CYP3cide, PF-04981517
99%
- Product Code: 101966
CAS:
1390637-82-7
Molecular Weight: | 456.59 g./mol | Molecular Formula: | C₂₆H₃₂N₈ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | -20℃ |
Product Description:
CYP3cide, also known as PF-04981517, is primarily used in research settings as a selective inhibitor of the cytochrome P450 3A enzyme. Its application is significant in drug metabolism studies, where it helps researchers understand the role of CYP3A in the breakdown of various pharmaceuticals. By inhibiting this enzyme, CYP3cide allows scientists to identify drug-drug interactions and assess the metabolic stability of new drug candidates. This compound is particularly valuable in early-stage drug development, where predicting and mitigating potential interactions is crucial for ensuring safety and efficacy. Additionally, CYP3cide is utilized in vitro to study the pharmacokinetics and pharmacodynamics of drugs metabolized by CYP3A, aiding in the optimization of therapeutic dosing regimens.
Product Specification:
Test | Specification |
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Appearance | Powder |
Purity (%) | 98.5-100 |
Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.001 | 10-20 days | ฿3,960.00 |
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0.005 | 10-20 days | ฿15,160.00 |
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CYP3cide, PF-04981517
CYP3cide, also known as PF-04981517, is primarily used in research settings as a selective inhibitor of the cytochrome P450 3A enzyme. Its application is significant in drug metabolism studies, where it helps researchers understand the role of CYP3A in the breakdown of various pharmaceuticals. By inhibiting this enzyme, CYP3cide allows scientists to identify drug-drug interactions and assess the metabolic stability of new drug candidates. This compound is particularly valuable in early-stage drug development, where predicting and mitigating potential interactions is crucial for ensuring safety and efficacy. Additionally, CYP3cide is utilized in vitro to study the pharmacokinetics and pharmacodynamics of drugs metabolized by CYP3A, aiding in the optimization of therapeutic dosing regimens.
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