| ²é¿´: 314 | »Ø¸´: 1 | ||
yuhe0920½ð³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
°ï²éϸÃÌìÈ»²úÎïYJ-23 µÄ΢Æ×Êý¾Ý£¬Ð»Ð»£¡ ÒÑÓÐ1È˲ÎÓë
|
| 22.1,23.2,23.6,25.6,30.0,43.8,46.8,57.1,59.4,169.0,171.4 |
» ²ÂÄãϲ»¶
288»·¾³×¨Ë¶,Çóµ÷²ÄÁÏ·½Ïò
ÒѾÓÐ12È˻ظ´
ÇóÉúÎïѧѧ˶µ÷¼Á¡ª¡ª364·Ö
ÒѾÓÐ7È˻ظ´
288Çóµ÷¼Á£¬Ò»Ö¾Ô¸»ªÄÏÀí¹¤´óѧ071005
ÒѾÓÐ4È˻ظ´
11408,335·Ö£¬±¾¿Æ211£¬Çóµ÷¼Á£¬¿Éתרҵ
ÒѾÓÐ5È˻ظ´
0817»¯Ñ§¹¤³ÌÓë¼¼ÊõÇóµ÷¼Á£¬Ò»Ö¾Ô¸Öк£Ñó319
ÒѾÓÐ7È˻ظ´
Äܶ¯µ÷¼Á326ר˶
ÒѾÓÐ4È˻ظ´
295Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
315Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ6È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú¼¸¸ö»¯ºÏÎï΢Æ×Êý¾Ý£¬¼±¼±£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
°ïÃ¦ÍÆ¼ö¸öºÃµÄÌìÈ»²úÎïºÍÒ©ÎﻯѧÔÓÖ¾£¬Ð»Ð»ÁË
ÒѾÓÐ5È˻ظ´
½ñÌìÔÙÇóÒ»´Î΢Æ× ³ê½ð20 ллÁË °´Õչ涨¸ñʽÕûÀíºÃ̼Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»df12
ÒѾÓÐ5È˻ظ´
΢Æ×Êý¾ÝÇóÖú¡ª¡ªÈý¸ö»¯ºÏÎï лл£¡
ÒѾÓÐ8È˻ظ´
Çó΢Æ×Êý¾Ý лл
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯһ¸ö»¯ºÏÎï~¼±~£¡Ð»Ð»
ÒѾÓÐ3È˻ظ´
Çó´óÉñ°ïæ²é΢Æ×Êý¾Ý лл£º£©
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
Çó²é΢Æ×Êý¾Ý¿â£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
¡¾ÇóÖú¡¿ÇëÓÐCCDCÊý¾Ý¿âÅóÓѰïæ²éÏÂÓÐûÓиýṹµÄÎïÖʵ¥¾§Òѱ»·¢±í£¿Ð»Ð»
ÒѾÓÐ5È˻ظ´

seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48394.9
- ºì»¨: 52
- Ìû×Ó: 6742
- 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 ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
yuhe0920: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2015-02-06 22:26:02
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
yuhe0920: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2015-02-06 22:26:02
|
1 . cyclo-[Leucyl-prolyl]2 ÏàËÆ¶È:81.8% Tetrahedron 2008 64 3147-3152 Cyclic tetrapeptides from marine bacteria associated with the seaweed Diginea sp. and the sponge Halisarca ectofibrosa Wimolpun Rungprom, Eric R.O. Siwu, Lynette K. Lambert, Chutiwan Dechsakulwatana, Michael C. Barden, Udom Kokpol, Joanne T. Blanchfield, Masaki Kita, Mary J. Garson Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 3-isobutyl-hexahydropyrrolo[1,22A]pyrazine-1,4-dione C11H18N2O2 ÏàËÆ¶È:81.8% Academic Journal of Second Military Medical University 2006 27 22-24 Bioactive cyclodipeptides extracted from marine microbes in East China Sea AI Feng, XU Qiang-zhi, YANG Yu, LIU Xiao-yu, SHI Xiao-qiong, SONG Zhi-gang, JIAO Bing-hua Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 3(R)-[(2(S)-pyrrolidinylcarbonyl)amino]-2-oxo-1-azetidineacetamide acetic acid C12H20N4O5 ÏàËÆ¶È:75% Journal of Medicinal Chemistry 1993 36 256-263 Synthesis and dopamine receptor modulating activity of lactam conformationally constrained analogs of Pro-Leu-Gly-NH2 Uma Sreenivasan, Ram K. Mishra, Rodney L. Johnson Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . cyclo-((S)-Pro-(R)-Leu) ÏàËÆ¶È:72.7% Helvetica Chimica Acta 2009 92 1112-1117 Proline-Containing Dipeptides from a Marine Sponge of a Callyspongia Species Bin Yang, Junde Dong, Xuefeng Zhou, Xianwen Yang, Kyung Jin Lee, Lishu Wang, Si Zhang, Yonghong Liu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . cyclo(L-Leu-L-Pro) ÏàËÆ¶È:72.7% China Journal of Chinese Materia Medica 2010 35 2852-2861 Constituents of Gymnadenia conopsea YUE Zhenggang; ZI Jiachen; ZHU Chenggen; LIN Sheng; YANG Yongchun; SHI Jiangong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . Cis-3-isobutyl-tetrahydroimidazo[1,2-a]pyridine-2,5-dione C11H18O2N2 ÏàËÆ¶È:72.7% Journal of Asian Natural products Research 2010 12 331-333 A new alkaloid from the stem of Sparganium stoloniferum Buch.