alpha-Humulene (BioDeep_00000000984)

 

Secondary id: BioDeep_00000175900, BioDeep_00000229350, BioDeep_00000859309, BioDeep_00001103689, BioDeep_00001892945

human metabolite PANOMIX_OTCML-2023 Endogenous


代谢物信息卡片


trans,trans,trans-2,6,6,9-Tetramethyl-1,4,8-cycloundecatriene

化学式: C15H24 (204.1878)
中文名称: α-律草烯, α-蛇麻烯, α-忽布烯, 香蛇麻烯, ALPHA-律草烯, α-蛇麻烯萜, 1,4,8-环十一碳烯,2,6,6,9-四甲基-(1E,4E,8E), α-石竹烯
谱图信息: 最多检出来源 Homo sapiens(feces) 28.6%

分子结构信息

SMILES: C/C1=C/CC/C(C)=C/CC(C)(C)/C=C/C1
InChI: InChI=1S/C15H24/c1-13-7-5-8-14(2)10-12-15(3,4)11-6-9-13/h6-7,10-11H,5,8-9,12H2,1-4H3/b11-6+,13-7+,14-10+

描述信息

alpha-Humulene, also known as alpha-caryophyllene, belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. Thus, alpha-humulene is considered to be an isoprenoid lipid molecule. alpha-Humulene is found in allspice. alpha-Humulene is a constituent of many essential oils including hops (Humulus lupulus) and cloves (Syzygium aromaticum).
(1E,4E,8E)-alpha-humulene is the (1E,4E,8E)-isomer of alpha-humulene.
Humulene is a natural product found in Nepeta nepetella, Teucrium montanum, and other organisms with data available.
See also: Caryophyllene (related).
α-Humulene is a main constituent of Tanacetum vulgare L. (Asteraceae) essential oil with anti-inflammation (IC50=15±2 μg/mL). α-Humulene inhibits COX-2 and iNOS expression[1].
α-Humulene is a main constituent of Tanacetum vulgare L. (Asteraceae) essential oil with anti-inflammation (IC50=15±2 μg/mL). α-Humulene inhibits COX-2 and iNOS expression[1].

同义名列表

63 个代谢物同义名

trans,trans,trans-2,6,6,9-Tetramethyl-1,4,8-cycloundecatriene; 1,4,8-Cycloundecatriene, 2,6,6,9-tetramethyl-, (1E,4E,8E)-; 2,6,6,9-Tetramethyl-1,4,8-cycloundecatriene-, (1E,4E,8E)-; Cycloundeca-1,4,8-triene,2,6,6,9-tetramethyl-, (E,E,E)-; 1,4,8-Cycloundecatriene, 2,6,6,9-tetramethyl-, (E,E,E)-; (1E,4E,8E)-2,6,6,9-tetramethyl-1,4,8-cycloundecatriene; 2,6,6,9-Tetramethyl-(1E,4E,8E)-1,4,8-Cycloundecatriene; (1E,4E,8E)-2,6,6,9-Tetramethyl-1,4-8-cycloundecatriene; (1E,4E,8E)-2,6,6,9-tetramethylcycloundeca-1,4,8-triene; 2,6,6,9-Tetramethyl-1,4,8-cycloundecatriene (E,E,E)-; (E,E,E)-2,6,6,9-tetramethyl-1,4,8-cycloundecatriene; 2,6,6,9-Tetramethyl-(E,E,E)-1,4,8-Cycloundecatriene; Cycloundeca-1,4,8-triene,2,6,6,9-tetramethyl-; 4-05-00-01171 (Beilstein Handbook Reference); 2,6,6,9-tetramethyl-cycloundeca-1,4,8-triene; 2,6,6,9-Tetramethyl-1,4,8-cycloundecatriene; alpha -humulene (alpha -caryophyllene); alpha-Humulene, analytical standard; (1E,4E,8E)-humula-1(11),4,8-triene; Alpha-caryophylla-2,8(14)-diene; Alpha-humulene alpha-humulene; alpha-Humulene, >=96.0\\% (GC); alpha-Caryophyllene (obsol.); minyak fraksi daun cengkeh; (1E,4E,8E)-alpha-humulene; Humulene; -Caryophyllene; a-Caryophyllene (obsol.); (+/-)-.ALPHA.-HUMULENE; (1E,4E,8E)-a-Humulene; (1E,4E,8E)-Α-humulene; .alpha.-Caryophyllene; (+/-)-alpha-HUMULENE; 3,7,10-Humulatriene; Alpha caryophyllene; alpha-caryophyllene; (±)-alpha-humulene; -)-alpha-Humulene; alpha -humulenen; .alpha.-Humulene; HUMULENE, ALPHA-; UNII-54W56MD2WD; α-Caryophyllene; alpha -humulene; a-Caryophyllene; (±)-α-humulene; alpha-humulene; Caryophyllene:; alpha -humulen; Alpha-humulol; HUMULENE [MI]; α-Humulene; 54W56MD2WD; a-humulene; -Humulene; CANNABIS; Humulene; Humulen; Weed; Hemp; V8Z; α-Humulene; 1,4,8-Cycloundecatriene, 2,6,6,9-tetramethyl-, (1E,4E,8E)-; Humulene



