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Phytosphingosine is a phospholipid with anti-inflammatory, antibacterial, and anti-cancer activities, and can induce apoptosis. It is an immune regulator and can be used in the study of inflammatory skin diseases. Phytosphingosine is also an activator of GPR120 with an IC50 value of 33.4 μM and can be used in the study of type II diabetes.
Phospholipid with anti-inflammatory, antibacterial, and anti-cancer activities.
Induces apoptosis.
Immune regulator.
Activator of GPR120.
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Methylamino-PEG4-Boc is a polyethylene glycol (PEG)-based PROTAC linker that can be used in the synthesis of PROTACs. PROTACs contain two different ligands connected by a linker: one for an E3 ubiquitin ligase and the other for the target protein. These molecules exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
PEG-based PROTAC linker
Can be used in the synthesis of PROTACs
Contains two different ligands connected by a linker
Exploits the ubiquitin-proteasome system
Selectively degrades target proteins
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Phytosphingosine (4-Hydroxysphinganine) is a phospholipid that exhibits anti-inflammatory, antibacterial, and anti-cancer properties. It functions as an immune regulator and an activator of GPR120 with an IC50 value of 33.4 μM. This compound is useful for research into inflammatory skin diseases and type II diabetes.
Induces apoptosis
Effective against inflammation
Possesses antibacterial activity
Exhibits anti-cancer activities
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6-(Dimethylamino)purine is a serine threonine protein kinase inhibitor that can affect various cellular processes. It is used in research to study cellular mechanisms.
Inhibits prolactin-induced expression of lactoprotein genes in rabbit mammary gland cells.
Affects the maturation of mammalian oocytes.
Leads to downregulation of genes related to cell proliferation and cell cycle progression.
Induces apoptosis in lymphoma cells.
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WCK-4234 is a research-grade β-lactamase inhibitor that targets class A, C, and D enzymes. It has no intrinsic antibacterial activity but enhances the effect of carbapenem antibiotics such as imipenem and meropenem against resistant Enterobacteriaceae, including strains with OXA-type carbapenemases. Intended for laboratory research use only.
Inhibits class A, C, and D β-lactamases.
Potentiates carbapenem activity against resistant Enterobacteriaceae.
Effective against OXA-type carbapenemase-mediated resistance.
Supplied with high purity suitable for biochemical and microbiological studies.
Molecular weight 269.21 g·mol⁻1 and formula C7H8N3NaO5S.
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3-Azetidinemethanol hydrochloride (CAS 928038-44-2) is a nitrogen-containing heterocyclic compound commonly utilized as an intermediate in the synthesis of SHP2 inhibitors SHP2 a protein tyrosine phosphatase plays a regulatory role in cellular signaling pathways that control cell proliferation differentiation and migration Dysregulation of SHP2 function has been implicated in the development of various diseases including cancer By enabling the preparation of SHP2 inhibitors 3-Azetidinemethanol hydrochloride supports research aimed at elucidating the effects of SHP2 inhibition on cellular signaling pathways and exploring novel therapeutic strategies
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