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HPLC of Formula: C7H4Cl2O2. Bye, fridends, I hope you can learn more about C7H4Cl2O2, If you have any questions, you can browse other blog as well. See you lster.

HPLC of Formula: C7H4Cl2O2. In 2019 SYNTHESIS-STUTTGART published article about RADIOIODINATION; ARYL; TRACERS in [Dubost, Emmanuelle; Babin, Victor; Benoist, Florian; Hebert, Alexandra; Fabis, Frederic; Cailly, Thomas] Normandie Univ, UNICAEN, CERMN, F-14000 Caen, France; [Pigree, Gilbert; Cailly, Thomas] Normandie Univ, UNICAEN, IMOGERE, F-14000 Caen, France; [Bouillon, Jean-Philippe] Normandie Univ, UNIROUEN, CNRS, INSA Rouen,COBRA UMR 6014, F-76000 Rouen, France; [Cailly, Thomas] CHU Cote Nacre, Dept Nucl Med, F-14000 Caen, France in 2019, Cited 17. The Name is 2,4-Dichlorobenzoic acid. Through research, I have a further understanding and discovery of 50-84-0.

An improved protocol to perform C-H radio-iodination is described. These new conditions allow rapid and clean formation of radio-iodinated N -acylsulfonamides using [ (125) I]NIS and catalytic amounts of palladium acetate and para -toluenesulfonic acid. No pre-functionalized precursors are required and the products are obtained with radiochemical conversions (RCC) of 27-84%.

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Reference:
Chloride – Wikipedia,
,Chlorides – an overview | ScienceDirect Topics

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An article Discovery and Structural Optimization of Acridones as Broad-Spectrum Antimalarials WOS:000464768300020 published article about PLASMODIUM-BERGHEI; CATALYZED AMINATION; CYTOCHROME-B; LIVER-STAGE; MALARIA; VIVAX; CHALLENGES; RESISTANT; PROPHYLAXIS; MUTATIONS in [Dodean, Rozalia A.; Kancharla, Papireddy; Li, Yuexin; Winter, Rolf W.; Riscoe, Michael K.; Kelly, Jane X.] Portland State Univ, Dept Chem, Portland, OR 97201 USA; [Dodean, Rozalia A.; Li, Yuexin; Smilkstein, Martin J.; Pou, Sovitj; Winter, Rolf W.; Riscoe, Michael K.; Kelly, Jane X.] Dept Vet Affairs Med Ctr, Portland, OR 97239 USA; [Melendez, Victor; Read, Lisa; Bane, Charles E.; Vesely, Brian; Kreishman-Deitrick, Mara; Black, Chad; Li, Qigui; Sciotti, Richard J.; Olmeda, Raul; Thu-Lan Luong; Gaona, Heather; Potter, Brittney; Sousa, Jason; Marcsisin, Sean; Caridha, Diana; Xie, Lisa; Vuong, Chau; Zeng, Qiang; Zhang, Jing; Zhang, Ping; Lin, Hsiuling; Butler, Kirk; Roncal, Norma; Gaynor-Ohnstad, Lacy; Leed, Susan E.; Nolan, Christina] Walter Reed Army Inst Res, Div Expt Therapeut, Silver Spring, MD 20910 USA; [Huezo, Stephanie J.; Rasmussen, Stephanie A.; Cooper, Roland A.] Dominican Univ Calif, Dept Nat Sci & Math, San Rafael, CA 94901 USA; [Stephens, Melissa T.; Tan, John C.] Univ Notre Dame, Genom Core Facil, Notre Dame, IN 46556 USA; [Tan, John C.] Univ Notre Dame, Eck Inst Global Hlth, Notre Dame, IN 46556 USA in 2019, Cited 53. The Name is 2,4-Dichlorobenzoic acid. Through research, I have a further understanding and discovery of 50-84-0. Recommanded Product: 2,4-Dichlorobenzoic acid

Malaria remains one of the deadliest diseases in the world today. Novel chemoprophylactic and chemotherapeutic antimalarials are needed to support the renewed eradication agenda. We have discovered a novel antimalarial acridone chemotype with dual-stage activity against both liver stage and blood-stage malaria. Several lead compounds generated from structural optimization of a large library of novel acridones exhibit efficacy in the following systems: (1) picomolar inhibition of in vitro Plasmodium falciparum blood-stage growth against multidrug-resistant parasites; (2) curative efficacy after oral administration in an erythrocytic Plasmodium yoelii murine malaria model; (3) prevention of in vitro Plasmodium berghei sporozoite-induced development in human hepatocytes; and (4) protection of in vivo P. berghei sporozoite-induced infection in mice. This study offers the first account of liver-stage antimalarial activity in an acridone chemotype. Details of the design, chemistry, structure-activity relationships, safety, metabolic/pharmacokinetic studies, and mechanistic investigation are presented herein.

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Reference:
Chloride – Wikipedia,
,Chlorides – an overview | ScienceDirect Topics

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Welcome to talk about 50-84-0, If you have any questions, you can contact Thakral, S; Singh, V or send Email.. Formula: C7H4Cl2O2

Recently I am researching about GLUCOSIDASE INHIBITORY-ACTIVITY; ALPHA-GLUCOSIDASE; BIOLOGICAL EVALUATION; BENZOTHIAZOLE DERIVATIVES; SULFONAMIDE; DOCKING; AMYLASE; BENZENESULFONAMIDE; AGENTS; POTENT, Saw an article supported by the Dr. A. P. J. Abdul Kalam Central Instrumentation laboratory, G. J. U.S. and T., Hisar under DST-PURSE programme. Published in BENTHAM SCIENCE PUBL LTD in SHARJAH ,Authors: Thakral, S; Singh, V. The CAS is 50-84-0. Through research, I have a further understanding and discovery of 2,4-Dichlorobenzoic acid. Formula: C7H4Cl2O2

Background: Postprandial hyperglycemia can be reduced by inhibiting major carbohydrate hydrolyzing enzymes, such as alpha-glucosidase and alpha-amylase which is an effective approach in both preventing and treating diabetes. Objective: The aim of this study was to synthesize a series of 2,4-dichloro-5-[(N-and/alkyl)sulfamoyl]benzoic acid derivatives and evaluate alpha-glucosidase and alpha-amylase inhibitory activity along with molecular docking and in silico ADMET property analysis. Method: Chlorosulfonation of 2,4-dichloro benzoic acid followed by reaction with corresponding anilines/amines yielded 2,4-dichloro-5-[(N-aryl/alkyl)sulfamoyl]benzoic acid derivatives. For evaluating their antidiabetic potential alpha-glucosidase and alpha-amylase inhibitory assays were carried out. In silico molecular docking studies of these compounds were performed with respect to these enzymes and a computational study was also carried out to predict the drug-likeness and ADMET properties of the title compounds. Results: Compound 3c (2,4-clichloro-5-[(2-nitrophenyl)sulfamoyl]benzoic acid) was found to be highly active having 3 fold inhibitory potential against alpha-amylase and 5 times inhibitory activity against alpha-glucosidase in comparison to standard drug acarbose. Conclusion: Most of the synthesized compounds were highly potent or equipotent to standard drug acarbose for inhibitory potential against alpha-glucosidase and alpha-amylase enzyme and hence this may indicate their antidiabetic activity. The docking study revealed that these compounds interact with active site of enzyme through hydrogen bonding and different pi interactions.

Welcome to talk about 50-84-0, If you have any questions, you can contact Thakral, S; Singh, V or send Email.. Formula: C7H4Cl2O2

Reference:
Chloride – Wikipedia,
,Chlorides – an overview | ScienceDirect Topics

Machine Learning in Chemistry about 2,4-Dichlorobenzoic acid

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An article Cost comparison of surgical management of nonsagittal synostosis: traditional open versus endoscope-assisted techniques WOS:000523190800003 published article about FRONTO-ORBITAL ADVANCEMENT; POSTOPERATIVE HELMET THERAPY; SAGITTAL SYNOSTOSIS; CORONAL SYNOSTOSIS; RIGID FIXATION; OPEN REPAIR; CRANIOSYNOSTOSIS; CRANIECTOMY; OUTCOMES; CARE in [Zubovic, Ema; Skolnick, Gary B.; Naidoo, Sybill D.; Patel, Kamlesh B.] Washington Univ, Sch Med, Dept Surg, Div Plast & Reconstruct Surg, St Louis, MO 63110 USA; [Lapidus, Jodi B.] Univ Calif San Francisco, Dept Surg, Div Plast & Reconstruct Surg, San Francisco, CA USA; [Smyth, Matthew D.] Washington Univ, Sch Med, Dept Neurosurg, St Louis, MO USA in 2020, Cited 41. The Name is 2,4-Dichlorobenzoic acid. Through research, I have a further understanding and discovery of 50-84-0. Recommanded Product: 50-84-0

OBJECTIVE Management of craniosynostosis at an early age is important for mitigating the risk of abnormal cranial development, but treatment can result in significant expenses. Previous research has shown that endoscope-assisted craniectomy (EAC) is less costly than open cranial vault remodeling (CVR) for patients with sagittal synostosis. The aim of this study was to strengthen the existing body of healthcare cost research by elucidating the charges associated with open and endoscopic treatment for patients with nonsagittal synostosis. METHODS The authors performed a retrospective analysis of data obtained in 41 patients who underwent open CVR and 38 who underwent EAC with postoperative helmet therapy for nonsagittal, single-suture craniosynostosis (metopic, coronal, and lambdoid) between 2008 and 2018. All patients were < 1 year of age at the time of surgery and had a minimum 1 year of follow-up. Inpatient charges, physician fees, helmet charges, and outpatient clinic visits in the 1st year were analyzed. RESULTS The mean ages of the children treated with EAC and open CVR were 3.5 months and 8.7 months, respectively. Patients undergoing EAC with postoperative helmet therapy required more outpatient clinic visits in the 1st year than patients undergoing CVR (4 vs 2; p < 0.001). Overall, 13% of patients in the EAC group required 1 helmet, 30% required 2 helmets, 40% required 3 helmets, and 13% required 4 or more helmets; the mean total helmeting charges were $10,072. The total charges of treatment, including inpatient charges, physician fees, outpatient clinic visit costs, and helmet charges, were significantly lower for the EAC group than they were for the open CVR group ($50,840 vs $95,588; p < 0.001). CONCLUSIONS Despite the additional charges for postoperative helmet therapy and the more frequent outpatient visits, EAC is significantly less expensive than open CVR for patients with metopic, coronal, and lambdoid craniosynostosis. In conjunction with the existing literature on clinical outcomes and perioperative resource utilization, these data support EAC as a cost-minimizing treatment for eligible patients with nonsagittal synostosis. Recommanded Product: 50-84-0. Bye, fridends, I hope you can learn more about C7H4Cl2O2, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Chloride – Wikipedia,
,Chlorides – an overview | ScienceDirect Topics

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Product Details of 50-84-0. Authors Jiang, S; Tian, XJ; Feng, SY; Li, JS; Li, ZW; Lu, CH; Li, CJ; Liu, WD in AMER CHEMICAL SOC published article about in [Jiang, Si; Tian, Xiao-Jing; Feng, Shu-Yao; Li, Jiang-Sheng; Li, Zhi-Wei; Lu, Cui-Hong] Changsha Univ Sci & Technol, Sch Chem & Food Engn, Hunan Prov Key Lab Mat Protect Elect Power & Tran, Changsha 410114, Peoples R China; [Li, Chao-Jun] McGill Univ, Dept Chem, Sherbrooke, PQ H3A 0B8, Canada; [Li, Chao-Jun] McGill Univ, FQRNT Ctr Green Chem & Catalysis, Sherbrooke, PQ H3A 0B8, Canada; [Liu, Wei-Dong] Hunan Res Inst Chem Ind, Natl Engn Res Ctr Agrochem, Changsha 410007, Peoples R China in 2021, Cited 45. The Name is 2,4-Dichlorobenzoic acid. Through research, I have a further understanding and discovery of 50-84-0

A visible-light photoredox catalyzed radical cascade cyclization of simple ethers with cyanamides is developed at room temperature. This strategy involves sequential inert C-sp3-H/C-sp2-H functionalizations through intermolecular addition reaction of oxyalkyl radicals to N-cyano groups followed by radical cyclization of iminyl radicals in situ generated with C-2 aryl rings. This method allows for efficient synthesis of tetracyclic benzo[4,5]imidazo[1,2-c]quinazolines. Importantly, this is the first example of an intermolecular-intramolecular radical cascade cyclization reaction of cyanamides.

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Reference:
Chloride – Wikipedia,
,Chlorides – an overview | ScienceDirect Topics

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I found the field of Agriculture; Chemistry; Food Science & Technology very interesting. Saw the article Rational Optimization and Action Mechanism of Novel Imidazole (or Imidazolium)-Labeled 1,3,4-Oxadiazole Thioethers as Promising Antibacterial Agents against Plant Bacterial Diseases published in 2019. Recommanded Product: 2,4-Dichlorobenzoic acid, Reprint Addresses Song, BA; Yang, S (corresponding author), Guizhou Univ, State Key Lab Breeding Base Green Pesticide & Agr, Key Lab Green Pesticide & Agr Bioengn, Minist Educ,Ctr R&D Fine Chem, Guiyang 550025, Guizhou, Peoples R China.; Yang, S (corresponding author), East China Univ Sci & Technol, Coll Pharm, Shanghai 200237, Peoples R China.. The CAS is 50-84-0. Through research, I have a further understanding and discovery of 2,4-Dichlorobenzoic acid

The emergence and widespread occurrence of plant bacterial diseases that cause global production constraints have become major challenges to agriculture worldwide. To promote the discovery and development of new bactericides, imidazole-labeled 1,3,4-oxadiazole thioethers were first fabricated by integrating the crucially bioactive scaffolds of the imidazole motif and 1,3,4-oxadiazole skeleton in a single molecular architecture. Subsequently, a superior antibacterial compound A(6) was gradually discovered possessing excellent competence against plant pathogens Xanthomonas oryzae pv oryzae and Xanthomonas axonopodis pv citri with EC50 values of 0.734 and 1.79 mu g/mL, respectively. These values were better than those of commercial agents bismerthiazol (92.6 mu g/mL) and thiodiazole copper (77.0 mu g/mL). Further modifying the imidazole moiety into the imidazolium scaffold led to the discovery of an array of potent antibacterial compounds providing the corresponding minimum EC50 values of 0.295 and 0.607 mu g/mL against the two strains. Moreover, a plausible action mechanism for attacking pathogens was proposed based on the concentration dependence of scanning electron microscopy, transmission electron microscopy, and fluorescence microscopy images. Given the simple molecular structures, easy synthetic procedure, and highly efficient bioactivity, imidazole (or imidazolium)-labeled 1,3,4-oxadiazole thioethers can be further explored and developed as promising indicators for the development of commercial drugs.

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Reference:
Chloride – Wikipedia,
,Chlorides – an overview | ScienceDirect Topics

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Welcome to talk about 50-84-0, If you have any questions, you can contact Zubovic, E; Lapidus, JB; Skolnick, GB; Naidoo, SD; Smyth, MD; Patel, KB or send Email.. Safety of 2,4-Dichlorobenzoic acid

An article Cost comparison of surgical management of nonsagittal synostosis: traditional open versus endoscope-assisted techniques WOS:000523190800003 published article about FRONTO-ORBITAL ADVANCEMENT; POSTOPERATIVE HELMET THERAPY; SAGITTAL SYNOSTOSIS; CORONAL SYNOSTOSIS; RIGID FIXATION; OPEN REPAIR; CRANIOSYNOSTOSIS; CRANIECTOMY; OUTCOMES; CARE in [Zubovic, Ema; Skolnick, Gary B.; Naidoo, Sybill D.; Patel, Kamlesh B.] Washington Univ, Sch Med, Dept Surg, Div Plast & Reconstruct Surg, St Louis, MO 63110 USA; [Lapidus, Jodi B.] Univ Calif San Francisco, Dept Surg, Div Plast & Reconstruct Surg, San Francisco, CA USA; [Smyth, Matthew D.] Washington Univ, Sch Med, Dept Neurosurg, St Louis, MO USA in 2020, Cited 41. The Name is 2,4-Dichlorobenzoic acid. Through research, I have a further understanding and discovery of 50-84-0. Safety of 2,4-Dichlorobenzoic acid

