Structure of Thiostrepton
CAS No.: 1393-48-2
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
Thiostrepton is a natural cyclic oligopeptide antibiotic, is a natural product of the ribosomally synthesized and post-translationally modified peptide (RiPP) class.
Synonyms: Bryamycin; Thiactin; Thiostreptin A
4.5
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CAS No. : | 1393-48-2 |
Formula : | C72H85N19O18S5 |
M.W : | 1664.89 |
SMILES Code : | O=C(N[C@@]1(CCC(C2=NC(C(NC(C(NC(C(N)=O)=C)=O)=C)=O)=CS2)=N[C@H]1C3=CSC([C@@H](NC(C4=CSC([C@@H](NC5=O)C(O)([C@@H](C)O)C)=N4)=O)[C@H](OC(C6=NC7=C(C([C@H](C)O)=C6)C=C[C@@H](N[C@H]8C(CC)C)[C@@H]7O)=O)C)=N3)C9=NC(C(N[C@H](C(N/C(C%10=N[C@@H]5CS%10)=C/C)=O)[C@@H](C)O)=O)=CS9)[C@@H](NC(C(NC([C@@H](NC8=O)C)=O)=C)=O)C |
Synonyms : |
Bryamycin; Thiactin; Thiostreptin A
|
MDL No. : | MFCD00135828 |
GHS Pictogram: |
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Signal Word: | Warning |
Hazard Statements: | H302-H312-H332 |
Precautionary Statements: | P280 |
In Vitro:
Cell Line
|
Concentration | Treated Time | Description | References |
E. coli 70S ribosomes | 0.15 μM | 10 minutes | To study the inhibitory effect of Thiostrepton on the GTPase activity of EF-G and EF4, the results showed that Thiostrepton significantly inhibited the GTPase activity of both EF-G and EF4. | PMC3245911 |
EL4 cells | 0.5 μM, 1 μM, 2 μM | 24 hours | To investigate the effect of TST on RORγt expression in EL4 cells, results showed that TST induced ubiquitination and degradation of RORγt by promoting the binding of Itch to RORγt. | PMC10616104 |
Human monocyte-derived macrophages (hMDMs) | 2.5 μM | 24 hours | Thiostrepton induced hMDMs to express proinflammatory cytokines TNFα and IL-1β and downregulate the M2 chemokine CCL24. Functional enrichment analysis showed that IFN/NFκB pathway, TNF-mediated pathway, oxidative-reduction process, protein polyubiquitination, and cellular response to LPS were upregulated, while DNA replication, cell cycle, and cell matrix adhesion were downregulated. | PMC7858590 |
Mouse bone marrow macrophages (BMMs) | 2.5 μM | 24 hours | Thiostrepton inhibited the expression of TAM/M2-associated genes Arg1, Fizz1, Vegfa, Ym1, and Tgfb but upregulated the expression of M1-associated genes Tnf, Il1b, Cxcl2, and Nos2. | PMC7858590 |
Human peripheral blood mononuclear cell (PBMC)-derived macrophages | 10 mM | 24 hours | To study the effect of Thiostrepton on macrophage polarization, results showed that Thiostrepton did not significantly promote M2 to M1 macrophage repolarization but caused slight reductions in CD86 and CD206 expression in M2 macrophages. | PMC10828769 |
70S ribosomes | 100 µM | 3 minutes | To study the effect of thiostrepton on EF-G-dependent GTP hydrolysis, results showed that thiostrepton inhibited the turnover of EF-G but did not affect single-round GTP hydrolysis. | PMC22252 |
H1299 cells | 5 μM | 48 hours | Reduced FOXM1 and PD-L1 expression, inhibited cell proliferation | PMC9561767 |
PC9 cells | 5 μM | 48 hours | Reduced FOXM1 and PD-L1 expression, inhibited cell proliferation | PMC9561767 |
HCT-8 cells | 2 μM | 48 hours | To test the anti-proliferative activity of Thiostrepton against CRC cells | PMC6988281 |
HCT116 cells | 2 μM | 48 hours | To test the anti-proliferative activity of Thiostrepton against CRC cells | PMC6988281 |
HCT-15 cells | 5 µM and 10 µM | 48 hours | Induced apoptosis in CRSC subpopulations and inhibited their sphere and colony formation capabilities. | PMC4650716 |
HT-29 cells | 5 µM and 10 µM | 48 hours | Induced apoptosis in CRSC subpopulations and inhibited their sphere and colony formation capabilities. | PMC4650716 |
Panc-1 | 0–250 μM | 48 hours | To evaluate the inhibitory effect of TST on the proliferation of pancreatic cancer cells, the results showed that TST significantly reduced the growth of pancreatic cancer cells in a dose-dependent manner. | PMC9300693 |
MIA PaCa-2 | 0–250 μM | 48 hours | To evaluate the inhibitory effect of TST on the proliferation of pancreatic cancer cells, the results showed that TST significantly reduced the growth of pancreatic cancer cells in a dose-dependent manner. | PMC9300693 |
BxPC-3 | 0–250 μM | 48 hours | To evaluate the inhibitory effect of TST on the proliferation of pancreatic cancer cells, the results showed that TST significantly reduced the growth of pancreatic cancer cells in a dose-dependent manner. | PMC9300693 |
