Campesterol (BioDeep_00000000527)

 

Secondary id: BioDeep_00000017530, BioDeep_00000173721, BioDeep_00000398246, BioDeep_00000618916, BioDeep_00000860621, BioDeep_00001893179

human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite


代谢物信息卡片


(8R,9S,10S,13R,14S,17R)-17-((2R,5R)-5,6-Dimethylheptan-2-yl)-10,13-dimethyl-4,5,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol

化学式: C28H48O (400.37049579999996)
中文名称: 菜油甾醇
谱图信息: 最多检出来源 Homo sapiens(blood) 0.02%

Reviewed

Last reviewed on 2024-07-01.

Cite this Page

Campesterol. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/campesterol (retrieved 2024-09-17) (BioDeep RN: BioDeep_00000000527). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

分子结构信息

SMILES: C1[C@@H](CC2=CC[C@@H]3[C@@H]([C@]2(C1)C)CC[C@]1([C@H]3CC[C@@H]1[C@@H](CC[C@H](C(C)C)C)C)C)O
InChI: InChI=1S/C28H48O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h9,18-20,22-26,29H,7-8,10-17H2,1-6H3/t19-,20+,22-,23-,24+,25-,26-,27-,28+/m0/s1

描述信息

Campesterol is a phytosterol, meaning it is a steroid derived from plants. As a food additive, phytosterols have cholesterol-lowering properties (reducing cholesterol absorption in intestines), and may act in cancer prevention. Phytosterols naturally occur in small amount in vegetable oils, especially soybean oil. One such phytosterol complex, isolated from vegetable oil, is cholestatin, composed of campesterol, stigmasterol, and brassicasterol, and is marketed as a dietary supplement. Sterols can reduce cholesterol in human subjects by up to 15\\\\\%. The mechanism behind phytosterols and the lowering of cholesterol occurs as follows : the incorporation of cholesterol into micelles in the gastrointestinal tract is inhibited, decreasing the overall amount of cholesterol absorbed. This may in turn help to control body total cholesterol levels, as well as modify HDL, LDL and TAG levels. Many margarines, butters, breakfast cereals and spreads are now enriched with phytosterols and marketed towards people with high cholesterol and a wish to lower it. -- Wikipedia.
Campesterol is a member of phytosterols, a 3beta-sterol, a 3beta-hydroxy-Delta(5)-steroid and a C28-steroid. It has a role as a mouse metabolite. It derives from a hydride of a campestane.
Campesterol is a natural product found in Haplophyllum bucharicum, Bugula neritina, and other organisms with data available.
Campesterol is a steroid derivative that is the simplest sterol, characterized by the hydroxyl group in position C-3 of the steroid skeleton, and saturated bonds throughout the sterol structure, with the exception of the 5-6 double bond in the B ring.

Campesterol. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=474-62-4 (retrieved 2024-07-01) (CAS RN: 474-62-4). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Campesterol is a plant sterol with cholesterol lowering and anticarcinogenic effects.
Campesterol is a plant sterol with cholesterol lowering and anticarcinogenic effects.

