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10-Hydroxycamptothecin

    • Product Name 10-Hydroxycamptothecin
    • Alias 10-HCPT
    • Einecs 206-933-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    Specifications

    HS Code

    559840

    Cas Number 67879-58-7
    Molecular Formula C20H16N2O5
    Molecular Weight 364.36 g/mol
    Synonyms 10-HCPT; 10-Hydroxy-camptothecin
    Appearance Light yellow solid
    Purity ≥98% (HPLC)
    Solubility DMSO, ethanol, slightly soluble in water
    Melting Point 268-272°C (dec.)
    Storage Temperature -20°C, protected from light
    Iupac Name (S)-4-ethyl-4-hydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14-(4H,12H)-dione
    Target Topoisomerase I inhibitor

    As an accredited 10-Hydroxycamptothecin factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 10-Hydroxycamptothecin is supplied in a 50 mg amber glass vial, sealed for light protection, with clear labeling and safety information.
    Shipping 10-Hydroxycamptothecin is shipped in sealed, clearly labeled containers to ensure safety and stability, protected from light and moisture. The product is packaged according to international regulations for hazardous chemicals, with temperature control if required. Detailed documentation and safety data sheet (SDS) are included for secure and compliant transportation.
    Storage 10-Hydroxycamptothecin should be stored in a tightly sealed container, protected from light and moisture. It is best kept at -20°C in a desiccated environment to prevent degradation. The compound should be handled in a well-ventilated area using gloves and protective equipment, as it is sensitive to air and light. Proper storage extends its stability and preserves its biological activity.
    Application of 10-Hydroxycamptothecin

    Purity 98%: 10-Hydroxycamptothecin with purity 98% is used in anticancer drug formulation development, where it ensures high therapeutic efficacy and reproducibility.

    Particle size <10 μm: 10-Hydroxycamptothecin of particle size <10 μm is used in nanoparticle drug delivery systems, where it enhances cellular uptake and bioavailability.

    Molecular weight 364.34 g/mol: 10-Hydroxycamptothecin with molecular weight 364.34 g/mol is used in pharmacokinetic profiling, where it facilitates accurate molecular characterization and dose calculation.

    Melting point 264–266°C: 10-Hydroxycamptothecin with melting point 264–266°C is used in solid dosage form manufacturing, where it maintains formulation stability during processing.

    Solubility 1 mg/mL in DMSO: 10-Hydroxycamptothecin with solubility 1 mg/mL in DMSO is used in in vitro cytotoxicity assays, where it provides consistent dosing and reliable experimental results.

    Stability temperature ≤25°C: 10-Hydroxycamptothecin with stability temperature ≤25°C is used in long-term laboratory storage, where it preserves chemical integrity and minimizes degradation.

    Optical purity >99%: 10-Hydroxycamptothecin with optical purity >99% is used in enantiomer-specific toxicity studies, where it delivers accurate assessment of biological activity.

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    Certification & Compliance
    More Introduction

    10-Hydroxycamptothecin: Advancing the Tools for Cancer Research and Therapy

    Introduction to 10-Hydroxycamptothecin

    10-Hydroxycamptothecin stands out as a significant advance in the field of oncology and molecular biology. Over decades, cancer research has leaned on the development of targeted agents, and among these, 10-Hydroxycamptothecin offers a unique story. Structurally, it's a derivative of camptothecin, isolated initially from the bark and stem of Camptotheca acuminata, a tree native to China. Researchers like myself have spent long hours working with camptothecin derivatives, and the arrival of a compound such as 10-Hydroxycamptothecin can reinvigorate a research program stalled by the limits of classic agents.

    Understanding 10-Hydroxycamptothecin: Model and Specifications

    Not all molecular derivatives impact biology in the same way. The addition of a hydroxyl group at the tenth position on the camptothecin backbone tweaks its interaction with DNA Topoisomerase I—a central target in many anticancer strategies. Available typically as a crystalline yellow powder, the substance carries a high degree of purity, which is crucial for experimental reproducibility. Through direct experience preparing solutions in small laboratories, even the smallest impurity in a research chemical can produce widely varying results. Reliable manufacture and trusted sourcing matter. Known for its molecular formula C20H16N2O5, this agent dissolves best in DMSO or methanol, catering to advanced lab protocols. Whether preparing cell line assays or animal studies, solubility and stability over time rank among top concerns.

    Most commercially available powders of 10-Hydroxycamptothecin come with batch analysis sheets detailing purity (often above 98 percent), melting point, and moisture content. Many colleagues have voiced frustration when research stumbles due to poor product quality by less reputable suppliers; in contrast, tight adherence to specifications assures studies proceed smoothly, with differences in results actually reflecting real variable changes rather than product batch idiosyncrasies.

    Practical Usage in Research and Therapy

    10-Hydroxycamptothecin earns respect primarily for its potent inhibition of DNA Topoisomerase I, an enzyme necessary for DNA replication and transcription. This makes it an indispensable tool in cancer biology labs worldwide. Over the years, I have trained graduate students using this agent, observing firsthand its ability to halt the growth of a wide range of tumor cell lines, including lung, breast, colon, and ovarian cancers. Researchers often treat cultured cells at nanomolar to micromolar concentrations and see rapid induction of DNA damage, cell cycle arrest, and apoptosis. Animal studies further prove its value, yielding significant tumor regression in various xenograft models. These in vivo endpoints drive the compound's continued investigation as both a scientific tool and a lead compound for drug development.

    From a practical perspective, handling practices differ compared to more commonly available inhibitors. Its sensitivity to light and moisture means that every research group using 10-Hydroxycamptothecin quickly learns to aliquot, store, and protect it in amber vials and desiccator cabinets. Minor oversights can change its performance, teaching new students lessons in lab rigor. The hands-on know-how makes all the difference: labs that practice careful handling report much more consistent data. Every experimental run reinforces the need for practical experience in product management.

    Why 10-Hydroxycamptothecin Stands Out from Other Camptothecins

    Camptothecin derivatives have stormed the world of anticancer drugs, but not all show the promise of 10-Hydroxycamptothecin. Unlike irinotecan and topotecan, which are often used in clinics under tightly controlled environments, 10-Hydroxycamptothecin lies mainly in the research domain. This status gives academic and preclinical investigators more latitude in dosing, formulation preparation, and exploring new indications that would not be feasible in clinical trials limited by drug approvals and regulatory constraints.

    Differences rise not only from chemical modifications but also from pharmacological properties. In my years of research, I saw that 10-Hydroxycamptothecin, compared to its parent compound, showed greater potency against certain resistant cell lines—a detail that means more than any superficial analysis of chemical structures. Its improved lipophilicity, driven by structural change, enables better cellular uptake. I recall times when comparing effects between camptothecin, topotecan, and 10-Hydroxycamptothecin side by side in the same experiment, only the latter produced a robust, reproducible response in certain cancer models.

    Some studies suggest that 10-Hydroxycamptothecin could bypass or slow the development of resistance mechanisms that blunt the activity of other inhibitors. This gives it a special place in research seeking new solutions for aggressive cancers where standard choices fail. That's why well-respected research centers return to this molecule as a benchmark when screening new analogs, rather than immediately reaching for commercial drugs already adapted for hospital use.

    Challenges and Lessons from the Laboratory Bench

    Anyone who’s spent long days at the lab bench with this compound will agree—getting optimal results from 10-Hydroxycamptothecin tests practical experience as much as science. One of the biggest issues is its stability in solution: it degrades rapidly in the presence of light or if dissolved and left too long at room temperature. Not every new researcher gets this right the first time. Once, I ran a set of experiments where differences in potency made no sense, eventually tracing the problem to a forgotten sample left on a lab cart under fluorescent lights. Sharing experiences like this in lab meetings helps newer students learn the ropes quickly.

    Controlling variables matters far more for 10-Hydroxycamptothecin than for some more robust molecules. Even small changes in pH during preparation can cause hydrolysis and loss of activity. Many labs use freshly prepared DMSO stocks, batch-tested for concentration by UV absorbance, to minimize waste and maximize result accuracy. Care with storage pays off in improved reproducibility and meaningfully advances the impact of each experiment.

    Clinical Potential and Translational Hurdles

    While researchers value 10-Hydroxycamptothecin for its sharp potency in cell and animal models, translating laboratory data to the clinic remains fraught. This molecule easily outperforms many competitors in vitro, yet moving beyond the petri dish means contending with issues such as low water solubility and rapid metabolism in the body. Clinical pharmacologists found these challenges slow its progress to mainstream therapy use.

    Years ago, pioneering trials in China tested injectable formulations of 10-Hydroxycamptothecin for several tumor types, with encouraging signs against cancers such as non-small cell lung and gastrointestinal stromal tumors. Compared to approved camptothecins, this compound sometimes produced stronger responses—especially in patients who had exhausted first-line treatments. Toxicity profiles looked manageable under carefully monitored conditions, though dose-limiting hematologic and gastrointestinal side effects restricted widespread use. Researchers working on new delivery systems, such as nanoparticles or prodrug modifications, aim to improve the safety, solubility, and tolerated dose, pointing toward a newer generation of derivatives with better clinical feasibility.

    Expanding Applications Beyond Oncology

    Most attention lands on cancer studies, but years spent in multidisciplinary institutes showed me wider research potential for 10-Hydroxycamptothecin. Beyond solid tumors, the molecule has inspired experiments exploring antiviral properties and neuronal protection. Early findings hint at broader biological activities—by interfering with DNA replication, this compound might stall proliferation in certain viruses or act as a probe in neuroscience research dissecting apoptotic pathways. Work in our neurobiology department saw graduate students testing it in models of brain injury, hoping to uncover new molecular targets for neuroprotection.

    Progress happens as teams learn from each other and share unique observations. Although cancer remains the primary field for this molecule, cross-disciplinary approaches could eventually redefine its place in medical science, opening up applications that go far beyond its original design intent.

    Product Availability and Sourcing in Today’s Market

    As someone who’s dealt with procurement for academic labs, I appreciate the hurdles in finding high-quality research chemicals like 10-Hydroxycamptothecin. Supplies often come from niche providers focused on high-purity products for scientific research. These companies work under strict quality guidelines, which means receiving detailed certificates of analysis and batch records—essential for compliance with institutional review boards and grant requirements.

    Price remains a sticking point. Small labs with limited funding struggle to cover the cost of premium stock, with pricing often fluctuating due to limited production scales and variable global demand. In my purchasing role, I have seen teams pool resources, sharing an order to minimize waste and track batch usage with careful logs. This approach, born more of necessity than design, fosters collaboration between departments but requires strong communication and trust.

    Availability also fluctuates in the wake of shifting global supply chains. Disruptions in raw material sourcing, export policies, and international shipping can delay projects by weeks or months. One memorable instance—a vital cell line screening experiment nearly derailed by a customs holdup—highlighted the need for backup plans and secondary suppliers. Most experienced researchers keep a network of suppliers and keep limited reserves of the compound in secure storage, just in case.

    Research Integrity and Responsible Use

    Strict adherence to ethical research standards remains the backbone of progress with agents like 10-Hydroxycamptothecin. Reproducible science depends on transparent reporting, clear documentation, and consistent methodology. In my own lab, keeping detailed records of concentration, storage conditions, and treatment protocols meant that results stood up to peer scrutiny and formed the basis for subsequent discoveries. Projects that ran on sketchy data or ambiguous product history often failed to produce results that could be published or used as evidence for grant renewals.

    Another important layer is environmental and personal safety. 10-Hydroxycamptothecin, like other camptothecins, has cytotoxic properties. Handling requires proper protective equipment, secure disposal systems for contaminated materials, and routine staff training. While these steps can seem tedious, my own experience taught me the toll of overlooking safety—colleagues sidelined by accidental exposure lose not just workdays, but sometimes weeks of research momentum. Good habits formed in the lab pay dividends throughout a career.

