T3813

20(R)-Ginsenoside Rh2 (Ginsenoside Rh2) is a minor stereoisomer of ginsenoside Rh2, possesses matrix metalloproteinase inhibitory.

3,5-Dihydroxyacetophenone is an endogenous metabolite widely used in biochemical experiments and drug synthesis research.

3,5-Dimethylbenzaldehyde has broad-spectrum antimicrobial activity, inhibiting Bacillus subtilis, Pseudomonas albicans, Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus and Streptococcus pneumoniae.

The diazomethyl ketone Z-LVG-CHN2 mimics part of the human cysteine proteinase-binding center, has been shown to be an irreversible inhibitor of this proteinase. The compound was also tested for antiviral activity against herpes simplex virus type 1 (HSV) and found to block the HSV replication. Irreversible inhibitor of streptopain.

(E)-10-Hydroxynortriptyline (E-10-OH-NT) is an active metabolite of Nortriptyline with anxiolytic activity and affinity for muscarinic acetylcholine receptors, which can be used in the study of neurological disorders.

(S)-O-Desmethyl Venlafaxine N-Oxide, an N-oxide derivative of (S)-O-Desmethyl Venlafaxine, is an active metabolite of the serotonin-norepinephrine reuptake inhibitor (SNRI) antidepressant Venlafaxine[1][2].

3,4-Dehydro Cilostazol (OPC-13015) is an active metabolite of Cilostazol used for pharmacokinetic studies. Cilostazol is a selective PDE3A inhibitor.

Orexin Receptor Antagonist 2 (compound 30), characterized by its potent antagonistic activity with pKis of 7.69 and 9.78, holds promise for insomnia research[1].