Works about LABDANES
Results: 61
Convergent Assembly of the Tricyclic Labdane Core Enables Synthesis of Diverse Forskolin‐like Molecules.
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- Angewandte Chemie, 2023, v. 135, n. 1, p. 1, doi. 10.1002/ange.202213183
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Biological Evaluation of Terrestrial and Marine Plant Originated Labdane Diterpenes (A Review).
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- Pharmaceutical Chemistry Journal, 2016, v. 50, n. 8, p. 558, doi. 10.1007/s11094-016-1490-2
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Biosynthesis of mercapturic acid derivative of the labdane-type diterpene, cyslabdan that potentiates imipenem activity against methicillin-resistant Staphylococcus aureus: cyslabdan is generated by mycothiol-mediated xenobiotic detoxification.
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- Journal of Industrial Microbiology & Biotechnology, 2016, v. 43, n. 2/3, p. 325, doi. 10.1007/s10295-015-1694-6
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Design, biological evaluation, and molecular modelling insights of cupressic acid derivatives as promising anti-inflammatory agents.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2023, v. 38, n. 1, p. 1, doi. 10.1080/14756366.2023.2187327
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- Article
Andrographolide inhibits HMGB1-induced inflammatory responses in human umbilical vein endothelial cells and in murine polymicrobial sepsis.
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- Acta Physiologica, 2014, v. 211, n. 1, p. 176, doi. 10.1111/apha.12264
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Functional characterization of ent-copalyl diphosphate synthase from Andrographis paniculata with putative involvement in andrographolides biosynthesis.
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- Biotechnology Letters, 2016, v. 38, n. 1, p. 131, doi. 10.1007/s10529-015-1961-7
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- Article
Neuroprotective and Antioxidant Constituents from Curcuma zedoaria Rhizomes.
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- Records of Natural Products, 2015, v. 9, n. 3, p. 349
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A New Labdane Diterpene and Other Constituents from Marrubium deserti Noe ex coss.
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- Records of Natural Products, 2011, v. 5, n. 4, p. 300
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- Article
Andrographolide exerted its antimicrobial effects by upregulation of human β-defensin-2 induced through p38 MAPK and NF-κB pathway in human lung epithelial cells.
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- Canadian Journal of Physiology & Pharmacology, 2012, v. 90, n. 5, p. 647, doi. 10.1139/y2012-050
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- Article
Anti-cancer labdane diterpenoids from adventitious roots of Andrographis paniculata: augmentation of production prospect endowed with pathway gene expression.
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- Protoplasma, 2018, v. 255, n. 5, p. 1387, doi. 10.1007/s00709-018-1211-7
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Andrographolide suppresses epithelial mesenchymal transition by inhibition of MAPK signalling pathway in lens epithelial cells.
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- Journal of Biosciences, 2015, v. 40, n. 2, p. 313, doi. 10.1007/s12038-015-9513-9
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- Article
Molecular Docking and Inhibition Kinetics of α-glucosidase Activity by Labdane Diterpenes Isolated from Tora Seeds ( Alpinia nigra B.L. Burtt.).
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- Applied Biochemistry & Biotechnology, 2015, v. 175, n. 3, p. 1477, doi. 10.1007/s12010-014-1366-4
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- Article
LCMS-DNP based dereplication of Araucaria cunninghamii Mudie gum-resin: identification of new cytotoxic labdane diterpene.
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- Natural Product Research, 2022, v. 36, n. 24, p. 6207, doi. 10.1080/14786419.2021.2024530
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A new diterpene and bioactivities of labdanes isolated from Buddleja marrubiifolia.
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- Natural Product Research, 2022, v. 36, n. 1, p. 71, doi. 10.1080/14786419.2020.1762184
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Labdanes: antifungal compounds isolates from the resinous exudate of Madia sativa against Phytophthora cinnamomi Rands.
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- Natural Product Research, 2020, v. 34, n. 16, p. 2310, doi. 10.1080/14786419.2018.1531402
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Antifungal activity against Botrytis cinerea of labdane-type diterpenoids isolated from the resinous exudate of Haplopappus velutinus Remy (Asteraceae).