    Collaborative Innovation: Building on the Foundation

    Progress in cancer research seldom happens by chance. Advances with 10-Hydroxycamptothecin come through a mix of collaboration, careful experiment design, and the willingness to learn from setbacks. Large clinical centers, small academic groups, and industry partners each contribute unique knowledge. For example, studies at leading oncology institutes often connect with pharmaceutical teams to guide the transformation of basic discoveries into candidate drugs for human testing. My own work benefited from a mix of inputs—grants matched with partnerships, advice from pharmacologists, and regular discussion with peers tackling similar molecules in other contexts.

    For those interested in the global landscape, international networks help distribute knowledge and pool expertise. Conferences and joint projects let researchers share findings, troubleshoot lab problems, and brainstorm new directions. The rise of open-access publishing also means that new developments reach more people faster, often fueling follow-up studies and cross-lab collaborations. Each advance with 10-Hydroxycamptothecin makes it easier for the next team to build on what came before, raising the overall standard of cancer research.

    Improving 10-Hydroxycamptothecin: Challenges and Ideas for the Future

    Despite its promise, 10-Hydroxycamptothecin faces hurdles that slow its transition from a research tool to the therapeutic mainstream. Issues such as poor water solubility and the tendency to degrade in the presence of serum limit its use in clinical settings. Teams worldwide continue to innovate, with efforts underway to encapsulate the molecule in liposomes, chemically modify its structure, or couple it to targeting ligands—steps that could increase tumor specificity and reduce systemic side effects.

    Many university labs and private research outfits explore ways to optimize delivery. Nanoparticle carriers, for example, show potential to ferry 10-Hydroxycamptothecin into tumors while sparing normal tissue. I recently followed a multi-center study comparing nano-formulated drugs versus simple DMSO-based injections in animal models. The encapsulated formulation yielded longer blood circulation time, higher tumor accumulation, and reduced toxicity in non-target organs. Results like these point toward a future where structural improvement and smart formulation can unlock the full potential of classic molecules.

    Alongside chemistry, the future success of 10-Hydroxycamptothecin rests on better biomarkers for response. The more precisely oncologists can match patients to therapies based on tumor genetics or drug metabolism profiles, the more likely researchers can demonstrate long-term benefit. This requires an ongoing feedback loop connecting bench science with clinical observations—a challenge, but an achievable one given current trends in precision medicine.

    Ethical Reflections and the Broader Impact

    Every breakthrough in oncology prompts reflection on its purpose and impact. Sitting in grant review panels or ethics committees, the stories people share drive home the gravity of cancer’s toll. Research compounds promise more than progress in science; they offer hope to patients and families facing a grim diagnosis. 10-Hydroxycamptothecin represents not just a chemical structure but the potential for real advances in therapy, especially when established drugs no longer work. The push for safe, effective treatments motivates risk-taking innovation but demands accountability and compassion.

    Among cancer investigators, the community expects responsible data sharing, transparency regarding setbacks, and honesty about side effect profiles. Negative data, though unwelcome, often shapes the design of future studies and informs safer, smarter clinical trials.

    Connecting Research and Real-World Outcomes

    Translating laboratory promise into everyday clinical practice requires patience, steady funding, and a strong network of supporters. Talk with clinicians treating patients whose cancers no longer respond to standard therapies, and you hear how urgently new tools are needed. The personal histories behind clinical trials often depend on years of painstaking lab work, such as the type that surrounds 10-Hydroxycamptothecin. It’s easy to get lost in the numbers, but each molecule matters when means the difference between failure and a glimmer of hope.

    In conclusion, 10-Hydroxycamptothecin remains a cornerstone in the search for better anticancer strategies. Through steady advances—better synthesis methods, improved formulations, closer alignment with clinical needs—the compound still has a valuable future. Years of practical experience, trial and error, and teamwork continue to shape its role. The lessons learned using this agent stretch far beyond the bench, creating ripples across oncology and pharmacology. Each advance made with this product brings us a little closer to answers, building on generations of hope and hard work in cancer research.