Tag: 300-400

Evaluation of the antibacterial and inhibitory activity of NorA and MepA efflux pumps from Staphylococcus aureus by diosgenin was written by do Socorro Costa, Maria;da Silva, Ana Raquel Pereira;Araujo, Nara Juliana Santos;Filho, Jose Maria Barbosa;Tavares, Josean Fechine;de Freitas, Thiago Sampaio;Pereira, Francisco Nascimento Junior;de Sousa, Erlanio Oliveira;Maia, Francisco Paulo Araujo;de Vasconcelos, John Eversong Lucena;Pinheiro, Jacqueline Cosmo Andrade;Coutinho, Henrique Douglas Melo. And the article was included in Life Sciences in 2022.COA of Formula: C16H18FN3O3 The following contents are mentioned in the article:

The increase in bacterial resistance to available antibiotics has driven several researchers to search for new agents with therapeutic properties. Diosgenin is a naturally occurring steroidal saponin that has demonstrated several pharmacol. properties. In the present study, we report the antimicrobial activity of diosgenin against the standard and multidrug-resistant bacteria of Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus, in addition to the efflux pump inhibitory activity against Staphylococcus aureus strains carrying NorA and MepA pumps. For this purpose, the broth microdilution method was used, from which the value of the Min. Inhibitory Concentration (MIC) was obtained, and this was associated with subinhibitory concentration (MIC/8) with antibiotic of clin. use and ethidium bromide for strains carrier by efflux pump. Diosgenin showed antimicrobial activity for standard S. aureus bacteria and potentiating activity in association with gentamicin and ampicillin for P. aeruginosa multidrug-resistant bacteria, it also showed potentiation in association with norfloxacin against the E. coli strain and gentamicin against the S. aureus strain. Antimicrobial activity against efflux pump-bearing strains revealed that saponin did not interfere with the efflux pump mechanism or intervened antagonistically. Thus, saponin has shown to be very promising against bacterial resistance in association with aminoglycoside, fluoroquinolones and beta-lactam, however addnl. studies should be carried out to better elucidate the mechanism of action of diosgenin. This study involved multiple reactions and reactants, such as 1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (cas: 70458-96-7COA of Formula: C16H18FN3O3).

1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (cas: 70458-96-7) belongs to piperazine derivatives. Piperazine was first introduced as an anthelmintic in 1953. Piperazine compounds mediate their anthelmintic action by generally paralyzing parasites, allowing the host body to easily remove or expel the invading organism. Piperazine is an anthelminthic especially useful in the treatment of partial intestinal obstruction caused by Ascaris worms, which is a condition primarily seen in children. Piperazine hydrate and piperazine citrate are the main anthelminthic piperazines.COA of Formula: C16H18FN3O3

Referemce:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics

Distribution of florfenicol and norfloxacin in ice during water freezing process: Dual effects by fluorine substituents was written by Sun, Heyang;Chen, Tianyi;Zhang, Liwen;Dong, Deming;Li, Yanchun;Guo, Zhiyong. And the article was included in Environmental Pollution (Oxford, United Kingdom) in 2022.Recommanded Product: 1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid The following contents are mentioned in the article:

Distribution in ice is regarded as one of important transport modes for pollutants in seasonal freeze-up waters in cold regions. However, the distribution characteristics and mechanisms of fluorinated antibiotics as emerging contaminants during the water freezing process remain unclear. Here, florfenicol and norfloxacin were selected as model fluorinated antibiotics to investigate their ice-water distribution. Effects of antibiotic mol. structure on the distribution were explored through comparative studies with their non-fluorinated structural analogs. Results showed that phase changes during the ice growth process redistributed the antibiotics, with antibiotic concentrations in water 3.0-6.4 times higher than those in ice. The solute-rich boundary layer with a concentration gradient was presented at the ice-water interface and controlled by constitutional supercooling during the freezing process. The ice-water distribution coefficient (KIW) values of antibiotics increased by 34.8%-38.0% with a doubling of the cooling area. The solute distribution coefficient (Kbs) values of antibiotics at -20°C were 65.6%-70.3% higher than at -10°C. The KIW and Kbs values of all antibiotics were neg. correlated with their water solubilities. The fluorine substituents influenced the binding energies between antibiotics and ice, resulting in a 1.1-fold increase in the binding energy of norfloxacin on the ice surface relative to its structural analog pipemidic acid. The results provide a new insight into the transport behaviors of fluorinated pharmaceuticals in ice-water systems. This study involved multiple reactions and reactants, such as 1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (cas: 70458-96-7Recommanded Product: 1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid).

