ICD inducer-2
ICD inducer-2 is a immunogenic cell death inducer. ICD inducer-2 binds to the colchicine binding site on tubulin to inhibit tubulin polymerization. ICD inducer-2 exhibits broad-spectrum antiproliferative activity across multiple cancer cell lines. ICD inducer-2 inhibits cells migration, causes G2/M phase and induces apoptosis. ICD inducer-2 promotes infiltration of CD4+ and CD8+ T cells into the tumor microenvironment. ICD inducer-2 downregulates antiapoptotic protein Bcl-2, upregulates proapoptotic proteins Bax and Bim-1, and increases cleaved caspase 3, cleaved caspase 9, and cleaved PARP levels. ICD inducer-2 overcomes paclitaxel resistance in xenograft models and achieves tumor growth inhibition. ICD inducer-2 can be used for the research of cancer, such as lung carcinoma.
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- CAS. Nr.: 3069681-35-9
- Formel: C22H15N3O2S
- Molecular Weight:385.44
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Speicherung:
Please store the product under the recommended conditions in the Certificate of Analysis.
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Biologische Aktivität
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Bcl-2 |
Bax |
Bim |
Caspase 9 |
Caspase 3 |
ICD inducer-2 (Compound 17) (1.25-5 μM; 60 min) inhibits purified tubulin polymerization in a dose-dependent manner[1].
ICD inducer-2 (0.2-25 μM; 2 h) binds to the colchicine-binding site on tubulin in A549 cells[1].
ICD inducer-2 (10-20 nM; 48 h) disrupts the microtubule network in A549 cells at 10 and 20 nM[1].
ICD inducer-2 (20-80 nM; 12 h) potently induces ICD in A549 cells[1].
ICD inducer-2 (8-64 nM; 12-24 h) exhibits immunostimulatory potential in vitro, reducing A549 cell viability in co-culture with Jurkat cells[1].
ICD inducer-2 (48 h) exhibits broad-spectrum antiproliferative activity across multiple cancer cell lines with IC50 values from 8 ± 3 nM (MCF-7) to 47 ± 12 nM (A549/TxR), and overcomes paclitaxel resistance in A549/TxR cells with an RI of 4.7[1].
ICD inducer-2 (5-20 nM; 48 h) induces dose-dependent G2/M phase arrest in A549 cells, with corresponding arrest rates of 20.16%, 32.83%, and 40.30%, and modulates cell cycle regulatory proteins[1].
ICD inducer-2 (5-20 nM; 48 h) induces dose-dependent mitochondria-mediated apoptosis in A549 cells, increasing late-stage apoptosis and modulating apoptosis-related protein expression[1].
ICD inducer-2 (5-20 nM; 24 h) inhibits A549 cell migration in a dose-dependent manner[1].
ICD inducer-2 (5-20 nM; 8 h) inhibits HUVEC tube formation in a dose-dependent manner[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:A549 cells
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Concentration:0.2, 1, 5, 25 μM
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Incubation Time:2 h
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Result:Effectively suppressed the formation of the EBI/β-tubulin complex band, confirming binding to the colchicine-binding site on tubulin.
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Cell Line:A549 cells
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Concentration:10, 20 nM
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Incubation Time:48 h
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Result:Induced obvious microtubule network depolymerization, characterized by disorganized structures and diminished fluorescence signal.
Induced more severe disruption than colchicine at 20 nM.
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Cell Line:A549 cells, Jurkat cells
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Concentration:8, 16, 32, 64 nM
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Incubation Time:12-24 h
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Result:Significantly reduced the viability of A549 cells in the co-culture group compared to the A549 monoculture group in a dose-dependent manner, indicating immunostimulatory potential.
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Cell Line:A549 cells
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Concentration:5, 10, 20 nM
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Incubation Time:48 h
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Result:Induced G2/M phase arrest with blocking rates of 20.16% (5 nM), 32.83% (10 nM), and 40.30% (20 nM) in a dose-dependent manner.
Regulated the expression of cell cycle proteins Cdc25c, CDK7, cyclin B1, and P21.
