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Table 1 In vitro data (1saturation binding assay, 2real-time radioligand binding) for the 64Cu-labeled compounds [64Cu]Cu-14–[64Cu]Cu-16 and their respective Log D7.4 values

From: Chelator impact: investigating the pharmacokinetic behavior of copper-64 labeled PD-L1 radioligands

Compound

KD [nM]1

Bmax [pmol/mg]

KD [nM]2

ka (M × s)–1

kd s–1

Log D7.4

[64Cu]Cu-14

100.4 ± 9.23

2.40 ± 0.48

23.3 ± 1.67

(5.06 ± 0.25) × 103

(1.17 ± 0.06) × 10–4

–3.00 ± 0.03

[64Cu]Cu-15

184.8 ± 15.4

2.58 ± 0.35

19.1 ± 1.69

(5.10 ± 0.55) × 103

(0.96 ± 0.02) × 10–4

–2.11 ± 0.02

[64Cu]Cu-16

265.0 ± 12.5

3.30 ± 0.46

24.2 ± 0.93

(5.55 ± 0.31) × 103

(1.35 ± 0.09) × 10–4

–2.79 ± 0.02