A dopamine decarboxylase inhibitor
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Labeled Version(s)
34884Carbidopa-d3 (hydrate)
Pro-drug Form(s)
43930Foscarbidopa
Technical Support & Resources

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Carbidopa (hydrate)

Item No. 23783

Technical Information
Formal Name
(αS)-α-hydrazinyl-3,4-dihydroxy-α-methyl-benzenepropanoic acid, monohydrate
CAS Number
38821-49-7
Molecular Formula
C10H14N2O4 • H2O
Formula Weight
Purity
≥98%
A solid
DMSO: Slightly SolubleMethanol: Slightly Soluble
SMILES
OC1=C(O)C=CC(C[C@](C)(NN)C(O)=O)=C1.O
InChi Code
InChI=1S/C10H14N2O4.H2O/c1-10(12-11,9(15)16)5-6-2-3-7(13)8(14)4-6;/h2-4,12-14H,5,11H2,1H3,(H,15,16);1H2/t10-;/m0./s1
InChi Key
QTAOMKOIBXZKND-PPHPATTJSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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Certificates of Analysis & Batch Specific Data

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    Product Description

    Carbidopa is a peripherally restricted inhibitor of dopamine decarboxylase, the enzyme that converts L-DOPA (Item No. 13248) to dopamine.1 Carbidopa (100 mg/kg) pretreatment in dog increases the plasma concentration of L-DOPA by 186% and prolongs the half-life in plasma by 48% and skeletal muscle extracellular fluid by 66%.2 Carbidopa also binds to and potentiates the activity of the aryl hydrocarbon receptor (AhR), which is a ligand-dependent transcription factor that mediates the toxicity of certain xenobiotics and polyaromatic hydrocarbons.3 It inhibits the proliferation of pancreatic cancer cells in vitro and tumor growth in vivo. Formulations containing carbidopa are used in combination with L-DOPA in the treatment of Parkinson’s disease to increase the amount of dopamine in the brain and reduce peripheral side effects associated with L-DOPA administration.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Clark, W.G., Oldendorf, W.H., and Dewhurst, W.G. Blood-brain barrier to carbidopa (MK-486) and Ro 4-4602, peripheral dopa decarboxylase inhibitors. J. Pharm. Pharmacol. 25(5), 416-418 (1973).

    2. Deleu, D., Sarre, S., Ebinger, G., et alThe effect of carbidopa on the pharmacokinetics and metabolism of intravenously administered levodopa in blood plasma and skeletal muscle. Naunyn Schmiedebergs Arch. Pharmacol. 348(6), 576-581 (1993).

    3. Ogura, J., Miyauchi, S., Shimono, K., et alCarbidopa is an activator of aryl hydrocarbon receptor with potential for cancer therapy. Biochem J. 474(20), 3391-3402 (2017).