1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (cas: 70458-96-7) belongs to piperazine derivatives. The piperazine scaffold is often found in biologically active compounds in different therapeutic areas. These therapeutic areas include antifungals, antidepressants, antivirals, and serotonin receptor (5-HT) antagonists/agonists. Outside the body, piperazine has a remarkable power to dissolve uric acid and producing a soluble urate, but in clinical experience it has not proved equally successful. Recommanded Product: 1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid

Referemce:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics

Genome mining reveals polysaccharide-degrading potential and new antimicrobial gene clusters of novel intestinal bacterium Paenibacillus jilinensis sp. nov. was written by Ma, Ke;Chen, Wei;Yan, Shi-Qing;Lin, Xiao-Qi;Liu, Zhen-Zhen;Zhang, Jia-Bao;Gao, Yu;Yang, Yong-Jun. And the article was included in BMC Genomics in 2022.Product Details of 70458-96-7 The following contents are mentioned in the article:

Drug-resistant bacteria have posed a great threat to animal breeding and human health. It is obviously urgent to develop new antibiotics that can effectively combat drug-resistant bacteria. The commensal flora inhabited in the intestines become potential candidates owing to the production of a wide range of antimicrobial substances. In addition, host genomes do not encode most of the enzymes needed to degrade dietary structural polysaccharides. The decomposition of these polysaccharides mainly depends on gut commensal-derived CAZymes. We report a novel species isolated from the chicken intestine, designated as Paenibacillus jilinensis sp. nov. and with YPG26T (= CCTCC M2020899T) as the type strain. The complete genome of P. jilinensis YPG26T is made up of a single circular chromosome measuring 3.97 Mb in length and containing 49.34% (mol%) G + C. It carries 33 rRNA genes, 89 tRNA genes, and 3871 protein-coding genes, among which abundant carbohydrate-degrading enzymes (CAZymes) are encoded. Moreover, this strain has the capability to antagonize multiple pathogens in vitro. We identified putative 6 BGCs encoding bacteriocin, NRPs, PKs, terpenes, and protcusin by genome mining. In addition, antibiotic susceptibility testing showed sensitivity to all antibiotics tested. This study highlights the varieties of CAZymes genes and BGCs in the genome of Paenibacillus jilinensis. These findings confirm the beneficial function of the gut microbiota and also provide a promising candidate for the development of new carbohydrate degrading enzymes and antibacterial agents. This study involved multiple reactions and reactants, such as 1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (cas: 70458-96-7Product Details of 70458-96-7).

1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (cas: 70458-96-7) belongs to piperazine derivatives. Piperazine is a fairly basic compound and is an amine solvent. Piperazines are very broad chemical group, covering a wide range of drugs from antidepressants to antihistamines. The connecting property of all these chemicals is the presence of a piperazine functional group.Product Details of 70458-96-7

Referemce:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics

Eradication of exotoxin A and its producer in freshwater by means of cold-vaporized hydrogen peroxide-enhanced SDBD: A sustainable processing was written by Sohbatzadeh, Farshad;Haqpanah, Hanieh;Shabannejad, Amir;Yazdanshenas, Homayoon. And the article was included in Aquaculture in 2022.Product Details of 70458-96-7 The following contents are mentioned in the article:

