Oncology pathway explorer
Glycolysis
Scientific explanation
Aerobic (Warburg metabolism) supports ATP, biomass and redox buffering even when oxygen is available. Hexokinase, PKM2 and lactate export are frequent nodes.
Cancers where relevant
Compounds that intersect this pathway
Modest complex I inhibition raises AMP:ATP, activating and restraining hepatic and -linked anabolism. Direct antineoplastic efficacy is not established from that pharmacology alone.
Evidence in mapped cancers: Clinical / Human Evidence · In Vivo · In Vitro · Mechanistically Plausible
Benzimidazole that binds β-. Mammalian disruption, mitotic arrest and related signalling in cancer models are preclinical and are not an approved anticancer use.
Veterinary benzimidazole with and experimental glucose-transport effects in cell models. Not an established human antineoplastic.
Evidence in mapped cancers: In Vitro · Hypothesis-Generating
Benzimidazole anthelmintic with effects; mammalian oncology readouts remain preclinical.
AMP mimetic that activates in experimental systems. Research tool, not an approved oncology medicine.
Berberine
Isoquinoline alkaloid that can inhibit complex I and activate in metabolic models, with additional -independent reports. Not an approved antineoplastic.
Convergence partners
Other pathways that co-occur with Glycolysis on mapped adjunct records: AMPK, mTOR, Apoptosis.
This oncology atlas is educational. Pathway maps, adjunctive strategies, and compound listings describe mechanistic relevance. They do not establish clinical efficacy, do not recommend treatment, and are not a substitute for oncology care. Evidence tiers are not equivalent.