Terpenol (BioDeep_00000396759)

Main id: BioDeep_00000007671

Secondary id: BioDeep_00000016706, BioDeep_00000396317, BioDeep_00000405615, BioDeep_00000859395

PANOMIX_OTCML-2023


代谢物信息卡片


3-Cyclohexene-1-methanol, .alpha.,.alpha.,4-trimethyl-, sodium salt, (1S)-

化学式: C10H18O (154.1358)
中文名称: 松脂醇, α-萜品醇, 松油醇, （-）-α-萜品醇, α-松油醇
谱图信息: 最多检出来源 Homo sapiens(lipidsearch) 25.23%

分子结构信息

SMILES: C=C(C)C1CCC(C)(O)CC1
InChI: InChI=1S/C10H18O/c1-8-4-6-9(7-5-8)10(2,3)11/h4,9,11H,5-7H2,1-3H3

描述信息

Alpha-terpineol is a terpineol that is propan-2-ol substituted by a 4-methylcyclohex-3-en-1-yl group at position 2. It has a role as a plant metabolite.
alpha-TERPINEOL is a natural product found in Nepeta nepetella, Xylopia aromatica, and other organisms with data available.
2-(4-Methyl-3-cyclohexen-1-yl)-2-propanol is a metabolite found in or produced by Saccharomyces cerevisiae.
See also: Coriander Oil (part of); Cannabis sativa subsp. indica top (part of); Peumus boldus leaf (part of).
A terpineol that is propan-2-ol substituted by a 4-methylcyclohex-3-en-1-yl group at position 2.
(-)-α-Terpineol ((S)-α-Terpineol), a monoterpene compound, is one of compounds in Melaleuca alternifolia[1].
(-)-α-Terpineol ((S)-α-Terpineol), a monoterpene compound, is one of compounds in Melaleuca alternifolia[1].
(-)-α-Terpineol ((S)-α-Terpineol), a monoterpene compound, is one of compounds in Melaleuca alternifolia[1].
(-)-α-Terpineol ((S)-α-Terpineol), a monoterpene compound, is one of compounds in Melaleuca alternifolia[1].
α-Terpineol is isolated from Eucalyptus globulus Labill, exhibits strong antimicrobial activity against periodontopathic and cariogenic bacteria[1]. α-Terpineol possesses antifungal activity against T. mentagrophytes, and the activity might lead to irreversible cellular disruption[2].
α-Terpineol is isolated from Eucalyptus globulus Labill, exhibits strong antimicrobial activity against periodontopathic and cariogenic bacteria[1]. α-Terpineol possesses antifungal activity against T. mentagrophytes, and the activity might lead to irreversible cellular disruption[2].

同义名列表

78 个代谢物同义名

3-Cyclohexene-1-methanol, .alpha.,.alpha.,4-trimethyl-, sodium salt, (1S)-; 3-Cyclohexene-1-methanol, .alpha.,.alpha.,4-trimethyl-, (S)-; alpha-Terpineol, primary pharmaceutical reference standard; 3-CYCLOHEXENE-1-METHANOL, ALPHA., .ALPHA., 4-TRIMETHYL-; 3-Cyclohexene-1-methanol, .alpha.,.alpha.,4-trimethyl-; 3-Cyclohexene-1-methanol, .alpha.,.alpha.4-trimethyl-; 3-CYCLOHEXENE-1-METHANOL, ALPHA., alpha, 4-TRIMETHYL-; (1)-alpha,alpha,4-Trimethylcyclohex-3-ene-1-methanol; 3-cyclohexene-1-methanol, alpha, alpha, 4-trimethyl-; 3-Cyclohexene-1-methanol, alpha,alpha,4-trimethyl-; alpha,alpha,4-Trimethyl-3-cyclohexene-1-methanol; (S)-2-(4-Methyl-3-cyclohexen-1-yl)-2-propanol; (1R)-a,a,4-trimethyl-3-cyclohexene-1-methanol; 3-Cyclohexene-1-methanol,.alpha.4-trimethyl-; TERPIN MONOHYDRATE IMPURITY A [EP IMPURITY]; TERPIN MONOHYDRATE IMPURITY A (EP IMPURITY); 2-(4-methyl-1-cyclohex-3-enyl)-propan-2-ol; 2-(4-methylcyclohex-3-en-1-yl)propan-2-ol; 1-Methyl-4-isopropyl-1-cyclohexene-8-ol; 2-(4-methylcyclohex-3-enyl)propan-2-ol; 1-Methyl-4-isopropyl-1-cyclohexen-8-ol; 2-(4-Methyl-3-cyclohexenyl)-2-propanol; alpha-Terpineol, 90\\%, technical grade; alpha-Terpineol, analytical standard; alpha-TERPINEOL (PROPYL METHYL-D3); alpha-terpineol, sodium salt; alpha-Terpineol, AldrichCPR; alpha-Terpineol (natural); .ALPHA.-TERPINEOL [FHFI]; ALFA-TERPINEOL [WHO-DD]; .ALPHA.-TERPINEOL [MI]; ALPHA-TERPINEOL [HSDB]; .ALPHA.-TERPINEOL [II]; ALPHA-TERPINEOL [FCC]; (+)-.alpha.-Terpineol; Terpineol schlechthin; alpha-TERPINEOL (II); (-​)​-​α-​Terpineol; DL-alpha-terpineol; Terpilenol, alpha-; .alpha.-Terpineol; p-menth-1-en-8-ol; D-alpha-terpineol; 1-alpha-terpineol; alpha-Terpinenol; TERPINEOL, ALPHA; alpha -Terpineol; .ALPHA.TERPINEOL; 1-p-Menthen-8-ol; 1-Menthene-8-ol; Terpene alcohol; alpha-terpineol; Menth-1-en-8-ol; UNII-R53Q4ZWC99; alphaTERPINEOL; Alfa_terpineol; CARVOMENTHENOL; ALFA-TERPINEOL; DL a-terpineol; 1-p-Menthen-8-; Menthen-8-ol; Tox21_200112; Tox21_302298; Tox21_112118; CAS-98-55-5; α-Terpineol; -terpineol; R53Q4ZWC99; TERPINEOLS; Terpineol; AI3-00275; Terpenol; (-)-alpha-Terpineol; (S?)?-?α-?Terpineol; (-?)?-?α-?Terpineol; alpha-Terpineol; (-)-alpha-Terpineol; alpha-Terpineol



数据库引用编号

30 个数据库交叉引用编号

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)

552 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。

亚细胞结构定位 关联基因列表
Cytoplasm 12 BCL2, CASP3, CASP9, CAT, CNR1, ELANE, HPGDS, PTGS2, RELA, SREBF1, TYR, VEGFA
Peripheral membrane protein 3 ACHE, CYP1B1, PTGS2
Endoplasmic reticulum membrane 4 BCL2, CYP1B1, PTGS2, SREBF1
Nucleus 8 ACHE, BCL2, CASP3, CASP9, MPO, RELA, SREBF1, VEGFA
cytosol 9 BCL2, CASP3, CASP9, CAT, ELANE, HPGDS, LIPE, RELA, SREBF1
phagocytic vesicle 1 ELANE
nucleoplasm 5 CASP3, HPGDS, MPO, RELA, SREBF1
Cell membrane 4 ACHE, CNR1, LIPE, TNF
Cell projection, axon 1 CNR1
Multi-pass membrane protein 2 CNR1, SREBF1
Golgi apparatus membrane 1 SREBF1
Synapse 1 ACHE
cell surface 4 ACHE, ELANE, TNF, VEGFA
glutamatergic synapse 3 CASP3, CNR1, RELA
Golgi apparatus 3 ACHE, ATRN, VEGFA
Golgi membrane 1 SREBF1
growth cone 1 CNR1
neuromuscular junction 1 ACHE
neuronal cell body 2 CASP3, TNF
presynaptic membrane 1 CNR1
Cytoplasm, cytosol 1 LIPE
Lysosome 2 MPO, TYR
Presynapse 1 CNR1
plasma membrane 4 ACHE, ATRN, CNR1, TNF
Membrane 6 ACHE, BCL2, CAT, CYP1B1, LIPE, VEGFA
axon 1 CNR1
caveola 2 LIPE, PTGS2
extracellular exosome 4 ATRN, CAT, ELANE, MPO
endoplasmic reticulum 4 BCL2, PTGS2, SREBF1, VEGFA
extracellular space 8 ACHE, ATRN, ELANE, IL4, IL6, MPO, TNF, VEGFA
perinuclear region of cytoplasm 2 ACHE, TYR
adherens junction 1 VEGFA
mitochondrion 4 BCL2, CASP9, CAT, CYP1B1
protein-containing complex 5 BCL2, CASP9, CAT, PTGS2, SREBF1
intracellular membrane-bounded organelle 5 CAT, CYP1B1, HPGDS, MPO, TYR
Microsome membrane 2 CYP1B1, PTGS2
postsynaptic density 1 CASP3
Single-pass type I membrane protein 2 ATRN, TYR
Secreted 4 ACHE, IL4, IL6, VEGFA
extracellular region 8 ACHE, CAT, ELANE, IL4, IL6, MPO, TNF, VEGFA
Mitochondrion outer membrane 2 BCL2, CNR1
Single-pass membrane protein 1 BCL2
mitochondrial outer membrane 2 BCL2, CNR1
[Isoform 2]: Secreted 1 ATRN
mitochondrial matrix 1 CAT
Extracellular side 1 ACHE
transcription regulator complex 1 RELA
Nucleus membrane 1 BCL2
Bcl-2 family protein complex 1 BCL2
nuclear membrane 1 BCL2
external side of plasma membrane 1 TNF
Secreted, extracellular space, extracellular matrix 1 VEGFA
actin cytoskeleton 1 CNR1
Melanosome membrane 1 TYR
Golgi-associated vesicle 1 TYR
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
Membrane raft 2 CNR1, TNF
pore complex 1 BCL2
focal adhesion 1 CAT
GABA-ergic synapse 1 CNR1
extracellular matrix 1 VEGFA
Peroxisome 1 CAT
basement membrane 1 ACHE
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
collagen-containing extracellular matrix 1 ELANE
secretory granule 3 ELANE, MPO, VEGFA
Nucleus inner membrane 1 PTGS2
Nucleus outer membrane 1 PTGS2
nuclear inner membrane 1 PTGS2
nuclear outer membrane 1 PTGS2
neuron projection 1 PTGS2
chromatin 2 RELA, SREBF1
phagocytic cup 1 TNF
Lipid-anchor, GPI-anchor 1 ACHE
[Isoform 3]: Secreted 1 ATRN
nuclear envelope 1 SREBF1
Lipid droplet 1 LIPE
Membrane, caveola 1 LIPE
Cytoplasmic vesicle membrane 1 SREBF1
Melanosome 1 TYR
side of membrane 1 ACHE
myelin sheath 1 BCL2
azurophil granule 1 MPO
ficolin-1-rich granule lumen 1 CAT
secretory granule lumen 1 CAT
endoplasmic reticulum lumen 2 IL6, PTGS2
transcription repressor complex 1 ELANE
platelet alpha granule lumen 1 VEGFA
specific granule lumen 1 ELANE
azurophil granule lumen 2 ELANE, MPO
ER to Golgi transport vesicle membrane 1 SREBF1
apoptosome 1 CASP9
phagocytic vesicle lumen 1 MPO
synaptic cleft 1 ACHE
death-inducing signaling complex 1 CASP3
[Isoform 1]: Cell membrane 1 ATRN
Cytoplasmic vesicle, phagosome 1 ELANE
Cytoplasmic vesicle, COPII-coated vesicle membrane 1 SREBF1
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
catalase complex 1 CAT
interleukin-6 receptor complex 1 IL6
BAD-BCL-2 complex 1 BCL2
[N-VEGF]: Cytoplasm 1 VEGFA
[VEGFA]: Secreted 1 VEGFA
[Isoform L-VEGF189]: Endoplasmic reticulum 1 VEGFA
[Isoform VEGF121]: Secreted 1 VEGFA
[Isoform VEGF165]: Secreted 1 VEGFA
VEGF-A complex 1 VEGFA
NF-kappaB p50/p65 complex 1 RELA
[Isoform H]: Cell membrane 1 ACHE
NF-kappaB complex 1 RELA
[Sterol regulatory element-binding protein 1]: Endoplasmic reticulum membrane 1 SREBF1
[Processed sterol regulatory element-binding protein 1]: Nucleus 1 SREBF1
[Isoform SREBP-1aDelta]: Nucleus 1 SREBF1
[Isoform SREBP-1cDelta]: Nucleus 1 SREBF1
caspase complex 1 CASP9
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF


文献列表

  • M Shiraiwa, T Fang, J Wei, Psj Lakey, Bch Hwang, K C Edwards, S Kapur, Jem Mena, Y-K Huang, M A Digman, S A Weichenthal, S Nizkorodov, M T Kleinman. Chemical and Cellular Formation of Reactive Oxygen Species from Secondary Organic Aerosols in Epithelial Lining Fluid. Research report (Health Effects Institute). 2023 Dec; ?(215):1-56. doi: ". [PMID: 38420854]
  • Wenhui Zeng, Tong Chen, Yong Chen, Xun Yan, Wenjing Wu, Shijun Zhang, Zhiqiang Li. α-Terpineol affects social immunity, increasing the pathogenicity of entomopathogenic nematodes to subterranean termites (Isoptera). Pesticide biochemistry and physiology. 2023 Nov; 196(?):105621. doi: 10.1016/j.pestbp.2023.105621. [PMID: 37945257]
  • 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]
  • Xiujuan Pan, He Xiao, Xinping Hu, Zhi Long Liu. Insecticidal activities of the essential oil of Rhynchanthus beesianus rhizomes and its constituents against two species of grain storage insects. Zeitschrift fur Naturforschung. C, Journal of biosciences. 2023 Jan; 78(1-2):83-89. doi: 10.1515/znc-2022-0017. [PMID: 36130869]
  • Azize Demirpolat. Chemical Composition of Essential Oils of Seven Polygonum Species from Turkey: A Chemotaxonomic Approach. Molecules (Basel, Switzerland). 2022 Dec; 27(24):. doi: 10.3390/molecules27249053. [PMID: 36558187]
  • Valtcho D Zheljazkov, Giuseppe Micalizzi, Solomon Yilma, Charles L Cantrell, Amber Reichley, Luigi Mondello, Ivanka Semerdjieva, Tzenka Radoukova. Melissa officinalis L. as a Sprout Suppressor in Solanum tuberosum L. and an Alternative to Synthetic Pesticides. Journal of agricultural and food chemistry. 2022 Nov; 70(44):14205-14219. doi: 10.1021/acs.jafc.2c05942. [PMID: 36306427]
  • Majid Mohammadhosseini, Alessandro Venditti, Behnam Mahdavi, Mohammad Reza Kianasab, Reyhaneh Shirazi. Profiling of the essential oil compositions from the flowers and leaves of Tanacetum fisherae Aitch. & Hemsl., an endemic plant in Kerman province, Iran. Natural product research. 2022 Oct; 36(20):5347-5352. doi: 10.1080/14786419.2021.1924711. [PMID: 33977845]
  • Emanuel Tenório Paulino, Amanda Karine Barros Ferreira Rodrigues, Maria Luiza Dal Pont Machado, Kelly Rayane Vital de Oliveira, Alessando César Bernardino, Lucindo José Quintans-Júnior, Aldeídia Pereira Oliveira, Êurica Adélia Nogueira Ribeiro. Alpha-terpineol prevents myocardial damage against isoproterenol-MI induced in Wistar-Kyoto rats: new possible to promote cardiovascular integrity. Life sciences. 2022 Feb; 290(?):120087. doi: 10.1016/j.lfs.2021.120087. [PMID: 34740575]
  • Guodong Zheng, Yingxin Chao, Mengshi Liu, Yuhua Yang, Dedong Zhang, Kanghui Wang, Yiwen Tao, Jianye Zhang, Yongmei Li, Minyan Wei. Evaluation of dynamic changes in the bioactive components in Citri Reticulatae Pericarpium (Citrus reticulata 'Chachi') under different harvesting and drying conditions. Journal of the science of food and agriculture. 2021 Jun; 101(8):3280-3289. doi: 10.1002/jsfa.10957. [PMID: 33222189]
  • José Manuel Pineda-Ríos, Juan Cibrián-Tovar, Luis Martín Hernández-Fuentes, Rosa María López-Romero, Lauro Soto-Rojas, Jesús Romero-Nápoles, Celina Llanderal-Cázares, Luis F Salomé-Abarca. α-Terpineol: An Aggregation Pheromone in Optatus palmaris (Coleoptera: Curculionidae) (Pascoe, 1889) Enhanced by Its Host-Plant Volatiles. Molecules (Basel, Switzerland). 2021 May; 26(10):. doi: 10.3390/molecules26102861. [PMID: 34065875]
  • Sunil Kumar Bose, Karuna Sharma, Sanjay Chhibber, Kusum Harjai. Therapeutic potential of nanolipoidal α-terpineol in combating keratitis induced by Pseudomonas aeruginosa in the murine model. International journal of pharmaceutics. 2021 Feb; 594(?):120175. doi: 10.1016/j.ijpharm.2020.120175. [PMID: 33338569]
  • Any Carolina Cardoso Guimarães Vasconcelos, Daniel Fernando Pereira Vasconcelos, Felipe Rodolfo Pereira da Silva, Luiz Felipe de Carvalho França, Even Herlany Pereira Alves, David Di Lenardo, Larissa Dos Santos Pessoa, Hélio Mateus Silva Nascimento, André Dos Santos Carvalho, Francisca Beatriz de Melo Sousa, André Luiz Dos Reis Barbosa, Jand-Venes Rolim Medeiros, Pedro Duarte Novaes, Flávia Sammartino Mariano, Bruno Dos Santos Lima, Adriano Antunes de Souza Araujo, Lucindo José Quintans Júnior, Aldeídia Pereira de Oliveira. Alpha-terpineol complexed with beta-cyclodextrin reduces damages caused by periodontitis in rats. Journal of periodontal research. 2020 Dec; 55(6):877-886. doi: 10.1111/jre.12780. [PMID: 32583890]
  • Xin-Sheng Liu, Bo Gao, Xin-Lu Li, Wan-Nan Li, Zi-An Qiao, Lu Han. Chemical Composition and Antimicrobial and Antioxidant Activities of Essential Oil of Sunflower (Helianthus annuus L.) Receptacle. Molecules (Basel, Switzerland). 2020 Nov; 25(22):. doi: 10.3390/molecules25225244. [PMID: 33187052]
  • Rosa M Ojeda-Amador, Giuseppe Fregapane, María Desamparados Salvador. Influence of cultivar and technological conditions on the volatile profile of virgin pistachio oils. Food chemistry. 2020 May; 311(?):125957. doi: 10.1016/j.foodchem.2019.125957. [PMID: 31864191]
  • Nicole G H Leferink, Kara E Ranaghan, Jaime Battye, Linus O Johannissen, Sam Hay, Marc W van der Kamp, Adrian J Mulholland, Nigel S Scrutton. Taming the Reactivity of Monoterpene Synthases To Guide Regioselective Product Hydroxylation. Chembiochem : a European journal of chemical biology. 2020 04; 21(7):985-990. doi: 10.1002/cbic.201900672. [PMID: 31682055]
  • Anand Kumar Chaudhari, Vipin Kumar Singh, Abhishek Kumar Dwivedy, Somenath Das, Neha Upadhyay, Akanksha Singh, Mumtaz S Dkhar, Highland Kayang, Bhanu Prakash, Nawal Kishore Dubey. Chemically characterised Pimenta dioica (L.) Merr. essential oil as a novel plant based antimicrobial against fungal and aflatoxin B1 contamination of stored maize and its possible mode of action. Natural product research. 2020 Mar; 34(5):745-749. doi: 10.1080/14786419.2018.1499634. [PMID: 30421964]
  • Carla Maria Mariano Fernandez, Maurício Ferreira da Rosa, Ana Claudia Aparecida Mariano Fernandez, Wanessa de Campos Bortolucci, Fabiana Borges Padilha Ferreira, Giani Andrea Linde, Nelson Barros Colauto, Márcia Regina Simões, Viviane da Silva Lobo, Zilda Cristiani Gazim. Essential oil and fractions isolated of Laurel to control adults and larvae of cattle ticks. Natural product research. 2020 Mar; 34(5):731-735. doi: 10.1080/14786419.2018.1495637. [PMID: 30445842]
  • Dlzar A Kheder, Omar A M Al-Habib, Gianluca Gilardoni, Giovanni Vidari. Components of Volatile Fractions from Eucalyptus camaldulensis Leaves from Iraqi-Kurdistan and Their Potent Spasmolytic Effects. Molecules (Basel, Switzerland). 2020 Feb; 25(4):. doi: 10.3390/molecules25040804. [PMID: 32069801]
  • J Tyler Ramsey, Yin Li, Yukitomo Arao, Ajanta Naidu, Laurel A Coons, Alejandro Diaz, Kenneth S Korach. Lavender Products Associated With Premature Thelarche and Prepubertal Gynecomastia: Case Reports and Endocrine-Disrupting Chemical Activities. The Journal of clinical endocrinology and metabolism. 2019 11; 104(11):5393-5405. doi: 10.1210/jc.2018-01880. [PMID: 31393563]
  • Joel Ljunggren, Felipe Borrero-Echeverry, Amrita Chakraborty, Tobias U T Lindblom, Erik Hedenström, Maria Karlsson, Peter Witzgall, Marie Bengtsson. Yeast Volatomes Differentially Affect Larval Feeding in an Insect Herbivore. Applied and environmental microbiology. 2019 11; 85(21):. doi: 10.1128/aem.01761-19. [PMID: 31444202]
  • 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]
  • Chuanbo Zhang, Man Li, Guang-Rong Zhao, Wenyu Lu. Alpha-Terpineol production from an engineered Saccharomyces cerevisiae cell factory. Microbial cell factories. 2019 Sep; 18(1):160. doi: 10.1186/s12934-019-1211-0. [PMID: 31547812]
  • Nilufar Z Mamadalieva, Fadia S Youssef, Mohamed L Ashour, Sobirdjan A Sasmakov, Antonio Tiezzi, Shahnoz S Azimova. Chemical composition, antimicrobial and antioxidant activities of the essential oils of three Uzbek Lamiaceae species. Natural product research. 2019 Aug; 33(16):2394-2397. doi: 10.1080/14786419.2018.1443088. [PMID: 29468889]
  • Mohamed E I Badawy, Gehan I Kh Marei, Entsar I Rabea, Nehad E M Taktak. Antimicrobial and antioxidant activities of hydrocarbon and oxygenated monoterpenes against some foodborne pathogens through in vitro and in silico studies. Pesticide biochemistry and physiology. 2019 Jul; 158(?):185-200. doi: 10.1016/j.pestbp.2019.05.008. [PMID: 31378356]
  • Q Kong, L Zhang, P An, J Qi, X Yu, J Lu, X Ren. Antifungal mechanisms of α-terpineol and terpene-4-alcohol as the critical components of Melaleuca alternifolia oil in the inhibition of rot disease caused by Aspergillus ochraceus in postharvest grapes. Journal of applied microbiology. 2019 Apr; 126(4):1161-1174. doi: 10.1111/jam.14193. [PMID: 30614164]
  • Yueting Chen, Yuanyuan Weng, Min Zhou, Yiyu Meng, Jialu Liu, Lin Yang, Zhaojiang Zuo. Linalool- and α-terpineol-induced programmed cell death in Chlamydomonas reinhardtii. Ecotoxicology and environmental safety. 2019 Jan; 167(?):435-440. doi: 10.1016/j.ecoenv.2018.10.062. [PMID: 30368137]
  • Yutian Zhang, Diying Li, Zhuo Wang, Wanting Zang, Pan Rao, Yunxiang Liang, Yuxia Mei. Alpha-terpineol affects synthesis and antitumor activity of triterpenoids from Antrodia cinnamomea mycelia in solid-state culture. Food & function. 2018 Dec; 9(12):6517-6525. doi: 10.1039/c8fo02079e. [PMID: 30474680]
  • Daniel Vázquez-Sánchez, Juliana Antunes Galvão, Marina Rodrigues Mazine, Eduardo Micotti Gloria, Marília Oetterer. Control of Staphylococcus aureus biofilms by the application of single and combined treatments based in plant essential oils. International journal of food microbiology. 2018 Dec; 286(?):128-138. doi: 10.1016/j.ijfoodmicro.2018.08.007. [PMID: 30099281]
  • Silan Chen, Tiefeng Zheng, Chaolin Ye, Wulan Huannixi, Zumulati Yakefu, Yiyu Meng, Xin Peng, Zhengfeng Tian, Junhao Wang, Yuandan Ma, Youyou Yang, Zhongqing Ma, Zhaojiang Zuo. Algicidal properties of extracts from Cinnamomum camphora fresh leaves and their main compounds. Ecotoxicology and environmental safety. 2018 Nov; 163(?):594-603. doi: 10.1016/j.ecoenv.2018.07.115. [PMID: 30077157]
  • Donato Colangelo, Fabrizio Torchio, Dante Marco De Faveri, Milena Lambri. The use of chitosan as alternative to bentonite for wine fining: Effects on heat-stability, proteins, organic acids, colour, and volatile compounds in an aromatic white wine. Food chemistry. 2018 Oct; 264(?):301-309. doi: 10.1016/j.foodchem.2018.05.005. [PMID: 29853380]
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