| ²é¿´: 348 | »Ø¸´: 1 | ||
fuxuetengгæ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú£¬¼±£¬Ð»Ð»¡£¡£¡£¡£ ÒÑÓÐ1È˲ÎÓë
|
| 109.88£¬110.77£¬115.59£¬116.16,121.35,123.73,125.33,127.17,131.43,146.19,149.41,151.82,152.68,152.83,195.50,196.52 |
» ²ÂÄãϲ»¶
071000ÉúÎïѧµ÷¼ÁÇóÖú
ÒѾÓÐ14È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ9È˻ظ´
277Çóµ÷¼Á
ÒѾÓÐ19È˻ظ´
344Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
»¯¹¤µ÷¼ÁÇóµ¼Ê¦ÊÕÁô£¡Ò»Ö¾Ô¸Ê§Àû£¬Ì¤Êµ¿Ï¸É£¬ÓÐÖ²ÎïÌáÈ¡¿ÆÑоÀú
ÒѾÓÐ13È˻ظ´
Ò»Ö¾Ô¸Î÷½»»úеר˶Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
277 ÊýÒ»104£¬Ñ§Ë¶£¬Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
Çóµ÷¼Á ²ÄÁÏÓ빤³Ì 324·Ö ר˶
ÒѾÓÐ17È˻ظ´
342µç×ÓÐÅϢר˶Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
0835ѧ˶299Çóµ÷¼Á 08´óÀà¿É½ÓÊÜ
ÒѾÓÐ7È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬¼±¼±¼±£¬Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
HETEROCYCLESͶ¸åÇóÖú
ÒѾÓÐ9È˻ظ´
½âÆ×ÇóÖú£¨Ö»ÓÐ̼Æ×£©£¬Ð»Ð»ÁË¡£
ÒѾÓÐ3È˻ظ´
ÇóÖú¡¢¡¢¡¢Ð»Ð»´óÉñ
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
¼±¼±¼±£¡ºË´ÅCÆ×ÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú¦Á-¼×»ù±½ÒÒÏ©Óë¹ýÁ¿±½·ÓÔÚÁòËá¼ÓÈÈÌõ¼þÏ·¢Éúʲô·´Ó¦£¿
ÒѾÓÐ5È˻ظ´
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻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´
¼±¼±¼±¡£¡£¡£¡£ÇóÖú΢Æ×Êý¾Ý£¨50%ÏàËÆ¶È¾ÍOKÁË£©£¬²»Ê¤¸Ðл£¡
ÒѾÓÐ8È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
ÇóÖú΢Æ×²éѯ½âÆ×
ÒѾÓÐ5È˻ظ´
Records of Natural Products
ÒѾÓÐ7È˻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
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
fuxueteng: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-01-31 23:10:24
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
fuxueteng: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-01-31 23:10:24
|
²éѯ½á¹û£º¹²²éµ½631¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (4-hydroxyphenyl)-3',4'-dimethoxyacetophenone C16H16O4 ÏàËÆ¶È:62.5% Journal of Natural Products 1994 Vol 57 1136 A Versatile Approach to the Synthesis of Combretastatins Manuel Medarde, Rafael Pel¨¢ez-Lamami¨¦ de Clairac, Jose Luis L¨®pez, Arturo San Feliciano Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 21-methyl ellipticine ÏàËÆ¶È:62.5% Tetrahedron 1978 34 2385-2388 ¨¦tude par rm13c d'alcaloïdes ¨¤ squelette acridinone 9(10h) et pyrido(4,3b) carbazole(6h) Alain Ahond, Christiane Popat, Pierre Potier Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 1-(2-fluorophenyl)-3-(2-hydroxy-4-nitrophenyl)urea C13H10FN3O4 ÏàËÆ¶È:62.5% Bioorganic & Medicinal Chemistry 2009 17 8102-8112 Structural optimization of a CXCR2-directed antagonist that indirectly inhibits ¦Ã-secretase and reduces A¦Â Pancham Bakshi, Chao Jin, Pierre Broutin, Beniam Berhane, Jon Reed, Michael Mullan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . N-(3,4-difluorophenyl)-3-hydroxy-2-naphthamide C17H11F2NO2 ÏàËÆ¶È:62.5% Bioorganic & Medicinal Chemistry 2012 20 6811-6820 Structure¨Cactivity relationship studies of naphthol AS-E and its derivatives as anticancer agents by inhibiting CREB-mediated gene