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Cat. No. Product Name Information
PC-62916

PSB-12379

CD73 inhibitor

PSB-12379 is an α,β-Methylene-ADP (AOPCP) derivative, potent, selective ecto-5′-Nucleotidase (eN, CD73) inhibitor with Ki of 9.03/2.21 nM for rat/human recombinant eN.
PC-62880

DDD85646

NMT1/NMT2 inhibitor

DDD 85646 is a potent, specific, dual N-Myristoyltransferase NMT1/NMT2 inhibitor with IC50 of 17 nM/22 nM respectively.
PC-62875

STK16-IN-1

STK16-IN-1 is a potent, highly selective ATP competitive STK16 inhibitor with IC50 of 0.295 uM, displays excellent selectivity across the kinome.
PC-62874

ARN726

NAAA inhibitor

ARN726 is a potent, selective, orally bioavailable N-acylethanolamine acid amidase (NAAA) inhibitor with IC50 of 63 nM (r-NAAA) and 27 nM (h-NAAA).
PC-62873

ARN077

NAAA inhibitor

ARN077 is the first potent, selective N-acylethanolamine acid amidase (NAAA) inhibitor with IC50 of 7 nM on both rat NAAA and human NAAA.
PC-62861

PNPLA4-IN-1

PNPLA4 inhibitor

PNPLA4-IN-1 is a potent, selective, and irreversible PNPLA4 (patatin-like phospholipase domain-containing protein 4) inhibitor with IC50 of 1.8 uM (separated membrane proteome fraction), shows in-cell inhibition of PNPLA4 with IC50 of 11.7 uM.
PC-62860

PF-6808472

PF-6808472 (XO44) is a sulfonyl fluoride chemical probe that covalently labels a broad swath of the intracellular kinome with high efficiency.
PC-62859

SB1301

Lin28 inhibitor

SB1301 (LIN28-Let-7 inhibitor) is a small-molecule inhibitor disrupting the protein-RNA interaction of LIN28 and Let-7 with FRET IC50 of 4 uM.
PC-62825

CCG-203971

Rho/MKL1/SRF inhibitor

CCG-203971(CCG203971) is a potent Rho/MKL1/SRF transcriptional pathway inhibitor, suppresses PC-3 cell migration in scratch wound assays (IC50=4.2 uM), blocks nuclear localization and activity of MRTF-A in SK-Mel-147 cells.
PC-62824

CCG-232601

MRTF/SRF inhibitor

CCG-232601 is a potent (IC50=0.55 uM), orally bioavailable inhibitor of Rho/MRTF/SRF transcriptional pathway that target transcriptional factor MRTF.
PC-62786

VU6001221

Choline transporter inhibitor

VU6001221 is a potent choline transporter (CHT) inhibitor with IC50 of 270 nM.
PC-62785

ML352

Choline transporter inhibitor

ML352 (VU0476201) is a potent, selective choline transporter (CHT) inhibitor with Ki of 92 nM.

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