(+)-Sabinene (BioDeep_00000014731)

human metabolite Endogenous

代谢物信息卡片

(1R,5R)-4-methylidene-1-(propan-2-yl)bicyclo[3.1.0]hexane

化学式: C10H16 (136.1251936)
中文名称: (+)-桧烯
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC(C)C12CCC(=C)C1C2
InChI: InChI=1S/C59H102O6/c1-4-7-10-13-16-19-22-25-27-29-31-34-37-40-43-46-49-52-58(61)64-55-56(54-63-57(60)51-48-45-42-39-36-33-24-21-18-15-12-9-6-3)65-59(62)53-50-47-44-41-38-35-32-30-28-26-23-20-17-14-11-8-5-2/h16-17,19-21,24-28,31,34,56H,4-15,18,22-23,29-30,32-33,35-55H2,1-3H3/b19-16-,20-17-,24-21-,27-25-,28-26-,34-31-/t56-/m0/s1

描述信息

Sabinene (CAS: 3387-41-5) belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. Thus, sabinene is considered to be an isoprenoid lipid molecule. Sabinene is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. (+)-Sabinene, also known as (+)-4(10)-thujene, is found in common sage and Myristica fragrans (nutmeg).

同义名列表

16 个代谢物同义名

(1R,5R)-4-methylidene-1-(propan-2-yl)bicyclo[3.1.0]hexane; (1R,5R)-4-Methylene-1-(1-methylethyl)bicyclo[3.1.0]hexane; (1R,5R)-1-isopropyl-4-methylenebicyclo[3.1.0]hexane; 4-methylene-1-(1-methylethyl)bicyclo[3.1.0]hexane; 1-Isopropyl-4-methylenebicyclo[3.1.0]hexane; (1R,5R)-(+)-4(10)-Thujene; (1R,5R)-(+)-Sabinene; (+)-4(10)-Thujene; (1R,5R)-Sabinene; d-4(10)-Thujene; 4(10)-Thujene; (+)-sabinene; d-Sabinene; Sabenene; Sabinene; Sabinen

数据库引用编号

12 个数据库交叉引用编号

ChEBI: CHEBI:50029
KEGG: C20230
PubChem: 10887971
HMDB: HMDB0036076
Wikipedia: Sabinene
MetaCyc: CPD-14013
KNApSAcK: C00000857
foodb: FDB097355
chemspider: 9063235
CAS: 2009-00-9
PubChem: 163311973
LipidMAPS: LMPR0102120036

分类词条

Bicyclic monoterpenoids

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)

115 个相关的物种来源信息

589713 Anthemis aciphylla: 10.1248/CPB.54.222
497760 Nicotiana mutabilis: 10.1016/J.PHYTOCHEM.2006.05.038
118694 Nicotiana bonariensis: 10.1016/J.PHYTOCHEM.2006.05.038
4087 Nicotiana alata: 10.1016/J.PHYTOCHEM.2006.05.038
118700 Nicotiana langsdorffii: 10.1016/J.PHYTOCHEM.2006.05.038
85571 Citrus reticulata:
558547 Citrus deliciosa:
37334 Citrus maxima: 10.1016/J.PHYTOCHEM.2009.07.031
170989 Citrus hystrix: 10.1016/J.PHYTOCHEM.2009.07.031
271192 Pimpinella anisum: 10.1016/S0031-9422(98)00022-3
16752 Houttuynia cordata: 10.3390/MOLECULES200610298
58041 Pinus cembra: 10.1016/S0031-9422(98)00105-8
305795 Oenanthe aquatica: 10.1055/S-0028-1097637
130381 Piper arboreum: 10.1016/S0031-9422(97)00762-0
425151 Piper fimbriulatum: 10.1016/S0031-9422(97)00762-0
169599 Porophyllum ruderale: 10.1016/S0031-9422(98)00189-7
176571 Porophyllum gracile: 10.1016/S0031-9422(98)00189-7
4047 Coriandrum sativum: 10.1055/S-0028-1100058
2878271 Thymus camphoratus: 10.1016/S0031-9422(97)00117-9
37690 Citrus trifoliata: 10.1007/BF00580068
55188 Citrus unshiu:
119949 Myrtus communis: 10.1016/J.PHYTOCHEM.2006.04.025
58039 Juniperus communis:
203015 Rhodiola rosea: 10.1016/S0031-9422(02)00004-3
264418 Hesperis matronalis: 10.1016/J.PHYTOCHEM.2006.12.009
4465 Acorus calamus: 10.1016/J.PHYTOCHEM.2005.01.007
43850 Schinus: 10.1016/S0031-9422(00)94384-X
3329 Picea abies:
183013 Espeletia timotensis: 10.1016/S0031-9422(99)00346-5
13216 Piper nigrum: 10.3390/MOLECULES24234244
40949 Angelica archangelica: 10.1002/(SICI)1099-1026(199711/12)12:6<397::AID-FFJ670>3.0.CO;2-Z
401942 Artemisia xerophytica: 10.1007/BF00568367
54477 Vitex agnus-castus: 10.1055/S-2006-957433
4039 Daucus carota: 10.1016/0031-9422(82)80129-5
1391945 Sideritis leucantha: 10.1016/S0031-9422(00)80325-8
155237 Sideritis chamaedryfolia: 10.1016/S0031-9422(00)80325-8
155267 Sideritis tragoriganum: 10.1016/S0031-9422(00)80325-8
103973 Juniperus drupacea: 10.1055/S-0028-1097977
45372 Abies alba: 10.1055/S-0028-1100131
758917 Juniperus excelsa: 10.1021/NP50050A053
13727 Thujopsis dolabrata: 10.1016/0031-9422(82)83156-7
19953 Valeriana officinalis: 10.1016/0031-9422(95)00492-P
76352 Hesperocyparis macrocarpa: 10.1021/JO01199A001
128002 Tanacetum vulgare: 10.1039/J39690000541
38860 Mentha suaveolens: 10.1055/S-0028-1097962
103974 Libocedrus bidwillii: 10.1002/JCTB.5000681208
107254 Molopospermum peloponnesiacum: 10.1016/0031-9422(81)85188-6
38868 Salvia officinalis: 10.1016/0003-9861(87)90436-X
4220 Artemisia vulgaris: 10.1055/S-0028-1097719
85223 Laurus nobilis: 10.1021/JF049033E
48117 Cryptotaenia japonica: 10.1246/BCSJ.42.3026
136217 Curcuma longa: 10.1021/JF00110A018
996322 Cantinoa mutabilis: 10.1002/JPS.3080240410
13415 Chamaecyparis obtusa:
282738 Achillea fragrantissima: 10.1002/JPS.2600531215
317702 Pittosporum eugenioides: 10.1002/JCTB.5000680110
60894 Saccharopolyspora spinosa: 10.1002/CBIC.201300329
589713 Anthemis aciphylla: 10.1248/CPB.54.222
497760 Nicotiana mutabilis: 10.1016/J.PHYTOCHEM.2006.05.038
118694 Nicotiana bonariensis: 10.1016/J.PHYTOCHEM.2006.05.038
4087 Nicotiana alata: 10.1016/J.PHYTOCHEM.2006.05.038
118700 Nicotiana langsdorffii: 10.1016/J.PHYTOCHEM.2006.05.038
85571 Citrus reticulata:
558547 Citrus deliciosa:
37334 Citrus maxima: 10.1016/J.PHYTOCHEM.2009.07.031
170989 Citrus hystrix: 10.1016/J.PHYTOCHEM.2009.07.031
271192 Pimpinella anisum: 10.1016/S0031-9422(98)00022-3
16752 Houttuynia cordata: 10.3390/MOLECULES200610298
58041 Pinus cembra: 10.1016/S0031-9422(98)00105-8
305795 Oenanthe aquatica: 10.1055/S-0028-1097637
130381 Piper arboreum: 10.1016/S0031-9422(97)00762-0
425151 Piper fimbriulatum: 10.1016/S0031-9422(97)00762-0
169599 Porophyllum ruderale: 10.1016/S0031-9422(98)00189-7
176571 Porophyllum gracile: 10.1016/S0031-9422(98)00189-7
4047 Coriandrum sativum: 10.1055/S-0028-1100058
2878271 Thymus camphoratus: 10.1016/S0031-9422(97)00117-9
37690 Citrus trifoliata: 10.1007/BF00580068
55188 Citrus unshiu:
119949 Myrtus communis: 10.1016/J.PHYTOCHEM.2006.04.025
58039 Juniperus communis:
203015 Rhodiola rosea: 10.1016/S0031-9422(02)00004-3
264418 Hesperis matronalis: 10.1016/J.PHYTOCHEM.2006.12.009
4465 Acorus calamus: 10.1016/J.PHYTOCHEM.2005.01.007
43850 Schinus: 10.1016/S0031-9422(00)94384-X
3329 Picea abies:
183013 Espeletia timotensis: 10.1016/S0031-9422(99)00346-5
13216 Piper nigrum: 10.3390/MOLECULES24234244
40949 Angelica archangelica: 10.1002/(SICI)1099-1026(199711/12)12:6<397::AID-FFJ670>3.0.CO;2-Z
401942 Artemisia xerophytica: 10.1007/BF00568367
54477 Vitex agnus-castus: 10.1055/S-2006-957433
4039 Daucus carota: 10.1016/0031-9422(82)80129-5
1391945 Sideritis leucantha: 10.1016/S0031-9422(00)80325-8
155237 Sideritis chamaedryfolia: 10.1016/S0031-9422(00)80325-8
155267 Sideritis tragoriganum: 10.1016/S0031-9422(00)80325-8
103973 Juniperus drupacea: 10.1055/S-0028-1097977
45372 Abies alba: 10.1055/S-0028-1100131
758917 Juniperus excelsa: 10.1021/NP50050A053
13727 Thujopsis dolabrata: 10.1016/0031-9422(82)83156-7
19953 Valeriana officinalis: 10.1016/0031-9422(95)00492-P
76352 Hesperocyparis macrocarpa: 10.1021/JO01199A001
128002 Tanacetum vulgare: 10.1039/J39690000541
38860 Mentha suaveolens: 10.1055/S-0028-1097962
103974 Libocedrus bidwillii: 10.1002/JCTB.5000681208
107254 Molopospermum peloponnesiacum: 10.1016/0031-9422(81)85188-6
38868 Salvia officinalis: 10.1016/0003-9861(87)90436-X
4220 Artemisia vulgaris: 10.1055/S-0028-1097719
85223 Laurus nobilis: 10.1021/JF049033E
48117 Cryptotaenia japonica: 10.1246/BCSJ.42.3026
136217 Curcuma longa: 10.1021/JF00110A018
996322 Cantinoa mutabilis: 10.1002/JPS.3080240410
13415 Chamaecyparis obtusa:
282738 Achillea fragrantissima: 10.1002/JPS.2600531215
317702 Pittosporum eugenioides: 10.1002/JCTB.5000680110
60894 Saccharopolyspora spinosa: 10.1002/CBIC.201300329
9606 Homo sapiens: -

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

Sung-Hee Kim, Young-Ah Jang, Yong-Jin Kwon. Anti-Inflammatory Effect of Chamaecyparis obtusa (Siebold & Zucc.) Endl. Leaf Essential Oil. Molecules (Basel, Switzerland). 2024 Mar; 29(5):. doi: 10.3390/molecules29051117. [PMID: 38474629]
Huizhong Hu, Dengwu Li, Ruxue Bai, Weiping Zhang, Hong Luo, Enping Yu. Chemodiversity and Bioactivity of the Essential Oils of Juniperus and Implication for Taxonomy. International journal of molecular sciences. 2023 Oct; 24(20):. doi: 10.3390/ijms242015203. [PMID: 37894884]
Yessenia E Maldonado, Omar Malagón, Nixon Cumbicus, Gianluca Gilardoni. A new essential oil from the native Ecuadorian species Steiractinia sodiroi (Hieron.) S.F. Blake (Asteraceae): chemical and enantioselective analyses. Scientific reports. 2023 Oct; 13(1):17180. doi: 10.1038/s41598-023-44524-6. [PMID: 37821569]
J W Walker, B M Shoemake, D G Quadros, J W Thorne, N C Cahill. Selecting goats for juniper consumption did not improve their liver Phase I detoxification. Journal of animal science. 2023 Jun; ?(?):. doi: 10.1093/jas/skad180. [PMID: 37328163]
Mahin Bashiri-Nahnjeh, Abdolrahman Sarihi, Ahmad Ebadi, Dara Dastan, Mojdeh Mohammadi. In silico molecular modeling, neuro-behavioral profile, and toxicity assessment of the essential oil of Ferula gummosa Boiss. as an anti-seizure agent. Journal of ethnopharmacology. 2023 Jun; 309(?):116347. doi: 10.1016/j.jep.2023.116347. [PMID: 36894108]
Meiyu Sun, Ningning Liu, Jiahui Miao, Yanan Zhang, Yuanpeng Hao, Jinzheng Zhang, Hui Li, Hongtong Bai, Lei Shi. Creation of New Oregano Genotypes with Different Terpene Chemotypes via Inter- and Intraspecific Hybridization. International journal of molecular sciences. 2023 Apr; 24(8):. doi: 10.3390/ijms24087320. [PMID: 37108486]
Bartłomiej Piasecki, Viktória L Balázs, Anna Kieltyka-Dadasiewicz, Péter Szabó, Béla Kocsis, Györgyi Horváth, Agnieszka Ludwiczuk. Microbiological Studies on the Influence of Essential Oils from Several Origanum Species on Respiratory Pathogens. Molecules (Basel, Switzerland). 2023 Mar; 28(7):. doi: 10.3390/molecules28073044. [PMID: 37049808]
Corinna Schmiderer, Ralf Steinborn, Johannes Novak. Monoterpene synthases of three closely related sage species (Salvia officinalis, S. fruticosa and S. pomifera, Lamiaceae). Plant physiology and biochemistry : PPB. 2023 Jan; 196(?):318-327. doi: 10.1016/j.plaphy.2023.01.034. [PMID: 36738511]
Souad El Hafidi, Khadija Bakhy, Mohammed Ouhssine, Abderrahim Benzakour, Hamid Khamar, Joseph Casanova, Mathieu Paoli, Félix Tomi. Composition and Chemical Variability of the Essential Oil from Aerial Parts of Cladanthus scariosus, an Endemic Species to the Moroccan High Atlas. Chemistry & biodiversity. 2023 Jan; 20(1):e202201022. doi: 10.1002/cbdv.202201022. [PMID: 36520049]
Daniela Gruľová, Beáta Baranová, Vincent Sedlák, Laura De Martino, Valtcho D Zheljazkov, Mária Konečná, Janka Poráčová, Lucia Caputo, Vincenzo De Feo. Juniperus horizontalis Moench: Chemical Composition, Herbicidal and Insecticidal Activities of Its Essential Oil and of Its Main Component, Sabinene. Molecules (Basel, Switzerland). 2022 Dec; 27(23):. doi: 10.3390/molecules27238408. [PMID: 36500500]
Lina M Barhoumi, Reem N Dabaibeh, Hala I Al-Jaber, Safwan M Obeidat, Ismaeil F Abaza, Nooman A Khalaf, Musa H Abu-Zarga, Fatma U Afifi. Aroma Profiles Analysis of Two Populations of Salvia palaestina Benth. Collected from Mediterranean and Irano-Turanian Zones in Jordan. Journal of oleo science. 2021 May; 70(5):713-719. doi: 10.5650/jos.ess20156. [PMID: 33840661]
