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Cat. No. Product Name Information
PC-45088

SP-420

Iron chelating agent

Petadeferitrin (SP-420) is a desferrithiocin analogue and iron chelating agent that has iron-clearing efficiency with ICE value of 26.7, SP-420 is more potent than desferrithiocin.
PC-45513

HQ-415

Metal chelator, TDP-43 modulator

HQ-415 is a derivative of 8-hydroxyquinoline that has selectivity for rescuing the distinct toxicities caused by the expression of TDP-43 with EC50 of 15 uM, α-synuclein or polyglutamine proteins.
PC-42072

BAPTA

Mg2+ chelator

BAPTA is a cell-permeant, calcium-specific chelator with high selectivity over Mg2+.
PC-45623

GW4869

nSMase inhibitor

GW-4869 (GW4869, GW 4869) is a cell-permeable, potent, specific, non-competitive inhibitor of neutral sphingomyelinase (nSMase) with IC50 of 1 uM.
PC-42082

TPEN

LIN28 inhibitor

TPEN (TPEDA) is a potent, cell-permeable inhibitor of LIN28 that abolishes LIN28-mediated oligouridylation with IC50 of 2.5 uM, also is a specific cell-permeable heavy metal chelator.
PC-42281

GGTI298

GGTase I inhibitor

GGTI298 (GGTI-298) is a CAAZ peptidomimetic geranylgeranyltransferase I (GGTase I) inhibitor that inhibits the processing of geranylgeranylated Rap1A with little effect on processing of farnesylated Ha-Ras (IC50s are 3 and >10 uM respectively).
PC-28178

Naringenin

DENV RdRp inhibitor, MARK4 inhibitor

Naringenin is a flavanone in Citrus reticulata Blanco within anti-inflammatory and antioxidant activities, monocarboxylate transporter 1 (MCT1) in Caco-2 cells with Ki of 15-20 uM, also inhibits DENV RNA-dependent RNA polymerase (RdRp), is also a potent inhibitor of MARK4 with IC50 of 4.11 uM.
PC-28145

FM029

FOXP3-T-bet stabliezer

FM029 is a direct FOXP3 targeting small molecule that binds to FOXP3 (SPR KD=1.13 uM), stabilizes the FOXP3-T-bet interaction to represses T-bet-driven IFN-γ production.
PC-28105

SEP-227900

DAAO inhibitor

SEP-227900 is an orally active small molecule D-amino-acid oxidase (DAAO) inhibitor.
PC-28104

AS057278

DAAO inhibitor

AS057278 (MPCA, U-19425) is a potent, selective, orally active and blood-brain barrier (BBB) penetrant D-amino acid oxidase (DAAO) inhibitor with IC50 of 0.91 uM, shows potential anti-psychotic properties, also inhibits adipocyte lipolysis.
PC-28054

MOG (35-55) mouse, rat

MOG peptide

MOG (35-55) mouse, rat is a myelin oligodendrocyte glycoprotein (MOG) peptide derived from the extracellular domain of MOG protein and key immunodominant epitope extensively utilized in the study of autoimmune demyelinating diseases of the central nervous system (CNS), induce experimental autoimmune encephalomyelitis (EAE) in susceptible animal models, particularly C57BL/6 mice.
PC-28053

MOG(35-55) amide Mouse, Rat

MOG peptide

MOG(35-55) peptide (mouse/rat sequence) is a myelin oligodendrocyte glycoprotein (MOG) peptide derived from the extracellular domain of MOG protein and key immunodominant epitope extensively utilized in the study of autoimmune demyelinating diseases of the central nervous system (CNS), induce experimental autoimmune encephalomyelitis (EAE) in susceptible animal models, particularly C57BL/6 mice.

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