FOH 8:0 (BioDeep_00000629771)
Secondary id: BioDeep_00000003253, BioDeep_00000004214, BioDeep_00000406241, BioDeep_00001867626, BioDeep_00001867656
PANOMIX_OTCML-2023
描述信息
D012997 - Solvents
1-Octanol (Octanol), a saturated fatty alcohol, is a T-type calcium channels (T-channels) inhibitor with an IC50 of 4 μM for native T-currents[1]. 1-Octanol is a highly attractive biofuel with diesel-like properties[2].
1-Octanol (Octanol), a saturated fatty alcohol, is a T-type calcium channels (T-channels) inhibitor with an IC50 of 4 μM for native T-currents[1]. 1-Octanol is a highly attractive biofuel with diesel-like properties[2].
同义名列表
37 个代谢物同义名
xi-2-Ethyl-1-hexanol; 2-Ethylhexan-1-ol; 2-Ethylhexanol; FOH 8:0; 4-methyl-2-heptanol; 4-methylheptan-2-ol; Octan-2-ol; 2-OCTANOL; (S)-3-Octanol; octan-3-ol; (2xi,4xi)-2,4-Dimethyl-1-hexanol; 2,4-dimethylhexan-1-ol; (2S)-2-octanol;(S)-(+)-2-octanol;(S)-2-octanol;d-octan-2-ol; (2S)-octan-2-ol; (2R)-2-octanol;(R)-(-)-2-octanol;(R)-2-octanol;l-octan-2-ol; (2R)-octan-2-ol; Octan-3S-ol; Octan-3R-ol; 6-Methylheptan-3-ol; 6-methyl-3-heptanol; 3-Methylheptan-2-ol; 2-Methylheptan-4R-ol; (3S,4S)-4-Methylheptan-3-ol; 4S-Methylheptan-3S-ol; (3R,4S)-4-Methylheptan-3-ol; 4S-Methylheptan-3R-ol; Octan-1-ol; n-octanol; 1-octanol; Octanol; 1-Octanol; 2-Ethylhexan-1-ol; 6-Methylheptan-3-ol; 4-Methyl-2-heptanol; 2-Ethylhexanol; 2-Octanol; 1-Octanol
数据库引用编号
62 个数据库交叉引用编号
- ChEBI: CHEBI:16011
- ChEBI: CHEBI:165509
- ChEBI: CHEBI:37869
- ChEBI: CHEBI:186745
- ChEBI: CHEBI:137757
- ChEBI: CHEBI:16188
- KEGG: C02498
- KEGG: C00756
- PubChem: 7720
- PubChem: 143345
- PubChem: 20083
- PubChem: 14753148
- PubChem: 6999002
- PubChem: 445789
- PubChem: 86783
- PubChem: 35784
- PubChem: 12650794
- PubChem: 6993196
- PubChem: 6993195
- PubChem: 957
- DrugBank: DB12452
- ChEMBL: CHEMBL31637
- ChEMBL: CHEMBL510068
- ChEMBL: CHEMBL26215
- LipidMAPS: LMFA05000703
- LipidMAPS: LMFA05000630
- LipidMAPS: LMFA05000620
- LipidMAPS: LMFA05000568
- LipidMAPS: LMFA05000553
- LipidMAPS: LMFA05000551
- LipidMAPS: LMFA05000547
- LipidMAPS: LMFA05000492
- LipidMAPS: LMFA05000490
- LipidMAPS: LMFA05000482
- LipidMAPS: LMFA05000479
- LipidMAPS: LMFA05000476
- LipidMAPS: LMFA05000473
- LipidMAPS: LMFA05000472
- LipidMAPS: LMFA05000130
- MeSH: 1-Octanol
- CAS: 104-76-7
- CAS: 56298-90-9
- CAS: 25339-16-6
- CAS: 4128-31-8
- CAS: 4128-32-9
- CAS: 123-96-6
- CAS: 3965-59-1
- CAS: 18720-66-6
- CAS: 67700-96-3
- CAS: 68603-15-6
- CAS: 111-87-5
- PubChem: 4018
- KNApSAcK: C00001264
- PDB-CCD: OC9
- 3DMET: B00168
- NIKKAJI: J2.459G
- PubChem: 5510
- NIKKAJI: J3.604H
- RefMet: n-Octanol
- medchemexpress: HY-W032013
- KNApSAcK: 16188
- KNApSAcK: 16011
分类词条
相关代谢途径
Reactome(0)
BioCyc(3)
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)
113 个相关的物种来源信息
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- 299928 - Alpinia latilabris: 10.1080/10412905.1994.9698447
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- 4442 - Camellia sinensis: 10.1021/JF00034A031
- 3483 - Cannabis sativa: 10.1021/NP50008A001
- 79829 - Capillipedium parviflorum: 10.1016/J.PHYTOCHEM.2004.04.003
- 114816 - Castanopsis cuspidata: 10.1021/JF60224A025
