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Structure of Membrane-Bound Amphidinol 3 in Isotropic Small Bicelles

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

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Merck molecular force field. I. Basis, form, scope, parameterization, and performance of MMFF94
inferredcites →https://doi.org/10.1002/jcc.540120908openalex-snapshot
An unbounded systematic search of conformational space
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Magnetically Oriented Phospholipid Bilayered Micelles for Structural Studies of Polypeptides. Does the Ideal Bicelle Exist?
inferredcites →https://doi.org/10.1016/0040-4039(95)01259-kopenalex-snapshot
Isolation and chemical structure of amphidinol 2, a potent hemolytic compound from marine dinoflagellate Amphidinium klebsii
inferredcites →https://doi.org/10.1016/0079-6565(94)80012-xopenalex-snapshot
Magnetically-oriented phospholipid micelles as a tool for the study of membrane-associated molecules
inferredcites →https://doi.org/10.1016/j.bbamem.2004.06.005openalex-snapshot
Direct observation and characterization of DMPC/DHPC aggregates under conditions relevant for biological solution NMR
inferredcites →https://doi.org/10.1016/j.bmc.2006.06.012openalex-snapshot
Structures of new amphidinols with truncated polyhydroxyl chain and their membrane-permeabilizing activities
inferredcites →https://doi.org/10.1016/j.bmc.2007.12.029openalex-snapshot
Effects of lipid constituents on membrane-permeabilizing activity of amphidinols
inferredcites →https://doi.org/10.1016/j.tet.2005.01.069openalex-snapshot
Hairpin conformation of amphidinols possibly accounting for potent membrane permeabilizing activities
inferredcites →https://doi.org/10.1016/j.tet.2005.07.004openalex-snapshot
Isolation and structure elucidation of a new amphidinol with a truncated polyhydroxyl chain from Amphidinium klebsii
inferredcites →https://doi.org/10.1016/j.tetlet.2004.05.067openalex-snapshot
Lingshuiols A and B, two new polyhydroxy compounds from the Chinese marine dinoflagellate Amphidinium sp.
inferredcites →https://doi.org/10.1016/j.tetlet.2006.02.045openalex-snapshot
Karatungiols A and B, two novel antimicrobial polyol compounds, from the symbiotic marine dinoflagellate Amphidinium sp.
inferredcites →https://doi.org/10.1016/s0005-2736(01)00358-3openalex-snapshot
Morphology of fast-tumbling bicelles: a small angle neutron scattering and NMR study
inferredcites →https://doi.org/10.1016/s0006-3495(01)75864-xopenalex-snapshot
Structural Evaluation of Phospholipid Bicelles for Solution-State Studies of Membrane-Associated Biomolecules
inferredcites →https://doi.org/10.1021/j100168a057openalex-snapshot
Structure of mixed short-chain lecithin/long-chain lecithin aggregates studied by small-angle neutron scattering
inferredcites →https://doi.org/10.1021/ja00026a027openalex-snapshot
Amphidinol, a polyhydroxy-polyene antifungal agent with an unprecedented structure, from a marine dinoflagellate, Amphidinium klebsii
inferredcites →https://doi.org/10.1021/ja00172a038openalex-snapshot
Semianalytical treatment of solvation for molecular mechanics and dynamics
inferredcites →https://doi.org/10.1021/ja017875dopenalex-snapshot
Micelle-Induced Curvature in a Water-Insoluble HIV-1 Env Peptide Revealed by NMR Dipolar Coupling Measurement in Stretched Polyacrylamide Gel
inferredcites →https://doi.org/10.1021/ja075024lopenalex-snapshot
Conformation and Location of Membrane-Bound Salinomycin−Sodium Complex Deduced from NMR in Isotropic Bicelles
inferredcites →https://doi.org/10.1021/ja983655xopenalex-snapshot
Absolute Configuration of Amphidinol 3, the First Complete Structure Determination from Amphidinol Homologues: Application of a New Configuration Analysis Based on Carbon−Hydrogen Spin-Coupling Constants
inferredcites →https://doi.org/10.1021/jm051210vopenalex-snapshot
Detailed Description of the Conformation and Location of Membrane-Bound Erythromycin A Using Isotropic Bicelles
inferredcites →https://doi.org/10.1021/jo970273lopenalex-snapshot
Luteophanol A, a New Polyhydroxyl Compound from Symbiotic Marine Dinoflagellate Amphidinium sp.
inferredcites →https://doi.org/10.1021/la053177lopenalex-snapshot
Size and Shape of Fast-tumbling Bicelles as Determined by Translational Diffusion
inferredcites →https://doi.org/10.1111/j.1432-1033.1996.00586.xopenalex-snapshot
Location of Cholesterol in Model Membranes by Magic‐Angle‐Sample‐Spinning NMR
inferredcites →https://doi.org/10.1529/biophysj.104.049817openalex-snapshot
Melittin-Induced Bilayer Leakage Depends on Lipid Material Properties: Evidence for Toroidal Pores

