Cat. No.: HY-100455

RK-33

Name: RK-33
Brand: MedChemExpress
SKU: HY-100455
Price: 60.00 USD
Availability: InStock
Rating: 5 (7 reviews)

7 Cited Publications

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Based on 7 publication(s) in Google Scholar

RK-33 is an RNA helicase inhibitor against DDX3, and inhibits its helicase activity.

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Pureté : 99.63%
CAS No.: 1070773-09-9
Formule: C₂₃H₂₀N₆O₃
Masse moléculaire:428.44

Stockage:

Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 2 years , -20°C, 1 year

RK-33 Chemical Structure

CAS No.: 1070773-09-9

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Top Publications Citing

Use of MCE Products

Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Activité biologique
- Description
- IC₅₀ & Target
- Cellular Effect
- In Vitro
- In Vivo
Chemical Information
Publications (7)
Solvant et solubilité
- In Vitro
- In Vivo
Pureté et documentation
Références
Help & FAQs
Classifications
Bioz

Activité biologique

Description

RK-33 is an RNA helicase inhibitor against DDX3, and inhibits its helicase activity.

IC₅₀ & Target

Helicase

Voir tous les produits spécifiques à Isoform DNA/RNA Synthesis :

Cellular Effect

Cell Line	Type	Value	Description	References
A549	IC₅₀	2.5 μM Compound: 1	Cytotoxicity against human A549 cells after 72 hrs by WST1 assay Cytotoxicity against human A549 cells after 72 hrs by WST1 assay	[PMID: 21572541]
A549	IC₅₀	2.56 μM Compound: 1	Cytotoxicity against human A549 cells after 72 hrs by WST1 assay Cytotoxicity against human A549 cells after 72 hrs by WST1 assay	[PMID: 23290252]
Daoy	IC₅₀	2.5 μM Compound: RK-33	Antiproliferative activity against human Daoy cells assessed as inhibition of cell proliferation incubated for 72 hrs by MTS assay Antiproliferative activity against human Daoy cells assessed as inhibition of cell proliferation incubated for 72 hrs by MTS assay	[PMID: 33636537]
Huh-7	CC₅₀	<10 μM Compound: 51	Cytotoxicity against human Huh-7 cells assessed as reduction in cell viability Cytotoxicity against human Huh-7 cells assessed as reduction in cell viability	[PMID: 35899912]
MCF7	IC₅₀	7.5 μM Compound: 1	Cytotoxicity against human MCF7 cells after 72 hrs by WST1 assay Cytotoxicity against human MCF7 cells after 72 hrs by WST1 assay	[PMID: 21572541]
MCF7	IC₅₀	7.59 μM Compound: 1	Cytotoxicity against human MCF7 cells after 72 hrs by WST1 assay Cytotoxicity against human MCF7 cells after 72 hrs by WST1 assay	[PMID: 23290252]
MDA-MB-231	IC₅₀	4.01 μM Compound: 1	Cytotoxicity against human MDA-MB-231 cells after 72 hrs by WST1 assay Cytotoxicity against human MDA-MB-231 cells after 72 hrs by WST1 assay	[PMID: 21572541]
MDA-MB-231	IC₅₀	4.05 μM Compound: 1	Cytotoxicity against human MDA-MB-231 cells after 72 hrs by WST1 assay Cytotoxicity against human MDA-MB-231 cells after 72 hrs by WST1 assay	[PMID: 23290252]
NCI-H460	IC₅₀	2.8 μM Compound: 1	Cytotoxicity against human H460 cells after 72 hrs by WST1 assay Cytotoxicity against human H460 cells after 72 hrs by WST1 assay	[PMID: 21572541]
NCI-H460	IC₅₀	2.87 μM Compound: 1	Cytotoxicity against human H460 cells after 72 hrs by WST1 assay Cytotoxicity against human H460 cells after 72 hrs by WST1 assay	[PMID: 23290252]
OVCAR-3	IC₅₀	14.5 μM Compound: 1	Cytotoxicity against human OVCAR3 cells after 72 hrs by WST1 assay Cytotoxicity against human OVCAR3 cells after 72 hrs by WST1 assay	[PMID: 21572541]
OVCAR-3	IC₅₀	14.5 μM Compound: 1	Cytotoxicity against human OVCAR3 cells after 72 hrs by WST1 assay Cytotoxicity against human OVCAR3 cells after 72 hrs by WST1 assay	[PMID: 23290252]
PC-3	IC₅₀	4.8 μM Compound: 1	Cytotoxicity against human PC3 cells after 72 hrs by WST1 assay Cytotoxicity against human PC3 cells after 72 hrs by WST1 assay	[PMID: 21572541]
PC-3	IC₅₀	4.9 μM Compound: 1	Cytotoxicity against human PC3 cells after 72 hrs by WST1 assay Cytotoxicity against human PC3 cells after 72 hrs by WST1 assay	[PMID: 23290252]
Vero	CC₅₀	29.7 μM Compound: 51	Cytotoxicity against African green monkey Vero cells assessed as reduction in cell viability incubated for 22 hrs by XTT assay Cytotoxicity against African green monkey Vero cells assessed as reduction in cell viability incubated for 22 hrs by XTT assay	[PMID: 35899912]
Vero C1008	CC₅₀	>30 μM Compound: 51	Cytotoxicity against African green monkey Vero E6 cells assessed as reduction in cell viability Cytotoxicity against African green monkey Vero E6 cells assessed as reduction in cell viability	[PMID: 35899912]