- 260595 - Cedronella canariensis: 10.1016/0031-9422(95)00241-X
- 114280 - Cichorium endivia: 10.1021/JF00068A014
- 3654 - Citrullus lanatus: 10.1271/BBB1961.49.3145
- 2706 - Citrus: 10.1080/10412905.1993.9698179
- 558547 - Citrus deliciosa:
- 79217 - Citrus iyo: 10.1271/BBB1961.47.1841
- 85571 - Citrus reticulata:
- 85571 - Citrus reticulata Blanco: -
- 37690 - Citrus trifoliata: 10.3390/MOLECULES13061333
- 55188 - Citrus unshiu:
- 4047 - Coriandrum sativum: 10.1021/JF00029A021
- 136209 - Curcuma aromatica: 10.1016/J.JPBA.2005.07.050
- 136221 - Curcuma wenyujin: 10.1016/J.JPBA.2005.07.050
- 329675 - Daphne odora: 10.1271/BBB1961.47.483
- 2715869 - Daphne papyracea: 10.1271/BBB1961.47.483
- 270439 - Erica manipuliflora: 10.1080/10412905.2000.9712044
- 102770 - Eupatorium cannabinum: 10.1055/S-2007-969599
- 52153 - Festuca rubra: 10.1016/0031-9422(91)84185-U
- 48119 - Glehnia littoralis: 10.1021/JF010219C
- 4397 - Hamamelis virginiana: 10.1055/S-2006-957420
- 261800 - Helichrysum pendulum: 10.1055/S-2006-957552
- 360619 - Heracleum antasiaticum: 10.1080/10412905.1993.9698208
- 360621 - Heracleum persicum: 10.1055/S-2007-969621
- 185542 - Ilex paraguariensis: 10.1021/JF00025A023
- 16719 - Juglans nigra: 10.1080/10412905.1993.9698259
- 1231670 - Leiocarpa semicalva: 10.1055/S-2006-957552
- 5353 - Lentinula edodes:
- 4606 - Lolium arundinaceum: 10.1016/0031-9422(91)84185-U
- 105884 - Lonicera japonica: 10.1186/1471-2164-13-195
- 3750 - Malus domestica: 10.1002/FOOD.19810250610
- 283210 - Malus pumila: 10.1002/FOOD.19810250610
- 389206 - Mandragora autumnalis: 10.1080/10412905.1998.9700991
- 33117 - Mandragora officinarum: 10.1080/10412905.1998.9700991
- 3879 - Medicago sativa: 10.1016/S0031-9422(97)00119-2
- 38859 - Mentha longifolia: 10.1080/10412905.1991.9697909
- 29719 - Mentha spicata: 10.1080/10412905.1991.9697909
- 39350 - Ocimum basilicum: 10.1080/10412905.1995.9698501
- 84561 - Oecophylla smaragdina: 10.1271/BBB1961.54.3335
- 4146 - Olea europaea: 10.1016/S0031-9422(97)00730-9
- 145953 - Ophrys sphegodes: 10.1016/S0031-9422(00)81276-5
- 371859 - Opuntia ficus-indica: 10.1021/JF60218A053
- 1268187 - Origanum cordifolium: 10.1016/0378-8741(91)90063-J
- 39352 - Origanum vulgare: 10.1080/10412905.1993.9698253
- 1477654 - Pectis elongata var. floribunda: 10.1080/10412905.1999.9701062
- 158596 - Pelargonium endlicherianum: 10.1055/S-2006-960872
- 3435 - Persea americana: 10.1021/JF00019A020
- 3885 - Phaseolus vulgaris: 10.1021/JF60199A053
- 3528 - Phytolacca acinosa: 10.1007/S10600-019-02670-2
- 260139 - Pimenta racemosa: 10.1080/10412905.1995.9698553
- 204156 - Platostoma africanum: 10.1055/S-2006-962093
- 204187 - Plectranthus glabratus: 10.1080/10412905.1993.9698226
- 5322 - Pleurotus ostreatus: 10.1021/JF960876I
- 62097 - Plumeria rubra: 10.1002/FFJ.2730070108
- 174549 - Polygala senega: 10.1002/FFJ.2730100408
- 3755 - Prunus dulcis: 10.1021/JF60228A025
- 120290 - Psidium guajava: 10.1016/0031-9422(82)80138-6
- 242839 - Rhodiola crenulata:
- 203015 - Rhodiola rosea: 10.1016/S0031-9422(02)00004-3
- 933131 - Salvia dorisiana:
- 39367 - Salvia rosmarinus: 10.1111/J.1365-2621.1985.TB10476.X
