Figures & data
![Figure 1. Chemical structures of kopetdaghin A (1), kopetdaghin C (3) and kopetdaghin E (5) isolated from D. kopetdaghense.](/cms/asset/d97a1121-ee43-40f4-bf1f-6f969605e072/cfai_a_950200_f0001_b.jpg)
![Figure 2. Effect of 10–100 μg/ml of kopetdaghin A (A), kopetdaghin C (B) and kopetdaghin E (C) on the viability of J774A.1 macrophages. Results are shown as mean ± SEM (n = 3). *P < 0.05, **P < 0.01 and ***P < 0.001 compared to untreated macrophages.](/cms/asset/9687690b-18b2-41a0-aee4-e57588924a0c/cfai_a_950200_f0002_b.jpg)
![Figure 3. Evaluation of NO production by J774A.1 macrophages stimulated for 24 h with LPS alone or in combination with 10–100 μg/ml of kopetdaghin A (A), kopetdaghin C (B) and kopetdaghin E (C). Results are shown as mean ± SEM (n = 3). *P < 0.05, **P < 0.01 and ***P < 0.001 compared to LPS-stimulated macrophages.](/cms/asset/d398a02c-0d40-4eea-8f84-bf170bacde04/cfai_a_950200_f0003_b.jpg)
![Figure 4. Effect of kopetdaghins A, C and E on LPS-induced iNOS expression. Lysates were prepared from control or LPS (1 μg/ml) stimulated macrophages alone or in combination with kopetdaghins for 24 h. Different lanes were represented as follow: (1) unstimulated macrophages, (2) LPS-stimulated macrophages, (3, 4) stimulated macrophages with 20 and 50 μg/ml of kopetdaghin A, (5, 6) stimulated macrophages with 20 and 50 μg/ml of kopetdaghin C, and (7, 8) stimulated macrophages with 20 and 50 μg/ml of kopetdaghin E.](/cms/asset/39aa4f51-eae0-49f6-9da7-87d37832ec5c/cfai_a_950200_f0004_b.jpg)
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