2. Immunology/Inflammation Metabolic Enzyme/Protease Cytoskeleton
  3. Aryl Hydrocarbon Receptor Cytochrome P450 Collagen
  4. 1-Hydroxypyrene

1-Hydroxypyrene, a biomarker of exposure to polycyclic aromatic hydrocarbons (PAHs), is analyzed in urine samples. 1-Hydroxypyrene is the major biomarker of exposure to pyrenes. 1-Hydroxypyrene is the orally active agonist for aryl hydrocarbon receptor (AhR) and can lead to renal fibrosis.

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1-Hydroxypyrene Chemical Structure

1-Hydroxypyrene Chemical Structure

CAS No. : 5315-79-7

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Based on 1 publication(s) in Google Scholar

Other Forms of 1-Hydroxypyrene:

Top Publications Citing Use of Products

View All Cytochrome P450 Isoform Specific Products:

View All Isoforms
CYP1 CYP2 CYP3 CYP4 CYP11 CYP17 Aromatase/CYP19A1 CYP26 CYP51 CYP1A2 CYP2D6 CYP2C9 CYP2C19 CYP3A4 CYP17A1

  • Biological Activity

  • Purity & Documentation

  • References

  • Customer Review

Description

1-Hydroxypyrene, a biomarker of exposure to polycyclic aromatic hydrocarbons (PAHs), is analyzed in urine samples. 1-Hydroxypyrene is the major biomarker of exposure to pyrenes. 1-Hydroxypyrene is the orally active agonist for aryl hydrocarbon receptor (AhR) and can lead to renal fibrosis[1][2].

IC50 & Target

Human Endogenous Metabolite

 

In Vitro

1-Hydroxypyrene (10 nM, 12-36 h) inhibits the cell viability of HK-2, increases the expression of AhR, Cyp1a1/Cyp1a2/Cyp1b1, collagen I, α-smooth muscle actin (α-SMA), and fibronectin, maintains the expression of E-cadherin, induces epithelial-mesenchymal transition (EMT) in cell HK-2[2].

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

Western Blot Analysis[2]

Cell Line: HK-2
Concentration: 10 nM
Incubation Time: 12 h
Result: Increased the mRNA expression of collagen I, α-SMA and fibronectin.

Real Time qPCR[2]

Cell Line: HK-2
Concentration: 10 nM
Incubation Time: 12 h
Result: Upregulated the mRNA expression of AhR, Cyp1a1, Cyp1a2, and Cyp1b1.
In Vivo

1-Hydroxypyrene (250 mg/kg, po, once daily for 4-12 weeks) increases the serum creatinine and urea levels, causing kidney injury and fibrosis in mouse models[2].

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

Animal Model: C57BL/6 mouse models[2]
Dosage: 250 mg/kg
Administration: po, once daily for 4-12 weeks
Result: Increased the serum creatinine and urea levels, caused kidney injury and fibrosis.
Molecular Weight

218.25

Formula

C16H10O
CAS No.
Appearance

Solid

Color

Light yellow to green yellow

SMILES

OC1=C(C2=C34)C=CC4=CC=CC3=CC=C2C=C1
Structure Classification
Initial Source
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 : 50 mg/mL (229.10 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 4.5819 mL 22.9095 mL 45.8190 mL
5 mM 0.9164 mL 4.5819 mL 9.1638 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.

  • Molarity Calculator

  • Dilution Calculator

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

Mass
=
Concentration
×
Volume
×
Molecular Weight *

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

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start)

C1

×
Volume (start)

V1

=
Concentration (final)

C2

×
Volume (final)

V2

In Vivo:

Select the appropriate dissolution method based on your experimental animal and administration route.

For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for in vivo experiments, it is recommended to prepare freshly and use it on the same day.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

  • Protocol 1

    Add each solvent one by one:  10% DMSO    40% PEG300    5% Tween-80    45% Saline

    Solubility: ≥ 2.5 mg/mL (11.45 mM); Clear solution

    This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.

    Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
  • Protocol 2

    Add each solvent one by one:  10% DMSO    90% (20% SBE-β-CD in Saline)

    Solubility: ≥ 2.5 mg/mL (11.45 mM); Clear solution

    This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.

    Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:

Dosage

mg/kg

Animal weight
(per animal)

g

Dosing volume
(per animal)

μL

Number of animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
%
DMSO +
% 
+
%
Tween-80 +
%
Saline
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
The co-solvents required include: DMSO, PEG300/PEG400, Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Purity & Documentation

Purity: 99.84%

Data Sheet (312 KB) SDS (393 KB)

COA (257 KB) HNMR (117 KB) RP-HPLC (189 KB)

Handling Instructions (2659 KB)
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 4.5819 mL 22.9095 mL 45.8190 mL 114.5475 mL
5 mM 0.9164 mL 4.5819 mL 9.1638 mL 22.9095 mL
10 mM 0.4582 mL 2.2910 mL 4.5819 mL 11.4548 mL
15 mM 0.3055 mL 1.5273 mL 3.0546 mL 7.6365 mL
20 mM 0.2291 mL 1.1455 mL 2.2910 mL 5.7274 mL
25 mM 0.1833 mL 0.9164 mL 1.8328 mL 4.5819 mL
30 mM 0.1527 mL 0.7637 mL 1.5273 mL 3.8183 mL
40 mM 0.1145 mL 0.5727 mL 1.1455 mL 2.8637 mL
50 mM 0.0916 mL 0.4582 mL 0.9164 mL 2.2910 mL
60 mM 0.0764 mL 0.3818 mL 0.7637 mL 1.9091 mL
80 mM 0.0573 mL 0.2864 mL 0.5727 mL 1.4318 mL
100 mM 0.0458 mL 0.2291 mL 0.4582 mL 1.1455 mL
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1-Hydroxypyrene Related Classifications

Keywords:

1-Hydroxypyrene5315-79-7Aryl Hydrocarbon ReceptorCytochrome P450CollagenAhRCYPspolycyclicaromatichydrocarbonsPAHsbiomarkerpyrenesInhibitorinhibitorinhibit

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