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1 . 5,20-Dioxo-A-nor-3,5-secopregnane-3-oic acid
ÏàËƶÈ:60%
Molecules 2012 17 355-368
Synthesis and 5¦Á-Reductase Inhibitory Activity of C21 Steroids Having 1,4-diene or 4,6-diene 20-ones and 4-Azasteroid 20-Oximes
Sujeong Kim, Yong-ung Kim and Eunsook Ma
Structure 13C NMR ̼Æ×Ä£Äâͼ
2 . 5¦Á-Androst-3-en-17¦Â-ol
ÏàËƶÈ:57.8%
Steroids 2008 73 1409-1415
Synthesis and biochemical studies of 17-substituted androst-3-enes and 3,4-epoxyandrostanes as aromatase inhibitors
Margarida M.D.S. Cepa, Elisi¨¢rio J. Tavares da Silva, Georgina Correia-da-Silva, Fernanda M.F. Roleira, Nat¨¦rcia A.A. Teixeira
Structure 13C NMR ̼Æ×Ä£Äâͼ
3 . (E)-10-methoxy-8-oxo-9-octadecenoate
C20H36O4 ÏàËƶÈ:57.8%
Phytochemistry 1994 35 1245-1247
Two aliphatic enone ethers from Hibiscus rosa-sinensis
Munehiro Nakatani, Kimi Matsuoka, Yasuto Uchio, Tsunao Hase
Structure 13C NMR ̼Æ×Ä£Äâͼ
4 . Methyl (Z)-8-(2-hexylcyclopropane-1-yl)-8-oxo-octanoate
C18H32O3 ÏàËƶÈ:57.8%
Organic Letters 2006 Vol. 8, No. 1 79-81
Configurational Analysis of Cyclopropyl Fatty Acids Isolated from Escherichia coli
Laura J. Stuart, James P. Buck, Amy E. Tremblay, and Peter H. Buist
Structure 13C NMR ̼Æ×Ä£Äâͼ
5 . 17¦Á-hydroxy-3¦Á,21-disulfooxy-5¦Â-pregnane-11,20-dione disodium salt
C21H30O11SNa2 ÏàËƶÈ:57.1%
Chemical & Pharmaceutical Bulletin 2010 58 344-353
Potential Corticoid Metabolites: Chemical Synthesis of 3- and 21-Monosulfates and Their Double-Conjugates of Tetrahydrocorticosteroids in the 5¦Á- and 5¦Â-Series
Rika Okihara, Kuniko Mitamura, Maki Hasegawa, Megumi Mori, Akina Muto, Genta Kakiyama, Shoujiro Ogawa, Takashi Iida, Miki Shimada, Nariyasu Mano and Shigeo Ikegawa
Structure 13C NMR ̼Æ×Ä£Äâͼ
6 . 13,16¦Â-dihydroxystemodan-2-one
ÏàËƶÈ:55%
Phytochemistry 2002 59 57-62
Biotransformation of terpenes from Stemodia maritima by Aspergillus niger ATCC 9142
Avril R.M. Chen, Paul B. Reese
Structure 13C NMR ̼Æ×Ä£Äâͼ
7 . diacarperoxide C
C20H34O6 ÏàËƶÈ:55%
Journal of Natural Products 2008 71(8) 1358-1364
Diacarperoxides, Norterpene Cyclic Peroxides from the Sponge Diacarnus megaspinorhabdosa
Sabrin R. M. Ibrahim, Rainer Ebel, Victor Wray, Werner E. G. M¨¹ller, RuAngelie Edrada-Ebel, and Peter Proksch
Structure 13C NMR ̼Æ×Ä£Äâͼ
8 . 20-Hydroxyimino-5-oxo-A-nor-3,5-secopregnan-3-oic acid
ÏàËƶÈ:55%
Molecules 2009 14 4655-4668
Synthesis of Pregnane Derivatives, Their Cytotoxicity on LNCap and PC-3 Cells, and Screening on 5¦Á-Reductase Inhibitory Activity
Sujeong Kim and Eunsook Ma
Structure 13C NMR ̼Æ×Ä£Äâͼ
9 . 3¦Á-Hydroxy-6-oxa-5¦Á-pregnan-20-one
