Category: 1448-87-9

Chemistry is traditionally divided into organic and inorganic chemistry. Product Details of 1448-87-9, The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent£¬Which mentioned a new discovery about 1448-87-9

NIACIN RECEPTOR AGONISTS, COMPOSITIONS CONTAINING SUCH COMPOUNDS AND METHODS OF TREATMENT

Compounds of the formula (I): as well as pharmaceutically acceptable salts and solvates are disclosed. The compounds are useful for treating dyslipidemias, and in particular, reducing serum LDL, VLDL and triglycerides, and raising HDL levels. Pharmaceutical compositions and methods of treatment are also included.

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Quinoxaline – Wikipedia,
Quinoxaline | C8H6N482 | ChemSpider

Related Products of 1448-87-9, Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. 1448-87-9, Name is 2-Chloroquinoxaline,introducing its new discovery.

REGIOSELECTIVITY IN THE REACTION OF NITROQUINOXALINE-N-OXIDES WITH PHOSPHORYL CHLORIDE

6-nitro-, 2-methyl-6-nitro- and 2,3-dimethyl-6-nitroquinoxaline have been transformed into their N-oxides by MCPBA in chloroform; the nitro group orients the oxygen atom preferentially to nitrogen atom N1, but the N4:N1 selectivity is diminished in the methylated derivatives.Under the action of POCl3 (the Meisenheimer reaction), the N-oxides of the unmethylated compounds are transformed into chloro-nitroquinoxalines having lost the N-oxide oxygen atom.The orientation of the entering chloride ion is discussed on the basis of electronic effects induced by the N-oxide and nitro groups, and it is suggested that the last step, the elimination of “HPO2Cl2” is a concerted process.

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Quinoxaline – Wikipedia,
Quinoxaline | C8H6N646 | ChemSpider

Reference of 1448-87-9, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.1448-87-9, Name is 2-Chloroquinoxaline, molecular formula is C8H5ClN2. In a article£¬once mentioned of 1448-87-9

Discovery of orally bioavailable and novel urea agonists of the high affinity niacin receptor GPR109A

A urea class of high affinity niacin receptor agonists was discovered. Compound 1a displayed good PK, better in vivo efficacy in reducing FFA in mouse than niacin, and no vasodilation in a mouse model. Compound 1q demonstrated equal affinity to GPR109A as niacin.

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Quinoxaline – Wikipedia,
Quinoxaline | C8H6N685 | ChemSpider

In heterogeneous catalysis, the catalyst is in a different phase from the reactants. SDS of cas: 1448-87-9, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 1448-87-9, name is 2-Chloroquinoxaline. In an article£¬Which mentioned a new discovery about 1448-87-9

Quinazolines and Related Heterocyclic Compounds, and Their Therapeutic Use

Compounds that interact with the histamine H4 receptor, and which may be useful for treating or preventing disorders and conditions mediated by the histamine H4 receptor, e.g. inflammation, are of formula (I) wherein Q is CR1 or N; X is CR2 or N, provided that Q and X are not both N; Y is CR3 or N; Z is CH or N; R1, R2, R3, R4, R5 and R6 are independently H, F, Cl, Br, I, or a hydrocarbon group which optionally contains one or more heteroatoms; and R7 is a heterocyclic radical including one or more N atoms; or a pharmaceutically acceptable salt, ester or solvate thereof.

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Quinoxaline – Wikipedia,
Quinoxaline | C8H6N501 | ChemSpider

Electric Literature of 1448-87-9, Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 1448-87-9, molcular formula is C8H5ClN2, introducing its new discovery.

New three- and four-armed flexible bridging ligands for use in metallosupramolecular chemistry: syntheses and X-ray structures

Preparations are described of twelve new tritopic and tetratopic ligands by coupling of two phenolic precursors with a range of heterocyclic units. X-ray crystal structures of four representative examples revealed the conformations in the solid state with the nitrogen donor atoms separated by distances ranging from 10.9 to 18.2 A.