Leila Gimenes, Júlio César R Lopes Silva, Roselaine Facanali, Leandro Wang Hantao, Walter José Siqueira, Marcia Ortiz Mayo Marques. Essential Oils of New Lippia alba Genotypes Analyzed by Flow-Modulated Comprehensive Two-Dimensional Gas Chromatography (GC×GC) and Chemometric Analysis. Molecules (Basel, Switzerland). 2021 Apr; 26(8):. doi: 10.3390/molecules26082332. [PMID: 33923848]
Carolina E Galvez, Cristina M Jimenez, Analía de Los A Gomez, Emilio F Lizarraga, Diego A Sampietro. Chemical composition and antifungal activity of essential oils from Senecio nutans, Senecio viridis, Tagetes terniflora and Aloysia gratissima against toxigenic Aspergillus and Fusarium species. Natural product research. 2020 May; 34(10):1442-1445. doi: 10.1080/14786419.2018.1511555. [PMID: 30456990]
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]
Hala I Al-Jaber, Safwan M Obeidat, Fatma U Afifi, Musa H Abu Zarga. Aroma Profile of Two Populations of Salvia verbenaca Collected from Two Bio-Geographical Zones from Jordan. Chemistry & biodiversity. 2020 Feb; 17(2):e1900553. doi: 10.1002/cbdv.201900553. [PMID: 31869516]
Amrita Yadav, Anupam Kujur, Akshay Kumar, Prem Pratap Singh, Vishal Gupta, Bhanu Prakash. Encapsulation of Bunium persicum essential oil using chitosan nanopolymer: Preparation, characterization, antifungal assessment, and thermal stability. International journal of biological macromolecules. 2020 Jan; 142(?):172-180. doi: 10.1016/j.ijbiomac.2019.09.089. [PMID: 31521660]
Godfried Dougnon, Michiho Ito. Sedative effects of the essential oil from the leaves of Lantana camara occurring in the Republic of Benin via inhalation in mice. Journal of natural medicines. 2020 Jan; 74(1):159-169. doi: 10.1007/s11418-019-01358-9. [PMID: 31446559]
Shamini Sharma, Jeena Gupta, Pranav Kumar Prabhakar, Pawan Gupta, Preeti Solanki, Anuradha Rajput. Phytochemical Repurposing of Natural Molecule: Sabinene for Identification of Novel Therapeutic Benefits Using In Silico and In Vitro Approaches. Assay and drug development technologies. 2019 Nov; 17(8):339-351. doi: 10.1089/adt.2019.939. [PMID: 31846362]
Shixing Zhou, Caixia Wei, Chi Zhang, Caixia Han, Nigora Kuchkarova, Hua Shao. Chemical Composition, Phytotoxic, Antimicrobial and Insecticidal Activity of the Essential Oils of Dracocephalum integrifolium. Toxins. 2019 10; 11(10):. doi: 10.3390/toxins11100598. [PMID: 31614937]
A C do Prado, H G Garces, E Bagagli, V L M Rall, A Furlanetto, A Fernandes Junior, F B Furtado. Schinus molle essential oil as a potential source of bioactive compounds: antifungal and antibacterial properties. Journal of applied microbiology. 2019 Feb; 126(2):516-522. doi: 10.1111/jam.14157. [PMID: 30431699]
Mei Wang, Amar G Chittiboyina, Jon F Parcher, Zulfiqar Ali, Paul Ford, Jianping Zhao, Bharathi Avula, Yan-Hong Wang, Ikhlas A Khan. Piper nigrum Oil - Determination of Selected Terpenes for Quality Evaluation. Planta medica. 2019 Feb; 85(3):185-194. doi: 10.1055/a-0782-0548. [PMID: 30440078]
Séverin Nguemezi Tchameni, Staelle Njamou Mbiakeu, Modeste Lambert Sameza, Pierre Michel Dongmo Jazet, François Tchoumbougnang. Using Citrus aurantifolia essential oil for the potential biocontrol of Colocasia esculenta (taro) leaf blight caused by Phytophthora colocasiae. Environmental science and pollution research international. 2018 Oct; 25(30):29929-29935. doi: 10.1007/s11356-017-0506-0. [PMID: 29150804]
