Tag: M.W=500-550

Polak, Jolanta published the artcileBioactive Properties of a Novel Antibacterial Dye Obtained from Laccase-Mediated Oxidation of 8-Anilino-1-naphthalenesulfonic Acid, Application of Ammonium 2,2′-(hydrazine-1,2-diylidene)bis(3-ethyl-2,3-dihydrobenzo[d]thiazole-6-sulfonate), the publication is Molecules (2022), 27(2), 487, database is CAplus and MEDLINE.

Fungal laccase obtained from a Cerrena unicolor strain was used as an effective biocatalyst for the transformation of 8-anilino-1-naphthalenesulfonic acid into a green-colored antibacterial compound, which can be considered as both an antimicrobial agent and a textile dye, simultaneously. The process of biosynthesis was performed in buffered solutions containing methanol as a co-solvent, allowing better solubilization of substrate. The transformation process was optimized in terms of the buffer pH value, laccase activity, and concentrations of the substrate and co-solvent. The crude product obtained exhibited low cytotoxicity, antibacterial properties against Staphylococcus aureus and Staphylococcus epidermidis, and antioxidant properties. Moreover, the synthesized green-colored compound proved non-allergenic and demonstrated a high efficiency of dyeing wool fibers.

Molecules published new progress about 30931-67-0. 30931-67-0 belongs to thiazole, auxiliary class Salt,Hydrazine,Amine,Benzothiazole, name is Ammonium 2,2′-(hydrazine-1,2-diylidene)bis(3-ethyl-2,3-dihydrobenzo[d]thiazole-6-sulfonate), and the molecular formula is C18H24N6O6S4, Application of Ammonium 2,2′-(hydrazine-1,2-diylidene)bis(3-ethyl-2,3-dihydrobenzo[d]thiazole-6-sulfonate).

Referemce:
https://pubchem.ncbi.nlm.nih.gov/compound/thiazole,
Thiazole | chemical compound | Britannica

Fonseca, I. published the artcileUndervalued Atlantic brown seaweed species (Cystoseira abies-marina and Zonaria tournefortii): influence of treatment on their nutritional and bioactive potential and bioaccessibility, Quality Control of 30931-67-0, the publication is European Food Research and Technology (2021), 247(1), 221-232, database is CAplus.

The brown seaweed species Cystoseira abies-marina and Zonaria tournefortii are abundant Atlantic resources that remain undervalued. This results from an insufficient knowledge of their nutrients’ and bioactive potential. There is also uncertainty regarding the adequate culinary treatment of these seaweeds prior to their consumption. Thus, the current study evaluated the composition, bioactivity, and bioaccessibility of target compounds and bioactivities of these two species as a function of two treatments, simple rehydration and steaming, in comparison to sun-dried seaweed. The proportion of SFA, MUFA, and PUFA differed between species. C. abies-marina was richer in PUFA (30-31% vs 20-21%) and Z. tournefortii was richer in SFA (53-57% vs 46-47%). Main contributors to ω3 PUFA content were different in each species: alpha-linolenic acid in C. abies-marina, 4.5-5.1%, and eicosapentaenoic acid in Z. tournefortii, 5.8-6.7%. The sum of Mg and Ca contents in Z. tournefortii was two-fold the same sum in the other species. Furthermore, rehydration led to an elemental concentration reduction in most instances. The As content in C. abies-marina was very high, ranging between 295 ± 5 mg/kg dw and 369 ± 2 mg/kg dw, in rehydrated and steam-cooked seaweed, resp. While aqueous extracts of C. abies-marina had the highest phenolic contents, 620-1280 mg GAE/100 g dw, aqueous extracts of Z. tournefortii contained 170-280 mg GAE/100 g dw. Regarding bioaccessibility, Mg, K, Ca, As, and Cd showed relatively high bioaccessibility levels and it was shown that only a limited part of the original antioxidant activity in both species is bioaccessible.

European Food Research and Technology published new progress about 30931-67-0. 30931-67-0 belongs to thiazole, auxiliary class Salt,Hydrazine,Amine,Benzothiazole, name is Ammonium 2,2′-(hydrazine-1,2-diylidene)bis(3-ethyl-2,3-dihydrobenzo[d]thiazole-6-sulfonate), and the molecular formula is C18H24N6O6S4, Quality Control of 30931-67-0.

