Date published: 2025-12-24

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HHCM Inhibitors

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 NameCAS #Catalog #QUANTITYPriceCitationsRATING

Sorafenib

284461-73-0sc-220125
sc-220125A
sc-220125B
5 mg
50 mg
500 mg
$56.00
$260.00
$416.00
129
(3)

Sorafenib is a kinase inhibitor that targets RAF/MEK/ERK signaling, VEGFR, and PDGFR.

Regorafenib

755037-03-7sc-477163
sc-477163A
25 mg
50 mg
$320.00
$430.00
3
(0)

Regorafenib is a multi-kinase inhibitor used for affecting HCC, targeting angiogenesis and oncogenic pathways.

Lenvatinib

417716-92-8sc-488530
sc-488530A
sc-488530B
5 mg
25 mg
100 mg
$178.00
$648.00
$1657.00
3
(0)

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

849217-68-1sc-364657
sc-364657A
5 mg
10 mg
$92.00
$204.00
1
(1)

Cabozantinib, a tyrosine kinase inhibitor, targets MET, VEGFR, and AXL, used for advanced HCC.

Trametinib

871700-17-3sc-364639
sc-364639A
sc-364639B
5 mg
10 mg
1 g
$112.00
$163.00
$928.00
19
(1)

Trametinib, a MEK inhibitor, may be used in experimental therapies for HCC.

Everolimus

159351-69-6sc-218452
sc-218452A
5 mg
50 mg
$128.00
$638.00
7
(1)

Everolimus is an mTOR inhibitor..

Oxaliplatin

61825-94-3sc-202270
sc-202270A
5 mg
25 mg
$110.00
$386.00
8
(1)

Oxaliplatin is sometimes used in combination therapies for HCC.

Fluorouracil

51-21-8sc-29060
sc-29060A
1 g
5 g
$36.00
$149.00
11
(1)

5-FU is an agent used for cancer, including HCC.