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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

https://doi.org/10.1021/acs.jnatprod.8b00908
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/hlca.201500110openalex-snapshot
Stereoselective Total Synthesis of Pectinolides A, C, and H
inferredcites →https://doi.org/10.1002/mrc.4178openalex-snapshot
DFT 1H–1H coupling constants in the conformational analysis and stereoisomeric differentiation of 6‐heptenyl‐2H‐pyran‐2‐ones: configurational reassignment of synargentolide A
inferredcites →https://doi.org/10.1007/978-1-4899-1778-2_5openalex-snapshot
Bioactive Natural Products from Traditionally used Mexican Plants
inferredcites →https://doi.org/10.1007/978-3-642-18617-2_11openalex-snapshot
Labiatae
inferredcites →https://doi.org/10.1007/s10126-013-9506-3openalex-snapshot
Marine-Derived Aspergillus Species as a Source of Bioactive Secondary Metabolites
inferredcites →https://doi.org/10.1016/j.bjp.2015.07.029openalex-snapshot
Evaluation of the orofacial antinociceptive profile of the ethyl acetate fraction and its major constituent, rosmarinic acid, from the leaves of Hyptis pectinata on rodents
inferredcites →https://doi.org/10.1016/j.chembiol.2004.03.028openalex-snapshot
The Anticancer Natural Product Pironetin Selectively Targets Lys352 of α-Tubulin
inferredcites →https://doi.org/10.1016/j.chroma.2016.12.053openalex-snapshot
Countercurrent chromatography separation of saponins by skeleton type from Ampelozizyphus amazonicus for off-line ultra-high-performance liquid chromatography/high resolution accurate mass spectrometry analysis and characterisation
inferredcites →https://doi.org/10.1016/j.fitote.2015.07.012openalex-snapshot
Antibacterial constituents of Neohyptis paniculata
inferredcites →https://doi.org/10.1016/j.phymed.2007.09.009openalex-snapshot
Antinociceptive activity of the volatile oils of Hyptis pectinata L. Poit. (Lamiaceae) genotypes
inferredcites →https://doi.org/10.1016/j.phytochem.2003.08.017openalex-snapshot
α-Pyrones and a 2(5H)-furanone from Hyptis pectinata
inferredcites →https://doi.org/10.1016/j.tcb.2018.05.001openalex-snapshot
Microtubule-Targeting Agents: Strategies To Hijack the Cytoskeleton
inferredcites →https://doi.org/10.1016/j.tetlet.2012.12.039openalex-snapshot
First stereoselective total synthesis of pectinolide C and total synthesis of pectinolide A
inferredcites →https://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
inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00565openalex-snapshot
Antibacterial 3,6-Disubstituted 4-Hydroxy-5,6-dihydro-2H-pyran-2-ones from Serratia plymuthica MF371-2
inferredcites →https://doi.org/10.1021/cr000665jopenalex-snapshot
The Assignment of Absolute Configuration by NMR
inferredcites →https://doi.org/10.1021/cr2003344openalex-snapshot
Assignment of the Absolute Configuration of Polyfunctional Compounds by NMR Using Chiral Derivatizing Agents
inferredcites →https://doi.org/10.1021/jo034470yopenalex-snapshot
Stereoselective Synthesis and Determination of the Cytotoxic Properties of Spicigerolide and Three of Its Stereoisomers
inferredcites →https://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
inferredcites →https://doi.org/10.1021/jo500420jopenalex-snapshot
Studies of (−)-Pironetin Binding to α-Tubulin: Conformation, Docking, and Molecular Dynamics
inferredcites →https://doi.org/10.1021/np200864mopenalex-snapshot
Reversal of Multidrug Resistance by Morning Glory Resin Glycosides in Human Breast Cancer Cells
inferredcites →https://doi.org/10.1021/np500897yopenalex-snapshot
α-Glucosidase Inhibitors from a Xylaria feejeensis Associated with Hintonia latiflora
inferredcites →https://doi.org/10.1021/np50094a019openalex-snapshot
Structure and Stereochemistry of Pectinolides A-C, Novel Antimicrobial and Cytotoxic 5,6-Dihydro-α-pyrones from Hyptis pectinata
inferredcites →https://doi.org/10.1021/np50100a011openalex-snapshot
Cytotoxic Constituents from Hyptis verticillata
inferredcites →https://doi.org/10.1021/np800568jopenalex-snapshot
Tubulin-Interactive Natural Products as Anticancer Agents
inferredcites →https://doi.org/10.1021/np980222zopenalex-snapshot
Novel Labdane Diterpenes from the Insecticidal Plant Hyptis spicigera
inferredcites →https://doi.org/10.1021/ol0062852openalex-snapshot
Absolute Configuration of 1,n-Diols by NMR: The Importance of the Combined Anisotropic Effects in Bis-Arylmethoxyacetates
inferredcites →https://doi.org/10.1038/aps.2014.34openalex-snapshot
Tubulin inhibitors: pharmacophore modeling, virtual screening and molecular docking
inferredcites →https://doi.org/10.1038/ncomms12103openalex-snapshot
Pironetin reacts covalently with cysteine-316 of α-tubulin to destabilize microtubule
inferredcites →https://doi.org/10.1038/nprot.2007.354openalex-snapshot
Mosher ester analysis for the determination of absolute configuration of stereogenic (chiral) carbinol carbons
inferredcites →https://doi.org/10.1039/9781849734684-00001openalex-snapshot
Chapter 1. Application of the Nuclear Overhauser Effect to the Structural Elucidation of Natural Products
inferredcites →https://doi.org/10.1055/s-2005-837831openalex-snapshot
Anti-Staphylococcal and Cytotoxic Compounds fromHyptis pectinata
inferredcites →https://doi.org/10.1080/10412905.2016.1210039openalex-snapshot
Essential oil constituents from high altitude Brazilian species with antimicrobial activity: Baccharis parvidentata Malag., Hyptis monticola Mart. ex Benth. and Lippia origanoides Kunth
inferredcites →https://doi.org/10.1093/jnci/82.13.1107openalex-snapshot
New Colorimetric Cytotoxicity Assay for Anticancer-Drug Screening
inferredcites →https://doi.org/10.1111/j.1601-0825.2007.01405.xopenalex-snapshot
Hyptis pectinata essential oil: chemical composition and anti‐Streptococcus mutans activity
inferredcites →https://doi.org/10.1590/s0100-40422008000700009openalex-snapshot
Chemical composition and antimicrobial activity of the essential oil of Hyptis pectinata (l.) Poit.
