Category: thiazole

Jing, Yingjun; Diao, Yujia; Yu, Xueqing published an article on February 28 ,2019. The article was titled 《Free radical-mediated conjugation of chitosan with tannic acid: Characterization and antioxidant capacity》, and you may find the article in Reactive & Functional Polymers.Related Products of 30931-67-0 The information in the text is summarized as follows:

Chitosan (CS) is a natural biopolymer with versatile applications. In this work, CS was functionalized with tannic acid (TA) by a free radical grafting procedure to improve its antioxidant capacity. The resulting TA-conjugated CS (TA-CS) showed a high TA equivalent content of 267.1 ± 5.4 mg TAE/g. The formation of TA-CS was verified by UV-vis, FTIR, and 1H NMR analyses. Moreover, TA-CS showed a lower thermal stability and crystallinity than CS and exhibited a good water-solubility of 15.0 ± 0.3 mg/mL. The DPPH radical scavenging activity of TA-CS reached a maximum of 91.6%, which was 6.4-fold higher than that of CS. Similar results were also observed in ABTS and hydroxyl radical scavenging assays. Moreover, TA-CS showed a higher superoxide radical scavenging activity and ferrous ion chelating activity than both TA and CS. These results suggest that conjugating with TA is an available way to enhance the antioxidant capacity of CS. In the experimental materials used by the author, we found ABTS Diammonium(cas: 30931-67-0Related Products of 30931-67-0)

ABTS Diammonium(cas: 30931-67-0) belongs to anime. Nitrous acid converts secondary amines (aliphatic or aromatic) to N-nitroso compounds (nitrosamines): R2NH + HNO2 → R2N―NO. Some nitrosamines are potent cancer-inducing substances, and their possible formation is a serious consideration when nitrites, which are salts of nitrous acid, are present in foods or pharmaceutical preparations. Tertiary amines give rise to nitrosamines more slowly; an alkyl group is eliminated as an aldehyde or ketone, along with nitrous oxide, N2O.Related Products of 30931-67-0

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica

Gong, Xiaobei; Luo, Hao; Wu, Xing; Liu, Hao; Sun, Chengwu; Chen, Shicheng published an article in Indian Journal of Microbiology. The title of the article was 《Production of Red Pigments by a Newly Isolated Talaromyces aurantiacus Strain with LED Stimulation for Screen Printing》.Related Products of 30931-67-0 The author mentioned the following in the article:

Microbial pigments have been widely applied to printing in food, textile, and paper industries as a sustainable alternative to synthetic dyes. Herein, we isolated a novel Talaromyces aurantiacus strain with a strong ability to produce red pigments. We further studied pigment production conditions, stability, screen printing application, and bioactivities. Our results showed that sucrose was a favorable carbon source and the addition of L-histidine significantly enhanced the production of red pigments. Pigment production was strictly photo-regulated with effective wavelengths around 450 nm (blue light). We mixed the red pigments with cellulosic materials and explored their application potentials for screen printing on paper, cotton fabrics, and polymeric carriers. The printing d. was significantly improved from 0.3 to 0.7 by overlay printing. T. aurantiacus pigments could be stably stored at pH 5-11, temperature – 10 to 70°C, and redox potential – 200 to 300 mV. Moreover, the stable ranges were extended to pH 1-11 and temperature over 100°C after screen-printed on paper. The red pigments exhibited antioxidant activity toward 2,2′-Azinobis-(3-ethylbenzthiazoline-6-sulfonate) (IC50 10.4 mg L-1 in solution). Our results further indicated the red pigments by T. aurantiacus was environmentally friendly based on acetylcholinesterase activity assay. In addition to this study using ABTS Diammonium, there are many other studies that have used ABTS Diammonium(cas: 30931-67-0Related Products of 30931-67-0) was used in this study.

