| ²é¿´: 393 | »Ø¸´: 1 | |||
badhuster½ð³æ (ÕýʽдÊÖ)
ѧǰ°à°à³¤
|
[ÇóÖú]
΢Æ×ÇóÖú£¬Ð»Ð»£¬¼± ÒÑÓÐ1È˲ÎÓë
|
| 13C NMR (Pyr, 151 MHz) ¦Ä 14.74, 23.41, 26.29, 27.13, 27.20, 29.98, 30.09, 30.29, 30.34, 30.39, 30.44, 30.48, 30.51, 30.65, 30.81, 32.59, 33.45, 33.77, 34.31, 34.63, 36.19, 53.46, 62.49, 62.52, 72.95, 73.38, 73.50, 77.27, 77.32, 131.17, 131.29, 175.73. |
» ²ÂÄãϲ»¶
һ־Ը³¶«´óѧ071000ÉúÎïѧѧ˶³õÊÔ·ÖÊý276Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
Ò»Ö¾Ô¸¹þ¹¤´ó 085600 277 12²Ä¿Æ»ùÇóµ÷¼Á
ÒѾÓÐ33È˻ظ´
Ò»Ö¾Ô¸Öйú¿ÆÑ§ÔºÉϺ£ÓлúËù£¬Óлú»¯Ñ§356·ÖÕÒµ÷¼Á
ÒѾÓÐ12È˻ظ´
071000ÉúÎïѧ£¬Ò»Ö¾Ô¸ÉîÛÚ´óѧ296·Ö£¬Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
0854µ÷¼Á
ÒѾÓÐ12È˻ظ´
²ÄÁÏÓ뻯¹¤µ÷¼Á
ÒѾÓÐ37È˻ظ´
271Çóµ÷¼Á
ÒѾÓÐ23È˻ظ´
²ÄÁÏÏà¹Ø×¨Òµ344Çóµ÷¼ÁË«·Ç¹¤¿ÆÑ§Ð£»ò¿ÎÌâ×é
ÒѾÓÐ11È˻ظ´
»¯¹¤Ñ§Ë¶294·Ö£¬Çóµ¼Ê¦ÊÕÁô
ÒѾÓÐ14È˻ظ´
2026 WRÇà°Î
ÒѾÓÐ5È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬¼±¼±¼±£¬Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬¼±£¡~~лл
ÒѾÓÐ3È˻ظ´
½âÆ×ÇóÖú£¨Ö»ÓÐ̼Æ×£©£¬Ð»Ð»ÁË¡£
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
΢Æ×Ò»¸ö£¬ÇóÖú£¬Ð»Ð»£¡
ÒѾÓÐ8È˻ظ´
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻ظ´
¼±£¡Î¢Æ×ÇóÖú£¡ÏÈлл°¡£¡
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬¸ø30J
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¡¼±¼±¼±£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
ÇóÖú΢Æ×²éѯ½âÆ×
ÒѾÓÐ5È˻ظ´

seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48433.9
- ºì»¨: 52
- Ìû×Ó: 6749
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
badhuster: ½ð±Ò+10 2015-04-08 22:15:13
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
badhuster: ½ð±Ò+10 2015-04-08 22:15:13
|
1 . ceramide ÏàËÆ¶È:78.1% Indian Journal of Chemistry Section B 2007 46B 1868-1872 Antifungal and phytochemical studies of Eupatorium birmanicum DC. Devi,L Reena; Singh,Th Shyamkeshor; Laitonjam,Warjeet S Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . phytoceramide C36H71NO4 ÏàËÆ¶È:78.1% Molecules 2011 16 9090-9100 Phytoceramide Shows Neuroprotection and Ameliorates Scopolamine-Induced Memory Impairment Jae-Chul Jung, Yeonju Lee, Sohyeon Moon, Jong Hoon Ryu and Seikwan Oh Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 5-deoxy-6-O-dodecanoyl-D-allose C18H34O6 ÏàËÆ¶È:70.5% Bioscience, Biotechnology, and Biochemistry 2014 78 190−194 Anti-proliferative activity of 6-O-acyl-d-allose against the human leukemia MOLT-4F cell line Ryo C. Yanagita, Katsuya Kobashi, Chisa Ogawa, Yoshiki Ashida, Haruka Yamaashi & Yasuhiro Kawanami Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 1-O-¦Â-D-glucopyranosyl-(2S,3R,4E,8E)-2-[(2-hydroxyicosanoyl)amido]-4,8-octadecadiene-1,3-diol ÏàËÆ¶È:70.2% Journal of Natural Products 1996 59 319-322 New Bioactive Cerebrosides from Arisaema amurense Jee H. Jung, Chong-Ock Lee, Young Choong Kim, Sam Sik Kang Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . emmyguyacin A C36H64O16 ÏàËÆ¶È:69.6% Journal of Natural Products 2002 65 108-114 Emmyguyacins A and B: Unusual Glycolipids from a Sterile Fungus Species That Inhibit the Low-pH Conformational Change of Hemagglutinin A during Replication of Influenza Virus Christie Boros, Barry Katz, Scott Mitchell, Cedric Pearce, Karra Swinbank, and Debra Taylor Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . agelasphin-13 C50H99NO10 ÏàËÆ¶È:68.7% Tetrahedron 1994 50 2771-2784 Agelasphins, novel antitumor and immunostimulatory cerebrosides from the marine sponge Agelas mauritianus Takenori Natori, Masahiro Morita, Kohji Akimoto, Yasuhiko Koezuka Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (2S,3S,4R)-2-hexacosanoylamino-1-O-(6-O-methyl-5a-carba-¦Á-D-galactopyranosyl)octadecane-1,3,4-triol C52H101NO8 ÏàËÆ¶È:68.7% Bioorganic & Medicinal Chemistry 2009 17 6360-6373 RCAI-37, 56, 59, 60, 92, 101, and 102, cyclitol and carbasugar analogs of KRN7000: Their synthesis and bioactivity for mouse lymphocytes to produce Th1-biased cytokines Takuya Tashiro, Ryusuke Nakagawa, Takatsugu Hirokawa, Sayo Inoue, Hiroshi Watarai, Masaru Taniguchi, Kenji Mori Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . diphlorethol ÏàËÆ¶È:68.7% Fisheries Science 1994 60 319-321 Phlorotannins and Sulfoquinovosyl Diacylglycerols: Promoters of Larval Metamorphosis in Ascidians, Isolated from the Brown Alga Sargassum thunbergii Sachiko Tsukamoto, Hiroshi Hirota, Haruko Kato, Nobuhiro Fusetani Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 5-O-dodecanoyl-D-ribose C17H32O6 ÏàËÆ¶È:68.7% Bioscience, Biotechnology, and Biochemistry 2014 78 190−194 Anti-proliferative activity of 6-O-acyl-d-allose against the human leukemia MOLT-4F cell line Ryo C. Yanagita, Katsuya Kobashi, Chisa Ogawa, Yoshiki Ashida, Haruka Yamaashi & Yasuhiro Kawanami Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 1-O-¦Â-D-glucopyranosyl-(2S,3S,4R,8E/Z)-2-(2'-hydroxylignoceroyl amino)-8-octadecene-1,3,4-triol ÏàËÆ¶È:68.5% Natural Product Sciences 2008 14 161-166 Phytochemical Studies on Paeoniae Radix (4);Cerebrosides and Other Constituents Kim, Yoon-Jung; Yean, Min-Hye; Lee, Eun-Ju; Kim, Ju-Sun; Lee, Je-Hyun; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 1-O-¦Â-D-glucopyranosyl-(2S,3S,4R,8E/Z)-2-(2'-hydroxytricosanoyl amino)-8-octadecene-1,3,4-triol ÏàËÆ¶È:68.5% Natural Product Sciences 2008 14 161-166 Phytochemical Studies on Paeoniae Radix (4);Cerebrosides and Other Constituents Kim, Yoon-Jung; Yean, Min-Hye; Lee, Eun-Ju; Kim, Ju-Sun; Lee, Je-Hyun; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . poke-weed