menthyl

Menthol glucuronide is a metabolite of L-(-)-Menthol, the natural form of Methanol.

2'-Deoxycytidine is one of the major nucleosides of DNA consisting of cytosine and deoxyribose and inhibits the biological effects of bromodeoxyuridine (Brdu). The nucleoside consists only of a pentose sugar attached to a purine or pyrimidine base and has no phosphate group. When N1 is attached to C1 of deoxyribose, deoxyribosides and nucleotides are formed from cytosine and deoxyribose; deoxycytidine monophosphate (dCMP), deoxycytidine diphosphate (dCDP), and deoxycytidine triphosphate (dCTP). cTP is the source of cytosine in RNA (ribonucleic acid) and deoxycytidine triphosphate (dCTP) is the source of deoxycytidine in DNA (deoxyribonucleic acid). Itaconic acid is a polymer.

(+)-Menthyl acetate, extracted from the essential oil of Cunila angustifolia Benth, exhibits selective cytotoxicity, demonstrating higher efficacy against the MCF-7 cell line with an IC50 of 34.0 μg/mL and lower efficacy against the SK-Mel-28 cell line, where the IC50 is 279.9 μg/mL, when tested on A549 cells without fatal consequences [1].

(1S)-(+)-Menthyl chloroformate is a natural product for research related to life sciences. The catalog number is TN6545 and the CAS number is 7635-54-3.

L-Monomenthyl glutarate is a monoterpene compound serving as a low-irritant alternative to menthol, suitable for biochemical experiments and medicinal synthesis research.

Compound Fr13236, with CAS No. 40248-63-3, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. Compound Fr13236 provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

Menthyl isovalerate is a bioactive chemical.

Aminomenthylnorepinephrine is a partial agonist of the beta-adrenoreceptor that causes irreversible inactivation.

Homosalate (Homomenthyl salicylate) is an organic compound and chemical UV filter, formed as an ester from salicylic acid and 3,3,5-trimethylcyclohexanol, a cyclohexanol derivative.

MSK-9 is an allosteric modulator of the P2X4 receptor, exhibiting dual actions of enhancing ion conductivity and delaying receptor desensitization. By stabilizing the receptor's open state, MSK-9 utilizes rigid 3-piperidinyl and hydrophobic menthyl substituents. MSK-9 is applicable in research related to multiple sclerosis (MS).