Catalog No.
Product Name
Application
Product Information
Citations
- cis-Urocanic acid is a major ultraviolet-absorbing component of the stratum corneum.
- a-Hydroxyglutaric acid (2-HG) is an a-hydroxy acid. It is normally metabolized to 2-oxoglutarate by D- and L-2-hydroxyglutarate dehydrogenases, and mutations in these enzymes cause 2-hydroxyglutaric aciduria, a neurometabolic disorder.
- Phloroglucinol is a hygroscopic biochemical that is also potentially useful for bone decalcification in microscopy specimens or the detection of wood fibers.
- Levomefolic acid is the primary biologically active form of folic acid used at the cellular level for DNA reproduction, the cysteine cycle and the regulation of homocysteine.
- Gemcitabine elaidate is a lipophilic, unsaturated fatty acid ester derivative of gemcitabine (dFdC), an antimetabolite deoxynucleoside analogue, with potential antineoplastic activity.
-
ENT1 inhibitor
NBMPR is a nucleoside analog that competitively inhibits the equilibrative nucleoside transporter 1 (Kd = 0.1-1.0 nM, IC50s = 4.6 and 3.6 nM in rat and human, respectively). -
rRNA modificator
5S rRNA modificator is a suitable electrophile for 2?€?-hydroxyl acylation on structured RNA molecules, yielding accurate structural information comparable to that obtained with existing probes; 5S rRNA RNA modification. - Cambendazole acts as an anthelmintic used in the treatment of Chagas?€? disease.
- ST 101 (ZSET1446) is a novel cognitive enhancer that promotes hippocampal neurogenesis and ameliorates depressive behavior in olfactory bulbectomized mice.
-
GPIIb/IIIa antagonist
Tirofiban, Hydrochloride Hydrate is a specific nonpeptide platelet fibrinogen receptor (GPIIb/IIIa) antagonist. -
Bioluminescent substrate
D-Luciferin is a popular bioluminescent substrate of luciferase in the presence of ATP, used in luciferase-based bioluminescence imaging and cell-based high-throughput screening applications. - Clodronate disodium is the disodium salt of a nitrogen-free bisphosphonate analog of naturally occurring pyrophosphate.
-
DCPS inhibitor
RG3039 (PF-06687859) is orally bioavailable, brain-penetrant small molecule that has been shown to be an inhibitor of the mRNA decapping enzyme, DcpS. -
morpholino antisense oligomer
Eteplirsen is an experimental drug, currently in clinical trials. - Desmethyldoxepin is the primary metabolite of doxepin, produced by metabolism at the liver. Doxepin is a tricyclic antidepressant.
-
sympathetic ganglioblocker
Fluorocurarine chloride is a short-acting selective sympathetic ganglioblocker with weak antagonist activity on the nicotinic receptor at the neuromuscular junction. - Fosfluconazole is a water-soluble phosphate prodrug of fluconazole - a triazole antifungal drug used in the treatment and prevention of superficial and systemic fungal infections.
-
Alpha-galactosidase inhibitor
Deoxygalactonojirimycin Hydrochloride is a potent and selective Alpha-gal A (Alpha-galactosidase) inhibitor. - Biotin hydrazide is a biotinyl derivative that can be used as a probe for the determination of protein carbonylation, which is a component of several diseases.
- 6-Maleimidocaproic acid is a sulfhydryl reactive heterobifunctional crosslinking reagent.
-
neuronal differentiation inducer
Neuropathiazol is a synthetic small molecule that induces neuronal differentiation of adult hippocampal neural progenitor cells. - Tomeglovir is a novel nonnucleosidic inhibitor of human cytomegalovirus replication.
- Cyclosporin D is a weak immunosuppressor but potent inhibitor of tumor promoting phorbol ester TPA/PMA.
- Thymalfasin is a chemically synthesized version of thymosin alpha 1 that is identical to human thymosin alpha 1. Thymosin alpha 1 is an acetylated polypeptide.
- Thymosin β4 is naturally occuring, potent regulator of actin polymerization present in human platelets at a concentration of 200 - 500 uM.
- CM 346 is an anxiolytic drug, produces anxiolytic and neuroprotective effects without any sedative or muscle relaxant actions.
- Picoplatin is a new generation organic platinum analog with an extended spectrum of antineoplastic activity.
- Tafamidis is a potent and selective transthyretin kinetic stabilizer that inhibits the amyloid cascade.
