Ophthalmic acid is a glutathione analog in which cysteine moiety is replaced by L-aminobutyrate.

Aurapten is a coumarin with anti-inflammatory, anti-carcinogenic, anti-bacterial, neuroprotective, and hepatoprotective activities. It inhibits leukocyte activation and induces phase II enzymes during the initiation phase of carcinogenesis. Aurapten may also be useful in the treatment of Alzheimer’s disease by inhibiting β-secretase (BACE1) activity.

Chromocarb is used to eliminate lipoperoxidation postvitrectomy.

Decalin-1,4-dione is a biochemical.

Auramine is a dye.

Pachycarpine may decrease hyperexcitability through the activation of the M2 and M4 subtypes of mAChRs, which is a probable mechanism of action that together with its systemic effects may favor its anticonvulsant effects against seizures and SE.

Piperitenone is a monoterpene that has been found in various plants, has antioxidant activity and inhibits peroxidation of linoleic acid

L-Dehydroascorbic acid is the oxidized form of L-Ascorbic acid. It selectively induces cell death in KRAS and BRAF mutant cells in vitro.

Iditol is a rare sugar alcohol (polyol).

Propargyl-PEG1-t-butyl ester is a PEG derivative containing a propargyl group and a t-butyl protected carboxyl group. The propargyl group can be reacted with azide-bearing compounds or biomolecules via copper catalyzed azide-alkyne Click Chemistry to yield a stable triazole linkage. The t-butyl protected carboxyl group can be deprotected under acidic conditions. The hydrophilic PEG spacer increases solubility in aqueous media.

Jasmone is an organic compound, which is a volatile portion of the oil from jasmine flowers. It is a colorless to pale yellow liquid. Jasmone can exist in two isomeric forms with differing geometry around the pentenyl double bond, cis-jasmone and trans-jasmone. The natural extract contains only the cis form, while synthetic material is often a mixture of both, with the cis form predominating. Both forms have similar odors and chemical properties.

VU 0650991 is a non-competitive GLP-1 antagonist that is orally bioavailable and acts as a brain penetrant.

Apovincamine is a vinca alkaloid and a chemical precursor of Vinpocetine, a derivative of Vincamine with vasodilating activity.

Indican is a natural protective agent to the liver.

Ononetin is a TRPM3 channel blocker.

(+)-Pinoresinol is a lignan that diverse biological activities, including antioxidant, anticancer, and anti-inflammatory properties. It is an inhibitor of α-glucosidase and maltase. (+)-Pinoresinol scavenges ABTS but not 2,2-diphenyl-1-picrylhydrazyl (DPPH) radicals in cell-free assays. It is cytotoxic to A549, HepG2, and MCF-7, but not U251 and Bcap-37 cells. (+)-Pinoresinol prevents cell death induced by glutamate in HT22 cells and inhibits LPS-induced nitric oxide production in RAW 264.7 cells.

Nicotyrine is a biochemical.

Harman is a beta-carboline.

Vasicinone is a quinazoline alkaloid that can be isolated from A. vasica leaves and demonstrates bronchodilatory activity. It also is reported to possess antioxidant activity in nitric oxide and ABTS radical scavenging assays.

Ochratoxin C is a toxic metabolite from Aspergillus orchraceus.

Fluorenone is an aromatic organic compound with the chemical formula C??H?O. It is used to make antimalaria drugs.

PMX464 is a cytocidal anti-trypanosomal inhibitor that acts by targeting trypanothione metabolism. It is also a putative inhibitor of the thioredoxin-thioredoxin reductase (Trx-TrxR) system.

Boc-NH-ethyl-SS-propionic acid is a cleavable PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.

t-Boc-Cystamine is a cleavable PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.

BDP TMR is a borondipyrromethene dye, analog of BODIPY? TMR. This is an amine-reactive NHS ester for the labeling of proteins, peptides, and other molecules with amino groups.

Lophine derivatives as chemiluminescent in vitro activators for detection of free radicals.

Neocuproine is a copper(I) chelator.

Aspergillin PZ is a fungal metabolite active against S. epidermidis but not S. aureus, E. coli, or B. cereus. It is cytotoxic to HL-60 promyelocytic leukemia cells but not THP-1 acute monocytic leukemia or PC3 prostate cancer cells.

Ginkgetin is a biflavonoid that has been isolated from G. biloba and has diverse biological activities, including pro-apoptotic, antiproliferative, anti-inflammatory, anti-atherosclerosis, and neuroprotective properties.

Santonin is an Anthelmintic isolated from the dried unexpanded flower heads of Artemisia maritima and other species of Artemisia found principally in Russian and Chinese Turkestan and the Southern Ural region.