Azelaic acid (BioDeep_00000000146)
Secondary id: BioDeep_00000400099, BioDeep_00000415737
human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite Chemicals and Drugs Antibiotics BioNovoGene_Lab2019
代谢物信息卡片
化学式: C9H16O4 (188.1048536)
中文名称: 壬二酸
谱图信息:
最多检出来源 Viridiplantae(plant) 0.5%
Last reviewed on 2024-06-29.
Cite this Page
Azelaic acid. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China.
https://query.biodeep.cn/s/azelaic_acid (retrieved
2024-11-08) (BioDeep RN: BioDeep_00000000146). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
分子结构信息
SMILES: C(=O)(CCCCCCCC(=O)O)O
InChI: InChI=1S/C9H16O4/c10-8(11)6-4-2-1-3-5-7-9(12)13/h1-7H2,(H,10,11)(H,12,13)
描述信息
Nonanedioic acid is an alpha,omega-dicarboxylic acid that is heptane substituted at positions 1 and 7 by carboxy groups. It has a role as an antibacterial agent, an antineoplastic agent, a dermatologic drug and a plant metabolite. It is a dicarboxylic fatty acid and an alpha,omega-dicarboxylic acid. It is a conjugate acid of an azelaate(2-) and an azelaate.
Azelaic acid is a saturated dicarboxylic acid found naturally in wheat, rye, and barley. It is also produced by Malassezia furfur, also known as Pityrosporum ovale, which is a species of fungus that is normally found on human skin. Azelaic acid is effective against a number of skin conditions, such as mild to moderate acne, when applied topically in a cream formulation of 20\\\\\%. It works in part by stopping the growth of skin bacteria that cause acne, and by keeping skin pores clear. Azelaic acids antimicrobial action may be attributable to inhibition of microbial cellular protein synthesis.
Azelaic acid is a metabolite found in or produced by Escherichia coli (strain K12, MG1655).
The physiologic effect of azelaic acid is by means of Decreased Protein Synthesis, and Decreased Sebaceous Gland Activity.
Azelaic Acid is a naturally occurring dicarboxylic acid produced by Malassezia furfur and found in whole grain cereals, rye, barley and animal products. Azelaic acid possesses antibacterial, keratolytic, comedolytic, and anti-oxidant activity. Azelaic acid is bactericidal against Proprionibacterium acnes and Staphylococcus epidermidis due to its inhibitory effect on the synthesis of microbial cellular proteins. Azelaic acid exerts its keratolytic and comedolytic effects by reducing the thickness of the stratum corneum and decreasing the number of keratohyalin granules by reducing the amount and distribution of filaggrin in epidermal layers. Azelaic acid also possesses a direct anti-inflammatory effect due to its scavenger activity of free oxygen radical. This drug is used topically to reduce inflammation associated with acne and rosacea.
Azelaic acid is a saturated dicarboxylic acid found naturally in wheat, rye, and barley. It is a natural substance that is produced by Malassezia furfur (also known as Pityrosporum ovale), a yeast that lives on normal skin. It is effective against a number of skin conditions, such as mild to moderate acne, when applied topically in a cream formulation of 20\\\\\%. It works in part by stopping the growth of skin bacteria that cause acne, and by keeping skin pores clear. Azelaic acids antimicrobial action may be attributable to inhibition of microbial cellular protein synthesis.
See also: Azelaic acid; niacinamide (component of) ... View More ...
Azelaic acid (AZA) is a naturally occurring saturated nine-carbon dicarboxylic acid (COOH (CH2)7-COOH). It possesses a variety of biological actions both in vitro and in vivo. Interest in the biological activity of AZA arose originally out of studies of skin surface lipids and the pathogenesis of hypochromia in pityriasis versicolor infection. Later, it was shown that Pityrosporum can oxidize unsaturated fatty acids to C8-C12 dicarboxylic acids that are cornpetitive inhibitors of tyrosinase in vitro. Azelaic acid was chosen for further investigation and development of a new topical drug for treating hyperpigmentary disorders for the following reasons: it possesses a middle-range of antityrosinase activity, is inexpensive, and more soluble to be incorporated into a base cream than other dicarboxylic acids. Azelaic acid is another option for the topical treatment of mild to moderate inflammatory acne vulgaris. It offers effectiveness similar to that of other agents without the systemic side effects of oral antibiotics or the allergic sensitization of topical benzoyl peroxide and with less irritation than tretinoin. Azelaic acid is less expensive than certain other prescription acne preparations, but it is much more expensive than nonprescription benzoyl peroxide preparations. Whether it is safe and effective when used in combination with other agents is not known. (PMID: 7737781, 8961845).
An alpha,omega-dicarboxylic acid that is heptane substituted at positions 1 and 7 by carboxy groups.
Plants biology
In plants, azelaic acid serves as a "distress flare" involved in defense responses after infection.[7] It serves as a signal that induces the accumulation of salicylic acid, an important component of a plant's defensive response.[8]
Human biology
The mechanism of action in humans is thought to be through the inhibition of hyperactive protease activity that converts cathelicidin into the antimicrobial skin peptide LL-37.[9]
Polymers and related materials
Esters of this dicarboxylic acid find applications in lubrication and plasticizers. In lubricant industries it is used as a thickening agent in lithium complex grease. With hexamethylenediamine, azelaic acid forms Nylon-6,9, which finds specialized uses as a plastic.[4]
Medical
Azelaic acid is used to treat mild to moderate acne, both comedonal acne and inflammatory acne.[10][11] It belongs to a class of medication called dicarboxylic acids. It works by killing acne bacteria that infect skin pores. It also decreases the production of keratin, which is a natural substance that promotes the growth[clarification needed] of acne bacteria.[12] Azelaic acid is also used as a topical gel treatment for rosacea, due to its ability to reduce inflammation.[11] It clears the bumps and swelling caused by rosacea.
In topical pharmaceutical preparations and scientific research AzA is typically used in concentrations between 15\\\% and 20\\\% but some research demonstrates that in certain vehicle formulations the pharmaceutical effects of 10\\\% Azelaic acid has the potential to be fully comparable to that of some 20\\\% creams.[13]
Acne treatment
Azelaic acid is effective for mild to moderate acne when applied topically at a 15\\\%-20\\\% concentration.[14][15][16][17] In patients with moderate acne, twice daily application over 3 months of 20\\\% AzA significantly reduced the number of comedones, papules, and pustules;[18][19] at this strength, it’s considered to be as effective as benzoyl peroxide 5\\\%, tretinoin 0.05\\\%, erythromycin 2\\\%, and oral tetracycline at 500 mg-1000 mg.[20][21] In a comparative review of effects of topical AzA, Salicylic acid, Nicotinamide, Sulfur, Zinc, and alpha-hydroxy acid, AzA had more high-quality evidence of effectiveness than the rest.[22] Results can be expected after 4 weeks of twice-daily treatment. The effectiveness of long term use is unclear, but it’s been recommended that AzA be used for at least 6 months continuously for maintenance.[20]
Whitening agent
Azelaic acid is used for treatment of skin pigmentation, including melasma and postinflammatory hyperpigmentation, particularly in those with darker skin types. It has been recommended as an alternative to hydroquinone.[23] As a tyrosinase inhibitor,[5] azelaic acid reduces synthesis of melanin.[24] According to one report in 1988, azelaic acid in combination with zinc sulfate in vitro was found to be a potent (90\\\% inhibition) 5α-reductase inhibitor, similar to the hair loss drugs finasteride and dutasteride.[25] In vitro research during mid-1980s evaluating azelaic acid's depigmenting (whitening) capability concluded it is effective (cytotoxic to melanocytes) at only high concentrations.[26]
A 1996 review claimed 20\\\% AzA is as potent as 4\\\% hydroquinone after a period of application of three months without the latter's adverse effects and even more effective if applied along with tretinoin for the same period of time.[27][19]
Azelaic acid is a nine-carbon dicarboxylic acid. Azelaic acid has antimicrobial activity against Propionibacterium acnes and Staphylococcus epidermidis through inhibition of microbial cellular prorein synthesis. Azelaic acid has hypopigmentation action resulting from its ability to scavenge free radicals[1][2].
Azelaic acid is a nine-carbon dicarboxylic acid. Azelaic acid has antimicrobial activity against Propionibacterium acnes and Staphylococcus epidermidis through inhibition of microbial cellular prorein synthesis. Azelaic acid has hypopigmentation action resulting from its ability to scavenge free radicals[1][2].
同义名列表
110 个代谢物同义名
InChI=1/C9H16O4/c10-8(11)6-4-2-1-3-5-7-9(12)13/h1-7H2,(H,10,11)(H,12,13; 4-02-00-02055 (Beilstein Handbook Reference); Dicarboxylic acid C9; Nonanedioic acid; AZA; Azelaic acid, Vetec(TM) reagent grade; 0C50D8EC-0DB0-4F24-8EFC-2919E1F0D9BF; Azelaic acid, technical, ~85\\% (GC); Azelaic acid, technical grade, 80\\%; Azelaic acid, analytical standard; azelaic acid, dipotassium salt; heptane-1,7-dicarboxylic acid; azelaic acid, monosodium salt; Azelaic acid, technical grade; Nonanedioic acid Azelaic acid; azelaic acid, potassium salt; Nonanedioic acid homopolymer; azelaic acid, dilithium salt; alpha,omega-Nonanedioic acid; 1,7-Heptanedicarboxylic acid; azelaic acid, disodium salt; Water-soluble azelaic acid; AZELAIC ACID [ORANGE BOOK]; azelaic acid, sodium salt; Acidum azelaicum (Latin); Acide azelaique [French]; Acido azelaico [Spanish]; Water-solubleazelaicacid; Heptanedicarboxylic acid; 1,7-Heptanedicarboxylate; Acidum azelaicum [Latin]; Poly(azelaic anhydride); Azelaic acid [USAN:INN]; Azelaic acid (USAN/INN); Polyazelaic anhydride; AZELAIC ACID [WHO-DD]; 1,7-Dicarboxyheptane; α,ω-Nonanedioic acid; AZELAIC ACID [MART.]; AZELAIC ACID (MART.); 1,9-Nonanedioic acid; AZELAIC ACID [VANDF]; AZELAIC ACID [HSDB]; AZELAIC ACID [INCI]; AZELAIC ACID [USAN]; monosodium azelate; AZelaic acid, 99\\%; Azelaic acid, 98\\%; n-Nonanedioic acid; AZELAIC ACID [INN]; AZELAIC ACID [MI]; acidum azelaicum; Azelaic Acid Gel; Acidum acelaicum; Spectrum3_000278; Spectrum4_000401; nonanedioic acid; Spectrum5_001304; 1,9-Nonanedioate; Spectrum2_000995; Lepargylic acid; Azelaicacidtech; acide azelaique; UNII-F2VW3D43YT; Acido azelaico; n-Nonanedioate; Azelainic acid; Tox21_110063_1; Azelainsaeure; Nonandisaeure; Lopac0_000051; DivK1c_000532; KBio3_001256; Nonandisaure; KBio2_003005; Nonanedioate; Finacea Foam; KBio2_005573; KBio2_000437; KBio1_000532; Azalaic Acid; Finacea (TN); Tox21_110063; EmeryS L-110; Tox21_303011; Anchoic acid; Tox21_500051; azelaic-acid; Azelaic Acid; Azelainsaure; Tox21_201989; Emerox 1110; IDI1_000532; Emerox 1144; Lepargylate; Azelex (TN); Azelic acid; F2VW3D43YT; AI3-06299; FA 9:1;O2; Skinorem; Anchoate; Azelaate; skinoren; D10AX03; Finevin; Azelaic; Finacea; azelate; Azelex; 1tuf; Azelaic acid
数据库引用编号
31 个数据库交叉引用编号
- ChEBI: CHEBI:48131
- KEGG: C08261
- KEGGdrug: D70171
- KEGGdrug: D03034
- PubChem: 2266
- HMDB: HMDB0000784
- Metlin: METLIN5750
- DrugBank: DB00548
- ChEMBL: CHEMBL1238
- Wikipedia: Azelaic_acid
- LipidMAPS: LMFA01170054
- MeSH: azelaic acid
- ChemIDplus: 0000123999
- MetaCyc: CPD0-1265
- KNApSAcK: C00045634
- foodb: FDB012192
- chemspider: 2179
- CAS: 123-99-9
- MoNA: KO000127
- MoNA: KO000123
- MoNA: KO000125
- MoNA: KO000126
- MoNA: KO000124
- PMhub: MS000000289
- MetaboLights: MTBLC48131
- PDB-CCD: AZ1
- 3DMET: B02152
- NIKKAJI: J10.058G
- RefMet: Azelaic acid
- medchemexpress: HY-B0704
- BioNovoGene_Lab2019: BioNovoGene_Lab2019-481
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
0 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
5 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
- Sara Álvarez-Rodríguez, Fabrizio Araniti, Marta Teijeira, Manuel J Reigosa, Adela M Sánchez-Moreiras. Azelaic acid can efficiently compete for the auxin binding site TIR1, altering auxin polar transport, gravitropic response, and root growth and architecture in Arabidopsisthaliana roots.
Plant physiology and biochemistry : PPB.
2024 May; 210(?):108592. doi:
10.1016/j.plaphy.2024.108592
. [PMID: 38569422] - Ahmed A Shibl, Michael A Ochsenkühn, Amin R Mohamed, Ashley Isaac, Lisa S Y Coe, Yejie Yun, Grzegorz Skrzypek, Jean-Baptiste Raina, Justin R Seymour, Ahmed J Afzal, Shady A Amin. Molecular mechanisms of microbiome modulation by the eukaryotic secondary metabolite azelaic acid.
eLife.
2024 Jan; 12(?):. doi:
10.7554/elife.88525
. [PMID: 38189382] - Agata Markiewicz-Tomczyk, Elżbieta Budzisz, Anna Erkiert-Polguj. Clinical evaluation of anti-aging effects of combined therapy-Azelaic acid, phytic acid, and vitamin C applied layer by layer in females with Fitzpatrick skin types II and III.
Journal of cosmetic dermatology.
2022 Dec; 21(12):6830-6839. doi:
10.1111/jocd.15359
. [PMID: 36056802] - Attila L Ádám, György Kátay, András Künstler, Lóránt Király. Detection of Lipid Peroxidation-Derived Free Azelaic Acid, a Biotic Stress Marker and Other Dicarboxylic Acids in Tobacco by Reversed-Phase HPLC-MS Under Non-derivatized Conditions.
Methods in molecular biology (Clifton, N.J.).
2022; 2526(?):191-200. doi:
10.1007/978-1-0716-2469-2_14
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Cell reports.
2021 04; 35(4):109040. doi:
10.1016/j.celrep.2021.109040
. [PMID: 33910017] - Hang Gao, Miaojie Guo, Jianbo Song, Yeye Ma, Ziqin Xu. Signals in systemic acquired resistance of plants against microbial pathogens.
Molecular biology reports.
2021 Apr; 48(4):3747-3759. doi:
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. [PMID: 33893927] - Supriya Kumari Singh, Saumya Chaubey, Anil Bansal, Gurpreet Kaur, Deepinder Singh Malik. Cosmeceutical Aptitudes of Azelaic Acid.
Current drug research reviews.
2021; 13(3):222-229. doi:
10.2174/2589977513666210526122909
. [PMID: 34042044] - Chunyan Wu, Mi-Young Jeong, Jung Yeon Kim, Giljae Lee, Ji-Sun Kim, Yu Eun Cheong, Hyena Kang, Chung Hwan Cho, Jimin Kim, Min Kyung Park, You Kyoung Shin, Kyoung Heon Kim, Geun Hee Seol, Seung Hoi Koo, GwangPyo Ko, Sung-Joon Lee. Activation of ectopic olfactory receptor 544 induces GLP-1 secretion and regulates gut inflammation.
Gut microbes.
2021 Jan; 13(1):1987782. doi:
10.1080/19490976.2021.1987782
. [PMID: 34674602] - Juan Bai, Renalison Farias-Pereira, Miran Jang, Yuan Zhang, Sang Mi Lee, Young-Suk Kim, Yeonhwa Park, Jun Bae Ahn, Gun-Hee Kim, Kee-Hong Kim. Azelaic Acid Promotes Caenorhabditis elegans Longevity at Low Temperature Via an Increase in Fatty Acid Desaturation.
Pharmaceutical research.
2021 Jan; 38(1):15-26. doi:
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. [PMID: 33449249] - Nabeelah Bibi Sadeer, Kouadio Ibrahime Sinan, Zoltán Cziáky, József Jekő, Gokhan Zengin, Rajesh Jeewon, Hassan H Abdallah, Kannan R R Rengasamy, Mohamad Fawzi Mahomoodally. Assessment of the Pharmacological Properties and Phytochemical Profile of Bruguiera gymnorhiza (L.) Lam Using in Vitro Studies, in Silico Docking, and Multivariate Analysis.
Biomolecules.
2020 05; 10(5):. doi:
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. [PMID: 32392806] - Robert T Streeper, Christopher Louden, Elzbieta Izbicka. Oral Azelaic Acid Ester Decreases Markers of Insulin Resistance in Overweight Human Male Subjects.
In vivo (Athens, Greece).
2020 May; 34(3):1173-1186. doi:
10.21873/invivo.11890
. [PMID: 32354907] - Gabriele Micheletti, Natalia Calonghi, Giovanna Farruggia, Elena Strocchi, Vincenzo Palmacci, Dario Telese, Silvia Bordoni, Giulia Frisco, Carla Boga. Synthesis of Novel Structural Hybrids between Aza-Heterocycles and Azelaic Acid Moiety with a Specific Activity on Osteosarcoma Cells.
Molecules (Basel, Switzerland).
2020 Jan; 25(2):. doi:
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. [PMID: 31963693] - Cristina Bez, Sree Gowrinadh Javvadi, Iris Bertani, Giulia Devescovi, Corrado Guarnaccia, David J Studholme, Alexander M Geller, Asaf Levy, Vittorio Venturi. AzeR, a transcriptional regulator that responds to azelaic acid in Pseudomonas nitroreducens.
Microbiology (Reading, England).
2020 01; 166(1):73-84. doi:
10.1099/mic.0.000865
. [PMID: 31621557] - Tobie D Lee, Olivia W Lee, Kyle R Brimacombe, Lu Chen, Rajarshi Guha, Sabrina Lusvarghi, Bethilehem G Tebase, Carleen Klumpp-Thomas, Robert W Robey, Suresh V Ambudkar, Min Shen, Michael M Gottesman, Matthew D Hall. A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
Molecular pharmacology.
2019 11; 96(5):629-640. doi:
10.1124/mol.119.115964
. [PMID: 31515284] - Eduardo J S Brás, Ana Margarida Fortes, Virginia Chu, Pedro Fernandes, João Pedro Conde. Microfluidic device for the point of need detection of a pathogen infection biomarker in grapes.
The Analyst.
2019 Aug; 144(16):4871-4879. doi:
10.1039/c9an01002e
. [PMID: 31298663] - Michael Maes, Buranee Kanchanatawan, Sunee Sirivichayakul, André F Carvalho. In Schizophrenia, Increased Plasma IgM/IgA Responses to Gut Commensal Bacteria Are Associated with Negative Symptoms, Neurocognitive Impairments, and the Deficit Phenotype.
Neurotoxicity research.
2019 Apr; 35(3):684-698. doi:
10.1007/s12640-018-9987-y
. [PMID: 30552634] - Francesca Nicolì, Carmine Negro, Eliana Nutricati, Marzia Vergine, Alessio Aprile, Erika Sabella, Gina Damiano, Luigi De Bellis, Andrea Luvisi. Accumulation of Azelaic Acid in Xylella fastidiosa-Infected Olive Trees: A Mobile Metabolite for Health Screening.
Phytopathology.
2019 Feb; 109(2):318-325. doi:
10.1094/phyto-07-18-0236-fi
. [PMID: 30566025] - Nicolás M Cecchini, Suruchi Roychoudhry, DeQuantarius J Speed, Kevin Steffes, Arjun Tambe, Kristin Zodrow, Katerina Konstantinoff, Ho Won Jung, Nancy L Engle, Timothy J Tschaplinski, Jean T Greenberg. Underground Azelaic Acid-Conferred Resistance to Pseudomonas syringae in Arabidopsis.
Molecular plant-microbe interactions : MPMI.
2019 01; 32(1):86-94. doi:
10.1094/mpmi-07-18-0185-r
. [PMID: 30156481] - Sree Gowrinadh Javvadi, Paola Cescutti, Roberto Rizzo, Valentina Lonzarich, Luciano Navarini, Danilo Licastro, Corrado Guarnaccia, Vittorio Venturi. The spent culture supernatant of Pseudomonas syringae contains azelaic acid.
BMC microbiology.
2018 11; 18(1):199. doi:
10.1186/s12866-018-1352-z
. [PMID: 30486794] - Jian-Jun Chen, Shun-Jie Bai, Wen-Wen Li, Chan-Juan Zhou, Peng Zheng, Liang Fang, Hai-Yang Wang, Yi-Yun Liu, Peng Xie. Urinary biomarker panel for diagnosing patients with depression and anxiety disorders.
Translational psychiatry.
2018 09; 8(1):192. doi:
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. [PMID: 30232320] - Claire Villette, Julie Zumsteg, Hubert Schaller, Dimitri Heintz. Non-targeted metabolic profiling of BW312 Hordeum vulgare semi dwarf mutant using UHPLC coupled to QTOF high resolution mass spectrometry.
Scientific reports.
2018 09; 8(1):13178. doi:
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. [PMID: 30181601] - A M Egorova, I A Tarchevsky. Azelaic Acid-Induced Enzymes of Phenolic Defense in Pea Roots.
Doklady. Biochemistry and biophysics.
2018 Sep; 482(1):252-254. doi:
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. [PMID: 30397886] - Aladdin Riad, Chandrakala Aluganti Narasimhulu, Pragney Deme, Sampath Parthasarathy. A Novel Mechanism for Atherosclerotic Calcification: Potential Resolution of the Oxidation Paradox.
Antioxidants & redox signaling.
2018 08; 29(5):471-483. doi:
10.1089/ars.2017.7362
. [PMID: 29237273] - Nadia Bouain, Santosh B Satbhai, Arthur Korte, Chorpet Saenchai, Guilhem Desbrosses, Pierre Berthomieu, Wolfgang Busch, Hatem Rouached. Natural allelic variation of the AZI1 gene controls root growth under zinc-limiting condition.
PLoS genetics.
2018 04; 14(4):e1007304. doi:
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. [PMID: 29608565] - Eun-Ji Seo, Young Joo Yeon, Joo-Hyun Seo, Jung-Hoo Lee, Jhoanne P Boñgol, Yuri Oh, Jong Moon Park, Sang-Min Lim, Choul-Gyun Lee, Jin-Byung Park. Enzyme/whole-cell biotransformation of plant oils, yeast derived oils, and microalgae fatty acid methyl esters into n-nonanoic acid, 9-hydroxynonanoic acid, and 1,9-nonanedioic acid.
Bioresource technology.
2018 Mar; 251(?):288-294. doi:
10.1016/j.biortech.2017.12.036
. [PMID: 29288957] - Arnaud T Djami-Tchatchou, Efficient N Ncube, Paul A Steenkamp, Ian A Dubery. Similar, but different: structurally related azelaic acid and hexanoic acid trigger differential metabolomic and transcriptomic responses in tobacco cells.
BMC plant biology.
2017 Nov; 17(1):227. doi:
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. [PMID: 29187153] - Takaomi Yaguchi, Tomohisa Kinami, Tetsuya Ishida, Takaomi Yasuhara, Kosaku Takahashi, Hideyuki Matsuura. Induction of plant disease resistance upon treatment with yeast cell wall extract.
Bioscience, biotechnology, and biochemistry.
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Gut.
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. [PMID: 26976734] - Archana Singh, Gah-Hyun Lim, Pradeep Kachroo. Transport of chemical signals in systemic acquired resistance.
Journal of integrative plant biology.
2017 May; 59(5):336-344. doi:
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Journal of the American Society for Mass Spectrometry.
2017 03; 28(3):443-451. doi:
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. [PMID: 27924497] - M I Mhlongo, F Tugizimana, L A Piater, P A Steenkamp, N E Madala, I A Dubery. Untargeted metabolomics analysis reveals dynamic changes in azelaic acid- and salicylic acid derivatives in LPS-treated Nicotiana tabacum cells.
Biochemical and biophysical research communications.
2017 Jan; 482(4):1498-1503. doi:
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. [PMID: 27956183] - Gah-Hyun Lim, Aardra Kachroo, Pradeep Kachroo. Role of plasmodesmata and plasmodesmata localizing proteins in systemic immunity.
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