Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing sales7@sinochem-nanjing.com 3389378665@qq.com
Follow us:

Kenpaullone

    • Product Name Kenpaullone
    • Alias KIAA1646
    • Einecs 602-705-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    925573

    Name Kenpaullone
    Cas Number 561456-14-6
    Molecular Formula C16H12N4O
    Molecular Weight 276.29
    Purity ≥98%
    Chemical Structure 2-(2-benzamido-1H-indol-3-yl)acetamide
    Appearance White to off-white solid
    Solubility DMSO, ethanol
    Storage Temperature -20°C
    Usage GSK-3β and CDK inhibitor

    As an accredited Kenpaullone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Kenpaullone is supplied in a 10 mg amber glass vial, sealed, labeled with product details, concentration, and storage instructions.
    Shipping Kenpaullone is shipped in compliance with chemical safety regulations, typically in sealed, labeled containers to prevent contamination or degradation. It is packaged with protective materials to avoid breakage or spills and transported under ambient or specified temperature conditions, ensuring product integrity during transit. Shipping documents ensure traceability and regulatory compliance.
    Storage Kenpaullone should be stored at -20°C, protected from light and moisture. It should be kept in a tightly sealed container in a dry and well-ventilated area. For long-term storage, minimize repeated freeze-thaw cycles. Proper labeling and adherence to laboratory safety protocols are essential to ensure chemical integrity and user safety.
    Application of Kenpaullone

    Applications of Kenpaullone in Industrial Manufacturing

    Kenpaullone serves as a high-purity chemical intermediate in specialized industrial production. As an experienced manufacturer, we supply Kenpaullone for verified segments where its performance, regulatory acceptance, and downstream integration have industrial validation. Below are the main application scenarios, their precise compliance frameworks, technical use ratios, process roles, and typical downstream products.

    1. Medicinal Chemistry Research and Small-Scale GMP Pilot Production

    Kenpaullone functions as a selective kinase inhibitor in pharmaceutical R&D pipelines. Medicinal chemistry teams use it during preclinical stages for target validation and hit-to-lead evaluation. Process engineers incorporate it in small-scale GMP-compliant synthesis for investigational new drug (IND) batches. Quality assurance teams monitor both raw material integrity and contamination risk under GMP protocols prior to advancing to clinical supply. Documentation for auditing incorporates lot tracking, testing reports, and supplier qualification modules.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • 21 CFR Parts 210–211 (FDA cGMP regulations)
    • EU GMP Part II (EudraLex Volume 4)
    • Certificate of Analysis (CoA) with impurity profiles and residual solvent analysis per USP & EP

    Typical usage ratio

    • 0.2–1.5% w/w relative to total reaction mass; adjusted by batch scale, target kinase, and required yield in screening versus pilot validation runs

    Downstream process integration

    • Introduced during the late-stage pathway of small molecule inhibitor synthesis
    • Filtered, assayed, and documented prior to pilot-scale blending
    • QC batch release for preclinical dosage form preparation

    Final product types

    • Investigational small molecule drugs (solid or solution form)
    • Reference standards for pharmacodynamic studies
    • Chemical reference libraries supplied for external R&D

    2. Diagnostic Reagent Production for Kinase Activity Assays

    Major diagnostic companies and life science suppliers use Kenpaullone as an in vitro standard in kinase activity assay kits. Reagent formulation teams require bulk supplies at consistent purity for manufacturing batch-controlled test kits. Stringent compatibility and contamination requirements govern both bulk storage and packaging processes. Stability studies and batch-to-batch consistency take priority for CE IVDR and FDA 21 CFR 820-compliant markets. Documentation supports full traceability and post-launch product recalls if needed.

    Industry compliance standards

    • CE-IVD Regulation (EU) 2017/746 for in vitro diagnostic medical devices
    • FDA 21 CFR Part 820 (Quality System Regulation for Devices)
    • ISO 13485:2016 (QMS for device manufacturers)
    • Certificate of Analysis aligned with ISO and FDA lot release requirements

    Typical usage ratio

    • 0.005–0.1% w/v in assay reagent concentrate; adjusted for sensitivity, substrate load, and detection method

    Downstream process integration

    • Formulation of lyophilized or stabilized assay master mixes
    • Portioning into single-use or bulk test kit formats
    • Labeling and serial number assignment based on regulatory geography

    Final product types

    • Enzyme activity assay kits (for research or diagnostics)
    • Cell-based screening reagent kits
    • In vitro kinase testing controls

