The marine environment is considered one of the most important ecosystems with high biodiversity. Microorganisms in this environment are variable and coexist with other marine organisms. The microbes associated with other marine organisms produce compounds with biological activity that may help the host's defense against invading organisms. The symbiotic association of bacteria with marine invertebrates is of ecological and biotechnological importance. Biologically active metabolites isolated from bacteria associated with marine invertebrates are considered potential sources of natural antimicrobial molecules for treating infectious diseases. Many studies have been conducted to screen the antimicrobial activity of metabolites produced by bacteria associated with marine invertebrates. This work provides an overview of the advancements in antimicrobial compound research on bacteria associated with marine invertebrates.
- MeSH
- antibakteriální látky * farmakologie MeSH
- antiinfekční látky * farmakologie metabolismus chemie MeSH
- Bacteria * metabolismus izolace a purifikace chemie MeSH
- bezobratlí * mikrobiologie MeSH
- symbióza MeSH
- vodní organismy * mikrobiologie MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
Monascus pigments having yellow, orange, and red colors are widely studied for their potential beneficial properties. Many different biological activities have been reported regarding Monascus pigments and their derivatives, but the usual method is to test complex extracts from the mycelium of the fungus or from a fungus-fermented substrate. However, this review is mainly concerned with the biological activities of purified Monascus pigments. Both yellow (ankaflavin, monascin) and red (rubropunctamine, monascorubramine) Monascus pigments are proven antioxidants if used in concentrations of 10 μg/mL or higher. Antimicrobial activity against Gram-positive and Gram-negative bacteria and fungi has been observed with all Monascus pigments. However, the best antimicrobials are red Monascus pigments, and their amino acid derivatives (l-cysteine derivatives have MIC 4 μg/mL against Enterococcus faecalis). Yellow monaphilones and orange monaphilols seem to have the highest anti-inflammatory activity (IC50 1.7 μM of monaphilol D) and, together with red Monascus pigment derivatives, have mild antiobesity and antidiabetic activities. Further, monascin and ankaflavin in daily doses of 0.5 and 0.08 mg, respectively, lowered serum blood levels of low-density lipoprotein cholesterol complexes in rats on a high-fat diet. Orange Monascus pigments, rubropunctatin and monaphilols A and C, exhibit cytotoxic and antitumor activities (IC50 8-10 μM).
- MeSH
- antibakteriální látky farmakologie chemie izolace a purifikace MeSH
- antiflogistika farmakologie chemie izolace a purifikace MeSH
- antiinfekční látky farmakologie chemie izolace a purifikace MeSH
- antioxidancia farmakologie chemie izolace a purifikace MeSH
- biologické pigmenty * farmakologie chemie izolace a purifikace MeSH
- flaviny farmakologie chemie MeSH
- grampozitivní bakterie účinky léků MeSH
- heterocyklické sloučeniny tricyklické MeSH
- lidé MeSH
- mikrobiální testy citlivosti MeSH
- molekulární struktura MeSH
- Monascus * chemie MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
Hydrazinecarboxamides (semicarbazides) are increasingly recognized as a versatile scaffold in developing potential antimicrobial agents. In addition to a brief overview of the synthetic methods to prepare them, this review comprehensively analyses their antimicrobial properties. These derivatives have demonstrated potent activity against a broad spectrum of mycobacteria, bacterial and fungal pathogens, highlighting their potential to address critical human health challenges, including neglected diseases, and to combat growing antimicrobial resistance. They have also been investigated for their antiviral and antiparasitic properties. The review also summarizes structure-activity relationships, known mechanisms of action and emphasizes the crucial role of the hydrazinecarboxamide moiety in facilitating interactions with biological targets. The combination of hydrazinecarboxamides with other bioactive scaffolds (primaquine, isoniazid, etc.) has led to an identification of promising drug candidates, including those active against resistant strains, offering a promising approach for future innovations in the field of antimicrobial therapy. Attention is also drawn to limitations of hydrazinecarboxamides (poor physicochemical properties, cytotoxicity to human cells, and insufficient target selectivity), which may hinder their clinical application.
