Amino Acids (AA)

Kentsin H-Thr-Pro-Arg-Lys-OH is a synthetic peptide that is used as a conditioning agent in vitro and in vivo. It was initially developed as an anti-viral to combat HIV, but has been found to possess contraceptive properties. Kentsin H-Thr-Pro-Arg-Lys-OH inhibits the proliferation of human granulosa cells by blocking ovulation and interfering with the regular development of ovarian follicles. It has been shown to be effective against Pim1, a progesterone receptor on granulosa cells. The concentration response curve for Kentsin H-Thr-Pro-Arg Lys OH shows that it can inhibit ovulation at concentrations as low as 1 μM.

Please enquire for more information about Methyl 1-cyclohexyl-5-(4-methylsulfanylphenyl)-1H-pyrazole-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

[(2S,3S,4S)-2-Methyl-4-[(2,2,2-Trifluoroacetyl)Amino]-3,4-Dihydro-2H-Pyran-3-Yl] Acetate is a compound that belongs to the class of pyran derivatives. It has been shown to interact with guanine in the DNA and form a complex. This interaction is dependent on the compressive force applied to the DNA as well as environmental effects such as aluminium concentration and temperature. [(2S,3S,4S)-2-Methyl-4-[(2,2,2-Trifluoroacetyl)Amino]-3,4-Dihydro-2H-Pyran-3-Yl] Acetate has been shown to be insensitive to deformation and temperatures up to about 100 degrees Celsius. The compound also inhibits the synthesis of

D-Threonine is a non-essential amino acid that is used in the synthesis of proteins. It is an essential amino acid for humans, and its production can be catalyzed by aldolase enzymes. D-Threonine has been shown to have anti-inflammatory properties, which may be due to its ability to inhibit the reaction mechanism of hydroxyl group enzymes. D-Threonine also inhibits cell lysis through the inhibition of certain bacterial enzymes, such as genus or kinetic. D-Threonine can also be synthetized from L-threonine by enzyme inhibitors or asymmetric synthesis.

4-Methoxystyrene is a monomer that can be polymerized to form poly(4-methoxystyrene). It is an ionic monomer that has been used in cationic polymerization reactions. 4-Methoxystyrene can also be used as a fluorescence detector and as a base for the synthesis of polymers with desired properties. The kinetic, radical, and cationic polymerization reactions are all possible with 4-methoxystyrene. This compound has been shown to have intermolecular hydrogen bonding and oxygen nucleophiles, which are both required for the reaction mechanism of this compound. X-ray crystal structures have revealed the structure of this compound.

Please enquire for more information about Methyl (4-amino-2-methoxyphenoxy)acetate including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Methyldecane is a nonionic surfactant that is used in detergent compositions. It has been shown to be effective as a skin cancer treatment and as an antimicrobial agent. 2-Methyldecane has been shown to have strong antifungal properties against dermatophytes, yeasts, and Gram-positive bacteria. The antimicrobial activity of 2-methyldecane may be due to its hydroxyl group that can act as a cross-linking agent or by its ability to form cationic ion pairs with anionic bacterial cell surfaces.

Please enquire for more information about [1-(2-Phenyl-1,3-thiazol-5-yl)ethyl]amine dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about N-(2-Phenylethyl)-1,3,5-triazine-2,4-diamine including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Fmoc-1-aminocyclohexane carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Iodo-2-methylanisole (4IM) is a naphthalene that is regiospecifically eliminated after activation by nitrate in an acidic medium. The hydrochloride salt of 4IM, koenigicine, has been shown to produce estrogen levels in the female rat similar to those produced by 17β-estradiol. The synthesis of 4IM involves the nitration of 2-methylanisole followed by iodine oxidation. This reaction produces a mixture of mono-, di-, and tri-iodonapthalenes. The product obtained from this reaction is purified with column chromatography or recrystallization. Theory predicts that 4IM will be oxidized to 4-iodo-2,6-dimethylanisole by terpene oxidants such as acetonitrile or ozone.