Category: 500-22-1

Authors Kazemnejadi, M; Sharafi, Z; Mahmoudi, B; Zeinali, A; Nasseri, MA in SPRINGER published article about ONE-POT SYNTHESIS; FRIEDLANDER SYNTHESIS; NANOPARTICLES; COMPLEX; SURFACE; ACID; NANOCATALYST; DERIVATIVES; QUINOLINES; PHOSPHINE in [Kazemnejadi, Milad; Zeinali, Atefeh; Nasseri, Mohammad Ali] Univ Birjand, Dept Chem, Fac Sci, Birjand 97175615, Iran; [Sharafi, Zeinab] Lorestan Univ Med Sci, Razi Herbal Med Res Ctr, Khorramabad, Iran; [Mahmoudi, Boshra] Sulaimani Polytech Univ, Res Ctr, Sulaimani 46001, Kurdistan Regio, Iraq in 2020.0, Cited 48.0. Computed Properties of C6H5NO. The Name is 3-Pyridinecarboxaldehyde. Through research, I have a further understanding and discovery of 500-22-1

A new, cheap, and accessible method has been used for the preparation of nano-belts from the chemical decomposition (top-down approach) of a cheap stainless steel screw and found as an efficient magnetically recyclable nanocatalyst for the preparation of quinolines and 1,8-dioxo-octahydroxanthenes under mild reaction conditions. The nano-belts, Fe-Cr-Ni oxide alloy, was prepared in a two-step synthesis and characterized with various instrumental methods. Due to magnetic property of the screw (a ferritic-alloy), the resultant nano-belts is magnetic. Magnetic Fe-Cr-Ni alloy nano-belts were applied toward efficient preparation of quinolines and 1,8-dioxo-octahydroxanthenes under mild conditions. The catalyst could be readily recovered and recycled for several consecutive runs, while it suffers from a very low metal leaching and subsequently efficiency drop. Graphic abstract

Welcome to talk about 500-22-1, If you have any questions, you can contact Kazemnejadi, M; Sharafi, Z; Mahmoudi, B; Zeinali, A; Nasseri, MA or send Email.. Computed Properties of C6H5NO

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

In 2020.0 J MED CHEM published article about NATURAL-PRODUCTS; INTRACELLULAR ZINC; CORRELATION-ENERGY; IRON CHELATORS; CELL-GROWTH; DNA-DAMAGE; APOPTOSIS; COMPLEXES; DEPLETION; ANALOGS in [Galiana-Rosello, Cristina; Gonzalez, Jorge; Martinez-Camarena, Alvaro; Garcia-Espana, Enrique] Univ Valencia, Inst Ciencia Mol ICMol, Dept Quim Inorgan, Valencia 46980, Spain; [Galiana-Rosello, Cristina; Eugenia Gonzalez-Rosende, Maria] Univ CEU Cardenal Herrera, Fac Ciencias Salud, Dept Farm, C Ramon y Cajal S-N, Valencia 46115, Spain; [Galiana-Rosello, Cristina; Fernandez de Mattos, Silvia; Villalonga, Priam] Univ Illes Balears, Inst Univ Invest Ctencies Salut IUNICS, Canc Cell Biol Lab, Illes Balears 07122, Spain; [Galiana-Rosello, Cristina; Fernandez de Mattos, Silvia; Villalonga, Priam] Inst Invest Sanitaria Illes Balears IdISBa, Illes Balears 07122, Spain; [Villalonga, Ruth] Univ Illes Balears, Dept Quim, Illes Balears 07122, Spain; [Fernandez de Mattos, Silvia] Univ Illes Balears, Dept Biol Fonamental, Illes Balears 07122, Spain; [Soriano, Concepcion; Llinares, Jose] Univ Valencia, Dept Quim Organ, E-46100 Valencia, Spain in 2020.0, Cited 79.0. The Name is 3-Pyridinecarboxaldehyde. Through research, I have a further understanding and discovery of 500-22-1. Category: pyridine-derivatives