Pseudomonas aeruginosa is a multidrug-resistant bacterial strain with the ability to produce exotoxin A which can pose a serious threat to freshwater ecosystems by having pathogenicity against eukaryotes. Detoxification of exotoxin A and disinfection of P. aeruginosa are the main aims of this study. Using a high dosage of antibiotics might have more toxic effects on ecosystems while cold atm. plasma (CAP) can promise reliable, rapid, and environmentally friendly detoxification and disinfection. In this study we produced CAP reinforced by H₂O₂/H₂O cold vapor to detoxify exotoxin A and inactivate P. aeruginosa in freshwater. We used Gammarus roeseli as the indicator of ecotoxicity in freshwater. The mortality of G. roeseli individuals elucidated that 420 s of CAP-based treatment under a surface dielec. barrier discharge (SDBD) set up can effectively passivize exotoxin A in freshwater. Meanwhile, a considerable decline in the concentration of exotoxin A was observed in treated samples due to the disruption of the protein structure. Ignorable side effects and changes to the physiochem. properties were observed On the other hand, 8.2-log reduction of P. aeruginosa viable cells was observed after 300 s of treatment by our CAP-based strategy. This study also showed that the combination of hydrogen peroxide and CAP can significantly increase the decontamination power of hydrogen peroxide and our strategy can eliminate the need of using high concentrations of H₂O₂ which decreases environmental concerns. This study involved multiple reactions and reactants, such as 1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (cas: 70458-96-7Product Details of 70458-96-7).

1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (cas: 70458-96-7) belongs to piperazine derivatives. The piperazine scaffold is often found in biologically active compounds in different therapeutic areas. These therapeutic areas include antifungals, antidepressants, antivirals, and serotonin receptor (5-HT) antagonists/agonists. Although many piperazine derivatives occur naturally, piperazine itself can be synthesized by reacting alcoholic ammonia with 1,2-dichloroethane, by the action of sodium and ethylene glycol on ethylene diamine hydrochloride, or by reduction of pyrazine with sodium in ethanol.Product Details of 70458-96-7

Referemce:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics

Antimicrobial resistance, virulence genes, and phylogenetic characteristics of pathogenic Escherichia coli isolated from patients and swine suffering from diarrhea was written by Do, Kyung-Hyo;Seo, Kwangwon;Lee, Wan-Kyu. And the article was included in BMC Microbiology in 2022.COA of Formula: C16H18FN3O3 The following contents are mentioned in the article:

Escherichia (E.) coli causes colibacillosis in swine and humans, and is frequently associated with antimicrobial resistance. In this study we aimed to compare antimicrobial resistance, O-serogroups, virulence genes, and multi-locus sequence type of E. coli between isolates from pigs and patients suffering from diarrhea, and the most prevalent pathogenic E. coli strain from swine isolates in Korea. We tested 64 and 50 E. coli strains from pigs and patients suffering from diarrhea for antimicrobial susceptibility test, virulence genes, O-serogroups, and multi-locus sequence typing. We confirmed that isolates from swine showed significantly higher resistance than from those from patients, especially to fluoroquinolone (ciprofloxacin: 37.5 and 10.0%; norfloxacin: 29.7 and 8.0%, resp.). Stx1 (46.0%) was most frequently detected in patients followed by stx2 (38.0%). There was no significant difference in stx2 (swine: 23.4%, patients: 38.0%). In isolates from patients, O157 (12.0%) was the most prevalent O-serogroup, and two isolates (3.1%) from pigs were confirmed to have O157. Addnl., sequence type (ST) 10 (swine: 6 isolates, patients: 2 isolates) and ST 88 (swine: 2 isolates, patients: 1 isolate) were simultaneously detected. We found that both isolates from swine and human had the stx2 gene, which could cause severe disease. Moreover, antimicrobial resistance was significantly higher in pigs than in patients. These results suggest that pig could act as a reservoir in human infection and antimicrobial resistance could be transferred to human from pigs. This study involved multiple reactions and reactants, such as 1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (cas: 70458-96-7COA of Formula: C16H18FN3O3).

1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (cas: 70458-96-7) belongs to piperazine derivatives. Piperazine was first introduced as an anthelmintic in 1953. Piperazine compounds mediate their anthelmintic action by generally paralyzing parasites, allowing the host body to easily remove or expel the invading organism. Outside the body, piperazine has a remarkable power to dissolve uric acid and producing a soluble urate, but in clinical experience it has not proved equally successful. COA of Formula: C16H18FN3O3

Referemce:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics

Antibiotics in urine from general adults in Shenzhen, China: Demographic-related difference in exposure levels was written by Zhong, Shihua;Wu, Xiaoling;Zhang, Duo;Du, Sijin;Shen, Junchun;Xiao, Lehan;Zhu, Ying;Xu, Yuanyuan;Lin, Yuli;Yin, Liuyi;Rao, Manting;Lu, Shaoyou. And the article was included in Science of the Total Environment in 2022.Related Products of 70458-96-7 The following contents are mentioned in the article:

Misuse or overuse of antibiotics can have a variety of detrimental microbial effects. However, the body burden of antibiotics in the general population is currently unclear. In this cross-sectional study, we determined four classes of widely-applied antibiotics (3 imidazoles, 2 sulfonamides, 5 quinolones, and 2 chloramphenicols) in urine samples from 1170 adult residents in Shenzhen, China. Antibiotics were detected in 30.8% of all urine samples with concentrations ranging from <LOD to 3517μg/mL, among which metronidazole, ofloxacin and florfenicol were predominant. Notably, antibiotics prohibited for human or veterinary use were detected in 21.0% of samples, indicating that these antibiotics may still be overused in daily life. We found that the presence of antibiotics in urine is associated with being overweight (OR: 1.386, 95% CI: 1.056-1.819, p = 0.019) and obesity (OR: 1.862, 95% CI: 1.103-3.146, p = 0.020) in the adult population. Multilinear regression anal. showed that a percent increase of hydroxy metronidazole was related to 9.86% pos. change of body mass index (p = 0.029). Interestingly, we also found total antibiotic concentration higher in the unmarried group (p = 0.006). Besides, consumption of smoked foods was correlated with urinary antibiotic levels (p = 0.001), indicating smoked meat may be a potential exposure source of veterinary antibiotics. These results highlight the need to reduce human exposure to banned antibiotics. Future research could focus on assessing the health risk and other outcomes of antibiotic overuse. This study involved multiple reactions and reactants, such as 1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (cas: 70458-96-7Related Products of 70458-96-7).

1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (cas: 70458-96-7) belongs to piperazine derivatives. The piperazine scaffold is often found in biologically active compounds in different therapeutic areas. These therapeutic areas include antifungals, antidepressants, antivirals, and serotonin receptor (5-HT) antagonists/agonists. Although many piperazine derivatives occur naturally, piperazine itself can be synthesized by reacting alcoholic ammonia with 1,2-dichloroethane, by the action of sodium and ethylene glycol on ethylene diamine hydrochloride, or by reduction of pyrazine with sodium in ethanol.Related Products of 70458-96-7

Referemce:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics

Copper exposure effects on antibiotic degradation in swine manure vary between mesophilic and thermophilic conditions was written by Lin, Hui;Cheng, Qilu;Sun, Wanchun;Yang, Fengxia;Ding, Yongzhen;Ma, Junwei. And the article was included in Science of the Total Environment in 2022.Synthetic Route of C16H18FN3O3 The following contents are mentioned in the article:

Antibiotic and heavy metal commonly coexist in manure. This study investigated the effect of Cu exposure on antibiotic dissipation in swine manure under two typical temperature (mesophilic and thermophilic) conditions in composting, focusing on biodegradation behaviors. The results showed that Cu promoted the dissipation of norfloxacin and sulfamethazine (SMZ) in solid swine manure under mesophilic conditions at initial concentrations ranging from 407.8 to 1353.0 mg·kg-1 but insignificantly influenced or even inhibited their dissipation under thermophilic conditions. A liquid manure suspension culture experiment was designed to elucidate the response of SMZ biodegradation to Cu. In this manure suspension, biodegradation was the major mechanism for SMZ removal, but SMZ biodegradation was decreased from 23.2% to 5.5% when the Cu concentration increased from 0 to 10 mg L^-1. Mesophilic and heat-resistant SMZ-degrading bacterial inoculants were subsequently prepared using 21 SMZ-degrading bacteria that were isolated and identified from manure suspension cultures. Inoculating both mesophilic and heat-resistant SMZ-degrading bacterial inoculants enhanced SMZ degradation in sterilized manure suspensions without Cu addition, however only mesophilic SMZ-degrading inoculum improved SMZ degradation after Cu addition In the presence of Cu, the heat-resistant SMZ-degrading inoculum failed to enhance SMZ removal in manure suspensions. Our findings can help to answer why Cu has varied effects on antibiotic degradation during manure composting. This study involved multiple reactions and reactants, such as 1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (cas: 70458-96-7Synthetic Route of C16H18FN3O3).

