Farnesol (BioDeep_00000001114)

Main id: BioDeep_00000406520

Secondary id: BioDeep_00000016571

human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite


代谢物信息卡片


InChI=1/C15H26O/c1-13(2)7-5-8-14(3)9-6-10-15(4)11-12-16/h7,9,11,16H,5-6,8,10,12H2,1-4H3/b14-9+,15-11

化学式: C15H26O (222.1983546)
中文名称: 金合欢醇, 法呢醇
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C/C(C)=C\CC/C(C)=C/CC/C(C)=C/CO
InChI: InChI=1S/C15H26O/c1-13(2)7-5-8-14(3)9-6-10-15(4)11-12-16/h7,9,11,16H,5-6,8,10,12H2,1-4H3

描述信息

Farnesol is a signaling molecule that is derived from farnesyl diphosphate, an intermediate in the isoprenoid/cholesterol biosynthetic pathway. Farnesol is a 15 carbon isoprenoid alcohol is the corresponding dephosphorylated form of the isoprenoid farnesyl diphosphate. Farnesol has a potential role in controlling the degradation of 3-hydroxy-3-methylglutaryl coenzyme A (HMGCoA) reductase (EC 1.1.1.34, NADPH-hydroxymethylglutaryl-CoA reductase). The enzyme is stabilized under conditions of cellular sterol depletion (e.g. statin-treated cells) and rapidly degraded in sterol-loaded cells. In mammalian cells, this enhanced degradation is dependent on the presence of both a sterol and a non-sterol derived from the isoprenoid pathway; farnesol, the dephosphorylated form of farnesyl diphosphate, can function as the non-sterol component. Farnesol has been shown to activate the farnesoid receptor (FXR), a nuclear receptor that forms a functional heterodimer with RXR. Thus, dephosphorylation of farnesyl diphosphate, an intermediate in the cholesterol synthetic pathway, might produce an active ligand for the FXR:RXR heterodimer. The physiological ligand for FXR remains to be identified; farnesol, may simply mimic the unidentified natural ligand(s). In addition, exogenous farnesol have an effect on several other physiological processes, including inhibition of phosphatidylcholine biosynthesis, induction of apoptosis, inhibition of cell cycle progression and actin cytoskeletal disorganization. Farnesol cellular availability is an important determinant of vascular tone in animals and humans, and provides a basis for exploring farnesyl metabolism in humans with compromised vascular function as well as for using farnesyl analogues as regulators of arterial tone in vivo. A possible metabolic fate for farnesol is its conversion to farnesoic acid, and then to farnesol-derived dicarboxylic acids (FDDCAs) which would then be excreted in the urine. Farnesol can also be oxidized to a prenyl aldehyde, presumably by an alcohol dehydrogenase (ADH), and that this activity resides in the mitochondrial and peroxisomal. Liver Endoplasmic reticulum and peroxisomal fractions are able to phosphorylate farnesol to Farnesyl diphosphate in a Cytosine triphosphate dependent fashion. (PMID: 9812197, 8636420, 9083051, 9015362). Prenol is polymerized by dehydration reactions; when there are at least four isoprene units (n in the above formula is greater than or equal to four), the polymer is called a polyprenol. Polyprenols can contain up to 100 isoprene units (n=100) linked end to end with the hydroxyl group (-OH) remaining at the end. These isoprenoid alcohols are also called terpenols These isoprenoid alcohols are important in the acylation of proteins, carotenoids, and fat-soluble vitamins A, E and K. They are also building blocks for plant oils such as farnesol and geraniol. Prenol is also a building block of cholesterol (built from six isoprene units), and thus of all steroids. Prenol has sedative properities, it is probably GABA receptor allosteric modulator.When the isoprene unit attached to the alcohol is saturated, the compound is referred to as a dolichol. Dolichols are important as glycosyl carriers in the synthesis of polysaccharides.(Wikipedia).
C26170 - Protective Agent > C275 - Antioxidant
Component of many flower absolutes [CCD]
Farnesol is a colorless liquid with a delicate floral odor. (NTP, 1992)
Farnesol is a farnesane sesquiterpenoid that is dodeca-2,6,10-triene substituted by methyl groups at positions 3, 7 and 11 and a hydroxy group at position 1. It has a role as a plant metabolite, a fungal metabolite and an antimicrobial agent. It is a farnesane sesquiterpenoid, a primary alcohol and a polyprenol.
trans,trans-Farnesol is a natural product found in Lonicera japonica, Psidium guajava, and other organisms with data available.
(2-trans,6-trans)-Farnesol is a metabolite found in or produced by Saccharomyces cerevisiae.
A colorless liquid extracted from oils of plants such as citronella, neroli, cyclamen, and tuberose. It is an intermediate step in the biological synthesis of cholesterol from mevalonic acid in vertebrates. It has a delicate odor and is used in perfumery. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 5th ed)
Farnesol is a sesquiterpene alcohol that modulates cell-to-cell communication in Candida albicans, and has the activity in inhibiting bacteria.
Farnesol is a sesquiterpene alcohol that modulates cell-to-cell communication in Candida albicans, and has the activity in inhibiting bacteria.