Referemce:
https://pubchem.ncbi.nlm.nih.gov/compound/thiazole,
Thiazole | chemical compound | Britannica

Ofosu, Fred Kwame published the artcilePhenolic profile, antioxidant, and antidiabetic potential exerted by millet grain varieties, Application of Ammonium 2,2′-(hydrazine-1,2-diylidene)bis(3-ethyl-2,3-dihydrobenzo[d]thiazole-6-sulfonate), the publication is Antioxidants (2020), 9(3), 254, database is CAplus and MEDLINE.

This study evaluated the potential antioxidant and antidiabetic properties in vitro of four millet grain varieties cultivated in South Korea. The free fractions were tested for their total antioxidant capacity using 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS+) and 2,2′-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging assays, followed by α-glucosidase, α-amylase, and advanced glycation endproducts (AGEs) formation inhibition assays. The total phenolics, flavonoids, and condensed tannins in the free fractions ranged from 107.8 to 136.4 mg ferulic acid equivalent (FAE)/100 g, 101.3 to 115.8 mg catechin equivalent (CE)/100 g, and 17.65 to 59.54 mg catechin equivalent (CE)/100 g, resp. Finger Italian millet had the highest total phenolic content (136.4 mg FAE/100 g) and flavonoid content (115.8 mg CE/100 g). Barnyard and finger Italian millet showed the highest DPPH (IC50 = 359.6μg/mL and 436.25μg/mL, resp.) and ABTS radical scavenging activity (IC50 = 362.40μg/mL and 381.65μg/mL, resp.). Similarly, finger Italian millet also exhibited significantly lower IC50 values for the percentage inhibition of α-glucosidase (18.07μg/mL) and α-amylase (10.56μg/mL) as compared with acarbose (IC50 = 59.34μg/mL and 27.73μg/mL, resp.) and AGEs formation (33.68μg/mL) as compared with aminoguanidine (AG) (52.30μg/mL). All eight phenolic compounds identified in finger Italian millet were flavonoids, with flavanols being the predominant subclass. Taken together, millet flavonoids play important roles in the prevention and management of type 2 diabetes, and hence finger Italian millet has the potential to be developed as a functional food.

Antioxidants published new progress about 30931-67-0. 30931-67-0 belongs to thiazole, auxiliary class Salt,Hydrazine,Amine,Benzothiazole, name is Ammonium 2,2′-(hydrazine-1,2-diylidene)bis(3-ethyl-2,3-dihydrobenzo[d]thiazole-6-sulfonate), and the molecular formula is C18H24N6O6S4, Application of Ammonium 2,2′-(hydrazine-1,2-diylidene)bis(3-ethyl-2,3-dihydrobenzo[d]thiazole-6-sulfonate).

Referemce:
https://pubchem.ncbi.nlm.nih.gov/compound/thiazole,
Thiazole | chemical compound | Britannica

Asif, Nida published the artcileBiofabrication and characterization of cyanobacteria derived ZnO NPs for their bioactivity comparison with commercial chemically synthesized nanoparticles, Product Details of C18H24N6O6S4, the publication is Bioorganic Chemistry (2021), 104999, database is CAplus and MEDLINE.

Due to unique properties of the nanoparticles (NPs) with biocompatibility, their application as drug in drug delievery and diagnostics, the recent scientific branch nanotechnol. has emerged as hope in modern medicine. Zinc oxide nanoparticles (ZnO NPs) have gained tremendous interest due to their potential use as chemotherapeutic and antimicrobial agents. They are included in the category of “generally recognized as safe (GRAS) metal oxide”. There is an urgent need for developing addnl. sources of ZnO NPs. Therefore, in the present study 30 cyanobacterial extracts were screened for ZnO NPs synthesis.. The color change of the reaction mixture from blue to pale white indicated the synthesis of ZnO NPs. It was further confirmed by UV-Visible spectroscopy that showed the absorption peak at 372 nm. The SEM anal. during screening revealed that Oscillatoria sp. synthesized smallest ZnO NPs (∼40 nm) that were further optimized for their higher yield by altering reaction conditions (pH, temperature, reaction time, concentration of extract and metal precursor). Best conditions for ZnO NPs synthesis are (0.02 M zinc nitrate, 10 mL of extract volume, pH 8, at 80°C for 3 h). The NPs were purified through calcination at 350°C and characterized by UV-Vis, FTIR, XRD, SEM-EDAX, TEM, Zeta potential and DLS anal. The comparative anal. of purified biogenic ZnO NPs with com. chem. synthesized ZnO NPs (CS), exhibited their superior nature as antioxidant and anti-bacterial agent against both gram-pos. and gram-neg. bacteria. Synergistic effects of biogenic ZnO NPs and streptomycin addnl. favored for their future use as a potential biomedical agent.

