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6 articles matched your search query. Search Parameters:
Authors = Yun-Sheng Lin

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YUN (963) , SHENG (975) , LIN (3140)

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Open AccessArticle New Briarane Diterpenoids from Taiwanese Soft Coral Briareum violacea
Mar. Drugs 2014, 12(8), 4677-4692; doi:10.3390/md12084677
Received: 28 May 2014 / Revised: 24 July 2014 / Accepted: 24 July 2014 / Published: 22 August 2014
Cited by 4 | Viewed by 1560 | PDF Full-text (1198 KB) | HTML Full-text | XML Full-text
Abstract
Ten new briarane diterpenoids, briaviolides A–J (110), together with six known briaranes, solenolides A and D, excavatolide A, briaexcavatolide I, 4β-acetoxy-9-deacetystylatulide lactone and 9-deacetylstylatulide lactone, were isolated from the Taiwanese soft coral, Briareum violacea. Their structures were determined
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Ten new briarane diterpenoids, briaviolides A–J (110), together with six known briaranes, solenolides A and D, excavatolide A, briaexcavatolide I, 4β-acetoxy-9-deacetystylatulide lactone and 9-deacetylstylatulide lactone, were isolated from the Taiwanese soft coral, Briareum violacea. Their structures were determined on the basis of spectroscopic data (1H- and 13C-NMR, 1H–1H COSY, HSQC, HMBC and NOESY), HR-MS and chemical methods. The absolute configuration of briaviolide A (1) was determined by X-ray crystallographic analysis. Compounds 5, 9 and derivative 11 showed moderate inhibitory activities on superoxide-anion generation and elastase release by human neutrophils in response to N-formyl-methionyl-leucyl-phenylalanine/ Cytochalasin B (fMLP/CB). Full article
(This article belongs to the collection Bioactive Compounds from Marine Invertebrates)
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Open AccessArticle Four New Briarane Diterpenoids from Taiwanese Gorgonian Junceella fragilis
Mar. Drugs 2013, 11(6), 2042-2053; doi:10.3390/md11062042
Received: 15 April 2013 / Revised: 22 May 2013 / Accepted: 27 May 2013 / Published: 10 June 2013
Cited by 10 | Viewed by 1634 | PDF Full-text (848 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
Four new 8-hydroxybriarane diterpenoids, frajunolides P–S (14), together with umbraculolide A, juncenolide C, junceellonoid A and juncin R, were isolated from the acetone extract of the gorgonian Junceella fragilis, collected from the southeast coast of Taiwan. Compound 1
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Four new 8-hydroxybriarane diterpenoids, frajunolides P–S (14), together with umbraculolide A, juncenolide C, junceellonoid A and juncin R, were isolated from the acetone extract of the gorgonian Junceella fragilis, collected from the southeast coast of Taiwan. Compound 1 contains an unusual pivaloyloxy group at C-2, while 3 is a rare compound having a chlorine atom on the olefinic carbon (C-6). The structures of the isolated compounds were established by extensive spectroscopic analysis, including 1D- and 2D-NMR, as well as HRMS data. Compound 1 was further confirmed by X-ray crystallographic analysis. In the anti-inflammatory test, compounds 1 and 2 exhibited moderate inhibition on superoxide anion generation and elastase release by human neutrophils in response to formylmethionylleucyl-phenylalanine/dihydrocytochalasin B (fMLP/CB). Full article
Open AccessArticle A New Spatane Diterpenoid from the Cultured Soft Coral Sinularia leptoclados
Mar. Drugs 2013, 11(1), 114-123; doi:10.3390/md11010114
Received: 27 November 2012 / Revised: 11 December 2012 / Accepted: 24 December 2012 / Published: 10 January 2013
Cited by 8 | Viewed by 2222 | PDF Full-text (611 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
A new spatane diterpenoid, leptoclalin A (1), along with two previously reported known norcembranoid diterpenes (2 and 3), were isolated from a cultured soft coral Sinularia leptoclados. The structures were determined by extensive spectroscopic analyses and by comparison