同义名列表

85 个代谢物同义名

(2-trans,6-trans)-3,7,11-trimethyldodeca-2,6,10-trien-1-ol; trans-1-Hydroxy-3,7,11-trimethyl-2,6,10-dodecatriene; 3,7,11-TRIMETHYLDODECA-2-TRANS,6-TRANS,10-TRIEN-1-OL; (2E,6E)-3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol; (2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-ol; (E,E)-3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol; 3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol; 3,7,11-Trimethyl-2,6,10-dodecen-1-ol; trans,trans-alpha-farnesol; Ditrans,polycis-polyprenol; 2-trans,6-trans-Farnesol; 2,6-trans,trans-Farnesol; trans-2,trans-6-Farnesol; 2-cis,6-trans-Farnesol; trans,trans-a-Farnesol; trans,trans-Α-farnesol; (E,E)-Farnesyl alcohol; 2,6-Di-trans-Farnesol; trans,trans-Farnesol; All-trans-Farnesol; (E)-beta-Farnesol; (2E,6E)-Farnesol; Farnesyl alcohol; trans-Farnesol; ALL-E-FARNESOL; (E)-β-Farnesol; (t,t)-Farnesol; (E,E)-Farnesol; (E)-farnesol; Nikkosome; FCI 119a; Farnesol; InChI=1/C15H26O/c1-13(2)7-5-8-14(3)9-6-10-15(4)11-12-16/h7,9,11,16H,5-6,8,10,12H2,1-4H3/b14-9+,15-11; trans,trans-3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol, (E,E)-3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol; 2,6,10-dodecatrien-1-ol, 3,7,11-trimethyl-, (2E,6E)-; trans,trans-3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol; 2,6,10-Dodecatrien-1-ol, 3,7,11-trimethyl- (8CI,9CI); 2,6,10-Dodecatrien-1-ol, 3,7,11-trimethyl-, (E,E)-; (2E,6E)-3,7,11-trimethyl-dodeca-2,6,10-trien-1-ol; (2E, 6E)-3,7,11-trimethyl2,6,10-dodecatrien-1-ol; (E,E,)-3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol; (2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-o; (E,E)-3,7,11-TRIMETHYL-2,6,10-DODECATNEN-1-OL; 2,6,10-Dodecatrien-1-ol, 3,7,11-trimethyl-; trans,trans-Farnesol, analytical standard; 3,7,11-trimethyldodeca-2,6,10-trien-1-ol; 3,7,11-Trimethyl-2,6,10-dodecatrienol; trans,trans-Farnesol; trans-Farnesol; FARNESOL TRANS,TRANS-FARNESOL [MI]; Farnesol, analytical standard; trans,trans-Farnesol, 96\\%; trans,trans-Farnesol, 97\\%; 2-trans-S-6-trans-farnesol; (2-trans,6-trans)-farnesol; Trimethyl dodecatrienol; Farnesol, trans, trans; 2E,6E-Farnesyl alcohol; trans, trans-Farnesol; trans,trans farnesol; (E)-.BETA.-FARNESOL; all-trans farnesol; FARNESOL, (2E,6E)-; CIS-TRANS-FARNESOL; Farnesol, (E,E)-; Spectrum5_002027; Farnesol (2E,6E); .beta.-Farnesol; UNII-EB41QIU6JL; UNII-X23PI60R17; trans- farnesol; (E,E,)-farnesol; Farnesol, 95\\%; Farnesol (6CI); 2E,6E-farnesol; (E,E)farnesol; transfarnesol; Tox21_302034; Inhibitor A2; E,E-farnesol; (E,)-arnesol; Polyprenol; EB41QIU6JL; X23PI60R17; AI3-44561; FOF