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- Natural Product Research, 2019, v. 33, n. 16, p. 2408, doi. 10.1080/14786419.2018.1443093
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Antioxidant and anti-inflammatory activity of Ocimum labiatum extract and isolated labdane diterpenoid.
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- Journal of Inflammation, 2015, v. 12, n. 1, p. 1, doi. 10.1186/s12950-015-0049-4
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Antioxidant and anti-inflammatory activity of Ocimum labiatum extract and isolated labdane diterpenoid.
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- Journal of Inflammation, 2015, v. 12, n. 1, p. 88, doi. 10.1186/s12950-015-0049-4
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Enantioselective reduction of prochiral aryl ketones using a novel chiral auxiliary derived from a labdane diterpene.
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- ARKIVOC: Online Journal of Organic Chemistry, 2011, p. 128
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Labdane-Type Diterpene and Two Flavones from Salvia Sharifii Rech. f. and Esfan. and their Biological Activities.
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- Iranian Journal of Pharmaceutical Research, 2013, v. 12, n. 2, p. 395
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- Article
A reduction of viral mRNA, proteins and induction of altered morphogenesis reveals the anti-HTLV-1 activity of the labdane-diterpene myriadenolide in vitro.
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- BMC Microbiology, 2014, v. 14, n. 1, p. 565, doi. 10.1186/s12866-014-0331-2
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Paecilomycines A and B, Novel Diterpenoids, Isolated from Insect-Pathogenic Fungi Paecilomyces sp. ACCC 37762.
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- Helvetica Chimica Acta, 2015, v. 98, n. 5, p. 642, doi. 10.1002/hlca.201400272
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- Article
Two New Labdane-Type Diterpene Acids from the Wood of Cunninghamia konishii.
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- Helvetica Chimica Acta, 2015, v. 98, n. 1, p. 123, doi. 10.1002/hlca.201400138
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Isomeric ent-Labdane-Type Diterpenoids from the Stems of Rhizophora mucronata.
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- Helvetica Chimica Acta, 2014, v. 97, n. 11, p. 1531, doi. 10.1002/hlca.201400022
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Labdane Diterpenoids from the Roots of Amomum maximum and Their Cytotoxic Evaluation.
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- Helvetica Chimica Acta, 2014, v. 97, n. 8, p. 1140, doi. 10.1002/hlca.201300426
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Synthesis of novel podocarpa-8,11,13-triene-7- and 13-nitriles and evaluation of their anti-inflammatory and cytotoxic activity.
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- Journal of Chemical Research, 2016, v. 40, n. 8, p. 502, doi. 10.3184/174751916X14682323381549
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Use of (+)-manool in the synthesis of natural products. Part II. Diterpenes and relatives.
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- Journal of Chemical Research, 2013, v. 37, n. 2, p. 63, doi. 10.3184/174751912X13563728953551
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A new labdane diterpene from Rauvolfia tetraphylla Linn. (Apocynaceae).
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- Journal of Chemical Research, 2011, v. 35, n. 12, p. 678, doi. 10.3184/174751911X13220462651507
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Application and Evaluation of the Antifungal Activities of Glandular Trichome Secretions from Air/Sun-Cured Tobacco Germplasms against Botrytis cinerea.
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- Plants (2223-7747), 2024, v. 13, n. 14, p. 1997, doi. 10.3390/plants13141997
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Critical role of the death receptor pathway in the antitumoral effects induced by hispanolone derivatives.
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- Oncogene, 2013, v. 32, n. 2, p. 259, doi. 10.1038/onc.2012.23
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- Article
Identification and evaluation of agents isolated from traditionally used herbs against Ophiophagus hannah venom.
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- Drug Discoveries & Therapeutics, 2012, v. 6, n. 1, p. 18, doi. 10.5582/ddt.2012.v6.1.18
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- Article
Labdane Aldehyde Diterpenoids from Curcuma mangga Rhizome.
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- Journal of Pure & Applied Chemistry Research, 2023, v. 12, n. 3, p. 157, doi. 10.21776/ub.jpacr.2023.012.03.694
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Effects of Juniperus species and stage of maturity on nutritional, in vitro digestibility, and plant secondary compound characteristics.
