Carboprost methyl

Analysis Note Assay (GC, area%): &#8805 99.0 % (a/a) Density (d 20&#8199&#176C/ 4&#8199&#176C): 0.

2-Methylpentane-d₁₄.

2-Methylserotonin·HCl, also known as α-Methyl-5-HT, is a SR-3 agonist. Studies show that α-Methyl-5-HT has low binding affinity for SR-1A, SR-1B, SR-1C, and SR-2 binding sites.

2-Methylserotonin·HCl, also known as α-Methyl-5-HT, is a SR-3 agonist. Studies show that α-Methyl-5-HT has low binding affinity for SR-1A, SR-1B, SR-1C, and SR-2 binding sites.

2-Methylstyrene

Biochem/physiol Actions 3-Hydroxyisovaleryl-L-carnitine is an endogenous metabolite that can result from impairment in the leucine catabolic pathway. 3-Hydroxyisovaleryl-L-carnitine was observed in plasma and urine of patient with isolated

6-(Methylamino)purine, 6-methylade is a reagent for substitution of adenine nucleotide analogs containing bicyclohexane ring system locked in northern conformation enhanced potency as py receptor antagonists. Adenine methylation as an epigenic mark

6-(Methylamino)purine, 6-methylade is a reagent for substitution of adenine nucleotide analogs containing bicyclohexane ring system locked in northern conformation enhanced potency as py receptor antagonists. Adenine methylation as an epigenic mark

6-(Methylamino)purine, 6-methylade is a reagent for substitution of adenine nucleotide analogs containing bicyclohexane ring system locked in northern conformation enhanced potency as py receptor antagonists. Adenine methylation as an epigenic mark

6-(Methylamino)purine, 6-methylade is a reagent for substitution of adenine nucleotide analogs containing bicyclohexane ring system locked in northern conformation enhanced potency as py receptor antagonists. Adenine methylation as an epigenic mark

An inhibitor of catechol-o-methyltransferase.

An inhibitor of catechol-o-methyltransferase.