| Cat.No. | Name | Information |
|---|---|---|
| M66454 | 3-Hydroxyhippuric acid | 3-Hydroxyhippuric acid inhibits homo sapiens kynureninase (Ki=60 μM). 3-Hydroxyhippuric acid is an acylglycine, it is one of the major metabolites of catechin-rich and wine polyphenol-rich diets. 3-Hydroxyhippuric acid is a biomarker for Clostridium and is positively correlated with the content of Clostridium. |
| M66453 | DSPE-PEG2000-SH | DSPE-PEG2000-SH is an amphiphilic thiol-functionalized DSPE-PEG molecule. DSPE-PEG2000-SH inserts into extracellular vesicle (EV) bilayer membranes via hydrophobic interactions, displaying surface thiol groups to form EV-SH crosslinkers. DSPE-PEG2000-SH can be used to encapsulate agents for drug delivery system, such as mRNA vaccine. |
| M66452 | Caracemide | Caracemide (NSC-253272) inhibits the enzyme ribonucleotide reductase of Escherichia coli. |
| M66450 | Tiludronate disodium | Tiludronate (Tiludronic Acid) disodium, an orally active bisphosphonate, can act an osteoregulator. Tiludronate is used for the research of the metabolic bone disorders. |
| M66449 | L-NIL dihydrochloride | L-NIL dihydrochloride is an inducible NO synthase inhibitor, with an IC 50 of 3.3 μM for miNOS. |
| M66448 | NFATc1-IN-1 | NFATc1-IN-1 is a potent inhibitor of RANKL-induced osteoclast formation, with an IC 50 of 1.57 μM. |
| M66447 | Petrelintide | Petrelintide (ZP8396) is a dual amylin and calcitonin receptor agonist (DACRA) Petrelintide elicits a selective reduction in high-fat diet intake in diet-induced obese (DIO) rats. |
| M66446 | VAF347 | VAF347 is a cell permeable and highly affinity aryl hydrocarbon receptor (AhR) agonist and induces AhR signaling. |
| M66445 | Darlifarnib | Darlifarnib (KO-2806) is an orally active farnesyl transferase inhibitor. Darlifarnib inhibits the mTORC1 signaling pathway. |
Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2026 AbMole BioScience. All Rights Reserved.