1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (cas: 70458-96-7) belongs to piperazine derivatives. Piperazine was first introduced as an anthelmintic in 1953. Piperazine compounds mediate their anthelmintic action by generally paralyzing parasites, allowing the host body to easily remove or expel the invading organism. Outside the body, piperazine has a remarkable power to dissolve uric acid and producing a soluble urate, but in clinical experience it has not proved equally successful. Synthetic Route of C16H18FN3O3

Referemce:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics

Occurrence and distribution of antibiotics and antibiotic resistance genes in water of Liaohe River Basin, China was written by Gao, Hui;Zhao, Fuqiang;Li, Ruijing;Jin, Shuaichen;Zhang, Haibo;Zhang, Keyu;Li, Shisheng;Shu, Qin;Na, Guangshui. And the article was included in Journal of Environmental Chemical Engineering in 2022.COA of Formula: C16H18FN3O3 The following contents are mentioned in the article:

Surface water environment is an important repository of antibiotics and antibiotic resistance genes (ARGs). It is of great significance to study the occurrence and distribution of antibiotics and ARGs in surface water environment. In this study, the Liaohe River Basin, China was taken as the study area, and the concentrations of antibiotics and ARGs in water were investigated by HPLC-MS/MS and HT-qPCR. The results showed that a total of 53 antibiotics of 6 types were detected in water, and the pollution level was at ND∼331.64 ng/L, where PCG was the highest. Totally 164 ARGs and 10 mobile genetic elements (MGEs) were detected in the water, and the absolute abundances were at 2.18 × 10⁴∼3.95 × 10⁷ copies/L and 1.82 × 10⁵-3.78 × 10⁷ copies/L, resp. The multidrug and aminoglycoside were the dominant ARG types. Amoxicillin, erythromycin, anhydroerythromycin and ofloxacin posed certain ecol. risks for sensitive aquatic organisms. In spatial distribution, the pollution of antibiotics and ARGs in the Daliao River system was higher than that in the Liaohe River system. There was a significant pos. correlation between total concentrations of antibiotics and total relative abundance of ARGs (r = 0.66, p < 0.05). The co-occurrence of multiple antibiotics promoted the pollution and spread of ARGs. In addition, the total relative abundance of MGEs and ARGs showed a significant pos. correlation (r = 0.946, p < 0.01), and MGEs played an important role in the occurrence and evolution of ARGs in water. This study involved multiple reactions and reactants, such as 1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (cas: 70458-96-7COA of Formula: C16H18FN3O3).

1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (cas: 70458-96-7) belongs to piperazine derivatives. Piperazine causes primary dermal irritation and skin burns at high concentrations. Piperazine also causes eye irritation in humans. Although many piperazine derivatives occur naturally, piperazine itself can be synthesized by reacting alcoholic ammonia with 1,2-dichloroethane, by the action of sodium and ethylene glycol on ethylene diamine hydrochloride, or by reduction of pyrazine with sodium in ethanol.COA of Formula: C16H18FN3O3

Referemce:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics

Molecularly imprinted polypyrrole film-coated poly(3,4-ethylenedioxythiophene):polystyrene sulfonate-functionalized black phosphorene for the selective and robust detection of norfloxacin was written by Li, Guangli;Wu, Jingtao;Qi, Xiaoman;Wan, Xuan;Liu, Ying;Chen, Yuwei;Xu, Lijian. And the article was included in Materials Today Chemistry in 2022.Computed Properties of C16H18FN3O3 The following contents are mentioned in the article:

An efficient molecularly imprinted polymer (MIP) voltammetric sensor was prepared based on polypyrrole (PPy) imprinted film-bearing poly(3,4-ethylenedioxythiophene):polystyrene sulfonate-functionalized black phosphorene (BP-PEDOT:PSS) for the selective recognition and robust determination of norfloxacin. BP-PEDOT:PSS was prepared via a simple ultrasonic-assisted liquid-phase exfoliation as an efficient support for use in MIP electrochem. sensors. The imprinted PPy film was deposited onto the surface of BP-PEDOT:PSS via the potentiodynamic technique in the presence of norfloxacin, with the imprinting factor of 3.86 for norfloxacin. The morphologies and microstructures of the sensing materials were investigated using SEM, energy dispersive X-ray spectroscopy, transmission electron microscopy, and Raman spectroscopy. Addnl., parameters including the BP-PEDOT:PSS loading volume, norfloxacin:pyrrole molar ratio, electropolymerization cycles, template removal, solution pH, and time of electrode exposure to the analyte were optimized. Under optimal conditions, the response peak currents of norfloxacin correlated linearly to norfloxacin concentrations from 0.001 to 10μM, with a limit of detection of 0.25 nM. The prepared imprinted sensor could effectively distinguish norfloxacin from other fluoroquinolone antibiotics with the selectivity coefficients of 5.4-17.3 and maintained stable, robust voltammetric responses for up to two weeks. Moreover, it successfully detected norfloxacin in pharmaceutical formulations and milk samples. This study involved multiple reactions and reactants, such as 1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (cas: 70458-96-7Computed Properties of C16H18FN3O3).

1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (cas: 70458-96-7) belongs to piperazine derivatives. Piperazine causes primary dermal irritation and skin burns at high concentrations. Piperazine also causes eye irritation in humans. Piperazine and its salts did not induce point mutations in a bacterial test. A series of mutagenicity studies in cells, both in vitro and in vivo, has been completed and showed no evidence of mutagenic effect.Computed Properties of C16H18FN3O3

Referemce:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics

Green and sustainable downscaled procedure using smartphone-based colorimetric determination of fluoroquinolones in extemporaneous syrup formulations was written by Apichai, Sutasinee;Thunyajaroen, Nuttharikar;Prajongsangsri, Tanyuta;Tananchai, Pimchanok;Pattananandecha, Thanawat;Ogata, Fumihiko;Kawasaki, Naohito;Grudpan, Kate;Saenjum, Chalermpong. And the article was included in Sustainable Chemistry and Pharmacy in 2022.COA of Formula: C16H18FN3O3 The following contents are mentioned in the article:

A green and sustainable downscaled procedure was developed to perform smartphone-based colorimetric determination of fluoroquinolones in extemporaneous syrup formulations. The procedure functioned by complexing fluoroquinolones with metal ions, the most suited of which is a ferric ion, to produce a colored product in a 96-well plate combined with smartphone detection and image processing. It performs on a microscale with 1 min detection time providing high throughput at 960 samples in triplicate/h/a well plate. Linear calibrations constituted the concentration of fluoroquinolones and the relative intensity of blue, yielding LODs (3.3σ) and LOQs (10σ) for ciprofloxacin, norfloxacin, ofloxacin and levofloxacin at 4.6, 8.3, 9.1 and 10.6μg/mL and 14.0, 25.1, 27.5 and 32.0μg/mL, resp., (where σ served as the standard deviation of the intercept, divided by the slope of the linear calibration graph). The developed procedure was applied to real extemporaneous oral ciprofloxacin syrup samples. The results obtained by the developed procedure agreed with that of a standard method, with no significant differences at a confidence level of 95%. The developed procedure is aimed at real-world applications in assays for quality and stability of the extemporaneous formulations in community and health-promoting hospitals. This promotes health and well-being for individuals of all ages by ensuring that everyone gains access to quality essential healthcare services as well as safe, effective, high-quality and affordable pharmaceuticals. This study involved multiple reactions and reactants, such as 1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (cas: 70458-96-7COA of Formula: C16H18FN3O3).

1-Ethyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid (cas: 70458-96-7) belongs to piperazine derivatives. Piperazine is a fairly basic compound and is an amine solvent. Piperazine is formed as a co-product in the ammoniation of 1,2-dichloroethane or ethanolamine. These are the only routes to the chemical used commercially.COA of Formula: C16H18FN3O3

Referemce:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics