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Cat. No. Product Name Information
PC-72887

FECH inhibitor 4e

Ferrochelatase inhibitor

FECH inhibitor 4e (FECH-IN-4e) is a potent, specifc, competitive inhibitor of ferrochelatase (FECH) with IC50 in the high-nanomolar range.
PC-72885

LCS3

GSR inhibitor

LCS3 is a small molecule that selectively impairs the growth of human lung adenocarcinoma (LUAD) cells, induces oxidative stress, inhibits glutathione disulfide reductase (GSR) and thioredoxin reductase 1 (TXNRD1) with IC50 of 3.3 and 3.8 uM, respectively.
PC-72877

CW5107

HSD17B7 inhibitor

CW5107 (CW 5107) is a small molecule HSD17B7 inhibitor that enhances oligodendrocyte formation.
PC-72876

CW4142

SC4MOL inhibitor

CW4142 (CW 4142) is a small molecule SC4MOL inhibitor that enhances oligodendrocyte formation.
PC-72871

NERx 329

RPA inhibitor

NERx 329 (RPAi 329, NERx329) is a novel potent, specific inhibitor of replication protein A (RPA), demonstrated potent RPA inhibitory activity in vitro, in vivo, and in cellular assays.
PC-72865

MN132.0262

APOBEC3G inhibitor

MN132.0262 is a small molecule, dual inhibitor of A3G (APOBEC3G, IC50=20 uM).
PC-72864

MN256.0102

APOBEC3G inhibitor

MN256.0102 is a small-molecule APOBEC3G DNA cytosine deaminase inhibitor with IC50 of 3.9 uM.
PC-72863

MN256.0105

APOBEC3G inhibitor

MN256.0105 is a small-molecule APOBEC3G DNA cytosine deaminase inhibitor with IC50 of 4.3 uM.
PC-72855

Pixatimod

Heparanase inhibitor

Pixatimod (PG545) is a heparan sulfate (HS) mimetic and anticancer agent and a potent inhibitor of heparanase.
PC-72846

Simufilam hydrochloride

Filamin A corrector

Simufilam hydrocloride (PTI-125) is a small molecule targeting scaffolding protein filamin A (FLNA), preferentially binds altered FLNA and restores its native conformation.
PC-72845

PTI-125

Filamin A corrector

PTI-125 (Simufilam, Sumifilam) is a small molecule targeting scaffolding protein filamin A (FLNA), preferentially binds altered FLNA and restores its native conformation.
PC-72843

RAGE229

RAGE inhibitor

RAGE229 (RAGE-229) is a specific antagonist of ctRAGE-DIAPH1 interaction, high potently binds to cytoplasmic tail of RAGE (ctRAGE) with KD of 2 nM.

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