Pilocarpine is a slowly hydrolyzed muscarinic agonist with no nicotinic effects. Pilocarpine is used as a miotic and in the treatment of glaucoma.

Obafluorin is a β-lactone antibiotic that has been found in P. fluorescens. It is active against S. aureus, S. faecalis, K. pneumoniae, and P. vulgaris.

Terphenyls are a group of closely related aromatic hydrocarbons. Also known as diphenylbenzenes or triphenyls, they consist of a central benzene ring substituted with two phenyl groups. The three isomers are ortho-terphenyl, meta-terphenyl, and para-terphenyl. Commercial grade terphenyl is generally a mixture of the three isomers.

C.I. Azoic Coupling Component 5 is a fluorescent indicator.

3-(Triethoxysilyl)propylamine is a biochemical.

Lck inhibitor II is a cell-permeable, ATP binding site-targeting, tri-substituted pyrimidine that acts as a highly potent Lck (lymphocyte specific kinase) inhibitor

Mepyramine, a histamine H1 antagonist. It has mild hypnotic properties and some local anesthetic action and is used for allergies (including skin eruptions) both parenterally and locally. It is a common ingredient of cold remedies.

UCL2077 is a selective slow-afterhyperpolarization (sAHP) channel blocker. UCL2077 suppresses the sAHP present in hippocampal neurons in culture and in the slice preparation. UCL2077 is selective and has minimal effects on Ca(2+) channels, action potentials, input resistance and the medium afterhyperpolarization.

t-Boc-Aminooxy-PEG3-bromide is a crosslinker containing a t-Boc-aminooxy group and a bromide group. The bromide (Br) is a very good leaving group for nucleophilic substitution reactions. Aminooxy PEGs may be useful in bioconjugation experiments.

t-Boc-Aminooxy-PEG4-alcohol is a PEG derivative containing a Boc-protected aminooxy group and an alcohol group. The protected aminooxy can be deprotected under mild acidic conditions and then can be reacted with an aldehyde or ketone group to form a stable oxime linkage. The hydroxyl group enables further derivatization or replacement with other reactive functional groups. Aminooxy PEG Linkers may be useful in bioconjugation experiments.

Decaphosphenonium bromide is a biochmeical.

TAN 420E is a bacterial metabolite that scavenges DPPH radicals and reduces thiobarbituric acid reactive substances (TBARS) liver microsomes. TAN 420E is active against B. brevis, B. cereus, M. flavus, and S. aureus. It is cytotoxic to P388 and KB lymphocytic leukemia cells.

Neratinib, also known as HKI-272 or PB272, is an orally available, irreversible inhibitor of the HER-2 receptor tyrosine kinase with potential antineoplastic activity. Neratinib binds to the HER-2 receptor irreversibly, thereby reducing autophosphorylation in cells, apparently by targeting a cysteine residue in the ATP-binding pocket of the receptor.

Momordicine I is a secondary metabolite from bitter melon (Momordica charantia L.) which significantly inhibits Spodoptera litura ovary cell line (SL-1 cell) proliferation.

2-Chloronaphthalene is an organochlorine chemical compound, a chlorinated derivative of naphthalene. Its chemical formula is C ??H ?Cl. The compound is an isomer for 1-chloronaphthalene.

A 33 is a potent and selective PDE4B inhibitor.

Flurbiprofen Axetil, also known as Ropion, is a prodrug of Flurbiprofen that provides better analgesia effects and few side effects.

lambda-Cyhalothrin is an insecticide and pesticide that has adverse effects on rats as well, including neurotoxic and hepatopancreatic effects.

PS372424 HCl is a specific agonist of human CXCR3. It has been shown to induce phosphorylation of ERK and block CXCL11 induced migration of CD45+ cells to air pouches generated on humanized mice.

Azido-PEG10-amine is a PEG derivative containing an amino group with an azide group. The amino group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. PEG Linkers may be useful in the development of antibody drug conjugates and drug delivery methods.

S-Diclofenac is a non-steroidal anti-inflammatory drug (NSAID). S-diclofenac may protect against doxorubicin-induced cardiomyopathy by ameliorating cardiac gap junction remodeling.

Naphthalene is an organic compound with formula C ??H ?. It is the simplest polycyclic aromatic hydrocarbon, and is a white crystalline solid with a characteristic odor that is detectable at concentrations as low as 0.08 ppm by mass.

Decahydronaphthalene

Veratrole is a building block for the organic synthesis of other aromatic compounds. Veratrole is relatively electron-rich and thus readily undergoes electrophilic substitution.

RBI-257 Maleate is a highly potent dopamine D4 receptor-selective ligand. RBI-257 Maleate may be a useful probe or radioligand for brain dopamine D4 receptors.

t-boc-N-amido-PEG5-azide is a PEG derivative containing an azide group and Boc-protected amino group. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. 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.

Dasatinib N-oxide is a major metabolite of the Abl and Src kinase inhibitor Dasatinib. It is also a potential impurity in commercial preparations of dasatinib.

Benzhydrylamine is a biochemical that may be used in grafting and peptide synthesis.

Chlorodiphenylmethane is an organic compound with two phenyl rings.

Neoxaline is an alkaloid fungal metabolite.