laurolitsine hydrochloride (MedChemExpress)
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Laurolitsine Hydrochloride, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/hy-n2352a/Laurolitsine+hydrochloride/pmc12563024-85-3-15
Average 93 stars, based on 1 article reviews
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1) Product Images from "Cinnamomum migao H.W. Li Ethanol-Water Extract Suppresses IL-6 Production in Cardiac Fibroblasts: Mechanisms Elucidated via UPLC-Q-TOF-MS, Network Pharmacology, and Experimental Assays"
Article Title: Cinnamomum migao H.W. Li Ethanol-Water Extract Suppresses IL-6 Production in Cardiac Fibroblasts: Mechanisms Elucidated via UPLC-Q-TOF-MS, Network Pharmacology, and Experimental Assays
Journal: Current Issues in Molecular Biology
doi: 10.3390/cimb47100798
Figure Legend Snippet: Molecular docking visualization. ( A ) Molecular docking mode diagram of Laurolitsine with ADRB2; ( B ) Molecular docking mode diagram of Hecogenin with MAPK8; ( C ) Molecular docking mode diagram of Hecogenin with MAPK9; ( D ) Molecular docking mode diagram of Hecogenin with MAPK10.
Techniques Used:
Figure Legend Snippet: Screening of the optimal intervention concentrations of MG-EWE, Laurolitsine, and Hecogenin. ( A ) Effects of different concentrations of Laurolitsine on CFs viability; ( B ) Effect of different concentrations of Hecogenin on CFs viability; ( C ) Effect of different concentrations of MG-EWE on CFs viability; ( D ) Effects of different concentrations of MG-EWE, Laurolitsine, and Hecogenin on ISO-induced CFs viability; ( E ) IL-6 content in the cell supernatant of each group. Compared to the control group, #### p < 0.0001. Compared to the ISO model group, * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001.
Techniques Used: Control
Figure Legend Snippet: The Migration ability of CFs in each group, original magnification: 200×. ( A ) Representative images from the Transwell assay showing the migration of CFs treated with MG-EWE, Laurolitsine, and Hecogenin; ( B ) Quantitative analysis of the effects of MG-EWE, Laurolitsine, and Hecogenin on the number of ISO-induced CFs migration. Compared to the control group, #### p < 0.0001. Compared to the ISO model group, ** p < 0.01, **** p < 0.0001.
Techniques Used: Migration, Transwell Assay, Control
Figure Legend Snippet: The schematic diagram illustrates the molecular mechanism through which MG suppresses IL-6 production in cardiac fibroblasts (CFs): in the isoproterenol (ISO)-induced CFs transdifferentiation model, MG-EWE and its active components Laurolitsine and Hecogenin can inhibit the abnormal activation of the ADRB2/JNK/c-Jun signaling pathway. When ISO binds to the ADRB2 receptor on the cell membrane surface of CFs, it initiates a downstream signaling cascade. Activation of this receptor leads to the phosphorylation of key signaling molecules, including JNK1/2/3 and c-Jun, thereby activating the JNK/c-Jun signaling pathway. The activated JNK1/2/3 translocates from the cytoplasm to the nucleus and further phosphorylates the transcription factor c-Jun within the nucleus, enhancing its transcriptional activity. This ultimately promotes the transcription of the IL-6 gene and increases its protein expression. Laurolitsine functions by inhibiting the activation of ADRB2 on the CFs cell membrane surface, while Hecogenin inhibits the phosphorylation of JNK, thereby blocking the subsequent phosphorylation of c-Jun. Together, these actions result in the joint inhibition of IL-6 production.
Techniques Used: Activation Assay, Membrane, Phospho-proteomics, Activity Assay, Expressing, Blocking Assay, Inhibition
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