In vitro viability assays against a representative panel of human cancer cell lines revealed that polyamines L1a and L5a displayed remarkable activity with IC50 values in the micromolar range. Preliminary research indicated that both compounds promoted G1 cell cycle arrest followed by cellular senescence and apoptosis. The induction of apoptotic cell death involved loss of mitochondrial outer membrane permeability and activation of caspases 3/7. Interestingly, L1a and L5a failed to activate cellular DNA damage response. The high intracellular zinc-chelating capacity of both compounds, deduced from the metal specific Zinquin assay and ZnL2+ stability constant values in solution, strongly supports their cytotoxicity. These data along with quantum mechanical studies have enabled to establish a precise structure-activity relationship. Moreover, L1a and L5a showed appropriate drug-likeness by in silico methods. Based on these promising results, L1a and L5a should be considered a new class of zinc-chelating anticancer agents that deserves further development.

Category: pyridine-derivatives. Bye, fridends, I hope you can learn more about C6H5NO, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

In 2020.0 RUSS CHEM B+ published article about HYDRAZONES in [Gorodnicheva, N. V.; Vasil’eva, O. S.; Ostroglyadov, E. S.; Baichurin, R. I.; Makarenko, S. V.] Herzen State Pedag Univ Russia, 48 Nab R Moiki, St Petersburg 191186, Russia; [Karamov, F. A.] Kazan Natl Res Tech Univ, 10 Ul K Marksa, Kazan 420111, Russia; [Lodochnikova, O. A.; Litvinov, I. A.] Russian Acad Sci, Kazan Sci Ctr, Fed Res Ctr, AE Arbuzov Inst Organ & Phys Chem, 8 Ul Akad Arbuzova, Kazan 420088, Russia in 2020.0, Cited 25.0. The Name is 3-Pyridinecarboxaldehyde. Through research, I have a further understanding and discovery of 500-22-1. SDS of cas: 500-22-1

4-Het(aryl)-2-pyrrolidone-3(5)-carboxylic acid hydrazides react with aromatic aldehydes, acetone, and acetophenone to give new representatives of N ‘-alkyl(hetaryl)idenecarbohydrazides of (3R*,4S*)-4-het(aryl)-2-pyrrolidone-3- and (4R*,5R*)-4-het(aryl)-2-pyrrolidone-5-carboxylic acids.

About 3-Pyridinecarboxaldehyde, If you have any questions, you can contact Gorodnicheva, NV; Vasil’eva, OS; Ostroglyadov, ES; Baichurin, RI; Makarenko, SV; Karamov, FA; Lodochnikova, OA; Litvinov, IA or concate me.. SDS of cas: 500-22-1

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

An article Microwave-assisted synthesis and antibacterial propensity of N ‘-s-benzylidene-2-propylquinoline-4-carbohydrazide and N ‘-((s-1H-pyrrol-2-yl)methylene)-2-propylquinoline-4-carbohydrazide motifs WOS:000505076000135 published article about QUINOLINE DERIVATIVES; ESCHERICHIA-COLI; BINDING; MECHANISMS; RESISTANCE; DOCKING; OVENS in [Ajani, Olayinka O.; Iyaye, King T.; Aderohunmu, Damilola V.; Olanrewaju, Ifedolapo O.] Covenant Univ, Dept Chem, CST, Km 10 Idiroko Rd,PMB 1023, Ota, Ogun State, Nigeria; [Germann, Markus W.; Bello, Babatunde L.] Georgia State Univ, Dept Chem, Atlanta, GA 30302 USA; [Olorunshola, Shade J.] Covenant Univ, Dept Biol Sci, CST, Km 10 Idiroko Rd,PMB 1023, Ota, Ogun State, Nigeria in 2020.0, Cited 53.0. The Name is 3-Pyridinecarboxaldehyde. Through research, I have a further understanding and discovery of 500-22-1. Product Details of 500-22-1

