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TES-1025

TES-1025
TES-1025 is an effective and selective inhibitor of human α-amino-β-carboxymuconate-ε-semialdehyde decarboxylase (IC50: 13 nM).
Catalog No. T17042Cas No. 1883602-21-8
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Purity:98.81%
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TES-1025

Catalog No. T17042Cas No. 1883602-21-8

TES-1025 is an effective and selective inhibitor of human α-amino-β-carboxymuconate-ε-semialdehyde decarboxylase (IC50: 13 nM).
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
Pack SizePriceAvailabilityQuantity
5 mg$58In Stock
10 mg$79In Stock
25 mg$122In Stock
50 mg$174In Stock
100 mg$254In Stock
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Product Introduction

Bioactivity
Description
TES-1025 is an effective and selective inhibitor of human α-amino-β-carboxymuconate-ε-semialdehyde decarboxylase (IC50: 13 nM).
Targets&IC50
ACMSD (human):13±3 nM
In vitro
TES-1025 increases NAD+ levels in cellular systems[1].
In vivo
TES-1025 (0.5 mg/kg; i.v.) shows low blood clearance, with low volumes of distribution and half-lives of about 5.33 h, although the blood concentration of TES-1025 (5 mg/kg) is quantifiable for up to 8 h after oral administration. A good systemic exposure is recorded for TES-1025, with a Cmax of 2570 ng/mL reaches at 2 h. The greater oral exposure of TES-1025 is AUC0-8h of 19 200 h•ng/mL and 36 600 h•ng/mL, respectively[1].
Chemical Properties
Molecular Weight383.44
FormulaC18H13N3O3S2
Cas No.1883602-21-8
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 95 mg/mL (247.76 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.6080 mL13.0398 mL26.0797 mL130.3985 mL
5 mM0.5216 mL2.6080 mL5.2159 mL26.0797 mL
10 mM0.2608 mL1.3040 mL2.6080 mL13.0398 mL
20 mM0.1304 mL0.6520 mL1.3040 mL6.5199 mL
50 mM0.0522 mL0.2608 mL0.5216 mL2.6080 mL
100 mM0.0261 mL0.1304 mL0.2608 mL1.3040 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
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Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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