- 49988 - Satureja montana: 10.1080/10412905.1991.9700495
- 375857 - Scolochloa festucacea: 10.1016/0031-9422(91)84185-U
- 138013 - Senegalia berlandieri: 10.1021/JF00120A008
- 155234 - Sideritis athoa: 10.1080/10412905.1993.9698303
- 155260 - Sideritis romana: 10.1076/1388-0209(200004)3821-1FT106
- 155267 - Sideritis tragoriganum: 10.1016/S0031-9422(00)80325-8
- 265416 - Solanum stuckertii: 10.1080/10412905.1997.9700728
- 80338 - Spondias mombin: 10.1080/10412905.1992.9698127
- 547782 - Symphyotrichum undulatum: 10.1021/JF00034A033
- 169607 - Tagetes minuta:
- 58860 - Tamarindus indica: 10.1080/10412905.1990.9697860
- 88032 - Taxus canadensis: 10.1080/10412905.1993.9698163
- 155022 - Terminalia chebula: 10.4103/0974-8490.112421
- 1194133 - Thymus longicaulis:
- 1132412 - Thymus zygioides: 10.1080/10412905.1996.9701028
- 489417 - Tordylium apulum: 10.1080/10412905.1993.9698167
- 40145 - Tricholoma matsutake:
- 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
- 103349 - Vitis rotundifolia: 10.1021/JF00112A014
- 29760 - Vitis vinifera:
- 29760 - Vitis vinifera: 10.3389/FMICB.2017.00457
- 36659 - Volvariella volvacea: 10.1021/JF9703314
- 328402 - Zanthoxylum simulans: 10.1021/JF950577D
- 4577 - Zea mays:
- 136225 - Zingiber mioga: 10.1271/BBB1961.55.1655
- 94328 - Zingiber officinale:
- 94328 - Zingiber officinale: 10.1021/JF00097A027
- 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
- Pierre-Alain van Griethuysen, Kelly R Redeker, Stuart A MacFarlane, Roy Neilson, Sue E Hartley. Virus-induced changes in root volatiles attract soil nematode vectors to infected plants.
The New phytologist.
2024 Mar; 241(5):2275-2286. doi:
10.1111/nph.19518
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Applied and environmental microbiology.
2023 Feb; ?(?):e0189222. doi:
10.1128/aem.01892-22
. [PMID: 36722969] - Wen Ouyang, Yaya Yu, Huajie Wang, Yongwen Jiang, Jinjie Hua, Jingming Ning, Haibo Yuan. Analysis of volatile metabolite variations in strip green tea during processing and effect of rubbing degree using untargeted and targeted metabolomics.
Food research international (Ottawa, Ont.).
2022 12; 162(Pt B):112099. doi:
10.1016/j.foodres.2022.112099
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The Journal of membrane biology.
2022 10; 255(4-5):423-435. doi:
10.1007/s00232-022-00231-3
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Chemistry & biodiversity.
2022 Oct; 19(10):e202200411. doi:
10.1002/cbdv.202200411
. [PMID: 36085355] - Vivek Kempraj, Soo Jean Park, Donald N S Cameron, Phillip W Taylor. 1-Octanol emitted by Oecophylla smaragdina weaver ants repels and deters oviposition in Queensland fruit fly.
Scientific reports.
2022 09; 12(1):15768. doi:
10.1038/s41598-022-20102-0
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Journal of agricultural and food chemistry.
2022 Aug; 70(34):10543-10551. doi:
10.1021/acs.jafc.2c04329
. [PMID: 35997264] - Yu-Liang Qin, Shuai-Bing Zhang, Yang-Yong Lv, Huan-Chen Zhai, Yuan-Sen Hu, Jing-Ping Cai. The antifungal mechanisms of plant volatile compound 1-octanol against Aspergillus flavus growth.