Bioorganic Chemistry published new progress about 30931-67-0. 30931-67-0 belongs to thiazole, auxiliary class Salt,Hydrazine,Amine,Benzothiazole, name is Ammonium 2,2′-(hydrazine-1,2-diylidene)bis(3-ethyl-2,3-dihydrobenzo[d]thiazole-6-sulfonate), and the molecular formula is C18H24N6O6S4, Product Details of C18H24N6O6S4.

Referemce:
https://pubchem.ncbi.nlm.nih.gov/compound/thiazole,
Thiazole | chemical compound | Britannica

Pandey, Deepshikha published the artcileBioremoval of toxic malachite green from water through simultaneous decolorization and degradation using laccase immobilized biochar, Application of Ammonium 2,2′-(hydrazine-1,2-diylidene)bis(3-ethyl-2,3-dihydrobenzo[d]thiazole-6-sulfonate), the publication is Chemosphere (2022), 134126, database is CAplus and MEDLINE.

In this study, decolorization and degradation of malachite green dye was studied using the laccase immobilized pine needle biochar. Successful immobilization of biochar was achieved by adsorption and confirmed through SEM and energy dispersive X-ray anal. (SEM-EDX), Fourier transform IR spectroscopy (FTIR). High laccase binding of 64.4 U/g and high immobilization yield of 78.1% was achieved using 4U of enzyme at pH3 and temperature 30 °C. The immobilized laccase retained >50% relative activity in the pH range 2-7, >45% relative activity at 65 °C and >55% relative activity at 4 °C for 4 wk. The re-usability of immobilized enzyme was checked with 2, 2′-azino-bis 3-ethylbenzothiazoline-6-sulfonic acid (ABTS) substrate and enzyme retained 53% of its activity after 6 cycles. Immobilized laccase was used for the degradation and decolorization of azo dye malachite green in aqueous solution More than 85% removal of malachite green dye (50 mg/L) was observed within 5 h. FTIR and high performance liquid chromatog. (HPLC) anal. clearly indicated the breakdown of dye and presence of metabolites (leuco malachite green, methanone, [4-(di-Me amino)pheny]phenyl and 3-dimethyl-Ph amine) in gas chromatog.-mass spectrometry (GC-MS) anal. confirmed the dye degradation Phytotoxicity anal. indicated that the enzymic degradation resulted in lesser toxic metabolites than the original dye. Thus, laccase immobilized biochar can be used as an efficient biocatalytic agent to remove dye from water.

Chemosphere published new progress about 30931-67-0. 30931-67-0 belongs to thiazole, auxiliary class Salt,Hydrazine,Amine,Benzothiazole, name is Ammonium 2,2′-(hydrazine-1,2-diylidene)bis(3-ethyl-2,3-dihydrobenzo[d]thiazole-6-sulfonate), and the molecular formula is C18H24N6O6S4, Application of Ammonium 2,2′-(hydrazine-1,2-diylidene)bis(3-ethyl-2,3-dihydrobenzo[d]thiazole-6-sulfonate).

Referemce:
https://pubchem.ncbi.nlm.nih.gov/compound/thiazole,
Thiazole | chemical compound | Britannica

Akhil published the artcileComparative evaluation of laccase mediated oxidized and unoxidized lignin of sugarcane bagasse for the synthesis of lignin-based formaldehyde resin, HPLC of Formula: 30931-67-0, the publication is Industrial Crops and Products (2020), 112385, database is CAplus.

Pretreatment using dilute acid is one of the strategies employed in a lignocellulosic biorefinery. The current study deals with the isolation, characterization, and oxidation of lignin from the enzymic residue of acid pre-treated sugarcane bagasse. The study also focused on evaluating the reactivity of Laccase mediated oxidized lignin with the non-oxidized one for the preparation of lignin-based formaldehyde (LF) resin. In the current study, 100% phenolic lignin was utilized for the synthesis of LF resin. Three different approaches (Alk. hydrolysis, mild acidolysis & organosolv) have been employed to evaluate the effect of isolation method on the physicochem. properties of lignin. The isolation method had a bearing on the properties of lignin and its reactivity towards formaldehyde for the synthesis of LF resin. Alkali and organosolv lignin were found as promising candidates for the preparation of LF resin. Oxidized lignin exhibited better reactivity than the non-oxidized one.

Industrial Crops and Products published new progress about 30931-67-0. 30931-67-0 belongs to thiazole, auxiliary class Salt,Hydrazine,Amine,Benzothiazole, name is Ammonium 2,2′-(hydrazine-1,2-diylidene)bis(3-ethyl-2,3-dihydrobenzo[d]thiazole-6-sulfonate), and the molecular formula is C18H24N6O6S4, HPLC of Formula: 30931-67-0.

