Odds for drugs being bilayer active or likely cytotoxic vs. ALogP/PSA
| Odds for drugs having 1.25 ≤ NormRate/NormRate < 1.25 | ||
|---|---|---|
| PSA ≤ 75 Å2 | PSA > 75 Å2 | |
| ALogP ≤ 3 | 6/38 = 0.16 | 32/61 = 0.52 |
| ALogP > 3 | 99/72 = 1.38 | 58/34 = 1.71 |
| Odds for drugs having | ||
| PSA ≤ 75 Å2 | PSA > 75 Å2 | |
| ALogP ≤ 3 | 25/19 = 1.32 | 59/34 = 1.74 |
| ALogP > 3 | 129/41 = 3.15 | 69/21 = 3.29 |
| Odds for drugs having 1.25 ≤ | ||
|---|---|---|
| PSA ≤ 75 Å2 | PSA > 75 Å2 | |
| ALogP ≤ 3 | 6/38 = 0.16 | 32/61 = 0.52 |
| ALogP > 3 | 99/72 = 1.38 | 58/34 = 1.71 |
| PSA ≤ 75 Å2 | PSA > 75 Å2 | |
| ALogP ≤ 3 | 25/19 = 1.32 | 59/34 = 1.74 |
| ALogP > 3 | 129/41 = 3.15 | 69/21 = 3.29 |
Top: The odds ratio for a drug being bilayer-modifying (having 1.25 ≤ NormRate) is 11-fold higher (95% CI: 4.1–28.2) for drugs with ALogP > 3 and PSA > 75 Å2, relative to drugs with ALogP ≤ 3 and PSA ≤ 75 Å2. Bottom: The odds ratio for a drug being cytotoxic (having HepG2 CC20 < 50 µM) is 2.5-fold higher (95% CI: 1.1–5.6) for drugs with ALogP > 3 and PSA > 75 Å2, relative to drugs with ALogP ≤ 3 and PSA ≤ 75 Å2. We only have HepG2 CC20 information for 397 of the 400 drugs in the Pathogen Box.
As a benefit of your subscription, you can share temporary access to restricted articles.
Each link will stop working after 30 days or 10 uses. You may create up to 10 links in a 30 day period.
Please sign in to your personal account to gift article access.
As a benefit of your subscription, you can share temporary access to restricted articles.
Each link will stop working after 30 days or 10 uses. You may create up to 10 links in a 30 day period.
Gift articles remaining: --
Each link will stop working after 30 days or 10 uses. You may create up to 10 links in a 30 day period.
Gift articles remaining: --
As a benefit of your subscription, you can share temporary access to restricted articles.
Each link will stop working after 30 days or 10 uses.
You have reached the limit of 10 links within a 30 day period.
Sharing content requires targeting cookies to be enabled. Please update your cookie preferences to use this feature.