In Vitro

RK-33 shows inhibition of many kinds of cancer cells with IC₅₀ of 3-6 μM, while PC3 is much less sensitive to RK-33 (IC₅₀ >12 μM). RK-33 treatment causes a significant accumulation in the G1 phase for DU145 and LNCaP, although treatment with RK-33 causes only a moderate accumulation of the G1 phase for 22Rv1, and the treated cells have significantly reduced G2 phase. RK-33 treatment also causes 12 moderate G1 accumulation in 22Rv1^[1]. RK-33-loaded NPs demonstrate cytotoxicity to MCF-7 cells in a dose-dependent manner, while equivalent doses of empty NPs have no killing effect. The IC₅₀ value of 5% RK-33 loaded NPs is 49 μg/mL, and the IC₅₀ value of 10% RK-33 loaded NPs is 25 μg/mL^[2].

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

In Vivo

There is more cell death (pyknotic or condensed nuclei) admixed with fibrin and interstitial edema in the tumors from mice from the combination RK-33 and radiation group compared to the control or single treatment groups. The treatment combination of RK-33 and radiation has an advantage in reducing tumor proliferation^[1]. In the mice treated with RK-33-PLGA, RK-33 can be detected in the plasma (34 μg/mL) and liver (28 μg/g), but not lungs^[2].

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

Chemical Information

CAS No. 1070773-09-9
Appearance Solid
Masse moléculaire 428.44
Formule C₂₃H₂₀N₆O₃
Color Light yellow to yellow
SMILES

O=C1N(CC2=CC=C(OC)C=C2)C3=NC=NC4=C(N=CN4CC5=CC=C(OC)C=C5)C3=N1
Livraison

Room temperature in continental US; may vary elsewhere.

Stockage

Powder	-20°C	3 years
	4°C	2 years
In solvent	-80°C	2 years
	-20°C	1 year

Publications (7)

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Journal Impact Factor

Sci Adv

2026 Aug 28;12(35):eaej5359. PMID: 42664359
Free Radic Biol Med

YAP-mediated DDX3X confers resistance to ferroptosis in breast cancer cells by reducing lipid peroxidation. [Abstract]

2025 May:232:330-339. PMID: 40089076

RK-33 purchased from MedChemExpress. Usage Cited in: Free Radic Biol Med. 2025 May:232:330-339. [Abstract]

RK-33 (5 μM; 24 h), a DDX3-specific inhibitor, reinforced increased lipid peroxidation levels in BT549 cells in the presence of hydrogen peroxide.

RK-33 purchased from MedChemExpress. Usage Cited in: Free Radic Biol Med. 2025 May:232:330-339. [Abstract]

RK-33 (5 μM; 24 h) elevated the levels of lipid peroxidation in MCF7/DDX3X-HA cells when they were exposed to hydrogen peroxide.

