1. Others Metabolic Enzyme/Protease
  2. Drug Metabolite Isotope-Labeled Compounds
  3. N-Deschlorobenzoyl indomethacin-d3

N-Deschlorobenzoyl indomethacin-d3 is the deuterium labeled N-Deschlorobenzoyl indomethacin (HY-W008567). N-Deschlorobenzoyl indomethacin (Compound 18), the primary metabolite of indomethacin (HY-14397), lacks the N-p-chlorobenzoyl group in its structure. Consequently, N-Deschlorobenzoyl indomethacin loses inhibitory activity against AKR1C2 and AKR1C3 (AKR1C2 IC50 =100 μM, AKR1C3 IC50 >100 μM), exhibiting no selectivity.

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N-Deschlorobenzoyl indomethacin-d<sub>3</sub> Chemical Structure

N-Deschlorobenzoyl indomethacin-d3 Chemical Structure

CAS No. : 3029090-15-8

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Description

N-Deschlorobenzoyl indomethacin-d3 is the deuterium labeled N-Deschlorobenzoyl indomethacin (HY-W008567). N-Deschlorobenzoyl indomethacin (Compound 18), the primary metabolite of indomethacin (HY-14397), lacks the N-p-chlorobenzoyl group in its structure. Consequently, N-Deschlorobenzoyl indomethacin loses inhibitory activity against AKR1C2 and AKR1C3 (AKR1C2 IC50 =100 μM, AKR1C3 IC50 >100 μM), exhibiting no selectivity[1].

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

222.26

Formula

C12H10D3NO3

CAS No.
Unlabeled CAS
SMILES

CC(NC1=C2C=C(OC([2H])([2H])[2H])C=C1)=C2CC(O)=O

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

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Product Name:
N-Deschlorobenzoyl indomethacin-d3
Cat. No.:
HY-W706737
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