数据库引用编号

26 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(1)

PlantCyc(1)

代谢反应

73 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(3)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(70)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

628 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 9 ABCB1, CBR1, HPGDS, MAPK14, MAPK8, MSMP, NFKB1, NOS2, PTGS2
Peripheral membrane protein 3 ACHE, CYP1B1, PTGS2
Endoplasmic reticulum membrane 4 CYP1B1, HMGCR, HMOX1, PTGS2
Nucleus 7 ACHE, HMOX1, MAPK14, MAPK8, NFKB1, NOS2, PARP1
cytosol 8 CBR1, HMOX1, HPGDS, MAPK14, MAPK8, NFKB1, NOS2, PARP1
nuclear body 1 PARP1
nucleoplasm 7 HMOX1, HPGDS, MAPK14, MAPK8, NFKB1, NOS2, PARP1
Cell membrane 3 ABCB1, ACHE, TNF
Cytoplasmic side 1 HMOX1
Multi-pass membrane protein 2 ABCB1, HMGCR
Synapse 2 ACHE, MAPK8
cell surface 3 ABCB1, ACHE, TNF
glutamatergic synapse 1 MAPK14
Golgi apparatus 2 ACHE, ATRN
lysosomal membrane 1 GAA
neuromuscular junction 1 ACHE
neuronal cell body 1 TNF
Cytoplasm, cytosol 2 NOS2, PARP1
Lysosome 1 GAA
plasma membrane 6 ABCB1, ACHE, ATRN, GAA, NOS2, TNF
Membrane 7 ABCB1, ACHE, CYP1B1, GAA, HMGCR, HMOX1, PARP1
apical plasma membrane 1 ABCB1
axon 1 MAPK8
caveola 1 PTGS2
extracellular exosome 4 ABCB1, ATRN, CBR1, GAA
Lysosome membrane 1 GAA
endoplasmic reticulum 3 HMGCR, HMOX1, PTGS2
extracellular space 8 ACHE, ATRN, CXCL8, HMOX1, IL10, IL6, MSMP, TNF
lysosomal lumen 1 GAA
perinuclear region of cytoplasm 3 ACHE, HMOX1, NOS2
mitochondrion 4 CYP1B1, MAPK14, NFKB1, PARP1
protein-containing complex 2 PARP1, PTGS2
intracellular membrane-bounded organelle 3 CYP1B1, GAA, HPGDS
Microsome membrane 2 CYP1B1, PTGS2
Single-pass type I membrane protein 1 ATRN
Secreted 6 ACHE, CXCL8, GAA, IL10, IL6, MSMP
extracellular region 8 ACHE, CXCL8, GAA, IL10, IL6, MAPK14, NFKB1, TNF
mitochondrial outer membrane 1 HMOX1
[Isoform 2]: Secreted 1 ATRN
Extracellular side 1 ACHE
transcription regulator complex 2 NFKB1, PARP1
external side of plasma membrane 1 TNF
Extracellular vesicle 1 CBR1
nucleolus 1 PARP1
Cytoplasm, P-body 1 NOS2
P-body 1 NOS2
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
Apical cell membrane 1 ABCB1
Cytoplasm, perinuclear region 1 NOS2
Membrane raft 1 TNF
Peroxisome 1 NOS2
basement membrane 1 ACHE
peroxisomal matrix 1 NOS2
peroxisomal membrane 1 HMGCR
nuclear speck 1 MAPK14
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 NFKB1, PARP1
phagocytic cup 1 TNF
Chromosome 1 PARP1
Nucleus, nucleolus 1 PARP1
spindle pole 1 MAPK14
nuclear replication fork 1 PARP1
chromosome, telomeric region 1 PARP1
Lipid-anchor, GPI-anchor 1 ACHE
site of double-strand break 1 PARP1
[Isoform 3]: Secreted 1 ATRN
nuclear envelope 1 PARP1
tertiary granule membrane 1 GAA
side of membrane 1 ACHE
Peroxisome membrane 1 HMGCR
ficolin-1-rich granule lumen 1 MAPK14
secretory granule lumen 2 MAPK14, NFKB1
endoplasmic reticulum lumen 2 IL6, PTGS2
specific granule lumen 1 NFKB1
azurophil granule membrane 1 GAA
Single-pass type IV membrane protein 1 HMOX1
synaptic cleft 1 ACHE
protein-DNA complex 1 PARP1
ficolin-1-rich granule membrane 1 GAA
external side of apical plasma membrane 1 ABCB1
basal dendrite 1 MAPK8
[Isoform 1]: Cell membrane 1 ATRN
site of DNA damage 1 PARP1
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
cortical cytoskeleton 1 NOS2
interleukin-6 receptor complex 1 IL6
[Poly [ADP-ribose] polymerase 1, processed N-terminus]: Chromosome 1 PARP1
[Poly [ADP-ribose] polymerase 1, processed C-terminus]: Cytoplasm 1 PARP1
autolysosome lumen 1 GAA
[Nuclear factor NF-kappa-B p105 subunit]: Cytoplasm 1 NFKB1
[Nuclear factor NF-kappa-B p50 subunit]: Nucleus 1 NFKB1
I-kappaB/NF-kappaB complex 1 NFKB1
NF-kappaB p50/p65 complex 1 NFKB1
[Isoform H]: Cell membrane 1 ACHE
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF


文献列表

  • Qianqian Cheng, Bin Lyu, Jingweng Hu, Zhiqiang Zhang, Yusheng Huang, Zhenhua Wang. Research on the antipruritic active ingredients of Mikania micrantha. Fitoterapia. 2024 Jan; 174(?):105837. doi: 10.1016/j.fitote.2024.105837. [PMID: 38286314]
  • John Staton Laws, Scott D Smid. Characterizing cannabis-prevalent terpenes for neuroprotection reveal a role for α and β-pinenes in mitigating amyloid β-evoked neurotoxicity and aggregation in vitro. Neurotoxicology. 2024 Jan; 100(?):16-24. doi: 10.1016/j.neuro.2023.12.004. [PMID: 38070653]
  • Naglaa S Ashmawy, Haidy A Gad, Heba A S El-Nashar. Comparative Study of Essential Oils from Different Organs of Syzygium cumini (Pamposia) Based on GC/MS Chemical Profiling and In Vitro Antiaging Activity. Molecules (Basel, Switzerland). 2023 Nov; 28(23):. doi: 10.3390/molecules28237861. [PMID: 38067590]
  • Tuan Quoc Doan, Dien Dinh, Thang Nam Tran, Phu Quynh Dinh Nguyen, Chau Bao Hoai Nguyen, Nhan Trong Le, Hung Quoc Vo, Duc Viet Ho, Anh Le Tuan, Hoai Thi Nguyen, Isiaka A Ogunwande. Chemical composition and acetylcholinesterase inhibitory activity of essential oil from the leaves of Mitrephora poilanei Weeras. & R.M.K. Saunders. Natural product research. 2023 Jun; ?(?):1-5. doi: 10.1080/14786419.2023.2227989. [PMID: 37357615]
  • Xiuyin Chen, Mindy Y Wang, Cecilia H Deng, Ron A Beatson, Kerry R Templeton, Ross G Atkinson, Niels J Nieuwenhuizen. The hops (Humulus lupulus) genome contains a mid-sized terpene synthase family that shows wide functional and allelic diversity. BMC plant biology. 2023 May; 23(1):280. doi: 10.1186/s12870-023-04283-y. [PMID: 37231379]
  • Bei Cui, Tao Zheng, Ping Deng, Sheng Zhang, Zhong Zhao. Chemotaxonomic Variation in Volatile Component Contents in Ancient Platycladus orientalis Leaves with Different Tree Ages in Huangdi Mausoleum. Molecules (Basel, Switzerland). 2023 Feb; 28(5):. doi: 10.3390/molecules28052043. [PMID: 36903288]
  • Qi Guo, Qian-Qian Peng, Ying-Ying Chen, Ping Song, Xiao-Jun Ji, He Huang, Tian-Qiong Shi. High-yield α-humulene production in Yarrowia lipolytica from waste cooking oil based on transcriptome analysis and metabolic engineering. Microbial cell factories. 2022 Dec; 21(1):271. doi: 10.1186/s12934-022-01986-z. [PMID: 36566177]
  • Qi Guo, Ya-Wen Li, Fang Yan, Ke Li, Yue-Tong Wang, Chao Ye, Tian-Qiong Shi, He Huang. Dual cytoplasmic-peroxisomal engineering for high-yield production of sesquiterpene α-humulene in Yarrowia lipolytica. Biotechnology and bioengineering. 2022 10; 119(10):2819-2830. doi: 10.1002/bit.28176. [PMID: 35798689]
  • Nurul Huda Alwakil, Mohamad Suffian Mohamad Annuar, Mahanom Jalil. Synergistic Effects of Plant Growth Regulators and Elicitors on α-Humulene and Zerumbone Production in Zingiber zerumbet Smith Adventitious Root Cultures. Molecules (Basel, Switzerland). 2022 Jul; 27(15):. doi: 10.3390/molecules27154744. [PMID: 35897918]
  • Silvia Di Giacomo, Alessia Mariano, Marco Gullì, Caterina Fraschetti, Annabella Vitalone, Antonello Filippi, Luisa Mannina, Anna Scotto d'Abusco, Antonella Di Sotto. Role of Caryophyllane Sesquiterpenes in the Entourage Effect of Felina 32 Hemp Inflorescence Phytocomplex in Triple Negative MDA-MB-468 Breast Cancer Cells. Molecules (Basel, Switzerland). 2021 Nov; 26(21):. doi: 10.3390/molecules26216688. [PMID: 34771097]
  • Xue-Long Yan, Jun-Sang, Xu Zhang, Yan Lin, Qing-De Long, Qin-Feng Zhu, Shang-Gao Liao. Euphorboside A, a cytotoxic meroterpenoid glycoside with an unusual humulene-phloroglucinol skeleton from Euphorbia kansuensis. Fitoterapia. 2021 Sep; 153(?):104966. doi: 10.1016/j.fitote.2021.104966. [PMID: 34144143]
  • Karolina Połeć, Karolina Olechowska, Amanda Klejdysz, Michał Dymek, Rafał Rachwalik, Elżbieta Sikora, Katarzyna Hąc-Wydro. The influence of ergosterol on the action of the hop oil and its major terpenes on model fungi membranes. Towards understanding the mechanism of action of phytocompounds for food and plant protection. Chemistry and physics of lipids. 2021 08; 238(?):105092. doi: 10.1016/j.chemphyslip.2021.105092. [PMID: 34000279]
  • Eduardo Valarezo, Génesis Gaona-Granda, Vladimir Morocho, Luis Cartuche, James Calva, Miguel Angel Meneses. Chemical Constituents of the Essential Oil from Ecuadorian Endemic Species Croton ferrugineus and Its Antimicrobial, Antioxidant and α-Glucosidase Inhibitory Activity. Molecules (Basel, Switzerland). 2021 Jul; 26(15):. doi: 10.3390/molecules26154608. [PMID: 34361759]
  • Sofia Milker, Anne Sydow, Ingrid Torres-Monroy, Guido Jach, Frederik Faust, Lea Kranz, Ljubov Tkatschuk, Dirk Holtmann. Gram-scale production of the sesquiterpene α-humulene with Cupriavidus necator. Biotechnology and bioengineering. 2021 07; 118(7):2694-2702. doi: 10.1002/bit.27788. [PMID: 33844284]
  • Fumin Wang, Yong-Lak Park, Michael Gutensohn. Glandular Trichome-Derived Mono- and Sesquiterpenes of Tomato Have Contrasting Roles in the Interaction with the Potato Aphid Macrosiphum euphorbiae. Journal of chemical ecology. 2021 Feb; 47(2):204-214. doi: 10.1007/s10886-021-01243-4. [PMID: 33447946]
  • Mohammad Firoznejhad, Abdollah Ghasemi Pirbalouti, Vahid Abdoosi, Atousa Aliahmadi. Chemical composition of essential oils from the underground parts of Glycyrrhiza echinata L. accessions growing wild in Northern Iran. Natural product research. 2021 Jan; 35(1):162-166. doi: 10.1080/14786419.2019.1616721. [PMID: 31165644]
  • Didjour Albert Kambiré, Acafou Thierry Yapi, Jean Brice Boti, Zana Adama Ouattara, Zanahi Félix Tonzibo, Jean-Jacques Filippi, Ange Bighelli, Félix Tomi. Two new eudesman-4α-ol epoxides from the stem essential oil of Laggera pterodonta from Côte d'Ivoire. Natural product research. 2020 Oct; 34(19):2765-2771. doi: 10.1080/14786419.2019.1586701. [PMID: 30908078]
  • Anh Duc Nguyen, Donghyuk Kim, Eun Yeol Lee. Unlocking the biosynthesis of sesquiterpenoids from methane via the methylerythritol phosphate pathway in methanotrophic bacteria, using α-humulene as a model compound. Metabolic engineering. 2020 09; 61(?):69-78. doi: 10.1016/j.ymben.2020.04.011. [PMID: 32387228]
  • T Soumya, P R Jayasree, M Deepak, P R Manish Kumar. Chemical composition, antioxidant and antiproliferative activities of essential oil from rhizome and leaves of Curcuma mutabilis Škorničk., M. Sabu & Prasanthk., endemic to Western Ghats of India. Natural product research. 2020 Aug; 34(16):2336-2340. doi: 10.1080/14786419.2018.1533826. [PMID: 30724591]
  • Amanda Moreno-Rodríguez, Rosario Santos-Castro, Josefina Vázquez-Medrano, Rafael E Quintanar-Zúñiga, Fernando A García-García, Luis B Hernández-Portilla, Cesar M Flores-Ortiz. Effect of jasmonic acid on major terpenes and density of glandular trichomes in Lippia graveolens kunth (Verbenaceae). Natural product research. 2020 Jul; 34(13):1942-1946. doi: 10.1080/14786419.2019.1566721. [PMID: 30724587]
  • Hye-In Jang, Ki-Jong Rhee, Yong-Bin Eom. Antibacterial and antibiofilm effects of α-humulene against Bacteroides fragilis. Canadian journal of microbiology. 2020 Jun; 66(6):389-399. doi: 10.1139/cjm-2020-0004. [PMID: 32073898]
  • Sonal Shah, Tushar Dhanani, Sonu Sharma, Raghuraj Singh, Satyanshu Kumar, Bhanu Kumar, Sharad Srivastava, Srikant Ghosh, Rajesh Kumar, Sanis Juliet. Development and Validation of a Reversed Phase High Performance Liquid Chromatography-Photodiode Array Detection Method for Simultaneous Identification and Quantification of Coumarin, Precocene-I, β-Caryophyllene Oxide, α-Humulene, and β-Caryophyllene in Ageratum Conyzoides Extracts and Essential Oils from Plants. Journal of AOAC International. 2020 Jun; 103(3):857-864. doi: 10.1093/jaoacint/qsz038. [PMID: 33241362]
  • Hao Chen, Jingquan Yuan, Ji Hao, Yanzhang Wen, Yibing Lv, Lu Chen, Xinzhou Yang. α-Humulene inhibits hepatocellular carcinoma cell proliferation and induces apoptosis through the inhibition of Akt signaling. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2019 Dec; 134(?):110830. doi: 10.1016/j.fct.2019.110830. [PMID: 31562948]
  • E A J Silva, E B B Estevam, T S Silva, H D Nicolella, R A Furtado, C C F Alves, E L Souchie, C H G Martins, D C Tavares, L C A Barbosa, M L D Miranda. Antibacterial and antiproliferative activities of the fresh leaf essential oil of Psidium guajava L. (Myrtaceae). Brazilian journal of biology = Revista brasleira de biologia. 2019 Oct; 79(4):697-702. doi: 10.1590/1519-6984.189089. [PMID: 30462815]
  • Abeer A Mohamed, Said I Behiry, Hosny A Younes, Nader A Ashmawy, Mohamed Z M Salem, Ofelia Márquez-Molina, Alberto Barbabosa-Pilego. Antibacterial activity of three essential oils and some monoterpenes against Ralstonia solanacearum phylotype II isolated from potato. Microbial pathogenesis. 2019 Oct; 135(?):103604. doi: 10.1016/j.micpath.2019.103604. [PMID: 31247257]
  • 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]
  • Alline L B Dias, Hellen R F Batista, Elisângela B B Estevam, Cassia C F Alves, Moacir R Forim, Heloiza D Nicolella, Ricardo A Furtado, Denise C Tavares, Thayna S Silva, Carlos H G Martins, Mayker L D Miranda. Chemical composition and in vitro antibacterial and antiproliferative activities of the essential oil from the leaves of Psidium myrtoides O. Berg (Myrtaceae). Natural product research. 2019 Sep; 33(17):2566-2570. doi: 10.1080/14786419.2018.1457664. [PMID: 29611435]
  • Gilcy George Kallivalappil, Girija Kuttan. Evaluation of the anti-inflammatory and urotoxicity ameliorative effects of γ-humulene containing active fraction of Emilia sonchifolia (L.) DC. Inflammopharmacology. 2019 Apr; 27(2):409-420. doi: 10.1007/s10787-017-0423-3. [PMID: 29224178]
  • Hai Ming Zhang, Shan Shan Guo, Bin Fan, Shu Shan Du, Yong Yan Wang, Zhi Wei Deng. Evaluation of efficacy of the essential oil from Ostericum viridiflorum (Turcz.) Kitagawa in control of stored product insects. Environmental science and pollution research international. 2019 Jan; 26(2):1406-1413. doi: 10.1007/s11356-018-3728-x. [PMID: 30426372]
  • Sandra Márcia Mazutti da Silva, Claudio Rodrigues Rezende Costa, Guilherme Martins Gelfuso, Eliete Neves Silva Guerra, Yanna Karla de Medeiros Nóbrega, Sueli Maria Gomes, Aline Pic-Taylor, Yris Maria Fonseca-Bazzo, Damaris Silveira, Pérola de Oliveira Magalhães. Wound Healing Effect of Essential Oil Extracted from Eugenia dysenterica DC (Myrtaceae) Leaves. Molecules (Basel, Switzerland). 2018 Dec; 24(1):. doi: 10.3390/molecules24010002. [PMID: 30577426]
  • Ekaterina Jeliazkova, Valtcho D Zheljazkov, Miroslava Kačániova, Tess Astatkie, Babu L Tekwani. Sequential Elution of Essential Oil Constituents during Steam Distillation of Hops (Humulus lupulus L.) and Influence on Oil Yield and Antimicrobial Activity. Journal of oleo science. 2018 Jul; 67(7):871-883. doi: 10.5650/jos.ess17216. [PMID: 29877222]
  • Giovanni Benelli, Mohan Rajeswary, Marimuthu Govindarajan. Towards green oviposition deterrents? Effectiveness of Syzygium lanceolatum (Myrtaceae) essential oil against six mosquito vectors and impact on four aquatic biological control agents. Environmental science and pollution research international. 2018 Apr; 25(11):10218-10227. doi: 10.1007/s11356-016-8146-3. [PMID: 27921244]
  • Raju Sripathi, Dharani Jayagopal, Subban Ravi. A study on the seasonal variation of the essential oil composition from Plectranthus hadiensis and its antibacterial activity. Natural product research. 2018 Apr; 32(7):871-874. doi: 10.1080/14786419.2017.1363748. [PMID: 28783957]
  • Thomas Krieg, Anne Sydow, Sonja Faust, Ina Huth, Dirk Holtmann. CO2 to Terpenes: Autotrophic and Electroautotrophic α-Humulene Production with Cupriavidus necator. Angewandte Chemie (International ed. in English). 2018 02; 57(7):1879-1882. doi: 10.1002/anie.201711302. [PMID: 29232490]
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