hTERT-HPNE | 0–250 μM | 48 hours | To evaluate the inhibitory effect of TST on the proliferation of normal pancreatic ductal epithelial cells, the results showed that TST had low toxicity to normal cells. | PMC9300693 |
Human neuroglioma H4 cells | 0.5, 5, 50 µM | 6 hours | Autophagy induction was assessed by measuring GFP-LC3 positive puncta, and 175 compounds were selected | PMC7206967 |
Human osteosarcoma U2OS cells | 50 µM | 6 hours | ATP release was assessed by measuring quinacrine positive dots, and Thiostrepton was identified as a potential ICD enhancer | PMC7206967 |
Th17 cells | 0.01 μM, 0.25 μM, 5 μM | 72 hours | To investigate the effect of TST on Th17 cell differentiation, results showed that TST significantly inhibited Th17 cell differentiation and reduced IL-17A production and RORγt expression. | PMC10616104 |
Acute myeloid leukemia (AML) cell lines | 1.91 mM to 38.67 mM (ED50) | 72 hours | To study the cytotoxicity of Thiostrepton on leukemic cells, results showed that Thiostrepton exhibited significant cytotoxicity against AML cell lines with ED50 values ranging from 1.91 mM to 38.67 mM. | PMC10828769 |
Yeast strain 6EA1 | 100 µM | To test the inhibitory effect of Thiostrepton on yeast strain 6EA1 expressing bacterial protein L11, results showed that the strain was sensitive to Thiostrepton with an IC50 of approximately 100 μM. | PMC2175356 | |
pulmonary fibroblasts | 10 µM | Inhibition of FOXM1 expression significantly reduced the expression of α-SMA and COL1A1 and impaired the migration ability of pulmonary fibroblasts. | PMC11409797 |
In Vivo:
Species
|
Animal Model
|
Administration | Dosage | Frequency | Description | References |
Mice | DSS-induced colitis model | Intraperitoneal injection | 20 mg/kg | Every other day, for 7 days | To investigate the therapeutic effect of TST on DSS-induced colitis, results showed that TST significantly alleviated colitis symptoms and controlled colonic inflammation by modulating dysbiosis. | PMC10616104 |
BALB/c Nude mice | H1299 and PC9 xenograft model | Intraperitoneal injection | 17 mg/kg | Every 2 days for 9 days | Significantly downregulated PD-L1 expression and reduced tumor volume | PMC9561767 |
Mice | B16F10 melanoma model | Intraperitoneal or subcutaneous injection | 150 or 300 mg/kg (intraperitoneal injection), 20 mg/kg (subcutaneous injection) | Administered on day 6 and day 12 | Thiostrepton significantly suppressed tumor growth and showed additive effects with TA99. Flow cytometry analysis revealed elevated levels of macrophages and monocytes in tumors from mice treated with thiostrepton or thiostrepton plus TA99, with upregulated expression of iNOS and CD86 and downregulated expression of Arg1 in TAMs. | PMC7858590 |
Nude mice | CRC xenograft model | Intraperitoneal injection | 500 mg/kg/day | Every three days for 21 days | To evaluate the anti-tumor effect of Thiostrepton on CRC xenograft model | PMC6988281 |
C57BL/6 mice | MCA205 or TC-1 tumor model | Intraperitoneal injection | 200 mg/kg | Once daily 1 day before, on, and 1 day after chemotherapy, then 40 mg/kg three times per week | Thiostrepton enhanced the anticancer activity of oxaliplatin, further diminishing tumor size and extending the survival of the animals | PMC7206967 |
Mice | BLM-induced pulmonary fibrosis models | intraperitoneal injection | 30 mg/kg | every other day for 2 weeks | Inhibition of FOXM1 expression significantly reduced pulmonary fibrosis, decreased collagen deposition, and lowered the expression of fibrotic markers such as α-SMA and COL1A1. | PMC11409797 |
BALB/c Nude mice | Subcutaneous tumour model | Intraperitoneal injection | 17 mg/kg | Three times a week for 3 weeks | To evaluate the inhibitory effect of TST on the growth of subcutaneous tumours, the results showed that TST significantly inhibited tumour growth, and Fer-1 reversed this effect. | PMC9300693 |
Bio Calculators | ||||
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1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
0.60mL 0.12mL 0.06mL |
3.00mL 0.60mL 0.30mL |
6.01mL 1.20mL 0.60mL |
Tags: Thiostrepton | Antibiotic | thiazole antibiotic | FOXM1 | YAP/TEAD complex | 1393-48-2
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