D-NMMA monoacetate, L-NMMA control compound (ab144315)

Overview

  • Product name

    D-NMMA monoacetate, L-NMMA control compound
  • Description

    Cell-permeable control compound for L-NMMA
  • Alternative names

    • NG-monomethyl-D-arginine monoacetate
  • Biological description

    Cell-permeable control compound for L-NMMA (ab120137). Inactive, shows no NOS inhibitor activity. Useful tool to investigate non-specific L-NMMA activity.
  • Purity

    > 98%
  • CAS Number

    137694-75-8
  • Chemical structure

    Chemical Structure

Properties

  • Chemical name

    (2R)-2-Amino-5-[(N'-methylcarbamimidoyl)amino]pentanoic acid acetate
  • Molecular weight

    248.28
  • Molecular formula

    C7H16N4O2.CH3CO2H
  • PubChem identifier

    2733509
  • 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

    CC(=O)O.CN=C(N)NCCC[C@H](C(=O)O)N
  • Source

    Synthetic

References

This product has been referenced in:

  • Kashiwagi S  et al. NO mediates mural cell recruitment and vessel morphogenesis in murine melanomas and tissue-engineered blood vessels. J Clin Invest 115:1816-27 (2005). Read more (PubMed: 15951843) »
  • Peterson DA  et al. The non specificity of specific nitric oxide synthase inhibitors. Biochem Biophys Res Commun 187:797-801 (1992). Read more (PubMed: 1382421) »
  • Rees DD  et al. Characterization of three inhibitors of endothelial nitric oxide synthase in vitro and in vivo. Br J Pharmacol 101:746-52 (1990). Read more (PubMed: 1706208) »

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Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES, NOT FOR USE IN HUMANS"
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