Adenine is a purine, one of the four nucleobases in the nucleic acid of DNA.

1,8-Cineole is an inhibitor of 5-HT3 receptor,potassium channel, TNF-α and IL-1β.

Tizanidine Hydrochloride is an α2‑adrenergic receptor agonist that inhibits the release of neurotransmitters from CNS norepinephrine‑activated neurons.

2''-O-Galloylhyperin upregulates SIRT1/Nrf2 signaling, inhibits NF-κB and MAPK (ERK1/2, p38, JNK) phosphorylation, suppresses TSHR activation, reduces ROS accumulation, and enhances SOD and GSH-Px activities.

N-Acetyltizanidine is the N-acetylated derivative of tizanidine and is designated as Tizanidine USP Related Compound B.

Hypericin is an inhibitor of PKC (protein kinase C), MAO (monoaminoxidase), dopamine-beta-hydroxylase, reverse transcriptase, telomerase and CYP.

1-Acetyl-2-imidazolidinone is an imidazolidinone pharmaceutical intermediate. It is designated as Clonidine EP Impurity A and serves as a reference standard for clonidine hydrochloride impurity profiling.

4'-O-beta-Glucopyranosyl-5-O-methylvisamminol is an active natural chromone glycoside with multiple biological activities.

Traxoprodil is a potent and selective NMDA NR2B antagonist.

6-Gingerol is an active compound isolated from Ginger (Zingiber officinale),.

(1E,4E)-1,5-Bis(2-methoxyphenyl)penta-1,4-dien-3-one, also known as TFEB Activator 1 or curcumin analog C1, is an activator of transcription factor EB (TFEB) and is used as a research tool compound in molecular and chemical biology.

Erianin could inhibit IDO-induced tumor angiogenesis.

Combretastatin A4 is a microtubule-targeting agent that binds β-tubulin.

L-Fucose is a naturally occurring methylpentose that exists in the L-configuration in nature. It is a component of the glycan chains in glycoproteins and glycolipids on the surface of mammalian cells and is involved in the determination of blood group antigen substructures.

Nonivamide is a synthetic derivative of natural capsaicin and a TRPV1 agonist.

(-)-Epigallocatechin is the most abundant flavonoid in green tea, can bind to unfolded native polypeptides and prevent conversion to amyloid fibrils.