7-Hydroxyaristolochic acid A, aristolochic acid derivative (ab142644)

Overview

  • Product name

    7-Hydroxyaristolochic acid A, aristolochic acid derivative
  • Description

    Mycotoxin. Aristolochic acid derivative.
  • Biological description

    Mycotoxin. Aristolochic acid derivative (ab142618. Possible mutagenic and nephrotoxin agent as an aristolochic acid constituent. Active in vivo.
  • Purity

    > 95%
  • CAS Number

    79185-75-4
  • Chemical structure

    Chemical Structure

Properties

  • Chemical name

    8-Hydroxy-9-methoxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylic acid
  • Molecular weight

    357.27
  • Molecular formula

    C17H11NO8
  • PubChem identifier

    147113
  • Storage instructions

    Store at -20°C. Store under desiccating conditions. The product can be stored for up to 12 months.
  • Solubility overview

    Soluble in water
  • Handling

    Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

    Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

  • SMILES

    COC1=C(C2=CC(=C3C(=CC4=C(C3=C2C=C1)OCO4)C(=O)O)[N+](=O)[O-])O
  • Source

    Synthetic

  • Research areas

References

This product has been referenced in:

  • Xie BB  et al. [A new aristolochic acid derivative from Asarum himalaicum]. Yao Xue Xue Bao 46:188-92 (2011). Read more (PubMed: 21542290) »
  • Hadjiolov D  et al. Effect of diallyl sulfide on aristolochic acid-induced forestomach carcinogenesis in rats. Carcinogenesis 14:407-10 (1993). Read more (PubMed: 8453716) »
  • Lou FC  et al. [Chemical studies on Aristolochia contorta Bunge. II. The structure of aristolochic acid E]. Yao Xue Xue Bao 21:702-5 (1986). Read more (PubMed: 3577793) »

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