| ²é¿´: 281 | »Ø¸´: 1 | |||
zhjy12345½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
Çó΢Æ×²éÒ»»¯ºÏÎï
|
| 13C NMR (101 MHz, DMSO) ¦Ä 9.77, 11.95, 28.45, 50.49, 56.22, 61.25, 70.40, 73.67, 74.07, 76.82, 77.34, 98.84, 99.62, 105.77, 119.82, 121.00, 125.97, 127.02, 129.06, 130.58, 142.57, 148.84, 149.33, 153.51, 155.01, 160.49, 199.00 |
» ²ÂÄãϲ»¶
085600²ÄÁÏÓ뻯¹¤329·ÖÇóµ÷¼Á
ÒѾÓÐ9È˻ظ´
283Çóµ÷¼Á 086004¿¼Ó¢¶þÊý¶þ
ÒѾÓÐ5È˻ظ´
ÉúÎïѧµ÷¼Á
ÒѾÓÐ5È˻ظ´
ũѧ0904 312Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
¸´ÊÔµ÷¼Á
ÒѾÓÐ9È˻ظ´
²ÄÁÏÓ뻯¹¤µ÷¼Á
ÒѾÓÐ35È˻ظ´
µ÷¼ÁÇóÊÕÁô
ÒѾÓÐ10È˻ظ´
Ò»Ö¾Ô¸¹þ¹¤´ó 085600 277 12²Ä¿Æ»ùÇóµ÷¼Á
ÒѾÓÐ18È˻ظ´
0831ÉúÒ½¹¤µÚÒ»ÂÖµ÷¼Áʧ°ÜÇóÖú
ÒѾÓÐ9È˻ظ´
ÉúÎïѧ308Çóµ÷¼Á£¨Ò»Ö¾Ô¸»ª¶«Ê¦´ó£©
ÒѾÓÐ6È˻ظ´
¶þÂȼ×Íé
½ð³æ (ÕýʽдÊÖ)
- Ó¦Öú: 105 (¸ßÖÐÉú)
- ½ð±Ò: 2190.7
- É¢½ð: 1870
- ºì»¨: 15
- Ìû×Ó: 538
- ÔÚÏß: 120.8Сʱ
- ³æºÅ: 1337209
- ×¢²á: 2011-07-04
- ÐÔ±ð: GG
- רҵ: ÌìȻҩÎﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
jiangchunyong: ½ð±Ò+1, лл 2012-07-03 15:55:28
zhjy12345: ½ð±Ò+15 2012-07-04 12:47:13
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
jiangchunyong: ½ð±Ò+1, лл 2012-07-03 15:55:28
zhjy12345: ½ð±Ò+15 2012-07-04 12:47:13
|
. compound 6 C32H40N2O12 ÏàËÆ¶È:80.6% Journal of the Chemical Society, Perkin Transactions 1 1995 583-587 Constituents of Nothapodytes foetida Angela Pirillo, Luisella Verotta, Pierluigi Gariboldi, Elisabetta Torregiani and Ezio Bombardelli Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 3 ÏàËÆ¶È:74.0% Journal of the Chemical Society, Perkin Transactions 1 1995 583-587 Constituents of Nothapodytes foetida Angela Pirillo, Luisella Verotta, Pierluigi Gariboldi, Elisabetta Torregiani and Ezio Bombardelli Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 4 ÏàËÆ¶È:64.5% Journal of the Chemical Society, Perkin Transactions 1 1995 583-587 Constituents of Nothapodytes foetida Angela Pirillo, Luisella Verotta, Pierluigi Gariboldi, Elisabetta Torregiani and Ezio Bombardelli Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . tetrasweroside B C26H30O15 ÏàËÆ¶È:62.9% Chinese Chemical Letters 2001 12 433-434 Two New Xanthone Glycosides from Swertia Tetraptera Zhi Xin LIAO, Yu Lin LI, Ming Kui WANG, Li Sheng DING,Yao Zu CHEN Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 5 C25H28N2O8 ÏàËÆ¶È:59.2% Journal of the Chemical Society, Perkin Transactions 1 1995 583-587 Constituents of Nothapodytes foetida Angela Pirillo, Luisella Verotta, Pierluigi Gariboldi, Elisabetta Torregiani and Ezio Bombardelli Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . effuside I C24H30O8 ÏàËÆ¶È:55.5% Phytochemistry 1995 40 533-535 Effusides I-V: 9, 10-dihydrophenanthrene glucosides from Juncus effusus Marina Della Greca, Antonio Fiorentino, Pietro Monaco, Lucio Previtera, Armando Zarrelli Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . henryoside ÏàËÆ¶È:55.5% Phytochemistry 1993 33 161-164 Two phenolic glucosides and an iridoid glucoside from Alangium platanifolium var. Trilobum Atsuko Itoh, Takao Tanahashi, Naotaka Nagakura Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . isoirigenin 7-O-¦Â-D-glucoside ÏàËÆ¶È:55.5% Chinese Pharmaceutical Journal 2006 41 1133-1135 Studies on Chemical Constituents of Belamcanda chinensis QIU Ying-kun, GAO Yu-bai, XU Bi-xia, LIU Ke Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . OPHR-17 ÏàËÆ¶È:55.5% Tetrahedron 2002 58 9169-9178 Camptothecin-related alkaloids from hairy roots of Ophiorrhiza pumila Mariko Kitajima, Satoshi Yoshida, Kyoko Yamagata, Mio Nakamura, Hiromitsu Takayama, Kazuki Saito, Hiroko Seki, Norio