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TOMATIDINE HYDROCHLORIDE

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Catalog No. T4592Cas No. 6192-62-7
Alias Tomatidine HCl

Tomatidine hydrochloride (Tomatidine HCl) is a steriodal alkaloid structurally similar to Cyclopamine but does not inhibit hedgehog pathway. May be used as a negative control for Cyclopamine and KAAD-Cyclopamine. Tomatidine protects against muscle atrophy and boosting muscle growth.

TOMATIDINE HYDROCHLORIDE

TOMATIDINE HYDROCHLORIDE

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🥰Excellent
Purity: 99.94%
Catalog No. T4592Alias Tomatidine HClCas No. 6192-62-7
Tomatidine hydrochloride (Tomatidine HCl) is a steriodal alkaloid structurally similar to Cyclopamine but does not inhibit hedgehog pathway. May be used as a negative control for Cyclopamine and KAAD-Cyclopamine. Tomatidine protects against muscle atrophy and boosting muscle growth.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
2 mg$30In StockIn Stock
5 mg$42In StockIn Stock
10 mg$58In StockIn Stock
25 mg$92In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.94%
Color:White
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Product Introduction

TOMATIDINE HYDROCHLORIDE AI Summary
TOMATIDINE HYDROCHLORIDE exhibits various bioactivities, most notably as an inhibitor of human tyrosyl-DNA phosphodiesterase 1 (TDP1) with a potency of 16360.1 nM, determined through a quantitative high-throughput screening (qHTS) assay conducted in the absence of camptothecin. It strongly inhibits sodium fluorescein uptake in OATP1B1-transfected and OATP1B3-transfected CHO cells at a 10 μM concentration, with inhibition rates of 108.76% and 99.59%, respectively. The compound demonstrates antimicrobial activity against Staphylococcus aureus ATCC 29213 with a MIC greater than 64.0 μg/mL and synergizes with gentamicin (FICI of 8.0). It is highly effective against hemB-deficient Staphylococcus aureus Newbould, showing an MIC of 0.06 μg/mL. Antifungal properties include a MIC of 20000.0 nM against Candida albicans, although it shows no significant activity against Cryptococcus neoformans or a range of bacteria, including Escherichia coli, Klebsiella pneumoniae, and Pseudomonas aeruginosa. Additionally, TOMATIDINE HYDROCHLORIDE has low hemolytic activity on human red blood cells at concentrations above 20.0 μM and shows low cytotoxicity against HEK293 cells (CC50 > 20000.0 nM)..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Tomatidine hydrochloride (Tomatidine HCl) is a steriodal alkaloid structurally similar to Cyclopamine but does not inhibit hedgehog pathway. May be used as a negative control for Cyclopamine and KAAD-Cyclopamine. Tomatidine protects against muscle atrophy and boosting muscle growth.
SynonymsTomatidine HCl
Chemical Properties
Molecular Weight452.11
FormulaC27H46ClNO2
Cas No.6192-62-7
SmilesC[C@@H]1[C@@]2(O[C@@]3([C@]1([C@]4(C)[C@@](C3)([C@]5([C@](CC4)([C@]6(C)[C@@](CC5)(C[C@@H](O)CC6)[H])[H])[H])[H])[H])[H])CC[C@H](C)CN2.Cl
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
Methanol: 12.5 mg/mL (27.65 mM), Sonication is recommended.
DMSO: 1.67 mg/mL (3.69 mM), Sonication is recommended.
Solution Preparation Table
DMSO/Methanol
1mg5mg10mg50mg
1 mM2.2119 mL11.0593 mL22.1185 mL110.5926 mL
Methanol
1mg5mg10mg50mg
5 mM0.4424 mL2.2119 mL4.4237 mL22.1185 mL
10 mM0.2212 mL1.1059 mL2.2119 mL11.0593 mL
20 mM0.1106 mL0.5530 mL1.1059 mL5.5296 mL

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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:
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.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | 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 DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent 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 ddH2OTargetMol | 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.
1 Enter information below:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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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

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