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TH5487 

Cat. No.: HY-125276 Purity: 98.10%
Handling Instructions

TH5487 is a potent 8-oxoguanine DNA glycosylase 1 (OGG1) inhibitor with an IC50 of 342 nM. TH5487 stops OGG1 from recognizing its DNA substrate, inhibits DNA repair and modifies OGG1 chromatin dynamics, which results in the inhibition of proinflammatory pathway genes.

For research use only. We do not sell to patients.

TH5487 Chemical Structure

TH5487 Chemical Structure

CAS No. : 2304947-71-3

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10 mM * 1 mL in DMSO USD 140 In-stock
Estimated Time of Arrival: December 31
5 mg USD 118 In-stock
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10 mg USD 200 In-stock
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50 mg USD 700 In-stock
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100 mg USD 1300 In-stock
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Based on 1 publication(s) in Google Scholar

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Description

TH5487 is a potent 8-oxoguanine DNA glycosylase 1 (OGG1) inhibitor with an IC50 of 342 nM. TH5487 stops OGG1 from recognizing its DNA substrate, inhibits DNA repair and modifies OGG1 chromatin dynamics, which results in the inhibition of proinflammatory pathway genes[1].

In Vitro

TH5487 (5 μM; 1 hour) decreases TNFα- and LPS-induced proinflammatory gene expression to near pretreatment levels[1].
TH5487 (0-10 μM; 1 hour) perturbs binding of NF-κB to 8-oxoG–containing synthetic DNA in nuclear extracts from MLE 12 or hSAEC cells[1].

RT-PCR[1]

Cell Line: Murine airway epithelial cell line (MLE 12); Diploid human small-airway epithelial cell (hSAECs)
Concentration: 5 μM
Incubation Time: 1 hour
Result: Inhibited proinflammatory gene expression dose-dependently.

Western Blot Analysis[1]

Cell Line: Murine airway epithelial cell line (MLE 12); Diploid human small-airway epithelial cell (hSAECs)
Concentration: 2.5 μM; 5 μM; 10 μM
Incubation Time: 1 hour
Result: Decreased p50-p65 and p50-p50 expression in a dose dependent manner.
In Vivo

TH5487 (prophylactic intraperitoneally injection; 8-30 mg/kg; 1-9 hours) decreases TNFα or LPS induced the robust recruitment of neutrophils to the airways, and reduces the pulmonary neutrophil count in a time-dependent manner[1].

Animal Model: Eightweek-old female and male BALB/c mice[1]
Dosage: 8 mg/kg, 15 mg/kg, 30 mg/kg
Administration: Prophylactic intraperitoneally injection; 8-30 mg/kg; 1-9 hours
Result: InterruptedTNFα-induced ongoing inflammatory processes.
Molecular Weight

541.18

Formula

C₁₉H₁₈BrIN₄O₂

CAS No.

2304947-71-3

SMILES

O=C(N1CCC(N(C2=CC=CC(Br)=C2N3)C3=O)CC1)NC4=CC=C(I)C=C4

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 : 25 mg/mL (46.20 mM; Need ultrasonic)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 1.8478 mL 9.2391 mL 18.4781 mL
5 mM 0.3696 mL 1.8478 mL 3.6956 mL
10 mM 0.1848 mL 0.9239 mL 1.8478 mL
*Please refer to the solubility information to select the appropriate solvent.
In Vivo:
  • 1.

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

    Solubility: ≥ 2.08 mg/mL (3.84 mM); Clear solution

*All of the co-solvents are provided by MCE.
References
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Keywords:

TH5487TH 5487TH-5487OthersInhibitorinhibitorinhibit

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TH5487
Cat. No.:
HY-125276
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