What points at this work

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

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inferred← citeshttps://doi.org/10.1002/asia.70353openalex-snapshot
Synthesis and Structure–Activity Relationship Studies of Truncated Artificial Analogues of Amphidinol 3
inferred← citeshttps://doi.org/10.1002/tcr.201402097openalex-snapshot
Bioactive Structure of Membrane Lipids and Natural Products Elucidated by a Chemistry‐Based Approach
inferred← citeshttps://doi.org/10.1007/978-981-97-6830-1_6openalex-snapshot
NMR Studies on Natural Product—Stereochemical Determination and Conformational Analysis in Solution and in Membrane
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Bioactive Metabolites from Marine Dinoflagellates
inferred← citeshttps://doi.org/10.1016/j.algal.2018.01.010openalex-snapshot
A pilot-scale bioprocess to produce amphidinols from the marine microalga Amphidinium carterae: Isolation of a novel analogue
inferred← citeshttps://doi.org/10.1016/j.bbamem.2018.07.010openalex-snapshot
Theonellamide A, a marine-sponge-derived bicyclic peptide, binds to cholesterol in aqueous DMSO: Solution NMR-based analysis of peptide-sterol interactions using hydroxylated sterol
inferred← citeshttps://doi.org/10.1016/j.bmc.2016.08.043openalex-snapshot
Sterol-dependent membrane association of the marine sponge-derived bicyclic peptide Theonellamide A as examined by 1H NMR
inferred← citeshttps://doi.org/10.1016/j.bmcl.2010.02.025openalex-snapshot
Sterol effect on interaction between amphidinol 3 and liposomal membrane as evidenced by surface plasmon resonance
inferred← citeshttps://doi.org/10.1016/j.bmcl.2023.129594openalex-snapshot
Truncated Derivatives of Amphidinol 3 Reveal the Functional Role of Polyol Chain in Sterol-Recognition and Pore Formation
inferred← citeshttps://doi.org/10.1016/j.pnmrs.2013.01.001openalex-snapshot
When detergent meets bilayer: Birth and coming of age of lipid bicelles
inferred← citeshttps://doi.org/10.1016/j.tet.2013.05.067openalex-snapshot
Iron-catalyzed cross-coupling between C-bromo mannopyranoside derivatives and a vinyl Grignard reagent: toward the synthesis of the C31–C52 fragment of amphidinol 3
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.11.033openalex-snapshot
Amdigenol A, a long carbon-backbone polyol compound, produced by the marine dinoflagellate Amphidinium sp
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.09.094openalex-snapshot
Amdigenols E and G, long carbon-chain polyol compounds, isolated from the marine dinoflagellate Amphidinium sp.
inferred← citeshttps://doi.org/10.1021/bi5002932openalex-snapshot
Direct and Stereospecific Interaction of Amphidinol 3 with Sterol in Lipid Bilayers
inferred← citeshttps://doi.org/10.1021/ja9091853openalex-snapshot
Structure and Absolute Configuration of Karlotoxin-2, an Ichthyotoxin from the Marine Dinoflagellate Karlodinium veneficum
inferred← citeshttps://doi.org/10.1021/jacs.9b11789openalex-snapshot
Total Synthesis of Amphidinol 3: A General Strategy for Synthesizing Amphidinol Analogues and Structure–Activity Relationship Study
