From: The drug likeness analysis of anti-inflammatory clerodane diterpenoids
No | Model/Method | Dose | Outcomes | Mechanisms | Ref |
---|---|---|---|---|---|
14 | LPS-induced murine microglial BV-2 cells | 30.9 μM | Inhibited NO production |  | [44] |
16 | 31.2 μM |  | |||
17 | 30.3 μM |  | |||
18 | 27.5 μM |  | |||
38 | 34.7 μM |  | |||
48 | 45.5 ± 3.6 μM |  | [47] | ||
49 | 34.0 ± 3.2 μM |  | |||
51 | 48.5 μM |  | [45] | ||
52 | 36.0 ± 0.8 μM | Directly interacted and suppressed iNOS | [43] | ||
53 | 30 μM | ||||
54 | 27.3 ± 1.3 μM | ||||
57 | 11.1 ± 0.8 μM | ||||
58 | 30 μM | ||||
60 | 25.3 μM |  | [46] | ||
61 | 27.2 μM |  | [45] | ||
22 | 25.8 ± 1.7 μM | Directly interacted and suppressed iNOS and COX2 | [47] | ||
50 | 27.0 ± 0.9 μM | ||||
59 | 20.2 ± 2.0 μM | ||||
1 | LPS-induced RAW264.7 macrophages | 31.4 μM | Inhibited NO production |  | [57] |
4 | 25.49 μM |  | [58] | ||
7 | 31.4 μM |  | [57] | ||
14 | 26.3 μM |  | [53] | ||
15 | 27.7 μM |  | |||
16 | 22.8 μM |  | |||
19 | 32.19 μM |  | [54] | ||
20 | 22.92 μM |  | [50] | ||
21 | 13.25 μM |  | |||
25 | 46.43 μM |  | [54] | ||
26 | 31.99 μM |  | |||
27 | 48.85 μM |  | |||
28 | 42.04 μM |  | |||
33 | 35.6 μM |  | [53] | ||
34 | 34.2 μM |  | |||
35 | 20.6 μM |  | |||
36 | 21.5 μM |  | |||
37 | 20.2 μM |  | |||
41 | 1.2 μM |  | [51] | ||
42 | 1.6 μM |  | |||
44 | 0.82 μM |  | [91] | ||
45 | 0.54 μM |  | |||
46 | 21.9 μM |  | [52] | ||
47 | 45.1 μM |  | [59] | ||
55 | 39.3 μM |  | [56] | ||
56 | 36.2 μM |  | [55] | ||
63 | 22.4 μM |  | [52] | ||
12 | 35.35 μM | Inhibited NO, IL-6, IL-1β and TNF-α production in a dose-responsive manner |  | [50] | |
13 | 17.49 μM |  | |||
2 | fMLP/CB induced neutrophils | 4.40 ± 0.83 μM | Suppressed superoxide generation |  | [64] |
3 | 1.81 ± 0.27 μM |  | |||
5 | 13.00 ± 1.77 μM |  | |||
6 | 23.95 ± 5.36 μM |  | |||
7 | 9.59 ± 3.55 μM |  | |||
8 | 4.40 ± 0.56 μM 3.67 ± 0.20 μM | Inhibited superoxide anion generation and elastase release |  | [65] | |
2 | 3.06 ± 0.20 μM | Attenuated the phosphorylation of AKT and p38 MAPK | [66] | ||
9 | TPA-induced CD-1 auricular pavilion mouse ear edema | 0.25, 0.5, 1Â mg/ear | Reduced edema to 64% | Â | [71] |
10 | 0.10Â mg/ear | exhibited 70-76% Inhibition of inflammation | Â | [70] | |
11 | 0.39Â mg/ear | Â | |||
40 | 200Â mg/kg | Dose-dependently inhibited ear edema | Â | [73] | |
62 | 0.50 μg/ear | Inhibited ear edema |  | [72] | |
10 | TPA-induced acute mouse ear edema | 2.03 μg/ear | Inhibited IL-1β production, reduced ear thickness, IL-6 and myeloperoxidase accumulation |  | [81] |
24 | carrageenan-induced paw edema in rats | 50–200 mg/kg | Dose-dependently inhibited paw edema. |  | [73] |
30 | 200Â mg/kg | Inhibited paw edema and cotton pellet granuloma | Â | [77] | |
43 | 20Â mg/kg | Inhibited inflammation in rat paw | Â | [78] | |
64 | 0.5, 2.5Â mg/kg | Reduced paw edema | Â | [76] | |
65 | Â | ||||
24 | Carrageenan-induced pleurisy in rats | 10Â mg/kg | Inhibited LTB4 production in exudates and phlogistic process in lung | Â | [79] |
31 | Teleocidin induced mouse ear inflammation | 5.6 μg/ear | Inhibited tropical inflammation in mouse ear |  | [92] |
32 | 3.0 μg/ear |  | |||
39 | Indomethacin-induced gastric ulcer in rats | 50Â mg/kg | Downregulated PGE2, IL-4, IL-10, VEGF, and EGF | Â | [83] |
7 | DSS/OAM induced IBD mice | 1.6, 6.4 mg/kg | Reduced iNOS, COX2 expression | Reduced NF-κB gene expression | [85] |
29 | Dextran- or histamine-induced edema | 50Â mg/kg | Reduced edema | Â | [80] |
24 | A23187-induced LTB4 biosynthesis | 1 μM | Dose-dependently inhibited LTB4 biosynthesis |  | [79] |
Zymosan-induced peritonitis | 10Â mg/kg | Inhibited myeloperoxidase activity, LTC4 production, cell infiltration, and vascular permeability in the peritoneal cavity, but not the production of PGE2 | Â |