4 Matching Annotations
  1. Apr 2025
    1. These results revealed that 6j is a potential drug candidate against MRSA infection, thus providing a reference for the development of anti-MRSA drugs

      QUESTION: Because this article talks about derivatives of an antibiotic that makes it harder for bacteria to resist, I would want to know how does the decay rate of this new derivative, more specifically 6j, compare to the decay rate of the original antibiotic. Therefore, would the drug have to be taken more or less frequently for optimum use. Also, if the 6j derivative stays in the blood stream, does the environment the bacteria could potentially create cause reversification back into the original form of the drug or into an ineffective form of the drug?

    2. Possible locations for modifications of the parent ring include the tricyclic structure, (22) C-2 methylene, (15) C-3 carbonyl, (23) C-8 methylene, (17) C-13 methylene, (24) and C-19 double bond.

      CONNECT: parent ring modification of pleuromutilin relates to the synthesis of thyroid hormone (T3 and T4) through parent ring modification. The parent ring undergoes ionization which adds either three or four iodines onto the benzene ring.

    3. Hydroxyl at the C-22 position of pleuromutilin was activated with p-toluenesulfonyl chloride (30) to obtain intermediate 2 via nucleophilic substitution.

      FACT: tosylation occurs with the use of TsCl which then adds a Ts onto O. Therefore, the O becomes a better leaving group which then allows for a better nucleophilic substitution to obtain the intermediate.