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camptothecin analogue

" in MedChemExpress (MCE) Product Catalog:

13

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1

Natural
Products

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-12486
    FL118
    3 Publications Verification

    10,11-(Methylenedioxy)-20(S)-camptothecin

    Survivin Apoptosis IAP Cancer
    FL118 (10,11-(Methylenedioxy)-20(S)-camptothecin), a Camptothecin (HY-16560) analogue, is a potent and orally active survivin inhibitor. FL118 binds to oncoprotein DDX5 (p68) to dephosphorylates and degrades DDX5. FL118 can be used for the research of cancer .
    FL118
  • HY-13566
    Belotecan
    2 Publications Verification

    CKD-602 free base

    Topoisomerase Apoptosis Cancer
    Belotecan (CKD-602 free base) is a DNA topoisomerase I inhibitor. Belotecan induces cell apoptosis and cell-cycle arrest. Belotecan is a camptothecin analogue with anti-tumor effects, it can be used for the research of cancer .
    Belotecan
  • HY-B0063

    ST1481

    Topoisomerase Cancer
    Gimatecan (ST1481) is a potent topoisomerase I inhibitor. Gimatecan is an orally bioavailable camptothecin analogue with antitumor activity .
    Gimatecan
  • HY-156513

    7-Hydroxyethyl carbamate-(10Me-11F-camptothecin)

    ADC Payload Cancer
    ZD06519 (7-Hydroxyethyl carbamate-(10Me-11F-Camptothecin)) is a camptothecin (HY-16560) analogue and a topoisomerase I inhibitor. ZD06519 is an ADC cytotoxin with a strong bystander effect, inhibiting a variety of malignancies such as HER2-positive and FRα-overexpressing tumors. ZD06519 inhibits DNA cleavage, relaxation, and reconnection processes, inducing tumor cell death. ZD06519 can be used for ADC synthesis and cancer research .
    ZD06519
  • HY-148058

    Topoisomerase Cancer
    Topoisomerase I inhibitor 8 is a potent topoisomerase I inhibitor. Topoisomerase I inhibitor 8 is a hexacyclic analogue of camptothecin, and displays cytotoxic effect against tumor cells .
    Topoisomerase I inhibitor 8
  • HY-156516

    ADC Payload Topoisomerase Cancer
    10NH2-11F-Camptothecin is a Camptothecin (HY-16560) analogue that serves as an ADC cytotoxin for the synthesis of antibody-drug conjugates (ADCs). 10NH2-11F-Camptothecin can inhibit tumor growth and is used in cancer research .
    10NH2-11F-Camptothecin
  • HY-13566R

    CKD-602 free base (Standard)

    Topoisomerase Apoptosis Reference Standards Cancer
    Belotecan (Standard) is the analytical standard of Belotecan. This product is intended for research and analytical applications. Belotecan (CKD-602 free base) is a DNA topoisomerase I inhibitor. Belotecan induces cell apoptosis and cell-cycle arrest. Belotecan is a camptothecin analogue with anti-tumor effects, it can be used for the research of cancer .
    Belotecan (Standard)
  • HY-156516A

    ADC Payload Topoisomerase Cancer
    10NH2-11F-Camptothecin TFA is a Camptothecin (HY-16560) analogue that serves as an ADC cytotoxin for the synthesis of antibody-drug conjugates (ADCs). 10NH2-11F-Camptothecin TFA has anticancer effects (WO2022246576A1; compound 140) .
    10NH2-11F-Camptothecin TFA
  • HY-156517

    ADC Payload Topoisomerase Cancer
    7Ethanol-10NH2-11F-Camptothecin is a Camptothecin (HY-16560) analogue that serves as an ADC cytotoxin for the synthesis of antibody-drug conjugates (ADCs). 7Ethanol-10NH2-11F-Camptothecin can inhibit tumor growth and is used in cancer research .
    7Ethanol-10NH2-11F-Camptothecin
  • HY-122014

    Topoisomerase Others
    39625 is a camptothecin ketone analogue, a stable, potent and selective topoisomerase I inhibitor, active against purified topoisomerase I and cytotoxic to cancer cells.
    S 39625
  • HY-N12944

    Drug Derivative Infection Cancer
    18-Hydroxycamptothecin is a camptothecin analogue that can be isolated from Camptotheca acuminata. Camptothecin compounds possess potential activities such as anti-cancer and anti-viral properties .
    18-Hydroxycamptothecin
  • HY-160829

    Cositecan-NH2; BNP 1350-NH2

    Drug Derivative Cancer
    Karenitecin-NH2 (Cositecan-NH2) (DB-173) is a Camptothecin (HY-16560) analogue with antitumor activity .
    Karenitecin-NH2
  • HY-12898

    LPL Receptor Apoptosis Inflammation/Immunology
    (S)-FTY-720 Vinylphosphonate is a chiral phosphonate analogue of Fingolimod (HY-11063). (S)-FTY-720 Vinylphosphonate can activate the S1P1 receptor with an EC50 value of 75 nM. (S)-FTY-720 Vinylphosphonate can significantly inhibit Camptothecin (HY-16560)-induced apoptosis in IEC-6 cells. (S)-FTY-720 Vinylphosphonate is applicable for the research of autoimmune diseases .
    (S)-FTY-720 Vinylphosphonate

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