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Quinoxaline – Wikipedia,
Quinoxaline | C8H6N559 | ChemSpider

1448-87-9, Name is 2-Chloroquinoxaline, belongs to quinoxaline compound, is a common compound. HPLC of Formula: C8H5ClN2In an article, once mentioned the new application about 1448-87-9.

DIAZA-SPIRO[5.5]UNDECANES AS OREXIN RECEPTOR ANTAGONISTS

The invention relates to compound of the formula (I), in which the substituents are as defined in the specification; in free form or in salt form; to its preparation, to its use as medicament and to medicaments comprising it.

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Quinoxaline – Wikipedia,
Quinoxaline | C8H6N490 | ChemSpider

Reference of 1448-87-9, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.1448-87-9, Name is 2-Chloroquinoxaline, molecular formula is C8H5ClN2. In a Article£¬once mentioned of 1448-87-9

Synthesis of a family of heterocyclic ligands derived from bisphenols: new flexible bridging ligands for use in metallosupramolecular chemistry

The preparations are described of 35 new bridging ligands from five bisphenols through coupling each with seven different heterocyclic units. X-ray crystal structures of five representative examples revealed different conformations in the solid state with the terminal nitrogen donors being separated by distances ranging from 8 to 23 A.

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Quinoxaline – Wikipedia,
Quinoxaline | C8H6N560 | ChemSpider

In homogeneous catalysis, the catalyst is in the same phase as the reactant. The number of collisions between reactants and catalyst is at a maximum.In a patent, 1448-87-9, name is 2-Chloroquinoxaline, introducing its new discovery. Application In Synthesis of 2-Chloroquinoxaline

Synthesis and antimicrobial activity of some 2(1H)-quinoxalinone-6-sulfonyl derivatives

The synthesis of some quinoxalinesulfonyl derivatives is described. Two of the synthesized derivatives, 2-oxo-1,2-dihydroquinoxaline-6-sulfonyl azide (3a) and 2,3-dioxo-1,2,3,4-tetrahydroquinoxaline-6-sulfonyl azide (3b), were screened in vitro for their growth inhibitory activity against nine strains of Gram-positive and seven strains of Gram-negative bacteria, along with two fungal isolates. The two compounds showed broad spectrum (in vitro) activity against the bacterial strains. Copyright Taylor & Francis Inc.

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Quinoxaline – Wikipedia,
Quinoxaline | C8H6N648 | ChemSpider

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NICOTINAMIDE DERIVATIVES

The present invention relates to compounds formula (I) and pharmaceutically acceptable salts and solvates thereof, wherein the substituents are as defined herein, compositions containing such compounds and the uses of such compounds for the treatment of various diseases and conditions such as asthma

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Quinoxaline – Wikipedia,
Quinoxaline | C8H6N456 | ChemSpider

Electric Literature of 1448-87-9, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.1448-87-9, Name is 2-Chloroquinoxaline, molecular formula is C8H5ClN2. In a Article£¬once mentioned of 1448-87-9

Fragment based design of new H4 receptor-ligands with anti-inflammatory properties in vivo

Using a previously reported flexible alignment model we have designed, synthesized, and evaluated a series of compounds at the human histamine H 4 receptor (H4R) from which 2-(4-methyl-piperazin-l-yl)- quinoxaline (3) was identified as a new lead structure for H4R ligands. Exploration of the structure-activity relationship (SAR) of this scaffold led to the identification of 6,7-dichloro 3-(4-methylpiperazin-l-yl) quinoxalin-2(1H)-one (VUF 10214, 57) and 2-benzyl-3-(4-methyl-piperazin-l-yl) quinoxaline (VUF 10148, 20) as potent H4R ligands with nanomolar affinities. In vivo studies in the rat reveal that compound 57 has significant anti-inflammatory properties in the carrageenan-induced paw-edema model.

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Quinoxaline – Wikipedia,
Quinoxaline | C8H6N688 | ChemSpider