HHCM inhibitors represent a specialized class of compounds designed to target and inhibit specific enzymatic or molecular mechanisms associated with the HHCM (Hypothetical Heterogeneous Catalytic Mechanism) pathway. The concept of inhibition in this context typically refers to the ability of these chemicals to bind to active sites or allosteric regions of enzymes or proteins within the HHCM pathway, thereby altering the normal catalytic function or modulating the structural dynamics of the involved biomolecules. The exact molecular interactions can vary based on the inhibitor's structure, which may include hydrogen bonding, hydrophobic interactions, van der Waals forces, and coordination with metal cofactors if applicable. The inhibition process often results in the alteration of downstream molecular processes, potentially leading to changes in the activity of catalytic centers or a decrease in the production of reaction intermediates.
The structural diversity of HHCM inhibitors is broad, encompassing both small organic molecules and larger macromolecular agents that have been engineered or designed to interfere with specific catalytic processes. These compounds may demonstrate selectivity for their targets through structural complementarity, whereby the inhibitor fits precisely into a binding pocket or interacts with key residues of the enzyme or molecular complex in question. Additionally, the inhibitory effect can vary between reversible and irreversible mechanisms, depending on how the inhibitor interacts with the target. Reversible inhibitors typically form non-covalent interactions, allowing for dissociation under certain conditions, while irreversible inhibitors form covalent bonds, leading to permanent deactivation of the catalytic function. The study of HHCM inhibitors provides valuable insights into the underlying biochemistry of complex catalytic processes and serves as a platform for developing more refined chemical agents to study specific molecular systems.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Sorafenib | 284461-73-0 | sc-220125 sc-220125A sc-220125B | 5 mg 50 mg 500 mg | $56.00 $260.00 $416.00 | 129 | |
Sorafenib is a kinase inhibitor that targets RAF/MEK/ERK signaling, VEGFR, and PDGFR. | ||||||
Regorafenib | 755037-03-7 | sc-477163 sc-477163A | 25 mg 50 mg | $320.00 $430.00 | 3 | |
Regorafenib is a multi-kinase inhibitor used for affecting HCC, targeting angiogenesis and oncogenic pathways. | ||||||
Lenvatinib | 417716-92-8 | sc-488530 sc-488530A sc-488530B | 5 mg 25 mg 100 mg | $178.00 $648.00 $1657.00 | 3 | |
Lenvatinib is a multi-targeted kinase inhibitor, effective in HCC, particularly against VEGFR1-3, FGFR1-4, PDGFR alpha, RET, and KIT. | ||||||
XL-184 free base | 849217-68-1 | sc-364657 sc-364657A | 5 mg 10 mg | $92.00 $204.00 | 1 | |
Cabozantinib, a tyrosine kinase inhibitor, targets MET, VEGFR, and AXL, used for advanced HCC. | ||||||
Trametinib | 871700-17-3 | sc-364639 sc-364639A sc-364639B | 5 mg 10 mg 1 g | $112.00 $163.00 $928.00 | 19 | |
Trametinib, a MEK inhibitor, may be used in experimental therapies for HCC. | ||||||
Everolimus | 159351-69-6 | sc-218452 sc-218452A | 5 mg 50 mg | $128.00 $638.00 | 7 | |
Everolimus is an mTOR inhibitor.. | ||||||
Oxaliplatin | 61825-94-3 | sc-202270 sc-202270A | 5 mg 25 mg | $110.00 $386.00 | 8 | |
Oxaliplatin is sometimes used in combination therapies for HCC. | ||||||
Fluorouracil | 51-21-8 | sc-29060 sc-29060A | 1 g 5 g | $36.00 $149.00 | 11 | |
5-FU is an agent used for cancer, including HCC. | ||||||