(S)-10-Hydroxycamptothecin CAS 19685-09-7

120580

Synonyms: 10-HCPT, Hydroxycamptothecine

500 mg € 120
1 g € 170
2,5 g € 320
5 g € 580
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Cat. No. NST-10-204
CAS 19685-09-7
Purity 98% (HPLC)
Appearance Yellow Powder
Molecular formula C20H16N2O5
Molecular weight 364,35
Storage store in a cool & dry place, keep away from strong light and heat

Certificate of analysis available by request to [email protected]

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Description

(S)-10-Hydroxycamptothecin: Potent Topoisomerase I Inhibitor for Advanced Cancer Research

1. Molecular Identity

  • Chemical Name: (S)-4-ethyl-4-hydroxy-1H-pyrano[3′,4′:6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione
  • CAS Number: 19685-09-7
  • Source: Semi-synthetic derivative of camptothecin, originally isolated from Camptotheca acuminata

2. Biochemical Significance

(S)-10-Hydroxycamptothecin is a potent topoisomerase I inhibitor with enhanced solubility compared to its parent compound, camptothecin. Its unique structure and mechanism of action make it a compound of significant interest in cancer research and drug development.

3. Key Properties

  • Topoisomerase I Inhibition: Potent activity against DNA topoisomerase I
  • Anticancer Potential: Exhibits strong cytotoxicity against various cancer cell lines
  • Improved Solubility: Enhanced aqueous solubility compared to camptothecin
  • S-Configuration: Demonstrates superior biological activity over the R-isomer

4. Potential Research Applications

  • Cancer drug development and optimization
  • Structure-activity relationship studies of camptothecin analogues
  • Investigation of topoisomerase I-mediated DNA damage and repair
  • Development of novel drug delivery systems for camptothecin derivatives

5. Current Research Focus

Ongoing studies are investigating (S)-10-Hydroxycamptothecin’s effects on:

  • Various cancer types, including drug-resistant tumors
  • Combination therapies with other anticancer agents
  • Nanoformulations for improved drug delivery
  • Mechanisms of resistance to topoisomerase I inhibitors

6. Formulation Challenges and Innovations

Researchers are actively working on:

  • Enhancing stability of the active lactone form
  • Developing targeted delivery systems for improved efficacy
  • Creating prodrug formulations for optimized pharmacokinetics

7. Regulatory Considerations

As a research compound, (S)-10-Hydroxycamptothecin (CAS 19685-09-7) is primarily used in preclinical studies. Its development for therapeutic use would require extensive safety and efficacy evaluations to meet regulatory standards.

8. Future Research Directions

The scientific community anticipates:

  • Advanced preclinical and potential clinical trials for specific cancer indications
  • Development of novel (S)-10-Hydroxycamptothecin conjugates and analogues
  • Exploration of its potential in non-cancer applications, such as antiviral research

9. Collaborative Opportunities

We invite cancer researchers, medicinal chemists, pharmaceutical scientists, and academic institutions to explore the research potential of (S)-10-Hydroxycamptothecin. For inquiries, collaborations, or to discuss how this compound can benefit your research projects, please contact us at [email protected].

Join us in advancing cancer research with (S)-10-Hydroxycamptothecin – a key player in the development of next-generation topoisomerase I inhibitors.