(S)-()-Camptothecin

≥99%(HPLC)

  • Product Code: 127033
  Alias:    Camptothecin; 4-Ethyl-4-hydroxy-1H-pyran[3',4':6,7]indolizine[1,2]quinoline-3,14(4H,12H)-dione
  CAS:    7689-03-4
Molecular Weight: 348.35 g./mol Molecular Formula: C₂₀H₁₆N₂O₄
EC Number: MDL Number: MFCD00081076
Melting Point: 260 °C (dec.)(lit.) Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: Used primarily in cancer treatment, it inhibits the enzyme topoisomerase I, which is crucial for DNA replication in cancer cells. This action leads to the interruption of DNA synthesis and induces apoptosis in malignant cells. It serves as a key precursor for synthesizing more potent chemotherapeutic agents like irinotecan and topotecan, which are FDA-approved for treating colorectal and ovarian cancers, respectively. Additionally, ongoing research explores its potential in combating other diseases, including viral infections and autoimmune disorders, due to its mechanism of action on cellular DNA processes.
Product Specification:
Test Specification
Purity (%) 99-100
Appearance Light Yellow To Brown Powder Or Crystals Or Solid
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days £40.26
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-
1.000 10-20 days £90.24
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5.000 10-20 days £290.85
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(S)-()-Camptothecin
Used primarily in cancer treatment, it inhibits the enzyme topoisomerase I, which is crucial for DNA replication in cancer cells. This action leads to the interruption of DNA synthesis and induces apoptosis in malignant cells. It serves as a key precursor for synthesizing more potent chemotherapeutic agents like irinotecan and topotecan, which are FDA-approved for treating colorectal and ovarian cancers, respectively. Additionally, ongoing research explores its potential in combating other diseases, including viral infections and autoimmune disorders, due to its mechanism of action on cellular DNA processes.
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