transcription Bingbing X. Li, Kinrin Yamanaka, Xiangshu Xiao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 3-(3,4-Dimethoxyphenyl)-4-(4'-methoxyphenyl)cyclobut-3-ene-1,2-dione C19H16O5 ÏàËÆ¶È:62.5% European Journal of Medicinal Chemistry 2013 65 187-194 Synthesis and antitumor activity of novel 3,4-diaryl squaric acid analogs Original Research Article Zong-ying Liu, Yue-ming Wang, Yan-xing Han, Ling Liu, Jie Jin, Hong Yi, Zhuo-rong Li, Jian-dong Jiang, David W. Boykin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 1-(3,4-Dimethoxybenzoyl)chromeno[3,4-c]pyrazol-4(3H)-one C19H14N2O5 ÏàËÆ¶È:62.5% Tetrahedron 2014 70 9321-9329 One-pot synthesis of polyfunctional pyrazoles: an easy access to ¦Á-diazoketones from arylglyoxal monohydrates and tosylhydrazine Wen-Ming Shu, Jun-Rui Ma, Kai-Lu Zheng, Hui-Ying Sun, Mei Wang, Yan Yang, An-Xin Wu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . crassifogenin B C17H12O6 ÏàËÆ¶È:58.8% Helvetica Chimica Acta 2004 Vol. 87 845 Four New Phenolic Compounds from Curculigo crassifolia (Hypoxidaceae) Ning Li, Ji-Jun Chen, and Jun Zhou Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 2-{N¡ä-[1-(Benzothiazol-2-yliminomethyl)-2-oxo-propylidene]-hydrazino}-benzonitrile C18H13N5OS ÏàËÆ¶È:58.8% Molecules 2007 12 2061-2079 Microwave Assisted Condensation Reactions of 2-Aryl Hydrazonopropanals with Nucleophilic Reagents and Dimethyl Acetylenedicarboxylate Khadijah M. Al-Zaydi and Rita M. Borik Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 62 ÏàËÆ¶È:58.8% Magnetic Resonance in Chemistry 1986 24 225-230 Carbon-13 nuclear magnetic resonance spectra of isoflavones M. Sree Rama Murthy, E. Venkata Rao and R. S. Ward Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . Z-3-(3,4-Dihydroxybenzylidene)-5-(3,4-dihydroxyphenyl)-2(3H)-furanone C17H12O6 ÏàËÆ¶È:58.8% Journal of Natural Products 2011 74 1421-1426 Phenolic Compounds from the Roots of Jordanian Viper's Grass, Scorzonera judaica Ammar Bader, Nunziatina De Tommasi, Roberta Cotugno, and Alessandra Braca Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 4-{[(2-Methoxyphenyl)amino]acetyl}-3,4-dihydroquinoxalin-2(1H)-one C17H17N3O2 ÏàËÆ¶È:58.8% Archives of Pharmacal Research 2011 34 1605-1614 Synthesis of Novel Quinoxalinone Derivatives by Conventional and Microwave Methods and Assessing their Biological Activity Waqar Nasir, Munawar Ali Munawar, Ejaz Ahmed, Ahsan Sharif, Saeed Ahmed, Amjad Ayub, Misbahul Ain Khan, and Faizul Hassan Nasim Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 5-hydroxy-6-methoxycleistopholine C15H11NO4 ÏàËÆ¶È:56.2% Journal of Natural Products 2001 64 240-242 Alkaloids from Porcelia macrocarpa1 Mariana H. Chaves, Luciana de A. Santos, João Henrique G. Lago, and Nidia F. Roque Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 2,5-dihydroxy-3,4-dimethoxyphenanthrene C16H14O4 ÏàËÆ¶È:56.2% Journal of Natural Products 1999 62 1175-1178 New Phenanthrene Derivatives from Maxillaria densa Samuel Estrada, Rub¨¦n A. Toscano, and Rachel