Applied microbiology and biotechnology.
2022 Jul; ?(?):. doi:
10.1007/s00253-022-12049-z
. [PMID: 35779097] - Richard Wibel, Patrick Knoll, Bao Le-Vinh, Gergely Kali, Andreas Bernkop-Schnürch. Synthesis and evaluation of sulfosuccinate-based surfactants as counterions for hydrophobic ion pairing.
Acta biomaterialia.
2022 05; 144(?):54-66. doi:
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International journal of environmental research and public health.
2022 03; 19(7):. doi:
10.3390/ijerph19073989
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Industrial health.
2021 Nov; 59(6):383-392. doi:
10.2486/indhealth.2020-0252
. [PMID: 34588381] - Nam Ah Kim, Hyun Woo Yu, Ga Yeon Noh, Sang-Koo Park, Wonku Kang, Seong Hoon Jeong. Protein microbeadification to achieve highly concentrated protein formulation with reversible properties and in vivo pharmacokinetics after reconstitution.
International journal of biological macromolecules.
2021 Aug; 185(?):935-948. doi:
10.1016/j.ijbiomac.2021.07.012
. [PMID: 34237365] - Ian Sofian Yunus, Zhixuan Wang, Pachara Sattayawat, Jonathan Muller, Fessehaye W Zemichael, Klaus Hellgardt, Patrik R Jones. Improved Bioproduction of 1-Octanol Using Engineered Synechocystis sp. PCC 6803.
ACS synthetic biology.
2021 06; 10(6):1417-1428. doi:
10.1021/acssynbio.1c00029
. [PMID: 34003632] - Christopher M Ranger, Marek Dzurenko, Jenny Barnett, Ruchika Geedi, Louela Castrillo, Matthew Ethington, Matthew Ginzel, Karla Addesso, Michael E Reding. Electrophysiological and Behavioral Responses of an Ambrosia Beetle to Volatiles of its Nutritional Fungal Symbiont.
Journal of chemical ecology.
2021 May; 47(4-5):463-475. doi:
10.1007/s10886-021-01263-0
. [PMID: 33761047] - David R Hall, Steven J Harte, Daniel P Bray, Dudley I Farman, Rob James, Celine X Silva, Michelle T Fountain. Hero Turned Villain: Identification of Components of the Sex Pheromone of the Tomato Bug, Nesidiocoris tenuis.
Journal of chemical ecology.
2021 May; 47(4-5):394-405. doi:
10.1007/s10886-021-01270-1
. [PMID: 33844148] - Poovarasan Neelakandan, Chiu-Chung Young, Asif Hameed, Yu-Ning Wang, Kui-Nuo Chen, Fo-Ting Shen. Volatile 1-octanol of tea (Camellia sinensis L.) fuels cell division and indole-3-acetic acid production in phylloplane isolate Pseudomonas sp. NEEL19.
Scientific reports.
2021 02; 11(1):2788. doi:
10.1038/s41598-021-82442-7
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Scientific reports.
2021 01; 11(1):2249. doi:
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Journal of medicinal chemistry.
2020 10; 63(20):11809-11818. doi:
10.1021/acs.jmedchem.0c00958
. [PMID: 32945672] - Néstor J Hernández Lozada, Trevor R Simmons, Ke Xu, Michael A Jindra, Brian F Pfleger. Production of 1-octanol in Escherichia coli by a high flux thioesterase route.
Metabolic engineering.
2020 09; 61(?):352-359. doi:
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Current drug metabolism.
2020; 21(9):714-721. doi:
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Contrast media & molecular imaging.
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Mikrochimica acta.
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International journal of nanomedicine.
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Journal of separation science.
2019 Jan; 42(2):566-573. doi:
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Xenobiotica; the fate of foreign compounds in biological systems.
2018 Nov; 48(11):1142-1156. doi:
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2018 Sep; 122(?):85-93. doi:
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Journal of computer-aided molecular design.
2018 08; 32(8):809-819. doi:
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. [PMID: 30019206] - Vanessa Hörmann, Klaus-Reinhard Brenske, Christian Ulrichs. Assessment of filtration efficiency and physiological responses of selected plant species to indoor air pollutants (toluene and 2-ethylhexanol) under chamber conditions.
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