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14.37,19.30,24.85,29.84,32.07,35.05,35.95,47.62,48.08,48.19,52.45,60.90,69.55,101.64,109.18,128.02,142.94,147.76,173.59
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1 .     phanginin G
C21H28O5     ÏàËÆ¶È:76.1%
Phytochemistry          2008          69          1242-1249
Phanginin A¨CK, diterpenoids from the seeds of Caesalpinia sappan Linn.
Orapun Yodsaoue,Sarot Cheenpracha, Chatchanok Karalai, Chanita Ponglimanont,Suchada Chantrapromma, Hoong-Kun Fun,Akkharawit Kanjana-Opas
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     phanginin G
C21H28O5     ÏàËÆ¶È:76.1%
Chinese Journal of Natural Medicines          2012          10          218-221
Two new cassane diterpenoids from the seeds of Caesalpinia sappan Linn.
Jing-Yu ZHANG, Fei-Hua WU, Wei QU, Jing-Yu LIANG
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     phanginin H
C21H28O4     ÏàËÆ¶È:71.4%
Phytochemistry          2008          69          1242-1249
Phanginin A¨CK, diterpenoids from the seeds of Caesalpinia sappan Linn.
Orapun Yodsaoue,Sarot Cheenpracha, Chatchanok Karalai, Chanita Ponglimanont,Suchada Chantrapromma, Hoong-Kun Fun,Akkharawit Kanjana-Opas
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     phanginin P
C21H28O5     ÏàËÆ¶È:66.6%
Phytochemistry Letters          2014          8          141-144
Three new cassane diterpenes from the seeds of Caesalpinia sappan
Guo-Xu Ma, Yin-Di Zhu, Zhong-Hao Sun, Jing-Quan Yuan, Yong Xie, Xiao-Po Zhang, Yu Tian, Jun-Shan Yang, Hai-Feng Wu, Xu-Dong Xu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     compound 7
C16H18O2I2     ÏàËÆ¶È:57.8%
Spectrochimica Acta Part A          2005          62          604-613
1H, 13C NMR and X-ray crystallographic studies of highly polyhalogenated derivatives of costunolide lactone
D. Corona, E. D¨ªaz, J.L. Nava, A. Guzm¨¢n, H. Barrios, A. Fuentes, S.A. Hernandez-Plata, J. Allard, C.K. Jankowsk
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     caesaljapin
C21H28O5     ÏàËÆ¶È:57.1%
Phytochemistry          1992          31          2897-2898
Caesaljapin, a cassane diterpenoid from Caesalpinia decapetala var. Japonica
Kazunori Ogawa, Izumi Aoki, Yutaka Sashida
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     curcucomosin A
C20H26O3     ÏàËÆ¶È:55%
Journal of Natural Products          2010          73          724-728
Labdane Diterpenes from the Aerial Parts of Curcuma comosa Enhance Fetal Hemoglobin Production in an Erythroid Cell Line
Ratchanaporn Chokchaisiri, Nattawara Chaneiam, Saovaros Svasti, Suthat Fucharoen, Jim Vadolas and Apichart Suksamrarn
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     ent-pimaric acid
C20H30O2     ÏàËÆ¶È:55%
Journal of China Pharmaceutical University          1989          20          203-207
Diterpenes From Pseuduvaria Indochinensis
Xie Ning; Zhong Shouming; Zhao Shouxun; Peter G. Waterman; He Cunheng and Zheng Qitai
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     compound 36b
C22H21NO5     ÏàËÆ¶È:55%
The Journal of Organic Chemistry          2012          77          7435-7470
Assembly of Four Diverse Heterocyclic Libraries Enabled by Prins Cyclization, Au-Catalyzed Enyne Cycloisomerization, and Automated Amide Synthesis
Jiayue Cui, David I. Chai, Christopher Miller, Jason Hao, Christopher Thomas, JingQi Wang, Karl A. Scheidt, and Sergey A. Kozmin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     (3'R)-Hydroxystemofoline
C22H29NO6     ÏàËÆ¶È:54.5%
Journal of Natural Products          2009          72          679-684
Semisynthesis and Biological Activity of Stemofoline Alkaloids
