Discovery of Potent and Selective 7-Ethyl-10-hydroxycamptothecin-Glucose Conjugates for Colorectal Cancer Treatment

Novel SN38-glucose conjugates offer enhanced efficacy and targeted delivery for colorectal cancer therapy.

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Key Advantages

Enhanced Potency

These novel anticancer agents for CRC treatment demonstrate significantly higher potency compared to existing therapies, offering a more effective approach to combating cancer.

Improved Selectivity

The conjugates exhibit improved selectivity, ensuring better delivery to tumor sites and minimizing damage to healthy tissues, a key aspect of selective chemotherapy for colorectal cancer.

Reduced Side Effects

By targeting cancer cells specifically, these compounds are expected to lead to fewer adverse effects, improving patient tolerance and quality of life during treatment.

Key Applications

Colorectal Cancer Therapy

Specifically designed for efficacy against colorectal cancer, these conjugates represent a new frontier in novel anticancer compound synthesis.

Targeted Drug Delivery

The application of glucose transporter targeted drug delivery principles opens avenues for treating various cancers with overexpressed glucose transporters.

Pharmaceutical Research

These compounds serve as valuable tools in pharmaceutical research, aiding the understanding of cancer metabolism and drug resistance mechanisms.

Oncology Drug Development

As promising candidates for preclinical oncology drug development, they offer a potential new treatment option for patients with limited therapeutic choices.