Aimi Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 10-O-coumaroyl-10-O-deacetyldaphylloside C26H30O13 ÏàËÆ¶È:51.8% Helvetica Chimica Acta 2006 Vol. 89 884 Study on the Chemical Constituents of Daphniphyllum angustifolium Haiyun Bai and Lihong Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . tetra-O-methylcurcapicycloside C27H34O11 ÏàËÆ¶È:51.8% Journal of Natural Products 1999 62 734-739 Three Novel Constituents from Curculigo capitulata and Revision of C-2 Stereochemistry in Nyasicoside Wen-Liang Chang, Chung-Hsiung Chen, and Shoei-Sheng Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . rhaponticin 2''-O-gallate C28H28O13 ÏàËÆ¶È:51.8% Chemical & Pharmaceutical Bulletin 1984 32 3501-3517 Studies on Rhubarb (Rhei Rhizoma). VI. Isolation and Characterization of Stilbenes YOSHIKI KASHIWADA,GENICHIRO NONAKA and ITSUO NISHIOKA Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 7-{[2-({[(1E)-2-(1H-Benzimidazol-1-yl)-1-phenylethylidene]amino}oxy)ethoxy]methyl}-1,3-dimethyl- 3,7-dihydro-1H-purine-2,6-dione C25H25N7O4 ÏàËÆ¶È:51.8% Helvetica Chimica Acta 2009 92 1760-1774 Design and Synthesis of Some Novel Oxiconazole-Like Carboacyclic Nucleoside Analogues, as Potential Chemotherapeutic Agents Mohammad Navid Soltani Rad, Ali Khalafi-Nezhad, Somayeh Behrouz Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 8-[3-(2,4-benzenediol)-propionic acid methyl ester]-coumarin-7-¦Â-D-glucoside C25H28O12 ÏàËÆ¶È:51.8% Natural Product Research 2009 23 1259-1264 Two new coumarins from Edgeworthia chrysantha Xiao-Jia Hu; Hui-Zi Jin; Wei-Dong Zhang; Wei Zhang; Shi-Kai Yan; Run-Hui Liu; Yun-Heng Shen; Wen-Zheng Xu Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 2,3,7-trimethoxy-1-O-primeverosyloxyxanthone ÏàËÆ¶È:51.8% China Journal of Chinese Materia Medica 2009 34 580-582 Xanthone glycosides from Tibetan herb Halenia elliptica LIU Xia, LIU Yong, SHI Yanping Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . schachristanoside C26H28O13 ÏàËÆ¶È:51.8% Chemistry of Natural Compounds 2011 Vol. 47, No. 4 547-549 A NEW FLAVONE GLYCOSIDE FROM THE AERIAL PART OF Scutellaria schachristanica Z. O. Tashmatov, K. A. Eshbakova,and Kh. M. Bobakulov Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 5,7,2'-trihydroxy-8-methoxyflavone 2'-O-¦Â-D-glucopyranoside C22H22O11 ÏàËÆ¶È:51.8% Chemical & Pharmaceutical Bulletin 2006 54 435-441 Studies on the Constituents of Scutellaria Species (XXII). Constituents of the Roots of Scutellaria amabilis HARA Yukinori Miyaichi, Eiji Hanamitsu, Haruhisa Kizu and Tsuyoshi Tomimori Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . henryoside C26H32O15 ÏàËÆ¶È:51.8% Phytochemistry 1989 28 3197-3200 Alangifolioside,a diphenylmethylene derivative,and other phenolics from the leaves of Alangium platanifolium var. trilobum Hideaki Otsuka,Kazuo Yamasaki,Tatsuo Yamauchi Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (+/-)O-benzylmappicine C26H24N2O ÏàËÆ¶È:51.8% Journal of Heterocyclic Chemistry 2003 40 601-605 Synthesis of (+/-) mappicine and mappicine ketone Kevin E. Henegar and Ted A. Baughman Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 5-hydroxy-6-methyl-2'-methoxy-[6'',6''-dimethylpyrano(2'',3'':7,8)][6''',6'''-dimethyl-pyrano(2''',3''':4',5')]-(2S)?avonone C27H28O6 ÏàËÆ¶È:51.8% Bioorganic & Medicinal Chemistry Letters 2007 17 6311-6315 A novel flavonoid from Lespedeza virgata (Thunb.) DC.: Structural elucidation and antioxidative activity Li Tan, Xiu-Feng Zhang, Bao-Zhen Yan, Hai-Ming Shi, Li-Bo Du, Ya-Zhou Zhang, Lan-Fen Wang, Ya-Lin