Category: naphthyridines

Catalysts are substances that increase the reaction rate of a chemical reaction without being consumed in the process. 39156-41-7, Name is 4-Methoxybenzene-1,3-diamine sulfate, SMILES is NC1=CC=C(OC)C(N)=C1.O=S(O)(O)=O, belongs to naphthyridines compound. In a document, author is Gerisch, Michael, introduce the new discover, Recommanded Product: 39156-41-7.

Biotransformation of Finerenone, a Novel Nonsteroidal Mineralocorticoid Receptor Antagonist, in Dogs, Rats, and Humans, In Vivo and In Vitro

Mass balance and biotransformation of finerenone, a nonsteroidal mineralocorticoid receptor antagonist, were investigated in four healthy male volunteers following a single oral administration of 10 mg (78 mu Ci) of [C-14]finerenone and compared with data from studies in dogs and rats. The total recovery of the administered radioactivity was 101% in humans, 94.7% in dogs, and 95.2% in rats. In humans, radioactivity was mainly excreted renally (80%); in rats, it was primarily the biliary/fecal route (76%); and in dogs, excretion was more balanced. Finerenone was extensively metabolized in all species by oxidative biotransformation, with minor amounts of unchanged drug in excreta (humans: 1%; dogs, rats: <9%). In vitro studies suggested cytochrome P450 3A4 was the predominant enzyme involved in finerenone metabolism in humans. Primary metabolic transformation involved aromatization of the dihydronaphthyridine moiety of metabolite M1 as a major clearance pathway with a second oxidative pathway leading to M4. These were both prone to further oxidative biotransformation reactions. Naphthyridine metabolites (M1-M3) were the dominant metabolites identified in human plasma, with no on-target pharmacological activity. In dog plasma, finerenone and metabolite M2 constituted the major components; finerenone accounted almost exclusively for drug-related material in rat plasma. For metabolites M1-M3, axial chirality was observed, represented by two atropisomers (e.g., M1a and M1b). Analysis of plasma and excreta showed one atropisomer (a-series, >79%) of each metabolite predominated in all three species. In summary, the present study demonstrates that finerenone is cleared by oxidative biotransformation, mainly via naphthyridine derivatives.

The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 39156-41-7 is helpful to your research. Recommanded Product: 39156-41-7.

Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem

Application of 89343-06-6, Catalysts allow a reaction to proceed via a pathway that has a lower activation energy than the uncatalyzed reaction. 89343-06-6, Name is Ethynyltriisopropylsilane, SMILES is CC([Si](C(C)C)(C#C)C(C)C)C, belongs to naphthyridines compound. In a article, author is Amalia Perillo, Isabel, introduce new discover of the category.

Synthesis and spectroscopic properties of novel polyfunctionally substituted 2,6-and 2,7-naphthyridines

Series of 5,6-dihydro-8-hydroxy-5-oxo-2,6-naphthyridine-7-carboxylic acid derivatives (2,4) and the isomeric 7,8-dihydro-5-hydroxy-8-oxo-2,7-naphthyridine-6-carboxylic acid derivatives (3,5) having potential pharmacological activity were synthesized from 3,4-pyridinedicarboxylic acid derivatives. Spectroscopic data (IR, H-1- and C-13-NMR, MS) are analyzed and support the enol-lactam structure of compounds 2-5 in Solution, solid state and gas phase. Results in the different series (2.6- vs 2,7-naphthyridines and N-unsubstituted lactam vs N-methyl derivatives) are compared. and common and differential features amongst them are indicated. (C) 2009 Elsevier B.V. All rights reserved.

Application of 89343-06-6, Consequently, the presence of a catalyst will permit a system to reach equilibrium more quickly, but it has no effect on the position of the equilibrium as reflected in the value of its equilibrium constant.I hope my blog about 89343-06-6 is helpful to your research.

Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem

Synthetic Route of 5089-22-5, As an important bridge between the micro and macro material world, chemistry is one of the main methods and means for humans to understand and transform the material world. 5089-22-5, Name is 1,4-Bis(benzo[d]oxazol-2-yl)naphthalene, SMILES is C1(C2=NC3=CC=CC=C3O2)=C4C=CC=CC4=C(C5=NC6=CC=CC=C6O5)C=C1, belongs to naphthyridines compound. In a article, author is Cheng, Yu, introduce new discover of the category.