    3. Cell Culture Reagent Manufacturing for Signal Transduction Studies

    Producers of customized cell culture supplements use Kenpaullone for applications in stem cell differentiation and signal transduction pathway modulation. Formulation chemists blend precise amounts of Kenpaullone with basal media or serum replacements under ISO-certified cleanroom conditions. This component helps research institutions conduct controlled pathway inhibition experiments. Traceability, batch segregation, and endotoxin control are enforced for all cGMP-grade reagents intended for cellular research relevant to pharmacological profiling or toxicological assessment.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • ISO 13485:2016 for production of research-use-only (RUO) reagents
    • USP Chapter <797> for sterile compounding (if supplied as media additive)
    • REACH Regulation EC 1907/2006 (if supplied in the EU as a lab chemical)

    Typical usage ratio

    • Final concentration 1–10 μM in culture medium; adjusted case-by-case after viability and cytotoxicity screening

    Downstream process integration

    • Direct addition to cell culture at experiment start or induction phase
    • Batched preparation as bulk cell culture additive under standard operating procedures
    • Documentation for lot tracking and research reporting

    Final product types

    • Stem cell induction media kits
    • Pathway modulation supplements for cell-based assays
    • High-content screening media for pharmaceutical research

    4. Chemical Biology Tool Manufacturing for Academic and CRO Supply

    Specialty chemical suppliers and contract research organizations (CROs) integrate Kenpaullone in chemical probe libraries used for pathway mapping, kinase selectivity testing, and target validation services. Bulk intermediates undergo repackaging under inert environments followed by analytical confirmation using NMR, MS, and HPLC systems. Products require labeling that meets local chemical safety, transport, and laboratory use regulations. Storage and handling follow ISO-based protocols for academic or CRO bulk supply. Compliance documentation supports both institutional procurement and grant-funded research.

    Industry compliance standards

    • REACH EC 1907/2006 chemical registration (for EU non-pharmaceutical supply)
    • OECD Good Laboratory Practice (GLP) Principles
    • GHS/CLP chemical labeling requirements
    • SDS in accordance with OSHA 29 CFR 1910.1200

    Typical usage ratio

    • 5–50 mg per library entry or probe batch; determined by inventory needs and planned experimental scale

    Downstream process integration

    • Formulation of chemical probe libraries for kinase selectivity panels
    • Packaging in sealed vials, with barcoding for inventory traceability
    • QC testing and third-party verification prior to release for academic and CRO shipment

    Final product types

    • Annotated chemical probe sets for research institutions
    • Kinase inhibitor panels for contract screening services
    • Reference materials for bioanalytical method validation
    Free Quote

    Competitive Kenpaullone prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to sales7@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: sales7@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Kenpaullone: A Closer Look from the Manufacturer’s Perspective

    Introduction to Kenpaullone

    Kenpaullone attracts attention across biotechnology and pharmaceutical research for its reliable inhibition of cyclin-dependent kinases and glycogen synthase kinase-3. Our production teams see consistent demand from scientists who explore cell cycle regulation and neurodegenerative disease pathways. Delivering this compound to labs with strict control over consistency has shown us what matters most: precise purity, traceable batch quality, and the practical needs of real working researchers.

    We recognize that the environment in which Kenpaullone performs is fast-moving and competitive. Each lot we produce follows detailed analytical protocols overseen by quality assurance chemists with decades behind them. The result is a product that meets the performance standards imposed by both regulatory authorities and leading research institutions.

    Understanding the Product

    Kenpaullone originates from the paullone family of small molecule inhibitors. Featuring the molecular formula C15H13N3O, this compound stands out for its selective inhibition profile targeting CDK1/cyclin B, CDK2/cyclin A, CDK5/p25, and GSK-3β. In our labs, chemists follow procedures that minimize batch-to-batch variability. We purify using state-of-the-art chromatographic techniques, and every lot comes through hands accustomed to spotting subtle impurities others might miss. Experience has shown that small differences in impurity profile can have broad consequences for reproducibility, especially in cell-based assay work.

    Researchers working with neuroblastoma, Alzheimer’s models, or β-catenin signaling appreciate Kenpaullone’s ability to cross into cell membranes without significant modification. We have seen labs prioritize this trait because they need compounds that perform in both in vitro and in vivo settings. To support such experiments, our product is delivered as an off-white crystalline powder, typically packaged in sealed, amber-glass vials under inert atmosphere. This packaging choice reflects the sensitivity of Kenpaullone to light and moisture, a factor we realized through years of field feedback rather than simply following standard shipping templates.

