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Cat. No.: HY-W745111

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S-Benzoylcaptopril-d₃

Name: S-Benzoylcaptopril-d3
Brand: MedChemExpress
SKU: HY-W745111
Availability: PreOrder

1 Cited Publications

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Based on 1 publication(s) in Google Scholar

S-Benzoylcaptopril-d₃ is the deuterium labeled S-Benzoylcaptopril (HY-137171).

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

Formula: C₁₆H₁₆D₃NO₄S
Molecular Weight:324.41

Storage:

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

Data Sheet (241 KB)

S-Benzoylcaptopril-d₃ Chemical Structure

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Top Publications Citing

Use of MCE Products

Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biological Activity
- Description
- Cellular Effect
- In Vitro
- Application
Chemical Information
Publications (1)
Purity & Documentation
Calculators
Help & FAQs
Classifications
Bioz

Biological Activity

Description

S-Benzoylcaptopril-d₃ is the deuterium labeled S-Benzoylcaptopril (HY-137171).

Cellular Effect

Cell Line	Type	Value	Description	References
Astrocyte	EC₅₀	1.182 μM Compound: 7	Antiproliferative activity against mouse astrocyte cells by MTT assay Antiproliferative activity against mouse astrocyte cells by MTT assay	[PMID: 17417631]
HEK293	IC₅₀	89.5 μM Compound: flupenthixol	Inhibition of 4-(4-(dimethylamino)styryl)-N-methylpyridinium uptake at human OCT1 expressed in HEK293 cells by confocal microscopy Inhibition of 4-(4-(dimethylamino)styryl)-N-methylpyridinium uptake at human OCT1 expressed in HEK293 cells by confocal microscopy	[PMID: 18788725]
Medulloblastoma cell	EC₅₀	0.187 μM Compound: 7	Antiproliferative activity against mouse medulloblastoma cells harboring heterozygous ptch1 gene by MTT assay Antiproliferative activity against mouse medulloblastoma cells harboring heterozygous ptch1 gene by MTT assay	[PMID: 17417631]
Vero C1008	IC₅₀	>2.0 × 10⁵ M Compound: COVC-1215041578	Antiviral activity determined as inhibition of SARS-CoV-2 induced cytotoxicity of VERO-6 cells at 10 uM after 48 hours exposure to 0.01 MOI SARS CoV-2 virus by high content imaging Antiviral activity determined as inhibition of SARS-CoV-2 induced cytotoxicity of VERO-6 cells at 10 uM after 48 hours exposure to 0.01 MOI SARS CoV-2 virus by high content imaging	10.6019/CHEMBL4651402

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.

Application

1. This compound can be used as a tracer
2. This compound can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.

Chemical Information

Unlabeled Cas 75107-57-2
Molecular Weight 324.41
Formula C₁₆H₁₆D₃NO₄S
SMILES

O=C(SC[C@@H](C)C(N1[C@]([2H])(C(O)=O)CCC1([2H])[2H])=O)C2=CC=CC=C2
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

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