| ²é¿´: 333 | »Ø¸´: 1 | ||
Artclassľ³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú£¬Ð»Ð»
|
|
ÈܼÁΪMeOH£¬ 4.9, 10.8, 21.2, 51.1, 75.2, 92.2, 92.4, 107.6, 107.6, 117.9, 128.2, 130.4, 133.5, 133.8, 143.5, 163.9, 167.9, 171.8, 195.8, 196.0 ллÁË~ |
» ²ÂÄãϲ»¶
0854Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
²ÄÁϹ¤³ÌרҵÈÕÓïÉúÇóµ÷¼Á
ÒѾÓÐ6È˻ظ´
071000ÉúÎïѧ£¬Ò»Ö¾Ô¸ÉîÛÚ´óѧ296·Ö£¬Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
µ÷¼Á
ÒѾÓÐ5È˻ظ´
±¾¿ÆÖ£ÖÝ´óѧ£¬Ò»Ö¾Ô¸»ª¶«Ê¦·¶´óѧ282Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
»¯¹¤Ñ§Ë¶ 285Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
312Çóµ÷¼Á
ÒѾÓÐ17È˻ظ´
ÉúÎïµ÷¼Á
ÒѾÓÐ6È˻ظ´
Ò»Ö¾Ô¸¹þ¹¤´ó£¬³õÊÔ329£¬Çó»·¾³¿ÆÑ§Ó빤³Ìµ÷¼Á£¡
ÒѾÓÐ9È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
»¯ºÏÎï΢Æ×ÇóÖú лл
ÒѾÓÐ9È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¡¼±¼±¼±£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл¡£¡£¡£
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻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 ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Artclass: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2013-09-26 14:29:59
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Artclass: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2013-09-26 14:29:59
|
²éѯ½á¹û£º¹²²éµ½15¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . Azaspirofurans A C22H21NO7 ÏàËÆ¶È:75% Archives of Pharmacal Research 2010 33 499-502 Two new hetero-spirocyclic ¦Ã-lactam derivatives from marine sediment-derived fungus Aspergillus sydowi D2¨C6 Hong Ren, Rui Liu, Li Chen, Tianjiao Zhu and Wei Ming Zhu, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . azaspirofuran A C22H21NO7 ÏàËÆ¶È:75% Chinese Pharmaceutical Journal 2011 46 569-575 Antitumor Metabolites from Fungus Aspergillus sydowi D2-6 REN Hong, CAO Xue-li, WANG Qiao-e, XV Chun-ming Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . Azaspirofurans B C21H19NO7 ÏàËÆ¶È:60% Archives of Pharmacal Research 2010 33 499-502 Two new hetero-spirocyclic ¦Ã-lactam derivatives from marine sediment-derived fungus Aspergillus sydowi D2¨C6 Hong Ren, Rui Liu, Li Chen, Tianjiao Zhu and Wei Ming Zhu, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . azaspirofuran B C21H19NO7 ÏàËÆ¶È:60% Chinese Pharmaceutical Journal 2011 46 569-575 Antitumor Metabolites from Fungus Aspergillus sydowi D2-6 REN Hong, CAO Xue-li, WANG Qiao-e, XV Chun-ming Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . synerazol C22H23NO7 ÏàËÆ¶È:60% The Journal of Antibiotics 1991 44 382-389 SYNERAZOL, A NEW ANTIFUNGAL ANTIBIOTIC OSAMU ANDO, HITOMI SATAKE, MUTSUO NAKAJIMA, AKIRA SATO, TAKEMICHI NAKAMURA, TAKESHI KINOSHITA, KOUHEI FURUYA, TATSUO HANEISHI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . pseurotin A ÏàËÆ¶È:60% Chinese Pharmaceutical Journal 2011 46 1154-1158 Metabolites of Aspergillus sp. HT-2 ZHANG, Li-min, LI, Zhan-lina, BAI, Jiao, Wu, Xinc, WANG, Yu, HUA, Hui-ming Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . pseurotin A ÏàËÆ¶È:57.1% Journal of Natural Products 2007 70 1672-1675 Pinpointing Pseurotins from a Marine-Derived