同义名列表

75 个代谢物同义名

(8R,9S,10S,13R,14S,17R)-17-((2R,5R)-5,6-Dimethylheptan-2-yl)-10,13-dimethyl-4,5,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol; (3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol; (1S,2R,5S,10S,11S,14R,15R)-14-[(2R,5R)-5,6-dimethylheptan-2-yl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-5-ol; CAMPESTEROL (CONSTITUENT OF SAW PALMETTO) [DSC]; CAMPESTEROL (CONSTITUENT OF SAW PALMETTO); CAMPESTEROL (CONSTITUENT OF PYGEUM) [DSC]; 24.alpha.-Methyl-5-cholesten-3.beta.-ol; 24 alpha-methylcholest-5-en-3 beta-ol; (24R)-24-methylcholest-5-en-3beta-ol; (24R)24-Methylcholest-5-en-3beta-ol; CAMPESTEROL (CONSTITUENT OF PYGEUM); (24R)-Methylcholest-5-en-3.beta.-ol; 24alpha-Methyl-5-cholesten-3beta-ol; Ergost-5-en-3-ol-, (24R, 3.beta.)-; .DELTA.5-24-Isoergosten-3.beta.-ol; (24R)-24-Methylcholest-5-en-3β-ol; ergost-5-en-3 beta- ol, 24 epimer; (24R)-Methylcholest-5-en-3beta-ol; campesterol, (3beta,24xi)-isomer; (24R)-Methylcholest-5-en-3β-ol; 24-Methylcholest-5-en-3beta-ol; (3.BETA.,24R)-ERGOST-5-EN-3-OL; (24R)-Methylcholest-5-en-3b-ol; Ergost-5-en-3-ol, (3beta,24R)-; delta5-24-Isoergosten-3beta-ol; (24S)-beta-Methyl cholesterol; (3-beta-24R)-Ergost-5-en-3-ol; cholest 5-en-3-ol, 24-methyl; 3 beta, 24R-ergost-5-en-3-ol; 24a-Methyl-5-cholesten-3b-ol; (3beta,24R)-ergost-5-en-3-ol; Ergost-5-en-3beta-ol, (24R)-; 24Α-methyl-5-cholesten-3β-ol; (24R)-Ergost-5-en-3-beta-ol; Ergost-5-en-3-ol, (3b,24R)-; 22,23-dihydrobrassicasterol; campesterol, (3beta)-isomer; 24.alpha.-Methylcholesterol; 24-methyl-5-Cholestene-3-ol; (24R)-Ergost-5-en-3beta-ol; 24-alpha-Methylcholesterol; (24R)-5-Ergosten-3-beta-ol; 24alpha-Methylcholesterol; (24R)-5-Ergosten-3beta-ol; (24R)ergost-5-en-3beta-ol; (3Β,24R)-ergost-5-en-3-ol; (3-beta)-Ergost-5-en-3-ol; (3b,24R)-Ergost-5-en-3-ol; 24(R)-methylcholesterol; (24R)-Ergost-5-en-3b-ol; (24R)-Ergost-5-en-3β-ol; Δ5-24-isoergosten-3β-ol; (24R)Ergost-5-en-3b-ol; (24R)-5-Ergosten-3β-ol; (24R)Ergost-5-en-3β-ol; (24R)-5-Ergosten-3b-ol; Campest-5-en-3beta-ol; Ergost-5-en-3-beta-ol; 24a-Methylcholesterol; 24Α-methylcholesterol; CAMPESTEROL [WHO-DD]; 24-methylcholesterol; Campest-5-en-3-ol; CAMPESTEROL [MI]; UNII-5L5O665639; Mieyajunsu A; Campesterin; Campasterol; Campesterol; 5L5O665639; ST 28:1;O; (3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5S)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol; (24R)-5-Ergosten-3-beta-ol (24R)-5-Ergosten-3b-ol; Ergost-5-en-3-ol; Campestrol



数据库引用编号

24 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(4)

PlantCyc(1)

代谢反应

164 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(10)

WikiPathways(1)

Plant Reactome(5)

INOH(0)

PlantCyc(147)

COVID-19 Disease Map(0)

PathBank(1)

  • Steroid Biosynthesis: Hydrogen Ion + Lathosterol + Oxygen + ferrocytochrome b5 ⟶ 7-Dehydrocholesterol + Water + ferricytochrome b5

PharmGKB(0)

985 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:

  • PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。



文献列表

  • Yu Chun Teng, Marie Claire Gielen, Nina M de Gruijter, Coziana Ciurtin, Elizabeth C Rosser, Kersti Karu. Phytosterols in human serum as measured using a liquid chromatography tandem mass spectrometry. The Journal of steroid biochemistry and molecular biology. 2024 Jul; 241(?):106519. doi: 10.1016/j.jsbmb.2024.106519. [PMID: 38614432]
  • Zhijie Qin, Yunliang Zhang, Song Liu, Weizhu Zeng, Jingwen Zhou, Sha Xu. Combining Metabolic Engineering and Lipid Droplet Assembly to Achieve Campesterol Overproduction in Saccharomyces cerevisiae. Journal of agricultural and food chemistry. 2024 Mar; 72(9):4814-4824. doi: 10.1021/acs.jafc.3c09764. [PMID: 38389392]
  • Jiarui Mi, Qingwei Jiang, Zhengwei Qi, Zhengye Liu, Xiaoyin Bai, Xia Zheng, Jiaguo Wu, Yanfei Fang, Aiming Yang, Haotian Chen. Plasma campesterol and ABCG5/ABCG8 gene loci on the risk of cholelithiasis and cholecystitis: evidence from Mendelian randomization and colocalization analyses. Human genomics. 2024 Feb; 18(1):19. doi: 10.1186/s40246-024-00583-y. [PMID: 38347599]
  • Adam Yasgar, Danielle Bougie, Richard T Eastman, Ruili Huang, Misha Itkin, Jennifer Kouznetsova, Caitlin Lynch, Crystal McKnight, Mitch Miller, Deborah K Ngan, Tyler Peryea, Pranav Shah, Paul Shinn, Menghang Xia, Xin Xu, Alexey V Zakharov, Anton Simeonov. Quantitative Bioactivity Signatures of Dietary Supplements and Natural Products. ACS pharmacology & translational science. 2023 May; 6(5):683-701. doi: 10.1021/acsptsci.2c00194. [PMID: 37200814]
  • Shanhui Xu, Xiaoxuan Teng, Yanran Li. Optimization of Campesterol-Producing Yeast Strains as a Feasible Platform for the Functional Reconstitution of Plant Membrane-Bound Enzymes. ACS synthetic biology. 2023 Mar; ?(?):. doi: 10.1021/acssynbio.2c00599. [PMID: 36972300]
  • Ahmed Jibrin Uttu, Muhammad Sani Sallau, Hamisu Ibrahim, Ogunkemi Risikat Agbeke Iyun. In silico modelling and NMR Characterization of some steroids from Strychnos innocua (Delile) root bark as potential antifungal agents. Steroids. 2023 Mar; 194(?):109222. doi: 10.1016/j.steroids.2023.109222. [PMID: 36924816]
  • Valéria Sutti Nunes, Edite Vieira Silva de Campos, Jamal Baracat, Victor França, Érica Ivana Lázaro Gomes, Raissa Peres Coelho, Edna Regina Nakandakare, Vanessa Helena Souza Zago, Eliana Cotta de Faria, Eder Carlos Rocha Quintão. Plasma Campesterol Is Positively Associated with Carotid Plaques in Asymptomatic Subjects. International journal of molecular sciences. 2022 Oct; 23(19):. doi: 10.3390/ijms231911997. [PMID: 36233298]
  • S Baumgartner, D Lütjohann, C Husche, A Kerksiek, A K Groen, R P Mensink, J Plat. Plasma oxyphytosterols most likely originate from hepatic oxidation and subsequent spill-over in the circulation. The Journal of steroid biochemistry and molecular biology. 2022 02; 216(?):106039. doi: 10.1016/j.jsbmb.2021.106039. [PMID: 34861389]
  • Madlen Reinicke, Judith Leyh, Silke Zimmermann, Soroth Chey, Ilijana Begcevic Brkovic, Christin Wassermann, Julia Landmann, Dieter Lütjohann, Berend Isermann, Ingo Bechmann, Uta Ceglarek. Plant Sterol-Poor Diet Is Associated with Pro-Inflammatory Lipid Mediators in the Murine Brain. International journal of molecular sciences. 2021 Dec; 22(24):. doi: 10.3390/ijms222413207. [PMID: 34948003]