ABTS Diammonium(cas: 30931-67-0) belongs to anime. Hydrogen peroxide (H2O2) and peroxy acids generally add an oxygen atom to the nitrogen of amines. With primary amines, this step is normally followed by further oxidation, leading to nitroso compounds, RNO, or nitro compounds, RNO2. Secondary amines are converted to hydroxylamines, R2NOH, and tertiary amines to amine oxides, R3NO.Related Products of 30931-67-0

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica

COA of Formula: C7H5ClN2SOn November 27, 2019 ,《Chagas Disease Drug Discovery: Multiparametric Lead Optimization against Trypanosoma cruzi in Acylaminobenzothiazole Series》 appeared in Journal of Medicinal Chemistry. The author of the article were Fleau, Charlotte; Padilla, Angel; Miguel-Siles, Juan; Quesada-Campos, Maria T.; Saiz-Nicolas, Isabel; Cotillo, Ignacio; Cantizani Perez, Juan; Tarleton, Rick L.; Marco, Maria; Courtemanche, Gilles. The article conveys some information:

Acylaminobenzothiazole hits were identified as potential inhibitors of T. cruzi replication, a parasite responsible for Chagas Disease. We selected compound 1, N-(6-chlorobenzo[d]thiazol-2-yl)cyclopropanecarboxamide, for lead optimization, aiming to improve in parallel its anti-T. cruzi activity (IC50 = 0.630μM) and its human metabolic stability (human clearance = 9.57mL/min/g). A total of 39 analogs of 1 were synthesized and tested in vitro. We established a multiparametric structure activity relationship, allowing optimization of both anti-parasite activity, physicochem. parameters and ADME properties. We identified compound 50, N-(5-Fluoro-6-(trifluoromethyl)benzothiazol-2-yl)cyclopropanecarboxamide, as an advanced lead with an improved anti-T. cruzi activity in vitro (IC50 = 0.079μM), an enhanced metabolic stability (Human Clearance = 0.413mL/min/g) and opportunity for oral route of administration. After tolerability assessment, compound 50 demonstrated a promising in vivo efficacy. In the experiment, the researchers used 6-Chlorobenzothiazol-2-ylamine(cas: 95-24-9COA of Formula: C7H5ClN2S)

6-Chlorobenzothiazol-2-ylamine(cas: 95-24-9) belongs to thiazoles. Thiazoles are a class of five-membered rings containing nitrogen and sulfur with excellent antitumor, antiviral and antibiotic activities.COA of Formula: C7H5ClN2SThiazoles can also be used as protected formyl groups, which can be released in later stages of complex natural product synthesis.

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica

In 2018,Liu, Juan-Juan; Lu, Yan-Ju; Zhao, Zhen-Dong; Xu, Shi-Chao; Bi, Liang-Wu published 《Synthesis and Cytotoxic Activity of Amides from Isopimaric Acid》.Chemistry of Natural Compounds published the findings.Name: 5-Bromothiazol-2-amine The information in the text is summarized as follows:

The amide derivatives were synthesized from isopimaric acid and characterized by spectroscopy. These amides were examined in vitro for their cytotoxic activity against four cancer cell lines. The majority of the screened compounds displayed better inhibitory activity than isopimaric acid, and many amides displayed promising cytotoxic activity against hepatocarcinoma (HepG-2), breast carcinoma (MDA-MB-231), and prostate adenocarcinoma (PC-3). The substituent type, number, and position in the benzene and heterocyclic rings have an important influence on cytotoxicity against the three tested cancer cell lines. In the experimental materials used by the author, we found 5-Bromothiazol-2-amine(cas: 3034-22-8Name: 5-Bromothiazol-2-amine)

5-Bromothiazol-2-amine(cas: 3034-22-8) belongs to anime. Acylation is one of the most important reactions of primary and secondary amines; a hydrogen atom is replaced by an acyl group (a group derived from an acid, such as RCOOH or RSO3H, by removal of ―OH, such as RC(=O)―, RS(O)2―, and so on). Reagents may be acid chlorides (RCOC1, RSO2C1), anhydrides ((RCO)2O), or even esters (RCOOR′); the products are amides of the corresponding acids.Name: 5-Bromothiazol-2-amine

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica

The author of 《Copper-catalyzed one-pot coupling reactions of aldehydes (ketones), tosylhydrazide and 2-amino(benzo)thiazoles: An efficient strategy for the synthesis of N-alkylated (benzo)thiazoles》 were Xie, Zengyang; Chen, Ruijiao; Ma, Mingfang; Kong, Lingdong; Liu, Jun; Wang, Cunde. And the article was published in Applied Organometallic Chemistry in 2019. Computed Properties of C7H5ClN2S The author mentioned the following in the article:

An efficient and practical C-N bond formation methodol. for the synthesis of N-(alkyl)benzothiazoles I [R = H, 4-Me, 6-Br, etc.; R1 = n-Pr, Ph, 4-MeOC6H4, etc.] and N-(alkyl)thiazoles II [R2 = H, Me; R3 = Ph, 2-MeC6H4, 2-naphthyl, etc.; R2R3 = (CH2)5; R4 = H, 4-Me, 5-Me] was developed via Cu-catalyzed one-pot two-step cross-coupling of 2-aminobenzothiazoles/2-aminothiazoles and aldehydes/ketones with tosylhydrazide. This cross-coupling reaction proceeded smoothly and tolerated a broad range of functional groups. A variety of functionalized benzothiazoles/thiazoles were obtained in moderate to high yields. Notably, gram-scale synthesis of fanetizole (anti-inflammatory drug) was also realized through this protocol. In the experimental materials used by the author, we found 6-Chlorobenzothiazol-2-ylamine(cas: 95-24-9Computed Properties of C7H5ClN2S)

6-Chlorobenzothiazol-2-ylamine(cas: 95-24-9) belongs to thiazoles. Thiazoles are a class of five-membered rings containing nitrogen and sulfur with excellent antitumor, antiviral and antibiotic activities.Computed Properties of C7H5ClN2SThe thiazole ring has been identified as a central feature of numerous natural products, perhaps the most famous example of which is epothilone.

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica

《Bee Pollen Extracts as Potential Antioxidants and Inhibitors of α-Amylase and α-Glucosidase Enzymes In Vitro Assessment》 was published in Journal of Apicultural Science in 2019. These research results belong to Daudu, Oluremi M.. Recommanded Product: ABTS Diammonium The article mentions the following:

The study was conducted to determine the antioxidant and anti-diabetic properties of bee pollen. The phenol content of extracts was 1.43, 2.04, 2.10 and 1.79 mg gallic acid g-1, resp. Total flavonoid content was 0.78, 1.39, 0.86 and 0.79 mg gallic acid g-1 resp. Bee pollen extracts have the potential to scavenge free radicals and lower blood glucose due to the presence of phenols and flavonoids. The aqueous-ethanol extract had the lowest IC50 for HRS and TAC, 0.53mg/mL and 0.25mg/mL resp., which depicts that this extract alleviates the destructive effect of hydroxyl radicals. Methanol extract had the lowest IC50 (0.21 mg/mL) for DPPH inhibition, hence it was able to scavenge the DPPH radicals. Ethanol extract had the lowest IC50 (0.04 mg/mL) for 2, 2-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) inhibition, hence it can protect living cells from ABTS cations. The aqueous-ethanol extract displayed higher inhibition of α-amylase (4.51 mg/mL) while the aqueous extract exhibited a higher inhibition of α-glucosidase (0.60 mg/mL), which slows down the breakdown of disaccharides and reduces sugar buildup in the bloodstream. Bee pollen has potential antioxidative and antidiabetic activity. The results came from multiple reactions, including the reaction of ABTS Diammonium(cas: 30931-67-0Recommanded Product: ABTS Diammonium)

ABTS Diammonium(cas: 30931-67-0) belongs to anime. Primary amines having a tertiary alkyl group (R3CNH2) are difficult to prepare with most methods but are made industrially by the Ritter reaction. In this method a tertiary alcohol reacts with hydrogen cyanide (HCN) in the presence of a concentrated strong acid; a formamide, RNH―CHO, is formed first, which then undergoes hydrolysis.Recommanded Product: ABTS Diammonium

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica

Saha, Rituparna; Mukhopadhyay, Mainak published an article on January 31 ,2022. The article was titled 《Electrochemical analysis of Catechol polymerization in presence of Trametes versicolor laccase and the mediator ABTS》, and you may find the article in Enzyme and Microbial Technology.Formula: C18H24N6O6S4 The information in the text is summarized as follows:

The phenolic compound catechol has found various applications in the industry but is often discharged untreated in industrial effluents. Catechol is highly toxic and adversely affects the environment. This has increased extensive investigation into elucidating the effects of various synthetic elements or different biocatalysts on catechol, thereby leading the way to its bioremediation. Hence, an electrochem.-based study on catechol in the presence of the enzyme laccase could provide a basic understanding of the unique characteristics exhibited by catechol, thus facilitating a distinct perspective to its subsequent treatment and removal. The present study focuses on the electrochem. characterization of catechol based on the oxidation of laccase and the redox mediator 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS). Catechol exhibited distinct electrochem. behavior across various concentrations The unique electroactive nature of ABTS assisted in the polymerization of catechol which was found to be concentration-dependent. Laccase produced a higher oxidation-reduction rate, thereby producing a much more stable condition for the polymerization of catechol. However, with the laccase-mediator system (LMS), the catechol polymerization rate was distinctly higher and more gradual with the enzyme utilizing the electroactive species produced by ABTS to increase the electron transfer and producing a combinatorial impact on the phenolic compound This study could rightly serve as the building block in developing future technologies like wastewater treatment and biosensors for catechol bioremediation. The experimental process involved the reaction of ABTS Diammonium(cas: 30931-67-0Formula: C18H24N6O6S4)

