2468639-37-2

Pimonidazole-d<sub>10</sub> Chemical Structure
2468639-37-2

Chemical Structure

Pimonidazole-d10

  • CAS No.: 2468639-37-2
  • Formula:C11H8D10N4O3
  • Molecular Weight:264.35

IUPAC Name: 1-(2-nitro-1H-imidazol-1-yl)-3-(piperidin-1-yl-d10)propan-2-ol

InChIKey: WVWOOAYQYLJEFD-RCNOUUCRSA-N

SMILES: OC(CN1C=CN=C1[N+]([O-])=O)CN2C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])C2([2H])[2H]

Biological Activity: Pimonidazole-d10 is the deuterium labeled Pimonidazole. Pimonidazole is a novel hypoxia marker for complementary study of tumor hypoxia and cell proliferation in tumor[1]. Pimonidazole accumulates in hypoxic cells via covalent binding with macromolecules or by forming reductive metabolites after reduction of its nitro group, it can be used for qualitative and quantitative assessment of tumor hypoxia [2].

Cat. No. Product Name Purity Description Pricing
HY-105129AS
Pimonidazole-d10 Pimonidazole-d10 is the deuterium labeled Pimonidazole. Pimonidazole is a novel hypoxia marker for complementary study of tumor hypoxia and cell proliferation in tumor. Pimonidazole accumulates in hypoxic cells via covalent binding with macromolecules or by forming reductive metabolites after reduction of its nitro group, it can be used for qualitative and quantitative assessment of tumor hypoxia .
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HY-105129AR
Pimonidazole (Standard) ≥98% Pimonidazole (Standard) is the analytical standard of Pimonidazole. This product is intended for research and analytical applications. Pimonidazole is a novel hypoxia marker for complementary study of tumor hypoxia and cell proliferation in tumor. Pimonidazole accumulates in hypoxic cells via covalent binding with macromolecules or by forming reductive metabolites after reduction of its nitro group, it can be used for qualitative and quantitative assessment of tumor hypoxia .
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HY-105129A
Pimonidazole 99.32% Pimonidazole is a novel hypoxia marker for complementary study of tumor hypoxia and cell proliferation in tumor. Pimonidazole accumulates in hypoxic cells via covalent binding with macromolecules or by forming reductive metabolites after reduction of its nitro group, it can be used for qualitative and quantitative assessment of tumor hypoxia .
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