Benzyl-PEG2-Tos is a Benzyl PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.

Boc-Gly-amido-(CH2)3-PEG3-(CH2)3-amine is an Amino PEG Linker. PEG Amines contain an amino group which can react with acids, succinimidyl-active esters, or pentafluorophenyl esters for labeling, chemical modification, surface or particle modifications. PEG Linkers may be useful in the development of antibody drug conjugates.

Azido-PEG5-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.

Amino-PEG11-amine is a PEG derivative containing two amino groups. The amino groups are reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. PEG Linkers may be useful in the development of antibody drug conjugates or drug delivery methods.

Amino-PEG9-amine is a PEG derivative containing two amino groups. The amino groups are reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. PEG Linkers may be useful in the development of antibody drug conjugates and drug delivery methods.

Propargyl-PEG2-acrylate is a PEG derivative containing a propargyl group and an acrylate 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 acrylate group enables Michael addition. PEG Linkers may be useful in the development of antibody drug conjugates and drug delivery.

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.

2-Iminothiolane HCl, or Traut's Reagent,is commonly used to convert primary amines into sulfhydryl groups in a one-step process is called thiolation. It is a useful RNA-protein crosslinking reagent and an effective thiolation reagent for polysaccharides.

CDI Crosslinker, or N,N'-Carbonyldiimidazole, is a zero-length crosslinker that is often employed in the coupling of amino acids for peptide synthesis and also in organic synthesis. CDI can be used to convert alcohols and amines into carbamates, esters, and ureas.

Betonicine can be found in herbs and spices and pulses, which makes betonicine a potential biomarker for the consumption of these food products. Betonicine can be found primarily in urine. This compound belongs to the class of organic compounds known as l-alpha-amino acids.

Dithiazanine iodide is a benzothiazole that has been used as an antinematodal agent. Also, it has been effective as a nanoparticle in treating glioblastoma.

Abietic acid has been investgated as an antimetastatic agent or as an adjuvant for anticancer therapy.

Blastomycin, also known as Antimycin A3, is an antigen for intradermal testing prepared from sterile filtrates of cultures of the filamentous form of Blastomyces dermatitidis. It acts as a fungicide, bactericide, and wood preservative.

Manumycin A is a Farnesyltransferase inhibitor which suppresses exosome biogenesis and secretion via targeted inhibition of Ras/Raf/ERK1/2 signaling and hnRNP H1 in castration-resistant prostate cancer cells, inhibiting IKKβ activity through covalent cross-linking of IKKβ monomers via C179.

Galnon is a selective, non-peptide agonist at the galanin receptors GALR.

Echimidine is one of the natural predominant pyrrolizidine alkaloids (PAs) found in honeys produced in Australia and New Zealand. Echimidine activates PXR and induces PXR-mediated CYP3A4 expression.

Ornithine-α-ketoglutarate is a modulator of the respiratory burst via nitric oxide and polyamine generation, thereby improving immune status during stress.

24-Methylenecholesterol is a natural marine sterol, which stimulates cholesterol acyl transferase (ACAT) in human macrophages.

Delphinidin Chloride is an inhibitor of BDNF-induced migration and invasion in SKOV3 ovarian cancer cells.

ATC0065 dihydrochloride is a novel nonpeptidic and potent melanin-concentrating hormone receptor 1 (MCHR1) selective antagonist.

Cerebrosterol is a major brain metabolite of cholesterol.

L-NMMA acetate is an endothelium-derived relaxing factor inhibitor. It acts by inhibiting the generation of NO from arginine.

A1899 is a potent and selective TASK-1 and TASK-3 antagonist.

8-Br-cGMP is an activator of cGMP-dependent protein kinase. It acts by inhibiting the intracellular calcium oscillations of tracheal smooth muscle cells in response to acetylcholine.

(R)-Pantetheine is a metabolite in carbapenem biosynthesis, pantothenate and CoA biosynthesis and biosynthesis of secondary metabolites.

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.

MMPIP HCl is an allosteric mGlu7-selective receptor antagonist.

Ononetin is a TRPM3 channel blocker.

MS438 is a potent agonist of the TSH receptor (TSHR).

BAMF is an acetylating agent for the chemical modification of proteins.