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danil1288
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zhangli1987: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл£¡ 2013-08-24 11:44:01
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zhangli1987: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл£¡ 2013-08-24 11:44:01
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²éѯ½á¹û£º¹²²éµ½116¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . deoxycorticosterone 21-O-¦Â-glucoside ÏàËÆ¶È:62.9% Steroids 2012 77 1373-1380 Biotransformation of 21-O-acetyl-deoxycorticosterone by cell suspension cultures of Digitalis lanata (strain W.1.4) Rodrigo Maia de P¨¢dua, Nadine Meitinger, Jos¨¦ Dias de Souza Filho, Reiner Waibel, Peter Gmeiner, Fernão Castro Braga, Wolfgang Kreis Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . tricalysioside I C26H42O10 ÏàËÆ¶È:61.5% Phytochemistry 2005 66 2857-2864 Tricalysiosides H¨CO: Ent-kaurane glucosides from the leaves of Tricalysia dubia Dong-Hui He, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato,Mitsunori Aramoto, Masahiko Bando, Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 16(S),22(S)-Dihydroxycholest-4-en-3-one ÏàËÆ¶È:59.2% Phytochemistry 1996 41 907-917 Cholestane- and pregnane-type glycosides from the roots of Tribulus cistoides Hans Achenbach, Harald H¨¹bner, Melchior Reiter Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (25S)-16(S),22(S),26-Trihydroxycholest-4-en-3-one ÏàËÆ¶È:59.2% Phytochemistry 1996 41 907-917 Cholestane- and pregnane-type glycosides from the roots of Tribulus cistoides Hans Achenbach, Harald H¨¹bner, Melchior Reiter Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (1¦Á,3S,4S,5S,7¦Á,9¦Á,10¦Á,11R)-1-acetyloxy-9-hydroxy-7-p-nitrobenzoyloxylongipinane C24H31O7N ÏàËÆ¶È:56.5% Journal of Natural Products 2002 65 1398-1411 Quirogane, Prenopsane, and Patzcuarane Skeletons Obtained by Photochemically Induced Molecular Rearrangements of Longipinene Derivatives Myriam Mel¨¦ndez-Rodr¨¦guez, Carlos M. Cerda-Garc¨¦a-Rojas, and Pedro Joseph-Nathan Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 11¦Á, 13-dihydro-4H-xanthalongin 4-O-¦Â-n-glucopyranoside C21H34O8 ÏàËÆ¶È:56.5% Planta Medica 1996 62 39-41 11¦Á, 13- and 11¦Â,13 -Dihydro-4H-xanthalongin 4-O-¦Â-Glucopyranosides: New Sesquiterpene Lactone Glycosides from Flowers of Arnica amplexicaulis and A. mollis ClausM. Passreiter, IrmgardMerfort, ChristophBestendonk. G¨¹nter Willuhn. andAloisSteigel Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . gonocaryoside A C22H32O14 ÏàËÆ¶È:56.5% Phytochemistry 1995 39 115-120 Secoiridoid and flavonoid glycosides from Gonocaryum calleryanum Tetsuo Kaneko, Mayumi Sakamoto, Kazuhiro Ohtani, Aiko Ito, Ryoji Kasai, Kazuo Yamasaki, William G. Padorina Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . gonocaryoside B C21H30O14 ÏàËÆ¶È:56.5% Phytochemistry 1995 39 115-120 Secoiridoid and flavonoid glycosides from Gonocaryum calleryanum Tetsuo Kaneko, Mayumi Sakamoto, Kazuhiro Ohtani, Aiko Ito, Ryoji Kasai, Kazuo Yamasaki, William G. Padorina Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 15¦Â-hydroxytestosterone ÏàËÆ¶È:56.5% Magnetic Resonance in Chemistry 2006 44 467-474 Structure and stereochemistry of products of hydroxylation of human steroid hormones by a housefly cytochrome P450 (CYP6A1) (pages 467¨C474) Neil E. Jacobsen, Katalin E. Köv¨¦r, Marat B. Murataliev, Ren¨¦ Feyereisen and F. Ann Walker Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . hemsleyanidine ÏàËÆ¶È:56.5% Heterocycles 1996 43 1243-1250 Hemsleyanidine and Isohemsleyanidine from Aconitum hemsleyanum var. circinatum Qing-Yan Xu, Zheng-Ban Li, Feng-Peng Wang, and Chun-Tao Che Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Gonocaryoside A C22H32O14 ÏàËÆ¶È:56.5% Chemical & Pharmaceutical Bulletin 2007 55 689-728 Naturally Occurring Secoiridoids and Bioactivity of Naturally Occurring Iridoids and Secoiridoids. A Review, Part 2 Biswanath DINDA, Sudhan DEBNATH and Yoshihiro HARIGAYA Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Gonocaryoside B C21H30O14 ÏàËÆ¶È:56.5% Chemical & Pharmaceutical Bulletin 2007 55 689-728 Naturally Occurring Secoiridoids and Bioactivity of Naturally Occurring Iridoids and Secoiridoids. A Review, Part 2 Biswanath DINDA, Sudhan DEBNATH and Yoshihiro HARIGAYA Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 17¦Â-(2',5'-Dihydro-5'-oxo-3'-furyl)-11¦Á-hydroxyandrost-4-en-3-one C23H30O4 ÏàËÆ¶È:56.5% Organic Magnetic Resonance 1977 9 439-464 13C n.m.r. spectra of steroids ¡ªa survey and commentary J. W. Blunt and J. B. Stothers Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Genkwanine I C27H36O9 ÏàËÆ¶È:56% Bioorganic & Medicinal Chemistry 2005 13 645-655 Novel diterpenoids with potent inhibitory activity against endothelium cell HMEC and cytotoxic activities from a well-known TCM plant Daphne genkwa Zha-Jun Zhan, Cheng-Qi Fan, Jian Ding, Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (20R,24S)-5¦Á-cholestane-3¦Â,6¦Â,15¦Á,24-tetraol C27H48O4 ÏàËÆ¶È:55.5% Russian Journal of Bioorganic Chemistry 2005 31 519-527 Steroid Compounds from Far Eastern Starfishes Henricia aspera and H.tumida E. V. Levina, A. I. Kalinovsky, V. A. Stonik, P. S. Dmiternok, and P. V. Andriyashchenko Structure 13C NMR ̼Æ×Ä£Äâͼ |

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