inferredcites →https://doi.org/10.1590/s0102-695x2007000100021openalex-snapshot
Synopsis of the plants known as medicinal and poisonous in Northeast of Brazil
inferredcites →https://doi.org/10.3891/acta.chem.scand.41b-0599openalex-snapshot
Molecular and Crystal Structure of Hyptolide, a Naturally Occurring alpha,beta-Unsaturated delta-Lactone.

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112481zenodo-depositor-declared
Dihydro-furanones from Hyptis species: Chemical correlations and DFT-NMR/ECD calculations for stereochemical assignments
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/10.1007/978-3-031-81728-1_5openalex-snapshot
Computational Approaches to Model Macromolecules
inferred← citeshttps://doi.org/10.1007/s00706-022-02923-xopenalex-snapshot
Multicomponent synthesis of a novel bicyclic pyran-2-one system
inferred← citeshttps://doi.org/10.1007/s40415-020-00582-yopenalex-snapshot
A review of the phytochemical profiling and biological activities of Hyptis Jacq.: a Brazilian native genus of Lamiaceae
inferred← citeshttps://doi.org/10.1007/s43450-020-00081-xopenalex-snapshot
Absolute Stereochemistry of Antifungal Limonene-1,2-diols from Lippia rubella
inferred← citeshttps://doi.org/10.1007/s43450-023-00424-4openalex-snapshot
Brazilian Medicinal Plants with Antiamyloidogenic Activity
inferred← citeshttps://doi.org/10.1007/s43450-024-00561-4openalex-snapshot
Recycling Preparative Liquid Chromatography, the Overlooked Methodology for the Purification of Natural Products
inferred← citeshttps://doi.org/10.1016/j.fct.2021.112095openalex-snapshot
Hyptis mociniana: phytochemical fingerprint and photochemoprotective effect against UV-B radiation-induced erythema and skin carcinogenesis
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.tet.2021.132004openalex-snapshot
Total synthesis of monticolides A and B
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.8b00975openalex-snapshot
Antifungal Phenylpropanoid Glycosides from Lippia rubella
inferred← citeshttps://doi.org/10.1080/14756366.2021.2022658openalex-snapshot
In vitro α-glucosidase inhibition by Brazilian medicinal plant extracts characterised by ultra-high performance liquid chromatography coupled to mass spectrometry
inferred← citeshttps://doi.org/10.12688/f1000research.161261.1openalex-snapshot
Nat-UV DB: A Natural Products Database Underlying of Veracruz-Mexico
inferred← citeshttps://doi.org/10.14710/jksa.22.6.305-309openalex-snapshot
Total Hyptolide of Indonesian Hyptis pectinata extracts in a various solvent using HPLC and UV-Vis spectroscopy and their toxicities
inferred← citeshttps://doi.org/10.3390/microorganisms9091807openalex-snapshot
Characterization of Pseudomonas aeruginosa Quorum Sensing Inhibitors from the Endophyte Lasiodiplodia venezuelensis and Evaluation of Their Antivirulence Effects by Metabolomics
inferred← citeshttps://doi.org/10.3390/molecules24213908openalex-snapshot
Computer-Aided Chemotaxonomy and Bioprospecting Study of Diterpenes of the Lamiaceae Family
inferred← citeshttps://doi.org/10.3390/molecules28196767openalex-snapshot
Antioxidant Properties and Secondary Metabolites Profile of Hyptis colombiana at Various Phenological Stages
inferred← citeshttps://doi.org/10.3390/plants12020296openalex-snapshot
Molecular Docking of Cryptoconcatones to α-Tubulin and Related Pironetin Analogues
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