Lovastatin


Curated chemical-phenotype interactions from CTD
GO IDGO nameInteraction typeReference
GO:0000165 Mapk cascade Affects phenotype PMID:16952276; PMID:9018116
GO:0000226 Microtubule cytoskeleton organization Decreases phenotype PMID:12405293
GO:0001516 Prostaglandin biosynthetic process Increases phenotype PMID:26863638
GO:0002537 Nitric oxide production involved in inflammatory response Increases phenotype PMID:18809656
GO:0004602 Glutathione peroxidase activity Decreases phenotype PMID:35734936
GO:0004666 Prostaglandin-endoperoxide synthase activity Increases phenotype PMID:35734936
GO:0004784 Superoxide dismutase activity Decreases phenotype PMID:29341888; PMID:35734936
GO:0006007 Glucose catabolic process Decreases phenotype PMID:26616219
GO:0006171 Camp biosynthetic process Increases phenotype PMID:38432573
GO:0006309 Apoptotic dna fragmentation Increases phenotype PMID:12843138; PMID:26863638; PMID:9141529; PMID:9872842
GO:0006641 Triglyceride metabolic process Affects phenotype PMID:35734936
GO:0006693 Prostaglandin metabolic process Affects phenotype PMID:35734936
GO:0006695 Cholesterol biosynthetic process Affects phenotype PMID:20578043; PMID:27208389; PMID:27208389; PMID:29852127; PMID:29852127; PMID:34890705
GO:0006749 Glutathione metabolic process Affects phenotype PMID:34165024; PMID:35734936
GO:0006809 Nitric oxide biosynthetic process Increases phenotype PMID:22185406
GO:0006915 Apoptotic process Affects phenotype PMID:10203554; PMID:18231920; PMID:9605009; PMID:10360474; PMID:10412747; PMID:10473109; PMID:10500066; PMID:10502407; PMID:11178870; PMID:11178870; PMID:16367743; PMID:16952276; PMID:11307620; PMID:11448925; PMID:11483865; PMID:11720884; PMID:11839765; PMID:12094262; PMID:12094262; PMID:15705602; PMID:16156861; PMID:12467231; PMID:12843138; PMID:12933658; PMID:15180944; PMID:15705602; PMID:15943032; PMID:16156861; PMID:16234849; PMID:16952276; PMID:17180086; PMID:17234346; PMID:17472962; PMID:17928957; PMID:18034278; PMID:18231920; PMID:18766339; PMID:18766339; PMID:20298590; PMID:18815881; PMID:19741129; PMID:19760159; PMID:20298590; PMID:20694854; PMID:7794281; PMID:9141529; PMID:9398081; PMID:9603146; PMID:9872842
GO:0006954 Inflammatory response Increases phenotype PMID:35734936
GO:0007049 Cell cycle Decreases phenotype PMID:10203554; PMID:11470239; PMID:9605009; PMID:10360474; PMID:10401660; PMID:10502407; PMID:11470239; PMID:11483865; PMID:12392621; PMID:12467231; PMID:15180944; PMID:17928957; PMID:18034278; PMID:7794281; PMID:9044834; PMID:9398081; PMID:9848777
GO:0007095 Mitotic g2 dna damage checkpoint signaling Increases phenotype PMID:26739623
GO:0007162 Negative regulation of cell adhesion Increases phenotype PMID:12405293
GO:0008177 Succinate dehydrogenase (ubiquinone) activity Decreases phenotype PMID:34165024
GO:0008203 Cholesterol metabolic process Affects phenotype PMID:32739440; PMID:35734936
GO:0008219 Cell death Increases phenotype PMID:10856525; PMID:11154978; PMID:16400415; PMID:20578043; PMID:24518598; PMID:29341888; PMID:9018116
GO:0008283 Cell population proliferation Decreases phenotype PMID:10203554; PMID:11470239; PMID:18231920; PMID:10360474; PMID:10401660; PMID:10412747; PMID:10856525; PMID:11178870; PMID:11483865; PMID:12094262; PMID:12094262; PMID:15705602; PMID:16156861; PMID:12392621; PMID:15160275; PMID:15180944; PMID:15705602; PMID:16156861; PMID:18034278; PMID:18199328; PMID:18231920; PMID:19260826; PMID:19760159; PMID:20298590; PMID:20578043; PMID:20948439; PMID:23718831; PMID:7794281; PMID:9605009; PMID:9848777
GO:0008285 Negative regulation of cell population proliferation Increases phenotype PMID:1988098; PMID:38432573
GO:0008361 Regulation of cell size Decreases phenotype PMID:29852127; PMID:9398081
GO:0009410 Response to xenobiotic stimulus Increases phenotype PMID:18809656
GO:0010942 Positive regulation of cell death Increases phenotype PMID:18809656; PMID:25578243; PMID:38432573
GO:0016042 Lipid catabolic process Affects phenotype PMID:29341888; PMID:35734936
GO:0018158 Protein oxidation Increases phenotype PMID:34165024
GO:0018342 Protein prenylation Affects phenotype PMID:10203554; PMID:11178870; PMID:16156861; PMID:17472962; PMID:9018116; PMID:9398081
GO:0019432 Triglyceride biosynthetic process Increases phenotype PMID:27208389; PMID:29852127
GO:0019722 Calcium-mediated signaling Decreases phenotype PMID:1827487
GO:0020027 Hemoglobin metabolic process Decreases phenotype PMID:28710503
GO:0030154 Cell differentiation Affects phenotype PMID:12843138; PMID:20694854; PMID:7794281
GO:0030336 Negative regulation of cell migration Increases phenotype PMID:12405293
GO:0030866 Cortical actin cytoskeleton organization Decreases phenotype PMID:12405293
GO:0032060 Bleb assembly Increases phenotype PMID:26863638
GO:0034440 Lipid oxidation Increases phenotype PMID:34165024
GO:0036273 Response to statin Increases phenotype PMID:32739440
GO:0036438 Maintenance of lens transparency Affects phenotype PMID:34890705
GO:0043065 Positive regulation of apoptotic process Increases phenotype PMID:26739623; PMID:28710503; PMID:9525472
GO:0044237 Cellular metabolic process Affects phenotype PMID:29341888; PMID:31311324
GO:0044818 Mitotic g2/m transition checkpoint Increases phenotype PMID:26739623
GO:0045541 Negative regulation of cholesterol biosynthetic process Increases phenotype PMID:21430599
GO:0045599 Negative regulation of fat cell differentiation Increases phenotype PMID:8773465
GO:0045648 Positive regulation of erythrocyte differentiation Decreases phenotype PMID:28710503
GO:0045931 Positive regulation of mitotic cell cycle Increases phenotype PMID:28710503
GO:0046209 Nitric oxide metabolic process Affects phenotype PMID:35734936
GO:0048709 Oligodendrocyte differentiation Increases phenotype PMID:20578043
GO:0050729 Positive regulation of inflammatory response Increases phenotype PMID:21430599
GO:0051881 Regulation of mitochondrial membrane potential Affects phenotype PMID:34165024
GO:0051895 Negative regulation of focal adhesion assembly Increases phenotype PMID:12405293
GO:0060305 Regulation of cell diameter Affects phenotype PMID:27208389
GO:0070085 Glycosylation Decreases phenotype PMID:10203554
GO:0070265 Necrotic cell death Increases phenotype PMID:35734936
GO:0070665 Positive regulation of leukocyte proliferation Decreases phenotype PMID:28710503
GO:0072593 Reactive oxygen species metabolic process Increases phenotype PMID:34165024
GO:0090315 Negative regulation of protein targeting to membrane Increases phenotype PMID:12405293
GO:1900127 Positive regulation of hyaluronan biosynthetic process Increases phenotype PMID:38432573
GO:1900745 Positive regulation of p38mapk cascade Increases phenotype PMID:26739623
GO:1903035 Negative regulation of response to wounding Increases phenotype PMID:36008464

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We have built a comprehensive resource which compiles potential endocrine disrupting chemicals (EDCs) based on the observed adverse effects or endocrine-mediated endpoints in published experiments on humans or rodents to support basic research. We are not responsible for any errors or omissions in the published research articles or supporting literature on potential EDCs compiled in this resource. Users are advised to exercise their own judgement on the weight of evidence for potential EDCs compiled in this resource. Importantly, our sole goal to build this resource on potential EDCs is to enable future basic research towards better understanding of the systems-level perturbations upon chemical exposure rather than influencing regulatory advice on chemical use.