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Liposome-based formulations for the antibiotic nonapeptide Leucinostatin A: Fourier transform infrared spectroscopy characterization and in vivo toxicologic study
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Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
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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/bip.360250307openalex-snapshot
Examination of the secondary structure of proteins by deconvolved FTIR spectra
inferredcites →https://doi.org/10.1002/bip.360280138openalex-snapshot
The crystal and molecular structure of the α‐helical nonapeptide antibiotic leucinostatin A
inferredcites →https://doi.org/10.1006/jcis.2000.6816openalex-snapshot
Antimicrobial Nonapeptide Leucinostatin A-Dependent Effects on the Physical Properties of Phospholipid Model Membranes
inferredcites →https://doi.org/10.1016/0003-9861(78)90457-5openalex-snapshot
Inhibition of energy conservation reactions in chromatophores of Rhodospirillum rubrum by antibiotics
inferredcites →https://doi.org/10.1016/0005-2736(85)90521-8openalex-snapshot
Production of large unilamellar vesicles by a rapid extrusion procedure. Characterization of size distribution, trapped volume and ability to maintain a membrane potential
inferredcites →https://doi.org/10.1016/0167-4889(94)90004-3openalex-snapshot
The nonapeptide leucinostatin A acts as a weak ionophore and as an immunosuppressant on T lymphocytes
inferredcites →https://doi.org/10.1016/0304-4157(84)90017-0openalex-snapshot
Polymorphic phase behaviour of phospholipid membranes studied by infrared spectroscopy
inferredcites →https://doi.org/10.1016/0928-0987(94)90011-6openalex-snapshot
Liposome-associated retinoids: production, characterization and antiproliferative activity on neoplastic cells
inferredcites →https://doi.org/10.1016/s0021-9258(19)35423-7openalex-snapshot
Lipid-induced changes in the secondary structure of snake venom cardiotoxins.
inferredcites →https://doi.org/10.1016/s0168-9452(97)00131-3openalex-snapshot
Acremonium sp.—a leucinostatin A producing endophyte of European yew (Taxus baccata)
inferredcites →https://doi.org/10.1016/s0174-3031(84)80082-7openalex-snapshot
Leucinostatins, Peptide Mycotoxins Produced by Paecilomyces lilacinus and their Possible Roles in Fungal Infection
inferredcites →https://doi.org/10.1073/pnas.79.24.7951openalex-snapshot
Peptaibol antibiotics: a study on the helical structure of the 2-9 sequence of emerimicins III and IV.
inferredcites →https://doi.org/10.1111/j.1399-3011.1989.tb00205.xopenalex-snapshot
Structural studies of leucinostatin A and its Boc‐Aib‐Leu‐Leu‐Aib‐OMe tetrapeptide fragment
inferredcites →https://doi.org/10.1247/csf.15.53openalex-snapshot
Dual inhibitory effects of the peptide antibiotics leucinostatins on oxidative phosphorylation in mitochondria.
inferredcites →https://doi.org/10.7164/antibiotics.36.1613openalex-snapshot
Studies on peptide antibiotics, leucinostatins. II. The structures of leucinostatins A and B.
inferredcites →https://doi.org/10.7164/antibiotics.40.130openalex-snapshot
Leucinostatin D. A novel peptide antibiotic from Paecilomyces marquandii.
inferredcites →https://doi.org/10.7164/antibiotics.40.714openalex-snapshot
Leucinostatins H and K, two novel peptide antibiotics with tertiay amine-oxide terminal group from Paecilomyces marquandii Isolation, structure and biological activity.
inferredcites →https://doi.org/10.7164/antibiotics.48.254openalex-snapshot
Structure Activity Studies on Chemically Modified Homologues of the Antibiotic Phytotoxic Leucinostatin A.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/ange.202102153openalex-snapshot
Antiprotozoische Struktur‐Aktivitäts‐Beziehungen von synthetischen Leucinostatin‐Derivaten und Aufklärung ihres Wirkprinzips
inferred← citeshttps://doi.org/10.1002/anie.202102153openalex-snapshot
Antiprotozoal Structure–Activity Relationships of Synthetic Leucinostatin Derivatives and Elucidation of their Mode of Action
inferred← citeshttps://doi.org/10.1002/bip.10493openalex-snapshot
Spectroscopic investigation on gel‐forming β‐sheet assemblage of peptide derivatives
inferred← citeshttps://doi.org/10.1007/s11274-016-2038-zopenalex-snapshot
Evidence for the involvement of nematocidal toxins of Purpureocillium lilacinum 6029 cultured on Karanja deoiled cake liquid medium
inferred← citeshttps://doi.org/10.1016/j.chphi.2024.100519openalex-snapshot
Facile one-pot electrochemical synthesis and encapsulation of carbon quantum dots in GUVs
inferred← citeshttps://doi.org/10.1016/j.ejpb.2014.01.008openalex-snapshot
Development of Process Analytical Technology (PAT) methods for controlled release pellet coating
inferred← citeshttps://doi.org/10.1016/j.ijpharm.2004.01.030openalex-snapshot
Leucinostatin-A loaded nanospheres: characterization and in vivo toxicity and efficacy evaluation
inferred← citeshttps://doi.org/10.1016/j.powtec.2010.09.006openalex-snapshot
Study of the preparation of a multiparticulate drug delivery system with a layering technique
inferred← citeshttps://doi.org/10.1016/s0731-7085(01)00365-xopenalex-snapshot
Microbiological and densitometric TLC analyses for peptides in liposomes
inferred← citeshttps://doi.org/10.1111/j.1472-765x.2004.01488.xopenalex-snapshot
Production of leucinostatins and nematicidal activity of Australian isolates of Paecilomyces lilacinus (Thom) Samson
inferred← citeshttps://doi.org/10.1186/s12940-024-01092-0openalex-snapshot
Toxicological evaluation of microbial secondary metabolites in the context of European active substance approval for plant protection products
inferred← citeshttps://doi.org/10.2174/1567201817666200115163506openalex-snapshot
Investigation on the Preparation, Characteristics, and Controlled Release Model of Paeonol-Loaded Liposome in Carbomer Hydrogel
inferred← citeshttps://doi.org/10.2533/chimia.2023.593openalex-snapshot
Key Contributions by the Swiss Tropical and Public Health Institute Towards New and Better Drugs for Tropical Diseases
inferred← citeshttps://doi.org/10.2903/sp.efsa.2017.en-1274openalex-snapshot
Database on the taxonomical characterisation and potential toxigenic capacities of microorganisms used for the industrial production of food enzymes and feed additives, which do not have a recommendation for Qualified Presumption of Safety
inferred← citeshttps://doi.org/10.48780/publications.aston.ac.uk.00033302openalex-snapshot
Liposomes:a multifaceted delivery system
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