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Cat. No. Product Name Information
PC-62028

BRD 8899

BRD 8899 is a potent and selective inhibitor of the serine/threonine kinase STK33 with IC50 of 0.11 nM (25 uM ATP).
PC-62025

FQI2

FQI2 is a small-molecule inhibitor of transcription factor LSF with IC50 of 0.71 uM.
PC-62024

(S)-FQI1

(S)-FQI1 is a small-molecule inhibitor of transcription factor LSF with IC50 of 0.93 uM, approximately 2-fold more active than the racemate FQI-1.
PC-62023

FQI1

FQI1 is a small-molecule inhibitor of transcription factor LSF with IC50 of 2.1 uM.
PC-61918

Cyclocreatine Phosphate

Cyclocreatine Phosphate (AM 285) is an analog of the creatine kinase CKMT1 substrate creatine and inhibitor of the creatine biosynthesis pathway.
PC-61883

PF-03382792

PF-03382792 (PF-3382792) is a clinical compound under phase 1 investigation for an unknown indication..
PC-61856

EPI 743

EPI 743 (Vatiquinone) is an orally bioavailable para-benzoquinone for treatment of inherited mitochondrial diseases, an analogue of the antioxidant ubidecarenone..
PC-61820

UK-396082

UK-396082 is a potent and selective inhibitor of activated thrombin-activatable fibrinolysis inhibitor (activated TAFI.
PC-61795

Cromoglicic acid

Cromoglicic acid is a mast cell stabilizer with anti-inflammatory activity that prevents the release of inflammatory chemicals such as histamine, leukotrienes from mast cells.
PC-61794

Sodium cromoglicate

Sodium cromoglicate is a mast cell stabilizer with anti-inflammatory activity that prevents the release of inflammatory chemicals such as histamine, leukotrienes from mast cells.
PC-61730

OX-14

OX-14 is a highly potent farnesyl pyrophosphate synthase (FPPS) inhibitor with IC50 of 2.46 nM, with significantly lower binding affinity to hydroxyapatite.
PC-61689

Fhit-IN-15

Fhit-IN-15 is a potent, competitive, reversible inhibitor of the enzymatic activity of tumor suppressor Fhit with IC50 of 49 nM, shows cytotoxicity in HEK293T cells..

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