Stephane L Ngahang Kamte, Farahnaz Ranjbarian, Kevin Cianfaglione, Stefania Sut, Stefano Dall'Acqua, Maurizio Bruno, Fariba Heshmati Afshar, Romilde Iannarelli, Giovanni Benelli, Loredana Cappellacci, Anders Hofer, Filippo Maggi, Riccardo Petrelli. Identification of highly effective antitrypanosomal compounds in essential oils from the Apiaceae family. Ecotoxicology and environmental safety. 2018 Jul; 156(?):154-165. doi: 10.1016/j.ecoenv.2018.03.032. [PMID: 29549739]
Pradeep Kumar Kamila, Asit Ray, Sudipta Jena, Pradipta Kumar Mohapatra, Pratap Chandra Panda. Chemical composition and antioxidant activities of the essential oil of Hypericum gaitii Haines - an endemic species of Eastern India. Natural product research. 2018 Mar; 32(6):739-742. doi: 10.1080/14786419.2017.1338283. [PMID: 28595453]
Emanuele Pallozzi, Ilaria Lusini, Lucia Cherubini, Ramilla A Hajiaghayeva, Paolo Ciccioli, Carlo Calfapietra. Differences between a deciduous and a conifer tree species in gaseous and particulate emissions from biomass burning. Environmental pollution (Barking, Essex : 1987). 2018 Mar; 234(?):457-467. doi: 10.1016/j.envpol.2017.11.080. [PMID: 29207297]
Gabriel Garcia, Adrien Garcia, Marc Gibernau, Ange Bighelli, Félix Tomi. Chemical compositions of essential oils of five introduced conifers in Corsica. Natural product research. 2017 Jul; 31(14):1697-1703. doi: 10.1080/14786419.2017.1285299. [PMID: 28278672]
Aida Lahmar, Ahmed Bedoui, Imen Mokdad-Bzeouich, Zaineb Dhaouifi, Zahar Kalboussi, Imed Cheraif, Kamel Ghedira, Leila Chekir-Ghedira. Reversal of resistance in bacteria underlies synergistic effect of essential oils with conventional antibiotics. Microbial pathogenesis. 2017 May; 106(?):50-59. doi: 10.1016/j.micpath.2016.10.018. [PMID: 27815129]
Mirjana Marčetić, Nada Kovačević, Dmitar Lakušić, Branislava Lakušić. Habitat-related variation in composition of the essential oil of Seseli rigidum Waldst. & Kit. (Apiaceae). Phytochemistry. 2017 Mar; 135(?):80-92. doi: 10.1016/j.phytochem.2016.12.004. [PMID: 27939243]
Jirakrit Leelarungrayub, Jiradej Manorsoi, Aranya Manorsoi. Anti-inflammatory activity of niosomes entrapped with Plai oil (Zingiber cassumunar Roxb.) by therapeutic ultrasound in a rat model. International journal of nanomedicine. 2017; 12(?):2469-2476. doi: 10.2147/ijn.s129131. [PMID: 28408818]
Elwira Sieniawska, Marta Swatko-Ossor, Rafał Sawicki, Krystyna Skalicka-Woźniak, Grazyna Ginalska. Natural Terpenes Influence the Activity of Antibiotics against Isolated Mycobacterium tuberculosis. Medical principles and practice : international journal of the Kuwait University, Health Science Centre. 2017; 26(2):108-112. doi: 10.1159/000454680. [PMID: 27883995]
Yaser Masoumi-Ardakani, Ali Mandegary, Khadijeh Esmaeilpour, Hamid Najafipour, Fariba Sharififar, Mahboobeh Pakravanan, Hamed Ghazvini. Chemical Composition, Anticonvulsant Activity, and Toxicity of Essential Oil and Methanolic Extract of Elettaria cardamomum. Planta medica. 2016 Nov; 82(17):1482-1486. doi: 10.1055/s-0042-106971. [PMID: 27433883]
Le D Hieua, Tran M Hoic, Tran D Thangda, Isiaka A Ogunwande. Volatile Constituents of Three Piper Species from Vietnam. Natural product communications. 2015 Nov; 10(11):1997-8. doi: . [PMID: 26749846]
Brigitte Lukas, Corinna Schmiderer, Johannes Novak. Essential oil diversity of European Origanum vulgare L. (Lamiaceae). Phytochemistry. 2015 Nov; 119(?):32-40. doi: 10.1016/j.phytochem.2015.09.008. [PMID: 26454793]
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