12-en-3¦Â-O-9E,12E-octadecadienoate C19H34O2 ÏàËÆ¶È:66.6% Journal of Asian Natural Products Research 2009 11 583-587 A new lipid and other constituents from the rhizomes of Nelumbo nucifera Prabir Kumar Chaudhuri and Deepika Singh Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . (3¦Â,5¦Á,6¦Â,22E)-ergosta-7,22-diene-3,5,6-triol 6-oleate ÏàËÆ¶È:65.9% Helvetica Chimica Acta 2007 Vol. 90 1165 New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . 11-oxoolean-12-en-3 -yl (9Z)-hexadec-9-enoate C46H76O3 ÏàËÆ¶È:65.9% Helvetica Chimica Acta 2004 Vol. 87 46 Palmitoleate (=(9Z)-Hexadeca-9-enoate) Esters of Oleanane Triterpenoids from the Golden Flowers of Tagetes erecta: Isolation and Autoxidation Products Shaheen Faizi and Aneela Naz Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . sitosteryl-9,10-dihydroxystearate C47H84O4 ÏàËÆ¶È:65.9% Steroids 2008 73 1098-1109 Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1] Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 22 . 7-Ketocholesteryl-9,10-dihydroxystearate C45H78O5 ÏàËÆ¶È:65.9% Steroids 2008 73 1098-1109 Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1] Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 23 . 3b-linoleyloxyergosta-7,24(28)-diene ÏàËÆ¶È:65.9% Phytochemistry 2000 54 603-610 Constituents of various wood-rotting basidiomycetes Joachim Rösecke, Wilfried A. König Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 24 . 3¦Â-stearoyl-panaxdiol C48H86O4 ÏàËÆ¶È:65.9% Chemical Research in Chinese Universities 2007 23 176-182 Synthesis and Primary Research on Antitumor Activity of Three New Panaxadiol Fatty Acid Esters ZHANG Chun-hong, LIXiang-gao,GAO Yu-gang,ZHANG Lian-xue and FU Xue-qi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 25 . ursa-12-dien-1¦Â,3¦Â-diol 3-O-palmitate ÏàËÆ¶È:65.9% Journal of Asian Natural Products Research 2011 13 105-110 Triterpenoids from Viburnum betulifolium Jiang Hu; Xuan-Qin Chen; Qin-Shi Zhao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 26 . dammar-9(11),24-dien-3¦Â-ol-3¦Á-L-arabinosyl-7¦Á-octanoate C43H74O7 ÏàËÆ¶È:65.9% Asian Journal of Chemistry 2013 25 4667-4669 New Compound from the Heat Processed Roots of Panax ginseng Ill-Min Chung, Mohd Ali, Youn-Pyo Hong and Ateeque Ahmad Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-02-05 17:16:50














»Ø¸´´ËÂ¥