Decanal (BioDeep_00000003252)
Secondary id: BioDeep_00000406211
human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite
代谢物信息卡片
化学式: C10H20O (156.151407)
中文名称: 癸醛
谱图信息:
最多检出来源 Homo sapiens(blood) 2.14%
分子结构信息
SMILES: CCCCCCCCCC([H])=O
InChI: InChI=1S/C10H20O/c1-2-3-4-5-6-7-8-9-10-11/h10H,2-9H2,1H3
描述信息
Decanal, also known as 1-decyl aldehyde or capraldehyde, belongs to the class of organic compounds known as medium-chain aldehydes. These are an aldehyde with a chain length containing between 6 and 12 carbon atoms. Thus, decanal is considered to be a fatty aldehyde lipid molecule. Decanal is a very hydrophobic molecule, practically insoluble in water, and relatively neutral. Decanal exists in all eukaryotes, ranging from yeast to humans. Decanal is a sweet, aldehydic, and citrus tasting compound. Decanal is found, on average, in the highest concentration within a few different foods, such as corianders, dills, and gingers and in a lower concentration in limes, sweet oranges, and safflowers. Decanal has also been detected, but not quantified, in several different foods, such as fishes, cauliflowers, citrus, fats and oils, and lemon grass. This could make decanal a potential biomarker for the consumption of these foods. Decanal is a potentially toxic compound. Decanal, with regard to humans, has been found to be associated with several diseases such as uremia, asthma, and perillyl alcohol administration for cancer treatment; decanal has also been linked to the inborn metabolic disorder celiac disease. Decanal occurs naturally and is used in fragrances and flavoring. Chronic exposure of uremic toxins can lead to a number of conditions including renal damage, chronic kidney disease and cardiovascular disease. Uremic toxins tend to accumulate in the blood either through dietary excess or through poor filtration by the kidneys.
Constituent of Cassia, Neroli and other oils especies citrus peel oilsand is also present in coriander leaf or seed, caviar, roast turkey, roast filbert, green tea, fish oil, hop oil and beer. Flavouring agent
Decyl aldehyde is a simple ten-carbon aldehyde. Decyl aldehyde is a bacterial luciferase substrate.
Decyl aldehyde is a simple ten-carbon aldehyde. Decyl aldehyde is a bacterial luciferase substrate.
同义名列表
20 个代谢物同义名
N-Decanal (capric aldehyde); 1-Decanal(mixed isomers); Decanal (acd/name 4.0); Caprinic aldehyde; 1-Decyl aldehyde; N-Decyl aldehyde; Decylic aldehyde; Capric aldehyde; Decyl aldehyde; Caprinaldehyde; N-Decaldehyde; Decanaldehyde; C-10 Aldehyde; Capraldehyde; Aldehyde C10; Decaldehyde; 1-Decanal; N-Decanal; FAL 10:0; Decanal
数据库引用编号
22 个数据库交叉引用编号
- ChEBI: CHEBI:31457
- KEGG: C12307
- PubChem: 8175
- HMDB: HMDB0011623
- Metlin: METLIN36572
- ChEMBL: CHEMBL2228377
- Wikipedia: Decanal
- LipidMAPS: LMFA06000052
- MetaCyc: CPD-8490
- KNApSAcK: C00030804
- KNApSAcK: C00030099
- foodb: FDB012768
- chemspider: 7883
- CAS: 112-31-2
- CAS: 112-81-2
- PMhub: MS000008622
- PubChem: 582698
- PDB-CCD: 8YP
- 3DMET: B04449
- NIKKAJI: J2.888F
- RefMet: Capraldehyde
- medchemexpress: HY-W012570
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)
84 个相关的物种来源信息
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- 589713 - Anthemis aciphylla: 10.1248/CPB.54.222
- 4217 - Arctium lappa: 10.1271/NOGEIKAGAKU1924.59.389
- 4458 - Arum maculatum: 10.1016/0305-1978(95)00026-Q
- 76974 - Atalantia buxifolia: 10.1080/10412905.1994.9698400
- 41492 - Bellis perennis: 10.1016/0031-9422(95)00183-8
- 3483 - Cannabis sativa: 10.1021/NP50008A001
- 79829 - Capillipedium parviflorum: 10.1016/J.PHYTOCHEM.2004.04.003
- 48032 - Carum carvi: 10.1021/JF00047A021
- 114816 - Castanopsis cuspidata: 10.1021/JF60224A025
- 114280 - Cichorium endivia: 10.1021/JF00068A014
- 2706 - Citrus: 10.1080/10412905.1993.9698179
- 558547 - Citrus deliciosa:
- 79217 - Citrus iyo: 10.1271/BBB1961.47.1841
