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°´´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£º¹²²éµ½558¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 8-methoxypsoralen ÏàËÆ¶È:100% Acta Pharmaceutica Sinica 1993 28 432-436 ISOLATION AND STRUCTURE ELUCIDATION OF QIANHUCOUMARIN A LY Kong; YH Pei; X Li; TR Zhu and T Okuyama Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . xanthotoxin ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2009 34 1231-1234 Coumarins from Peucedanum harry- smithii var. subglabrum LIWen, FENG Shilan, HU Fangdi, CHEN Erlin Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . xanthotoxin C12H8O4 ÏàËÆ¶È:100% Chemical & Pharmaceutical Bulletin 1999 47 96-100 Antiproliferative Constituents from Umbelliferae Plants. V. A New Furanocoumarin and Falcarindiol Furanocoumarin Ethers from the Root of Angelica japonica Toshihiro FUJIOKA,Kazuhiro FURUMI,Hiroko FUJII,Hikaru OKABE,Kunihide MIHASHI,Yukitaka NAKANO,Hisashi MATSUNAGA,Mitsuo KATANO and Masato MORI Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Xanthotoxin C12H8O4 ÏàËÆ¶È:100% Phytochemistry 1998 47 13-16 Psoralen and other linear furanocoumarins as phytoalexins in Glehnia littoralis Takahiro Masuda, Mitsuo Takasugi, Masaki Anetai Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . xanthotoxin C12H8O4 ÏàËÆ¶È:100% Phytochemistry 1987 26 2063-2069 Chromones and coumarins from Skimmia laureola E.S. Waight,T.K. Razdan,B. Qadri,S. Harkar Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . xanthotoxin ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2010 35 58-62 Chemical constituents of Incarvillea younghusbandii FU Yu; BAI Yang; DAWA Zhuoma; BAI Bingru; DING Lisheng Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . xanthotoxin ÏàËÆ¶È:100% Phytochemistry 1979 18 139-143 13 C NMR Chemical shifts and carbon-proton coupling constants of some furocoumarins and furochromones M. H. A. Elgamal, N. H. Elewa, E. A. M. Elkhrisy, Helmut Duddeck Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . xanthotoxin C12H8O4 ÏàËÆ¶È:100% Phytochemistry 1984 23 419-426 Steroids, chromone and coumarins from angelica officinalis S. Harkar, T.K. Razdan, E.S. Waight Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Xanthotoxin ÏàËÆ¶È:100% Archives of Pharmacal Research 2002 25 824-830 Constituents of the fruits and leaves of Euodia daniellii Sang Woo Yoo, Ju Sun Kim, Sam Sik Kang, Kun Ho Son and Hyeun Wook Chang, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Xanthotoxin ÏàËÆ¶È:100% Archives of Pharmacal Research 2004 27 1211-1215 Cytotoxic coumarins from the root of Angelica dahurica Pham Ngoc Thanh, WenYi Jin, GyuYong Song, KiHwan Bae and Sam Sik Kang Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Xanthotoxin ÏàËÆ¶È:100% Archives of Pharmacal Research 2006 29 617-623 Chemical constituents of the root of Dystaenia takeshimana and their anti-inflammatory activity Ju Sun Kim, Jin Cheul Kim, Sang Hee Shim, Eun Ju Lee and Wen Yi Jin, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . xanthotoxin ÏàËÆ¶È:100% Bioscience, Biotechnology, and Biochemistry 2000 64 420-423 Coumarin-related Compounds as Plant Growth Inhibitors from Two Rutaceous Plants in Thailand Suratwadee JIWAJINDA, Vilai SANTISOPASRI, Hajime OHIGASHI Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-07-22 21:47:43
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ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
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ħÁ¦Äñ: ½ð±Ò+15 2013-07-22 23:11:28
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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£º¹²²éµ½669¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . mutisiphenone A C19H26O2 ÏàËÆ¶È:94.7% Zeitschrift f¨¹r Naturforschung C 2003 58 533-540 Antifungal Methylphenone Derivatives and 5-Methylcoumarins from Mutisia friesiana C. I. Viturro, J. R. de la Fuente, and M. S. Maier Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3-(3,7-dimethylocta-2,6-diemyl)-4-hydroxy-2H-chromeme-2-thiome (depremyl thioferulemol) C19H22O2S ÏàËÆ¶È:68.4% Journal of Heterocyclic Chemistry 2007 44 411-418 Cyclization reactions of coumarin derivatives: Chemo-and regioselectivity effects of oxygen/sulfur isosteric replacement Giovanni Palmisano,Lucio Toma,Rita Annunziata,Silvia Tagliapietra,Alessandro Barge and Giancarlo Cravotto Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 1 C36H53O5SNa ÏàËÆ¶È:68.4% Experientia 1987 43 1233-1234 Isolation of a hexaprenylhydroquinone sulfate from the marine spongeDysidea sp. as an H, K-ATPase inhibitor N. Fusetani, M. Sugano, S. Matsunaga, K. Hashimoto and H. Shikama, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 9 ÏàËÆ¶È:66.6% Phytochemistry 1993 34 1603-1607 Sapelenins A, B and C, acyclic triterpenoids from the stem bark of Entandrophragma cylindricum David Ngnokam, Georges Massiot, Jean-Marc Nuzillard, Joseph D. Connolly, Etienne Tsamo, Christophe Morin Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Sesquilavandulal C15H25O ÏàËÆ¶È:66.6% Phytochemistry 2010 71 1545-1557 Irregular sesquiterpenoids from Ligusticum grayi roots Laurence G. Cool, Karl E. Vermillion, Gary R. Takeoka, Rosalind Y. Wong Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . agelasidine-A C18H33N3O2 ÏàËÆ¶È:66.6% Tetrahedron letters 1983 24 4105-4108 Agelasidine-A, a novel sesquiterpene possessing antispasmodic activity from the okinawa sea sponge Agelas sp. Hideshi Nakamura, Houming Wu, Jun'ichi Kobayashi, Yasushi Ohizumi, Yoshimasa Hirata, Tsutomu Higashijima, Tatsuo Miyazawa Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Dimethyl [4,8,12-trimethyl-(E,E)-3,7,11-tridecatrienyl]phosphonate C18H34O3P ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry 1998 6 687-694 Phosphonate and bisphosphonate analogues of farnesyl pyrophosphate as potential inhibitors of farnesyl protein transferase Sarah A Holstein, Diana M Cermak, David F Wiemer, Kriste Lewis, Raymond J Hohl Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (E,E)-5,9,13-Trimethyl-4,8,12-tetradecatrienoic acid ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry 2000 8 2729-2737 2-(Acyloxy)ethylphosphonate analogues of prenyl pyrophosphates: synthesis and biological characterization Diana M. Cermak, David F. Wiemer, Kriste Lewis, Raymond J. Hohl Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Geranyllinaloisocyanide C21H33N ÏàËÆ¶È:66.6% Journal of the Chemical Society, Perkin Transactions 1 1993 2429-2432 Novel, regioselective allylamine construction; first synthesis of geranyllinaloisocyanide, a diterpene from the marine sponge, Halichondria sp. Yoshiyasu Ichikawa, Masatugu Yamazaki and Minoru Isobe Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (4E,8E)-5,9,13-Trimethyltetradeca-4,8,12-trien-1-al C17H28O ÏàËÆ¶È:66.6% Journal of the Chemical Society, Perkin Transactions 1 1999 489-496 Synthesis of rac-hippospongic acid A and revision of the structure Munetaka Tokumasu, Hiroshi Ando, Yoshikazu Hiraga, Satoshi Kojima and Katsuo Ohkata Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Agelasidine A C18H33N3O2S ÏàËÆ¶È:66.6% Journal of the American Chemical Society 1984 106 1819-1822 Antimicrobial metabolites from a Pacific sponge, Agelas sp Robert J. Capon, D. John Faulkner Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (5E,9E)-6,10,14-Trimethylpentadeca-5,9,13-trien-2-one C18H30O ÏàËÆ¶È:66.6% Australian Journal of Chemistry 1982 35 171-182 C18 terpenoid metabolites of the brown alga Cystophora moniliformis BN Ravi, PT Murphy, RO Lidgard, RG Warren and RJ Wells Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Yalongene B C20H30 ÏàËÆ¶È:65% Helvetica Chimica Acta 2012 95 235-239 YalongenesA and B, Two New Cembranoids with Cytoprotective Effects from the Hainan Soft Coral Sarcophyton trocheliophorum Marenzeller Li-Gong Yao, Hai-Yan Zhang, Lin-Fu Liang, Xian-Jun Guo, Shui-Chun Mao, and Yue-Wei Guo Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 2-(Dimethoxyphosphinyl)ethyl (E,E)-5,9,13-trimethyl-4,8,12-tetradecatrienoate C21H37O5P ÏàËÆ¶È:65% Bioorganic & Medicinal Chemistry 2000 8 2729-2737 2-(Acyloxy)ethylphosphonate analogues of prenyl pyrophosphates: synthesis and biological characterization Diana M. Cermak, David F. Wiemer, Kriste Lewis, Raymond J. Hohl Structure 13C NMR ̼Æ×Ä£Äâͼ |

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