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HM03

Name: HM03
Brand: TargetMol
SKU: T8668
Price: 40 USD
Availability: InStock
Rating: 5 (10 reviews)

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Catalog No. T8668Cas No. 500565-15-1

HM03 is a potent and selective inhibitor of HSPA5 and exhibits anticancer activity.

HM03

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Purity: 97.15%

Catalog No. T8668Cas No. 500565-15-1

HM03 is a potent and selective inhibitor of HSPA5 and exhibits anticancer activity.

Pack Size	Price	USA Warehouse	Global Warehouse
5 mg	$40	In Stock	In Stock
10 mg	$64	In Stock	In Stock
25 mg	$129	In Stock	In Stock
50 mg	$213	In Stock	In Stock
100 mg	$347	In Stock	In Stock
200 mg	$515	-	In Stock
1 mL x 10 mM (in DMSO)	$44	In Stock	In Stock

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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]

All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.

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Batch Information

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Purity:97.15%

Appearance:Solid

Color:Red

Resource Download

COA LCMS HNMR

Product Introduction

HM03 AI Summary

HM03 exhibits a broad range of bioactivities. It has significant antibacterial properties against Escherichia coli and Staphylococcus aureus, showing MIC values between 32.0 to 256.0 µg/mL, and inhibits Escherichia coli DdlB with a Ki value of 218,000 nM and an IC50 of 162,000 nM. It also binds selectively to HIV1 RNA, with dissociation constants of 670 nM for the 20mer stem loop 3, 870 nM for duplex RNA, and 3000 nM for single-stranded RNA, displaying a selectivity ratio of 4.4 for single-stranded RNA over the 20mer stem loop 3. Additionally, HM03 shows cytotoxicity against various human cell lines, inhibiting 50% growth of DK1 cells at 25 µM and reducing HCT116 cell survival to 18% at the same concentration after 72 hours. It also impacts several cellular processes including caspase inhibition, IMPase activity, DNA repair enzymes, polymerase and helicase activities, glucose metabolism, and chromatin regulation. Pharmacokinetically, it has a log D value of 3.86 at pH 7.4, and an efflux ratio of 11.18 in human Caco2 cells. It inhibits multiple cytochrome P450 enzymes such as CYP1A2, CYP2C9, CYP2C19, CYP2D6, and CYP3A4, with varying IC50 values indicating potential drug interaction risks. HM03 also affects membrane integrity in Staphylococcus aureus and shows activity against Giardia lamblia. Furthermore, it inhibits human ERCC1-XPF endonuclease with an IC50 value of 1860 nM, binding affinity (Kd) of 140 nM, and induces varied intracellular responses including TGF-beta signaling modulation, Vif-A3F interactions, and synthetic lethality in specific cell lines..

Note: Summary generated by AI. Data source: ChEMBL

Bioactivity

Description

HM03 is a potent and selective inhibitor of HSPA5 and exhibits anticancer activity.

Chemical Properties

Molecular Weight	462.97
Formula	C₂₆H₂₇ClN₄O₂
Cas No.	500565-15-1
Smiles	COc1ccc2nc3cc(Cl)ccc3c(Nc3ccc(O)c(CN4CCN(C)CC4)c3)c2c1
Relative Density.	1.327 g/cm3 (Predicted)

Storage & Solubility Information

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: 125 mg/mL (270 mM), Sonication is recommended.

In Vivo Formulation

10% DMSO+40% PEG300+5% Tween 80+45% Saline: 5 mg/mL (10.8 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

DMSO

	1mg	5mg	10mg	50mg
1 mM	2.1600 mL	10.7998 mL	21.5997 mL	107.9984 mL
5 mM	0.4320 mL	2.1600 mL	4.3199 mL	21.5997 mL
10 mM	0.2160 mL	1.0800 mL	2.1600 mL	10.7998 mL
20 mM	0.1080 mL	0.5400 mL	1.0800 mL	5.3999 mL
50 mM	0.0432 mL	0.2160 mL	0.4320 mL	2.1600 mL
100 mM	0.0216 mL	0.1080 mL	0.2160 mL	1.0800 mL

Calculator

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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:

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 DMSO TargetMol | 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 DMSO TargetMol | reagent 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 TargetMol | 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.

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