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Cat. No.: HY-122163

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MK-3901

MK-3901 is a selective P2X3 receptor antagonist with an IC₅₀ of 24 nM. MK-3901 inhibits UGT1A1 (with an IC₅₀ of 1 μM) and CYP2C9 (with an IC₅₀ of 5.7 μM). MK-3901 activates PXR. MK-3901 induces hyperbilirubinemia. MK-3901 can be used for the research of inflammatory pain.

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CAS No.: 1149750-69-5
화학식: C₂₈H₂₄FN₅O₂
분자량:481.53

보관:

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

MK-3901 Chemical Structure

CAS No.: 1149750-69-5

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Use of MCE Products

Fluorescent Dye

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

Biological Activity
- 제품 설명
- IC₅₀ & Target
- In Vitro
- In Vivo
Chemical Information
순도&문서
References
Calculators
Help & FAQs
Classifications
Bioz

Biological Activity

제품 설명

IC₅₀ & Target^[1]

P2X3 Receptor

24 nM (IC₅₀)

CYP2C9

5.7 μM (IC₅₀)

UGT1A1

1 μM (IC₅₀)

All P2X Receptor Isoforms :

All Cytochrome P450 Isoforms :

In Vitro

MK-3901 potently antagonizes the P2X3 receptor in a cell-based patch clamp electrophysiology assay with an IC₅₀ of 24 nM^[1].
MK-3901 inhibits UGT1A1 enzyme activity in a cell-free biochemical assay with an IC₅₀ of 1 μM^[1].
MK-3901 inhibits CYP2C9 enzyme activity in a human liver microsome-based cell-free biochemical assay with an IC₅₀ of 5.7 μM^[1].
MK-3901 (10 μM) activates the pregnane X receptor (PXR) by 47%^[1].

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

In Vivo

MK-3901 is demonstrated to induce hyperbilirubinemia in multiple species in preclinical studies^[1].

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

Chemical Information

CAS No. 1149750-69-5
분자량 481.53
화학식 C₂₈H₂₄FN₅O₂
SMILES

C(N[C@H](C)C1=CC=C(F)C=N1)(=O)C2=CC(=CC(=C2)C3=CC=C(C)C=N3)C=4C[C@H](ON4)C5=CC=CC=N5
선적

Room temperature in continental US; may vary elsewhere.
보관

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

순도&문서

Handling Instructions (2659 KB)

References

[1]. Ginnetti AT, et al. Identification of second-generation P2X3 antagonists for treatment of pain. Bioorg Med Chem Lett. 2018;28(8):1392-1396. [Content Brief]

Calculators

몰농도 계산기

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Concentration Concentration

Volume Volume

Molecular Weight Molecular Weight

농도 희석 계산기

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

Concentration _(start) Concentration _(start)

Volume _(start) Volume _(start)

Concentration _(final) Concentration _(final)

Volume _(final) Volume _(final)

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

MOQ

Minimum order quantity

100 mg

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Amount: USD 0.00

Biological Activity
- 제품 설명
- IC₅₀ & Target
- In Vitro
- In Vivo
Chemical Information
순도&문서
References

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MK-3901

All P2X Receptor Isoforms

All Cytochrome P450 Isoforms

Biological Activity

Chemical Information

순도&문서

References

Calculators

Help & FAQs

MK-3901 Related Classifications

HY-122163 Related Classifications