Deiodoamiodarone is an intermediate of amiodarone, which is an α/β-adrenergic receptor antagonist and coronary vasodilator.

Alloxan Monohydrate is a glucose analog used to induce diabetes by destroying beta-cells.

Phenylethyl isothiocyanate is an HDAC inhibitor potentially for the treatment of benign prostatic hypertrophy.

Oxymetazoline is a selective α1 adrenergic receptor agonist and α2 adrenergic receptor partial agonist. It is a topical decongestant, used in the form of oxymetazoline hydrochloride in products such as Afrin, Dristan, Nasivin, Nezeril, Nostrilla, Logicin, Vicks Sinex, Visine L.R., Sudafed OM, Zicam, SinuFrin and Mucinex Sinus-Max. It was developed from xylometazoline at E. Merck Darmstadt by Fruhstorfer in 1961. Oxymetazoline is generally available as a nasal spray.

Metribuzin is a triazine herbicide.

JWH-022 is a cannabimimetic indole that is structurally related to JWH 018, a mildly selective agonist of the peripheral cannabinoid (CB2) receptor.

JWH 072 is a synthetic cannabinoid (CB) that displays a higher affinity for the peripheral CB2 receptor (Ki = 170 nM) than the central CB1 receptor (Ki = 1,050 nM). The physiological and toxicological properties of this compound are not known.

JS-K is a Nitric oxide donor; antiproliferative.

D&C Red No. 8 is a dye.

Amarogentin displays immunomodulatory effects in human Mast Cells and Keratinocytes.

Cauloside C, also known as Hederoside D2, is a triterpenoid saponin that induces potassium release and hemolysis in mouse erythrocytes in a pH-dependent manner. Hederoside D2 is cytotoxic to N1E-115 neuroblastoma cells at low pH. It induces proliferation of human embryonic fibroblasts in acidic medium, an effect that can be blocked by the calcium channel blockers verapamil, diltiazem, and nitrendipine.

AI3-17602 is a biochemical.

Benzyl lactate is a biochemical.

Myristyl glycol is a type of glycol.

Tafluprost acid is a selective agonist at the prostaglandin F receptor, increasing outflow of aqueous fluid from the eyes and thus lowering intraocular pressure.

IDO-IN-3 is an inhibitor of indoleamine-2,3-dioxygenase 1.

Mahanimbine is a major carbazole alkaloid from Murraya koenigii (curry leaves) that may alleviate development of HFD-induced metabolic alterations.

WEHI-539 has high affinity (IC50=1.1 nM) and selectivity for BCL-XL and potently kills cells by selectively antagonizing its prosurvival activity. It has more than a 400-fold higher affinity for BCL-XL versus other prosurvival BCL-2 family members.

3-hydroxy Darifenacin is a metabolite of darifenacin. It is an antagonist of M1-5 muscarinic receptors.

Feglymycin is a 13-amino acid peptide that has antibacterial and antiviral activities. It is active against Gram-positive bacteria and inhibits HIV viral replication.

CAY10737 is a turn-on fluorescent probe for the detection of carbon monoxide (CO). It is selective for CO over a variety of anions, amino acids, amines, biothiols, and reactive species. In the presence of palladium (Pd) and CO, CAY10737 undergoes the Pd0-mediated Tsuji-Trost reaction to release a fluorescent compound that has absorption and emission maxima of 678/714 nm, respectively. This fluorescence can be used to detect CO production in vitro and in vivo.

Pasiniazid is a biochemical used in the treatment of tuberculosis

Gallein is a Gβγ subunit signalling inhibitor which has been shown to inhibit metastatic spread of tumour cells expressing OR51E2 and exposed to its odorant ligand.

AMBMP hydrochloride is a Wnt canonical signaling activator and tubulin polymerization inhibitor.

APHS is a cyclooxygenase-2 (COX-2) inhibitor with anti-inflammatory action. It also more potent than aspirin in the inhibition of COX-1.

m-PEG8-(CH2)12-phosphonic acid ethyl ester is a PEG Linker.

m-PEG8-(CH2)12-phosphonic acid is a PEG Linker.

m-PEG9-phosphonic acid is a PEG Linker.

Fmoc-PEG3-Ala-Ala-Asn(Trt)-PAB-PNP is a peptide reagent for ADC conjugation that possesses a cleavable peptide sequence. The hydrophilic PEG spacer increases solubility in aqueous media.

Azido-PEG4-Ala-Ala-Asn(Trt)-PAB is a PEG derivative conjugated with a peptide via an amide bond. The azide group on the PEG end enables Click Chemistry. The hydrophilic PEG spacer increases solubility in aqueous media.