数据库引用编号

29 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(2)

PlantCyc(1)

代谢反应

145 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(7)

WikiPathways(1)

Plant Reactome(0)

INOH(0)

PlantCyc(135)

COVID-19 Disease Map(0)

PathBank(2)

PharmGKB(0)

166 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

  • Anton Möllerke, Diogo Montes Vidal, Hans Petter Leinaas, Stefan Schulz. Socialane, a Nonaprenyl Terpene Hydrocarbon Surface Lipid from the Collembola Hypogastrura socialis. Chemistry (Weinheim an der Bergstrasse, Germany). 2024 May; 30(27):e202400272. doi: 10.1002/chem.202400272. [PMID: 38445549]
  • Raissa Bayker Vieira Silva, Valdeci Geraldo Coelho Júnior, Adolfo de Paula Mattos Júnior, Henrique Julidori Garcia, Ester Siqueira Caixeta Nogueira, Talita Sarah Mazzoni, Juliana Ramos Martins, Lívia Maria Rosatto Moda, Angel Roberto Barchuk. Farnesol, a component of plant-derived honeybee-collected resins, shows JH-like effects in Apis mellifera workers. Journal of insect physiology. 2024 05; 154(?):104627. doi: 10.1016/j.jinsphys.2024.104627. [PMID: 38373613]
  • Ting Shen, Baocheng Tian, Wei Liu, Xuesong Yang, Qi Sheng, Mengxin Li, Haiyan Wang, Xiuwen Wang, Huihui Zhou, Yanchun Han, Chen Ding, Sixiang Sai. Transdermal administration of farnesol-ethosomes enhances the treatment of cutaneous candidiasis induced by Candida albicans in mice. Microbiology spectrum. 2024 Apr; 12(4):e0424723. doi: 10.1128/spectrum.04247-23. [PMID: 38415658]
  • Pei Wang, Miao Liu, Changhong Lv, Zhen Tian, Ruichi Li, Yifan Li, Yalin Zhang, Jiyuan Liu. Identifying the Key Role of Plutella xylostella General Odorant Binding Protein 2 in Perceiving a Larval Attractant, (E,E)-2,6-Farnesol. Journal of agricultural and food chemistry. 2024 Mar; 72(11):5690-5698. doi: 10.1021/acs.jafc.4c00621. [PMID: 38447177]
  • Carlos Jonnathan Castro-Juárez, Silvia Luna-Suárez, Flor de Fátima Rosas-Cárdenas, Nemesio Villa-Ruano. Hernandulcin Production in Elicited Hairy Roots of Phyla scaberrima: Toward Sustainable Production of a Non-Caloric Sweetener with Nutraceutical Properties. Chemistry & biodiversity. 2024 Mar; 21(3):e202302095. doi: 10.1002/cbdv.202302095. [PMID: 38334300]
  • Jill Romer, Katharina Gutbrod, Antonia Schuppener, Michael Melzer, Stefanie J Müller-Schüssele, Andreas J Meyer, Peter Dörmann. Tocopherol and phylloquinone biosynthesis in chloroplasts requires the phytol kinase VTE5 and the farnesol kinase FOLK. The Plant cell. 2023 Dec; ?(?):. doi: 10.1093/plcell/koad316. [PMID: 38124486]
  • Guglielmina Froldi, Francesco Benetti, Andrea Mondin, Marco Roverso, Elisa Pangrazzi, Francine Medjiofack Djeujo, Paolo Pastore. Pterodon emarginatus Seed Preparations: Antiradical Activity, Chemical Characterization, and In Silico ADMET Parameters of β-caryophyllene and Farnesol. Molecules (Basel, Switzerland). 2023 Nov; 28(22):. doi: 10.3390/molecules28227494. [PMID: 38005216]
  • Rodrigo Santos-Pascual, Iván Campoy, David Sanz Mata, María Jesús Martínez, Alicia Prieto, Jorge Barriuso. Deciphering the molecular components of the quorum sensing system in the fungus Ophiostoma piceae. Microbiology spectrum. 2023 Oct; ?(?):e0029023. doi: 10.1128/spectrum.00290-23. [PMID: 37796004]
