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Oxythiamine

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Catalog No. T12354Cas No. 136-16-3
Alias Hydroxythiamin

Oxythiamine (Hydroxythiamin) is an antivitamin of thiamine and a transketolase (TK) inhibitor. Oxythiamine inhibits cancer cell proliferation and induces cell cycle arrest. Oxythiamine has potential anticancer activity, inhibits non-oxidative synthesis of ribose, and induces apoptosis.

Oxythiamine

Oxythiamine

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Purity: 99.51%
Catalog No. T12354Alias HydroxythiaminCas No. 136-16-3
Oxythiamine (Hydroxythiamin) is an antivitamin of thiamine and a transketolase (TK) inhibitor. Oxythiamine inhibits cancer cell proliferation and induces cell cycle arrest. Oxythiamine has potential anticancer activity, inhibits non-oxidative synthesis of ribose, and induces apoptosis.
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10 mg$29-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.51%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Oxythiamine (Hydroxythiamin) is an antivitamin of thiamine and a transketolase (TK) inhibitor. Oxythiamine inhibits cancer cell proliferation and induces cell cycle arrest. Oxythiamine has potential anticancer activity, inhibits non-oxidative synthesis of ribose, and induces apoptosis.
Targets&IC50
MIAPaCa2 cells:14.95 μM
In vitro
Oxythiamine for MIA PaCa-2 cells 5-320 μM for 2 days IC50 is 14.95 μM MTT, MIA PaCa-2 cells concentrations of Oxythiamine (0 μM, 5 μM, 50 μM and 500 μM) for 48 hours two-dimensional gel electrophoresis (2DE). Oxythiamine altered protein expression in a dose dependent manner.[1]
The MIC and MFC values of Oxythiamine were in the range 0.08 × 103 to 10 × 103 mg/L. [2]
A549 cells were co-cultured with Oxythiamine (from 0.1 to 100 μM) for 6–12 h CCK-8 assay
Oxythiamine contributes to a significant reduction of A549 cell viability of 11.7%, 23.6%, and 28.2% at 12, 24, and 48 h. [3]
Oxythiamine arrests the cell growth in G1 phase of cell cycle. [3]
Oxythiamine inhibits the growth of A549 cells by initially slowing-down cell cycle and by leading to apoptosis. [3]
In vivo
s.c. injection C57BL/6 mice with LLC cells and supplemented the mice with a low- or a high-dose of Oxythiamine (250 or 500 mg/kg BW) daily for 5 wk. During the 5-wk period, Oxythiamine supplementation decreased plasma MMP-2 activity in a dose-dependent manner, and this effect was significant after 4 wk of tumor cell implantation. [4]
SynonymsHydroxythiamin
Chemical Properties
Molecular Weight266.34
FormulaC12H16N3O2S
Cas No.136-16-3
SmilesO=C1NC(=NC=C1C[N+]2=CSC(=C2C)CCO)C
Relative Density.1.2416 g/cm3 (Estimated)
Storage & Solubility Information
Storagekeep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 40 mg/mL (150.18 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (7.51 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
1mg5mg10mg50mg
1 mM3.7546 mL18.7730 mL37.5460 mL187.7300 mL
5 mM0.7509 mL3.7546 mL7.5092 mL37.5460 mL
10 mM0.3755 mL1.8773 mL3.7546 mL18.7730 mL
20 mM0.1877 mL0.9386 mL1.8773 mL9.3865 mL
50 mM0.0751 mL0.3755 mL0.7509 mL3.7546 mL
100 mM0.0375 mL0.1877 mL0.3755 mL1.8773 mL

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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:
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2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
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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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