Mata Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 6-methyl-6,12-epoxy-6H,12H-dibenzo[b,f][1,5]dioxocin C15H12O3 ÏàËÆ¶È:56.2% Molecules 2009 14 4065-4078 Sulphated Zirconia as an Eco-Friendly Catalyst in Acylal Preparation under Solvent-Free Conditions, Acylal Deprotection Assisted by Microwaves, and the Synthesis of Anhydro-Dimers of o-Hydroxybenzaldehydes Laura N. Palacios-Grijalva, Deysi Y. Cruz-Gonz¨¢lez, Leticia Lomas-Romero, Eduardo Gonz¨¢lez-Zamora, Gerardo Ulibarri and Guillermo E. Negr¨®n-Silva Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . ¦×-baptigenin ÏàËÆ¶È:56.2% China Journal of Chinese Materia Medica 2008 33 1292-1294 Studies on Chemical Constituents of Oxytropis falcata WANG Dong, YANG Huan, DAI Yan-peng, TONG Li, CAI Bao-chang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . trans-2-[3-(3,4-dihydroxyphenylpropenoyl)amino)-3,5-dihydroxybenzoic acid C16H13NO7 ÏàËÆ¶È:56.2% Journal of Natural Products 1994 Vol 57 90 Isolation, Identification, and Synthesis of Miriamides, New Hostmarkers from Eggs of Pieris brassicae Anton Blaakmeer, Andr¨¦ Stork, Albertus van Veldhuizen, Teris A. van Beek, Aede de Groot, Joop J. A. van Loon, Louis M. Schoonhoven Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . Okanin ÏàËÆ¶È:56.2% Korean Journal of Pharmacognosy 2009 40(4) 345-350 Antioxidative and Hepatoprotective Effect of Compounds from the Flowers of Bidens bipinnata L. Kwon, Ji-Wung; Byun, Erisa; Lee, Eoh-Jin; Kim, Youn-Chul; Jeong, Gil-Saeng; An, Ren-Bo; Kwon, Tae-Oh Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . S-2-(4-hydroxyphenyl)-5-(2-hydroxypropyl)-3-methylbenzofuran ÏàËÆ¶È:56.2% Phytochemistry 1989 28 1959-1962 Neolignans and nor-neolignans from Krameria lanceolata Hans Achenbach,Johann Groß,Peter Bauereiß,Xorge A. Dominguez,Humberto Sanchez Vega,Julia Verde Star,Carlos Romboldt Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . 2'-hydroxy-2-aminobenzanilide C13H12N2O2 ÏàËÆ¶È:56.2% Journal of Heterocyclic Chemistry 2010 47 268-271 On the purity of 2-[ortho-anilinyl]-1,3-benzoxazole derived from 2H-3,1-benzoxazine-2,4(1H)dione (isatoic anhydride) [1,2] Karen M. Button, Robert A. Gossage, Hilary A. Jenkins, Tayseer Mahdi and Sanja Resanović Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . 2',4'-dimethyl-2-phenyl-2H-1-benzopyran C17H14O ÏàËÆ¶È:56.2% Heterocycles 2010 82 843-850 Efficient Transformation of Flav-3-enes Using Reductive Elimination of Flav-4-triflate Yoshihito Kohari, Yukio Hoshino, Haruo Matsuyama, and Hiroto Nakano Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . 7,8-Dihydroxy-3-[(3,4-dihydroxyphenyl)methylene]-chro-man-4-one C16H12O6 ÏàËÆ¶È:56.2% Bioorganic & Medicinal Chemistry Letters 2007 17 1288-1290 Synthesis, structural revision, and antioxidant activities of antimutagenic homoisoflavonoids from Hoffmanosseggia intricata Vidavalur Siddaiah, Muchchintala Maheswara, Chunduri Venkata Rao, Somepalli Venkateswarlu, Gottumukkala V. Subbaraju Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-01-30 08:42:51













»Ø¸´´ËÂ¥