- MeSH
- antiinfekční látky * farmakologie chemie MeSH
- Bacteria účinky léků MeSH
- lidé MeSH
- semikarbazidy * farmakologie chemie MeSH
- vztahy mezi strukturou a aktivitou MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
This research paper presents a novel approach to the green synthesis of silver nanoparticles (AgNPs) using viticultural waste, allowing to obtain NP dispersions with distinct properties and morphologies (monodisperse and polydisperse AgNPs, referred to as mAgNPs and pAgNPs) and to compare their biological activities. Our synthesis method utilized the ethanolic extract of Vitis vinifera pruning residues, resulting in the production of mAgNPs and pAgNPs with average sizes of 12 ± 5 nm and 19 ± 14 nm, respectively. Both these AgNPs preparations demonstrated an exceptional stability in terms of size distribution, which was maintained for one year. Antimicrobial testing revealed that both types of AgNPs inhibited either the growth of planktonic cells or the metabolic activity of biofilm sessile cells in Gram-negative bacteria and yeasts. No comparable activity was found towards Gram-positives. Overall, pAgNPs exhibited a higher antimicrobial efficacy compared to their monodisperse counterparts, suggesting that their size and shape may provide a broader spectrum of interactions with target cells. Both AgNP preparations showed no cytotoxicity towards a human keratinocyte cell line. Furthermore, in vivo tests using a silkworm animal model indicated the biocompatibility of the phytosynthesized AgNPs, as they had no adverse effects on insect larvae viability. These findings emphasize the potential of targeted AgNPs synthesized from viticultural waste as environmentally friendly antimicrobial agents with minimal impact on higher organisms.
- MeSH
- antiinfekční látky farmakologie chemie MeSH
- biofilmy účinky léků MeSH
- bourec MeSH
- buněčné linie MeSH
- gramnegativní bakterie účinky léků MeSH
- keratinocyty účinky léků MeSH
- kovové nanočástice * chemie MeSH
- kvasinky účinky léků MeSH
- larva účinky léků MeSH
- lidé MeSH
- mikrobiální testy citlivosti * MeSH
- rostlinné extrakty farmakologie chemie MeSH
- stříbro * farmakologie chemie metabolismus MeSH
- technologie zelené chemie MeSH
- velikost částic MeSH
- viabilita buněk účinky léků MeSH
- Vitis * chemie MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- MeSH
- antiinfekční látky chemie klasifikace terapeutické užití MeSH
- antisepse * MeSH
- asepse * MeSH
- dezinfekce klasifikace metody MeSH
- hygiena rukou metody MeSH
- lidé MeSH
- sterilizace klasifikace metody MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- přehledy MeSH
Essential oils can be used in a variety of ways to treat microorganisms that have evolved antibiotic resistance. The research assessed the antimicrobial and antioxidant activities of essential oil obtained from Citrus Limonum, Citrus reticulate, and Citrus sinensis fresh peels using the hydro-distillation method. Their chemical compositions were analyzed by Gas Chromatography-Mass Spectrometer. Citrus oils had antimicrobial and antioxidant properties and their activity was increased with increasing concentrations. Oils had a significant antimicrobial effect on tested bacteria except on P. aeruginosa only C. Limonum had significant (p≤0.05) inhibitory effects at both 100 and 200 mg/ml. There was no significant (p>0.05) difference in the inhibition zone of tested oils against A. baumannii and ciprofloxacin at 25 mg/ml, which was the same as against E. coli at 200 mg/ml. The oil inhibitory effect on K. pneumoniae, P. mirabilis, and S. aureus was less than that obtained from ciprofloxacin at concentrations used. At 100 mg/mL, C. reticulate oil had a 23 mm inhibitory zone, while C. sinensis oil had a 23 mm inhibitory zone at 200 mg/mL, which was the same as the inhibitory area of ciprofloxacin against S. marcescens. Oils had convergent antifungal activity against Candida albicans that increased with increasing concentrations. The extracts competed favorably with voriconazole being used as a positive control. Citrus oils had convergent scavenging activities at the concentrations used. The studies confirmed the medicinal and industrial use of citrus essential oils as a therapeutic and antioxidant agent.
- MeSH
- antifungální látky analýza chemie farmakologie MeSH
- antiinfekční látky analýza chemie farmakologie MeSH
- antioxidancia analýza chemie farmakologie MeSH
- biomedicínský výzkum MeSH
- chemické techniky analytické metody přístrojové vybavení MeSH
- Citrus * chemie MeSH
- destilace metody přístrojové vybavení MeSH
- epidermis rostlin chemie MeSH
- farmakologické účinky MeSH
- fytonutrienty analýza chemie farmakologie MeSH
- oleje prchavé * analýza chemie farmakologie MeSH
- plynová chromatografie s hmotnostně spektrometrickou detekcí MeSH
- scavengery volných radikálů MeSH
- Geografické názvy
- Irák MeSH
This review comprehensively describes the recent advances in the synthesis and pharmacological evaluation of steroid polyamines squalamine, trodusquemine, ceragenins, claramine, and their diverse analogs and derivatives, with a special focus on their complete synthesis from cholic acids, as well as an antibacterial and antiviral, neuroprotective, antiangiogenic, antitumor, antiobesity and weight-loss activity, antiatherogenic, regenerative, and anxiolytic properties. Trodusquemine is the most-studied small-molecule allosteric PTP1B inhibitor. The discovery of squalamine as the first representative of a previously unknown class of natural antibiotics of animal origin stimulated extensive research of terpenoids (especially triterpenoids) comprising polyamine fragments. During the last decade, this new class of biologically active semisynthetic natural product derivatives demonstrated the possibility to form supramolecular networks, which opens up many possibilities for the use of such structures for drug delivery systems in serum or other body fluids.