cerebroside C48H93NO10 ÏàËÆ¶È:67.5% Chemical & Pharmaceutical Bulletin 2001 49 321-323 Cyclooxygenase-2 Inhibitory Cerebrosides from Phytolaccae Radix Sam Sik KANG, Ju Sun KIM, Kun Ho SON, Hyun Pyo KIM, Hyeun Wook CHANG Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . hylodendroside-I C48H91NO9 ÏàËÆ¶È:66.6% Phytochemistry 2008 69 2400-2405 A triterpenoidal saponin and sphingolipids from Pteleopsis hylodendron Atta-ur-Rahman,Seema Zareen,M. Iqbal Choudhary,M. Nadeem Akhtar,F.N. Ngounou Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 1-O-¦Â-D-glucopyranosyl-(2S,3S,4R,8E/Z)-2-(2'-hydroxypalmitoyl amino)-8-octadecene-1,3,4-triol ÏàËÆ¶È:66.6% Natural Product Sciences 2008 14 161-166 Phytochemical Studies on Paeoniae Radix (4);Cerebrosides and Other Constituents Kim, Yoon-Jung; Yean, Min-Hye; Lee, Eun-Ju; Kim, Ju-Sun; Lee, Je-Hyun; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . AGL-588 C56H108NO14 ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry 1997 5 2245-2249 Immunostimulatory activities of monoglycosylated ¦Á-d-pyranosylceramides Akira Uchimura, Toshiyuki Shimizu, Masahiro Morita, Hitomi Ueno, Kazuhiro Motoki, Hideaki Fukushima, Takenori Natori, Yasuhiko Koezuka Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 1-O-¦Â-D-glucopyranosyl-(2S,3R,4E,8Z)-2-N-palmitoyloctadecasphinga-4,8-dienine C40H75NO8 ÏàËÆ¶È:65.6% Journal of Natural Products 1997 60 274-276 New Antihepatotoxic Cerebroside from Lycium chinense Fruits Sun Yeou Kim, Young-Hee Choi, Hoon Huh, Jinwoong Kim, Young Choong Kim, and Heum Sook Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (2S)-1-O-hexadecanoyl-2-O-(9z,l 2z-octadecadienoyl)-3-O-¦Â-D- galacatopyranosyl glycerol ÏàËÆ¶È:65.6% Phytochemistry 1996 42 447-452 Diacylglycerylgalactosides from Arisaema amurense Jee H. Jung, Hongkum Lee, Sam Sik Kang Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . N-palmitoyl-D-erythro-(2S,3R)-17-methyl-octadecasphinga-4(E),8(E)-dienine C35H67NO3 ÏàËÆ¶È:65.6% Journal of Natural Products 1995 Vol 58 948-953 Isolation of New Ceramides from the Gorgonian Acabaria undulata Jongheon Shin, Youngwan Seo Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . fraction A ÏàËÆ¶È:65.6% Phytochemistry 1989 28 3047-3050 Glycerol tridehydrocrepenynate from the basidiomycete Craterellus cornucopioides Volker Magnus,Goran Laćan,Robin T. Aplin,Viktor Thaller Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . cerebroside ÏàËÆ¶È:65.6% Indian Journal of Chemistry Section B 2007 46B 1868-1872 Antifungal and phytochemical studies of Eupatorium birmanicum DC. Devi,L Reena; Singh,Th Shyamkeshor; Laitonjam,Warjeet S Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-03-11 16:57:43













»Ø¸´´ËÂ¥