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Anti-Staphylococcal and Cytotoxic Compounds fromHyptis pectinata

https://doi.org/10.1055/s-2005-837831
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inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112706zenodo-depositor-declared
Distribution of 5,6-dihydro-α-pyrones by electrospray ionization ion trap mass spectrometry in different aerial parts of Hyptis monticola
inferred← citeshttps://doi.org/10.1002/ejoc.201300913openalex-snapshot
The First Total Synthesis of Synparvolide C
inferred← citeshttps://doi.org/10.1002/hlca.201500110openalex-snapshot
Stereoselective Total Synthesis of Pectinolides A, C, and H
inferred← citeshttps://doi.org/10.1007/978-94-007-6603-7_7openalex-snapshot
Antimicrobial Activity of Plants Used in México for Gastrointestinal and Respiratory Disorders
inferred← citeshttps://doi.org/10.1007/s11418-012-0693-4openalex-snapshot
Two new cembranoids from the leaves of Croton longissimus Airy Shaw
inferred← citeshttps://doi.org/10.1007/s11418-023-01698-7openalex-snapshot
Crotofolanes, rearranged crotofolanes, and a novel diterpene: isocrotofolane from Croton cascarilloides, collected in Okinawa
inferred← citeshttps://doi.org/10.1007/s43450-022-00333-yopenalex-snapshot
From Relative to Absolute Stereochemistry of Secondary Metabolites: Applications in Plant Chemistry
inferred← citeshttps://doi.org/10.1016/j.fitote.2006.06.001openalex-snapshot
Antinociceptive effect of Hyptis pectinata leaves extracts
inferred← citeshttps://doi.org/10.1016/j.hermed.2015.09.001openalex-snapshot
Chemical composition and antimicrobial, antioxidant activities and anti-inflammatory potential of Achillea millefolium L., Anethum graveolens L., and Carum copticum L. essential oils
inferred← citeshttps://doi.org/10.1016/j.indcrop.2013.08.052openalex-snapshot
Phytotoxic, DPPH scavenging, insecticidal activities and essential oil composition of Achillea vermicularis, A. teretifolia and proposed chemotypes of A. biebersteinii (Asteraceae)
inferred← citeshttps://doi.org/10.1016/j.indcrop.2017.04.046openalex-snapshot
Chemical composition and allelopathic, antibacterial, antifungal and in vitro acetylcholinesterase inhibitory activities of yarrow ( Achillea millefolium L.) native to India
inferred← citeshttps://doi.org/10.1016/j.jep.2010.11.055openalex-snapshot
Mexican medicinal plants used for cancer treatment: Pharmacological, phytochemical and ethnobotanical studies
inferred← citeshttps://doi.org/10.1016/j.jep.2016.04.045openalex-snapshot
Antibacterial activities of medicinal plants used in Mexican traditional medicine
inferred← citeshttps://doi.org/10.1016/j.jep.2020.113225openalex-snapshot
Subtribe Hyptidinae (Lamiaceae): A promising source of bioactive metabolites
inferred← citeshttps://doi.org/10.1016/j.jphotobiol.2009.04.002openalex-snapshot
In vitro phototoxic activity of Eugenia jambolana L. and Hyptis martiusii Benth
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112481openalex-snapshot
Dihydro-furanones from Hyptis species: Chemical correlations and DFT-NMR/ECD calculations for stereochemical assignments
inferred← citeshttps://doi.org/10.1016/j.tetasy.2014.09.009openalex-snapshot
The stereoselective total syntheses of pectinolides A, B, and C
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.06.033openalex-snapshot
A crotofolane-type diterpenoid and a rearranged nor-crotofolane-type diterpenoid with a new skeleton from the stems of Croton cascarilloides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.12.122openalex-snapshot
First stereoselective total synthesis of pectinolide H
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c00965openalex-snapshot
Hyptolactones and Their Biological Potential: A Systematic Review
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00953openalex-snapshot
Complementarity of DFT Calculations, NMR Anisotropy, and ECD for the Configurational Analysis of Brevipolides K–O from Hyptis brevipes
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00908openalex-snapshot
Structure Elucidation, Conformation, and Configuration of Cytotoxic 6-Heptyl-5,6-dihydro-2H-pyran-2-ones from Hyptis Species and Their Molecular Docking to α-Tubulin
inferred← citeshttps://doi.org/10.1021/jo200637gopenalex-snapshot
Vicinal 1H–1H NMR Coupling Constants from Density Functional Theory as Reliable Tools for Stereochemical Analysis of Highly Flexible Multichiral Center Molecules
inferred← citeshttps://doi.org/10.1021/jo500420jopenalex-snapshot
Studies of (−)-Pironetin Binding to α-Tubulin: Conformation, Docking, and Molecular Dynamics
inferred← citeshttps://doi.org/10.1021/np300740hopenalex-snapshot
Absolute Configuration and Conformational Analysis of Brevipolides, Bioactive 5,6-Dihydro-α-pyrones from Hyptis brevipes
inferred← citeshttps://doi.org/10.1080/14786419.2019.1628747openalex-snapshot
Evaluation of the cytotoxicity on breast cancer cell of extracts and compounds isolated from Hyptis pectinata (L.) poit
inferred← citeshttps://doi.org/10.1128/aac.00737-18openalex-snapshot
Argentilactone Molecular Targets in Paracoccidioides brasiliensis Identified by Chemoproteomics
inferred← citeshttps://doi.org/10.1248/cpb.53.1577openalex-snapshot
New Labdane Diterpenoids from Hyptis fasciculata
inferred← citeshttps://doi.org/10.1248/cpb.c12-01002openalex-snapshot
Eight New Diterpenoids and Two New Nor-Diterpenoids from the Stems of Croton cascarilloides
inferred← citeshttps://doi.org/10.1248/cpb.c15-00635openalex-snapshot
Crotocascarins I–K: Crotofolane-Type Diterpenoids, Crotocascarin γ, Isocrotofolane Glucoside and Phenolic Glycoside from the Leaves of Croton cascarilloides
inferred← citeshttps://doi.org/10.1248/cpb.c16-00500openalex-snapshot
Crotofolane-Type Diterpenoids, Crotocascarins L–Q, and a Rearranged Crotofolane-Type Diterpenoid, Neocrotocascarin, from the Stems of Croton cascarilloides
inferred← citeshttps://doi.org/10.1248/yakushi.19-00180openalex-snapshot
Structural Diversity of Chemical Constituents from Okinawan Plants
inferred← citeshttps://doi.org/10.1590/s0102-695x2008000500005openalex-snapshot
In vitro anti-staphylococcal activity of Hyptis martiusii Benth against methicillin-resistant Staphylococcus aureus: MRSA strains
inferred← citeshttps://doi.org/10.1590/s1517-83822012000400009openalex-snapshot
Antimicrobial activity of some medicinal plants from the cerrado of the central-western region of Brazil
inferred← citeshttps://doi.org/10.3109/13880200903382686openalex-snapshot
In vitroadditive effect ofHyptis martiusiiin the resistance to aminoglycosides of methicillin-resistantStaphylococcus aureus
inferred← citeshttps://doi.org/10.5155/eurjchem.6.1.93-97.1150openalex-snapshot
Stereoselective total synthesis of pectinolide H and 4'-epi-pectinolide H
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