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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T27995 | MDK-3046 | HK-inhibitor-2,MDK3046,HK inhibitor 2 | |
MDK-3046 is a YycG histidine kinase (HK) inhibitor with potent antibiofim activity against Staphylococcus epidermidis. | |||
T6835 | Fenoldopam mesylate | Fenoldopam methanesulfonate,SKF-82526 mesylate,Corlopam mesylate,mesylate,SKF 82526 | Dopamine Receptor |
Fenoldopam mesylate (Corlopam mesylate) is a selective dopamine-1 receptor (DA1) agonist with natriuretic/diuretic properties. It lowers blood pressure through arteriolar vasodilation. | |||
T2O2701 | L-Ornithine hydrochloride | L(+)-Ornithine hydrochloride,(S)-2,5-Diaminopentanoic acid | Others , Endogenous Metabolite |
L-Ornithine hydrochloride ((S)-2,5-Diaminopentanoic acid) has an antifatigue effect by increasing the efficiency of energy consumption and promoting the excretion of ammonia. It is one of the key reactants in the urea cy... | |||
T81120 | SP4f | PPAR | |
SP4f, an activator of PPAR-γ, exhibits an EC50 value of 826 nM in HK-2 cells. In Swiss albino mice, it diminishes blood glucose levels and lipid peroxidation while enhancing glutathione levels and catalase activity [1]. | |||
T83392 | 2a,3a,23-Trihydroxyurs-12,20(30)-dien-28-oic acid | ||
2a,3a,23-Trihydroxyurs-12,20(30)-dien-28-oic acid (compound 3), a triterpenoid, markedly reduces fibronectin levels by 27.66% at a concentration of 10 μM in HK-2 cells subjected to high-glucose and TGF-b1 induction [1]. | |||
T81121 | SP4e | PPAR | |
SP4e, a PPAR-γ activator, exhibits an EC50 of 739 nM in HK-2 cells. In Swiss albino mice, it diminishes blood glucose and lipid peroxidation while enhancing glutathione levels and catalase activity [1]. | |||
T81267 | RIPK3-IN-4 | RIP kinase | |
RIPK3-IN-4 (Compound 42) is a RIPK3 inhibitor that mitigates necroptosis, inflammatory responses, and HK-2 cell damage. It alleviates acute kidney injury by attenuating Cisplatin- and I/R-induced kidney damage, along wit... | |||
T21978 | P-nitro-Pifithrin-α | ||
p-nitro-Pifithrin-α is a cell-permeable analog of pifithrin-α, a potent p53 inhibitor. It suppresses p53-mediated TGF-β1 expression in HK-2 cells and inhibits the activation of caspase-3 by Zika virus (ZIKV) strains. Mor... |