Microwave-assisted approach was utilized as green approach to access a series of 2-pro pylquinoline-4-carbohydrazide hydrazone derivatives 10a-j of aromatic and heteroaromatic aldehydes in highly encouraging yields. It involved four steps reaction which was initiated with ring opening reaction of isatin in a basified environment and subsequent cross-coupling with pentan-2-one to produce compound 7. Esterification of 7 in acid medium led to the formation of compound 8 which was reacted with hydrazine hydrate to access 9 which upon microwave-assisted condensed with aromatic and heteroaromatic aldehydes furnished the targeted compounds 10a-j. The structures of 10aj were confirmed by physico-chemical, elemental analyses and spectroscopic characterization which include UV, FT-IR, H-1 and C-13 NMR as well as DEPT-135. The targeted compounds 10a-j, alongside with gentamicin clinical standard, were investigated for their antibacterial efficacies using agar diffusion method. 2-Propyl-N’-(pyridine-3-ylmethylene) quinoline-4-carbohydrazide 10j emerged as the best antibacterial hydrazide-hydrazone with lowest MIC value of 0.39 +/- 0.02 – 1.56 +/- 0.02 mu g/ mL across all the organisms screened. (C) 2018 Production and hosting by Elsevier B.V. on behalf of King Saud University.

Welcome to talk about 500-22-1, If you have any questions, you can contact Ajani, OO; Iyaye, KT; Aderohunmu, DV; Olanrewaju, IO; Germann, MW; Olorunshola, SJ; Bello, BL or send Email.. Product Details of 500-22-1

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

Application In Synthesis of 3-Pyridinecarboxaldehyde. I found the field of Chemistry very interesting. Saw the article Probing the Effects of Heterocyclic Functionality in [(Benzene)Ru(TsDPENR)Cl] Catalysts for Asymmetric Transfer Hydrogenation published in 2019.0, Reprint Addresses Wills, M (corresponding author), Univ Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, England.; Xu, YJ (corresponding author), GoldenKeys High Tech Mat Co Ltd, Bldg B,Innovat & Entrepreneurship Pk, Guian New Area 550025, Guizhou, Peoples R China.. The CAS is 500-22-1. Through research, I have a further understanding and discovery of 3-Pyridinecarboxaldehyde.

A range of TsDPEN catalysts containing heterocyclic groups on the amine nitrogen atom were prepared and evaluated in the asymmetric transfer hydrogenation of ketones. Bidentate and tridentate ligands demonstrated a mutual exclusivity directly related to their function as catalysts. A broad series of ketones were reduced with these new catalysts, permitting the ready identification of an optimal catalyst for each substrate and revealing the subtle effects that changes to nearby donor groups can exhibit.

Bye, fridends, I hope you can learn more about C6H5NO, If you have any questions, you can browse other blog as well. See you lster.. Application In Synthesis of 3-Pyridinecarboxaldehyde

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

Authors Zhang, SY; Li, YM; Wang, JA; Hao, XY; Jin, K; Zhang, R; Duan, CY in PERGAMON-ELSEVIER SCIENCE LTD published article about ASYMMETRIC TRANSFER HYDROGENATION; NONCONVENTIONAL METHODOLOGIES; COUPLING REACTIONS; RADICAL-ADDITION; ALKYLATION; 4-ALKYL-1,4-DIHYDROPYRIDINES; TRIFLUOROMETHYLATION; ALKENYLATION; CLEAVAGE; ALCOHOLS in [Zhang, Siyu; Li, Yaming; Wang, Jiaao; Hao, Xinyu; Jin, Kun; Zhang, Rong; Duan, Chunying] Dalian Univ Technol, Sch Chem Engn, State Key Lab Fine Chem, Dalian 116024, Peoples R China in 2020.0, Cited 50.0. Quality Control of 3-Pyridinecarboxaldehyde. The Name is 3-Pyridinecarboxaldehyde. Through research, I have a further understanding and discovery of 500-22-1

A photocatalyst-free stereoselectively photo-induced strategy for the denitroalkylation of beta-nitrostyrenes using 4-alkyl substituted Hantzsch esters as the alkyl source under xenon lamp irradiation is developed. The reaction proceeds at room temperature and affords the corresponding products in moderate to excellent yields. The oxidant di-t-butyl peroxide serves as an efficient radical initiator under irradiation of a Xenon lamp, initiating alkyl radicals from the 4-alkyl substituted Hantzsch esters. (C) 2020 Elsevier Ltd. All rights reserved.