Referemce:
https://pubchem.ncbi.nlm.nih.gov/compound/thiazole,
Thiazole | chemical compound | Britannica

Pajnik, Jelena published the artcileZeolite/Chitosan/Gelatin Films: Preparation, Supercritical CO₂ Processing, Characterization, and Bioactivity, Category: thiazole, the publication is Macromolecular Materials and Engineering (2022), 307(8), 2200009, database is CAplus.

Chitosan/gelatin and chitosan/gelatin/zeolite films prepared by solvent casting method are impregnated with a mixture of thymol and carvacrol using a green solvent, supercritical carbon dioxide at 35 °C and 30 MPa, during 18 h. Proposed method enables preparation of biocompatible and biodegradable blends with strong antioxidant and antibacterial activity, whereby amounts of loaded thymol/carvacrol (TC) mixture are in the range from 3.3% to 6%. After initial burst release, both types of films exhibit gradual release of bioactive compounds, with around 72% and 96% of impregnated TC mixture released in water and phosphate buffered saline solution (pH 7.4) during tested period of 10 days, resp. Results of water vapor transmission rate (>76 g m^-2 day^-1) confirm that prepared composites are suitable for wound dressing application. Thermal anal. shows superior properties of prepared TC loaded films compared to control samples. In addition, mech. and structural properties, as well as solubility and swelling behavior of the obtained films are investigated in detail.

Macromolecular Materials and Engineering published new progress about 30931-67-0. 30931-67-0 belongs to thiazole, auxiliary class Salt,Hydrazine,Amine,Benzothiazole, name is Ammonium 2,2′-(hydrazine-1,2-diylidene)bis(3-ethyl-2,3-dihydrobenzo[d]thiazole-6-sulfonate), and the molecular formula is C18H24N6O6S4, Category: thiazole.

Referemce:
https://pubchem.ncbi.nlm.nih.gov/compound/thiazole,
Thiazole | chemical compound | Britannica

Tian, Qiaopeng published the artcileCharacterization of a robust cold-adapted and thermostable laccase from Pycnoporus sp. SYBC-L10 with a strong ability for the degradation of tetracycline and oxytetracycline by laccase-mediated oxidation, Application In Synthesis of 30931-67-0, the publication is Journal of Hazardous Materials (2020), 121084, database is CAplus and MEDLINE.

A native laccase (Lac-Q) with robust cold-adapted and thermostable characteristics from the white-rot fungus Pycnoporus sp. SYBC-L10 was purified, characterized, and used in antibiotic treatments. Degradation experiments revealed that Lac-Q at 10.0 U mL^-1 coupled with 1.0 mmol L^-1 ABTS could degrade 100% of the tetracycline or oxytetracycline (50 mg L^-1) within 5 min with a static incubation at 0 °C (pH 6.0). The presence of the Mn²⁺ ion inhibited the removal rate of tetracycline and oxytetracycline by the Lac-Q-ABTS system, and the presence of Al³⁺, Cu²⁺, and Fe³⁺ accelerated the removal rate of tetracycline and oxytetracycline by the Lac-Q-ABTS system. Furthermore, seven transformation products of oxytetracycline (namely TP 445, TP 431, TP 413, TP 399, TP 381, TP 367, and TP 351) were identified during the Lac-Q-mediated oxidation process by using UPLC-MS/MS. A possible degradation pathway including deamination, demethylation, and dehydration was proposed. Furthermore, the growth inhibition of Bacillus altitudinis SYBC hb4 and E. coli by tetracycline antibiotics revealed that the antimicrobial activity was significantly reduced after treatment with the Lac-Q-ABTS system. Finally, seven transformation products of oxytetracycline (namely TP 445, TP 431, TP 413, TP 399, TP 381, TP 367, and TP 351) were identified during the Lac-Q-mediated oxidation process by using UPLC-MS/MS. A possible degradation pathway including deamination, demethylation, and dehydration was proposed. These results suggest that the Lac-Q-ABTS system shows a great potential for the treatment of antibiotic wastewater containing different metal ions at various temperatures

Journal of Hazardous Materials published new progress about 30931-67-0. 30931-67-0 belongs to thiazole, auxiliary class Salt,Hydrazine,Amine,Benzothiazole, name is Ammonium 2,2′-(hydrazine-1,2-diylidene)bis(3-ethyl-2,3-dihydrobenzo[d]thiazole-6-sulfonate), and the molecular formula is C11H11NO2, Application In Synthesis of 30931-67-0.

