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Cat. No. Product Name Information
PC-26664

CNS-11D

Alpha-synuclein inhibitor

CNS-11D is a small molecule pathological tau tibrils disassembler that disaggregates brain-extracted tau fibrils in vitro and in vivo.
PC-26657

Gαo-IN-1

Gαo inhibitor

Gαo-IN-1 is a specific small-molecule inhibitor of neuronal G protein Gαo (encoded by GNAO1 gene), decreases the GTP binding rate of Gαo.
PC-26649

mtCI modulator C273

Mitochondrial complex I inhibitor/modulator

mtCI modulator C273 is a selective, brain-penetrant, orally bioavailable small molecule modulator/ weak inhibitor of mitochondrial complex I (mtCI) with IC50 of 201.5 uM, protects against Aβ toxicity through mtCI modulation.
PC-26639

Auxinole

Auxin antagonist

Auxinole is a potent auxin antagonist of TIR1/AFB receptors, binding TIR1 to block the formation of the TIR1-IAA-Aux/IAA complex and inhibits auxin-responsive gene expression.
PC-26624

S720-2261

FIBCD1 inhibitor

S720-2261 is a small molecule inhibitor of FIBCD1 (Fibrinogen C domain-containing protein 1) with SPR KD of 585 uM.
PC-26623

CTI-2

PNC inhibitor

CTI-2 is a small molecule inhibitor of perinucleolar compartment (PNC), shows potential anti-AML activity against FLT3-ITD mutant AML.
PC-26621

BCAT2 inhibitor C11

BACT2 inhibitor

BCAT2 inhibitor C11 is a potent, selective branched-chain amino acid transaminase 2 (BCAT2) inhibitor with IC50 of 54 nM.
PC-26620

BCAT2 inhibitor C10

BACT2 inhibitor

BCAT2 inhibitor C10 is a potent, selective branched-chain amino acid transaminase 2 (BCAT2) inhibitor with IC50 of 44 nM.
PC-26619

BCAT2-IN-2

BACT2 inhibitor

BCAT2-IN-2 is a potent, selective, in-vivo efficacious BCATm (BCAT2) inhibitor with pIC50 of 7.3, 100-fold selective for BCATm over BCATc.
PC-26618

BCAT2-IN-1

BACT2 inhibitor

BCAT2-IN-1 is a potent, selective, in-vivo efficacious BCATm (BCAT2) inhibitor with pIC50 of 7.3, 100-fold selective for BCATm over BCATc.
PC-26617

BAY-771

BAY-069 control

BAY-771 is a negative control compound of dual BCAT1/2 inhibitor BAY-069.
PC-26616

BAY-252

BACT1/BACT2 inhibitor

BAY-252 is a potent branched-chain amino acid transaminases 1 (BCAT1) and BCAT2 inhibitor with IC50s of 2 μM and 2 μM, respectively.

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