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Cat. No. Product Name Information
PC-61225

DFPM

Abscisic acid inhibitor

DFPM is a small molecule that rapidly downregulates abscisic acid (ABA)-dependent gene expression (IC50=3 and 1.5 uM for RD29B and RAB18 promoters), also inhibits ABA-induced stomatal closure.
PC-61214

Pyrimidinone 8

DMT1 inhibitor

Pyrimidinone 8 is a novel allosteric, non-competitive divalent metal transporter-1 (SLC11A2/DMT1) inhibitor with Ki of 20 uM.
PC-61208

Ferristatin II

Iron transport inhibitor

Ferristatin II (NSC 8679, NSC8679, Chlorazol Black) is a small molecule iron transport inhibitor that promotes degradation of transferrin receptor-1 in vitro and in vivo, through a nystatin-sensitive lipid raft pathway.
PC-61207

NSC 306711

Iron transport inhibitor

NSC 306711 (Ferristatin, NSC306711) is a small-molecule iron transport inhibitor that promotes degradation of the transferrin receptor independent of clathrin and dynamin, is sensitive to the cholesterol-depleting agents filipin and nystatin.
PC-70268

Shz-1

Nkx2.5 inducer

Shz-1 is a small cardiogenic molecule that potently induces Nkx2.5 and a subset of other cardiac markers, including myocardin, troponin-I, and sarcomeric α-tropomyosin (SαTM) in a variety of different stem/progenitor cells.
PC-70267

Shz-3

Nkx2.5 inducer

Shz-3 is a small cardiogenic molecule that potently induces Nkx2.5 and a subset of other cardiac markers, including myocardin, troponin-I, and sarcomeric α-tropomyosin (SαTM) in a variety of different stem/progenitor cells.
PC-70265

RNase L-IN-2

RNase L-IN-2 is a small-molecule activator of RNase L with EC50 of 22 uM.
PC-70260

Compound A5

AP-1 inhibitor

Compound 5431942 (Compound 5431942) is a small molecule that specifically inhibits the clathrin adaptor complex AP-1-dependent traffic, does not significantly affect other pathways through the trans-Golgi network (TGN).
PC-70257

Furin-IN-1d

Furin inhibitor

Furin-IN-1d is a small molecule furin inhibitor with Ki of 22 nM.
PC-70255

INP-0400

INP-0400 is a small-molecule inhibitor of type III secretion in Y. pseudotuberculosis, without affecting in vitro multiplication, causes a dose- and growth phase-dependent inhibition of C. trachomatis RB multiplication.
PC-70254

AUDA

sEH inhibitor

AUDA is a potent inhibitor of sEH (soluble epoxide hydrolase) with IC50 of 18 nM and 69 nM for mouse sEH and human sEH, respectively.
PC-70252

CUDA

sEH inhibitor

CUDA is a potent inhibitor of sEH (soluble epoxide hydrolase) with IC50 of 11.1 nM and 112 nM for mouse sEH and human sEH, respectively.

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