Aspergillus as Tools for Chemical Genetics Using a Synthetic Lethality Yeast Screen Claudia M. Boot,Nadine C. Gassner, Jennifer E. Compton, Karen Tenney, Craig M. Tamble,R. Scott Lokey, Theodore R. Holman, and Phillip Crews Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . pseurotin A C22H25NO8 ÏàËÆ¶È:55% Helvetica Chimica Acta 1981 64 304-315 Isolation and Structure of Pseurotin A, a Microbial Metabolite of Pseudeurotium ovalis STOLK with an Unusual Heterospirocyclic System Peter Bloch, Christoph Tamm Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . pseurotin A ÏàËÆ¶È:55% The Journal of Antibiotics 1991 44 382-389 SYNERAZOL, A NEW ANTIFUNGAL ANTIBIOTIC OSAMU ANDO, HITOMI SATAKE, MUTSUO NAKAJIMA, AKIRA SATO, TAKEMICHI NAKAMURA, TAKESHI KINOSHITA, KOUHEI FURUYA, TATSUO HANEISHI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . Pseurotin A ÏàËÆ¶È:54.5% Canadian Journal of Chemistry 2011 89 72¨C76 Pseurotin A1 and A2, two new 1-oxa-7-azaspiro[4.4]non-2-ene-4, 6-diones from the holothurian-derived fungus Aspergillus fumigatus WFZ-25 Fa-Zuo Wang, De-Hai Li, Tian-Jiao Zhu, Min Zhang, and Qian-Qun Gu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . xanthohumol G C21H24O7 ÏàËÆ¶È:50% Journal of Natural Products 2004 67 2024-2032 Estrogens and Congeners from Spent Hops (Humulus lupulus) Lucas R. Chadwick, Dejan Nikolic, Joanna E. Burdette, Cassia R. Overk, Judy L. Bolton, Richard B. van Breemen, Roland Frhlich, Harry H. S. Fong, Norman R. Farnsworth, and Guido F. Pauli Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 11-Omethylpseurotin A C23H27NO8 ÏàËÆ¶È:50% Journal of Natural Products 2007 70 1672-1675 Pinpointing Pseurotins from a Marine-Derived Aspergillus as Tools for Chemical Genetics Using a Synthetic Lethality Yeast Screen Claudia M. Boot,Nadine C. Gassner, Jennifer E. Compton, Karen Tenney, Craig M. Tamble,R. Scott Lokey, Theodore R. Holman, and Phillip Crews Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . pseurotin A C22H25NO8 ÏàËÆ¶È:50% Helvetica Chimica Acta 1981 64 304-315 Isolation and Structure of Pseurotin A, a Microbial Metabolite of Pseudeurotium ovalis STOLK with an Unusual Heterospirocyclic System Peter Bloch, Christoph Tamm Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . methyl 2-(2-hydroxy-5-methyl-phenyl)-1-methoxymethyl-1H-indole-3-carboxylate C19H19NO4 ÏàËÆ¶È:50% Heterocycles 2003 60 1615-1623 Photochemistry of 2-Indolyl Aryl Ethers: An Unexpected Rearrangement Leading to C-C Bond Formation Ken S. Feldman* and Daniela Boneva Vidulova Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . dimethyl 2-[3,3-dimethyl-6-oxo-8-(4-methylphenyl)-3,4,6,7-tetrahydro-2H-pyrrolo-[2,1-b]-1,3-oxazin-7-yl]malonate C21H25NO5 ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2011 48 577-581 Reaction of cyclic imidates with ,¦Â-unsaturated esters: Synthesis of new pyrrolo[2,1-b]-1,3-oxazine and pyrido[2,1-b]-1,3-oxazine derivatives Shogo Ihara, Takashi Soma, Daigo Yano, Shunichi Aikawa and Yasuhiko Yoshida Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- |
2Â¥2013-09-26 11:14:21














»Ø¸´´ËÂ¥