| ²é¿´: 228 | »Ø¸´: 1 | ||
mojiaoliгæ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
| 20.9,38.2,39.1,51.3,56.8,66.3,127.7,127.9,128.6,129.6,129.6,129.6,130.4,130.5,133.0,135.4,138.6,139.1,170.1,172.7,173.4 |
» ²ÂÄãϲ»¶
0703×Ü·Ö331Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
085600£¬321·ÖÇóµ÷¼Á
ÒѾÓÐ7È˻ظ´
325Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
085600£¬320·ÖÇóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Ò»Ö¾Ô¸0817»¯Ñ§¹¤³ÌÓë¼¼Êõ£¬Çóµ÷¼Á
ÒѾÓÐ27È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤085600 310·ÖÇóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸¹þ¶û±õ¹¤Òµ´óѧ085600Ó¢Ò»Êý¶þ337·ÖÇóµ÷¼Á
ÒѾÓÐ10È˻ظ´
22408Çóµ÷¼Á 354·Ö ¿É¿çרҵ
ÒѾÓÐ3È˻ظ´
277¹¤¿ÆÇóµ÷¼Á
ÒѾÓÐ4È˻ظ´
Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á£¬326·Ö
ÒѾÓÐ3È˻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
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
1 . trichosanatine C27H28N2O4 ÏàËÆ¶È:85.7% Acta Pharmaceutica Sinica 1995 30 517-520 STRUCTURE DETERMINATION OF TRICHOSANATINE FROM TRICHOSANTHES ROSTHORNII ZM Chao and JM Liu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . aurantiamide acetate ÏàËÆ¶È:85.7% Journal of Shenyang Pharmaceutical University 2011 28 364-367 Isolation and identification of chemical constituents of root of Girardinia suborbiculata C. J. Chen subsp. Triloba FENG Bao-min, LIU Jing-yan, WANG Hui-guo, SHI Li-ying, TANG Ling, WANG Yong-qi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . aurantiamide acetate C27H28N2O4 ÏàËÆ¶È:85.7% Molecules 2012 17 13673-13686 Chemical Constituents from Stem Bark and Roots of Clausena anisata Jules Lobe Songue, Kouam, Etienne Dongo, Theophile Ngando Mpondo and Robert L. White Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . trichosanatine ÏàËÆ¶È:85.7% Chemistry of Natural Compounds 2013 49 983-984 Chemical Constituents of Dioscorea collettii var. hyplauca G. M. She, X. Xiao, Y. Y. Ba, R. B. Shi, L. Z. Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . aurantiamide acetate ÏàËÆ¶È:80.9% Journal of Chinese Medicinal Materials 2009 32 1220-1223 Studies on the Chemical Constituents of the Fruit of Xylocarpus granatum CHENG Fan, ZHOU Yuan, ZOU Kun, WU Jun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . N-(N-3''-chloro-benzoyl-L-phenylalanyl)-L-phenylalanol C25H25ClN2O3 ÏàËÆ¶È:76.1% Bioorganic & Medicinal Chemistry 2009 17 3118-3125 Synthesis and anti-hepatitis B virus activities of Matijing-Su derivatives Bixue Xu, Zhengming Huang, Changxiao Liu, Zegui Cai, Weidong Pan, Peixue Cao, Xiaojiang Hao, Guangyi Liang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . aurantiamide acetate ÏàËÆ¶È:76.1% Pharmaceutical and Clinical Research 2014 22 339-341 Non-Steroidal Constituents from the Leaves of Dregea volubilis LI Jia, ZHAO Ceng, ZHANG Chao-feng, ZHANG Mian Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 19 ÏàËÆ¶È:71.4% Molecules 2004 9 349-364 Polymer-Supported Cinchona Alkaloid-Derived Ammonium Salts as Recoverable Phase-Transfer Catalysts for the Asymmetric Synthesis of ¦Á-Amino Acids Rafael Chinchilla, Patricia Maz¨®n and Carmen N¨¢jera Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . methyl 2-(4-chlorophenyl)-3-(4-methoxyphenyl)-1-oxo-1,2,3(RS),4-(SR),4a(SR),7,8,8a(SR)-octahydroisoquinoline-4-carboxylate C24H24ClNO4 ÏàËÆ¶È:71.4% European Journal of Organic Chemistry 2011 2697-2704 ¦Â-Lactam-Synthon-Interceded, Facile, One-Pot, Diastereoselective Synthesis of Functionalized Tetra/Octahydroisoquinolone Derivatives Raghu Raj, Vishu Mehra, Pardeep Singh, Vipan Kumar, Gaurav Bhargava, Mohinder P. Mahajan, Sachin Handa and LeGrande M. Slaughter Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . asperphnamate C32H30N2O4 ÏàËÆ¶È:71.4% Journal of Chinese Medicinal Materials 2008 31 1343-1347 Studies on the Anti-tumor Activity Principles of a Marine-derived Fungus BZYT-21 GAO Zong-hua, MA Li-ying, SHEN Yun-xiu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 20 ÏàËÆ¶È:66.6% Canadian Journal of Chemistry 2006 84 1487-1503 An examination of VANOL, VAPOL, and VAPOL derivatives as ligands for asymmetric catalytic Diels-Alder reactions1 Douglas P. Heller, Daniel R. Goldberg, Hongqiao Wu, and William D. Wulff Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . Methyl-2-(3-[2-(5-benzyl-4-phenyl-4H-[1,2,4]triazol-3-thio)-acetylamino]-propionylamino)-acetate C23H25N5O4S ÏàËÆ¶È:66.6% Molecules 2010 15 6759-6772 Convenient Synthesis and Antimicrobial Activity of Some Novel Amino Acid Coupled Triazoles S. M. El Rayes Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . Compond 6b ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 2003 41 193-201 1H, 13C, 17O NMR and quantum-chemical study of the stereochemistry of the sulfoxide and sulfone derivatives of 3-arylidene-1-thioflavan-4-one epoxides J¨®zsef Kov¨¢cs, G¨¢bor T¨®th, Andr¨¢s Simon, Albert L¨¦vai, Andreas Koch and Erich Kleinpeter Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 7a ÏàËÆ¶È:66.6% Tetrahedron Letters 2004 45 4755-4758 Crystallization-induced asymmetric transformation. Application to conjugate addition of benzylamine to amides of benzoylacrylic acid Pavol Jakubec, Dušan Berkeš, František Považanec Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . (S,S,R)-1-(2-(N-Morpholinocarbonyl)amino-2-benzyl-lhydroxypropyl)-N-methyl-N-benzylaminobenzoylimide ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry 1996 4 1545-1558 A new class of HIV-1 protease inhibitor: The crystallographic structure, inhibition and chemical synthesis of an aminimide peptide isostere Earl E. Rutenber, Fiona McPhee, Alan P. Kaplan, Steven L. Gallion, Joseph C. Hogan Jr., Charles S. Craik, Robert M. Stroud Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-03-26 14:40:07














»Ø¸´´ËÂ¥