1. Others Metabolic Enzyme/Protease Autophagy
  2. Isotope-Labeled Compounds Phosphodiesterase (PDE) Autophagy
  3. Cilostazol-d4

Cilostazol-d4 is deuterium labeled Cilostazol. Cilostazol (OPC 13013) is a potent and selective inhibitor of phosphodiesterase (PDE) 3A, the isoform of PDE 3 in the cardiovascular system, with an IC50 of 0.2 μM[1][2].

For research use only. We do not sell to patients.

Cilostazol-d<sub>4</sub> Chemical Structure

Cilostazol-d4 Chemical Structure

CAS No. : 1215541-47-1

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Description

Cilostazol-d4 is deuterium labeled Cilostazol. Cilostazol (OPC 13013) is a potent and selective inhibitor of phosphodiesterase (PDE) 3A, the isoform of PDE 3 in the cardiovascular system, with an IC50 of 0.2 μM[1][2].

In Vitro

Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molecular Weight

373.49

Formula

C20H23D4N5O2

CAS No.
Unlabeled CAS
SMILES

O=C1NC2=CC=C(C=C2CC1)OCCCCC3=NN=NN3C4C([2H])([2H])CCCC4([2H])[2H]

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Room temperature in continental US; may vary elsewhere.

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Please store the product under the recommended conditions in the Certificate of Analysis.

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Product Name:
Cilostazol-d4
Cat. No.:
HY-17464S1
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