Quality Control of 3-Pyridinecarboxaldehyde. Welcome to talk about 500-22-1, If you have any questions, you can contact Zhang, SY; Li, YM; Wang, JA; Hao, XY; Jin, K; Zhang, R; Duan, CY or send Email.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

I found the field of Chemistry; Science & Technology – Other Topics very interesting. Saw the article Efficient iron catalyzed ligand-free access to acridines and acridinium ions published in 2020.0. Quality Control of 3-Pyridinecarboxaldehyde, Reprint Addresses Roy, BG (corresponding author), Sikkim Univ, Dept Chem, 6th Mile, Gangtok 737102, Sikkim, India.. The CAS is 500-22-1. Through research, I have a further understanding and discovery of 3-Pyridinecarboxaldehyde

Acridines and acridinium ions are one of the important classes of compounds in terms of their usefulness in pharmaceuticals, materials, dyes and photo-catalysis. Here we present an unconventional FeCl3-alcohol catalysed one-pot method for their synthesis directly from aldehydes, 1,3-cyclohexanedione and amines. This method efficiently merged high atom-economy and diversity of multicomponent reaction with novel iron catalyzed dehydrogenation, using aerobic oxygen as the terminal oxidant, in alcoholic solvent to produce water as the only by-product. Easy scaling up of the method has been successfully demonstrated.

Quality Control of 3-Pyridinecarboxaldehyde. Bye, fridends, I hope you can learn more about C6H5NO, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

Computed Properties of C6H5NO. Recently I am researching about TETRAHYDRO-BETA-CARBOLINES; EUDISTOMIN-U; BIOLOGICAL EVALUATION; ASSISTED SYNTHESIS; ALKALOIDS; NORHARMANE; HARMANE; DERIVATIVES; UTILITY; OXIDATIONS, Saw an article supported by the UGC-BSR, UGC-New Delhi [F.4-3/2006(BSR)]; EUPHRATES, an Erasmus Mundus Lot 13 project (Europe, India) [2013-2540/001-001]; Council of Scientific & Industrial Research (CSIR), IndiaCouncil of Scientific & Industrial Research (CSIR) – India [02(0357)/19/EMR-II]; UGCUniversity Grants Commission, India; University Grant Commission (UGC) Faculty Research Program, New Delhi, IndiaUniversity Grants Commission, India. Published in WILEY-V C H VERLAG GMBH in WEINHEIM ,Authors: Gaikwad, SV; Nadimetla, DN; Al Kobaisi, M; Devkate, M; Joshi, R; Shinde, RG; Gaikwad, MV; Nikalje, MD; Bhosale, SV; Lokhande, PD. The CAS is 500-22-1. Through research, I have a further understanding and discovery of 3-Pyridinecarboxaldehyde

A new protocol for the chemoselective aromatization of tetrahydro-beta-carboline-3-carboxylic acids to direct biomimetic one step synthesis of beta-carboline-3-carboxylic acids 2 A-L using catalytic amount of I-2 in DMSO/H+ produces very good yield. This method was also successfully extended for the aromatization of tetrahydro-beta-carboline-3-methyl esters 5 A-G as well as one-step synthesis of Marinacarbolines-D analog, respectively. Further, the mechanism and role of iodine-DMSO in aromatization has been studied by Density Functional Theory Calculation.

Computed Properties of C6H5NO. Bye, fridends, I hope you can learn more about C6H5NO, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

Recently I am researching about BIOLOGICAL-ACTIVITIES; ASSISTED SYNTHESIS; GLUTAMIC-ACID; IN-SILICO; DESIGN; COMPLEXES; DERIVATIVES; THALIDOMIDE; COPPER(II); TOXICITY, Saw an article supported by the . Category: pyridine-derivatives. Published in ELSEVIER in AMSTERDAM ,Authors: Al-Sodies, SA; Aouad, MR; Ihmaid, S; Aljuhani, A; Messali, M; Ali, I; Rezki, N. The CAS is 500-22-1. Through research, I have a further understanding and discovery of 3-Pyridinecarboxaldehyde

Novel task dicationic ionic liquids (Ts-DilLs) 6-29 were designed and synthesized, under both conventional and microwave conditions; through molecular hybridization of the appropriate bispyridines having a hydrazone linkage as spacer with some alkyl functionalized esters forming the counter cations. Beside the synthesized halogenated DilLs 6-11, fluorinated metal anions were introduced via metathesis reaction in order to create new dipyridinium ionic liquid-hydrazone hybrids 12-29. All newly synthesized DilLs were fully characterized using different spectroscopic tools such as H-1, C-13, F-19, P-31, B-11 NMR and Mass experiment. The DNA binding, anticancer and docking studies of the synthesized ionic liquids were also carried out. The DNA binding constants ranged from 4.5 x 10(4) to 7.2 x 10(4) M-1, indicating good DNA binding tendencies. The most active ionic liquids were 28 and 29 with 99.99 and 99.86% anticancer activities, respectively. The docking studies indicated DNA binding in the outer grooves of DNA. The reported ionic liquids may be used as future anticancer drugs. (C) 2020 Elsevier B.V. All rights reserved.

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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

An article Synthesis, molecular docking analysis and carbonic anhydrase I-II inhibitory evaluation of new sulfonamide derivatives WOS:000487812000049 published article about BIOLOGICAL EVALUATION; ISOZYMES I; ISOFORMS I; DRUG DESIGN; HYDRAZONE; POTENT; COMPLEXES; XII; SOLUBILITY; ANALOGS in [Saglik, Begum Nurpelin; Cevik, Ulviye Acar; Osmaniye, Derya; Levent, Serkan; Cavusoglu, Betul Kaya; Ozkay, Yusuf; Kaplancikli, Zafer Asim] Anadolu Univ, Fac Pharm, Dept Pharmaceut Chem, TR-26470 Eskisehir, Turkey; [Saglik, Begum Nurpelin; Cevik, Ulviye Acar; Osmaniye, Derya; Levent, Serkan; Ozkay, Yusuf] Anadolu Univ, Fac Pharm, Doping & Narcot Cpds Anal Lab, TR-26470 Eskisehir, Turkey; [Demir, Yeliz] Ardahan Univ, Nihat Delibalta Gole Vocat High Sch, Dept Pharm Serv, TR-75700 Ardahan, Turkey; [Ilgin, Sinem] Anadolu Univ, Fac Pharm, Dept Toxicol, TR-26470 Eskisehir, Turkey; [Koparal, Ali Savas] Anadolu Univ, Open Educ Fac, TR-26470 Eskisehir, Turkey; [Beydemir, Sukru] Anadolu Univ, Fac Pharm, Dept Biochem, TR-26470 Eskisehir, Turkey in 2019.0, Cited 60.0. Application In Synthesis of 3-Pyridinecarboxaldehyde. The Name is 3-Pyridinecarboxaldehyde. Through research, I have a further understanding and discovery of 500-22-1

New sulfonamide-hydrazone derivatives (3a-3n) were synthesized to evaluate their inhibitory effects on purified human carbonic anhydrase (hCA) I and II. The inhibition profiles of the synthesized compounds on hCA I-II isoenzyme were investigated by comparing their IC50 and K-i values. Acetazolamide (5-acetamido-1,3,4-thia-diazole-2-sulfonamide, AZA) has also been used as a standard inhibitor. The compound 3e demonstrated the best hCA I inhibitory effect with a K-i value of 0.1676 +/- 0.017 mu M. Besides, the compound 3m showed the best hCA II inhibitory effect with a K-i value of 0.2880 +/- 0.080 mu M. Cytotoxicity of the compounds 3e and 3m toward NIH/3T3 mouse embryonic fibroblast cell line was observed and the compounds were found to be non-cytotoxic. Molecular docking studies were performed to investigate the interaction types between active compounds and hCA enzymes. Pharmacokinetic profiles of compounds were assessed by theoretical ADME predictions. As a result of this study a novel and potent class of CA inhibitors were identified with a good activity potential.

Application In Synthesis of 3-Pyridinecarboxaldehyde. Welcome to talk about 500-22-1, If you have any questions, you can contact Saglik, BN; Cevik, UA; Osmaniye, D; Levent, S; Cavusoglu, BK; Demir, Y; Ilgin, S; Ozkay, Y; Koparal, AS; Beydemir, S; Kaplancikli, ZA or send Email.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem