| ²é¿´: 943 | »Ø¸´: 4 | ||
| µ±Ç°Ö»ÏÔʾÂú×ãÖ¸¶¨Ìõ¼þµÄ»ØÌû£¬µã»÷ÕâÀï²é¿´±¾»°ÌâµÄËùÓлØÌû | ||
xzhfoodÈÙÓþ°æÖ÷ (ÖøÃûдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý1¸ö ÒÑÓÐ2È˲ÎÓë
|
|
|
ww-11 ÈܼÁ£º¼×´¼ Ö»ÓÐÁ½¸ö̼£¬ÒªÇ°10Ïî¼Ç¼£º 63.0,72.4 |
» ²ÂÄãϲ»¶
262Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
0856µ÷¼Á
ÒѾÓÐ6È˻ظ´
ÕÅ·¼Ãú-Öйúũҵ´óѧ-»·¾³¹¤³Ìר˶-298
ÒѾÓÐ6È˻ظ´
¿¼ÑÐÉúÎïÓëÒ½Ò©µ÷¼Á
ÒѾÓÐ3È˻ظ´
274Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
»¯Ñ§¹¤³Ì085602 305·ÖÇóµ÷¼Á
ÒѾÓÐ26È˻ظ´
334Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸ ÄϾ©º½¿Õº½Ìì´óѧ £¬080500²ÄÁÏ¿ÆÑ§Ó빤³Ìѧ˶
ÒѾÓÐ5È˻ظ´
¿´¿´ÎÒ£¡301Çóµ÷¼Á 081700
ÒѾÓÐ3È˻ظ´
Çóµ÷¼Á ÉúÎïѧ 377·Ö
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý1¸ö
ÒѾÓÐ3È˻ظ´
ÔÚÄĸöÍøÕ¾¿ÉÒԲ鵽»¯ºÏÎïµÄͼÆ×
ÒѾÓÐ3È˻ظ´
×öÒ»¸ö½çÃæ»¯µÄÊý¾Ý¿â£¬ÓÃʲôÓïÑԺã¿
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯһ¸ö»¯ºÏÎï~¼±~£¡Ð»Ð»
ÒѾÓÐ3È˻ظ´
MESTRENOVA 7 ½â̼Æ×£¬ÈçºÎÈÃÊä³öµÄÊý¾Ý±£ÁôһλСÊý£¨Ä¬ÈÏÊÇÁ½Î»£©£¿
ÒѾÓÐ12È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
¹òÇóÄÜÓÃ΢Æ×Êý¾Ý¿âµÄ³æ×ÓÃÇ£¬°ïæ²éÒ»ÏÂ̼Æ×Êý¾Ý£¬±¾ÈËËÍ6¸ö½ð±Ò£¡£¡£¡
ÒѾÓÐ7È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
Chem. Pharm. Bull. ÊÇÄǸöÊý¾Ý¿âÀïµÄ£¿
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿Ì¼Æ×ÖÐȱÉÙÒÔôÊ»ù̼Êý¾Ý
ÒѾÓÐ12È˻ظ´
xzhfood
ÈÙÓþ°æÖ÷ (ÖøÃûдÊÖ)
- Ó¦Öú: 5 (Ó×¶ùÔ°)
- ¹ó±ö: 22.859
- ½ð±Ò: 712.2
- É¢½ð: 31
- ºì»¨: 23
- Ìû×Ó: 1820
- ÔÚÏß: 837Сʱ
- ³æºÅ: 6596
- ×¢²á: 2003-04-11
- רҵ: ʳƷ¿ÆÑ§»ù´¡
5Â¥2014-01-11 17:48:48
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
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
²éѯ½á¹û£º¹²²éµ½77¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . glycerol ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 1991 16 421-423 Studies on the Chemical Constituents of Acanthopanax giraldii Harms Zhao Yuqing and Yuan Changlu Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 6-O-L-isoleucyl-D-fructose ÏàËÆ¶È:100% Indian Journal of Chemistry Section B 2007 46B 2026-2044 Enzymatic syntheses of L-valyl,L-leucyl and L-isoleucyl esters of carbohydrates using Candida rugosa lipase Somashekar,Bhandya R; Divakar,Soundar Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ³àÞº´¼ ÏàËÆ¶È:100% Chinese Traditional and Herbal Drugs 2007 38 650-652 Chemical constituents of Xuezhikang Capsula MA Xue-min; GUO Shu-ren; DUAN Zhen-wen; WANG Xiang-yun Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . glycerol C3H8O3 ÏàËÆ¶È:100% Chinese Journal of Natural Medicines 2008 6 268-270 Chemical Constituents from the Seeds of Ziziphus jujuba var.spinosa WANG Jian-Rong; ZHANG Jian; YIN Zhi-Qi; LIANG Jing-Yu; YE Wen-Cai Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . erythritol ÏàËÆ¶È:100% Chinese Journal of Natural Medicines 2009 7 203-205 Chemical Constituents from Solanum lyratum REN Yan; ZHANG De-Wu; DAI Sheng-Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . adonitol ÏàËÆ¶È:100% Natural Product Research and Development 2010 22 594-596 Chemical Constituents of Adonis coerulea Maxim. DAI Yuan; ZHANG Bei-bei; XU You; LIAO Zhi-xin Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . erythrol ÏàËÆ¶È:100% Medicinal Chemistry Research 2012 21 4324-4329 Antioxidant and a-glucosidase inhibitory compounds from Pimpinella candolleana Wight et Arn. Xing Chang • Wenyi Kang Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . meso-erythritol ÏàËÆ¶È:100% Carbohydrate Research 2011 346 1842-1847 Enzymatic synthesis of novel branched sugar alcohols mediated by the transglycosylation reaction of pullulan-hydrolyzing amylase II (TVA II) cloned from Thermoactinomyces vulgaris R-47 Yoichiro Shimura, Keimei Oh, Misaki Kon, Eri Yamamoto, Yoshinori Mizuno, Takashi Adachi, Tomomi Abe, Shigeru Tamogami, Jun Fukushima, Tamio Inamoto, Takashi Tonozuka Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . meso-erythritol C4H10O4 ÏàËÆ¶È:100% Acta Scientiarum Naturalium Universitatis Sunyatseni 1989 28(1) 51-54 Studies on the Chemical Constituents of Chinese Soft Coral¡ªLobophtum chevalieri (Tixier Durivault) (XIX) Li Ruisheng Di Li Long Kanghou Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . erythritol C4H10O4 ÏàËÆ¶È:100% Chinese Journal of Marine Drugs 2012 31 7-10 Secondary metabolites of marine fungus zp6 and their antifungal bioactivities GAO Chang-song; ZHONG Hui-min; CAO Jun-wei; CHEN Hao Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2014-01-11 10:01:15
