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- Catálogos PDF
Chemical Hay 28543 productos.
Alprenolol hydrochloride
Alprenolol (hydrochloride) is a non-selective beta blocker as well as 5-HT1A receptor antagonist. The reference for administration is 10 mg/kg.
Agomelatine (L(+)-Tartaric acid)
Agomelatine L(+)-Tartaric acid (S-20098 L(+)-Tartaric acid) is a specific agonist of MT1 and MT2 receptors with Kis of 0.1, 0.06, 0.12, and 0.27 nM for CHO-hMT1, HEK-hMT1, CHO-hMT2, and HEK-hMT2, respectively.
Umeclidinium bromide
Umeclidinium bromide is a novel mAChR antagonist. The affinity (Ki) of Umeclidinium bromide for the cloned human M1-M5 mAChRs ranges from 0.05 to 0.16 nM.
Taraxasterol
Taraxasterol is a pentacyclic triterpenoid compound isolated from Taraxacum mongolicum. Taraxasterol is an LXRα activator, with metabolic and anti-inflammatory effects.
Taraxasterol
Taraxasterol is a pentacyclic triterpenoid compound isolated from Taraxacum mongolicum. Taraxasterol is an LXRα activator, with metabolic and anti-inflammatory effects.
D-(+)-Fucose
D-(+)-Fucose prevents growth of Escherichia coli B/r on a mineral salts medium plus l-arabinose by inhibiting induction of the l-arabinose operon. D-fucose is a potent inducer of beta-methylgalactoside permease (MGP).
D-(+)-Fucose
D-(+)-Fucose prevents growth of Escherichia coli B/r on a mineral salts medium plus l-arabinose by inhibiting induction of the l-arabinose operon. D-fucose is a potent inducer of beta-methylgalactoside permease (MGP).
Tetramethyluric Acid
Tetramethyluric Acid is a purine alkaloid found in the leaves of wild bitter tea (Camellia kucha Hung T. Chang) with a molecular structure that has one more methyl group than the caffeine commonly found in tea leaves.
Cytidine-5'-monophospho-N-acetylneuraminic acid
Cytidine-5'-monophospho-N-acetylneuraminic acid is a nucleotide.
Cytidine-5'-monophospho-N-acetylneuraminic acid
Cytidine-5'-monophospho-N-acetylneuraminic acid is a nucleotide.
Clopidogrel thiolactone
Clopidogrel thiolactone
