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meitianyxs°æÖ÷
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| 13C NMR (101 MHz, MeOD) ¦Ä: 10.0, 12.9, 22.6, 23.5, 28.7, 30.2, 38.7, 53.9, 54.3, 55.0, 55.3, 60.1, 61.1, 67.7, 69.9, 71.3, 71.5, 72.4, 73.5, 76.4, 76.7, 85.7,85.8, 86.0, 101.5, 102.8, 109.6, 111.0, 114.7, 116.2, 118.6, 119.3, 128.4, 131.0, 132.1, 132.3, 134.6, 136.1, 137.6, 145.8, 145.9, 147.7, 149.0, 153.1, 167.9. |
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meitianyxs: ½ð±Ò+20, ¡ï¡ï¡ïºÜÓаïÖú 2014-07-02 21:16:39
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meitianyxs: ½ð±Ò+20, ¡ï¡ï¡ïºÜÓаïÖú 2014-07-02 21:16:39
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½13¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . coniferyl alcohol ÏàËÆ¶È:57.7% Phytochemistry 2009 70 147-155 On the role of the monolignol ¦Ã-carbon functionality in lignin biopolymerization Anders Holmgren, Magnus Norgren , Liming Zhang , Gunnar Henriksson Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . triallyl Et 770 C49H54N4O10S ÏàËÆ¶È:57.4% Bioorganic & Medicinal Chemistry 2011 19 4421-4436 Chemistry of ecteinascidins. Part 3: Preparation of 2'-N-acyl derivatives of ecteinascidin 770 and evaluation of cytotoxicity Panithi Saktrakulkla, Satoru Toriumi, Mitsuhiro Tsujimoto, Chamnan Patarapanich, Khanit Suwanborirux, Naoki Saito Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 18,6'-O-Bisallyl Et 770 C46H50N4O10S ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry 2011 19 4421-4436 Chemistry of ecteinascidins. Part 3: Preparation of 2'-N-acyl derivatives of ecteinascidin 770 and evaluation of cytotoxicity Panithi Saktrakulkla, Satoru Toriumi, Mitsuhiro Tsujimoto, Chamnan Patarapanich, Khanit Suwanborirux, Naoki Saito Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . respinomycin D C51H70N2O22 ÏàËÆ¶È:52% The Journal of Antibiotics 1993 46 942-951 RESPINOMYCINS A1, A2, B, C AND D, A NOVEL GROUP OF ANTHRACYCLINE ANTIBIOTICS II. PHYSICO-CHEMICAL PROPERTIES AND STRUCTURE ELUCIDATION MAKOTO UBUKATA, JUN UZAWA, HIROYUKI OSADA, KIYOSHI ISONO Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . jolkinin C47H36O34 ÏàËÆ¶È:51.1% Journal of Natural Products 2004 67 1018-1022 Structure and Biogenesis of Jolkinin, a Highly Oxygenated Ellagitannin from Euphorbia jolkinii Seung-Ho Lee, Takashi Tanaka, Gen-ichiro Nonaka, and Itsuo Nishioka Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . jolkinin C47H36O34 ÏàËÆ¶È:51.1% Korean Journal of Pharmacognosy 2005 36(1) 9-16 Isolation of 5¦Á-reducise Inhibitors from Euphorbia jolkinii Park, Sung-Hee; Kim, Jeong-Ah; Xu, Guang-Hua; Lee, Chong-Gu; Choi, Ji-Young; Oh, In-Suk; Son, Ae-Ryang; Chung, See-Ryun; Lee, Seung-Ho Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Zanthpodocarpins B C41H44O14 ÏàËÆ¶È:51.1% Bioorganic & Medicinal Chemistry Letters 2011 21 373-376 Two dimeric lignans with an unusual a,¦Â-unsaturated ketone motif from Zanthoxylum podocarpum and their inhibitory effects on nitric oxide production Xiao-Jiang Zhou, Xiao-Liang Chen, Xue-Song Li, Jia Su, Jiang-Bo He, Yue-Hu Wang, Yan Li,Yong-Xian Cheng Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . PF-1042 C45H55O16 ÏàËÆ¶È:51.1% The Journal of Antibiotics 1996 49 596-598 Discovery of Saricandin, a Novel Papulacandin, from a Fusarium Species RANDAL H. CHEN, SHAUN TENNANT, DAVID FROST, MICHAEL J. O'BEIRNE, JAMES P. KARWOWSKI, PATRICK E. HUMPHREY, LI-HONG MALMBERG, WON CHOI, KIM D. BRANDT, PAUL WEST, SUNIL K. KADAM, JACOB J. CLEMENT, JAMES B. MCALPINE Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . furanocandin C45H64O17 ÏàËÆ¶È:51.1% The Journal of Antibiotics 1996 49 599-602 Structure of Furanocandin, a New Antifungal Antibiotic from Tricothecium sp. EMIKO MAGOME, KENZO HARIMAYA, SHUICHI GOMI, MASAO KOYAMA, NORIKO CHIBA, KUNIHIKO OTA, TAKASHI MIKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . di-p-bromobenzoate ÏàËÆ¶È:51.0% Chemical & Pharmaceutical Bulletin 1990 38 2409-2418 Marine Natural Products. XXII. : The Absolute Stereostructure of Swinholide A, a Potent Cytotoxic Dimeric Macrolide from the Okinawan Marine Sponge Theonella swinhoei Motomasa KOBAYASHI,Jun-ichi TANAKA,Taketo KATORI,Miki MATSUURA,Megumi YAMASHITA and Isao KITAGAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . oleoacetoside C46H58O25 ÏàËÆ¶È:50% Journal of the Chinese Chemical Society 1996 43 171-176 Secoiridoid Glycosides from Jasminum Polyanthum ÉòÑž´(Ya-Ching Shen);ÁÖÉÙÁê(Shao-Ling Lin);Öx«˜ÎÄ(Pei-Wen Hsieh);º†Ö¾ÖÒ(Chyh-Chung Chein) Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . NeoC-1027 Chr-I C43H46N3O13Cl ÏàËÆ¶È:50% The Journal of Antibiotics 1999 52 415-421 C-1027 Enediyne Chromophore: Presence of Another Active Form and Its Chemical Structure TOSHIO OTANI, KEN-ICHIRO YOSHIDA, TORU SASAKI, YOSHINORI MINAMI Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 3 C46H48O17 ÏàËÆ¶È:50% Journal of Agricultural and Food Chemistry 2007 55 6460-6465 Inhibitory Activity against Tobacco Mosaic Virus (TMV) Replication of Pinoresinol and Syringaresinol Lignans and Their Glycosides from the Root of Rhus javanica var. roxburghiana Ming-An Ouyang, Yung-Shung Wein, Zhen-Kun Zhang, and Yueh-Hsiung Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2014-06-30 20:11:59
meitianyxs
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3Â¥2014-07-02 21:16:46
wangkaibo123
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ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
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- ×¢²á: 2012-10-26
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4Â¥2014-07-02 22:19:28














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