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  • Fabio Ferrini, Daniele Fraternale, Sabrina Donati Zeppa, Giancarlo Verardo, Andrea Gorassini, Vittoria Carrabs, Maria Cristina Albertini, Piero Sestili. Yield, Characterization, and Possible Exploitation of Cannabis Sativa L. Roots Grown under Aeroponics Cultivation. Molecules (Basel, Switzerland). 2021 Aug; 26(16):. doi: 10.3390/molecules26164889. [PMID: 34443479]
  • Teruo Jojima, Shintaro Sakurai, Sho Wakamatsu, Toshie Iijima, Masahiro Saito, Takuya Tomaru, Takahiko Kogai, Isao Usui, Yoshimasa Aso. Empagliflozin increases plasma levels of campesterol, a marker of cholesterol absorption, in patients with type 2 diabetes: Association with a slight increase in high-density lipoprotein cholesterol. International journal of cardiology. 2021 05; 331(?):243-248. doi: 10.1016/j.ijcard.2021.01.063. [PMID: 33556413]
  • Sławomira Drzymała-Czyż, Patrycja Krzyżanowska-Jankowska, Krzysztof Dziedzic, Aleksandra Lisowska, Szymon Kurek, Joanna Goździk-Spychalska, Victoria Kononets, Dagmara Woźniak, Edyta Mądry, Jarosław Walkowiak. Severe Genotype, Pancreatic Insufficiency and Low Dose of Pancreatic Enzymes Associate with Abnormal Serum Sterol Profile in Cystic Fibrosis. Biomolecules. 2021 02; 11(2):. doi: 10.3390/biom11020313. [PMID: 33669566]
  • Tabea Jahn, Christopher Clark, Anja Kerksiek, Piotr Lewczuk, Dieter Lütjohann, Julius Popp. Cholesterol metabolites and plant sterols in cerebrospinal fluid are associated with Alzheimer's cerebral pathology and clinical disease progression. The Journal of steroid biochemistry and molecular biology. 2021 01; 205(?):105785. doi: 10.1016/j.jsbmb.2020.105785. [PMID: 33171206]
  • Yujiro Nakano, Chikara Komiya, Hitomi Shimizu, Hiroyuki Mishima, Kumiko Shiba, Kazutaka Tsujimoto, Kenji Ikeda, Kenichi Kashimada, Sumito Dateki, Koh-Ichiro Yoshiura, Yoshihiro Ogawa, Tetsuya Yamada. A case of ezetimibe-effective hypercholesterolemia with a novel heterozygous variant in ABCG5. Endocrine journal. 2020 Nov; 67(11):1099-1105. doi: 10.1507/endocrj.ej20-0044. [PMID: 32641618]
  • Beibei Zhao, Yan Zhang, Hua Li, Jiawen Deng, Haodi Gong, Zhicheng Chen. Nutritional Component and Chemical Characterization of Chinese Highland Barley Bran Oil. Journal of oleo science. 2020 Nov; 69(11):1339-1347. doi: 10.5650/jos.ess19318. [PMID: 33055435]
  • Ivana Semova, Amy E Levenson, Joanna Krawczyk, Kevin Bullock, Kathryn A Williams, R Paul Wadwa, Philip R Khoury, Thomas R Kimball, Elaine M Urbina, Sarah D de Ferranti, David M Maahs, Lawrence M Dolan, Amy S Shah, Clary B Clish, Sudha B Biddinger. Markers of cholesterol synthesis are elevated in adolescents and young adults with type 2 diabetes. Pediatric diabetes. 2020 11; 21(7):1126-1131. doi: 10.1111/pedi.13097. [PMID: 32738021]
  • Takeru Koga, Takaiku Sakamoto, Eiji Sakuradani, Akihiro Tai. Neurite Outgrowth-Promoting Activity of Compounds in PC12 Cells from Sunflower Seeds. Molecules (Basel, Switzerland). 2020 Oct; 25(20):. doi: 10.3390/molecules25204748. [PMID: 33081156]
  • Ya Dan Qian, Si Yuan Tan, Gui Ru Dong, Yong Jie Niu, Ching Yuan Hu, Yong Hong Meng. Increased campesterol synthesis by improving lipid content in engineered Yarrowia lipolytica. Applied microbiology and biotechnology. 2020 Aug; 104(16):7165-7175. doi: 10.1007/s00253-020-10743-4. [PMID: 32592029]
  • Valéria Sutti Nunes, Isabela M Bensenor, Paulo A Lotufo, Marisa Passarelli, Edna Regina Nakandakare, Eder Carlos Rocha Quintão. The coronary artery calcium score is linked to plasma cholesterol synthesis and absorption markers: Brazilian Longitudinal Study of Adult Health. Bioscience reports. 2020 07; 40(7):. doi: 10.1042/bsr20201094. [PMID: 32579186]
  • Fang Liu, Xiaoping Zhang, Mingdao Wang, Lele Guo, Yingyue Yang, Mingqin Zhao. Biosorption of sterols from tobacco waste extract using living and dead of newly isolated fungus Aspergillus fumigatus strain LSD-1. Bioscience, biotechnology, and biochemistry. 2020 Jul; 84(7):1521-1528. doi: 10.1080/09168451.2020.1742089. [PMID: 32183612]
  • Josep M Llop-Talaveron, Elisabet Leiva-Badosa, Ana Novak, Raúl Rigo-Bonnin, Josep R Ticó-Grau, Josep M Suñé-Negre, Ana Suárez-Lledó, Toni Lozano-Andreu, Maria B Badía-Tahull. Phytosterolaemia associated with parenteral nutrition administration in adult patients. The British journal of nutrition. 2020 06; 123(12):1365-1372. doi: 10.1017/s0007114520000574. [PMID: 32077392]
  • Adchara Prommaban, Niramon Utama-Ang, Anan Chaikitwattana, Chairat Uthaipibull, John B Porter, Somdet Srichairatanakool. Phytosterol, Lipid and Phenolic Composition, and Biological Activities of Guava Seed Oil. Molecules (Basel, Switzerland). 2020 May; 25(11):. doi: 10.3390/molecules25112474. [PMID: 32471050]
  • Abdirahman Elmi, Rosella Spina, Arnaud Risler, Stéphanie Philippot, Ali Mérito, Raphaël E Duval, Fatouma Mohamed Abdoul-Latif, Dominique Laurain-Mattar. Evaluation of Antioxidant and Antibacterial Activities, Cytotoxicity of Acacia seyal Del Bark Extracts and Isolated Compounds. Molecules (Basel, Switzerland). 2020 May; 25(10):. doi: 10.3390/molecules25102392. [PMID: 32455580]
  • Asmita Poudel, George Gachumi, Ildiko Badea, Zafer Dallal Bashi, Anas El-Aneed. The simultaneous quantification of phytosterols and tocopherols in liposomal formulations using validated atmospheric pressure chemical ionization- liquid chromatography -tandem mass spectrometry. Journal of pharmaceutical and biomedical analysis. 2020 May; 183(?):113104. doi: 10.1016/j.jpba.2020.113104. [PMID: 32058287]
  • Cathelijne Heymans, Lara R Heij, Kaatje Lenaerts, Marcel den Dulk, Mhamed Hadfoune, Chantal van Heugten, Owen B Spiller, Michael L Beeton, Sarah J Stock, Alan H Jobe, Matthew S Payne, Matthew W Kemp, Boris W Kramer, Jogchum Plat, Wim G van Gemert, Tim G A M Wolfs. Prophylactic Intra-Uterine β-Cyclodextrin Administration during Intra-Uterine Ureaplasma parvum Infection Partly Prevents Liver Inflammation without Interfering with the Enterohepatic Circulation of the Fetal Sheep. Nutrients. 2020 May; 12(5):. doi: 10.3390/nu12051312. [PMID: 32380648]
  • Hiroshi Yoshida, Hayato Tada, Kumie Ito, Yoshimi Kishimoto, Hidekatsu Yanai, Tomonori Okamura, Katsunori Ikewaki, Kyoko Inagaki, Tetsuo Shoji, Hideaki Bujo, Takashi Miida, Masayuki Yoshida, Masafumi Kuzuya, Shizuya Yamashita. Reference Intervals of Serum Non-Cholesterol Sterols by Gender in Healthy Japanese Individuals. Journal of atherosclerosis and thrombosis. 2020 May; 27(5):409-417. doi: 10.5551/jat.50187. [PMID: 31484845]
  • Ivy W Chen, Robert J Grebenok, Hubert Schaller, Keyan Zhu-Salzman, Spencer T Behmer. Aphid growth and reproduction on plants with altered sterol profiles: Novel insights using Arabidopsis mutant and overexpression lines. Journal of insect physiology. 2020 May; 123(?):104054. doi: 10.1016/j.jinsphys.2020.104054. [PMID: 32275907]
