1. Apoptosis Autophagy Epigenetics
  2. Apoptosis Autophagy Histone Acetyltransferase
  3. MC4033

MC4033 shows IC50s of 39.4 μM, 52.1 μM, 41 μM and 30.1 μM in HCT116, H1299, A549 and U937, respectively.
MC4033 (25, 50, 100, and 200 μM, 72 h) reduces the level of H4K16Ac in HT29 cells, suggesting its ability to inhibit KAT8 in cells.

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

MC4033 Chemical Structure

MC4033 Chemical Structure

CAS No. : 28532-21-0

Size Price Stock Quantity
1 mg USD 40 In-stock
5 mg USD 87 In-stock
10 mg USD 140 In-stock
25 mg USD 281 In-stock
50 mg USD 450 In-stock
100 mg USD 720 In-stock
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Description

MC4033 shows IC50s of 39.4 μM, 52.1 μM, 41 μM and 30.1 μM in HCT116, H1299, A549 and U937, respectively[1].
MC4033 (25, 50, 100, and 200 μM, 72 h) reduces the level of H4K16Ac in HT29 cells, suggesting its ability to inhibit KAT8 in cells[1].

IC50 & Target

12.1μM (lysine acetyltransferase 8, KAT8)[1]

In Vitro

MC4033 shows IC50s of 39.4 μM, 52.1 μM, 41 μM and 30.1 μM in HCT116, H1299, A549 and U937, respectively[1].
MC4033 (25, 50, 100, and 200 μM, 72 h) reduces the level of H4K16Ac in HT29 cells, suggesting its ability to inhibit KAT8 in cells[1].

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

Cell Proliferation Assay[1]

Cell Line: HT29, HCT116, HeLa, H1299, A549, H460, MCF7, U937, and U251 cells
Concentration: 10, 25, 50, and 100 μM
Incubation Time: 72 h
Result: Displayed dose-dependent antiproliferative effects in HCT116, H1299, A549, and U937 cell lines.
The inhibition rate of cell proliferation was 70% at 50 μM and >80% at 100 μM in U937 cells.

Cell Cycle Analysis[1]

Cell Line: HT29, HCT116, and HeLa cells
Concentration: 50 μM and 100 μM
Incubation Time: 72 h
Result: Propidium iodide (PI) staining showed a slight increase in the percentage of cells with DNA hypodiploid peak, indicative of apoptosis.

RT-PCR[1]

Cell Line: HCT116 cells
Concentration: 100 μM
Incubation Time: 48h
Result: Reduced the mRNA levels of oncogenes UCP2.

Immunofluorescence[1]

Cell Line: HT29 cells
Concentration: 50 μM
Incubation Time: 24 h
Result: Reduced H4K16Ac signal intensity by 80%.

Western Blot Analysis[1]

Cell Line: HCT116 cells
Concentration: 0,10, 25, 50,100 μM
Incubation Time: 48 h
Result: Showed that the altered ratio of LC3-II/-I and the regulation of p62 autophagy markers indicated the activation of autophagy in HCT116 cells.

Apoptosis Analysis[1]

Cell Line: HCT116 cells
Concentration: 100 μM or 10 μM (MC4033/CQ)
Incubation Time: 72 h
Result: Showed that exposure of HCT116 cells to CQ increased the apoptotic effect of KAT8i.
Molecular Weight

295.29

Formula

C16H13N3O3

CAS No.
Appearance

Solid

Color

Light yellow to yellow

SMILES

CC1=NN(C2=CC=C(C=C2)C(O)=O)C(/C1=C\C3=CC=CN3)=O

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 (84.66 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 3.3865 mL 16.9325 mL 33.8650 mL
5 mM 0.6773 mL 3.3865 mL 6.7730 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.

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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    90% Corn Oil

    Solubility: ≥ 2.5 mg/mL (8.47 mM); Clear solution

    This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown). If the continuous dosing period exceeds half a month, please choose this protocol carefully.

    Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL Corn oil, and mix evenly.

In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:

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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
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Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Calculation results:
Working solution concentration: mg/mL
Method for preparing stock solution: mg drug dissolved in μL  DMSO (Stock solution concentration: mg/mL).
The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only. If necessary, please contact MedChemExpress (MCE).
Method for preparing in vivo working solution for animal experiments: Take μL DMSO stock solution, add μL . μL , mix evenly, next add μL Tween 80, mix evenly, then add μL Saline.
 If the continuous dosing period exceeds half a month, please choose this protocol carefully.
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
Purity & Documentation
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 3.3865 mL 16.9325 mL 33.8650 mL 84.6625 mL
5 mM 0.6773 mL 3.3865 mL 6.7730 mL 16.9325 mL
10 mM 0.3387 mL 1.6933 mL 3.3865 mL 8.4663 mL
15 mM 0.2258 mL 1.1288 mL 2.2577 mL 5.6442 mL
20 mM 0.1693 mL 0.8466 mL 1.6933 mL 4.2331 mL
25 mM 0.1355 mL 0.6773 mL 1.3546 mL 3.3865 mL
30 mM 0.1129 mL 0.5644 mL 1.1288 mL 2.8221 mL
40 mM 0.0847 mL 0.4233 mL 0.8466 mL 2.1166 mL
50 mM 0.0677 mL 0.3387 mL 0.6773 mL 1.6933 mL
60 mM 0.0564 mL 0.2822 mL 0.5644 mL 1.4110 mL
80 mM 0.0423 mL 0.2117 mL 0.4233 mL 1.0583 mL
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MC4033
Cat. No.:
HY-149302
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