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Chengdu Beite Denuo Pharmaceutical Co., Ltd.

  • Founded in:

    2018-01-30
  • Country:

    China China
  • Address:

    No. 66, Kelin Road West Section, Chengdu Cross-Strait Science and Technology Industrial Development Park, Wenjiang District, Chengdu
  • Tax NO.:

    91510115MA6CA1BY4U
  • Registered Funds:

    182.776863 yuan
  • Email:

Related Drugs
Hydroxycamptothecin injection
The main ingredient of this product is hydroxycamptothecin. Chemical name: (S)-4,9-dihydroxy-4-ethyl-1H-pyrano[3',4':6,7]indolizine[1,2b]quinoline-3,14-(4H,12H)-dione. Chemical structure: Molecular formula: C20H16N2O5 Molecular weight: 364.36 Auxiliary materials: sodium hydroxide, l-cysteine.
Name Description Content CAS NO. Registered Holders
Hydroxyl camptothecine

Cell cycle specific drugs mainly act on the S phase and selectively inhibit DNA topoisomerase I (TOPOI). By inhibiting the activity of TOPOI, it blocks DNA replication and transcription, interfering with the proliferation cycle of tumor cells. It may also induce tumor cell differentiation and apoptosis.

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Cell cycle specific drugs mainly act on the S phase and selectively inhibit DNA topoisomerase I (TOPOI). By inhibiting the activity of TOPOI, it blocks DNA replication and transcription, interfering with the proliferation cycle of tumor cells. It may also induce tumor cell differentiation and apoptosis.

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Etoposide Injection
Active ingredient: Etoposide.
Name Description Content CAS NO. Registered Holders
Etoposide

This product is a cell cycle-specific anti-tumor drug that acts on DNA topoisomerase II to form a stable reversible complex of drug-enzyme-DNA, which hinders DNA repair. Experiments have found that this complex can be reversed with the elimination of the drug, allowing the damaged DNA to be repaired and reducing cytotoxicity. Therefore, extending the drug administration time may increase the anti-tumor activity.

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This product is a cell cycle-specific anti-tumor drug that acts on DNA topoisomerase II to form a stable reversible complex of drug-enzyme-DNA, which hinders DNA repair. Experiments have found that this complex can be reversed with the elimination of the drug, allowing the damaged DNA to be repaired and reducing cytotoxicity. Therefore, extending the drug administration time may increase the anti-tumor activity.

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