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- Journal of Animal Science, 2015, v. 93, n. 8, p. 4034, doi. 10.2527/jas.2015-9274
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First synthesis of macrocyclic furanolabdanoids via cycloaddition of diacetylenic derivatives of lambertianic acid to 1,5-diazidopentane.
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- Doklady Chemistry, 2012, v. 446, n. 1, p. 174, doi. 10.1134/S0012500812090042
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- Article
New Diterpenoids from the Aerial Parts of Salvia reuterana.
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- Iranian Journal of Pharmaceutical Research, 2019, v. 18, n. 1, p. 406
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Labdane and Abietane Diterpenoids from Juniperus oblonga and Their Cytotoxic Activity.
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- Molecules, 2019, v. 24, n. 8, p. 1561, doi. 10.3390/molecules24081561
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Labdane-Type Diterpenes, Galangalditerpenes A-C, with Melanogenesis Inhibitory Activity from the Fruit of Alpinia galanga.
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- Molecules, 2017, v. 22, n. 12, p. 2279, doi. 10.3390/molecules22122279
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New Cytotoxic Seco-Type Triterpene and Labdane-Type Diterpenes from Nuxia oppositifolia.
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- Molecules, 2017, v. 22, n. 3, p. 389, doi. 10.3390/molecules22030389
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Labdane Diterpenes from the Fruits of Sinopodophyllum emodi.
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- Molecules, 2016, v. 21, n. 4, p. 434, doi. 10.3390/molecules21040434
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- Article
A Bicyclic Diterpenoid with a New 15,16-Dinorlabdane Carbon Skeleton from Leonurus japonicus and Its Coagulant Bioactivity.
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- Molecules, 2013, v. 18, n. 11, p. 13904, doi. 10.3390/molecules181113904
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Diterpenylquinone Hybrids: Synthesis and Assessment of Gastroprotective Mechanisms of Action in Human Cells.
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- Molecules, 2013, v. 18, n. 9, p. 11044, doi. 10.3390/molecules180911044
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Dimeric Labdane Diterpenes: Synthesis and Antiproliferative Effects.
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- Molecules, 2013, v. 18, n. 5, p. 5936, doi. 10.3390/molecules18055936
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Communic Acids: Occurrence, Properties and Use as Chirons for the Synthesis of Bioactive Compounds.
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- Molecules, 2012, v. 17, n. 2, p. 1448, doi. 10.3390/molecules17021448
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Chemical and transcriptomic analyses of leaf trichomes from Cistus creticus subsp. creticus reveal the biosynthetic pathways of certain labdane-type diterpenoids and their acetylated forms.
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- Journal of Experimental Botany, 2024, v. 75, n. 11, p. 3431, doi. 10.1093/jxb/erae098
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Evaluating Andrographolide as a Potent Inhibitor of NS3-4A Protease and Its Drug-Resistant Mutants Using In Silico Approaches.
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- Advances in Virology, 2015, p. 1, doi. 10.1155/2015/972067
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Antifilarial activity of diterpenoids from Taxodium distichum.
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- Parasites & Vectors, 2016, v. 9, p. 1, doi. 10.1186/s13071-016-1592-4
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Frontispiece: seco‐Labdanes: A Study of Terpenoid Structural Diversity Resulting from Biosynthetic C−C Bond Cleavage.
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- Chemistry - A European Journal, 2021, v. 27, n. 21, p. 1, doi. 10.1002/chem.202004574
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New Labdane-Type Diterpenoids from Leonurus heterophyllus.
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- Helvetica Chimica Acta, 2012, v. 95, n. 4, p. 618, doi. 10.1002/hlca.201100407
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Crystallization and X-ray diffraction analysis of a putative bacterial class I labdane-related diterpene synthase.
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- Acta Crystallographica: Section F, Structural Biology Communications, 2015, v. 71, n. 9, p. 1194, doi. 10.1107/S2053230X15014363
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- Article
Transformation of sclareol under ritter reaction conditions.
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- Russian Journal of Organic Chemistry, 2013, v. 49, n. 2, p. 303, doi. 10.1134/S1070428013020218
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