  • Claudia Aparecida Silva Almeida, Sueli Regina Baggio, Lilian Regina Barros Mariutti, Neura Bragagnolo. One-step rapid extraction of phytosterols from vegetable oils. Food research international (Ottawa, Ont.). 2020 04; 130(?):108891. doi: 10.1016/j.foodres.2019.108891. [PMID: 32156349]
  • April Davis, Laura K Cole, Kevin Kyung-Jun Min, Sidney Chow, Patrick C Choy, David Mymin, Grant M Hatch. A Phytosterolemic Mixture of Sterols Inhibits Cholesterol Synthesis, Esterification, and Low-Density Lipoprotein Receptor mRNA Abundance in HepG2 Cells. Lipids. 2020 03; 55(2):193-198. doi: 10.1002/lipd.12223. [PMID: 32065674]
  • Paweł Górnaś, Magdalena Rudzińska, Anna Grygier, Pravin Kumar Sahu, Khageshwar Singh Patel. Tephrosia apollinea seed: a new rich source of essential polyunsaturated fatty acids, tocopherols, sterols, and squalene. Natural product research. 2020 Jan; 34(2):296-299. doi: 10.1080/14786419.2018.1525373. [PMID: 30406669]
  • Joon Hee Lee, Da Young Song, Sun-Hee Jun, Sang Hoon Song, Choong Ho Shin, Chang-Seok Ki, Kyunghoon Lee, Junghan Song. High prevalence of increased sitosterol levels in hypercholesterolemic children suggest underestimation of sitosterolemia incidence. PloS one. 2020; 15(8):e0238079. doi: 10.1371/journal.pone.0238079. [PMID: 32845916]
  • Manon Le Goff, Eric Le Ferrec, Claire Mayer, Virginie Mimouni, Dominique Lagadic-Gossmann, Benoît Schoefs, Lionel Ulmann. Microalgal carotenoids and phytosterols regulate biochemical mechanisms involved in human health and disease prevention. Biochimie. 2019 Dec; 167(?):106-118. doi: 10.1016/j.biochi.2019.09.012. [PMID: 31545993]
  • Atsuko Chihara, Atsushi Tanaka, Takeshi Morimoto, Mio Sakuma, Michio Shimabukuro, Takashi Nomiyama, Osamu Arasaki, Shinichiro Ueda, Koichi Node. Differences in lipid metabolism between anagliptin and sitagliptin in patients with type 2 diabetes on statin therapy: a secondary analysis of the REASON trial. Cardiovascular diabetology. 2019 11; 18(1):158. doi: 10.1186/s12933-019-0965-3. [PMID: 31733647]
  • Ulrich Pecks, Verena Bornemann, Anika Klein, Laura Segger, Nicolai Maass, Ibrahim Alkatout, Christel Eckmann-Scholz, Mohamed Elessawy, Dieter Lütjohann. Estimating fetal cholesterol synthesis rates by cord blood analysis in intrauterine growth restriction and normally grown fetuses. Lipids in health and disease. 2019 Oct; 18(1):185. doi: 10.1186/s12944-019-1117-1. [PMID: 31653257]
  • M A Nurseitova, F B Amutova, A A Zhakupbekova, A S Omarova, A B Kondybayev, G A Bayandy, N N Akhmetsadykov, B Faye, G S Konuspayeva. Comparative study of fatty acid and sterol profiles for the investigation of potential milk fat adulteration. Journal of dairy science. 2019 Sep; 102(9):7723-7733. doi: 10.3168/jds.2018-15620. [PMID: 31255261]
  • Stefania Giammarioli, Concetta Boniglia, Luigia Di Stasio, Raffaella Gargiulo, Maurizio Mosca, Brunella Carratù. Phytosterols in supplements containing Serenoa repens: an example of variability of active principles in commercial plant based products. Natural product research. 2019 Aug; 33(15):2257-2261. doi: 10.1080/14786419.2018.1490910. [PMID: 30295072]
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