- 37334 - Citrus maxima: 10.1271/BBB1961.55.2571
- 85571 - Citrus reticulata:
- 85571 - Citrus Reticulata: -
- 55188 - Citrus unshiu:
- 475932 - Citrus wilsonii: 10.1007/BF00579447
- 4047 - Coriandrum sativum:
- 3661 - Cucurbita maxima: 10.1021/JF00073A014
- 79835 - Cymbopogon flexuosus: 10.1080/10412905.1994.9698332
- 329675 - Daphne odora: 10.1271/BBB1961.47.483
- 2715869 - Daphne papyracea: 10.1271/BBB1961.47.483
- 477864 - Eryngium foetidum: 10.1080/10412905.1997.9700731
- 188493 - Etlingera elatior: 10.1080/10412905.1993.9698191
- 102770 - Eupatorium cannabinum: 10.1055/S-2007-969599
- 87257 - Evernia prunastri: 10.1021/JF60201A022
- 5314 - Ganoderma: -
- 5315 - Ganoderma lucidum: 10.1016/J.PHYTOCHEM.2005.10.025
- 1770161 - Griffitharia pallescens: 10.1248/CPB.54.936
- 671128 - Gymnodinium nagasakiense: 10.1016/0031-9422(92)80160-G
- 4397 - Hamamelis virginiana: 10.1055/S-2006-957420
- 261800 - Helichrysum pendulum: 10.1055/S-2006-957552
- 261805 - Helichrysum stoechas: 10.1055/S-2006-957641
- 9606 - Homo sapiens: -
- 16752 - Houttuynia cordata:
- 16752 - Houttuynia cordata Thunb.: -
- 282542 - Hypericum japonicum: 10.1016/J.PHYTOCHEM.2004.08.014
- 65561 - Hypericum perforatum: 10.1016/J.PHYTOCHEM.2004.08.014
- 225107 - Karenia mikimotoi: 10.1016/0031-9422(92)80160-G
- 1231670 - Leiocarpa semicalva: 10.1055/S-2006-957552
- 3750 - Malus domestica: 10.1021/JF00025A025
- 283210 - Malus pumila: 10.1021/JF00025A025
- 1898872 - Micromeria biflora: 10.1080/10412905.1997.9700709
- 1127086 - Mikania cordifolia: 10.1016/S0031-9422(00)80558-0
- 54731 - Nepeta racemosa: 10.1080/10412905.1993.9698205
- 35924 - Paeonia lactiflora: 10.1016/S0031-9422(00)94541-2
- 158596 - Pelargonium endlicherianum: 10.1055/S-2006-960872
- 48386 - Perilla Frutescens: -
- 488003 - Persicaria minor: 10.3390/MOLECULES191119220
- 1155347 - Persicaria mitis: 10.3390/MOLECULES191119220
- 580473 - Persicaria odorata: 10.1080/10412905.1995.9698534
- 260139 - Pimenta racemosa: 10.1080/10412905.1991.9697952
- 268869 - Pinus sabiniana: 10.1002/JPS.3080240509
- 1546318 - Piper sylvestre: 10.1055/S-2006-959506
- 43073 - Pittosporum tobira: 10.1016/0031-9422(89)80285-7
- 992772 - Pittosporum viridiflorum: 10.1080/10412905.2000.9712178
- 6359 - Platynereis dumerilii: 10.1002/JEZ.1402460308
- 174549 - Polygala senega: 10.1002/FFJ.2730100408
- 169599 - Porophyllum ruderale: 10.1002/(SICI)1099-1026(199911/12)14:6<393::AID-FFJ849>3.0.CO;2-5
- 3755 - Prunus dulcis: 10.1021/JF60228A025
- 32242 - Prunus laurocerasus: 10.1016/J.FOODCHEM.2013.11.092
- 3760 - Prunus persica: 10.1016/J.FOODCHEM.2013.11.092
- 203015 - Rhodiola rosea: 10.1016/S0031-9422(02)00004-3
- 74632 - Rosa gallica: 10.1111/J.1600-0536.1991.TB01726.X
- 37565 - Ruta graveolens: 10.1080/10412905.1989.9697787
- 374729 - Siphonostegia chinensis Benth.: -
- 103871 - Solanum acaule: 10.1186/1471-2229-14-140
- 4081 - Solanum lycopersicum: 10.1186/1471-2229-14-140
- 4558 - Sorghum bicolor: 10.1021/NP50053A034
- 169607 - Tagetes minuta: 10.1080/10412905.1992.9698123
- 1194133 - Thymus longicaulis: 10.1080/10412905.1992.9698070
- 489417 - Tordylium apulum: 10.1080/10412905.1993.9698167
- 4565 - Triticum aestivum: 10.1016/S0031-9422(00)82634-5
- 13750 - Vaccinium macrocarpon: 10.3891/ACTA.CHEM.SCAND.21-2076
- 180772 - Vaccinium vitis-idaea: 10.3891/ACTA.CHEM.SCAND.21-0945
- 361442 - Vitex negundo: 10.1055/S-2006-959580
- 29760 - Vitis vinifera: 10.3389/FMICB.2017.00457
- 4577 - Zea mays:
- 136225 - Zingiber mioga: 10.1271/BBB1961.55.1655
- 94328 - Zingiber officinale:
- 94328 - Zingiber officinale Rosc.: -
- 94328 - Zingiber Officinale Roscoe: -
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
- Zelong Zhang, Minghong Liu, Xiaoyan Wang, Jianyu Gou, Tianliang Li, Te Zhao, Lin Zhou, Fulong Zhang, Fujia Cheng. Plant volatiles mediated the orientation preference of slugs to different plant species.
Pest management science.
2023 Sep; ?(?):. doi:
10.1002/ps.7757
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ACS pharmacology & translational science.
2023 May; 6(5):683-701. doi:
10.1021/acsptsci.2c00194
. [PMID: 37200814] - Marzieh Babashpour-Asl, Elnaz Farajzadeh-Memari-Tabrizi, Afsaneh Yousefpour-Dokhanieh. Foliar-applied selenium nanoparticles alleviate cadmium stress through changes in physio-biochemical status and essential oil profile of coriander (Coriandrum sativum L.) leaves.
Environmental science and pollution research international.
2022 Nov; 29(53):80021-80031. doi:
10.1007/s11356-022-19941-1
. [PMID: 35397029] - Juliah W Jacob, David P Tchouassi, Zipporah O Lagat, Evan M Mathenge, Collins K Mweresa, Baldwyn Torto. Independent and interactive effect of plant- and mammalian- based odors on the response of the malaria vector, Anopheles gambiae.
Acta tropica.
2018 Sep; 185(?):98-106. doi:
10.1016/j.actatropica.2018.04.027
. [PMID: 29709631] - Valentina Lazazzara, Michele Perazzolli, Ilaria Pertot, Franco Biasioli, Gerardo Puopolo, Luca Cappellin. Growth media affect the volatilome and antimicrobial activity against Phytophthora infestans in four Lysobacter type strains.
Microbiological research.
2017 Aug; 201(?):52-62. doi:
10.1016/j.micres.2017.04.015
. [PMID: 28602402] - Elin Isberg, Daniel Peter Bray, Ylva Hillbur, Rickard Ignell. Evaluation of Host-Derived Volatiles for Trapping Culicoides Biting Midges (Diptera: Ceratopogonidae).
Journal of chemical ecology.
2017 Jul; 43(7):662-669. doi:
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Journal of medical microbiology.
2016 Jul; 65(7):688-695. doi:
10.1099/jmm.0.000286
. [PMID: 27259704] - Ken-Ichi Fujita, Warinthorn Chavasiri, Isao Kubo. Anti-Salmonella Activity of Volatile Compounds of Vietnam Coriander.
Phytotherapy research : PTR.
2015 Jul; 29(7):1081-7. doi:
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Molecules (Basel, Switzerland).
2015 Jun; 20(6):10298-312. doi:
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Natural product research.
2015; 29(15):1473-6. doi:
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. [PMID: 25605295] - Perng-Kuang Chang, Leslie L Scharfenstein, Brian Mack, Jiujiang Yu, Kenneth C Ehrlich. Transcriptomic profiles of Aspergillus flavus CA42, a strain that produces small sclerotia, by decanal treatment and after recovery.
Fungal genetics and biology : FG & B.
2014 Jul; 68(?):39-47. doi:
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. [PMID: 24780887] - Kehai Liu, Qiulin Chen, Yanjun Liu, Xiaoyan Zhou, Xichang Wang. Isolation and biological activities of decanal, linalool, valencene, and octanal from sweet orange oil.
Journal of food science.
2012 Nov; 77(11):C1156-61. doi:
10.1111/j.1750-3841.2012.02924.x
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Proceedings. Biological sciences.
2012 Jun; 279(1737):2314-22. doi:
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Journal of dairy science.
2012 Jun; 95(6):2848-62. doi:
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Parasitology research.
2012 Apr; 110(4):1427-33. doi:
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Journal of chemical ecology.
2012 Apr; 38(4):378-88. doi:
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Plant foods for human nutrition (Dordrecht, Netherlands).
2012 Mar; 67(1):57-63. doi:
10.1007/s11130-011-0270-0
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Immunopharmacology and immunotoxicology.
2012 Feb; 34(1):152-6. doi:
10.3109/08923973.2011.589030
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PloS one.
2012; 7(5):e37479. doi:
10.1371/journal.pone.0037479
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International journal of molecular sciences.
2012; 13(3):2827-2845. doi:
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TheScientificWorldJournal.
2012; 2012(?):354019. doi:
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Journal of hazardous materials.
2011 Oct; 193(?):139-48. doi:
10.1016/j.jhazmat.2011.07.042
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Plant physiology and biochemistry : PPB.
2011 Sep; 49(9):1059-63. doi:
10.1016/j.plaphy.2011.06.008
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Proceedings. Biological sciences.
2011 Aug; 278(1716):2303-10. doi:
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Respiratory research.
2011 Jul; 12(?):92. doi:
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Drug development and industrial pharmacy.
2011 Jul; 37(7):841-8. doi:
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. [PMID: 21244220] - John J Beck, Noreen E Mahoney, Daniel Cook, Wai S Gee. Volatile analysis of ground almonds contaminated with naturally occurring fungi.
Journal of agricultural and food chemistry.
2011 Jun; 59(11):6180-7. doi:
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. [PMID: 21528918] - Shao-Hua Gu, Wei-Xuan Wang, Gui-Rong Wang, Xue-Ying Zhang, Yu-Yuan Guo, Ziding Zhang, Jing-Jiang Zhou, Yong-Jun Zhang. Functional characterization and immunolocalization of odorant binding protein 1 in the lucerne plant bug, Adelphocoris lineolatus (GOEZE).
Archives of insect biochemistry and physiology.
2011 Jun; 77(2):81-99. doi:
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Journal of food science.
2011 Mar; 76(2):C212-7. doi:
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Journal of dairy science.
2011 Mar; 94(3):1185-93. doi:
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. [PMID: 21338784] - Dong H Cha, Charles E Linn, Peter E A Teal, Aijun Zhang, Wendell L Roelofs, Gregory M Loeb. Eavesdropping on plant volatiles by a specialist moth: significance of ratio and concentration.
PloS one.
2011 Feb; 6(2):e17033. doi:
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Natural product communications.
2011 Feb; 6(2):267-70. doi:
"
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Evidence-based complementary and alternative medicine : eCAM.
2011; 2011(?):985832. doi:
10.1155/2011/985832
. [PMID: 21660258] - Sunday Oluwafemi, Toby J A Bruce, John A Pickett, Jurriaan Ton, Michael A Birkett. Behavioral responses of the leafhopper, Cicadulina storeyi China, a major vector of maize streak virus, to volatile cues from intact and leafhopper-damaged maize.
Journal of chemical ecology.
2011 Jan; 37(1):40-8. doi:
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. [PMID: 21191806] - Jun Tabata, Consuelo M De Moraes, Mark C Mescher. Olfactory cues from plants infected by powdery mildew guide foraging by a mycophagous ladybird beetle.
PloS one.
2011; 6(8):e23799. doi:
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. [PMID: 21876772] - Kartik Neog, Balagopalan Unni, Giasuddin Ahmed. Studies on the influence of host plants and effect of chemical stimulants on the feeding behavior in the muga silkworm, Antheraea assamensis.
Journal of insect science (Online).
2011; 11(?):133. doi:
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PloS one.
2011; 6(5):e20302. doi:
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. [PMID: 21637850] - Atsushi Muroi, Abdelaziz Ramadan, Masahiro Nishihara, Masaki Yamamoto, Rika Ozawa, Junji Takabayashi, Gen-ichiro Arimura. The composite effect of transgenic plant volatiles for acquired immunity to herbivory caused by inter-plant communications.
PloS one.
2011; 6(10):e24594. doi:
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International journal of molecular sciences.
2011; 12(11):7626-34. doi:
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BMC microbiology.
2010 Dec; 10(?):313. doi:
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. [PMID: 21138563] - Poluru G Padmaja, Christine M Woodcock, Toby J A Bruce. Electrophysiological and behavioral responses of sorghum shoot fly, Atherigona soccata, to sorghum volatiles.
Journal of chemical ecology.
2010 Dec; 36(12):1346-53. doi:
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Journal of Ayurveda and integrative medicine.
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