Cyclohexane, decyl-

Zearalenone is a mycotoxin produced by Fusarium. It acts by binding the estrogen receptor (ER).

Decarboxyl ofloxacin, (S)- is a degradation product of Levofloxacin.

Citiolone is a mucolytic agent for the treatment of certain hepatic disorders.

Prothioconazole is a chiral triazole fungicide.

Azide-PEG3-Tos is a PEG derivative containing an azide group and a tosyl group. The hydrophilic PEG spacer increases solubility in aqueous media. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The tosyl group is a good leaving group for nucleophilic substitution reactions.

Biotin-PEG3-oxyamine HCl salt is an aldehyde-reactive biotinylation reagent. It reacts with an aldehyde to form an oxime bond. If a reductant is used, it will form a hydroxylamine linkage. The hydrophilic PEG spacer arm imparts water solubility that is transferred to the biotinylated molecule.

ACT-678689 is a potent inhibitor of tryptophan hydroxylase 1 (TPH1).

Palmitoyl-L-aspartic acid is a natural N-acylaspartate that inhibits Hedgehog signaling after stimulation with Smoothened agonist or non-sterol-modified Sonic Hedgehog. It does not alter the activity of cannabinoid receptors or fatty acid amide hydrolase.

SB-747651A dihydrochloride is a potent MSK1 inhibitor; also inhibiting other AGC group kinases.

Bacopasaponin C is a triterpenoid saponin that inhibits the ATPase activity of P-glycoprotein.

Benomyl is a is a fungicide. It is a systemic benzimidazole fungicide that is selectively toxic to microorganisms and invertebrates, especially earthworms. Benomyl binds to microtubules, interfering with cell functions, such as meiosis and intracellular transportation. The selective toxicity of benomyl as a fungicide is possibly due to its heightened effect on fungal rather than mammalian microtubules.

Galloflavin Potassium is an inhibitor of lactate dehydrogenase.

AI3-15932 is a component of a tetrahydroquinoline analog.

Phenylphosphinic acid is an additive used with Noyori's catalyst for oxidation of sulfides to sulfones.

Acridine hydrochloride is a fluorescent indicator.

m-PEG3-t-butyl ester is a PEG derivative containing a t-butyl ester. The t-butyl protected carboxyl group can be deprotected under acidic conditions. The hydrophilic PEG spacer increases solubility in aqueous media.

ML230 is a specific inhibitor of the ABC-binding cassette trasporter BCRP (MRP-1; ABCG2). The compound ML 230 is 36-fold selective for BCRP over MDR-1 (Pgp; ABCB1) with IC50 values of 0.013 and 4.7 mM, respectively.

Rac-Efavirenz is a non stereospecific structure of Efavirenz.

Benthiavalicarb isopropyl is a fungicide, specifically targeting blight and downy mildew.

Decaborane, also called decaborane(14), is the borane with the chemical formula B10H14. This white crystalline compound is one of the principal boron hydride clusters, both as a reference structure and as a precursor to other boron hydrides. On its own, Decaborane is able to undergo reduction via acetate as a neat liquid.

Metergoline is a psychoactive drug of the ergoline chemical class which acts as a ligand for various serotonin and dopamine receptors. A dopamine agonist and serotonin antagonist. It has been used similarly to BROMOCRIPTINE as a dopamine agonist and also for MIGRAINE DISORDERS therapy.

Decyl cyanoacetate is a biochemical.

Bisindolylmaleimide I HCl, also known as GF-109203X HCl, is a specific ATP-competitive PKC inhibitor.

Fucosterol has been reported to have antioxidant, antidiabetic, and anti-inflammatory effects. In one study, fucosterol exhibited a protective effect on LPS-induced acute lung injury with a possible mechanism inhibiting NF-κB activation, thereby inhibiting LPS-induced inflammatory response.

1,3-Didecanoylglycerol is a saturated diacylglycerol with decanoic acid (Item No. 20838) at the sn-1 and sn-3 positions. It has been used in the formation of lipid monolayers in the study of lipases.

Biotin-PEG2-NH-Boc is a Biotin PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates (ADCs).

Amino-Tri-(t-butoxycarbonylethoxymethyl)-methane is a PEG derivative containing an amine group with three t-butyl esters. The amine groups 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.

AGN-192403 hydrochloride is an I1 imidazoline binding site selective ligand with a potency at I1 comparable to moxonidine, but devoid of affinity for adrenoceptors and the I2 binding site.

Silthiofam is very effective against Ggt, and recently it has been widely used for the control of take-all in China. Gaeumannomyces graminis var. tritici (Ggt) causes Wheat take-all.