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Results for "

hydroxylamine

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    15
    TargetMol | Inhibitors_Agonists
  • Recombinant Protein
    1
    TargetMol | Recombinant_Protein
  • Cell Research
    5
    TargetMol | Inhibitors_Agonists
Hydroxylamine
Nitroxide
T88947803-49-8
Hydroxylamine (Nitroxide) solution is an inorganic compound used in organic synthesis and as a reducing agent
  • $50
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Hydroxylamine hydrochloride
Hydroxylammonium chloride, Hydroxylamine hydrochloride
T115875470-11-1
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.
  • $31
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N-Boc-O-tosyl hydroxylamine
T19446105838-14-0
N-Boc-O-tosyl hydroxylamine serves as a nitrogen source for the N-amination of aryl and alkyl amines.
  • $29
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Dapsone hydroxylamine
DDS-NOH
T7851732695-27-5
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].
  • $98
35 days
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O-(4-Nitrobenzyl)hydroxylamine hydrochloride
TXB-005242086-26-2
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.
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7-10 days
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O-Benzoylhydroxylamine
T7991154495-98-6
O-Benzoyl hydroxylamine exhibits properties as a dipeptidyl peptidase-IV (DPP-IV) inhibitor and demonstrates antidiabetic effects[1].
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8-10 weeks
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O-Benzylhydroxylamine (hydrochloride)
T380202687-43-6
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)
  • $178
35 days
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N-Benzylhydroxylamine hydrochloride
TYD-0128929601-98-7
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.
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7-10 days
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N,O-Dimethylhydroxylamine hydrochloride
TYD-013436638-79-5
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.
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7-10 days
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OT-551 HCl
OT-551 HCl(627085-11-4 Free base)
T28273L627085-15-8In house
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).
  • $117
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Tretazicar
NSC 115829, CB1954, 5-Aziridino-2,4-dinitrobenzamide
T679821919-05-1
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.
  • $47
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Fmoc-L-Lys(Pentynoyl-DIM)-OH
T897072408993-33-7
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.
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10-14 weeks
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Fmoc-L-Lys(N3-Aca-DIM)-OH
T898212408993-39-3
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.
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10-14 weeks
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Aminooxy-PEG2-amine hydrochloride
TCL-010632582757-03-5
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.
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10-14 weeks
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Aminooxy-PEG1-amine
TYD-020521510385-08-6
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.
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10-14 weeks
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