RK-33 purchased from MedChemExpress. Usage Cited in: Free Radic Biol Med. 2025 May:232:330-339. [Abstract]

RK-33 (5-10 μM; 24 h) dose-dependently suppressed GPX4 protein levels in BT549 and MCF7 cells.
Int J Mol Sci

2026 Aug 12;27(16):7192. PMID: 42653197
Int Immunopharmacol

Inhibition of DDX3X alleviates persistent inflammation, immune suppression and catabolism syndrome in a septic mice model. [Abstract]

2023 Apr:117:109779. PMID: 36806038

RK-33 purchased from MedChemExpress. Usage Cited in: Int Immunopharmacol. 2023 Apr:117:109779. [Abstract]

RK-33 (20 mg/kg; i.p.; once daily) down-regulated the levels of CRP, IL-6 and TNF-α in the peripheral blood of CLP-induced septic mice.

RK-33 purchased from MedChemExpress. Usage Cited in: Int Immunopharmacol. 2023 Apr:117:109779. [Abstract]

RK-33 (20 mg/kg; i.p.; once daily) improved the total number of CD4⁺ and CD8⁺ T cells in septic mice reduced by CLP.
NonCoding RNA

DEAD-Box Helicase 3 Modulates the Non-Coding RNA Pool in Ribonucleoprotein Condensates During Stress Granule Formation. [Abstract]

2025 Aug 1;11(4):59. PMID: 40863725
Brain Res

DDX3X promotes ILF3 stability to accelerate neuroblastoma progression via M2 macrophage polarization. [Abstract]

2026 Jan 15:1871:150071. PMID: 41314490
bioRxiv

2024 October 16.

Solvant et solubilité

In Vitro:

DMSO : 25 mg/mL (58.35 mM; ultrasonic and warming and heat to 60°C; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

View the Complete Stock Solution Preparation Table

Preparing Stock Solutions

View the Complete Stock Solution Preparation Table

Concentration Solvent Mass

1 mg

5 mg

10 mg

Concentration

Solvent

Mass

1 mM

2.3340 mL

11.6702 mL

23.3405 mL

5 mM

0.4668 mL

2.3340 mL

4.6681 mL

10 mM

0.2334 mL

1.1670 mL

2.3340 mL

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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

Calculateur de molarité

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Concentration Concentration

Volume Volume

Molecular Weight Molecular Weight

Calculateur de dilution

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

Concentration _(start) Concentration _(start)

Volume _(start) Volume _(start)

Concentration _(final) Concentration _(final)

Volume _(final) Volume _(final)

In Vivo:

Working Solution

For the following dissolution methods, please prepare the working solution directly:

It is recommended to prepare fresh solutions and use them promptly within a short period of time.

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: 50% PEG300 50% Saline

Solubility: 2 mg/mL (4.67 mM); Suspended solution; Need ultrasonic

Pureté et documentation

Select Batch:

Pureté: 99.98%

Assay: 99.98%

ee.: 99.98%

Fiche technique (280 KB)
SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Instruction de manipulation (2659 KB)

Références

[1]. Xie M,et al. RK-33 radiosensitizes prostate cancer cells by blocking the RNA helicase DDX3. Cancer Res. 2016 Sep 12. [Content Brief]

[2]. Bol GM, e tal. PLGA nanoparticle formulation of RK-33: an RNA helicase inhibitor against DDX3. Cancer Chemother Pharmacol. 2015 Oct;76(4):821-7. [Content Brief]

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Complete Stock Solution Preparation Table

Storage method and period of stock solution: -80°C, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.

Optional Solvent	Concentration Solvent Mass	1 mg	5 mg	10 mg	25 mg
DMSO	1 mM	2.3340 mL	11.6702 mL	23.3405 mL	58.3512 mL
	5 mM	0.4668 mL	2.3340 mL	4.6681 mL	11.6702 mL
	10 mM	0.2334 mL	1.1670 mL	2.3340 mL	5.8351 mL
	15 mM	0.1556 mL	0.7780 mL	1.5560 mL	3.8901 mL
	20 mM	0.1167 mL	0.5835 mL	1.1670 mL	2.9176 mL
	25 mM	0.0934 mL	0.4668 mL	0.9336 mL	2.3340 mL
	30 mM	0.0778 mL	0.3890 mL	0.7780 mL	1.9450 mL
	40 mM	0.0584 mL	0.2918 mL	0.5835 mL	1.4588 mL
	50 mM	0.0467 mL	0.2334 mL	0.4668 mL	1.1670 mL

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RK-33

Publications Citing Use of MedChemExpress (MCE) RK-33

Voir tous les produits spécifiques à Isoform DNA/RNA Synthesis