  • Marta Balsells-Llauradó, Núria Vall-Llaura, Josep Usall, Christian J Silva, Barbara Blanco-Ulate, Neus Teixidó, Maria Caballol, Rosario Torres. Transcriptional profiling of the terpenoid biosynthesis pathway and in vitro tests reveal putative roles of linalool and farnesal in nectarine resistance against brown rot. Plant science : an international journal of experimental plant biology. 2023 Feb; 327(?):111558. doi: 10.1016/j.plantsci.2022.111558. [PMID: 36493930]
  • Liliane Sena Pinheiro, Valter Viana Andrade-Neto, Marcio Mantuano-Barradas, Elisa Cavalcante Pereira, Rodrigo Cesar Fernandes Barbosa, Marcia Cristina Campos de Oliveira, Rubem Figueiredo Sadok Menna-Barreto, Edézio Ferreira Cunha-Júnior, Eduardo Caio Torres-Santos. Biological effects of trans, trans-farnesol in Leishmania amazonensis. Frontiers in cellular and infection microbiology. 2023; 13(?):1221246. doi: 10.3389/fcimb.2023.1221246. [PMID: 38035328]
  • Bruna Colombari, Davide Tagliazucchi, Alessandra Odorici, Eva Pericolini, Ismaela Foltran, Diego Pinetti, Aida Meto, Samuele Peppoloni, Elisabetta Blasi. Pomegranate Extract Affects Fungal Biofilm Production: Consumption of Phenolic Compounds and Alteration of Fungal Autoinducers Release. International journal of environmental research and public health. 2022 10; 19(21):. doi: 10.3390/ijerph192114146. [PMID: 36361021]
  • Varun Dwivedi, Sarma Rajeev Kumar, H B Shilpashree, Ram Krishna, Srinivas Rao, Ajit K Shasany, Shannon B Olsson, Dinesh A Nagegowda. An inducible potato (E,E)-farnesol synthase confers tolerance against bacterial pathogens in potato and tobacco. The Plant journal : for cell and molecular biology. 2022 09; 111(5):1308-1323. doi: 10.1111/tpj.15890. [PMID: 35778946]
  • Sayoko Oiki, Ryo Nasuno, Syun-Ichi Urayama, Hiroshi Takagi, Daisuke Hagiwara. Intracellular production of reactive oxygen species and a DAF-FM-related compound in Aspergillus fumigatus in response to antifungal agent exposure. Scientific reports. 2022 08; 12(1):13516. doi: 10.1038/s41598-022-17462-y. [PMID: 35933435]
  • Yuyang Ma, Xue Liu, Defu Liu, Zihao Yin, Xinyi Yang, Mingyong Zeng. Oyster (Crassostrea gigas) Polysaccharide Ameliorates High-Fat-Diet-Induced Oxidative Stress and Inflammation in the Liver via the Bile Acid-FXR-AMPKα Pathway. Journal of agricultural and food chemistry. 2022 Jul; 70(28):8662-8671. doi: 10.1021/acs.jafc.2c02490. [PMID: 35797440]
  • Mohammed Ali, Elsayed Nishawy, Walaa A Ramadan, Mohamed Ewas, Mokhtar Said Rizk, Ahmed G M Sief-Eldein, Mohamed Abd S El-Zayat, Ahmed H M Hassan, Mingquan Guo, Guang-Wan Hu, Shengwei Wang, Fatma A Ahmed, Mohamed Hamdy Amar, Qing-Feng Wang. Molecular characterization of a Novel NAD+-dependent farnesol dehydrogenase SoFLDH gene involved in sesquiterpenoid synthases from Salvia officinalis. PloS one. 2022; 17(6):e0269045. doi: 10.1371/journal.pone.0269045. [PMID: 35657794]
  • Gopalakrishnan Balaraman, Jagan Sundaram, Ashok Mari, Palanisamy Krishnan, Sharmila Salam, Nirmala Subramaniam, Immaduddin Sirajduddin, Devaki Thiruvengadam. Farnesol alleviates diethyl nitrosamine induced inflammation and protects experimental rat hepatocellular carcinoma. Environmental toxicology. 2021 Dec; 36(12):2467-2474. doi: 10.1002/tox.23359. [PMID: 34473392]
  • Luz Díaz-Storani, Anaelle A Clary, Diego M Moreno, María Sol Ballari, Exequiel O J Porta, Andrea B J Bracca, Jonathan B Johnston, Guillermo R Labadie. Synthesis and interaction of terminal unsaturated chemical probes with Mycobacterium tuberculosis CYP124A1. Bioorganic & medicinal chemistry. 2021 08; 44(?):116304. doi: 10.1016/j.bmc.2021.116304. [PMID: 34289431]