Referemce:
https://pubchem.ncbi.nlm.nih.gov/compound/thiazole,
Thiazole | chemical compound | Britannica

Sriset, Yollada published the artcileIn vitro antioxidant potential of Mallotus repandus (Willd.) Muell. Arg stem extract and its active constituent bergenin, Product Details of C18H24N6O6S4, the publication is Songklanakarin Journal of Science and Technology (2021), 43(1), 24-30, database is CAplus.

Mallotus repandus (MR) is used in Thai traditional medicine recipes for anti-inflammation and adaptive homeostasis. Bergenin is the bioactive constituent in MR stem. This study evaluated the in vitro antioxidant activity of bergenin and the methanol, ethanol, and water extracts of MR stem prepared by maceration and Soxhlet extraction by assaying 2,2-azino-bis-(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS•⁺), hydroxyl (•OH), superoxide (•O₂), and nitric oxide (NO•) radical scavenging activities and ferric reducing antioxidant power. Bergenin had the highest ferric reducing power and all the MR extracts showed concentration-dependent ferric reducing power. Methanol and water extracts showed superior radical scavenging activities compared to ethanol extract The water and methanol Soxhlet extracts demonstrated the highest ABTS•⁺ and •OH radical scavenging activities, resp., and the macerated water extract had the lowest •O₂ and NO•; IC₅₀ values. Therefore, MR stem and bergenin are promising natural candidates for developing antioxidant supplements.

Songklanakarin Journal of Science and Technology published new progress about 30931-67-0. 30931-67-0 belongs to thiazole, auxiliary class Salt,Hydrazine,Amine,Benzothiazole, name is Ammonium 2,2′-(hydrazine-1,2-diylidene)bis(3-ethyl-2,3-dihydrobenzo[d]thiazole-6-sulfonate), and the molecular formula is C16H20N2, Product Details of C18H24N6O6S4.

Referemce:
https://pubchem.ncbi.nlm.nih.gov/compound/thiazole,
Thiazole | chemical compound | Britannica

Xing, Yanyan published the artcileTriple-enzyme mimetic activity of Fe₃O₄ @C@MnO₂ composites derived from metal-organic frameworks and their application to colorimetric biosensing of dopamine, Product Details of C18H24N6O6S4, the publication is Microchimica Acta (2022), 189(1), 12, database is CAplus and MEDLINE.

Novel Fe₃O₄ @C@MnO₂ composites were successfully synthesized for the first time via an interfacial reaction between magnetic porous carbon and KMnO4, in which the magnetic porous carbon was derived from the pyrolysis of Fe-MIL-88A under N₂ atmosphere. Interestingly, the obtained Fe₃O₄ @C@MnO₂ composites were found to have triple-enzyme mimetic activity including peroxidase-like, catalase-like, and oxidase-like activity. As a peroxidase mimic, Fe₃O₄ @C@MnO₂ composites could catalyze the oxidation of TMB into a blue oxidized product by H2O2. As a catalase mimic, Fe₃O₄ @C@MnO₂ could catalyze the decomposition of H2O2 to generate O2 and H2O. As an oxidase mimic, Fe₃O₄ @C@MnO₂ could catalyze the direct oxidation of TMB to produce a blue oxidized product without H2O2. Reactive oxygen species measurements revealed that the oxidase-like activity originated from 1O2 and O2-•and little•OH generated by the dissolved oxygen, which was catalyzed by the Fe₃O₄ @C@MnO₂ in the TMB oxidation reaction. The oxidase-like activity of Fe₃O₄ @C@MnO₂ was investigated in detail. Under the optimized conditions, a rapid, sensitive, visual colorimetric method for dopamine detection was developed based on the inhibitory effect of dopamine on the oxidase-like activity. The proposed method allows for dopamine detection with a limit of detection of 0.034μM and a linear range of 0.125-10μM. This new colorimetric method was successfully used for the determination of dopamine in human blood samples.

Microchimica Acta published new progress about 30931-67-0. 30931-67-0 belongs to thiazole, auxiliary class Salt,Hydrazine,Amine,Benzothiazole, name is Ammonium 2,2′-(hydrazine-1,2-diylidene)bis(3-ethyl-2,3-dihydrobenzo[d]thiazole-6-sulfonate), and the molecular formula is C9H22OSi, Product Details of C18H24N6O6S4.

Referemce:
https://pubchem.ncbi.nlm.nih.gov/compound/thiazole,
Thiazole | chemical compound | Britannica