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Tranilast 100 mg | Purity Not Available
TargetMol
Tranilast, an antiallergic drug, suppresses lipid mediator and cytokine release from inflammatory cells, therefore utilized in the treatment of allergic disorders.
More Information Supplier PageTranilast 10 mg | Purity Not Available
TargetMol
Tranilast, an antiallergic drug, suppresses lipid mediator and cytokine release from inflammatory cells, therefore utilized in the treatment of allergic disorders.
More Information Supplier PageChembridge-5861528 100 mg | 100.00%
TargetMol
Chembridge-5861528 (TCS 5861528) is a TRPA1 channel blocker that antagonizes AITC- and 4-HNE-evoked calcium influx with IC50 values of 14.3 and 18.7 μM, respectively.
More Information Supplier PageChembridge-5861528 10 mg | 100.00%
TargetMol
Chembridge-5861528 (TCS 5861528) is a TRPA1 channel blocker that antagonizes AITC- and 4-HNE-evoked calcium influx with IC50 values of 14.3 and 18.7 μM, respectively.
More Information Supplier PageChembridge-5861528 5 mg | 100.00%
TargetMol
Chembridge-5861528 (TCS 5861528) is a TRPA1 channel blocker that antagonizes AITC- and 4-HNE-evoked calcium influx with IC50 values of 14.3 and 18.7 μM, respectively.
More Information Supplier PageL-(R,S)-Tetrahydropalmatine 50 mg | 99.97%
TargetMol
L-(R,S)-Tetrahydropalmatine (Rotundine) is extracted from Corydalis yanhusuo W. T. Wang.
More Information Supplier PageUsnic Acid 100 mg | 99.98%
TargetMol
Usnic Acid (Usniacin) is an antimicrobial, antitumor and enzyme inhibiting agent shown to uncouple oxidative phosphorylation in mouse-liver mitochondria. Usnic acid induces necrosis in certain cells.
More Information Supplier PageUsnic Acid 10 mg | 99.98%
TargetMol
Usnic Acid (Usniacin) is an antimicrobial, antitumor and enzyme inhibiting agent shown to uncouple oxidative phosphorylation in mouse-liver mitochondria. Usnic acid induces necrosis in certain cells.
More Information Supplier Pagetrans-Cinnamic acid 100 mg | 99.96%
TargetMol
trans-Cinnamic acid (Myricitrine) exerts anti-diabetic activity by improving glucose tolerance in vivo and by stimulating insulin secretion in vitro.
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