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S-1 single

Sun Yat-sen University · Phase 3 active Small molecule

S-1 is an oral combination chemotherapy agent that inhibits thymidylate synthase and other folate metabolism enzymes to disrupt DNA synthesis in cancer cells.

S-1 is an oral combination chemotherapy agent that inhibits thymidylate synthase and other folate metabolism enzymes to disrupt DNA synthesis in cancer cells. Used for Gastric cancer, Colorectal cancer, Pancreatic cancer.

At a glance

Generic nameS-1 single
Also known asS-1
SponsorSun Yat-sen University
Drug classOral fluoropyrimidine combination
TargetThymidylate synthase, dihydrofolate reductase
ModalitySmall molecule
Therapeutic areaOncology
PhasePhase 3

Mechanism of action

S-1 combines tegafur (a prodrug of 5-fluorouracil), gimeracil (an inhibitor of dihydropyrimidine dehydrogenase), and oteracil potassium (an inhibitor of orotate phosphoribosyltransferase). This triple combination enhances 5-FU bioavailability and reduces gastrointestinal toxicity by modulating fluoropyrimidine metabolism, leading to prolonged anti-tumor effects.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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