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PHGDH-inactive
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Catalog No. T23150Cas No. 1914971-16-6
PHGDH inactive is inactive against PHGDH and serves as a negative control for NCT-502 and NCT-503 [1].
PHGDH-inactive
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Purity: 99.83%
Catalog No. T23150Cas No. 1914971-16-6
PHGDH inactive is inactive against PHGDH and serves as a negative control for NCT-502 and NCT-503 [1].
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 5 mg | $32 | In Stock | In Stock | |
| 10 mg | $55 | In Stock | In Stock | |
| 25 mg | $119 | In Stock | In Stock | |
| 50 mg | $191 | In Stock | In Stock | |
| 100 mg | $275 | In Stock | In Stock | |
| 200 mg | $386 | In Stock | In Stock | |
| 1 mL x 10 mM (in DMSO) | $39 | In Stock | In Stock |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Batch Information
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Purity:99.83%
Appearance:Solid
Color:White
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Product Introduction
PHGDH-inactive AI Summary
PHGDH-inactive exhibits bioactivity as an inhibitor of 15-hydroxyprostaglandin dehydrogenase (HPGD) and demonstrates a potency of 30401.6 nM against ALDH1A1 (Aldehyde dehydrogenase 1 family member A1) according to PubChem BioAssay data. Additionally, it shows inhibitory effects on human liver N-terminal His6-tagged PHGDH enzyme expressed in Escherichia coli Rosetta (DE3)pLysS, with an IC50 value greater than 57000.0 nM, indicating moderate to weak inhibition. In specific assays, PHGDH-inactive has an inhibitory effect of 33.0% against PHGDH and exhibits high kinetic solubility in pH 7.4 buffer and aqueous solubility. Furthermore, the compound has a half-life of more than 0.5 hours in rat liver microsomes, suggesting potential stability in this biological environment..
Note: Summary generated by AI. Data source: ChEMBL 
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | PHGDH inactive is inactive against PHGDH and serves as a negative control for NCT-502 and NCT-503 [1]. |
| Molecular Weight | 327.45 |
| Formula | C17H21N5S |
| Cas No. | 1914971-16-6 |
| Smiles | Cc1cc(C)nc(NC(=S)N2CCN(CC2)c2ccncc2)c1 |
| Relative Density. | 1.268 g/cm3 (Predicted) |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||
| Solubility Information | DMSO: 8 mg/mL (24.43 mM), Sonication is recommended.  | |||||||||||||||||||||||||
| In Vivo Formulation | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 1 mg/mL (3.05 mM), Sonication is recommended. Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions. | |||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||
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Calculator
In Vivo Formulation Calculator (Clear solution)
Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, and a total of 10 animals are to be administered, using a formulation of 
10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.Stock Solution Preparation:
Dissolve 2 mg of the compound in 100 μL DMSO to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
Preparation of the In Vivo Formulation:
1) Add 100 μL of the DMSO stock solution to 400 μL PEG300 and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O and mix thoroughly until a homogeneous solution is obtained.
This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
Dose Conversion
You can also refer to dose conversion for different animals. More Dose Conversion
Tech Support
Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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