Triflupromazine is a phenothiazine that binds to muscarinic receptors and inhibits serotonin (5-HT) uptake by synaptosomes. Formulations containing triflupromazine were previously used as antipsychotics.

Zaldaride maleate is an intestinal calmodulin inhibitor which has been shown to decrease the severity and duration of travelers' diarrhea and research suggests that calmodulin and intracellular calcium may serve as mediators of diarrhea in bacterial enteric infection.

Ms-PEG8-Ms is a PEG Linker.

Triphenyltetrazolium bromide may be useful in the detection of experimental cerebral infarction and biochemical analysis.

Allylthiourea inhibits of 11β-hydroxysteroid dehydrogenase type 1.

Englerin A is a natural potent activator of ion channels formed by Transient Receptor Potential Canonical 4 and 5 proteins (TRPC4 and TRPC5).

Boc-LRR-AMC is a fluorogenic substrate for the trypsin-like activity of the 26S proteasome or 20S proteolytic core. Upon enzymatic cleavage by the 26S proteasome or 20S proteolytic core, amino-4-methylcoumarin (AMC) is released and its fluorescence can be used to quantify 26S proteasome or 20S proteolytic core trypsin-like activity. AMC displays excitation/emission maxima of 340-360/440-460 nm, respectively.

Hexadecanolide is a bioactive chemical.

Azido-PEG3-CH2CO2-NHS is a PEG Linker.

Bis-propargyl-PEG9 is a crosslinker containing two propargyl groups at each terminal end. The propargyl groups can be reacted with azide-bearing compounds or biomolecules via copper catalyzed azide-alkyne Click Chemistry to yield stable triazole linkages.

t-Boc-N-amido-PEG6-amine is a PEG derivative containing an amino group and Boc-protected amino group. The amino group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The Boc group can be deprotected under mild acidic conditions to form the free amine. PEG Linkers may be useful in the development of antibody drug conjugates.

Thiophenol is an organosulfur compound with the formula C?H?SH, sometimes abbreviated as PhSH. This foul-smelling colorless liquid is the simplest aromatic thiol. Thiophenols are used in the production of pharmaceuticals including of sulfonamides. The antifungal agents butoconazole merthiolate are derivatives of thiophenols.

Toluene, also known as toluol, is an aromatic hydrocarbon. It is a colorless, water-insoluble liquid with the smell associated with paint thinners. It is a mono-substituted benzene derivative, consisting of a CH? group attached to a phenyl group.

Lumiflavine is a riboflavin uptake inhibitor. Lumiflavine is produced by the photolysis of vitamin B2 (Riboflavin).

ACS67 is an F-series prostaglandin (PG) analog for treatment of glaucoma. ACS 67 reduces intra-ocular pressure (IOP) and increases levels of reduced glutathione and cGMP in the aqueous humor of glaucomatous pigmented rabbits. ACS67 also acts as a neuroprotectant that stimulates GSH levels.

Cyanuric acid is a chlorine stabilizer. It is a precursor to N-chlorinated cyanurates, which are used to disinfect water and crosslink agents for polyurethane resins.

2,4,6-Trichloro-s-triazine leads to immobilization of a pancreatic lipase.

Metaldehyde is a Polymer of acetaldehyde.

AC-93253 iodide is a SIRT2 selective inhibitor. It acts by significantly enhancing acetylation of tubulin, p53, and histone H4.

Glycine, N-(2,4-dinitrophenyl)- is a biochemical.

t-Boc-N-amido-PEG2-CH2CO2H is a PEG derivative containing a terminal carboxylic acid and Boc-protected amino group. The terminal carboxylic acid can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine.

Meticrane is a diuretic.

meta-Cresol, also 3-methylphenol, is an organic compound with the formula CH?C?H?. It is a colourless, viscous liquid that is used as an intermediate in the production of other chemicals.

Syntide-2 is a synthetic peptide recognized as a substrate by Ca2+/calmodulin-dependent protein kinase II (CaMKII; Km = 12 μM).1 Its sequence is derived from the phosphorylation site 2 on glycogen synthase, a target of CaMKII action.1 This peptide has been used as a probe to assay CaMKII activity; however, protein kinase C, CaMKV, Raf-1, and other kinases are also known to recognize syntide-2 as a substrate.

Dihydrochalcone Cognitive Deficits and Neuropathology. It is also known to reduced periplaque activated microglia and astrocytes, indicating the inhibition of neuroinflammation.

Temafloxacin is an antibiotic and antimycobacterial agent. It was approved to treat lower respiratory tract infections, genital and urinary infections like prostatitis, and skin infections in 1992.

γ-Valerolactone is a prodrug form of γ-hydroxyvaleric acid.

Migalastat is a potent inhibitor of glycolipid biosynthesis.

Sarcosine is an amino acid intermediate in the metabolism of choline.

Butyric acid is a flavor and fragrance agent.