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Results for "

hydroxylamine

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    10
    TargetMol | Inhibitors_Agonists
  • Recombinant Protein
    1
    TargetMol | Recombinant_Protein
Hydroxylamine
Nitroxide
T88947803-49-8
Hydroxylamine (Nitroxide) solution is an inorganic compound used in organic synthesis and as a reducing agent
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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].
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8-10 weeks
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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.
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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)
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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).
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TargetMol | Inhibitor Sale
Hydroxyamine hydrochloride
Hydroxylammonium chloride, Hydroxylamine hydrochloride
T115875470-11-1
Hydroxyamine hydrochloride(Hydroxylammonium chloride) is a selective and potent monoamine oxidase (MAO) inhibitor with inhibitory effects on platelet aggregation.Hydroxyamine hydrochloridee is an intermediate in organic synthesis and can be used to synthesize other active compounds.
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7-10 days
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Tretazicar
5-Aziridino-2,4-dinitrobenzamide, CB1954, NSC 115829
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.
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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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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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