| ²é¿´: 869 | »Ø¸´: 6 | ||||
| µ±Ç°Ö»ÏÔʾÂú×ãÖ¸¶¨Ìõ¼þµÄ»ØÌû£¬µã»÷ÕâÀï²é¿´±¾»°ÌâµÄËùÓлØÌû | ||||
mrdone.0907½ð³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
ÇóÖúÁ½¸ö΢Æ×
|
|||
|
13C NMR (101 MHz, CDCl3) ¦Ä 14.23,20.52,24.91,25.50,25.59,27.17,29.06,29.09,29.12,29.54,34.07,51.39,127.09,127.71,128.23,128. 25,130.23,131.92,174.27 13C NMR (101 MHz, CDCl3) ¦Ä 14.03,22.55,24.92,25.61,27.17,29.07,29.10,29.13,29.33,29.57,31.51,34.08,51.39,127.89,128.03,130.0 2,130.19,174.26 |
» ²ÂÄãϲ»¶
ÇëÎÊÓÐÆÀÖ°³Æ£¬°Ñ¿ÆÑнÌѧҵ¼¨Ëã·ÖÅÅÐòµÄ¸ßУÂð
ÒѾÓÐ6È˻ظ´
2025ÀäÞøÑ§Ê²Ã´Ê±ºò³ö½á¹û
ÒѾÓÐ6È˻ظ´
Bioresource TechnologyÆÚ¿¯£¬µÚÒ»´Î·µÐÞµÄʱºò±»Í˻غü¸´ÎÁË
ÒѾÓÐ7È˻ظ´
Õæ³ÏÇóÖú£ºÊÖÀïµÄÊ¡Éç¿ÆÏîÄ¿½áÏîÒªÇóÖ÷³ÖÈËһƪÖÐÎĺËÐÄ£¬ÓÐʲôÇþµÀÄÜ·¢ºËÐÄÂð
ÒѾÓÐ8È˻ظ´
ѰÇóÒ»ÖÖÄÜ¿¸×¡Ç¿Ñõ»¯ÐÔ¸¯Ê´ÐÔµÄÈÝÆ÷ÃÜ·â¼þ
ÒѾÓÐ5È˻ظ´
ÇëÎÊÄÄÀï¿ÉÒÔÓÐÇàBÉêÇëµÄ±¾×Ó¿ÉÒÔ½è¼øÒ»Ï¡£
ÒѾÓÐ4È˻ظ´
ÇëÎÊÏ´ó¼ÒΪʲôÕâ¸öÁåľżÁª¼¸ºõ²»·´Ó¦ÄØ
ÒѾÓÐ5È˻ظ´
Ìì½ò¹¤Òµ´óѧ֣Áø´ºÍŶӻ¶Ó»¯Ñ§»¯¹¤¡¢¸ß·Ö×Ó»¯Ñ§»òÓлúºÏ³É·½ÏòµÄ²©Ê¿ÉúºÍ˶ʿÉú¼ÓÈë
ÒѾÓÐ4È˻ظ´
¿µ¸´´óѧ̩ɽѧÕßÖÜì÷»ÝÍŶÓÕÐÊÕ²©Ê¿Ñо¿Éú
ÒѾÓÐ6È˻ظ´
AIÂÛÎÄд×÷¹¤¾ß£ºÊÇ¿ÆÑмÓËÙÆ÷»¹ÊÇѧÊõ×÷±×Æ÷£¿
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
JYN-33 ΢Æ×ÇóÖú£¬¼±Çó£¬Ð»Ð»£¬×·¼Ó½ð±Ò¡£¡£¡£
ÒѾÓÐ6È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
Á½¸ö»¯ºÏÎï-----ÇóÖú¿ÉÒÔ²é΢Æ×Êý¾ÝµÄ³æ×Ó~
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
ÇóÖúÒ»¸öÓÃ΢Æ×½âÎöµÄ½á¹¹ 85%ÏàËÆÒ²ÐÐ
ÒѾÓÐ3È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
½ô¼±ÇóÖú£¡£¡Àë×Ó½»»»É«Æ×µÄÁ½¸öСÎÊÌâ
ÒѾÓÐ7È˻ظ´
ÇóÖúÈçϵÄÁ½¸ö»¯ºÏÎïÈçºÎͨ¹ýÆ×ͼÐÅÏ¢À´È·Ö¤¾ßÌåÊÇÄĸö½á¹¹£¿ лл
ÒѾÓÐ27È˻ظ´
¡¾ÇóÖú¡¿±£Áôʱ¼ä²»Ò»ÑùµÄÁ½¸ö»¯ºÏÎïµÄÇâÆ×̼Æ×Ò»Ñù£¿
ÒѾÓÐ13È˻ظ´
¡¾ÇóÖú¡¿Í¬Ò»ÎïÖÖÁ½¸öxrdÆ×ͼ·ÖÎö
ÒѾÓÐ5È˻ظ´
¡¾ÇóÖú¡¿ÈçºÎ°ÑÁ½¸öºìÍâÆ×ͼ·ÅÔÚÒ»Æð×÷±È½Ï
ÒѾÓÐ4È˻ظ´

mrdone.0907
½ð³æ (ÕýʽдÊÖ)
- PhEPI: 1
- Ó¦Öú: 21 (СѧÉú)
- ½ð±Ò: 817.5
- É¢½ð: 104
- ºì»¨: 16
- Ìû×Ó: 556
- ÔÚÏß: 161.4Сʱ
- ³æºÅ: 868670
- ×¢²á: 2009-10-11
- ÐÔ±ð: GG
- רҵ: º£ÑóÒ©Îï

3Â¥2013-07-24 14:41:49
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
-

ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
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%) ²éѯ½á¹û£º¹²²éµ½1195¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . linolenic acid ÏàËÆ¶È:100% Journal of the Chinese Chemical Society 2000 47 1131-1136 The Low Polar Constituents from Bidens Pilosa L. var. minor (Blume) Sherff Ming-Huey Chang, Guei-Jane Wang,Yueh-Hsiung Kuo and Ching-Kuo Lee* Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound B ÏàËÆ¶È:94.7% Zeitschrift f¨¹r Naturforschung C 2010 65 571-576 Feeding Stimulant in Cinnamomum camphora for the Common Bluebottle, Graphium sarpedon nipponum (Lepidoptera: Papilionidae) J. Li, R. Wakui, M. Horie, Y. Nishimura, Y. Nishiyama, Y. Ikeno, S.-i. Tebayashi, and C.-S. Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ¦Á-linolenic acid ÏàËÆ¶È:94.7% Zeitschrift f¨¹r Naturforschung C 2010 65 571-576 Feeding Stimulant in Cinnamomum camphora for the Common Bluebottle, Graphium sarpedon nipponum (Lepidoptera: Papilionidae) J. Li, R. Wakui, M. Horie, Y. Nishimura, Y. Nishiyama, Y. Ikeno, S.-i. Tebayashi, and C.-S. Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . ethyl linolenate ÏàËÆ¶È:90% Journal of the Chinese Chemical Society 2000 47 1131-1136 The Low Polar Constituents from Bidens Pilosa L. var. minor (Blume) Sherff Ming-Huey Chang, Guei-Jane Wang,Yueh-Hsiung Kuo and Ching-Kuo Lee* Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Methyl(7Z,10Z,13Z)-hexadecatrienoate ÏàËÆ¶È:89.4% Phytochemistry 1995 40 1433-1437 Anti-tumour-promoting glyceroglycolipids from the green alga, Chlorella vulgaris Takashi Morimoto, Akito Nagatsu, Nobutoshi Murakami, Jinsaku Sakakibara, Harukuni Tokuda, Hoyoku Nishino, Akio Iwashima Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . methyl hexadeca-7Z,10Z,13Z-trienoate ÏàËÆ¶È:89.4% Phytochemistry 1983 22 1445-1446 Fatty acid composition in Lemna minor-characterization of a novel hydroxy C16 acid Lucio Previtera, Pietro Monaco Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 2e ÏàËÆ¶È:89.4% Magnetic Resonance in Chemistry 2012 50 823-828 1H, 13C and 15N NMR assignments for N- and O-acylethanolamines, important family of naturally occurring bioactive lipid mediators Roberta Ottria, Silvana Casati and Pierangela Ciuffreda Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Khotimchenko C18H30O2 ÏàËÆ¶È:89.4% Chinese Journal of Antibiotics 2010 35 877-879 Study on the secondary metabolites from Mariannaea campospora SIIA-F12361 Qin, Chuan-ping, Wang, Xin-rong, Tian, Yong-qiang, and, Wang, Lu Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . linolenic acid methyl ester C21H36O4 ÏàËÆ¶È:85% Korean Journal of Pharmacognosy 2007 38(4) 403-408 Isolation of Chemical Compounds from xBrassicoraphanus Rhee, Yun-Hee; Ahn, Kyoo-Seok; Lee, Soo-Seong; Park, Young-Doo; Ryu, Shi-Yong; Kim, Sung-Hoon Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . glycerol 1-(9,12,15-pctadecatrienoate C21H36O4 ÏàËÆ¶È:85% Korean Journal of Pharmacognosy 2004 35(3) 255-258 Chemical Constituents of Brassica campestris ssp pekinensis Choi, Yeon-Hee; Kim, Jung-Sook; Seo, Jee-Hee; Lee, Jung-Won; Kim, Young-Sup; Ryu, Shi-Yong; Lee, Kang-Ro; Kim, Young-Kyoon; Kim, Sung-Hoon Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ¦Á-linolenic ÏàËÆ¶È:84.2% Chemistry of Natural Compounds 1987 23 168-173 POLYUNSATURATED FATTY ACIDS OF THE a-LINOLENIC SERIES FROM INSULIN PRODUCTION WASTES G. A. Frangulyan, A. V. Komkov, E. P. Prokof'ev, V. M. Belotserkovets, E. E. Lavut, and V. I. Panov Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 9,12,15-octadecatrienoic acid ÏàËÆ¶È:84.2% Natural Product Sciences 2004 10 335-340 Phytochemical Constituents of the Aerial Parts from Aster hispidus Lee, Sung-Ok; Choi, Sang-Zin; Choi, Sang-Un; Ryu, Shi-Yong; Lee, Kang-Ro Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 9,12,15-Octadecatrienoic acid ÏàËÆ¶È:84.2% Archives of Pharmacal Research 2002 25 628-635 Phytochemical constituens of Cirsium setidens Nakai and their cytotoxicity against human cancer cell lines Won Bin Lee, Hak Cheol Kwon, Ock Ryun Cho, Kang Choon Lee and Sang Un Choi, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . ¦Á-linolenic acid C18H30O2 ÏàËÆ¶È:84.2% Bioscience, Biotechnology, and Biochemistry 2005 69 2186-2192 Isolation and Structure Determination of Algicidal Compounds from Ulva fasciata Mochammad Amin ALAMSJAH, Shotaro HIRAO, Fumito ISHIBASHI and Yuji FUJITA Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . linolenic acid ÏàËÆ¶È:84.2% Journal of the Chinese Chemical Society 1995 42 573-577 Chemical Constituents from the Root and Aerial Parts of Rosa taiwanensis —î„Ù¿¡(Shen-Chyun Yang);·½¿¡Ãñ(Jim-Min Fang);à?Óñè¦(Yu-Shia Cheng) Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-07-24 14:35:46
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
-

ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ

4Â¥2013-07-24 14:44:25
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
-

ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
mrdone.0907: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, Ëٶȿ죬£¬ºÜ¸øÁ¦ 2013-07-24 14:51:49
mrdone.0907: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, Ëٶȿ죬£¬ºÜ¸øÁ¦ 2013-07-24 14:51:49
|
°´´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%) ²éѯ½á¹û£º¹²²éµ½3532¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . methyl linoleate ÏàËÆ¶È:94.7% Biological and Pharmaceutical Bulletin 2010 33 1242-1245 Melanogenesis Inhibitory Effect of Fatty Acid Alkyl Esters Isolated from Oxalis triangularis Sungran Huh, Young-Soo Kim, Eunsun Jung, Jihee Lim, Kwang Sun Jung, Myeong-Ok Kim, Jongsung Lee, Deokhoon Park Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (9Z,12Z)-1,3-Dihydroxypropan-2-yl octadeca-9,12-dienoate C21H38O4 ÏàËÆ¶È:89.4% Tetrahedron 2012 68 5422-5428 Application of chemoenzymatic hydrolysis in the synthesis of 2-monoacylglycerols Kyle M. Whitten, Alexandros Makriyannis, Subramanian K. Vadivel Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Ê®°ËÍé¶þÏ©Ëá¼×õ¥ ÏàËÆ¶È:89.4% China Journal of Chinese Materia Medica 2011 36 2515-2519 Studies on metabolites from marine microorganism Aspergillus terreus collected from nature reserve region of mangrove SHEN, Yi, ZOU, Jianhua, DAI, Jungui Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . linoleic acid ÏàËÆ¶È:88.8% Chemical & Pharmaceutical Bulletin 1988 36 4453-4461 Limonoids and Quinolone Alkaloids from Evodia rutaecarpa BENTHAM TOHRU SUGIMOTO,TOSHIO MIYASE,MASANORI KUROYANAGI and AKIRA UENO Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . linoleic acid,9Z,12Z-octadecadienoic acid ÏàËÆ¶È:88.8% Korean Journal of Pharmacognosy 1997 28(2) 75-79 A Study on the Constituents from the Roots of Astragalus membranaceus (II) Kim, Jin-Sook; Kim, Chung-Sook Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Methyl linoleate ÏàËÆ¶È:88.8% Archives of Pharmacal Research 1988 11 159-162 Studies on the chemical constituents of Acanthopanax koreanum (II) Young Ho Kim, Bo Sup Chung, Young Su Ko and Hee Ja Han Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Linoleic acid ÏàËÆ¶È:88.8% Organic Letters 2011 13 6228-6231 Echinopsacetylenes A and B, New Thiophenes from Echinops transiliensis Hiroshi Nakano, Charles L. Cantrell, Leonid K. Mamonov, Weste L. A. Osbrink, and Samir A. Ross Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . linoleic acid ÏàËÆ¶È:88.8% Tetrahedron 2007 63 8174-8180 Musanahol: a new aureonitol-related metabolite from a Chaetomium sp. Ruchi G. Marwah, Majekodunmi O. Fatope, Mike L. Deadman, Yousif Mohammed Al-Maqbali, John Husband Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . linoleic ÏàËÆ¶È:88.8% Organic Magnetic Resonance 1982 18 98-103 13C NMR spectra of 1-stearoyl-2-linoleyl-sn-glycero-3-phosphorylcholine and 1-stearoyl-2-arachidonoyl-sn-glycero-3-phosphorylcholine in CDCl3 solution and in sonicated dispersions in 2H2O Juan F. Santar¨¦n, M. Rico, J. Guilleme and A. Ribera Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 2d ÏàËÆ¶È:88.8% Magnetic Resonance in Chemistry 2012 50 823-828 1H, 13C and 15N NMR assignments for N- and O-acylethanolamines, important family of naturally occurring bioactive lipid mediators Roberta Ottria, Silvana Casati and Pierangela Ciuffreda Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . linoleic acid C18H32O2 ÏàËÆ¶È:88.8% Chinese Journal of Medicinal Chemistry 2012 22 47-50 Chemical constituents of Lysimachia stenosepala CAO Xian-ping; LIANG Xin; ZHONG Hui-min Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ÑÇÓÍËá ÏàËÆ¶È:88.8% Lishizhen Medicine and Materia Medica Research 2011 22 2144-2145 ´óÇàÒ¶µÄ»¯Ñ§³É·ÖµÄÑо¿ ÀîÑ©»¢; Áº½£Æ½; ½Îýºê Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Linoleic acid ÏàËÆ¶È:88.8% Lishizhen Medicine and Materia Medica Research 2011 22 2643-2644 Chemical Constituents of Leaves of Jatropha curcas in Hainan XU Miao; WANG Jun; CHEN Yi-ping; DENG Shi-ming; LIANG Zhen-yi; ZHENG Ru-gang Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 9,12-octadecadienoic acid methyl ester C19H34O2 ÏàËÆ¶È:88.8% Chinese Traditional and Herbal Drugs 2012 43 2356-2360 Chemical constituents from sporophore of Hericium coralloides (¢ñ) ZHANG Peng; BAO Hai-ying; Tolgor Structure 13C NMR ̼Æ×Ä£Äâͼ |

5Â¥2013-07-24 14:46:11













»Ø¸´´ËÂ¥