Morwenna C.Baird,Stephen G. Pyne, Alison T. Ung, Wilford Lie, Thanapat Sastraruji, Araya Jatisatienr, Chaiwat Jatisatienr, Srisulak Dheeranupattana, Jaturong Lowlam, and Sukanya Boonchalermkit
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     monomethyl ester of caesaljapin
    ÏàËÆ¶È:54.5%
Phytochemistry          1992          31          2897-2898
Caesaljapin, a cassane diterpenoid from Caesalpinia decapetala var. Japonica
Kazunori Ogawa, Izumi Aoki, Yutaka Sashida
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     dehydroretrofractamide C
C20H29NO3     ÏàËÆ¶È:52.6%
Phytochemistry          2007          68          899-903
ACAT inhibition of alkamides identified in the fruits of Piper nigrum
Mun-Chual Rho, Seung Woong Lee, Hye Ran Park, Jung-Ho Choi, Ji Yun Kang,Koanhoi Kim, Hyun Sun Lee, Young Kook Kim
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     compound 16
C17H26O6     ÏàËÆ¶È:52.6%
Journal of Natural Products          2005          68          1274-1276
Antifungal Activity of Artemisinin Derivatives
Ahmed M. Galal, Samir A. Ross, Melissa Jacob, and Mahmoud A. ElSohly
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     3¦Â,7¦Â-dihydroxyandrost-5-en-17-one
    ÏàËÆ¶È:52.6%
Phytochemistry          1998          49          2355-2358
The hydroxylation of ¦¤5-androstenes by Cephalosporium aphidicola
Caroline M. Bensasson, James R. Hanson, A. Christy Hunter
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     bryopterin B
C17H22O5     ÏàËÆ¶È:52.6%
Phytochemistry          1994          37          433-439
Sesqui- and diterpenoids from the panamanian liverwort Bryopteris filicina
Fumihiro Nagashima, Hiromi Izumo, Shigeru Takaoka, Motoo Tori, Yoshinori Asakawa
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     ethyl(-)-4-(4'-heptanoyloxyphenyl)-6-methyl-3,4-dihydropyrimidin-2-one-5-carboxylate
C21H28N2O5     ÏàËÆ¶È:52.6%
Indian Journal of Chemistry Section B          2009          48B          1738-1748
Synthesis and lipase-catalysed enantioselective acylation studies on ethyl 4-aryl-3,4-dihydropyrimidin-2(1H)-ones
Prasad,Ashok K; Arya,Pragya; Bhatia,Sumati; Sharma,Raman K; Singh,Rishipal; Singh,Brajendra K; Eycken,Erik Van der; Singh,Rajpal; Olsen,Carl E; Parmar,Virinder S
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     androsta-3,5-dien-17-one
    ÏàËÆ¶È:52.6%
Steroids          1998          63          650-664
The scope and limitations of the reaction of ¦Ä5-steroids with mercury(II) trifluoroacetate
Peter L. D. Ruddock, David J. Williams, Paul B. Reese
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     3¦Â,4¦Â-dihydroxyandrost-5-en-17-one
    ÏàËÆ¶È:52.6%
Steroids          1998          63          650-664
The scope and limitations of the reaction of ¦Ä5-steroids with mercury(II) trifluoroacetate
Peter L. D. Ruddock, David J. Williams, Paul B. Reese
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     4¦Â,5¦Â-Epoxyandrostane-6,17-dione
    ÏàËÆ¶È:52.6%
Steroids          1995          60          499-505
Competing pathway involved in allylic acetoxylation of androst-5-en-17-one, and oxidation of allylic alcohols with chromium oxides
Mitsuteru Numazawa, Mii Tachibana, Miyako Kamiza
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     androst-3,17-dione-4-eno[6,5,4-c,d]isoxazole
C19H23NO3     ÏàËÆ¶È:52.6%
Bioorganic & Medicinal Chemistry          1998          6          1525-1529
Synthesis of new steroidal isoxazoles: inhibitors of estrogen synthase
Shengrong Li, Edward J. Parish, Carla Rodriguez-Valenzuela, Angela M.H. Brodie
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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