OBJECTIVE Management of craniosynostosis at an early age is important for mitigating the risk of abnormal cranial development, but treatment can result in significant expenses. Previous research has shown that endoscope-assisted craniectomy (EAC) is less costly than open cranial vault remodeling (CVR) for patients with sagittal synostosis. The aim of this study was to strengthen the existing body of healthcare cost research by elucidating the charges associated with open and endoscopic treatment for patients with nonsagittal synostosis. METHODS The authors performed a retrospective analysis of data obtained in 41 patients who underwent open CVR and 38 who underwent EAC with postoperative helmet therapy for nonsagittal, single-suture craniosynostosis (metopic, coronal, and lambdoid) between 2008 and 2018. All patients were < 1 year of age at the time of surgery and had a minimum 1 year of follow-up. Inpatient charges, physician fees, helmet charges, and outpatient clinic visits in the 1st year were analyzed. RESULTS The mean ages of the children treated with EAC and open CVR were 3.5 months and 8.7 months, respectively. Patients undergoing EAC with postoperative helmet therapy required more outpatient clinic visits in the 1st year than patients undergoing CVR (4 vs 2; p < 0.001). Overall, 13% of patients in the EAC group required 1 helmet, 30% required 2 helmets, 40% required 3 helmets, and 13% required 4 or more helmets; the mean total helmeting charges were $10,072. The total charges of treatment, including inpatient charges, physician fees, outpatient clinic visit costs, and helmet charges, were significantly lower for the EAC group than they were for the open CVR group ($50,840 vs $95,588; p < 0.001). CONCLUSIONS Despite the additional charges for postoperative helmet therapy and the more frequent outpatient visits, EAC is significantly less expensive than open CVR for patients with metopic, coronal, and lambdoid craniosynostosis. In conjunction with the existing literature on clinical outcomes and perioperative resource utilization, these data support EAC as a cost-minimizing treatment for eligible patients with nonsagittal synostosis. Welcome to talk about 50-84-0, If you have any questions, you can contact Zubovic, E; Lapidus, JB; Skolnick, GB; Naidoo, SD; Smyth, MD; Patel, KB or send Email.. Safety of 2,4-Dichlorobenzoic acid

Reference:
Chloride – Wikipedia,
,Chlorides – an overview | ScienceDirect Topics

Our Top Choice Compound:2,4-Dichlorobenzoic acid

Bye, fridends, I hope you can learn more about C7H4Cl2O2, If you have any questions, you can browse other blog as well. See you lster.. Computed Properties of C7H4Cl2O2

Computed Properties of C7H4Cl2O2. In 2020 CHEM COMMUN published article about C-H ACTIVATION; DIRECT ARYLATION; EFFICIENT; DIHYDROPHENANTHRENE; FUNCTIONALIZATION; PHENANTHRENES; EXTENSION; ARYNES in [Gu, Yichao; Sun, Xueliang; Wan, Bin; Lu, Zhuoer; Zhang, Yanghui] Tongji Univ, Sch Chem Sci & Engn, Shanghai Key Lab Chem Assessment & Sustainabil, 1239 Siping Rd, Shanghai 200092, Peoples R China in 2020, Cited 63. The Name is 2,4-Dichlorobenzoic acid. Through research, I have a further understanding and discovery of 50-84-0.

A palladium-catalyzed cross-coupling reaction of aryl halides with 2-chlorobenzoic acids has been developed. The reaction forms C(sp(3)), C(sp(2))-palladacycles through C(sp(3))-H activation. The palladacycles react with 2-chlorobenzoic acids through two successive C-C cross-couplings, and two C-C bonds are formed with high chemoselectivity. The reaction provides an innovative method for the synthesis of 9,10-dihydrophenanthrenes.

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Reference:
Chloride – Wikipedia,
,Chlorides – an overview | ScienceDirect Topics

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Recommanded Product: 2,4-Dichlorobenzoic acid. Authors Anastassiadou, M; Bernasconi, G; Brancato, A; Cabrera, LC; Ferreira, L; Greco, L; Jarrah, S; Kazocina, A; Leuschner, R; Magrans, JO; Miron, I; Nave, S; Pedersen, R; Reich, H; Rojas, A; Sacchi, A; Santos, M; Scarlato, AP; Theobald, A; Vagenende, B; Verani, A in EUROPEAN FOOD SAFETY AUTHORITY-EFSA published article about in [Anastassiadou, Maria; Bernasconi, Giovanni; Brancato, Alba; Cabrera, Luis Carrasco; Ferreira, Lucien; Greco, Luna; Jarrah, Samira; Kazocina, Aija; Leuschner, Renata; Magrans, Jose Oriol; Miron, Ileana; Nave, Stefanie; Pedersen, Ragnor; Reich, Hermine; Rojas, Alejandro; Sacchi, Angela; Santos, Miguel; Scarlato, Alessia Pia; Theobald, Anne; Vagenende, Benedicte; Verani, Alessia] European Food Safety Author EFSA, Parma, Italy in 2021, Cited 4. The Name is 2,4-Dichlorobenzoic acid. Through research, I have a further understanding and discovery of 50-84-0

The applicant Syngenta Crop Protection AG submitted a request to the competent national authority in Finland to evaluate the confirmatory data that were identified for propiconazole in the framework of the MRL review under Article 12 of Regulation (EC) No 396/2005 as not available. Following the decision on the non-renewal of the approval of propiconazole and the decision to lower the maximum residue levels (MRLs) for propiconazole to the limit of quantification (LOQ) for all commodities, the data gaps identified in the MRL review are no longer relevant. EFSA summarised some new studies on the toxicological profile of propiconazole metabolites CGA91305, SYN547889 and NOA436613, which were assessed by the rapporteur Member State. Overall, the available information is not sufficient to characterise the toxicological profile of metabolites convertible to 2,4-dichlorobenzoic acid as data gaps still exist for SYN547889, NOA436613, CGA118244, CGA118245, CGA91304 and CGA91305. (C) 2021 European Food Safety Authority. EFSA Journal published by John Wiley and Sons Ltd on behalf of European Food Safety Authority.

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Reference:
Chloride – Wikipedia,
,Chlorides – an overview | ScienceDirect Topics

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Recently I am researching about NIPECOTIC ACID-DERIVATIVES; ANTIEPILEPTIC DRUGS; DESIGN; MODEL; 1,3,4-OXADIAZOLE; TRANSPORTER; MECHANISMS; EPILEPSY, Saw an article supported by the . Name: 2,4-Dichlorobenzoic acid. Published in ELSEVIER in AMSTERDAM ,Authors: Singh, RB; Das, N; Singh, GK; Singh, SK; Zaman, K. The CAS is 50-84-0. Through research, I have a further understanding and discovery of 2,4-Dichlorobenzoic acid

In the present study, we have synthesized a series of fifteen nipecotic acid 1,3,4-oxadiazole based hybrids with significant (60-78%) yields. All the compounds were characterized by using different spectroanalytical techniques such as FT-IR, H-1 NMR, C-13 NMR, and elemental analysis. This design strategy was validated by using in vivo anti-epileptic and anti-depressant bioassay models. Anti-convulsant activity was evaluated using subcutaneous pentylenetetrazol (scPTZ) in mice and MES induced seizure. Among a spectrum of activities, three compounds (4i, 4m, and 4n) displayed significant activity against pentylenetetrazole (scPTZ) induced seizures. No disruptions in motor co-ordination were observed in mice pretreated with the test compounds in the rotarod test. Their influence on the safety profile of elevated serum levels of biochemical markers such as hepatic and renal toxicity has been found to be safe. The derivatives also show marked anti-depressant activity, devoid of serotonergic augmentation as assessed using the despair swim test, 5-hydroxytryptophan (5-HTP)-induced head twitch test and learned helplessness test. In silico docking studies targeted on homology modelled GABA transporter 1 (GAT1) protein shows the critical enzyme-ligand interactions leading to the inhibition of the GAT1 transporter. The compound 4m was found to be the most active compound among all the synthesized compounds. (C) 2020 Published by Elsevier B.V. on behalf of King Saud University.

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Reference:
Chloride – Wikipedia,
,Chlorides – an overview | ScienceDirect Topics