  • Brad R Baker, Callum M Ives, Ashley Bray, Martin Caffrey, Stephen A Cochrane. Undecaprenol kinase: Function, mechanism and substrate specificity of a potential antibiotic target. European journal of medicinal chemistry. 2021 Jan; 210(?):113062. doi: 10.1016/j.ejmech.2020.113062. [PMID: 33310291]
  • Hui Huang, Qinhui Liu, Ting Zhang, Jinhang Zhang, Jian Zhou, Xiandan Jing, Qin Tang, Cuiyuan Huang, Zijing Zhang, Yingnan Zhao, Guorong Zhang, Jiamin Yan, Yan Xia, Ying Xu, Jiahui Li, Yanping Li, Jinhan He. Farnesylthiosalicylic Acid-Loaded Albumin Nanoparticle Alleviates Renal Fibrosis by Inhibiting Ras/Raf1/p38 Signaling Pathway. International journal of nanomedicine. 2021; 16(?):6441-6453. doi: 10.2147/ijn.s318124. [PMID: 34584410]
  • Diego Santos Souza, Tatiane de Oliveira Barreto, José Evaldo Rodrigues de Menezes-Filho, Luana Heimfarth, Paula Rhana, Thallita Kelly Rabelo, Michael Nadson Santos Santana, Aimée Obolari Durço, Michael Ramon de Lima Conceição, Lucindo José Quintans-Júnior, Adriana Gibara Guimarães, Jader Santos Cruz, Carla Maria Lins de Vasconcelos. Myocardial hypertrophy is prevented by farnesol through oxidative stress and ERK1/2 signaling pathways. European journal of pharmacology. 2020 Nov; 887(?):173583. doi: 10.1016/j.ejphar.2020.173583. [PMID: 32956645]
  • Lin Marcellin Messi, Olivier Placide Noté, Joséphine Ngo Mbing, Marieke Vansteelandt, Pierre Lavedan, Marc Vedrenne, Dieudonné Emmanuel Pegnyemb, Mohamed Haddad. Farnesyl glycosides and one new triterpenoid saponin from the roots of Lecaniodiscus cupanioides Planch. ex Benth. Carbohydrate research. 2020 Sep; 495(?):108092. doi: 10.1016/j.carres.2020.108092. [PMID: 32755723]
  • Pulu Sun, Clément Dégut, Stéphane Réty, Jean-Claude Caissard, Laurence Hibrand-Saint Oyant, Aurélie Bony, Saretta N Paramita, Corentin Conart, Jean-Louis Magnard, Julien Jeauffre, Ahmed M Abd-El-Haliem, Jordan Marie-Magdelaine, Tatiana Thouroude, Raymonde Baltenweck, Carine Tisné, Fabrice Foucher, Michel Haring, Philippe Hugueney, Robert C Schuurink, Sylvie Baudino. Functional diversification in the Nudix hydrolase gene family drives sesquiterpene biosynthesis in Rosa × wichurana. The Plant journal : for cell and molecular biology. 2020 09; 104(1):185-199. doi: 10.1111/tpj.14916. [PMID: 32639596]
  • Mohammad H Abukhalil, Omnia E Hussein, May Bin-Jumah, Sultan A M Saghir, Mousa O Germoush, Hassan A Elgebaly, Nermeen M Mosa, Ismail Hamad, Moath M Qarmush, Emad M Hassanein, Emadeldin M Kamel, Rene Hernandez-Bautista, Ayman M Mahmoud. Farnesol attenuates oxidative stress and liver injury and modulates fatty acid synthase and acetyl-CoA carboxylase in high cholesterol-fed rats. Environmental science and pollution research international. 2020 Aug; 27(24):30118-30132. doi: 10.1007/s11356-020-09296-w. [PMID: 32449150]
  • Anna Wróblewska-Kurdyk, Katarzyna Dancewicz, Anna Gliszczyńska, Beata Gabryś. New insight into the behaviour modifying activity of two natural sesquiterpenoids farnesol and nerolidol towards Myzus persicae (Sulzer) (Homoptera: Aphididae). Bulletin of entomological research. 2020 Apr; 110(2):249-258. doi: 10.1017/s0007485319000609. [PMID: 31559933]
