Unlock high‑purity, GMP‑certified ERK1/2 inhibitor signaling research reagents for your next discovery project. Designed for corporate purchasing managers, technical directors, and operations leaders who demand speed, consistency, and regulatory compliance.
In 2025, 70 % of R&D teams reported delays caused by reagent‑related issues. The most common pain points are:
Imagine a scenario where your team spends three weeks just waiting for a 100 mg batch of ERK1/2 inhibitor, only to discover it fails HPLC purity checks. The downstream impact? Missed grant deadlines, delayed clinical‑stage decisions, and lost competitive advantage.
Solution? Partner with a supplier that guarantees high‑purity, on‑time delivery, and full regulatory documentation—all at a cost structure that respects your ROI.
| Parameter | Specification | Unit |
|---|---|---|
| Chemical Name | ERK1/2 Inhibitor (Compound X‑001) | — |
| Purity (HPLC) | ≥99.5 % | % |
| Molecular Weight | 384.44 | g mol⁻¹ |
| Form | Free base / Hydrochloride salt | — |
| Packaging | Amber glass vial, 50 mg‑10 kg | — |
| Stability | ≥24 months at 25 °C (sealed) | — |
| Regulatory Docs | GMP, ISO 9001, FDA DMF, CE, RoHS | — |
Case Study 1 – Oncology Target Validation (USA)
Acme Oncology used 200 mg of our ERK1/2 inhibitor to validate MAPK pathway blockade in KRAS‑mutant cell lines. Within 10 days, they reported a 45 % reduction in phospho‑ERK levels, enabling a fast‑track IND filing. Cost per gram: $1,650 (vs. market average $2,500).
Case Study 2 – High‑Throughput Screening (Europe)
BioScreen Ltd. ordered 5 kg of bulk inhibitor for a 384‑well HTS campaign. Delivery time: 7 days from order to receipt. The assay showed a Z′‑factor of 0.78, meeting their stringent QC thresholds.
Case Study 3 – Custom Salt Form for In‑Vivo Studies (Asia)
PharmaX required a hydrochloride salt to improve solubility for mouse dosing. Our ODM team delivered 500 g of the custom salt in 14 days, complete with GLP‑compliant batch records.
Standard orders (≤5 kg) are dispatched within 48 hours after payment confirmation. Customs clearance in the U.S. averages 4‑6 days. Express shipping can reduce total door‑to‑door time to 7 days.

Yes. Our ODM team can synthesize hydrochloride, mesylate, or deuterated versions. Lead time for 500 g custom batches is 14 days, with full batch records and GMP documentation.
Each lot undergoes HPLC, LC‑MS, and NMR verification. Results are documented in a detailed Certificate of Analysis (CoA) and a batch‑specific GMP batch record. Our internal CV% for purity is ≤0.2 %.
We accept T/T, L/C, PayPal, and corporate credit cards. For orders > 5 kg, we can negotiate 30‑day net terms after the first successful shipment.
All shipments include GMP certificates, FDA DMF references, ISO 9001 compliance statements, and a full Material Safety Data Sheet (MSDS). Additional documentation (e.g., GLP batch records) can be supplied on request.
Limited‑time Offer: Order before 31 May 2026 and receive Free 100 mg sample plus a Money‑Back Guarantee if the purity does not meet the stated specifications.
Choose the contact method that works best for you:
Laura M., Procurement Lead – MedTech Corp. “The on‑time delivery and transparent pricing allowed us to stay within our FY budget while achieving 99.7 % assay reproducibility.”
Tom S., Technical Director – BioInnovate “Custom salt‑form synthesis was completed in two weeks, a timeline we thought impossible. The documentation satisfied our FDA audit without extra work.”
Angela R., Operations Manager – PharmaGen “Switching to Global Technology cut our logistics cost by 28 % and eliminated unexpected customs fees.”
Global Technology Co., Ltd | No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China | Contact Page
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All products are manufactured in a GMP‑certified, FDA‑registered facility and hold the following certifications: