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PAB-O-¦Â-D-glucopyranoside ÏàËÆ¶È:70% Journal of Separation Science 2009 32 309-313 Preparative isolation of pseudolaric acids A and B, and their glucosides from the root bark of Pseudolarix kaempferi using high-speed counter-current chromatography Quan-Bin Han, Lina Wong, Fanny Lai, Nian-Yun Yang, Jing-Zheng Song, Chun-Feng Qiao and Hong-Xi Xu Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 2',3'-dihydroxy-1'-propoxypseudolarate B C26H34O10 ÏàËÆ¶È:66.6% Journal of Natural Products 2002 65 1041-1044 Five New Diterpenoids from Pseudolarix kaempferi Sheng-Ping Yang, Yan Wu, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 6'-O-acetylpseudolaric acid B O-¦Â-D-glucopyranoside C31H40O14 ÏàËÆ¶È:64.5% Journal of Natural Products 2002 65 1041-1044 Five New Diterpenoids from Pseudolarix kaempferi Sheng-Ping Yang, Yan Wu, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3-(2-chlorobenzyl)androsta-3,5-dien-17-yl acetate ÏàËÆ¶È:63.3% Russian Journal of Organic Chemistry 2008 44 785-790 noaccess785-790 Pd-catalyzed alkylation of halogen-substituted steroids with organozinc compounds Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . N-((tert-butylcarbamoyl)methyl)-N-benzyl-3¦Â-hydroxyandrost-5-en-17¦Â-carboxamide C33H48N2O3 ÏàËÆ¶È:60% Steroids 2010 75 659-664 Synthesis and preliminary biological screening of sterol analogues as new antifungal agents against plant pathogens Fernando Alonso, Adriana M. Cirigliano, Gabriela M. Cabrera, Javier A. Ram¨ªrez Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . N-((tert-butylcarbamoyl)methyl)-N-(4-chlorophenyl)-3¦Â-hydroxyandrost-5-en-17¦Â-carboxamide C32H45ClN2O3 ÏàËÆ¶È:60% Steroids 2010 75 659-664 Synthesis and preliminary biological screening of sterol analogues as new antifungal agents against plant pathogens Fernando Alonso, Adriana M. Cirigliano, Gabriela M. Cabrera, Javier A. Ram¨ªrez Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . N-((tert-butylcarbamoyl)methyl)-N-phenyl-3¦Â-hydroxyandrost-5-en-17¦Â-carboxamide C32H46N2O3 ÏàËÆ¶È:60% Steroids 2010 75 659-664 Synthesis and preliminary biological screening of sterol analogues as new antifungal agents against plant pathogens Fernando Alonso, Adriana M. Cirigliano, Gabriela M. Cabrera, Javier A. Ram¨ªrez Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 6,12,13,14,21,22-triepoxycytochalasin B C29H37NO8 ÏàËÆ¶È:60% Magnetic Resonance in Chemistry 2008 46 650-659 Synthesis, complete 1H and 13C NMR assignment and crystal structure of novel epoxide derivatives of cytochalasin B (pages 650¨C659) Pieter S. Steyn, Jaco C. Breytenbach, Jeanne H. Botha, Manuel A. Fernandes and Philippus L. Wessels Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . N-{2-[3-(2,3-Dimethylphenylaminosulfonyl)phenylamino-carbonyl]ethyl}-(Z)-9-octadecenoic acid amide C35H53N3O4S ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry 2000 8 1991-2006 Design, synthesis and early structure¨Cactivity relationship of farnesyltransferase inhibitors which mimic both the peptidic and the prenylic substrate Martin Schlitzer, Markus Böhm, Isabel Sattler, Hans-Martin Dahse Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 3-(4-methylbenzyl)androsta-3,5-dien-17-yl acetate ÏàËÆ¶È:60% Russian Journal of Organic Chemistry 2008 44 785-790 noaccess785-790 Pd-catalyzed alkylation of halogen-substituted steroids with organozinc compounds Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (N-(3-Methoxyquinolinyl-2-carbonyl)-D-Ser-Pip-Gly-Sar-NMe-Val)2(serine hydroxyl) dilactone C62H80N12O16 ÏàËÆ¶È:58.0% Bioorganic & Medicinal Chemistry 1998 6 85-102 Synthesis of key sandramycin analogs: systematic examination of the intercalation chromophore Dale L. Boger, Jyun-Hung Chen, Kurt W. Saionz, Qing Jin Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . euphorbia factor L7b C33H40O9 ÏàËÆ¶È:58.0% Bioorganic & Medicinal Chemistry 2009 17 4786-4792 Lathyrane diterpenes from Euphorbia lathyris as modulators of multidrug resistance and their crystal structures Wei Jiao, Weiwei Dong, Zhefeng Li, Meicai Deng, Runhua Lu Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 7 ÏàËÆ¶È:56.6% Journal of Natural Products 1999 62 949-953 18, 20-Hemiacetal-type and Other Withanolides from Dunalia brachyacantha Gloria L. Silva, Gerardo Burton, and Juan C. Oberti Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . physachenolide B ÏàËÆ¶È:56.6% Planta Medica 2004 70 59-64 18-Acetoxywithanolides from Physalis chenopodifolia Emma Maldonado,Fernando R. Torres, Mahinda Mart¨ªnez,Ana L. P¨¦rez-Castorena Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . N-((tertbutylcarbamoyl)methyl)-N-phenyl-3¦Â-hydroxypregn-5-ene-20-carboxamide C34H50N2O3 ÏàËÆ¶È:56.6% Steroids 2010 75 659-664 Synthesis and preliminary biological screening of sterol analogues as new antifungal agents against plant pathogens Fernando Alonso, Adriana M. Cirigliano, Gabriela M. Cabrera, Javier A. Ram¨ªrez Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 16-(4-nitro-benzylidene)-3¦Â-morpholino-5¦Á-androstan-17¦Â-yl acetate C32H44N2O5 ÏàËÆ¶È:56.6% Steroids 2011 76 709-723 Synthesis, characterization and biological evaluation of some 16E-arylidene androstane derivatives as potential anticancer agents Hao Guo, Haotian Wu, Jin Yang, Yuling Xiao, Hans-Josef Altenbach, Guofu Qiu,Hao Hu, Zhongyuan Wu, Xianran He, Dingshan Zhou, Xianming Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 16-(4-chloro-benzylidene)-3¦Â-piperidino-5¦Á-androstan-17¦Â-yl acetate C33H46ClNO2 ÏàËÆ¶È:56.6% Steroids 2011 76 709-723 Synthesis, characterization and biological evaluation of some 16E-arylidene androstane derivatives as potential anticancer agents Hao Guo, Haotian Wu, Jin Yang, Yuling Xiao, Hans-Josef Altenbach, Guofu Qiu,Hao Hu, Zhongyuan Wu, Xianran He, Dingshan Zhou, Xianming Hu Structure 13C NMR ̼Æ×Ä£Äâͼ |

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