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A new spatane diterpenoid, leptoclalin A (1), along with two previously reported known norcembranoid diterpenes (2 and 3), were isolated from a cultured soft coral Sinularia leptoclados. The structures were determined by extensive spectroscopic analyses and by comparison with the spectral data of related known compounds. Metabolite 1 is rarely found in spatane skeletons reported from soft corals. In addition, compound 1 exhibited weak cytotoxicity towards human tumor cell lines T-47 D and K-562. Full article
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Open AccessCommunication A New Cubitane Diterpenoid from the Soft Coral Sinularia crassa
Molecules 2012, 17(9), 10072-10078; doi:10.3390/molecules170910072
Received: 12 July 2012 / Revised: 10 August 2012 / Accepted: 15 August 2012 / Published: 24 August 2012
Cited by 6 | Viewed by 2223 | PDF Full-text (376 KB)
Abstract
A new cubitane diterpenoid, crassalone A (1), was isolated from the marine soft coral Sinularia crassa. The structure was determined by extensive spectroscopic analyses. Compound 1 is not cytotoxic (IC50 > 20 μg/mL) toward the four human cancer cell
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A new cubitane diterpenoid, crassalone A (1), was isolated from the marine soft coral Sinularia crassa. The structure was determined by extensive spectroscopic analyses. Compound 1 is not cytotoxic (IC50 > 20 μg/mL) toward the four human cancer cell lines tested (HL60, MDA-MB-231, HCT-116 and DLD-1). Full article
(This article belongs to the Section Natural Products)
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Open AccessArticle Two New Cembrane-Based Diterpenoids from the Marine Soft Coral Sinularia crassa
Molecules 2012, 17(5), 5422-5429; doi:10.3390/molecules17055422
Received: 10 January 2012 / Revised: 4 May 2012 / Accepted: 8 May 2012 / Published: 8 May 2012
Cited by 11 | Viewed by 2428 | PDF Full-text (311 KB) | Supplementary Files
Abstract
Two new cembrane diterpenes, sicrassarines A and B (compounds 1 and 2), were isolated from the Taiwanese soft coral Sinularia crassa. The structures of the new metabolites were determined on the basis of extensive spectroscopic analysis, particularly mass spectroscopy and 2D
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Two new cembrane diterpenes, sicrassarines A and B (compounds 1 and 2), were isolated from the Taiwanese soft coral Sinularia crassa. The structures of the new metabolites were determined on the basis of extensive spectroscopic analysis, particularly mass spectroscopy and 2D NMR (1H–1H COSY, HMQC, HMBC, and NOESY) spectroscopy. Full article
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Open AccessArticle Frajunolides L–O, Four New 8-Hydroxybriarane Diterpenoids from the Gorgonian Junceella fragilis
Mar. Drugs 2011, 9(9), 1477-1486; doi:10.3390/md9091477
Received: 8 July 2011 / Revised: 23 August 2011 / Accepted: 25 August 2011 / Published: 2 September 2011
Cited by 11 | Viewed by 2841 | PDF Full-text (1085 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
Four new 8-hydroxybriarane diterpenoids, frajunolides L–O (14), were isolated from the Taiwanese gorgonian Junceella fragilis. The structures of compounds 14 were elucidated based on spectroscopic analysis, especially 2D NMR (1H-1H COSY, HSQC,
[...] Read more.
Four new 8-hydroxybriarane diterpenoids, frajunolides L–O (14), were isolated from the Taiwanese gorgonian Junceella fragilis. The structures of compounds 14 were elucidated based on spectroscopic analysis, especially 2D NMR (1H-1H COSY, HSQC, HMBC and NOESY) and HRMS. Compounds 1 and 4 showed weak anti-inflammatory activity as tested by superoxide anion generation and elastase release by human neutrophil in response to fMLP/CB. Compound 3 showed selective inhibition on elastase release in vitro. Full article

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