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thiosemicarbazide CAS:6610-29-3

Thiosemicarbazide is an organic compound with the molecular formula CH₅N₃S, featuring a thiosemicarbazide functional group characterized by the presence of a thiol (-SH) and a semicarbazide moiety. This compound is known for its diverse biological activities, including antimicrobial, antitumor, and antiviral properties. Thiosemicarbazide acts as a versatile building block in medicinal chemistry, facilitating the synthesis of various bioactive derivatives. Its ability to form coordination complexes with metal ions further enhances its significance in pharmacology and materials science. Ongoing research continues to explore its potential applications in drug development and therapeutic interventions.


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Application and Effect:

Thiosemicarbazide is a member of the thiosemicarbazone family, characterized by the presence of a thiourea-like structure that incorporates a thioamide and a hydrazine derivative. With the molecular formula CH₅N₃S, this compound has gained attention in both academic and industrial settings due to its unique properties and a wide range of biological activities. One of the most significant aspects of thiosemicarbazide is its pharmacological potential. Research has revealed that it exhibits notable antimicrobial, antifungal, and antiviral activities, making it a candidate for therapeutic applications. For example, thiosemicarbazide has demonstrated efficacy against various bacterial strains, showcasing its potential as an antimicrobial agent. Additionally, studies have indicated that it may possess antitumor properties, potentially inhibiting cancer cell proliferation through multiple mechanisms, including apoptosis induction and cell cycle arrest. Thiosemicarbazide’s ability to form stable complexes with transition metals further enhances its utility in medicinal chemistry. These metal-thiosemicarbazide complexes have been investigated for their biological activity, including enhanced anticancer effects and improved selectivity towards cancer cells. The ability to modify the thiosemicarbazide structure allows researchers to develop a plethora of derivatives, expanding its role as a versatile scaffold in drug discovery. Moreover, the compound’s reactivity enables it to participate in various organic reactions, such as condensation and cyclization, leading to the formation of more complex structures with tailored biological properties. Despite its promising applications, thorough safety evaluations are essential, as some derivatives may exhibit toxicity or adverse effects. Comprehensive studies into its pharmacokinetics, mechanisms of action, and optimal dosing regimens will be crucial for advancing thiosemicarbazide-based compounds into clinical use. Overall, thiosemicarbazide stands out as a significant compound in the field of medicinal chemistry, offering potential pathways for new therapeutic agents across various health conditions.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition 6610-29-3
Assay 99%
Appearance white powder
CAS No.  6610-29-3
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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