Results 201 to 210 of about 2,095 (251)
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A semi-synthetic analog of the cembranoid sarcophine
Acta Crystallographica Section C Crystal Structure Communications, 2003The title molecule, 2(R)-[(1E,3E,7S,8S,11E,13R)-13-hydroxy-4,8,12-trimethyl-7,8-epoxycyclotetradeca-1,3,11-trien-1-yl]propane-1,2-diol, C(20)H(32)O(4), is a semi-synthetic analog of sarcophine, the natural cembranoid of marine origin, isolated from the soft coral Sarcophyton glaucum.
Jordan K. Zjawiony+3 more
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A cembranoid diterpene from Cleome viscosa
Phytochemistry, 1990Abstract A new macrocyclic diterpene (3 E ,7 E ,11 E )-20-oxocembra-3,7,11,15-tetraen-19-oic acid (cleomaldeic acid), has been isolated from Cleome viscosa .
Jasmin Jakupovic+3 more
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ChemInform Abstract: Total Synthesis of Sarcophytol A, an Anticarcinogenic Marine Cembranoid.
ChemInform, 1994AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Hisao Takayanagi+2 more
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Two New Cembranoids from Croton oblongifolius
Journal of Natural Products, 1998Two new cembranoids, crotocembraneic acid (1) and neocrotocembraneic acid (2), were isolated from the stem bark of Croton oblongifolius. Their structures were established on the basis of spectroscopic analysis.
Sitthisak Achayindee+6 more
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A study on the sulfenylchlorination of cembrene and the related cembranoids
Chinese Journal of Chemistry, 1990Abstractp‐Tolylsulfenyl chloride adds regioselectively at the C(11) C(12) bond of cembrene 1 to give 11‐(R)‐p‐tolylthio‐1‐(S)‐cembra‐2E, 4Z, 7E, 12(20)‐tetraene 2 following a rapid HCl elimination. Two new cembranoids, 1‐(S)‐cembra‐2E, 4Z, 7E, 12(20)‐tetraene 3 and 1‐(S)‐cembra‐2E, 4Z, 7E, 11Z‐tetraen‐20‐ol 4 are prepared from 2.
Wang Wei‐Qi+3 more
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Cembranoids from the Octocoral Sarcophyton ehrenbergi
Journal of Natural Products, 2010Chemical investigation of the octocoral Sarcophyton ehrenbergi led to the isolation of six new cembranoids, (+)-12-carboxy-11Z-sarcophytoxide (1), (+)-12-methoxycarbonyl-11Z-sarcophine (3), ehrenberoxides A-C (4-6), and lobophynin C (2), along with two known compounds, (+)-sarcophytoxide (7) and (+)-sarcophine (8).
Cheng, S. Y.+6 more
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Chemistry and Biodiversity
Hepatitis B Virus (HBV) infection is a global public health challenge that seriously endangers human health. Soft coral, as a major source of terpenoids, contains many structurally novel and highly bioactive compounds.
Chao Huang+7 more
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Hepatitis B Virus (HBV) infection is a global public health challenge that seriously endangers human health. Soft coral, as a major source of terpenoids, contains many structurally novel and highly bioactive compounds.
Chao Huang+7 more
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Bioactive Natural, Biocatalytic, and Semisynthetic Tobacco Cembranoids
Planta Medica, 2010The two major Nicotiana tabacum tobacco cembranoids, (1 S,2 E,4 R,6 R,7 E,11 E)-2,7,11-cembratriene-4,6-diol (1) and its C-4 epimer, exhibit a wide range of interesting biological activities. Although the tumorigenesis inhibition activity of tobacco cembranoids have been known since the mid 1980's, only a limited number of investigations have targeted ...
Mohammad A. Khanfar+4 more
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Natural product reports (Print), 2020
Covering: 2010 to 2020The class of 2,11-cyclized cembranoids is particularly widespread in marine Octocorallia, especially Alcyonacea and Gorgonacea, and has been extensively studied.
Geng Li+2 more
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Covering: 2010 to 2020The class of 2,11-cyclized cembranoids is particularly widespread in marine Octocorallia, especially Alcyonacea and Gorgonacea, and has been extensively studied.
Geng Li+2 more
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Polycyclic diterpenoids biogenetically related to the cembranoids
Chemistry of Natural Compounds, 1987This review describes cyclocembrane compounds isolated from plants, marine organisms, and insects. A systematization of cyclized diterpenoids according to the types of carbon skeletons is given.
S. A. Shevtsov, V. A. Raldugin
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