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MK-0873

Catalog No. T33422   CAS 500355-52-2
Synonyms: MK 0873, MK0873

MK-0873 is a novel and potent selective phosphodiesterase 4 (PDE4) inhibitor.

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MK-0873 Chemical Structure
MK-0873, CAS 500355-52-2
Pack Size Availability Price/USD Quantity
1 mg In stock $ 146.00
5 mg In stock $ 350.00
10 mg In stock $ 530.00
25 mg In stock $ 859.00
50 mg In stock $ 1,180.00
100 mg In stock $ 1,590.00
500 mg In stock $ 3,190.00
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Purity: 99.29%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description MK-0873 is a novel and potent selective phosphodiesterase 4 (PDE4) inhibitor.
In vitro Eight healthy, non-smoking male subjects participated in this randomized, open-label, 2-period, cross-over study. In one period subjects received an oral dose of 2.5mg MK-0873 for 6 days co-administered with a single oral dose of 250 mg theophylline on day 5. The other period consisted of a single dose of 250 mg of theophylline on day 1. In each period, blood samples were collected at predefined time points. In this study, in a limited number of subjects, co-administration of oral MK-0873 did not affect the pharmacokinetics, safety, and tolerability of oral theophylline in non-smoking healthy male subjects.[3]
Synonyms MK 0873, MK0873
Molecular Weight 422.44
Formula C25H18N4O3
CAS No. 500355-52-2

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 1mg/ml, Sonication is recommended.

TargetMolReferences and Literature

1. Mitra A, et al. Use of minipig skin biopsy model as an innovative tool to design topical formulation to achieve desired pharmacokinetics in humans. J Pharm Sci. 2015 May;104(5):1701-8. 2. Guay D, et al. Optimization and structure-activity relationship of a series of 1-phenyl-1,8-naphthyridin-4-one-3-carboxamides: identification of MK-0873, a potent and effective PDE4 inhibitor. Bioorg Med Chem Lett. 2008 Oct 15;18(20):5554-8. 3. Boot JD, et al. MK-0873, a PDE4 inhibitor, does not influence the pharmacokinetics of theophylline in healthy male volunteers. Pulm Pharmacol Ther. 2008;21(3):573-7.

Related compound libraries

This product is contained In the following compound libraries:
Drug Repurposing Compound Library Inhibitor Library Bioactive Compound Library Bioactive Compounds Library Max Clinical Compound Library

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Keywords

MK-0873 500355-52-2 Metabolism PDE MK 0873 MK0873 inhibitor inhibit

 

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