׿Խ_ÏÈ·æ
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
ºýÍ¿³æ
- Ó¦Öú: 990 (²©ºó)
- ¹ó±ö: 2.955
- ½ð±Ò: 6796.4
- É¢½ð: 12161
- ºì»¨: 82
- ɳ·¢: 17
- Ìû×Ó: 3017
- ÔÚÏß: 2457Сʱ
- ³æºÅ: 1713223
- ×¢²á: 2012-03-24
- ÐÔ±ð: GG
- רҵ: ÁÙ´²Ò©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
xzhfood: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2014-01-11 12:22:04
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
xzhfood: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2014-01-11 12:22:04
|
ÈܼÁΪCD3ODʱ£¬²éµ½7¸ö½á¹û Ã²ËÆ¶¼ÊÇ4¸ö̼ ²éѯ½á¹û£º¹²²éµ½7¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . manntol C6H14O6 ÏàËÆ¶È:66.6% Mycosystema 2010 29 739-745 The endophytic fungus strain ZD6 isolated from the stem of Bruguiera gymnorrhiza and the antibacterial activity of its metabolites LI Ming-Yue CHANG Min ZHANG Qing-Hua HE Ren-Fa YE Bo-Ping Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 10,16-Dihydroxyhexadecanoic Acid ÏàËÆ¶È:66.6% Molecules 2013 18 9317-9333 Oligomerization of 10,16-Dihydroxyhexadecanoic Acid and Methyl 10,16-Dihydroxyhexadecanoate Catalyzed by Lipases M. Beatriz G¨®mez-Patiño, Julia Cassani, Mar¨ªa Eugenia Jaramillo-Flores, L. Gerardo Zepeda-Vallejo, Georgina Sandoval, Manuel Jimenez-Estrada and Daniel Arrieta-Baez Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 2-thiocyanatopropane-1,3-diol ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2010 18 1942-1947 S-Arachidonoyl-2-thioglycerol synthesis and use for fluorimetric and colorimetric assays of monoacylglycerol lipase John E. Casida, Alexander G. Gulevich, Richmond Sarpong, Eric M. Bunnelle Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . anti-3-chloro-2-hydroxybutane ÏàËÆ¶È:50% Phytochemistry 2013 87 140-147 Microtropins A¨CI: 6¡ä-O-(2¡åS,3¡åR)-2¡å-Ethyl-2¡å,3¡å-dihydroxybutyrates of aliphatic alcohol ¦Â-d-glucopyranosides from the branches of Microtropis japonica Yuka Uemura, Sachiko Sugimoto, Katsuyoshi Matsunami, Hideaki Otsuka, Yoshio Takeda, Masatoshi Kawahata, Kentaro Yamaguchi Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . syn-3-chloro-2-hydroxybutane ÏàËÆ¶È:50% Phytochemistry 2013 87 140-147 Microtropins A¨CI: 6¡ä-O-(2¡åS,3¡åR)-2¡å-Ethyl-2¡å,3¡å-dihydroxybutyrates of aliphatic alcohol ¦Â-d-glucopyranosides from the branches of Microtropis japonica Yuka Uemura, Sachiko Sugimoto, Katsuyoshi Matsunami, Hideaki Otsuka, Yoshio Takeda, Masatoshi Kawahata, Kentaro Yamaguchi Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . cerebroside D ÏàËÆ¶È:50% Journal of Guangdong Phamaceutical University 2011 27 256-259 Chemical constituents of the mycelia of Guignardia mangiferae,an endophyte from Smilax glabra LIANG Fa-liang, LI Dong-li, TAO Mei-hua, ZHANG De-zhi, ZHANG Wei-min Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . but-2-ene-1,4-diol ÏàËÆ¶È:50% European Journal of Organic Chemistry 2002 2002 4217-4221 Synthetic Scheme for the Preparation of 13C-Labeled 2,7-Dimethylocta2,4,6-triene-1,8-dial, the Central Part of Carotenoids Arjan A. C. van Wijk and Johan Lugtenburg Structure 13C NMR ̼Æ×Ä£Äâͼ |

3Â¥2014-01-11 10:08:20
xzhfood
ÈÙÓþ°æÖ÷ (ÖøÃûдÊÖ)
- Ó¦Öú: 5 (Ó×¶ùÔ°)
- ¹ó±ö: 22.859
- ½ð±Ò: 712.2
- É¢½ð: 31
- ºì»¨: 23
- Ìû×Ó: 1820
- ÔÚÏß: 837Сʱ
- ³æºÅ: 6596
- ×¢²á: 2003-04-11
- רҵ: ʳƷ¿ÆÑ§»ù´¡
4Â¥2014-01-11 16:58:32














»Ø¸´´ËÂ¥