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Cat. No. Product Name Information
PC-22666

Myeloperoxidase inhibitor RL6

Myeloperoxidase inhibitor

Myeloperoxidase inhibitor RL6 is a potent, reversible inhibitor of myeloperoxidase (MPO) and hypochlorous acid (HOCl) scavenger, inhibits neutrophil extracellular trap release (NETosis).
PC-22644

TAK-683

KISS1R agonist

TAK-683 is a potent and full KISS1R (metastin receptor) agonist and kisspeptin analogue with IC50 of 3 pM in radioimmunoassay.
PC-22643

TAK-683 acetate

KISS1R agonist

TAK-683 acetate is a potent and full KISS1R (metastin receptor) agonist and kisspeptin analogue with IC50 of 3 pM in radioimmunoassay.
PC-22642

TAK-448 acetate

KISS1R agonist

TAK-448 (MVT-602) acetate is a potent and full KISS1R (metastin receptor) agonist and kisspeptin analogue with IC50 of 3 pM in radioimmunoassay.
PC-22640

(S)-PHA533533

Ube3a unsilencer

(S)-PHA533533 is a potent, small molecule unsilencer of paternal UBE3A in mouse primary neurons with EC50 of 0.54 uM, Emax=80%, effectively downregulates Ube3a-ATS/UBE3A ATS and epigenetically unsilences paternal Ube3a/UBE3A in both mouse and human neuron.
PC-22636

Delphinidin chloride

Hyaluronidase inhibitor

Delphinidin chloride is a natural plant compound found in fruits and vegetables, a potent hyaluronidase inhibitor, increases high molecular weight hyaluronic acid (HMW-HA) and inhibits cancer metastasis.
PC-22628

GGTI-2154 hydrochloride

GGTase I inhibitor

GGTI-2154 hydrochloride is a potent, selective inhibitor geranylgeranyltransferase I (GGTase I) with IC50 f 21 nM, >250-fold selective over FTase.
PC-22627

GGTI-2154

GGTase I inhibitor

GGTI-2154 is a potent, selective inhibitor geranylgeranyltransferase I (GGTase I) with IC50 f 21 nM, >250-fold selective over FTase.
PC-22615

2-BDBPQD

α-glucosidase inhibitor

2-BDBPQD is a potent anti-diabetic agent and inhibitor of carbohydrate-degrading enzyme α-glucosidase with IC50 of 63.7 uM, moderately reduces cholesterol and LDL levels, exhibits superior efficacy in reducing glucose levels compared to acarbose.
PC-22607

Orpinolide

OSBP inhibitor

Orpinolide is a synthetic withanolide analog with potent antileukemic properties, directly targets oxysterol-binding protein OSBP, disrupts Golgi homeostasis via a mechanism that requires active phosphatidylinositol 4-phosphate (PtdIns4P, PI4P) signaling at ER-Golgi membrane interface.
PC-22606

SABRAC

Acid ceramidase inhibitor

SABRAC is a highly potent, irreversible inhibitor of acid ceramidase with Ki of 29.7 nM, induces apoptosis and provides a benefit in mice survival in IDH1 mut oligodendroglioma.
PC-22604

Oxybipin-2

OSBP inhibitor

Oxybipin-2 is a potent and selective inhibitor of oxysterol-binding protein (OSBP), inhibits OSBP–22-NBD-Chol interaction with IC50 of 13 nM, impair retrograde trafficking.

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