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Cat. No. Product Name Information
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.
PC-72839

BOS-318

Furin inhibitor

BOS-318 (BOS318) is a potent, highly selective, cell-permeable furin inhibitor with IC50 of 1.9 nM, Ki of 0.4 nM.
PC-72838

KM04794

UPR inhibitor

KM04794 (KM-04794) is a chemical chaperone-like small molecule modulator of endoplasmic reticulum (ER) proteostasis and alleviates ER stress, inhibits UPR signaling with IC50 of 10 uM.
PC-72833

ChemR23 inhibitor 14f

ChemR23 inhibitor

ChemR23 inhibitor 14f is a potent and orally active inhibitor of ChemR23 (IC80=12 nM), a G protein-coupled receptor (GPCR) expressed on the surface of plasmacytoid dendritic cells (pDCs).
PC-72831

Nek1 inhibitor 10f

Nek1 inhibitor

Nek1 inhibitor 10f is a potent, selective NIMA-related kinase 1 (Nek1) inhibitor with IC50 of 330 nM.
PC-72819

SID7969543

SF-1/NR5A1 inhibitor

SID7969543 is a potent, selective and cell penetrant inhibitor of steroidogenic factor 1 (SF-1/NR5A1) with IC50 of 760 nM, also selectively targets KMT2A-rearranged (KMT2A-r) leukemia cells.
PC-72817

BACH2 inhibitor compound 8

BACH2/BACH1 inhibitor

BACH2 inhibitor compound 8 is a potent, dual BACH2/BACH1 inhibitor.
PC-72813

SOCS1 inhibitor 20

SOCS1 inhibitor

SOCS1 inhibitor 20 is a specific, cell-permeable phosphotyrosine peptide that target the SH2 domain of SOCS1 (Suppressor of cytokine signaling 1) with IC50 of 20 nM (hSOCS1)
PC-72812

TLX agonist 10

TLX (NR2E1) agonist

TLX agonist 10 is potent, selective agonist of the orphan nuclear receptor tailless homologue (TLX, NR2E1) with pEC50 of 6.6.
PC-72801

HB007

SUMO1 degrader

HB007 (HB-007) is a small-molecule degrader of the small ubiquitin-related modifier 1 (SUMO1) with anticancer potency in vitro and in vivo.

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