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NSC 694621 (Synonyms: NSC694621)

Catalog No. T60018 Copy Product Info
Purity: 99.7%
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NSC 694621 is a PCAF and histone acetyltransferase (HAT) inhibitor that forms a covalent bond with Cys574, the active site of PCAF, thereby irreversibly inhibiting its acetyltransferase activity, and is able to inhibit the proliferation of SK-N-SH and HCT116 cells, which has anticancer potential.

NSC 694621

Copy Product Info
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Catalog No. T60018
Synonyms NSC694621

NSC 694621 is a PCAF and histone acetyltransferase (HAT) inhibitor that forms a covalent bond with Cys574, the active site of PCAF, thereby irreversibly inhibiting its acetyltransferase activity, and is able to inhibit the proliferation of SK-N-SH and HCT116 cells, which has anticancer potential.

NSC 694621
Cas No. 104857-29-6
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Pack SizePriceUSA StockGlobal StockQuantity
2 mg$53-In Stock
5 mg$85-In Stock
10 mg$133-In Stock
25 mg$218-In Stock
50 mg$325-In Stock
100 mg$483-In Stock
200 mg$691-In Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Purity:99.7%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
NSC 694621 is a PCAF and histone acetyltransferase (HAT) inhibitor that forms a covalent bond with Cys574, the active site of PCAF, thereby irreversibly inhibiting its acetyltransferase activity, and is able to inhibit the proliferation of SK-N-SH and HCT116 cells, which has anticancer potential.
Targets&IC50
SK-N-SH neuroblastoma cells:19.2 ± 1.22 μM (GI₅₀), PCAF (HAT) H4 (2–24):1.59 μM, PCAF (HAT) H3 (1–21): 5.19 μM
In vitro
NSC 694621 inhibits PCAF HAT activity with an IC₅₀ of 5.19 μM for H3 and 1.59 μM for H4, showing stronger inhibition for H4[1]. NSC 694621 shows moderate antiproliferative effects, with a GI₅₀ of 19.2 ± 1.22 μM in SK-N-SH neuroblastoma cells. In HCT116 colorectal cancer cells, NSC 694621 inhibits growth by 29% at 25 μM[1].
SynonymsNSC694621
Chemical Properties
Molecular Weight258.3
FormulaC13H10N2O2S
Cas No.104857-29-6
SmilesO=C1C2=CC=CN=C2SN1C3=CC=C(OC)C=C3
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 1 mg/mL (3.87 mM), Sonication and heating are recommended
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.8715 mL19.3573 mL38.7147 mL193.5734 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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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:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 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 DMSOTargetMol | reagent 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 DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent 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 ddH2OTargetMol | reagent 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.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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%
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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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