Thiostrepton

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Thiostrepton
Details
CAS: 1393-48-2
Core structure: Natural polycyclic thiopeptide antibiotic derived from *Streptomyces*, containing multiple thiazole rings, thiazoline rings and dehydroamino acids to form a highly rigid fused-ring structure. It targets bacterial ribosomal 23S rRNA to inhibit protein synthesis elongation, and also inhibits proteasome activity and the FOXM1 transcriptional pathway in eukaryotic cells.
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Related documents
COA/MS/HPLC Report
Peptide Dissolution and Storage Guide
Category
Drug Peptides
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Description

Shanghai Sonyt Biotechnology Co., Ltd. is one of the leading manufacturers and suppliers of thiostrepton in China, also supports custom service. Welcome to wholesale bulk high quality thiostrepton from our factory. Contact us for more details.

 

Description Thiostrepton is a classic thiopeptide antibiotic. By specifically binding to the 23S rRNA of the 50S ribosomal subunit in bacteria, it inhibits the translocation reaction of aminoacyl-tRNA, blocks bacterial protein synthesis, and exerts potent antibacterial activity against Gram-positive bacteria. In eukaryotic cells, it inhibits the chymotrypsin-like activity of the proteasome and downregulates the expression of transcription factor FOXM1, exerting anti-proliferative and pro-apoptotic effects on tumor cells. It is widely used in bacterial protein synthesis mechanism research, proteasome function study, tumor targeted therapy research and antibacterial drug development, and is a classic tool reagent for microbiology and oncology research.
Peptide purity (HPLC, %) 95%/98%/99%
Molecular formula C₇₂H₈₅N₁₉O₁₈S₅
Molecular weight (Da) 1664.9
Structure type Polycyclic thiopeptide with multiple thiazole rings, free peptide

 

Product Basic Information Table

 

Product Standard English Name Product Abbreviation / Alias Function Tags (comma-separated) Core Structure Molecular Formula Exact Mass (Da) Average MW (Da) Salt Form Length (aa)
Thiostrepton Thiostrepton Thiopeptide antibiotic, ribosome inhibitor, antitumor, FoxM1 inhibition Natural polycyclic thiopeptide with multiple thiazole/thiazoline rings and dehydroamino acids; targets bacterial 23S rRNA to inhibit protein synthesis C₇₂H₈₅N₁₉O₁₈S₅ 1663.54 1664.9 Free peptide Polycyclic thiopeptide

 

Physicochemical Solubility & Storage Parameters

 

Product Code Appearance Long-term Storage Short-term Storage Solution Stability Solid Powder Stability
PEP-THI001 Yellow to tan crystalline powder Store at -20°C, sealed, dry and protected from light. Aliquot for storage. Stable for 1 month at 2–8°C in sealed dry condition; ship on ice pack recommended. Stable for 7 days at 4°C. Freely soluble in DMSO, DMF and methanol. Very low water solubility; requires co-solvent. Unstable under strong acid and alkali. Stable for 2 years at -20°C, dry and protected from light.

 

Functional Description

 

Product Code Frontend Short Summary (for search list display) Detailed Biological Function Description Applicable Research Areas (comma-separated) Targets / Pathways
PEP-THI001 Polycyclic thiopeptide antibiotic inhibits ribosome and proteasome with antibacterial and antitumor activities Thiostrepton is a classic thiopeptide antibiotic. By specifically binding to the 23S rRNA of the 50S ribosomal subunit in bacteria, it inhibits aminoacyl-tRNA translocation, blocks bacterial protein synthesis, and exerts potent antibacterial activity against Gram-positive bacteria. In eukaryotic cells, it inhibits the chymotrypsin-like activity of the proteasome and downregulates the expression of transcription factor FOXM1, arresting tumor cell cycle and inducing apoptosis. It is widely used in bacterial protein synthesis mechanism research, proteasome function study, tumor targeted therapy research and antibacterial drug development. Bacterial protein synthesis research, proteasome function study, tumor targeted therapy research, antibacterial drug development, FoxM1 pathway study Bacterial 23S rRNA, eukaryotic proteasome, FOXM1; Protein synthesis inhibition and tumor proliferation regulatory pathway

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