Structure-based optimization and derivatization of 2-substituted quinolone-based non-nucleoside HCV NS5B inhibitors with submicromolar cellular replicon potency

HCV NS5B polymerase is an attractive and validated target for anti-HCV therapy. Starting from our previously identified 2-aryl quinolones as novel non-nucleoside NS5B polymerase inhibitors, structure-based optimization furnished 2-alkyl-N-benzyl quinolones with improved antiviral potency by employing privileged fragment hybridization strategy. The N-(4-chlorobenzyl)-2-(methoxymethyl) quinolone derivative 5f proved to be the best compound of this series, exhibiting a selective sub-micromolar antiviral effect (EC50 = 0.4 mu M, SI = 10.8) in Huh7.5.1 cells carrying a HCV genotype 2a. Considering the undesirable pharmacokinetic property of the highly substituted quinolones, a novel chemotype of 1,6-naphthyridine-4,5-diones were evolved via scaffold hopping, affording brand new structure HCV inhibitors with compound 6h (EC50 (gt2a) = 2.5 mu M, SI = 7.2) as a promising hit. Molecular modeling studies suggest that both of 2-alkyl quinolones and 1,6-naphthyridine-4,5-diones function as HCV NS5B thumb pocket II inhibitors. (C) 2016 Elsevier Ltd. All rights reserved.

Synthetic Route of 5089-22-5, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 5089-22-5.

Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem

In an article, author is Joyce, Eamonn, once mentioned the application of 40138-16-7, Recommanded Product: (2-Formylphenyl)boronic acid, Name is (2-Formylphenyl)boronic acid, molecular formula is C7H7BO3, molecular weight is 149.9397, MDL number is MFCD00151822, category is naphthyridines. Now introduce a scientific discovery about this category.

Acetic Anhydride Generated Imidazolium Ylide in Ring Closures onto Carboxylic Acids; Part of the Synthesis of New Potential Bioreductive Antitumor Agents

Acetic anhydride behaves as a traceless activating agent allowing thermal intramolecular condensation of 2-(benzimidazol-1-ylmethyl) benzoic and nicotinic acids. Autoxidation gives benzimidazo[1,2-b]isoquinoline-6,11-diones (intermediates characterized) and benzimidazo[2,1-g]-1,7-naphthyridine-5,12-diones in a facile, one-pot transformation. The 1,4-dimethoxy analogue of the former is converted into benzimidazo[1,2-b]isoquinoline-1,4,6,11-tetrone using cerium ammonium nitrate (CAN). The 1,7-naphthyridine-5,12-dione system readily ring-opens, and an X-ray crystal structure of the methanol adduct was obtained.

If you are interested in 40138-16-7, you can contact me at any time and look forward to more communication. Recommanded Product: (2-Formylphenyl)boronic acid.

Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem

Chemistry is the experimental and theoretical study of materials on their properties at both the macroscopic and microscopic levels. 5089-22-5, Name is 1,4-Bis(benzo[d]oxazol-2-yl)naphthalene, molecular formula is C24H14N2O2. In an article, author is Dey, Swapan,once mentioned of 5089-22-5, Product Details of 5089-22-5.

Naphthyridine based fluorescent receptors for the recognition of uric acid

Naphthyridine based fluorogenic receptors (R1, R2, R3 and R4) have been synthesised for the recognition of uric acid (UA). The receptors are very useful for potential applications arising from complexation reactions as demonstrated by H-1 NMR, UV-vis and fluorescence studies. The association constants (K-a) between the receptors and UA have been reported using UV and fluorescence techniques. The minimisation energy calculations and molecular modelling studies for the host-guest assemblies have been discussed in this context.

Interested yet? Keep reading other articles of 5089-22-5, you can contact me at any time and look forward to more communication. Product Details of 5089-22-5.

Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem

Reference of 149022-15-1, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 149022-15-1, Name is 3-Methyl-2-benzothiazolinone hydrazone hydrochloride hydrate(1:1:x), SMILES is CN1/C(SC2=CC=CC=C12)=N/N.[H]Cl.[H]O[H], belongs to naphthyridines compound. In a article, author is Gavrin, LK, introduce new discover of the category.

Inhibition of Tpl2 kinase and TNF-alpha production with 1,7-naphthyridine-3-carbonitriles: Synthesis and structure-activity relationships

The synthesis and structure-activity studies of a series of 6-substituted-4-anilino-[1,7]-naphthyridine-3-carbonitriles as inhibitors of Tpl2 kinase are described. The early exploratory work described here may lead to the discovery of compounds with significant therapeutic potential for treating rheumatoid arthritis and other inflammatory diseases. (c) 2005 Elsevier Ltd. All rights reserved.

Reference of 149022-15-1, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 149022-15-1.

Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem

In an article, author is Nakamori, Masayuki, once mentioned the application of 754-05-2, HPLC of Formula: C5H12Si, Name is Trimethyl(vinyl)silane, molecular formula is C5H12Si, molecular weight is 100.2343, MDL number is MFCD00008606, category is naphthyridines. Now introduce a scientific discovery about this category.

A slipped-CAG DNA-binding small molecule induces trinucleotide-repeat contractions in vivo

In many repeat diseases, such as Huntington’s disease (HD), ongoing repeat expansions in affected tissues contribute to disease onset, progression and severity. Inducing contractions of expanded repeats by exogenous agents is not yet possible. Traditional approaches would target proteins driving repeat mutations. Here we report a compound, naphthyridine-azaquinolone (NA), that specifically binds slipped-CAG DNA intermediates of expansion mutations, a previously unsuspected target. NA efficiently induces repeat contractions in HD patient cells as well as en masse contractions in medium spiny neurons of HD mouse striatum. Contractions are specific for the expanded allele, independently of DNA replication, require transcription across the coding CTG strand and arise by blocking repair of CAG slip-outs. NA-induced contractions depend on active expansions driven by MutS beta. NA injections in HD mouse striatum reduce mutant HTT protein aggregates, a biomarker of HD pathogenesis and severity. Repeat-structure-specific DNA ligands are a novel avenue to contract expanded repeats. Naphthyridine-azaquinolone specifically binds slipped-CAG DNA intermediates, induces contractions of expanded repeats and reduces mutant HTT protein aggregates in cell and animal models of Huntington’s disease.

If you are interested in 754-05-2, you can contact me at any time and look forward to more communication. HPLC of Formula: C5H12Si.

Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem

91-76-9, Name is 2,4-Diamino-6-phenyl-1,3,5-triazine, molecular formula is C9H9N5, Recommanded Product: 91-76-9, belongs to naphthyridines compound, is a common compound. In a patnet, author is Ma, Wenpeng, once mentioned the new application about 91-76-9.

Ruthenium-Catalyzed Enantioselective Hydrogenation of 1,8-Naphthyridine Derivatives

The first asymmetric hydrogenation of 2,7-disubstituted 1,3-naphthyridines catalyzed by chiral cationic ruthenium diamine complexes has been developed. A wide range of U-naphthyridine derivatives were effectively hydro-genated to give 1,2,3,4-tetrahydro-1,8-naphthyridines with up to 99% ee and full conversions. The method provides a practical and facile approach to the preparation of valuable chiral heterocyclic building blocks and useful motifs for a new kind of P,N-ligand.

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 91-76-9 help many people in the next few years. Recommanded Product: 91-76-9.

Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 1118-61-2, Name is 3-Aminocrotononitrile, molecular formula is C4H6N2. In an article, author is Bera, Jitendra K.,once mentioned of 1118-61-2, COA of Formula: C4H6N2.

1,8-Naphthyridine Revisited: Applications in Dimetal Chemistry

The diverse applications of functionalized 1,8-naphthyridine (NP) ligands is the focus of this microreview. Simpler synthetic routes and the pliant nature of NP-R steered us towards their utilization in dimetal chemistry, The ongoing research on NP chemistry in our laboratory is highlighted. The topics include the comprehensive study of the ligand disposition around the quadruply bonded Mo-2 core, modulation of the metal-metal distance by axial donors in paddlewheel complexes, facile cyclometalation and C-C bond formation at axial sites of the diruthenium(I) core, building metallosupramolecular architectures, and the formation of novel unsupported iridium(II) climer aided by redox-active NP-R ligands. (C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)

Interested yet? Keep reading other articles of 1118-61-2, you can contact me at any time and look forward to more communication. COA of Formula: C4H6N2.

Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem

286961-14-6, Name is tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate, molecular formula is C16H28BNO4, Quality Control of tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate, belongs to naphthyridines compound, is a common compound. In a patnet, author is Wang, Xiang-Shan, once mentioned the new application about 286961-14-6.

Efficient Method for the Synthesis of Pyranoquinoline, Thiopyranoquinoline, Thienoquinoline, and Naphtho[2,7]naphthyridine Derivatives Catalyzed by Iodine

A mild and efficient method for the synthesis of pyranoquinoline, thiopyranoquinoline, thienoquinoline, and naplitho[2,7]naphthyridine derivatives via three-component reaction of aromatic aldehyde, naphthalen-2-amine, and heterocycloketones, including tetrahydropyran-4-one. tetrahydrothiopyran-4-one, pyridinone, and thiophenone, is described using iodine as catalyst. The features of this procedure are mild reaction conditions, good to high yields, and operational simplicity.

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 286961-14-6 help many people in the next few years. Quality Control of tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate.

Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem