| ²é¿´: 305 | »Ø¸´: 1 | |||||
swaucq½ð³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×²éѯ»¯ºÏÎï½á¹¹
|
| 17.9,18.0,19.9,25.7,25.8,27.8,29.9,29.4,31.4,34.6,39.0,50.8,54.6,104.1,112.3,115.1,122.88,122.92,123.4,124.5,129.0,131.6,132.3,132.9,133.9,141.4,145.8,167.8,168.4 |
» ²ÂÄãϲ»¶
¸´ÊÔµ÷¼Á£¬Ò»Ö¾Ô¸Ö£ÖÝ´óѧ²ÄÁÏÓ뻯¹¤289·Ö
ÒѾÓÐ23È˻ظ´
»¯Ñ§¹¤³ÌÓë¼¼Êõרҵһ־Ը¹þ¹¤³Ì 291·ÖBÇø ¹ú¼Ò¼¶´ó´´¸ºÔðÈË ÓÐÒ»×÷ÂÛÎÄ
ÒѾÓÐ6È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ10È˻ظ´
314Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
µ÷¼Á »¯Ñ§ 307
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸211 0703»¯Ñ§ 346·ÖÇóµ÷¼Á
ÒѾÓÐ11È˻ظ´
086003µ÷¼ÁÇóÖú
ÒѾÓÐ14È˻ظ´
085400 328·Ö Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
083200 ³õÊÔ305·Ö Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
284Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
[ÇóÖú] ÇóÖú΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Ò»Ö¬ÈÜÐÔ»¯ºÏÎïµÄ½á¹¹
ÒѾÓÐ9È˻ظ´
ÇóÖúÒ»»¯ºÏÎï΢Æ×½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
΢Æ×ÇóÖúÒ»»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»»¯ºÏÎï΢Æ×Êý¾Ý½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú¡¡Î¢Æ×Êý¾Ý¿â £Ã£Î£Í£ÒÊý¾Ý²éδ֪»¯ºÏÎï½á¹¹
ÒѾÓÐ6È˻ظ´
ÇóÖúHÆ× ´ó¼Ò°ïæ¿´Ï»¯ºÏÎïµÄ½á¹¹¹Ç¼Ü
ÒѾÓÐ13È˻ظ´
¡¾ÇóÖú¡¿»¯ºÏÎï½á¹¹ÎÊÌâ
ÒѾÓÐ5È˻ظ´

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 ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
swaucq: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-06-23 10:22:51
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
swaucq: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-06-23 10:22:51
|
²éѯ½á¹û£º¹²²éµ½206¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . echinulin ÏàËÆ¶È:96.5% Helvetica Chimica Acta 2008 Vol. 91 1888 Dioxopiperazine Alkaloids Produced by the Marine Mangrove Derived Endophytic Fungus Eurotium rubrum Dong-Li Li, Xiao-Ming Li, Tie-Gang Li, Hong-Yue Dang, and Bin-Gui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . Peduncin C29H37O4N ÏàËÆ¶È:96.5% Chinese Chemical Letters 2001 12 899-902 Peduncin, A New Indole Alkaloid from Pueraria peduncualris Na LI, Qi Tai ZHENG, Zhi Da MIN Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . arestrictin B C29H39N3O2 ÏàËÆ¶È:86.2% Chemical & Pharmaceutical Bulletin 2006 54(12) 1639-1641 Two New Dioxopiperazine Derivatives, Arestrictins A and B, Isolated from Aspergillus restrictus and Aspergillus penicilloides Takeshi ITABASHI,Natsuna MATSUISHI,Tomoo HOSOE,Norihiro TOYAZAKI,Shun-ichi UDAGAWA, Toshimichi IMAI,Mitsuru ADACHI,and Ken-ichi KAWAI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . cristatumin B C29H39N3O3 ÏàËÆ¶È:86.2% Bioorganic & Medicinal Chemistry Letters 2012 22 4650-4653 Cristatumins A¨CD, new indole alkaloids from the marine-derived endophytic fungus Eurotium cristatum EN-220 Feng-Yu Du, Xiao-Ming Li, Chun-Shun Li, Zhuo Shang, Bin-Gui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . variecolorin L ÏàËÆ¶È:72.4% Helvetica Chimica Acta 2008 Vol. 91 1888 Dioxopiperazine Alkaloids Produced by the Marine Mangrove Derived Endophytic Fungus Eurotium rubrum Dong-Li Li, Xiao-Ming Li, Tie-Gang Li, Hong-Yue Dang, and Bin-Gui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . variecolorin L C29H39N3O2 ÏàËÆ¶È:72.4% Journal of Natural Products 2007 70 1558-1564 Isoechinulin-type Alkaloids, Variecolorins A¨CL, from Halotolerant Aspergillus Wariecolor Wen-Liang Wang, Zhen-Yu Lu, Hong-Wen Tao, Tian-Jiao Zhu, Yu-Chun Fang, Qian-Qun Gu, and Wei-Ming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . dehydroechinulin C29H37N3O2 ÏàËÆ¶È:68.9% Helvetica Chimica Acta 2008 Vol. 91 1888 Dioxopiperazine Alkaloids Produced by the Marine Mangrove Derived Endophytic Fungus Eurotium rubrum Dong-Li Li, Xiao-Ming Li, Tie-Gang Li, Hong-Yue Dang, and Bin-Gui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . dehydrovariecolorin