    Precision and Reliability: Manufacturing Considerations

    Sourcing high-quality Kenpaullone requires more than reacting precursors together. Our facility relies on validated synthetic routes, using high-purity solvents and reagents certified by our internal quality team. Early attempts at production showed us the pitfalls—side products and unwanted isomers cropped up, affecting both shelf life and performance. To address this, we invested in high-resolution mass spectrometry and NMR for final product verification. Every release hits a minimum of 98% HPLC purity, with water content and residual solvent levels controlled to parts per million. These decisions grew from witnessing the frustration researchers faced with off-the-shelf material from less rigorous suppliers.

    Years of batch history have proven the value of detailed tracking. Each batch we ship carries a full certificate of analysis and a unique identifier. No matter how far Kenpaullone travels, researchers can always trace it back to the day it was made and the controls it went through. This transparency gives confidence to labs who need absolute reliability for cell signaling pathway studies.

    Key Differences from Similar Molecules

    Kenpaullone often gets mentioned alongside other kinase inhibitors like roscovitine, purvalanol, and indirubin derivatives. We receive questions daily from customers comparing potency, selectivity, and solubility. Our technical support team regularly discusses how, while roscovitine shows good CDK inhibition, Kenpaullone provides stronger and broader GSK-3 inhibition. In side-by-side trials, Kenpaullone displays lower IC50 values for GSK-3β (around 23 nM) versus a few alternatives. This extra potency finds value in studies of tau phosphorylation and Wnt signaling, where subtle changes in enzyme activity tell the story of health or disease.

    Another important distinction comes through the handling and formulation of the compound. Some related molecules, as we have observed, suffer from lower solubility or greater sensitivity to oxidation in standard storage conditions. In our facility, we witnessed reduced shelf life in comparable products due to exposure to ambient light and humidity. By double-layer packaging and vacuum-sealing, we helped researchers avoid experimental inconsistencies due to material degradation.

    Usage in the Laboratory

    Scientists in our network often use Kenpaullone to disrupt cell cycle progression in cancer cell lines. The compound’s ability to stall cells in G2/M phase supports mechanistic studies in oncology, while the inhibition of GSK-3 opens exploration of neuronal differentiation, apoptosis, and metabolic signaling. Our team receives regular feedback on how Kenpaullone helps clarify signaling ambiguities in both stem cell and neurobiology experiments.

    Some researchers use concentrations ranging from micromolar to sub-micromolar, depending on their assay. Solubility in DMSO, confirmed by our direct testing, means Kenpaullone dissolves quickly and completely before dilution in culture media. We advise users to avoid extended storage of DMSO stock solutions at room temperature, after observing degradation patterns in our own stability studies. Many lessons in the handling of Kenpaullone came not from literature, but from years of supporting labs who needed their controls to remain consistent week after week.

    Our customers often emphasize the importance of precise weighing and solution preparation. Even minor errors lead to significant changes in final results, given Kenpaullone’s potency. We recommend calibrating balances regularly and using low-binding tubes, based on what we saw during our own in-house protocol development.

    Safety and Handling

    Kenpaullone is a research chemical, not intended for therapeutics or food. We stress the importance of following solid laboratory safety procedures. Our facility’s occupational health protocols require gloves, safety glasses, and use of chemical fume hoods during weighing and solution preparation. These recommendations evolved from real incidents—a minor skin exposure many years ago in our plant led to updated guidelines and extra attention to personal protective equipment.

    We emphasize careful waste disposal. Organic solvents used to dissolve Kenpaullone, along with contaminated tips or vials, go through approved disposal streams, reducing risk to people and the environment. Sharing what worked in our production lab proved to be a useful guide for many partners developing their laboratory management plans.

    Supporting Reproducibility in Life Science Research

    Manufacturers have a responsibility to support reproducibility, especially with high-impact tools like Kenpaullone. We observed that inconsistencies in critical reagents contribute to irreproducible results, something that damages trust across the scientific ecosystem. Our own stability testing uses forced degradation studies over months, uncovering hidden vulnerabilities. For Kenpaullone, we found light-induced breakdown occurs faster than literature suggests, prompting us to overhaul our packaging and handling recommendations.

    Every time we revise our protocols, the goal remains clear: minimize risks for scientists, regardless of whether their research involves oncology, neurology, or developmental biology. Customers rely on manufacturers to flag known issues before they derail projects. We learned early that close collaboration, not just sales, closes gaps in the supply chain.

    From Our Quality Control Archive

    Tracking Kenpaullone production for a decade shows patterns invisible to newcomers. In our earliest years, we underestimated the impact of trace residual acids on NMR spectra—only after extensive feedback rounds with users did we modify our neutralization and solvent-removal steps. The shift improved HPLC chromatograms and eliminated unexplained peaks.

