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Cat. No. Product Name Information
PC-26403

GPR61 inverse agonist 15

GPR61 inverse agonist

GPR61 inverse agonist 15 is a potent, selective, and brain-penetrant GPR61 inverse agonist with cAMP functional IC50 of 6.2 nM and 20 nM for human and mouse GPR61 respectively.
PC-26402

GPR61 inverse agonist 23

GPR61 inverse agonist

GPR61 inverse agonist 23 is a potent, selective, and brain-penetrant GPR61 inverse agonist with cAMP functional IC50 of 4.0 nM and 8.8 nM for human and mouse GPR61 respectively.
PC-26391

ONO-7068506

GCLC inhibitor

ONO-7068506 (GCLCi1) is a potent, selective glutamylcysteine ligase catalytic subunit (GCLC) inhibitor, shows potent anti-tumor effects in SMARCB1-deficient cancer cells.
PC-26390

ONO-6428513

GCLC inhibitor

ONO-6428513 (GCLCi0) is a potent, selective glutamylcysteine ligase catalytic subunit (GCLC) inhibitor, shows potent anti-tumor effects in SMARCB1-deficient cancer cells.
PC-26378

Z-5891

COPS3 inhibitor

Z-5891 is a highly selective COPS3 inhibitor, exhibits concentration-dependent proliferation-inhibitory activity against 143B cells with IC50 of 3.28 uM.
PC-26374

Aflatoxin B1

1162-65-8

Aflatoxin B1 (AFB1) is a Group 1A carcinogen and a secondary metabolite produced by Aspergillus flavus and A. parasiticus, can induces mutations by causing a G to T transversion at the third nucleotide of codon 249 in the tumor suppressor gene p53.
PC-26340

Mezodriton

Mitochondrial uncoupler

Mezodriton is a small molecule mitochondrial oxidative phosphorylation uncoupler.
PC-26323

Dinifedriton

Mitochondrial uncoupler

Dinifedriton is a small molecule mitochondrial uncoupler for regulating mitochondria activity and reducing adiposity in the treatment of diseases.
PC-26308

GIT1/β-Pix inhibitor 14-5-18

GIT1/β-Pix inhibitor

GIT1/β-Pix inhibitor 14-5-18 is a small-molecule inhibitor to interrupt the protein–protein interaction (PPI) of GIT1/β-Pix complex with Ki of 1.8 uM in FP assays, directly binds to GIT1 with BLI KD of 7.7 uM, inhibits gastric cancer metastasis.
PC-26306

GIT1 inhibitor Compound 3

GIT1 inhibitor

GIT1 inhibitor Compound 3 (GIT1-IN-C3) is a selective small molecule inhibitor of ARF GTPase protein 1 (GIT1) with MST KD of 6.2 uM, effectively disrupts GIT1 from interacting with MAT2B and RAF/MEK/ERK to halt cancer cell growth in vitro and in vivo.
PC-26292

STK189682

RNA helicase inhibitor

STK189682 is a potent small molecule inhibitor of RNA helicases MDA5, LGP2, and DDX1 with IC50 of 7 uM, 7 uM and 5 uM in ATPase assays.
PC-26275

Rebaudioside N

SBK2 agonist

Rebaudioside N is a terpenoid glycoside isolated from the leaves of Stevia rebaudiana Bertoni, is a potent SH3 domain-binding kinase 2 (SBK2) agonist, effectively suppresses NLRP3-mediated IL-1β/IL-18 secretion, reduces inflammatory responses, and diminishes atherosclerotic burden.

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