L C29H37N3O2 ÏàËÆ¶È:65.5% Helvetica Chimica Acta 2008 Vol. 91 1888 Dioxopiperazine Alkaloids Produced by the Marine Mangrove Derived Endophytic Fungus Eurotium rubrum Dong-Li Li, Xiao-Ming Li, Tie-Gang Li, Hong-Yue Dang, and Bin-Gui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . arestrictin A C29H39N3O3 ÏàËÆ¶È:65.5% Chemical & Pharmaceutical Bulletin 2006 54(12) 1639-1641 Two New Dioxopiperazine Derivatives, Arestrictins A and B, Isolated from Aspergillus restrictus and Aspergillus penicilloides Takeshi ITABASHI,Natsuna MATSUISHI,Tomoo HOSOE,Norihiro TOYAZAKI,Shun-ichi UDAGAWA, Toshimichi IMAI,Mitsuru ADACHI,and Ken-ichi KAWAI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . chabrolohydroxybenzoquinone D C28H38O4 ÏàËÆ¶È:65.5% Journal of Natural Products 2004 67 2048-2052 Novel Meroditerpenoid-Related Metabolites from the Formosan Soft Coral Nephthea chabrolii Jyh-Horng Sheu, Jui-Hsin Su, Ping-Jyun Sung, Guey-Horng Wang, and Chang-Feng Dai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . Z,E,E-cupaniopsin A 29-methylester C31H44O5 ÏàËÆ¶È:64.5% Tetrahedron 2005 61 845-851 New biologically active linear triterpenes from the bark of three new-caledonian Cupaniopsis species H. Bousserouel, M. Litaudon, B. Morleo, M.-T. Martin, O. Thoison, O. Nosjean, J.A. Boutin, P. Renard, T. S¨¦venet Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . cristatin A ÏàËÆ¶È:62.0% Chemical & Pharmaceutical Bulletin 2006 54(12) 1639-1641 Two New Dioxopiperazine Derivatives, Arestrictins A and B, Isolated from Aspergillus restrictus and Aspergillus penicilloides Takeshi ITABASHI,Natsuna MATSUISHI,Tomoo HOSOE,Norihiro TOYAZAKI,Shun-ichi UDAGAWA, Toshimichi IMAI,Mitsuru ADACHI,and Ken-ichi KAWAI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . MT-6 C24H31N3O2 ÏàËÆ¶È:62.0% Chemical & Pharmaceutical Bulletin 1999 47 1426-1432 Immunomodulatory Constituents from an Ascomycete, Microascus tardifaciens Haruhiro FUJIMOTO,Toshiyuki FUJIMAKI,Emi OKUYAMA and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . MT-7 C24H31N3O2 ÏàËÆ¶È:62.0% Chemical & Pharmaceutical Bulletin 1999 47 1426-1432 Immunomodulatory Constituents from an Ascomycete, Microascus tardifaciens Haruhiro FUJIMOTO,Toshiyuki FUJIMAKI,Emi OKUYAMA and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . Methyl 2-{[(2E)-3-(4-{[(2E)-2,7-dimethylocta-2,6-die-nyl]oxy}-3-methoxyphenyl)prop-2-enoyl]oxy}benzoate C28H32O6 ÏàËÆ¶È:62.0% Bioorganic & Medicinal Chemistry Letters 2007 17 5709-5714 Synthesis and anti-inflammatory activity of 3-(4¡ä-geranyloxy-3¡ä-methoxyphenyl)-2-trans propenoic acid and its ester derivatives Francesco Epifano, Salvatore Genovese, Silvio Sosa, Aurelia Tubaro, Massimo Curini Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . Terpeptin A C28H40N4O4 ÏàËÆ¶È:62.0% Magnetic Resonance in Chemistry 2008 46 1212-1216 1H and 13C NMR assignments of two new indolic enamide diastereomers from a mangrove endophytic fungus Aspergillus sp. (pages 1212¨C1216) Zhenjian Lin, Tianjiao Zhu, Yuchun Fang and Qianqun Gu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . Terpeptin B C28H40N4O4 ÏàËÆ¶È:62.0% Magnetic Resonance in Chemistry 2008 46 1212-1216 1H and 13C NMR assignments of two new indolic enamide diastereomers from a mangrove endophytic fungus Aspergillus sp. (pages 1212¨C1216) Zhenjian Lin, Tianjiao Zhu, Yuchun Fang and Qianqun Gu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 19-nor-cucurbita-5(10),6,8,22-(E),24-pentaen-3¦Â-ol C29H42O ÏàËÆ¶È:62.0% Journal of Agricultural and Food Chemistry 2011 59 4553-4561 Isolation and Identification of Cucurbitane-Type Triterpenoids with Partial Agonist/Antagonist Potential for Estrogen Receptors from Momordica charantia Chin Hsu, Chin-Lin Hsieh, Yueh-Hsiung Kuo, and Ching-jang Huang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . clusiachromene D acetyl derivative ÏàËÆ¶È:61.2% Heterocycles 2002 56 589-597 A Biphenyl, a Dihydrophenanthrene and a Xanthone from Clusia paralycola Franco Delle Monache,* Giuliano Delle Monache, Bruno Botta, and Eszter Gacs-Baitz Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . Z,E,Z-cupaniopsin A methyl ester C31H44O5 ÏàËÆ¶È:61.2% Tetrahedron 2005 61 845-851 New biologically active linear triterpenes from the bark of three new-caledonian Cupaniopsis species H. Bousserouel, M. Litaudon, B. Morleo, M.