CA19-9 inhibitors, a class of compounds in the field of medicinal chemistry, are designed to target and modulate the activity of the CA19-9 antigen, a carbohydrate antigen that is overexpressed in certain pathological conditions, particularly pancreatic and gastrointestinal cancers. These inhibitors belong to a broader category of biomarker-targeting agents, which are of immense significance in the early diagnosis and monitoring of cancer progression. CA19-9 itself is a sialylated Lewis blood group antigen, primarily found on the surface of epithelial cells and circulating glycoproteins. Elevated levels of CA19-9 in the bloodstream are commonly associated with malignant tumors, making it a valuable biomarker for cancer detection and management.
The development of CA19-9 inhibitors typically involves the design and synthesis of small molecules or macromolecules that can specifically interact with CA19-9 antigens, hindering their detection or impeding their biological function. This interaction can occur through various mechanisms, including competitive binding, structural modification of the antigen, or interference with its production and release. Researchers employ a range of chemical and biochemical strategies to create these inhibitors, often incorporating functional groups that enhance binding affinity and selectivity. The ultimate goal is to produce compounds that can effectively reduce CA19-9 levels. CA19-9 inhibitors represent an important facet of cancer research, with the ability to revolutionize the early detection and management of malignancies.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
2′-Deoxy-2′,2′-difluorocytidine | 95058-81-4 | sc-275523 sc-275523A | 1 g 5 g | $56.00 $128.00 | ||
Incorporates into DNA and inhibits replication | ||||||
Fluorouracil | 51-21-8 | sc-29060 sc-29060A | 1 g 5 g | $37.00 $152.00 | 11 | |
Inhibits thymidylate synthase, disrupting DNA synthesis | ||||||
Erlotinib, Free Base | 183321-74-6 | sc-396113 sc-396113A sc-396113B sc-396113C sc-396113D | 500 mg 1 g 5 g 10 g 100 g | $87.00 $135.00 $293.00 $505.00 $3827.00 | 42 | |
Targets EGFR tyrosine kinase, inhibiting cell growth | ||||||
Regorafenib | 755037-03-7 | sc-477163 sc-477163A | 25 mg 50 mg | $320.00 $430.00 | 3 | |
Multi-kinase inhibitor, including VEGFR, PDGFR, and RAF | ||||||
Lapatinib | 231277-92-2 | sc-353658 | 100 mg | $420.00 | 32 | |
Dual EGFR and HER2 inhibitor | ||||||
Sorafenib | 284461-73-0 | sc-220125 sc-220125A sc-220125B | 5 mg 50 mg 500 mg | $57.00 $100.00 $250.00 | 129 | |
Multi-kinase inhibitor, including VEGFR, PDGFR, and RAF | ||||||
Oxaliplatin | 61825-94-3 | sc-202270 sc-202270A | 5 mg 25 mg | $112.00 $394.00 | 8 | |
Forms DNA cross-links, disrupting replication and transcription | ||||||