  • Tejas Barot, Deepak Rawtani, Pratik Kulkarni, Chaudhery Mustansar Hussain, Satyaprasad Akkireddy. Physicochemical and biological assessment of flowable resin composites incorporated with farnesol loaded halloysite nanotubes for dental applications. Journal of the mechanical behavior of biomedical materials. 2020 04; 104(?):103675. doi: 10.1016/j.jmbbm.2020.103675. [PMID: 32174431]
  • A Špičáková, V Bazgier, L Skálová, M Otyepka, P Anzenbacher. beta-caryophyllene oxide and trans-nerolidol affect enzyme activity of CYP3A4 - in vitro and in silico studies. Physiological research. 2019 11; 68(Suppl 1):S51-S58. doi: 10.33549/physiolres.934323. [PMID: 31755290]
  • Michaela Šadibolová, Tomáš Zárybnický, Tomáš Smutný, Petr Pávek, Zdeněk Šubrt, Petra Matoušková, Lenka Skálová, Iva Boušová. Sesquiterpenes Are Agonists of the Pregnane X Receptor but Do Not Induce the Expression of Phase I Drug-Metabolizing Enzymes in the Human Liver. International journal of molecular sciences. 2019 Sep; 20(18):. doi: 10.3390/ijms20184562. [PMID: 31540101]
  • Mummadireddy Ramya, Pue Hee Park, Yu-Chen Chuang, Oh Keun Kwon, Hye Ryun An, Pil Man Park, Yun Su Baek, Byoung-Chorl Kang, Wen-Chieh Tsai, Hong-Hwa Chen. RNA sequencing analysis of Cymbidium goeringii identifies floral scent biosynthesis related genes. BMC plant biology. 2019 Aug; 19(1):337. doi: 10.1186/s12870-019-1940-6. [PMID: 31375064]
  • Miklós Tóth, Lorenzo Furlan, István Szarukán, Antal Nagy, József Vuts, Teodora Toshova, Dimitar Velchev, Zsófia Lohonyai, Zoltán Imrei. The Addition of a Pheromone to a Floral Lure Increases Catches of Females of the Click Beetle Agriotes ustulatus (Schaller) (Coleoptera: Elateridae). Journal of chemical ecology. 2019 Aug; 45(8):667-672. doi: 10.1007/s10886-019-01087-z. [PMID: 31313134]
  • Zohreh Nassimi, Parissa Taheri, Saeed Tarighi. Farnesol altered morphogenesis and induced oxidative burst-related responses in Rhizoctonia solani AG1-IA. Mycologia. 2019 May; 111(3):359-370. doi: 10.1080/00275514.2019.1600315. [PMID: 31021706]
  • Asmita Pant, Elizabeth A Rondini, Thomas A Kocarek. Farnesol induces fatty acid oxidation and decreases triglyceride accumulation in steatotic HepaRG cells. Toxicology and applied pharmacology. 2019 02; 365(?):61-70. doi: 10.1016/j.taap.2019.01.003. [PMID: 30611723]
  • Emine Sekerdag, Sevda Lüle, Sibel Bozdağ Pehlivan, Naile Öztürk, Aslı Kara, Abbas Kaffashi, Imran Vural, Ilkay Işıkay, Burҫin Yavuz, Kader Karlı Oguz, Figen Söylemezoğlu, Yasemin Gürsoy-Özdemir, Melike Mut. A potential non-invasive glioblastoma treatment: Nose-to-brain delivery of farnesylthiosalicylic acid incorporated hybrid nanoparticles. Journal of controlled release : official journal of the Controlled Release Society. 2017 09; 261(?):187-198. doi: 10.1016/j.jconrel.2017.06.032. [PMID: 28684169]
  • Abbas Kaffashi, Sevda Lüle, Sibel Bozdağ Pehlivan, Can Sarısözen, İmran Vural, Hüsnü Koşucu, Taner Demir, Kadir Emre Buğdaycı, Figen Söylemezoğlu, Kader Karlı Oğuz, Melike Mut. Farnesylthiosalicylic acid-loaded lipid-polyethylene glycol-polymer hybrid nanoparticles for treatment of glioblastoma. The Journal of pharmacy and pharmacology. 2017 Aug; 69(8):1010-1021. doi: 10.1111/jphp.12740. [PMID: 28471040]
  • Rui-Huan Liu, Zhi-Chun Shang, Tian-Xiao Li, Ming-Hua Yang, Ling-Yi Kong. In Vitro Antibiofilm Activity of Eucarobustol E against Candida albicans. Antimicrobial agents and chemotherapy. 2017 08; 61(8):. doi: 10.1128/aac.02707-16. [PMID: 28584159]
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