Q9: Voxelotor's structure is shown below. What would you expect the overall charge of the molecule to be in the blood (pH = 7.4) Pyridinium pka = 2.6 Phenol pka = 8.3 H. N OH N'

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**Q9: Voxelotor's structure is shown below. What would you expect the overall charge of the molecule to be in the blood (pH = 7.4)?**

- Pyridinium pKa = 2.6
- Phenol pKa = 8.3

The image displays the chemical structure of Voxelotor:

- The central structure features a bicyclic aromatic ring containing nitrogen atoms, indicating a pyridinium moiety.
- Connected to the pyridinium ring is a phenol group, characterized by a hydroxyl (-OH) group bonded to an aromatic ring.

**Explanation:**

In the context of blood at physiological pH (7.4), the following considerations apply:

- **Pyridinium Group:** With a pKa of 2.6, this group will likely be protonated at pH 7.4, as the pH is higher than the pKa. This would impart a positive charge to the molecule.
  
- **Phenol Group:** With a pKa of 8.3, this group will largely remain un-ionized at pH 7.4, as the pH is below the pKa. Thus, it is likely to remain neutral.

Overall, the molecule would likely have a positive charge under physiological conditions due to the protonation of the pyridinium group.
Transcribed Image Text:**Q9: Voxelotor's structure is shown below. What would you expect the overall charge of the molecule to be in the blood (pH = 7.4)?** - Pyridinium pKa = 2.6 - Phenol pKa = 8.3 The image displays the chemical structure of Voxelotor: - The central structure features a bicyclic aromatic ring containing nitrogen atoms, indicating a pyridinium moiety. - Connected to the pyridinium ring is a phenol group, characterized by a hydroxyl (-OH) group bonded to an aromatic ring. **Explanation:** In the context of blood at physiological pH (7.4), the following considerations apply: - **Pyridinium Group:** With a pKa of 2.6, this group will likely be protonated at pH 7.4, as the pH is higher than the pKa. This would impart a positive charge to the molecule. - **Phenol Group:** With a pKa of 8.3, this group will largely remain un-ionized at pH 7.4, as the pH is below the pKa. Thus, it is likely to remain neutral. Overall, the molecule would likely have a positive charge under physiological conditions due to the protonation of the pyridinium group.
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