Dicamba is a chlorinated organic herbicide. It is used to selectively control broadleaf weeds.

Lawesson's reagent is a thiation agent.

PHGDH-inactive is an inactive analog of the 3-phosphoglycerate dehydrogenase (PHGDH) inhibitors NCT-502 and NCT-503. PHGDH-inactive is intended to serve as a negative control for NCT-502 and NCT-503.

Atrazine is an herbicide of the triazine class. Atrazine functions by binding to the plastoquinone-binding protein in photosystem II, which animals lack. Plant death results from starvation and oxidative damage caused by breakdown in the electron transport process.

Mevalonolactone is a chemical that can be used in the preparation of a vitamin E.

Methisazone is an antiviral agent effective against pox viruses.

TAMRA-PEG4-acid is a TAMRA red-fluorescent dye derivative with excitation/emission maximum 553/575 nm, This molecule contains a carboxylic acid group which can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond.

AT-1015 HCl anhydrous is a serotonin (5-HT)2 receptor antagonist that blocks vascular and platelet 5-HT2A receptors.

Aspartyl adenylate is the adenyl derivative of succinic acid that plays a part in nucleotide metabolism.

Amino-PEG3-CH2CO2-t-butyl ester is a PEG derivative containing an amino group with a t-butyl protected carboxyl group. The amino group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The t-butyl protected carboxyl group can be deprotected under acidic conditions. PEG Linkers may be useful in the development of antibody drug conjugates and drug delivery methods.

Chlorothalonil is a an organochlorine, broad-spectrum and non-systemic fungicide[2], which can be widely used in agriculture, in order to have a control on foliar pathogens. Chlorothalonil is a broad spectrum fungicide with carcinogenic and aquatic toxicity properties.

t-Boc-aminooxy-PEG4-propargyl is a PEG derivative containing a propargyl group and t-Boc-aminooxy 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 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. PEG Linkers may be useful in the development of antibody drug conjugates.

t-Boc-Aminooxy-PEG3-thiol is an Aminooxy PEG Linker. Aminooxy PEG Linkers may be useful in bioconjugation experiments.

Aminooxy-PEG3-bromide HCl salt is a PEG derivative containing an aminooxy group and a bromide group. The aminooxy group can be used in bioconjugation. It reacts with an aldehyde to form an oxime bond. If a reductant is used, it will form a hydroxylamine linkage. The bromide (Br) is a very good leaving group for nucleophilic substitution reactions.

t-Boc-aminooxy-PEG1-propargyl is a PEG derivative containing a propargyl group and t-Boc-aminooxy 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. PEG Linkers can be useful in the development of antibody drug conjugates.

Fmoc-aminooxy-PEG4-acid is an Aminooxy PEG Linker. Aminooxy-PEGs may be useful in bioconjugation experiments.

Aminooxy-PEG1-propargyl HCl salt is a PEG derivative containing a propargyl group and an aminooxy group. The aminooxy group reacts with an aldehyde or ketone group to form a stable oxime linkage. 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. PEG derivatives may be useful in the development of antibody drug conjugates as well as drug delivery.

t-Boc-N-amido-PEG3-thiol is a PEG derivative containing a Boc-protected amino group and a thiol group. The Boc group can be deprotected under mild acidic conditions to form the free amine. The thiol group reacts with maleimide, OPSS, vinylsulfone and transition metal surfaces including gold, silver, etc.

Acid-PEG9-NHS ester is a PEG derivative containing a carboxylic acid and an NHS ester. The hydrophilic PEG spacer increases solubility in aqueous media. The terminal carboxylic acid can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond. The NHS ester can be used to label the primary amines (-NH2) of proteins, amine-modified oligonucleotides, and other amine-containing molecules.

TAMRA-PEG4-DBCO is a PEG derivative containing a TARMA dye and a DBCO group, which enables Click Chemistry. The TAMRA dye has achieved prominence as a dye for oligonucleotide labeling and automated DNA sequencing applications. DBCO will react with azide functionalized compounds or biomolecules without catalyst to form a stable triazole linkage, which is an ideal alternative to copper intolerant applications. The hydrophilic PEG spacer increases solubility in aqueous media.

Biotin-PEG5-NH-Boc is a Biotin PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.

t-boc-N-amido-PEG5-amine is a PEG derivative containing an amino group and Boc-protected amino group. The amino group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. 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.

Magnesium lactate is a buffering agent and magnesium donor

Desmethylselegiline is an Enzyme Inhibitor.

ZINC05626394 is a Cytochrome b5 reductase 3 (CYB5R3) inhibitor. It acts by increasing NO bioavailability.

Cbz-B3A inhibits the phosphorylation of eIF4E-binding protein 1 (4EBP1) and blocks 68% of translation. Cbz-B3A binds to ubiquilins 1, 2, and 4.

Diazo Biotin-PEG3-alkyne is useful for introducing a biotin moiety to azide-containing biomolecules using Cu(I)-catalyzed Click Chemistry. The hydrophilic spacer arm provides better solubility to the labeled molecules in aqueous media. Diazo allows efficient release of captured biotinylated molecules from streptavidin using sodium dithionite (Na2S2O4).

JTP 103237 is a potent and selective monoacyglycerol acyltransferase 2 (MOGAT2) inhibitor.

FHZ is a highly selective, cell-permeable, non-cytotoxic probe for dual channel detection of (OH radical) and HOCl in live cells and zebrafish embryos.

AA-5HT, also known as Arachidonoyl serotonin or N-arachidonoyl-serotonin, is an inhibitor of fatty acid amide hydrolase (FAAH). It has analgesic properties and acts as an antagonist of the TRPV1 receptor. It was shown to be present in the ileum and jejunum of the gastrointestinal tract and modulate glucagon-like peptide-1 (GLP-1) secretion.