inferred← citeshttps://doi.org/10.1021/la500231zopenalex-snapshot
Characterization of the Morphology of Fast-Tumbling Bicelles with Varying Composition
inferred← citeshttps://doi.org/10.1038/s41429-021-00468-5openalex-snapshot
Marine natural products targeting the eukaryotic cell membrane
inferred← citeshttps://doi.org/10.1038/s41598-017-11135-xopenalex-snapshot
Channel Formation and Membrane Deformation via Sterol-Aided Polymorphism of Amphidinol 3
inferred← citeshttps://doi.org/10.1038/s41598-024-68669-0openalex-snapshot
Sterolysin from a 1950s culture of Karlodinium veneficum (aka Gymnodinium veneficum Ballantine) forms lethal sterol dependent membrane pores
inferred← citeshttps://doi.org/10.1039/b906091jopenalex-snapshot
Marine natural products
inferred← citeshttps://doi.org/10.1039/c0np00002gopenalex-snapshot
3D structures of membrane-associated small molecules as determined in isotropic bicelles
inferred← citeshttps://doi.org/10.1039/c0ob00685hopenalex-snapshot
Synthesis of 6-F-ergosterol and its influence on membrane-permeabilization of amphotericin B and amphidinol 3
inferred← citeshttps://doi.org/10.1039/c2ob26641eopenalex-snapshot
Diastereoselective synthesis of the C17–C30 fragment of amphidinol 3
inferred← citeshttps://doi.org/10.1039/c3ob41569dopenalex-snapshot
Diastereoselective synthesis of the C14–C29 fragment of amphidinol 3
inferred← citeshttps://doi.org/10.1039/c9np00059copenalex-snapshot
Chemical diversity and mode of action of natural products targeting lipids in the eukaryotic cell membrane
inferred← citeshttps://doi.org/10.1039/np9900700269openalex-snapshot
Marine natural products
inferred← citeshttps://doi.org/10.1201/b13868-13openalex-snapshot
Bioactive Molecules from Symbiotic Marine Dinoflagellates
inferred← citeshttps://doi.org/10.1246/bcsj.20220273openalex-snapshot
Formation of a Tight Complex between Amphidinol 3 and Sterols in Lipid Bilayers Revealed by Short-Range Energy Transfer
inferred← citeshttps://doi.org/10.1246/cl.170050openalex-snapshot
Synthesis of a Truncated Analog of Amphidinol 3 Corresponding to the C21–C39/C52–C67 Section
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Membrane permeabilizing action of amphidinol 3 and theonellamide A in raft-forming lipid mixtures
inferred← citeshttps://doi.org/10.2183/pjab.101.016openalex-snapshot
Conformational dynamics and molecular interactions of natural products: unveiling functional structures in biological membranes
inferred← citeshttps://doi.org/10.3390/md19080432openalex-snapshot
Isolation and Structural Elucidation of New Amphidinol Analogues from Amphidinium carterae Cultivated in a Pilot-Scale Photobioreactor
inferred← citeshttps://doi.org/10.3987/com-10-s(e)86openalex-snapshot
Structural Reevaluations of Amphidinol 3, a Potent Antifungal Compound from Dinoflagellate
inferred← citeshttps://doi.org/10.3987/com-18-13927openalex-snapshot
Synthesis of an Analog of Amphidinol 3 Corresponding to the C31–C67 Section
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Structure and Interaction in Lipid Bilayers Analyzed Using Bicelles
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