Date published: 2025-10-10

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OIP106 Inhibitors

OIP106 Inhibitors represent a class of chemical compounds that have garnered significant attention in the field of biomedical research and drug discovery due to their potential role in modulating specific cellular processes. These inhibitors are characterized by their ability to selectively target and block the activity of OIP106, a specific protein or enzyme found within biological systems. The acronym "OIP" likely stands for "Overexpressed in Psoriasis," indicating a potential link between OIP106 and dermatological conditions, although it is essential to note that the exact biological functions of OIP106 remain an active area of investigation.

The development and study of OIP106 Inhibitors have primarily revolved around understanding the structural and biochemical properties of OIP106, as well as elucidating its functional significance within cells and tissues. Researchers have employed various techniques, including X-ray crystallography and computational modeling, to gain insights into the three-dimensional structure of OIP106 and to design inhibitors that can specifically bind to and inhibit its activity. These inhibitors may function by disrupting key interactions between OIP106 and its cellular substrates, potentially leading to alterations in signaling pathways or other cellular processes. As a result, OIP106 Inhibitors hold promise as research tools for studying the biology of OIP106.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Ibrutinib

936563-96-1sc-483194
10 mg
$153.00
5
(0)

Ibrutinib is a covalent inhibitor that irreversibly binds to and inhibits the Bruton's tyrosine kinase (BTK), a key enzyme involved in B-cell signaling. This disruption of signaling pathways leads to decreased B-cell proliferation and survival.

Imatinib

152459-95-5sc-267106
sc-267106A
sc-267106B
10 mg
100 mg
1 g
$25.00
$117.00
$209.00
27
(1)

Imatinib is a tyrosine kinase inhibitor targeting the BCR-ABL fusion protein in chronic myeloid leukemia (CML). It also inhibits other kinases like KIT and PDGF receptors, reducing cell proliferation and angiogenesis.

Gefitinib

184475-35-2sc-202166
sc-202166A
sc-202166B
sc-202166C
100 mg
250 mg
1 g
5 g
$62.00
$112.00
$214.00
$342.00
74
(2)

Gefitinib inhibits the epidermal growth factor receptor (EGFR) tyrosine kinase, hindering signal transduction pathways that promote cell growth.

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 multi-kinase inhibitor that targets RAF kinases and the vascular endothelial growth factor receptor (VEGFR), among others.

Olaparib

763113-22-0sc-302017
sc-302017A
sc-302017B
250 mg
500 mg
1 g
$206.00
$299.00
$485.00
10
(1)

Olaparib is a poly(ADP-ribose) polymerase (PARP) inhibitor, interfering with DNA repair mechanisms in cancer cells. It is studied in the research of BRCA-mutated ovarian and breast cancers.

Ruxolitinib

941678-49-5sc-364729
sc-364729A
sc-364729A-CW
5 mg
25 mg
25 mg
$246.00
$490.00
$536.00
16
(1)

Ruxolitinib inhibits Janus kinases (JAK1 and JAK2), downregulating cytokine signaling and reducing inflammation.

Lapatinib

231277-92-2sc-353658
100 mg
$412.00
32
(1)

Lapatinib is a dual tyrosine kinase inhibitor targeting both EGFR and HER2. It disrupts signaling pathways involved in cell proliferation.

Dasatinib

302962-49-8sc-358114
sc-358114A
25 mg
1 g
$47.00
$145.00
51
(1)

Dasatinib inhibits multiple tyrosine kinases, including BCR-ABL, SRC, and others.