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HDAC-IN-100

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Catalog No. TP4413 Copy Product Info
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HDAC-IN-100 is a histone deacetylase inhibitor with IC50 values of 0.038 μM for HDAC1, 0.283 μM for HDAC2, and 0.586 μM for HDAC3. It functions as a chemosensitizer and apoptosis (apoptosis) inducer, activating caspase3/7 and counteracting Cisplatin resistance. HDAC-IN-100 exhibits antiproliferative effects in ovarian cancer and squamous carcinoma cells. It is valuable for research on ovarian cancer, squamous cell carcinoma, and Cisplatin-resistant squamous cell carcinoma.

HDAC-IN-100

Cas No. 2390474-88-9
Pack SizePriceUSA StockGlobal StockQuantity
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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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Product Introduction

Bioactivity
Description
HDAC-IN-100 is a histone deacetylase inhibitor with IC50 values of 0.038 μM for HDAC1, 0.283 μM for HDAC2, and 0.586 μM for HDAC3. It functions as a chemosensitizer and apoptosis (apoptosis) inducer, activating caspase3/7 and counteracting Cisplatin resistance. HDAC-IN-100 exhibits antiproliferative effects in ovarian cancer and squamous carcinoma cells. It is valuable for research on ovarian cancer, squamous cell carcinoma, and Cisplatin-resistant squamous cell carcinoma.
Targets & IC50
HDAC1:0.038 μM
In vitro
HDAC-IN-100 (compound 2a) reduces the viability of human cancer cells A2780 (IC 50 2.40 μM) and Cal27 (IC 50 1.60 μM) over 72 hours. When applied at concentrations of 0-100 μM for 18 hours, HDAC-IN-100 potently inhibits cell HDAC activity in A2780 (IC 50 0.48 μM) and Cal27 (IC 50 0.11 μM) cancer cells. The compound at 0.5 μM for 48 hours exhibits a strong synergistic effect with Cisplatin, decreasing viability of Cal27 cells and Cisplatin-resistant Cal27CisR cells, while completely reversing the Cisplatin resistance in Cal27CisR cells. Additionally, HDAC-IN-100 at 0.5 μM for 48 hours significantly increases apoptosis levels in both Cal27 and Cal27CisR cells. It also induces high acetylation of histone H3 within 24 hours in Cal27 and Cisplatin-resistant Cal27CisR cells.
Chemical Properties
Molecular Weight535.64
FormulaC32H33N5O3
Cas No.2390474-88-9
SmilesO=C(NC=1C=CC=CC1N)C2=CC=C(C=C2)CN(C(=O)C3=CC=C(C=C3)N(C)C)CC(=O)NCC=4C=CC=CC4
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.

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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.
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Preparation of the In Vivo Formulation:

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Related Tags: HDAC-IN-100 in vitro | HDAC-IN-100 formula | HDAC-IN-100 molecular weight