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ATM-3507 trihydrochloride (1861449-70-8 free base)

Catalog No. T10395
Alias ATM-3507 trihydrochloride

ATM-3507 trihydrochloride is a potent tropomyosin inhibitor (IC50s: 3.83-6.84 μM in human melanoma cell lines).

ATM-3507 trihydrochloride (1861449-70-8 free base)

ATM-3507 trihydrochloride (1861449-70-8 free base)

Catalog No. T10395Alias ATM-3507 trihydrochloride
ATM-3507 trihydrochloride is a potent tropomyosin inhibitor (IC50s: 3.83-6.84 μM in human melanoma cell lines).
Pack SizePriceAvailabilityQuantity
5 mg$122Backorder
10 mg$206Backorder
50 mg$619Backorder
100 mg$1,058Backorder
200 mgInquiryBackorder
500 mgInquiryBackorder
1 mL x 10 mM (in DMSO)$191Backorder
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Product Introduction

Bioactivity
Description
ATM-3507 trihydrochloride is a potent tropomyosin inhibitor (IC50s: 3.83-6.84 μM in human melanoma cell lines).
Targets&IC50
Tropomyosin (human melanoma cell lines):3.83-6.84 μM
In vivo
The maximal tolerance dose (MTD) for TR100 and ATM-3507 is 60 and 150 mg/kg, respectively. The median survival of mice increased from 18 days for mice treated with ATM-3507 to more than 49 days for mice treated with the combination. It is also found that twice-weekly intravenous administration of ATM-3507 also shows combination efficacy. The impact of each treatment or the combination of body weight is minimal. Drug levels are measured following the intravenous administration of ATM-3507 at 30 mg/kg in Balb/c mice (n=3 per time point). The mean half-life of ATM-3507 is 5.01 hrs for the terminal elimination phase. The mean AUC0-t in the plasma is 14,548 ng/h/mL. The Cmax of ATM-3507 is 5,758 ng/mL and the t1/2 is 5.01 h. The observed plasma clearance and volume of distribution at steady state of ATM-3507 is 33.8 mL/min/kg and 7.23 L/kg, respectively.
AliasATM-3507 trihydrochloride
Chemical Properties
Molecular Weight721.17
FormulaC37H49Cl3FN5O2
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 250 mg/mL (346.66 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.3866 mL6.9332 mL13.8664 mL69.3318 mL
5 mM0.2773 mL1.3866 mL2.7733 mL13.8664 mL
10 mM0.1387 mL0.6933 mL1.3866 mL6.9332 mL
20 mM0.0693 mL0.3467 mL0.6933 mL3.4666 mL
50 mM0.0277 mL0.1387 mL0.2773 mL1.3866 mL
100 mM0.0139 mL0.0693 mL0.1387 mL0.6933 mL

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TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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