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Used in a more general sense, the term X,Y-acetal also refers to any functional group that consists of a carbon bearing two heteroatoms X and Y. For example, N,O-acetal refers to compounds of type R 1 R 2 C(OR)(NR' 2) (R,R' ≠ H) also known as a hemiaminal ether or Aminal, a.k.a. aminoacetal.
N-acetylcysteine, also known as Acetylcysteine and NAC, is a medication that is used to treat paracetamol (acetaminophen) overdose and to loosen thick mucus in individuals with chronic bronchopulmonary disorders, such as pneumonia and bronchitis. [9]
The product, CH 3 CH(OCH 2 CH 3) 2, is formally named 1,1-diethoxyethane but is commonly referred to as "acetal". [39] This can cause confusion as "acetal" is more commonly used to describe compounds with the functional groups RCH(OR') 2 or RR'C(OR'') 2 rather than referring to this specific compound — in fact, 1,1-diethoxyethane is also ...
Acetylfentanyl (acetyl fentanyl) is an opioid analgesic drug that is an analog of fentanyl. [4] Studies have estimated acetylfentanyl to be 15 times more potent than morphine , [ 5 ] [ 6 ] which would mean that despite being somewhat weaker than fentanyl, it is nevertheless still several times stronger than pure heroin .
The example below depicts the acetalisation reaction of D-ribose 1. With acetone or 2,2-dimethoxypropane as the acetalisation reagent the reaction is under thermodynamic reaction control and results in the pentose 2. The latter reagent in itself is an acetal and therefore the reaction is actually a cross-acetalisation.
Acetyl-CoA is an intermediate in the biological synthesis and in the breakdown of many organic molecules. Acetyl-CoA is also created during the second stage of cellular respiration (pyruvate decarboxylation) by the action of pyruvate dehydrogenase on pyruvic acid. [8] Proteins are often modified via acetylation, for various purposes.
Polyoxymethylene (POM), also known as acetal, [4] polyacetal, and polyformaldehyde, is an engineering thermoplastic used in precision parts requiring high stiffness, low friction, and excellent dimensional stability.
Because of the acetyl-group in 3-position, 3-MAM has relatively weak affinity to μ-opioid receptors. As 3-O-acetylmorphine-6-O-sulfate (C 19 H 23 NO 7 S), where 6-OH is changed to 6-O-SO 3, it can act as a potent, centrally acting morphine derivative and has important analgesic properties. [1] [2] [3] 3-MAM-6-Sulfate (M3A6S) Acetyl
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