ÏàËƶÈ:55%
Steroids 2000 65 349-356
Synthesis and GABAA receptor activity of 6-oxa-analogs of neurosteroids
Daniel Nicoletti, Alberto A. Ghini, Roman Furtm¨¹ller, Werner Sieghart, Robert H. Dodd, Gerardo Burton
Structure 13C NMR ̼Æ×Ä£Äâͼ
10 . 3-(3,17¦Â-Dihydroxyestra-1,3,5(10)-trien-4-yl)thiopropanoic acid
ÏàËƶÈ:55%
Steroids 2006 71 618-631
Estrogen conjugation and antibody binding interactions in surface plasmon resonance biosensing
John S. Mitchell, Yinqiu Wu, Christian J. Cook, Lyndsay Main
Structure 13C NMR ̼Æ×Ä£Äâͼ
11 . eduenone
C20H30O ÏàËƶÈ:55%
Journal of Natural Products 1995 Vol 58 226-232
Additional Dolabellane Diterpenes from the Caribbean Gorgonian Octocoral Eunicea laciniata
Abimael D. Rodr¨ªguez, Eduvigis Gonz¨¢lez, Cynthia Gonz¨¢lez
Structure 13C NMR ̼Æ×Ä£Äâͼ
12 . 11¦Î-hydroxystemodinone
ÏàËƶÈ:55%
Phytochemistry 1994 36 1391-1393
Biotransformation of some stemodane diterpenoids by Cephalosporium aphidicola
James R. Hanson, Paul B. Reese, Jacqueline A. Takahashi, Maureen R. Wilson
Structure 13C NMR ̼Æ×Ä£Äâͼ
13 . Methyl 10-ketolactobacillate (Methyl (Z)-10-(2-hexylcyclopropane-1-yl)-10-oxodecanoate)
C20H36O3 ÏàËƶÈ:55%
Organic Letters 2006 Vol. 8, No. 1 79-81
Configurational Analysis of Cyclopropyl Fatty Acids Isolated from Escherichia coli
Laura J. Stuart, James P. Buck, Amy E. Tremblay, and Peter H. Buist
Structure 13C NMR ̼Æ×Ä£Äâͼ
14 . Methyl 13-ketolactobacillate (Methyl (Z)-10-(2-(1-oxo)-hexylcyclopropane-1-yl)-decanoate)
C20H36O3 ÏàËƶÈ:55%
Organic Letters 2006 Vol. 8, No. 1 79-81
Configurational Analysis of Cyclopropyl Fatty Acids Isolated from Escherichia coli
Laura J. Stuart, James P. Buck, Amy E. Tremblay, and Peter H. Buist
Structure 13C NMR ̼Æ×Ä£Äâͼ
15 . Cyanthiwigin AC
C20H30O3 ÏàËƶÈ:55%
Organic Letters 2003 Vol. 5, No. 24 4575-4578
Cyanthiwigin AC and AD, Two Novel Diterpene Skeletons from the Jamaican Sponge Myrmekioderma styx
Jiangnan Peng, Mitchell A. Avery, and Mark T. Hamann
Structure 13C NMR ̼Æ×Ä£Äâͼ
16 . Neolaxiflorin F
C20H24O6 ÏàËƶÈ:55%
Tetrahedron Letters 2012 53 2777-2781
Biogenetically related caged ent-kaurane diterpenoids from Isodon eriocalyx var.laxiflora
Wei-Guang Wang, Xiao-Nian Li, Xue Du, Ke Dong, Wei Zhao, Hai-Yan Wu, Ling-Mei Kong,Yan Li, Jian-Xin Pu, Han-Dong Sun
Structure 13C NMR ̼Æ×Ä£Äâͼ
17 . 17¦Â-Acetylamino-10¦Â-hydroxyestr-4-en-3-one
ÏàËƶÈ:55%
Steroids 1998 63 484-495
Microbial hydroxylation of acetylaminosteroids
HerbertL Holland, Gingipalli Lakshmaiah, PeterL Ruddock
Structure 13C NMR ̼Æ×Ä£Äâͼ |
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