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Merulidial

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Catalog No. TN11385Cas No. 68053-32-7
Alias (-)-Merulidial

Merulidial (Compound 1) is an antibiotic and cytotoxic agent characterized by a sesquiterpene dialdehyde structure. It effectively inhibits the spore germination and mycelial growth of the wood-decaying basidiomycete Heterobasidion annosum (H. annosum) and the saprophytic fungus Cladosporium cucumerinum (C. cucumerinum). Additionally, Merulidial suppresses DNA synthesis in various bacteria, algae, and ECA cells. It exhibits strong anticancer activity, with IC50 values of 20 μg/mL for ECA cells and 10 μg/mL for L1210 cells.

Merulidial

Merulidial

😃Good
Catalog No. TN11385Alias (-)-MerulidialCas No. 68053-32-7
Merulidial (Compound 1) is an antibiotic and cytotoxic agent characterized by a sesquiterpene dialdehyde structure. It effectively inhibits the spore germination and mycelial growth of the wood-decaying basidiomycete Heterobasidion annosum (H. annosum) and the saprophytic fungus Cladosporium cucumerinum (C. cucumerinum). Additionally, Merulidial suppresses DNA synthesis in various bacteria, algae, and ECA cells. It exhibits strong anticancer activity, with IC50 values of 20 μg/mL for ECA cells and 10 μg/mL for L1210 cells.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mgInquiry10-14 weeks10-14 weeks
50 mgInquiry10-14 weeks10-14 weeks
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction

Bioactivity
Description
Merulidial (Compound 1) is an antibiotic and cytotoxic agent characterized by a sesquiterpene dialdehyde structure. It effectively inhibits the spore germination and mycelial growth of the wood-decaying basidiomycete Heterobasidion annosum (H. annosum) and the saprophytic fungus Cladosporium cucumerinum (C. cucumerinum). Additionally, Merulidial suppresses DNA synthesis in various bacteria, algae, and ECA cells. It exhibits strong anticancer activity, with IC50 values of 20 μg/mL for ECA cells and 10 μg/mL for L1210 cells.
In vitro
Merulidial (Compound 1), at a concentration of 25 mg/mL, significantly inhibits the growth of mycelium over 3-5 days, forming inhibition zones of 4-7 mm in width for [C. cucumerinum] and 15-19 mm for [H. annosum]. Additionally, Merulidial at 6.3-25 μg/mL over 24 hours strongly hinders the germination of [H. annosum] mycelial spores at concentrations of 12.5 and 25 μg/mL, and delays germination at 6.3 μg/mL, while it has a weaker effect on [C. cucumerinum], delaying spore germination by at least 48 hours. In the Ames test, Merulidial (50 μg/plate) demonstrates mutagenic activity against mutant strains TA98, TA2637, and TA100, with mutation rates of 0.62, 0.28, and 1.5 revertants/nmol, respectively.
Synonyms(-)-Merulidial
Chemical Properties
Molecular Weight248.32
FormulaC15H20O3
Cas No.68053-32-7
SmilesC(=O)[C@@]12[C@@](C)(C1)[C@@H](O)[C@]3(C(=C2C=O)CC(C)(C)C3)[H]
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

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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:
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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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