Converts to 5-FU (5-fluorouracil) via thymidine phosphorylase
Induces apoptosis through caspase activation
Down-regulates NF-κB
Upregulates caspase-3 and caspase-9
May down-regulate p53 in single treatment
[1]
An orally administered chemotherapeutic agent that is metabolized to 5-fluorouracil (5-FU) in the body
[2]
Chemotherapeutic agent for colorectal cancer
Part of regimens like FOLFOX or as monotherapy
Combination with irinotecan and 17-AAG for enhanced apoptosis
Treatment of HT-29 colon cancer cells
[1]
First-line treatment for metastatic colorectal cancer (mCRC); used in combination therapy with PD-1 inhibitors
[2]
Classification by use
Chemicals used in cancer chemotherapy
Chemicals used as prodrugs
Chemicals used as apoptosis inducers
[1]
Chemotherapy agent
[2]
A trustworthy factory and manufacturer
[Cite:1] Combination effects of capecitabine, irinotecan and 17-AAG on colorectal cancer cell line (HT-29), Annals of Medicine and Surgery, Volume 78, June 2022, 103850
[Cite:2] Intratumoral microbiota-derived S1P sensitizes the combination therapy of capecitabine and PD-1 inhibitors, Iscience, Volume 28, Issue 12, 19 December 2025, 114202