hydroxylamine

Hydroxylamine (Nitroxide) solution is an inorganic compound used in organic synthesis and as a reducing agent

(Nz)-n-(6-fluoro-2,3-dihydrothiochromen-4-ylidene)hydroxylamine ,with CAS No. 50596-11-7, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. (Nz)-n-(6-fluoro-2,3-dihydrothiochromen-4-ylidene)hydroxylamine provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

Dapsone hydroxylamine (DDS-NOH) promotes methemoglobinemia, impedes catalase (CAT) activity, and suppresses the generation of reactive oxygen species, while also exhibiting anti-inflammatory properties [1].

Hydroxylamine hydrochloride(Hydroxylammonium chloride) is a selective and potent monoamine oxidase (MAO) inhibitor with inhibitory effects on platelet aggregation.Hydroxylamine hydrochloride is an intermediate in organic synthesis and can be used to synthesize other active compounds.

N-Boc-O-tosyl hydroxylamine serves as a nitrogen source for the N-amination of aryl and alkyl amines.

Hydroxylamine-D3 hydrochloride is the deuterated form of Hydroxylamine hydrochloride, which serves as a selective monoamine oxidase (MAO) inhibitor and can be used to prevent platelet aggregation. Additionally, Hydroxylamine hydrochloride (T11587) acts as an intermediate in organic synthesis.

O-(4-Nitrobenzyl)hydroxylamine hydrochloride is a biochemical assay reagent used in the synthesis of N-(4-nitrobenzyloxy) amino acids, which serve as specific substrates for the preparation of N-hydroxy peptide.

CB1954(Tretazicar (NSC-115829)), an anticancer prodrug, is activated by NAD(P)H quinone oxidoreductase 2. It is converted in the presence of the enzyme NQO2 and co-substrate caricotamide ( EP-0152R) (EP) into a potent cytotoxic bifunctional alkylating agent.

O-benzylhydroxylamine ,with CAS No. 622-33-3, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. O-benzylhydroxylamine provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

o-Diphenylphosphinylhydroxylamine ,with CAS No. 72804-96-7, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. o-Diphenylphosphinylhydroxylamine provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

O-Benzoyl hydroxylamine exhibits properties as a dipeptidyl peptidase-IV (DPP-IV) inhibitor and demonstrates antidiabetic effects[1].

O-Benzylhydroxylamine is a building block.1,2It has been used in the synthesis of β-lactam inhibitor precursors and fluoroquinolone derivatives with antibiotic activity. 1.Bellettini, J.R., and Miller, M.J.A short synthesis of an important precursor to a new class of bicyclic β-lactamase inhibitorsTetrahedron Lett.38(2)167-168(1997) 2.Asadipour, A., Moshafi, M.H., Khosravani, L., et al.N-substituted piperazinyl sarafloxacin derivatives: synthesis and in vitro antibacterial evaluationDaru.26(2)199-207(2018)

N-Benzylhydroxylamine hydrochloride is a biochemical reagent that can be used as a biomaterial for life science related research and as a sulfonylation reagent for organic synthesis and drug discovery.

N,O-Dimethylhydroxylamine hydrochloride is a biochemical reagent that can be used as a biomaterial for life science related research and as a sulfonylation reagent for organic synthesis and drug discovery.

OT-551 HCl is an NF-Κb inhibitor, a disubstituted hydroxylamine with antioxidant properties can be used for the treatment of cataracts and age-related macular degeneration and geographic atrophy (GA).

DBNBS is a free radical spin trapping agent. It rapidly reacts with the Cys-34 residue in BSA, forming a hydroxylamine. Additionally, DBNBS captures protein-centered radicals generated from the porphyrin photosensitization of BSA.

Fmoc-L-Lys(Pentynoyl-DIM)-OH is a click chemistry reagent containing an azide group. Serving as a building block in Solid Phase Peptide Synthesis (SPPS), it is utilized in the helping hand strategy for purifying highly insoluble peptides. The solubilizing residue is attached to the lysine side chain through click chemistry. The solubilization tag can be removed with a 1M solution of hydrazine or hydroxylamine.

Fmoc-L-Lys(N3-Aca-DIM)-OH is a click chemistry reagent featuring an azide group. This SPPS building block is utilized in the helper strategy for purifying highly insoluble peptides. The solubilizing residue is attached to the lysine side chain through click chemistry. The solubility tag can be removed using a 1M solution of hydrazine or hydroxylamine.

Aminooxy-PEG2-amine hydrochloride (compound L3) is a crosslinking agent. The aminooxy group facilitates bioconjugation, reacting with aldehydes to form oxime bonds, and in the presence of a reducing agent, forming hydroxylamine bonds. The amine group can react with carboxylic acids, activated NHS esters, and carbonyls (ketones, aldehydes). Aminooxy compounds possess high reactivity and sensitivity; thus, they are unsuitable for long-term storage.

Aminooxy-PEG1-amine is a chemical reagent containing an aminooxy group and a primary amine. The aminooxy group can react with aldehydes to form oxime bonds, and with reductive agents, it can create hydroxylamine bonds. The amine group can interact with activated NHS esters or carboxylic acids in the presence of the coupling agent EDC. Compounds with aminooxy groups are highly reactive and sensitive, and should not be stored for long periods.