10 Results for "

N-oxide form

" in MedChemExpress (MCE) Product Catalog:
Products (10)

10 Results for "N-oxide form" in MCE Product Catalog:

Cat. No.: HY-Y1101B
CAS No.: 7529-22-8
Synonyms: N-Methylmorpholine N-oxide; MMNO; 4-Methylmorpholine 4-oxide
Research Areas:  

Others

4-Methylmorpholine N-oxide (N-Methylmorpholine N-Oxide; MMNO; 4-Methylmorpholine 4-oxide) is an amine oxide ligand and ozonation reagent. 4-Methylmorpholine N-oxide forms coordination complexes with lanthanum (III) nitrate and yttrium (III) nitrate via its nitroso oxygen atom. The metal-ligand bonds are dominated by electrostatic interactions with a small covalent component. 4-Methylmorpholine N-oxide is applicable in ozonation reactions for the synthesis of methyl 9-oxononanoate .
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Cat. No.: HY-169466
CAS No.: 4006-02-4
Target:  

Drug Derivative

Research Areas:  

Neurological Disease

5-Methoxy-N,N-dimethyltryptamine Nb-oxide is an indole alkaloid. 5-Methoxy-N,N-dimethyltryptamine Nb-oxide is the N-oxide form of 5-Methoxy-N,N-dimethyltryptamine (5-MeO-DMT), which is a known psychoactive substance .
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Cat. No.: HY-100644
CAS No.: 27653-68-5
Synonyms: Trimethoprim 1-N-oxide
Target:  

Drug Metabolite

Research Areas:  

Infection

Trimethoprim N-oxide (Trimethoprim 1-N-oxide) belongs to human urinary metabolites. Trimethoprim N-oxide is generated by oxidation of nitrogen atoms in the pyrimidine ring. Trimethoprim N-oxide is formed predominantly by CYP1A2 in human liver microsomes .
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Cat. No.: HY-100664
CAS No.: 43200-96-0
Synonyms: RP 29753
Research Areas:  

Neurological Disease

Zopiclone N-oxide (RP 29753) is a less active metabolite of Zopiclone. Zopiclone N-oxide is also an impurity of Eszopiclone and is formed by the oxidation of Eszopiclone .
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Cat. No.: HY-Z2493
CAS No.: 573691-09-5
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

Aripiprazole N-oxide is a metabolite of the atypical antipsychotic Aripiprazole (HY-14546). Aripiprazole N-oxide is formed from aripiprazole by the cytochrome P450 (CYP) isoforms CYP2D6 and CYP3A4.
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Cat. No.: HY-N15616
CAS No.: 72213-98-0
Parsonsine is ananalog of pyrrolizidine alkaloid that can be isolated in the N-oxide forms from adult bodies of the Apocynaceae-feeding danaine butterfly, Idea leuconoe .
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Cat. No.: HY-N16484
CAS No.: 55727-46-3
Trichodesmine N-oxide is the oxidized form of a pyrrolizidine alkaloid (PA) that can be isolated from the sunn hemp (Crotalaria juncea) teas. PAs are secondary metabolites in plants, which may exhibit toxicity and carcinogenicity .
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Cat. No.: HY-D3075
CAS No.: 2490504-23-7
Target:  

Fluorescent Dye

Research Areas:  

Others

TPE-2E N-oxide is a fluorescent probe used for hypoxia detection and tumor hypoxia imaging. Due to its active intramolecular motion, TPE-2E N-oxide shows no fluorescence in aqueous solution. In hypoxic environments, its N-oxide group undergoes two-electron reduction by CYP450 reductase and other heme protein reductases expressed under hypoxia, forming hydrophobic aggregates that trigger aggregation-induced emission through the restriction of intramolecular motion. TPE-2E N-oxide exhibits selective lipid droplet localization in cells. The absorption wavelength of TPE-2E N-oxide in dichloromethane is 313 nm; in a 99% hexane/dichloromethane mixed system, its excitation wavelength is 330 nm and emission wavelength is 460 nm. For in vitro cell imaging, excitation is performed at 405 nm, with an emission wavelength range of 430-560 nm .
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Cat. No.: HY-P82247
Synonyms: FMO3; Dimethylaniline monooxygenase [N-oxide-forming] 3; Dimethylaniline oxidase 3; FMO II; FMO form 2; Hepatic flavin-containing monooxygenase 3; FMO 3; Trimethylamine monooxygenase

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-N21955
CAS No.: 96657-94-2
Merenskine is a chlorinated 1,2-unsaturated senecionine-type pyrrolizidine alkaloid and serves as a substrate for epoxidation reactions. Merenskine forms merepoxine N-oxide upon evaporation in ammoniated solvents, while it generates merepoxine under alkaline sample preparation conditions. Merenskine exhibits a pH-dependent transfer rate in black tea infusion, and the transfer rate decreases sharply under alkaline conditions .
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