Buy Methyl thieno[3,2-d]thiadiazole-6-carboxylate (BT-254812)

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Methyl thieno[3,2-d]thiadiazole-6-carboxylate

Catalog Number: BT-254812

CAS Number: 152467-47-5

Molecular Formula: C6H4N2O2S2

Molecular Weight: 200.2 g/mol

The product is for non-human research only. Not for therapeutic or veterinary use.

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Product Introduction

Description

Methyl thieno[3,2-d]thiadiazole-6-carboxylate is a heterocyclic compound that has gained significant attention in recent years due to its potential therapeutic and industrial applications. This paper aims to provide a comprehensive review of the synthesis, chemical structure, biological activity, and applications of methyl thieno[3,2-d]thiadiazole-6-carboxylate.

Properties

CAS Number

152467-47-5

Product Name

Methyl thieno[3,2-d]thiadiazole-6-carboxylate

IUPAC Name

methyl thieno[3,2-d]thiadiazole-6-carboxylate

Molecular Formula

C6H4N2O2S2

Molecular Weight

200.2 g/mol

InChI

InChI=1S/C6H4N2O2S2/c1-10-5(9)3-2-11-6-4(3)7-8-12-6/h2H,1H3

InChI Key

FMCBCIKSEQJAGA-UHFFFAOYSA-N

SMILES

COC(=O)C1=CSC2=C1N=NS2

Synonyms

methylthieno[3,2-d][1,2,3]thiadiazole-6-carboxylate

Canonical SMILES

COC(=O)C1=CSC2=C1N=NS2

Method of Synthesis or Extraction

Methyl thieno[3,2-d]thiadiazole-6-carboxylate can be synthesized using various methods, including the reaction of thieno[3,2-d]thiadiazole-6-carboxylic acid with methanol in the presence of a catalyst. The efficiency and yield of each method vary depending on the reaction conditions, such as temperature, pressure, and reaction time. Environmental and safety considerations must also be taken into account during the synthesis process to minimize the production of hazardous waste and ensure worker safety.

Chemical Structure and Biological Activity

Methyl thieno[3,2-d]thiadiazole-6-carboxylate has a unique chemical structure that confers its biological activity. It acts as a potent inhibitor of various enzymes and receptors, including protein kinases, phosphodiesterases, and adenosine receptors. Its mechanism of action involves binding to the active site of these targets, thereby preventing their activation and downstream signaling. Methyl thieno[3,2-d]thiadiazole-6-carboxylate has shown promising bioactivity and potency in preclinical studies, making it a potential candidate for drug development.

Biological Effects

Methyl thieno[3,2-d]thiadiazole-6-carboxylate has been shown to have various effects on cell function and signal transduction. It can induce apoptosis, inhibit cell proliferation, and modulate immune responses. Its potential therapeutic effects include the treatment of cancer, inflammation, and cardiovascular diseases. However, it also has potential toxic effects, such as hepatotoxicity and nephrotoxicity, which must be carefully evaluated in preclinical and clinical studies.

Applications

Methyl thieno[3,2-d]thiadiazole-6-carboxylate has various applications in medical, environmental, and industrial research. In medical research, it can be used as a lead compound for drug development, with several clinical trials currently underway to evaluate its safety and efficacy. In environmental research, it can be used to study its effects on ecosystems and its role in pollution management. In industrial research, it can be used to improve product quality and efficiency, with health and safety considerations being of utmost importance.

Future Perspectives and Challenges

Despite its potential applications, there are still limitations in the use and study of methyl thieno[3,2-d]thiadiazole-6-carboxylate. These include its limited solubility and stability, as well as its potential toxicity. Possible solutions and improvements include the development of more efficient synthesis methods and the optimization of its chemical structure to improve its bioactivity and reduce its toxicity. Future trends and prospects in the application of methyl thieno[3,2-d]thiadiazole-6-carboxylate in scientific research include its potential use in personalized medicine and the development of novel therapeutic agents.

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