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Cell Line:A549 cells
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Concentration:5, 10, 20 nM
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Incubation Time:48 h
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Result:Significantly increased late-stage apoptosis in a dose-dependent manner.
Downregulated antiapoptotic protein Bcl-2, upregulated proapoptotic proteins Bax and Bim-1, and increased cleaved caspase 3, cleaved caspase 9, and cleaved PARP levels.
| Species | Dose | Route | T1/2 | Tmax | Cmax | AUC0-24 | AUC0-∞ | MRT0-∞ | F |
|---|---|---|---|---|---|---|---|---|---|
| Rat[1] | 25 mg/kg | i.v. | 2.14 ± 0.33 h | 0.08 ± 0.00 h | 35188.87 ± 7938.18 ng/mL | 22694.09 ± 3190.36 ng·h/mL | 23328.92 ± 3029.44 ng·h/mL | 1.40 ± 0.19 h | / |
| Rat[1] | 25 mg/kg | i.p. | 1.71 ± 0.18 h | 0.33 ± 0.14 h | 5208.96 ± 96.58 ng/mL | 14481.33 ± 1309.32 ng·h/mL | 15062.86 ± 1271.55 ng·h/mL | 2.53 ± 0.19 h | 64.57 % |
ICD inducer-2 (10-15 mg/kg; i.v.; once every two days; 14 days) achieves dose-dependent tumor growth inhibition of up to 81.6% in a Lewis lung carcinoma xenograft mice models, while effectively activating antitumor immune responses via increased T cell infiltration and pro-inflammatory cytokine production, with a favorable safety profile at tested doses[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:BALB/c-nu nude mice with A549/TxR xenograft (male)[1]
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Dosage:5 mg/kg; 10 mg/kg; 15 mg/kg
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Administration:i.v.; once every two days; 28 days
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Result:Achieved tumor growth inhibition rates of 67.3%, 77.1%, and 82.0% at doses of 5, 10, and 15 mg/kg, respectively.
Showed a tumor growth inhibition rate of 77.1% at 10 mg/kg, which was markedly greater than that of the same dose of Paclitaxel (HY-B0015) (17.6%).
Revealed no evident toxicity in major organs at the maximal dose of 15 mg/kg.
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Animal Model:C57BL/6N mice with Lewis lung carcinoma xenograft[1]
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Dosage:10 mg/kg; 15 mg/kg
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Administration:i.v.; once every two days; 14 days
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Result:Achieved tumor growth inhibition rates of 72.4% at 10 mg/kg and 81.6% at 15 mg/kg.
Showed a tumor growth inhibition rate of 72.4% at 10 mg/kg, which surpassed that of the same dose of paclitaxel (64.2%).
Increased the proportions of CD4+ and CD8+ T cells in tumor tissue to 7.008% and 7.439% at 10 mg/kg, respectively, significantly higher than the blank control group (3.334% and 3.658%) and slightly greater than the Paclitaxel group (6.627% and 6.559%).
Increased the proportions of CD4+ and CD8+ T cells in tumor tissue to 9.239% and 8.604% at 15 mg/kg, respectively.
Significantly increased serum levels of IFN-γ, IL-2, and IL-12, with higher levels than paclitaxel at the 10 mg/kg dose.
Induced marked calreticulin exposure and HMGB1 release in tumor cells, with greater effects than paclitaxel at the 10 mg/kg dose.
Showed no significant changes in body weight and no obvious toxicity in major organ tissues at 15 mg/kg.
Chemical Information
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CAS. Nr. 3069681-35-9
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Molecular Weight 385.44
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Formel C22H15N3O2S
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SMILES
N#CC1=C(NC2=CC(C3=CC=CS3)=CC=C2)C4=CC5=C(C=C4N=C1)OCCO5
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Versand
Room temperature in continental US; may vary elsewhere.
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Speicherung
Please store the product under the recommended conditions in the Certificate of Analysis.
Reinheit & Dokumentation
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Calculators
Konzentration (Stammlösung) × Volumen (Stammlösung) = Konzentration (Ziellösung) × Volumen (Ziellösung)
ICD inducer-2 Related Classifications
HY-181673 Related Classifications
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