Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Shwu Jen Wu"'
Autor:
Shwu-Jen Wu, Yu-Yi Chan
Publikováno v:
Molecules, Vol 19, Iss 10, Pp 15521-15534 (2014)
Five new iridoids, salvialosides A–E (compounds 1–5), together with fifty known compounds were isolated from the roots of Salvia digitaloides. The structures of the new compounds were completely elucidated using a combination of 2D NMR techniques
Externí odkaz:
https://doaj.org/article/bcbf3060860b4a6ab7a1ad1af633f219
Autor:
Chieh-Hung Huang, Yu-Yi Chan, Ping-Chung Kuo, Yu-Fon Chen, Ren-Jie Chang, Ih-Sheng Chen, Shwu-Jen Wu, Tian-Shung Wu
Publikováno v:
International Journal of Molecular Sciences, Vol 15, Iss 8, Pp 13424-13436 (2014)
Phytochemical investigation of the roots and stems of Illigera luzonensis afforded two new aporphine alkaloids (1) and (2), one new bisdehydroaporphine alkaloid (3), and one new benzenoid (4), along with 28 known structures. The structures of new com
Externí odkaz:
https://doaj.org/article/86afd0882c7f4169914f7960ccc391a7
Publikováno v:
International Journal of Molecular Sciences, Vol 15, Iss 7, Pp 11566-11577 (2014)
Two new glucosides, salviadigitoside A (1) and salviatalin A-19-O-β-glucoside (2), belonging to the salviatalin type diterpenoids, and a new cyclopenta[c]pyridine, salviadiginine A (3), were isolated from the roots of Salvia digitaloids. Structures
Externí odkaz:
https://doaj.org/article/7494300098ce46c28a6ce7f9ffb3e72f
Autor:
Tian Shung Wu, Mopur Vijaya Bhaskar Reddy, Yu Yi Chan, Ping Chung Kuo, Kuo Hsiung Lee, Shwu Jen Wu, Hsin Yi Hung, Shiow Chyn Huang, Guan-Jhong Huang, Susan L. Morris-Natschke
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 27:1547-1550
Twenty-one chalcones were prepared via aldol condensation and subsequent reduction of these compound led to the corresponding dihydrochalcone and 1,3-diphenylpropane derivatives. The synthetic products were examined for their effects on NO inhibition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::413fb0ee9183e2e796e4f8fd59400542
https://doi.org/10.1016/j.bmcl.2017.02.038
https://doi.org/10.1016/j.bmcl.2017.02.038
Autor:
De Yang Shen, Tian Shung Wu, Daih Huang Kuo, Hsin Yi Hung, Ping Chung Kuo, Tran Dinh Thang, Thi Ngan Nguyen, Shwu Jen Wu, Young Ji Shiao
Publikováno v:
Journal of Natural Products. 78:2521-2530
Eight new clausenamides, including three γ-lactams (1-3), four δ-lactams (4-7), and an amide (8), and seven known lactams, including compounds 9-11, which were purified from natural sources for the first time, were characterized from the leaves of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01af56c75758407ae6d7f45478c466d2
https://doi.org/10.1021/acs.jnatprod.5b00148
https://doi.org/10.1021/acs.jnatprod.5b00148
Autor:
Ih-Sheng Chen, Chieh-Hung Huang, Yu-yi Chan, Ren-Jie Chang, Yu Fon Chen, Tian Shung Wu, Shwu-Jen Wu, Ping Chung Kuo
Publikováno v:
International Journal of Molecular Sciences, Vol 15, Iss 8, Pp 13424-13436 (2014)
International Journal of Molecular Sciences
International Journal of Molecular Sciences; Volume 15; Issue 8; Pages: 13424-13436
International Journal of Molecular Sciences
International Journal of Molecular Sciences; Volume 15; Issue 8; Pages: 13424-13436
Phytochemical investigation of the roots and stems of Illigera luzonensis afforded two new aporphine alkaloids (1) and (2), one new bisdehydroaporphine alkaloid (3), and one new benzenoid (4), along with 28 known structures. The structures of new com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4910f274d7875c5510cd404d4b1fbc3
http://www.mdpi.com/1422-0067/15/8/13424
http://www.mdpi.com/1422-0067/15/8/13424
Autor:
Hsin Yi Hung, Tian Shung Wu, Shwu Jen Wu, Qiong Gu, Po Chuen Shieh, Hung Cheng Shih, De Yang Shen, E-Jian Lee, Ping Chung Kuo, Tsong-Long Hwang, Yu Ren Liao, Kuo Hsiung Lee
Publikováno v:
Bioorganicmedicinal chemistry. 24(7)
Nine neolignan derivatives (1-9) were characterized from the roots of Magnolia officinalis, and their structures were elucidated based on spectroscopic and physicochemical analyses. Among them, houpulins E (1) and M (9) possess novel homo- and trinor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e678ce306dca089e537d191eba0faa9b
https://pubmed.ncbi.nlm.nih.gov/26928286
https://pubmed.ncbi.nlm.nih.gov/26928286
Autor:
Yu Ren Liao, Yuh-Chiang Shen, Yann Lii Leu, Chou Hsiung Chen, Chih Hua Chao, Shwu Jen Wu, Keduo Qian, Kuo Hsiung Lee, Tian Shung Wu, Li Shian Shi, De Yang Shen, Yao-Haur Kuo, E-Jian Lee, Hsiu Hui Chan
Publikováno v:
Bioorganic & Medicinal Chemistry. 19:677-683
Five new benzenoids, benzocamphorins A–E ( 1 – 5 ), and 10 recently isolated triterpenoids, camphoratins A–J ( 16 – 25 ), together with 23 known compounds including seven benzenoids ( 6 – 12 ), three lignans ( 13 – 15 ), and 13 triterpeno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f75e35995640956a616819ab2bd1248
https://doi.org/10.1016/j.bmc.2010.10.032
https://doi.org/10.1016/j.bmc.2010.10.032
Autor:
Chou Hsiung Chen, Shwu Jen Wu, Kenneth F. Bastow, Keduo Qian, E-Jian Lee, Hsiu Hui Chan, De Yang Shen, Yea Hwey Wang, Yuh-Chiang Shen, Kuo-Hsiung Lee, Yann Lii Leu, Chih Hua Chao, Tian Shung Wu
Publikováno v:
Journal of Natural Products. 73:1756-1762
Ten new triterpenoids, camphoratins A–J (1–10), along with 12 known compounds were isolated from the fruiting body of Taiwanofungus camphoratus. Their structures were established by spectroscopic analysis and chemical methods. Compound 10 is the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f32070b6a57f7f85e14b5cccb1d8083
https://doi.org/10.1021/np1002143
https://doi.org/10.1021/np1002143
Publikováno v:
Journal of the Chinese Chemical Society. 49:263-268
Three new benzenoid compounds, namely cryptamygin-A, -B and -C together with eleven known compounds were isolated from the stem bark of Cryptocarya amygadalina. Their structures were elucidated by spectral analysis. The synthesis of cryptamygin-A is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6af798e66234d15f3f4e29d4e9d8a456
https://doi.org/10.1002/jccs.200200041
https://doi.org/10.1002/jccs.200200041