-T. Martin, O. Thoison, O. Nosjean, J.A. Boutin, P. Renard, T. S¨¦venet Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . kazinol C C30H40O4 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1986 34 1968-1979 Components of Broussonetia kazinoki SIEB. I. : Structures of Two New Isoprenylated Flavans and Five New Isoprenylated 1, 3-Diphenylpropane Derivatives JUNKO IKUTA(nee MATSUMOTO),YOSHIO HANO,TARO NOMURA,YOSHIYUKI KAWAKAMI and TADASHI SATO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . cristatin A C29H37N3O2 ÏàËÆ¶È:58.6% Phytochemistry 2001 58 1263-1266 An immunosuppressive tryptophan-derived alkaloid from Lepidagathis cristata V. Ravikanth, V. L. Niranjan Reddy, P. Ramesh, T. Prabhakar Rao,P. V. Diwan, Ashok Khar, Y. Venkateswarlu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . Anthyllisone C25H26O4 ÏàËÆ¶È:58.6% Phytochemistry 1996 42 1455-1458 Isoflavonoids and chalcones from Anthyllis hermanniae Luisa Pistelli, Katya Spera, Guido Flamini, Salvatore Mele, Ivano Morelli Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . compound 7a C28H38O4 ÏàËÆ¶È:58.6% Bulletin of the Chemical Society of Japan 2008 81 1125-1130 Antibacterial Quinone Metabolites from the Brown Alga, Sargassum sagamianum Shohei Horie, Shinsuke Tsutsumi, Yuuki Takada, Junji Kimura Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . 3,4-dihydroxy-5-(11'-carboxyl-3',7',15'-trimethylhexadeca-2'E,6'E,10'E,14'-tetraenyl)benzoic acid C27H36O6 ÏàËÆ¶È:58.6% Qu¨ªmica Nova 2010 33 802-804 Caldensinic acid, a benzoic acid derivative and others compounds from Piper carniconnectivum Alves, Harley da Silva; Souza, Maria de F¨¢tima Vanderlei de; Chaves, Maria C¨¦lia de Oliveira Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . (S)-MTPA ester C22H30O4 ÏàËÆ¶È:58.0% Bioscience, Biotechnology, and Biochemistry 2003 66 655-659 Myrsinoic Acids B, C and F, Anti-inflammatory Compounds from Myrsine seguinii Mitsuru HIROTA, Shintaro MIYAZAKI, Tomomi MINAKUCHI, Tomoko TAKAGI and Hisao SHIBATA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . plukenetione F C33H40O4 ÏàËÆ¶È:58.0% Tetrahedron 1999 55 1581-1596 Prenylated benzophenone derivatives from Caribbean Clusia species (Guttiferae). Plukenetiones B-G and xerophenone A Geneive E Henry, Helen Jacobs, C.M.Sean Carrington, Stewart McLean, William F Reynolds Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . compound 12 ÏàËÆ¶È:58.0% The Journal of Antibiotics 2001 54 105-108 Short and Convergent Synthesis of Asterriquinone B1 and Demethylasterriquinone B1 KUNIAKI TATSUTA,HIROSHI MUKAI and KAZUKI MITSUMOTO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . 3¦Â-hydroxy-lanosra-8,24-dien-21-al ÏàËÆ¶È:56.6% Planta Medica 1984 50 197-198 3¦Â-Hydroxy-lanosra-8,24-dien-21-al, a New Triterpene from Inonotus obliquus Kirsti Kahlos, R. Hiltunen and M. v. Schantz Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . Z,E,E-cupaniopsin A C30H42O5 ÏàËÆ¶È:56.6% Tetrahedron 2005 61 845-851 New biologically active linear triterpenes from the bark of three new-caledonian Cupaniopsis species H. Bousserouel, M. Litaudon, B. Morleo, M.-T. Martin, O. Thoison, O. Nosjean, J.A. Boutin, P. Renard, T. S¨¦venet Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-06-21 21:16:15













»Ø¸´´ËÂ¥
5