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zhangli1987

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13.5,18.0,18.9,22.1,33.7,34.9,36.7,37.0,40.3,44.5,55.2,56.0,72.4,74.5,75.3,75.5,78.0,78.4,100.8,124.0,175.8,198.0,203
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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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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
Tobeastriver
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