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Thiacetazone

Cat. No. M3705

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Thiacetazone  Structure
Synonym:

TAC

Size Price Availability Quantity
5mg USD 90 In stock
10mg USD 120 In stock
50mg USD 400 In stock
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Quality Control & Documentation
Biological Activity

Thioacetazone inhibits mycolic acid cyclopropane synthase but the exact binding site accounting for such inhibition is presently unknown. Thiacetazone (TAC) inhibits the conversion of double bonds of mycolic acid precursors into cyclopropyl rings in Mycobacterium bovis var BCG, M. marimum and M. chelonae by affecting the cyclopropyl mycolic acid synthases (CMASs) as judged by the build-up of unsaturated mycolate precursors.

Chemical Information
Molecular Weight 236.29
Formula C10H12N4OS
CAS Number 104-06-3
Solubility (25°C) DMSO 10 mM
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Coxon GD, et al. PLoS One. Synthesis, antitubercular activity and mechanism of resistance of highly effective thiacetazone analogues.

[2] Banerjee D, et al. Bioinformation. Isoniazid and thioacetazone may exhibit antitubercular activity by binding directly with the active site of mycolic acid cyclopropane synthase: Hypothesis based on computational analysis.

[3] Belardinelli JM, et al. Mol Microbiol. Mutations in the essential FAS II β-hydroxyacyl ACP dehydratase complex confer resistance to thiacetazone in Mycobacterium tuberculosis and Mycobacterium kansasii.

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Keywords: Thiacetazone , TAC supplier, Antibiotic, inhibitors, activators

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