- MeSH
- antiinfekční látky chemická syntéza chemie farmakologie MeSH
- biologické přípravky chemie farmakologie MeSH
- cholestanoly chemie MeSH
- cholestany chemie MeSH
- inhibitory angiogeneze chemická syntéza chemie farmakologie MeSH
- lidé MeSH
- neuroprotektivní látky chemická syntéza chemie farmakologie MeSH
- protinádorové látky chemická syntéza chemie farmakologie MeSH
- spermin analogy a deriváty chemie MeSH
- steroidy chemická syntéza chemie farmakologie MeSH
- triterpeny chemická syntéza chemie farmakologie MeSH
- vodní organismy chemie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
Naphthoquinones isolated from Quambalaria cyanescens (quambalarines) are natural pigments possessing significant cytotoxic and antimicrobial properties. Determining the structure of naphthoquinone compounds is important for the understanding of their biological activities and the informed synthesis of related analogues. Identifying quambalarines is challenging, because they contain a hydroxylated naphthoquinone scaffold and have limited solubility. Here, we report a detailed structural study of quambalarine derivatives, which form strong intramolecular hydrogen bonds (IMHBs) that enable the formation of several tautomers; these tautomers may complicate structural investigation due to their fast interconversion. To investigate tautomeric equilibria and identify new quambalarines, we complemented the experimental NMR spectroscopy data with density functional theory (DFT) calculations.
- MeSH
- antiinfekční látky chemie izolace a purifikace farmakologie MeSH
- Basidiomycota chemie MeSH
- magnetická rezonanční spektroskopie MeSH
- magnetická rezonanční tomografie MeSH
- molekulární struktura MeSH
- naftochinony chemie izolace a purifikace farmakologie MeSH
- protinádorové látky chemie izolace a purifikace farmakologie MeSH
- vodíková vazba MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Production of particles and their adaptation in the pharmacology became an object of interest, and they are the currently introduced therapies based on the use of micro and nanoparticles. The use of gold particles is not an exception. This review has focused on the application of gold micro and nanoparticles in pharmacology and biomedicine. The particles can be used for diagnosis respective theranostic of cancer, rheumatoid arthritis and as antimicrobial means. Besides these applications, specifications of gold, gold particles, and colloidal gold manufacturing and their comparison with the solid gold, are described as well. This review is based on a survey of actual scientific literature.
- MeSH
- antiflogistika chemie farmakologie MeSH
- antiinfekční látky chemie farmakologie MeSH
- Bacteria účinky léků MeSH
- biomedicínský výzkum MeSH
- houby účinky léků MeSH
- lidé MeSH
- nádory diagnóza farmakoterapie MeSH
- nanočástice chemie MeSH
- protinádorové látky chemie farmakologie MeSH
- revmatoidní artritida diagnóza farmakoterapie MeSH
- zlato chemie farmakologie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
In this review, we summarize the published data on squaric acid analogues with a special focus on their use in medicinal chemistry and as potential drugs. Squaric acid is an interesting small molecule with an almost perfectly square shape, and its analogues have a variety of biological activities that are enabled by the presence of significant H-bond donors and acceptors. Unfortunately, most of these compounds also exhibit reactive functionalities, and this deters the majority of medicinal chemists and pharmacologists from trying to use them in drug development. However, this group of compounds is experiencing a renaissance, and large numbers of them are being tested for antiprotozoal, antibacterial, antifungal, and antiviral activities. The most useful of these compounds exhibited IC50 values in the nanomolar range, which makes them promising drug candidates. In addition to these activities, their interactions with living systems were intensively explored, revealing that squaric acid analogues inhibit various enzymes and often serve as receptor antagonists and that the squaric acid moiety may be used as a non-classical isosteric replacement for other functional groups such as carboxylate. In summary, this review is focused on squaric acid and its analogues and their use in medicinal chemistry and should serve as a guide for other researchers in the field to demonstrate the potential of these compounds based on previous research.
- MeSH
- antiinfekční látky chemie farmakologie MeSH
- cyklobutany chemie farmakologie MeSH
- farmaceutická chemie MeSH
- inhibitory enzymů chemie farmakologie MeSH
- lidé MeSH
- objevování léků * MeSH
- protinádorové látky chemie farmakologie MeSH
- receptory N-methyl-D-aspartátu antagonisté a inhibitory MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
