2. Membrane Transporter/Ion Channel
  3. Ferroportin
  4. Pyrimidinone 8

Pyrimidinone 8 is a reversible linear non-competitive inhibitor of divalent metal transporter 1 (DMT1), with a Ki of 20 μM (hDMT1). Pyrimidinone 8 does not affect hDMT1 cell surface expression and shows no dependence with the extracellular pH. Pyrimidinone 8 can inhibit hDMT1-mediated iron uptake, with an IC50 of 13.8 μM.

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Pyrimidinone 8

Pyrimidinone 8 Chemical Structure

CAS No. : 65004-42-4

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Pyrimidinone 8 Related Antibodies

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Description

Pyrimidinone 8 is a reversible linear non-competitive inhibitor of divalent metal transporter 1 (DMT1), with a Ki of 20 μM (hDMT1). Pyrimidinone 8 does not affect hDMT1 cell surface expression and shows no dependence with the extracellular pH. Pyrimidinone 8 can inhibit hDMT1-mediated iron uptake, with an IC50 of 13.8 μM[1].

Cellular Effect
Cell Line Type Value Description References
Vero IC50
325 μM
Compound: 11
Cytotoxicity against African green monkey Vero cells assessed as reduction in cell viability by MTT assay
Cytotoxicity against African green monkey Vero cells assessed as reduction in cell viability by MTT assay
[PMID: 33395287]
Molecular Weight

204.23

Formula

C10H12N4O
CAS No.
Appearance

Solid

Color

White to off-white

SMILES

O=C1N=C(N2N=C(C)C=C2C)NC(C)=C1
Shipping

Room temperature in continental US; may vary elsewhere.
Storage
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
Solvent & Solubility
In Vitro: 

DMSO : 100 mg/mL (489.64 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 4.8964 mL 24.4822 mL 48.9644 mL
5 mM 0.9793 mL 4.8964 mL 9.7929 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

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

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

This equation is commonly abbreviated as: C1V1 = C2V2

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In Vivo Dissolution Calculator
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Calculation results:
Working solution concentration: mg/mL
Purity & Documentation
References

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 4.8964 mL 24.4822 mL 48.9644 mL 122.4110 mL
5 mM 0.9793 mL 4.8964 mL 9.7929 mL 24.4822 mL
10 mM 0.4896 mL 2.4482 mL 4.8964 mL 12.2411 mL
15 mM 0.3264 mL 1.6321 mL 3.2643 mL 8.1607 mL
20 mM 0.2448 mL 1.2241 mL 2.4482 mL 6.1206 mL
25 mM 0.1959 mL 0.9793 mL 1.9586 mL 4.8964 mL
30 mM 0.1632 mL 0.8161 mL 1.6321 mL 4.0804 mL
40 mM 0.1224 mL 0.6121 mL 1.2241 mL 3.0603 mL
50 mM 0.0979 mL 0.4896 mL 0.9793 mL 2.4482 mL
60 mM 0.0816 mL 0.4080 mL 0.8161 mL 2.0402 mL
80 mM 0.0612 mL 0.3060 mL 0.6121 mL 1.5301 mL
100 mM 0.0490 mL 0.2448 mL 0.4896 mL 1.2241 mL
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Pyrimidinone 8 Related Classifications

Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

Pyrimidinone 865004-42-4Pyrimidinone8Pyrimidinone-8FerroportinIron-regulated Transporter 1HEK293Inhibitorinhibitorinhibit

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