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Maytansine

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Catalog No. T21351Cas No. 35846-53-8
Alias NSC-153858, NSC153858, NSC 153858, Maitansine, Maitansina

Maytansine (NSC-153858), an ansamycin antibiotic originally isolated from the Ethiopian shrub Maytenus serrata, inhibits the assembly of microtubules by binding to tubulin at the rhizoxin binding site.

Maytansine

Maytansine

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Purity: 99.62%
Catalog No. T21351Alias NSC-153858, NSC153858, NSC 153858, Maitansine, MaitansinaCas No. 35846-53-8
Maytansine (NSC-153858), an ansamycin antibiotic originally isolated from the Ethiopian shrub Maytenus serrata, inhibits the assembly of microtubules by binding to tubulin at the rhizoxin binding site.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$30In StockIn Stock
5 mg$56In StockIn Stock
10 mg$77In StockIn Stock
25 mg$183In StockIn Stock
50 mgPreferential-In Stock
1 mL x 10 mM (in DMSO)$87In StockIn 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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Purity:99.62%
Appearance:Solid
Color:White
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Product Introduction

Maytansine AI Summary
Maytansine exhibits a range of bioactivities, effectively targeting multiple pathways and viruses. It inhibits Nrf2 with a potency of 517.4 nM and demonstrates cytotoxicity against VEEV compounds with a CC50 of less than 50.0 nM. This compound also inhibits Lassa Virus binding or entry into cells with a potency of 141.3 nM and blocks Hepatitis C Virus (HCV) activity at 2818.4 nM. It remarkably inhibits ATXN expression with a potency of 6.7 nM. Additionally, it induces synthetic lethality in tumor cells producing 2HG in the HT-1080-IDH1KD cell line at 32642.7 nM and in the HT-1080-NT fibrosarcoma cell line at 4.1 nM. For human tyrosyl-DNA phosphodiesterase 1 (TDP1) inhibition, it shows a potency of 130.0 nM in the absence of CPT and 46.1 nM in the presence of CPT. Lastly, it serves as a stage-specific inhibitor of Vaccinia Orthopoxvirus with a potency of 3548.1 nM..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Maytansine (NSC-153858), an ansamycin antibiotic originally isolated from the Ethiopian shrub Maytenus serrata, inhibits the assembly of microtubules by binding to tubulin at the rhizoxin binding site.
SynonymsNSC-153858, NSC153858, NSC 153858, Maitansine, Maitansina
Chemical Properties
Molecular Weight692.2
FormulaC34H46ClN3O10
Cas No.35846-53-8
Smiles[H][C@@]12O[C@@]1(C)[C@H](CC(=O)N(C)c1cc(C\C(C)=C/C=C\[C@@H](OC)[C@@]3(O)C[C@]([H])(OC(=O)N3)[C@H]2C)cc(OC)c1Cl)OC(=O)[C@H](C)N(C)C(C)=O
Relative Density.1.1049 g/cm3 (Estimated)
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
H2O: Insoluble
DMSO: 60 mg/mL (86.68 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (2.89 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 mM1.4447 mL7.2233 mL14.4467 mL72.2335 mL
5 mM0.2889 mL1.4447 mL2.8893 mL14.4467 mL
10 mM0.1445 mL0.7223 mL1.4447 mL7.2233 mL
20 mM0.0722 mL0.3612 mL0.7223 mL3.6117 mL
50 mM0.0289 mL0.1445 mL0.2889 mL1.4447 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:
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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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