-Ham Shu-Xian Li; Feng Wang; Xiao-Hui Deng; Sheng-Wang Liang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . Cyclo-(Leu-Pro) ÏàËÆ¶È:72.7% Chemistry of Natural Compounds 2010 46 828-830 Secondary metabolites from green algae Ulva pertusa Chang-Yun Wang, Lei Han, Kai Kang, Chang-Lun Shao and Yu-Xi Wei, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . cyclo(L-Leu-L-Pro) C11H18N2O2 ÏàËÆ¶È:72.7% Bioorganic & Medicinal Chemistry 2012 20 2002-2009 Cyclic dipeptides exhibit potency for scavenging radicals Tadashi Furukawa, Takashi Akutagawa, Hitomi Funatani, Toshikazu Uchida, Yoshihiro Hotta, Masatake Niwa, Yoshiaki Takaya Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . cyclo(L-Pro-L-Leu) ÏàËÆ¶È:72.7% Heterocycles 2013 87 1537-1543 Whitmanoside A, a New ¦Á-Pyrone Glycoside from the Leech Whitmania pigra Tao Li, Guo-Cai Wang,* Xiao-Jun Huang, and Wen-Cai Ye* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . Perhydrospiro[4H-pyrrolo[1,2-a]pyrazine-3,4'-(4'H)thiopyran]-1,4-dione C11H16N2O2S ÏàËÆ¶È:72.7% Heterocycles 2004 64 417-435 Synthesis of Perhydropyrrolo[1,2-a]pyrazine-1,4-diones and Their Sulfur-Analogues by Ring-Enlargement of N-(2H-Azirin-3-yl)-L-prolinates Artur Budzowski, Anthony Linden, and Heinz Heimgartner* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . cyclo-(S-Pro-S-Leu) ÏàËÆ¶È:72.7% Journal of Zhejiang University of Technology 2014 42 487-490 Researches on the secondary metabolites of marine-derived fungus Mucor circinelloides MNP 12010102 WANG Hong, FENG Yu-mei, WU Qi-hao, ZHAO Mei-rong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 14 ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 1992 30 183-185 13C NMR chemical shift assignments for substituted 2-azabicyclo[3.3.1] nonan-7-ones N¨²ria Casamitjana, Josep Bonjoch, Jordi Gr¨¤cia and Joan Bosch Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . cyclo-(L-prolyl-L-lecine) ÏàËÆ¶È:63.6% Natural Product Research 1995 6 241-246 Three Diketopiperazines from the Cultivated Fungus Fusarium oxysporum Angel Trigos; Silvia Reyna; Lourdes Cervantes Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . cyclo[L-(4-hydroxyprolinyl)-D-leucine] C11H19N2O3 ÏàËÆ¶È:63.6% Natural Product Research 1998 11 271-278 Plant Growth Promoters Isolated from a Marine Bacterium Associated with Palythoa sp John M. Cronan Jr.; Tammy R. Davidson; Fred L. Singleton; Rita R. Colwell; John H. Cardellina II Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 14 ÏàËÆ¶È:63.6% Tetrahedron Letters 2002 43 7565-7568 Asymmetric synthesis of myrioxazines A and B, novel alkaloids of Myrioneuron nutans Van Cuong Pham, Akino Jossang, Ang¨¨le Chiaroni, Thierry S¨¦venet, Bernard Bodo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . (5R,9R,10S)-decahydroquinolin-9-yl]methanol C10H19NO ÏàËÆ¶È:63.6% The Journal of Organic Chemistry 2008 73 7565-7573 Structure and Total Synthesis of (− -Myrionidine and (− -Schoberine, Antimalarial Alkaloids from Myrioneuron nutansVan Cuong Pham, Akino Jossang, Philippe Grellier, Thierry Sevenet, Van Hung Nguyen and Bernard Bodo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . trans-8-acetamido-o-menthone ÏàËÆ¶È:63.6% Russian Journal of Organic Chemistry 2006 42 1141-1145 Verbanone in the synthesis of amidoketones from o-menthane series S. S. Koval¡¯skaya, N. G. Kozlov and A. V. Tkachev Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . trans-2-(propylthio)cyclohexyl acetate C11H20O2S ÏàËÆ¶È:63.6% Tetrahedron 2012 68 2728-2735 Enantioselective oxysulfenylation and oxyselenenylation of olefins catalyzed by chiral Brønsted acids Huan Guan, Haining Wang, Deshun Huang, Yian Shi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-02-06 21:31:46














»Ø¸´´ËÂ¥
-Myrionidine and (−