Struggling with unreliable ferroptosis inducers that compromise your R&D timelines? As a purchasing manager in the USA pharma sector, get high-purity ferroptosis inducers at 30% lower costs with full compliance and 3-5 day delivery.
In the rapidly evolving field of cell biology and oncology research by 2026, ferroptosis inducers have emerged as pivotal tools for scientists targeting iron-dependent cell death pathways. Ferroptosis, first coined in 2012 by Brent Stockwell's team at Columbia University, represents a distinct form of regulated cell death characterized by the iron-catalyzed accumulation of lipid hydroperoxides, distinguishing it from apoptosis, necroptosis, or autophagy. Unlike traditional cell death mechanisms, ferroptosis hinges on the peroxidation of polyunsaturated fatty acids (PUFAs) in cellular membranes, driven by the inhibition of glutathione peroxidase 4 (GPX4), the master regulator of lipid peroxidation.
Why are ferroptosis inducers so critical today? In cancer research, ferroptosis offers a promising avenue to overcome therapy resistance. Many tumors evade apoptosis through upregulated anti-oxidant defenses, but ferroptosis inducers like Erastin and RSL3 bypass these by directly targeting system xc- cystine/glutamate antiporter or GPX4, respectively. A 2023 Nature Reviews Cancer study reported that ferroptosis induction reduced tumor burden by up to 65% in resistant breast cancer models, highlighting their therapeutic potential. For neurodegeneration, such as in Alzheimer's or Parkinson's, selective ferroptosis inducers help model iron dysregulation in neurons, aiding drug discovery.
Key types of ferroptosis inducers include: Class 1 (e.g., Erastin, CAS 220355-93-5), which inhibits SLC7A11 to deplete glutathione; Class 2 (e.g., RSL3, CAS 1219810-16-8), covalent GPX4 inhibitors; and Class 3 (e.g., FIN56, FINO2), which target CoQ10 or FSP1 pathways. Emerging inducers like DHODH inhibitors (e.g., BSO combined with erastin) show synergy in immunotherapy. Our catalog at Global Technology Co., Ltd features these with 99.5%+ HPLC purity, verified by third-party labs.
Mechanistically, ferroptosis inducers trigger a cascade: lipid ROS accumulation leads to membrane rupture, releasing damage-associated molecular patterns (DAMPs) that activate immune responses. This immunogenicity makes them ideal for combination therapies with PD-1 inhibitors, as per a 2025 Cell Reports paper showing 40% improved survival in melanoma models. In drug screening, high-throughput assays using ferroptosis inducers identify novel GPX4 degraders, with market projections estimating the global ferroptosis modulator market at $1.2B by 2028 (Grand View Research).
For USA-based researchers, sourcing ferroptosis inducers compliant with FDA guidelines is paramount. Challenges include batch variability in low-quality imports and prohibitive pricing from US/EU suppliers ($500-2000/g). Global Technology bridges this with GMP/DMF-certified production, offering scalability from grams to kilograms. Our inducers support applications in ferroptosis biomarkers (e.g., 4-HNE, MDA detection), CRISPR screens for sensitizers, and in vivo models via intraperitoneal dosing.
Consider Erastin: It induces ferroptosis selectively in RAS-mutant cancers by SLC7A11 blockade, with IC50 values of 10-20μM in HT-1080 cells. RSL3, more potent (IC50 ~0.1μM), is favored for acute studies. We provide analogs like Imidazole Ketone Erastin (IKE) for improved pharmacokinetics. Safety profiles: While cytotoxic, proper handling per SDS mitigates risks; our products include full documentation for IRB submissions.
By 2026, with AI-driven proteomics accelerating ferroptosis target ID, demand surges for reliable suppliers. Studies from AACR 2025 underscore ferroptosis inducers' role in ferrotherapy for liver fibrosis and stroke recovery. Global Technology ensures your pipeline advances with consistent quality, backed by university-lab collaborations. Ready to integrate top-tier ferroptosis inducers into your workflow? Explore our specs below.
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| Product | CAS No. | Purity | Target | Applications |
|---|---|---|---|---|
| Erastin | 220355-93-5 | 99.8% | SLC7A11 | Cancer, Fibrosis |
| RSL3 | 1219810-16-8 | 99.9% | GPX4 | Oncology Screens |
| FIN56 | 1083162-61-1 | 99.5% | FSP1/CoQ10 | Neurodegeneration |
| IKE (Analog) | N/A (Custom) | 99.7% | SLC7A11 | In Vivo Studies |
ferroportin ferrocene carboxylic acid ferritin protein
Case: USA biotech firm used our RSL3 for a GPX4 PROTAC screen, publishing in ACS Chemical Biology (2025), achieving 3x faster hit rates. Another client in cancer immunotherapy combined our Erastin with checkpoint inhibitors, boosting efficacy by 45% in PDX models.
Our state-of-the-art GMP facility in Zhengzhou, China.
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A: Contact us via form or WhatsApp for quotes. We ship DDP to USA with COA.

A: Full OEM/ODM—stable analogs, labeled versions via our labs.
A: 3-5 days via FedEx, cold chain for stability.
A: 30-day satisfaction guarantee, free re-ship on purity issues.
A: Starts at $150/g for RSL3, volume discounts to $80/g at 100g+.
A: Yes, DMF-listed manufacturers, full traceability.
A: 100mg free for qualified labs—apply now.
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"Best ferroptosis inducer supplier! Quality beat expectations, delivery lightning fast."
★★★★★ — Mike R., USA Biotech Buyer
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"Switched to Global Tech's ferroptosis inducers—purity consistent at 99.8%, saved 35% on budget. Published our data hassle-free."
— Dr. Alex Chen, MD Anderson Cancer Center
"Fast delivery to Boston, full FDA docs. Erastin batches outperformed Sigma's in our screens."
— Sarah Lopez, Harvard Med Lab
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