Tang, Yang Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . rhodiosin ÏàËÆ¶È:51.8% Chinese Traditional and Herbal Drugs 1995 26 177-179+223 Studies on the Chemical Constituents Bigflower Rhodiola (Rhodiola crenulata) Peng Jiangnan; Ma Chengyu; Ge Yongchao; et al (Institute of Radiation Medicine; Academy of Military Medical Sciences; Beijing); Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . quercetin-3,7-di-O-¦Â-D-glucopyranoside ÏàËÆ¶È:51.8% Archives of Pharmacal Research 1999 22 81-85 Antioxidative flavonoids from the leaves of Morus alba Sun Yeou Kim, Jian Jun Gao, Won-Chu Lee, Kang Sun Ryu and Kang Ro Lee, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . herbacet in 7-O-(3''-O-¦Â-D-D-glucopyranosyl)-¦Á-L-rhamnopyranoside ÏàËÆ¶È:51.8% Journal of Shenyang Pharmaceutical University 2007 24 402-406 Chemical constituents of Rhodiola rosea L. and the inhibitiory effect on UV-induced A375-S2 cell death WANG Fang-yu, LI Dan, HAN Zhi-chao, GAO Hui-yuan, WU Li-jun Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 9-¦Â-D-glucosyloxycamptothecin C26H26N2O10 ÏàËÆ¶È:51.8% Journal of the Chemical Society, Perkin Transactions 1 1998 389-390 Synthesis and absolute configuration of 9-¦Â-D-glucosyloxycamptothecin, a new gluco camptothecin isolated from Ophiorrhiza pumila regenerated plants Mariko Kitajima, Mio Nakamura, Akihito Watanabe, Hiromitsu Takayama and Norio Aimi Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . kaempferol-3,7-di-O-¦Â-D-glucopyranoside ÏàËÆ¶È:51.8% Food Chemistry 2009 115 592-595 Novel acetylated flavonoid glycosides from the leaves of Allium ursinum Hou Wu, Slavik Dushenkov, Chi-Tang Ho, Shengmin Sang Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . 10-O-p-Coumaroyl-10-O-deacetyldaphylloside C26H30O13 ÏàËÆ¶È:51.8% Chemical & Pharmaceutical Bulletin 2009 57 765-796 Naturally Occurring Iridoids, Secoiridoids and Their Bioactivity. An Updated Review, Part 3 Biswanath DINDA,* Debashis ROY CHOWDHURY, and Bikas Chandra MOHANTA Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . Phlomoidoside (6-O-(4'-O-p-Coumaroyl-¦Â-D-xylopyranosyl)-aucubin) C29H36O15 ÏàËÆ¶È:51.8% Chemical & Pharmaceutical Bulletin 2007 55 159-222 Naturally Occurring Iridoids. A Review, Part 1 Biswanath DINDA, Sudhan DEBNATH and Yoshihiro HARIGAYA Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . rhamnazin-3,4'-di-O-glucoside ÏàËÆ¶È:51.7% Chemical & Pharmaceutical Bulletin 1989 37 1300-1303 Studies on the Constituents of the Japanese Mistletoe, Viscum album L. var. coloratum OHWI Grown on Different Host Trees Takehiko FUKUNAGA,Ikuko KAJIKAWA,Koichi NISHIYA,Koichi TAKEYA and Hideji ITOKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . Herbacetin-3-sophoroside-8-¦Â-glucoside C33H40O22 ÏàËÆ¶È:51.7% Chemistry of Natural Compounds 2011 Vol. 47, No. 3 363-365 FERULOYL, CAFFEOYL, AND FLAVONOL GLUCOSIDES FROM Equisetum hyemale Byoung-Jae Park and Matsuta Tomohiko Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . compound XXVII ÏàËÆ¶È:51.7% Chinese Traditional and Herbal Drugs 1997 28 517-522 Flavonoids from Stringy Stonecrop (Sedum sarmentosum) He Aimin; Wang Mingshi (He Aimin; China Pharmaceutical University; Nanjing); Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . demethoxy egonol gentiobioside C30H36O14 ÏàËÆ¶È:50% Fitoterapia 2007 78 211-214 2-Aryl benzofurans and their derivatives from seeds of Styrax macranthus Yinggang Luo , Zhiheng He , Hongjuan Li Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2012-07-03 14:56:34













»Ø¸´´ËÂ¥
5