Lidocaine is a selective inverse peripheral histamine H1-receptor agonist with an IC50 of >32 μM.
2,5-Dihydroxyacetophenone possess anti-anxiety, and neuroprotective qualities.
2,5-Dihydroxyacetophenone treatment can induce a sustained activation of JNK, ERK1/2, and p38 MAPKs, it also can potentiate the pro-apoptotic and...
Xanthocillin is a marine agent extracted from Penicillium commune, inducesautophagythrough inhibition of theMEK/ERKpathway.
Corynoxeine, which could be isolated from Uncaria rhynchophylla, is a useful and prospective compound in the prevention and treatment for vascular diseases. It is a potent ERK1/2 inhibitor of key PDGF-BB-induced VSMC ...
Enniatin B is aFusariummycotoxin. Enniatin B inhibits acyl-CoA: cholesterol acyltransferase (ACAT) activity with an IC50 of 113μM in an enzyme assay using rat liver microsomes. Enniatins B decreases the activation ofERK(...
Urolithin B inhibits NF-κB activity by reducing the phosphorylation and degradation of IκBα. Urolithin B suppresses the phosphorylation of JNK, ERK, and Akt, and enhances the phosphoryla...
Trans-Zeatina is the member of the plant growth hormone family known as cytokinins, which regulate cell division, development, and nutrient processing.
TBHQ (tert-Butylhydroquinone) is a widely used Nrf2 activator, protects against Doxorubicin (DOX)-induced cardiotoxicity through activation ofNrf2. TBHQ (tert-Butylhydroquinone) is also an ERK activator; rescues Dehydroc...
Enniatin A1 isolated fromFusariummycotoxins is a cyclic hexadepsipeptide consisting of alternating D-α-hydroxyisovaleric acids and N-methyl-L-amino acids. Enniatin A1 possesses anticarcinogenic properties by induction ofapoptosis...
Pamoic acid disodium
Pamoic acid disodium is a potentGPR35agonist with an EC50 value of 79nM. Pamoic acid disodium inducesGPR35internalization and activatesERK1/2withEC50values of 22nM and 65nM, respectively. Pamoic acid disodium potently...
Tauroursodeoxycholic acid (TUDCA) is the taurine conjugate of ursodeoxycholic acid (UDCA) and acts as a mitochondrial stabilizer and anti-apoptotic agent in several models of neurodegenerative diseases, including AD, Parkinson'...
Enniatin B1 is aFusariummycotoxin. Enniatin B1 inhibits acyl-CoA: cholesterol acyltransferase (ACAT) activity with an IC50 of 73μM in an enzyme assay using rat liver microsomes. Enniatin B1 crosss the blood-brain barrier. E...
Asperulosidic Acid (ASPA), a bioactive iridoid glycoside, is extracted from the herbs of Hedyotis diffusa Willd. Asperulosidic Acid (ASPA) has anti-tumor, anti-oxidant, and anti-inflammatory activities.
ASPA is related t...
Pseudocoptisine acetate, a quaternary alkaloid with a benzylisoquinoline skeleton, is isolated from the tubers ofCorydalis turtschaninovii. Pseudocoptisine acetate shows anti-inflammatory properties.
Theaflavin 3,3'-digallate (TF3), the typical pigment in black tea, is a good antitumor agent. Theaflavin 3,3'-digallate is generally regarded as the effective component for the inhibitory effects against carcinogenesis without adverse s...
Magnolin reduces the renal oxidative stress, suppresses caspase-3 activity, and increases Bcl-2 expression in vivo and in vitro. Magnolin has anti-inflammatory and antioxidative effects.
Honokiol is the active principle of magnolia extract that inhibits Akt-phosphorylation and promotes ERK1/2 phosphorylation. Phase 3.
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