ABTS Diammonium(cas: 30931-67-0) belongs to anime. Many important products require amines as part of their syntheses. Methylamine is utilized in the production of the analgesic meperidine (trade name Demerol) and the photographic developer Metol (trademark), and dimethylamine is used in the synthesis of the antihistamine diphenhydramine (trade name Benadryl), the solvent dimethylformamide (DMF), and the rocket propellant 1,1-dimethylhydrazine. The synthesis of the insect repellent N,N-diethyl-m-toluamide (DEET) incorporates diethylamine while that of the synthetic fibre Kevlar requires aromatic amines.Formula: C18H24N6O6S4

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica

Laghezza, Antonio; Luisi, Grazia; Caradonna, Alessia; Di Pizio, Antonella; Piemontese, Luca; Loiodice, Fulvio; Agamennone, Mariangela; Tortorella, Paolo published an article on February 1 ,2020. The article was titled 《Virtual screening identification and chemical optimization of substituted 2-arylbenzimidazoles as new non-zinc-binding MMP-2 inhibitors》, and you may find the article in Bioorganic & Medicinal Chemistry.Safety of 6-Chlorobenzothiazol-2-ylamine The information in the text is summarized as follows:

Matrix metalloproteinases (MMPs) are a large family of zinc-dependent endoproteases known to exert multiple regulatory roles in tumor progression and invasiveness. This encouraged over the years the approach of MMP, and particularly MMP-2, targeting for anticancer treatment. Early generations of MMP inhibitors, based on aspecific zinc binding groups (ZBGs) assembled on (pseudo)peptide scaffolds, have been discontinued due to the clin. emergence of toxicity and further drawbacks, giving the way to inhibitors with alternative zinc-chelator moieties or not binding the catalytic zinc ion. In the present paper, we continue the search for new non-zinc binding MMP-2 inhibitors: exploiting previously identified compounds, a virtual screening (VS) campaign was carried out and led to the identification of a new class of ligands. The structure-activity relationship (SAR) of the benzimidazole scaffold was explored by synthesis of several analogs whose inhibition activity was tested with enzyme inhibition assays. By performing the mol. simplification approach, we disclosed different sets of single-digit micromolar inhibitors of MMP-2, with up to a ten-fold increase in inhibitory activity and ameliorated selectivity towards off-target MMP-8, compared to selected lead compound Mol. dynamics calculations conducted on complexes of MMP-2 with docked privileged structures confirmed that analyzed inhibitors avoid targeting the zinc ion and dip inside the S1′ pocket. Present results provide a further enrichment of our insights for the design of novel MMP-2 selective inhibitors. After reading the article, we found that the author used 6-Chlorobenzothiazol-2-ylamine(cas: 95-24-9Safety of 6-Chlorobenzothiazol-2-ylamine)

6-Chlorobenzothiazol-2-ylamine(cas: 95-24-9) belongs to thiazoles. Thiazoles are a class of five-membered rings containing nitrogen and sulfur with excellent antitumor, antiviral and antibiotic activities.Safety of 6-Chlorobenzothiazol-2-ylamineThe thiazole ring has been identified as a central feature of numerous natural products, perhaps the most famous example of which is epothilone.

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica

In 2021,New Journal of Chemistry included an article by Borthakur, Priyakshree; Boruah, Purna K.; Das, Punamshree; Das, Manash R.. Computed Properties of C18H24N6O6S4. The article was titled 《CuS nanoparticles decorated MoS2 sheets as an efficient nanozyme for selective detection and photocatalytic degradation of hydroquinone in water》. The information in the text is summarized as follows:

The development of cost effective and efficient nanomaterials with enzyme mimetics and photocatalytic activity has achieved tremendous research interest in the quant. detection as well as removal of toxic environmental pollutants. CuS nanoparticles decorated MoS2 sheets were successfully synthesized adopting a simple hydrothermal technique and using low-cost materials. The nanocomposite was successfully used as an efficient catalyst for the selective detection and removal of a toxic phenolic compound like hydroquinone (HQ). The CuS-MoS2 nanocomposite catalyzed the oxidation of different chromogenic substrates like 3,3′,5,5′-tetramethylbenzidine, 2,2′-azino-bis(3-ethylbenzo-thiazoline-6-sulfonic acid)diammonium salt, and o-phenylenediamine in the presence of H2O2, indicating its peroxidase-like activity as natural Horseradish peroxidase (HRP). The catalytic performance of the nanozyme was further investigated through the typical Michaelis-Menten kinetics. The results showed that the proposed sensor exhibited improved catalytic properties with a wide linear relationship (0.4-50μM) and a low detection limit of 3.68μM for HQ detection in aqueous medium. Meanwhile, the mechanism of HQ sensing in the presence of CuS-MoS2 nanozyme was systematically investigated. Moreover, the CuS-MoS2 nanozyme possessed significant photocatalytic activity and 83% HQ decomposition was achieved within 240 min under irradiation of natural sunlight. The mechanism of enhanced photocatalytic degradation of HQ through the formation of OH radicals as reactive species was evidenced by analyzing the formation of fluorescent active mols. on the addition of terephthalic acid and by high-resolution mass spectrometry. Thus CuS-MoS2 represents a new and promising HQ sensing material in a highly sensitive and fast manner as well as an efficient photocatalyst for the degradation of HQ to its non-toxic products under natural sunlight irradiation The experimental part of the paper was very detailed, including the reaction process of ABTS Diammonium(cas: 30931-67-0Computed Properties of C18H24N6O6S4)

ABTS Diammonium(cas: 30931-67-0) belongs to anime. Amines characteristically form salts with acids; a hydrogen ion, H+, adds to the nitrogen. With the strong mineral acids (e.g., H2SO4, HNO3, and HCl), the reaction is vigorous. Salt formation is instantly reversed by strong bases such as NaOH. Neutral electrophiles (compounds attracted to regions of negative charge) also react with amines; alkyl halides (R′X) and analogous alkylating agents are important examples of electrophilic reagents.Computed Properties of C18H24N6O6S4

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica

In 2021,Journal of Veterinary Research included an article by Szponder, Tomasz; Zdziennicka, Joanna; Nowakiewicz, Aneta; Swieca, Michal; Sobczynska-Rak, Aleksandra; Zylinska, Beata; Patkowski, Krzysztof; Junkuszew, Andrzej; Wessely-Szponder, Joanna. Formula: C18H24N6O6S4. The article was titled 《Effects of topical treatment of foot rot in sheep using ozonated olive ointment》. The information in the text is summarized as follows:

Foot rot in small ruminants is highly contagious, causes severe lameness, and impairs fertility and wool and meat production It is usually treated with parenteral antibiotics, with attendant antibiotic resistance risk, and with bactericidal footbaths, potentially harmful to humans and the environment. An alternative treatment in sheep is proposed based on repeated topical ozonated ointment application. Its effectiveness and safety were evaluated by estimation of acute-phase response, biochem. indicators of organic damage, and antioxidant/oxidant balance (AOB). The study was conducted on ten sheep with Egerton scale 2-3 lesions. Ozone application was repeated every day for seven days. Blood was drawn first (T0) after foot cleaning and before ozonation, then (T1) seven days after the first ozone application, and finally (T2) four days after the last application. High clin. effectiveness was observed, with total recovery by 28 days from the start of treatment. A significant increase in antiradical activity was noted on the basis of a 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) assay from 1.16 ± 0.04 μmolTe/mL at T0 to 1.23 ± 0.03 μmolTe/mL at T1, with a slight decrease in oxidative stress. Calculated on the basis of antiradical capacity, AOB was higher at T1 (130 ± 19%) and decreased to 110 ± 16% at T2. Calculated on the basis of reducing power, it was 169 ± 22% at T1 and 131 ± 17% at T2. These results indicated that the AOB is efficient enough to prevent oxidative organ injury and the applied doses of ozone are safe for animals. The experimental process involved the reaction of ABTS Diammonium(cas: 30931-67-0Formula: C18H24N6O6S4)

ABTS Diammonium(cas: 30931-67-0) belongs to anime. Left-handed and right-handed forms (mirror-image configurations, known as optical isomers or enantiomers) are possible when all the substituents on the central nitrogen atom are different (i.e., the nitrogen is chiral). With amines, there is extremely rapid inversion in which the two configurations are interconverted.Formula: C18H24N6O6S4

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica