Maslinic acid

Maslinic acid is a lipid of Prenol Lipids (PR) class.

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There are no associated biomedical information in the current reference collection.

Current reference collection contains 541 references associated with Maslinic acid in LipidPedia. Due to lack of full text of references or no associated biomedical terms are recognized in our current text-mining method, we cannot extract any biomedical terms related to diseases, pathways, locations, functions, genes, lipids, and animal models from the associated reference collection.

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Authors Title Published Journal PubMed Link
Yadav VR et al. Targeting inflammatory pathways by triterpenoids for prevention and treatment of cancer. 2010 Toxins (Basel) pmid:22069560
Mooi LY et al. Chemopreventive properties of phytosterols and maslinic acid extracted from Coleus tuberosus in inhibiting the expression of EBV early-antigen in Raji cells. 2010 Chem. Biodivers. pmid:20491082
Allouche Y et al. Triterpenic content and chemometric analysis of virgin olive oils from forty olive cultivars. 2009 J. Agric. Food Chem. pmid:19326867
Martín R et al. Natural triterpenic diols promote apoptosis in astrocytoma cells through ROS-mediated mitochondrial depolarization and JNK activation. 2009 PLoS ONE pmid:19543395
Cheng K et al. Practical synthesis of bredemolic acid, a natural inhibitor of glycogen phosphorylase. 2008 J. Nat. Prod. pmid:18847277
Lee IK et al. Triterpenoic acids of Prunella vulgaris var. lilacina and their cytotoxic activities in vitro. 2008 Arch. Pharm. Res. pmid:19099227
Wen X et al. Naturally occurring pentacyclic triterpenes as inhibitors of glycogen phosphorylase: synthesis, structure-activity relationships, and X-ray crystallographic studies. 2008 J. Med. Chem. pmid:18517260
Kim JM et al. Aldose-reductase- and protein-glycation-inhibitory principles from the whole plant of Duchesnea chrysantha. 2008 Chem. Biodivers. pmid:18293434
Xie Y et al. Medicinal flowers. XXIII. New taraxastane-type triterpene, punicanolic acid, with tumor necrosis factor-alpha inhibitory activity from the flowers of Punica granatum. 2008 Chem. Pharm. Bull. pmid:18981621
Juan ME et al. Antiproliferative and apoptosis-inducing effects of maslinic and oleanolic acids, two pentacyclic triterpenes from olives, on HT-29 colon cancer cells. 2008 Br. J. Nutr. pmid:18298868
Saimaru H et al. Production of triterpene acids by cell suspension cultures of Olea europaea. 2007 Chem. Pharm. Bull. pmid:17473469
Jovel EM et al. Bioactivity-guided isolation of the active compounds from Rosa nutkana and quantitative analysis of ascorbic acid by HPLC. 2007 Can. J. Physiol. Pharmacol. pmid:18066132
Liu J et al. Maslinic acid reduces blood glucose in KK-Ay mice. 2007 Biol. Pharm. Bull. pmid:17978478
Sultana N and Lee NH Antielastase and free radical scavenging activities of compounds from the stems of Cornus kousa. 2007 Phytother Res pmid:17661332
Martín R et al. Acidic triterpenes compromise growth and survival of astrocytoma cell lines by regulating reactive oxygen species accumulation. 2007 Cancer Res. pmid:17440087
Wang R et al. Constituents of the flowers of Punica granatum. 2006 Fitoterapia pmid:16887296
Reyes FJ et al. (2Alpha,3beta)-2,3-dihydroxyolean-12-en-28-oic acid, a new natural triterpene from Olea europea, induces caspase dependent apoptosis selectively in colon adenocarcinoma cells. 2006 FEBS Lett. pmid:17083937
Marquez-Martin A et al. Modulation of cytokine secretion by pentacyclic triterpenes from olive pomace oil in human mononuclear cells. 2006 Cytokine pmid:17292619
Juan ME et al. Olive fruit extracts inhibit proliferation and induce apoptosis in HT-29 human colon cancer cells. 2006 J. Nutr. pmid:16988125
Wang D et al. New triterpenoids isolated from the root bark of Ulmus pumila L. 2006 Chem. Pharm. Bull. pmid:16755042
García-Granados A et al. Epoxides, cyclic sulfites, and sulfate from natural pentacyclic triterpenoids: theoretical calculations and chemical transformations. 2003 J. Org. Chem. pmid:12790588
Gao H et al. Antitumor-promoting constituents from Chaenomeles sinensis KOEHNE and their activities in JB6 mouse epidermal cells. 2003 Chem. Pharm. Bull. pmid:14600382
Kim YK et al. Cytotoxic triterpenes from stem bark of Physocarpus intermedius. 2000 Planta Med. pmid:10909277
Xu HX et al. Anti-HIV triterpene acids from Geum japonicum. 1996 J. Nat. Prod. pmid:8759159
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