    More recently, a routine audit flagged a mild uptick in ethanol residue across several batches. Rather than dismiss it, our analytical team traced the issue to a change in glassware washing solvents. By returning to our previous rinse protocol, we restored product cleanliness and, just as important, preserved trust among our most detail-oriented customers.

    Only manufacturers with long operational memory develop this type of sensitivity to batch quirks. Each adjustment, whether in raw material sourcing or drying time tweaks, translates to more reliable Kenpaullone for researchers who cannot afford experimental surprises.

    Feedback and Ongoing Partnership

    The best advice about Kenpaullone often comes from the users themselves. We hold annual focus groups for chemists, biologists, and academic partners. From this process, two common concerns arise—batch consistency and transparency in product history. We take these seriously, offering not just batch traceability, but raw analytical data when requested.

    Feedback has shaped more than production. At the urging of several research groups, we began offering custom aliquoting to match specific experimental needs. Many researchers appreciated smaller, ready-to-use vials, which reduced freeze-thaw cycles and kept their studies on schedule.

    By embedding feedback into our process, Kenpaullone’s properties continue to support its role in research, not just as a product on a shelf, but as a tool trusted by its most demanding users.

    Storage and Stability Insights

    Stability ranks high among researcher concerns. Over the years, we have learned how much temperature swings and improper storage can erode the predictability of Kenpaullone. Our plant maintains a rigorous cold chain, with dedicated storage areas kept between 2°C and 8°C. In the rare case of power interruptions, backup systems engage immediately. Early in our journey, a single temperature incident taught us the cost—a portion of production needed to be scrapped, and going forward, every lot shipped is tracked with temperature indicators.

    We recommend storing Kenpaullone in closed vials, away from direct light and humidity. This advice stems from actual degradation studies carried out in our facility, where we subjected samples to high humidity and found visible changes within weeks. Real-world data leads us to recommend opening vials only when ready to prepare solutions, and aliquoting larger supplies into single-use portions.

    If researchers track inventory turnover closely, our team provides planning support, ensuring laboratories receive quantities that match consumption rates. Avoiding unnecessary open-vial storage mitigates risk and preserves both physical and chemical stability.

    Environmental Footprint and Sustainable Practices

    Manufacturing advanced research chemicals carries environmental responsibilities. We noticed early that solvent usage and energy demand during production cycles contribute to emissions and waste streams. Years ago, inefficient washing processes created excess solvent waste. By installing in-line solvent recyclers and updating purification columns, we slashed solvent use while maintaining purity standards. Every small adjustment accumulates—saving water, reducing energy draw, and ultimately making each batch of Kenpaullone with less environmental impact.

    Many of our institutional clients ask about sourcing and environmental stewardship. We share audit summaries from our sustainability team, covering everything from solvent recycling rates to waste neutralization. These steps came from internal targets, set after we examined our impact and found room for improvement. Sharing both successes and shortcomings with the research community spurs better practices industry-wide.

    The journey toward sustainability continues. Investments in closed-loop water cooling and smart energy control help keep our operations efficient, ensuring that progress in the life sciences does not come at the environment’s expense.

    Commitment to Research and Development

    In-house R&D enables us to constantly refine our Kenpaullone offerings. Our chemists experiment with greener synthesis routes, alternative raw materials, and automated process controls. Discoveries from this work directly influence the experience researchers have at the bench.

    Last year, a trial to incorporate flow chemistry showed promise, reducing reaction times and boost yields. Although not yet implemented at full scale, these studies continue. Our technical team remains committed to continuous improvement, driven by what we have learned from scientists using Kenpaullone in cutting-edge applications.

    We remain searchable and accountable. Engaged collaboration with universities and research consortia keeps us adaptable and informed about new scientific directions. This ongoing dialogue ensures Kenpaullone meets the shifting needs of life science research, not just today, but well into tomorrow.

    Conclusion: What Years of Manufacturing Kenpaullone Teach

    Every gram of Kenpaullone shipped connects us to research on the front lines of disease biology and cellular signaling. We take pride in supporting breakthroughs, drawing from a history of meticulous attention to detail, transparent process controls, and conversations with those who use what we manufacture. Each change, every lesson learned, and all feedback channels amount to more than incremental upgrades—they build a foundation of trust between manufacturer and scientist.

    Kenpaullone’s strength as a kinase inhibitor remains closely linked to how it’s made, handled, and delivered. It builds its reputation in real laboratories, under real working conditions, where reproducibility and trust matter more than brochures or datasheets. As manufacturers, our greatest contribution lies in the reliability, safety, and partnership we provide to the scientific community. We welcome inquiries, ideas, and demands for ever-better performance—the push and pull that moves research forward.