(S)-(-)-Carbidopa monohydrate, Aromatic-L-amino-acid decarboxylase inhibitor (ab142497)

Overview

  • Product name

    (S)-(-)-Carbidopa monohydrate, Aromatic-L-amino-acid decarboxylase inhibitor
  • Description

    Aromatic-L-amino-acid decarboxylase inhibitor
  • Biological description

    Aromatic-L-amino-acid decarboxylase inhibitor. Extends half-life of L-DOPA in blood plasma and skeletal muscle.
  • Purity

    > 98%
  • CAS Number

    38821-49-7
  • Chemical structure

    Chemical Structure

Properties

  • Chemical name

    (2S)-3-(3,4-Dihydroxyphenyl)-2-hydrazinyl-2-methylpropanoic acid hydrate
  • Molecular weight

    244.24
  • Molecular formula

    C10H14N2O4.H2O
  • PubChem identifier

    38101
  • Storage instructions

    Store at Room Temperature. The product can be stored for up to 12 months.
  • Solubility overview

    Soluble in ethanol to 10mM.
  • 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(CC1=CC(=C(C=C1)O)O)(C(=O)O)NN.O
  • Source

    Synthetic

  • Research areas

References

This product has been referenced in:

  • Ung RV  et al. Functional and physiological effects of treadmill training induced by buspirone, carbidopa, and L-DOPA in clenbuterol-treated paraplegic mice. Neurorehabil Neural Repair 26:385-94 (2012). Read more (PubMed: 22157146) »
  • Jenner P  et al. Receptor changes during chronic dopaminergic stimulation. J Neural Transm Suppl 27:161-75 (1988). Read more (PubMed: 2900291) »
  • Johansson P Comparative aspects of central cardiovascular control with special reference to adrenergic mechanisms. Comp Biochem Physiol C 74:239-48 (1983). Read more (PubMed: 6133681) »

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