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Cat. No. Product Name Information
PC-38614

GPR7 antagonist 9i

GPR7 antagonist 9i

GPR7 antagonist 9i a highly potent antagonist of NPBWR1 (GPR7) with binding and cAMP IC50 of 0.20 and 0.86 nM for mouse GPR7, respectively.
PC-38613

GPR7 antagonist 21a

GPR7 antagonist

GPR7 antagonist 21a is a highly potent small molecule antagonist of NPBWR1 (GPR7) antagonist with cAMP IC50 of 30 nM, dose-dependently increased [125I]-hNPW23 dissociation rate constants from NPBWR1 in kinetic binding assays.
PC-38612

ML181

GPR7 antagonist

ML181 (CYM50557) is a potent and selective GPR7 (Neuropeptides B/W receptor 1, NPBW1) antagonist probe with IC50 of 270 nM for inhibition of NPW-induced GPR7 activation.
PC-38611

ML250

GPR7 antagonist

ML250 (CYM 50769) is a potent and selective GPR7 (Neuropeptides B/W receptor 1, NPBWR1) antagonist probe, inhibits human GPR7 expression in the presence of GPR7 agonist NPW with IC50 value of 124 nM-244 nM, displays 82- >161 fold selectivity over MCH1.
PC-38609

MYLS22

Opa1 inhibitor

MYLS22 is a specific, nontoxic small molecule inhibitor of the inner mitochondrial membrane mitochondrial fusion protein optic atrophy 1 (OPA1), curtails tumor growth and metastasisin vitro and in vivo.
PC-38607

ML145

GPR35 inhibitor

ML145 (CID-2286812) is a selective GPR35 antagonist with IC50 of 20.1 nM, >1000-fold selectivity over GPR55.
PC-38606

CID 2745687

GPR35 inhibitor

CID-2745687 is a potent, selective and competitive GPR35 antagonist with pIC50 of 6.7 against human GPR35.
PC-38605

FPPS-IN-11

FPPS inhibitor

FPPS-IN-11 is a potent, allosteric, non-bisphosphonate farnesyl pyrophosphate synthase (FPPS) inhibitor with IC50 of 200 nM.
PC-38601

VK-28

Iron chelator

VK-28 is a novel brain permeable neuroprotective iron chelator with anti-Alzheimer's disease activities, inhibits both basal and Fe/ascorbate-induced mitochondrial membrane lipid peroxidation with IC50 of 12.7 uM.
PC-38593

Synucleozid hydrochloride

α-synuclein inhibitor

Synucleozid hydrochloride (NSC 377363) is a small molecule that targets the IRE structure and inhibits SNCA gene translation in cells, directly targets the α-synuclein mRNA 5'UTR at the designed site.
PC-38581

HyT36

Hydrophobic tag

HyT36 is a small-molecule hydrophobic tag compound for the degradation of stabilized proteins, induces an acute, resolvable ER stress that results in transient UPR activation without induction of apoptosis in ERHT-expressing cells.
PC-38576

ElteN378

FKBP12 inhibitor

ElteN378 is a highly potent synthetic inhibitor of FKBP12 with Ki of 0.5 nM, a low atomic weight ligand with affinity comparable to that of the macrolide Rapamycin

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