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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T23004 | ML-SA1 | Mucolipin synthetic agonist 1 | Others , TRP/TRPV Channel |
ML-SA1 (Mucolipin synthetic agonist 1) is a selective TRPML agonist, inhibits Dengue virus 2 (DENV2) and Zika virus (ZIKV) by promoting lysosomal acidification and protease activity. The IC50 value of ML-SA1 against DENV... | |||
T38089 | 2F-Peracetyl-Fucose | 1,3,4-Tri-O-acetyl-2-deoxy-2-fluoro-L-fucopyranos | Others |
2F-Peracetyl-Fucose (1,3,4-Tri-O-acetyl-2-deoxy-2-fluoro-L-fucopyranos) is a potent fucosyltransferase (FUT) inhibitor that inhibits salivary acidification and fucosylation in an in vitro inflammatory model. | |||
T11191 | EN6 | Proton pump , Autophagy | |
EN6-mediated ATP6V1A modification decouples the v-ATPase from the Rags, leading to inhibition of mTORC1 signaling, increased lysosomal acidification and activation of autophagy. EN6 clears TDP-43 aggregates, a causative ... | |||
T69550 | NS-3736 | ||
NS-3736 is a chloride channel inhibitor that has been shown to prevent osteoclastic acidification and resorption. | |||
T72003 | SKF-104557 | ||
N-Despropyl ropinirole is an active metabolite of the dopamine D2 receptor agonist ropinirole. It increases extracellular acidification rates in CHO cells expressing human dopamine D2, D3, and D4 receptors (EC50s = 0.63,... | |||
T36116 | Concanamycin B | ||
Concanamycin B is a macrolide antibiotic that selectively inhibits vacuolar type H+-ATPases, also known as V-ATPases (IC50 = 5 nM). In this way, it blocks the acidification of vacuolar organelles as well as early to late... | |||
T37547 | Trans-Urocanic Acid | ||
trans-Urocanic acid is a major epidermal chromophore for the immunosuppressive effects of UV radiation that is produced in mammalian stratum corneum by the action of histidine ammonialyase on L-histidine. It contributes ... | |||
T80516 | Human GALP (3-32) | Galanin-like peptide (3-32) | Neuropeptide Y Receptor |
Human GALP (3-32) (Galanin-like peptide (3-32)) serves as a high-affinity agonist for galanin receptors GalR1 (IC50 = 33 nM) and GalR2 (IC50 = 15 nM), as evidenced by competitive binding studies. It demonstrates signific... | |||
T76042 | Angiopeptin TFA | ||
Angiopeptin TFA, a cyclic octapeptide analogue of somatostatin, acts as a partial agonist at sst 2/sst 5 receptors, exhibiting IC50 values of 0.26 nM and 6.92 nM, respectively. This compound effectively inhibits the rele... | |||
T83889 | C-02 | ||
C-02, a proteolysis-targeting chimera (PROTAC) that combines the hexokinase inhibitor lonidamine with the cereblon ligand thalidomide, effectively induces the degradation of hexokinase 2 in 786-O and PANC-1 cells at a co... |