Lauric aldehyde (BioDeep_00000001081)
Secondary id: BioDeep_00000860740
human metabolite PANOMIX_OTCML-2023 Endogenous
代谢物信息卡片
化学式: C12H24O (184.1827)
中文名称: 十二醛, 十二烷醛
谱图信息:
最多检出来源 Homo sapiens(feces) 20.98%
分子结构信息
SMILES: C(CC)CCCCCCCCC([H])=O
InChI: InChI=1S/C12H24O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h12H,2-11H2,1H3
描述信息
Dodecanal is a long-chain fatty aldehyde that is dodecane in which two hydrogens attached to a terminal carbon are replaced by an oxo group. It has a role as a plant metabolite. It is a 2,3-saturated fatty aldehyde, a medium-chain fatty aldehyde and a long-chain fatty aldehyde. It derives from a hydride of a dodecane.
Dodecanal is a natural product found in Mikania cordifolia, Zingiber mioga, and other organisms with data available.
Occurs in peel oil from Citrus subspecies and kumquatand is also present in ginger, coriander, chervil and scallop. Flavouring agent. Lauric aldehyde is found in many foods, some of which are mollusks, rocket salad (sspecies), sweet orange, and fruits.
Lauric aldehyde is found in citrus. Lauric aldehyde occurs in peel oil from Citrus species and kumquat. Also present in ginger, coriander, chervil and scallop. Lauric aldehyde is a flavouring agent.
A long-chain fatty aldehyde that is dodecane in which two hydrogens attached to a terminal carbon are replaced by an oxo group.
同义名列表
42 个代谢物同义名
InChI=1/C12H24O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h12H,2-11H2,1H; 4-01-00-03380 (Beilstein Handbook Reference); Lauric aldehyde, >=95\\%, stabilized, FCC, FG; Lauric aldehyde, analytical standard; Lauric aldehyde, natural, >=95\\%, FG; DODECANAL (STABILIZED WITH BHT); Lauric aldehyde (natural); LAURYL ALDEHYDE [FHFI]; Dodecyl aldehyde, 92\\%; C-12 aldehyde, lauric; Dodecanal, stabilized; LAURYL ALDEHYDE [FCC]; Aldehyde C-12, lauric; C-12 lauric aldehyde; n-Dodecylic aldehyde; Duodecylic aldehyde; LAURALDEHYDE [INCI]; Lauraldehyde (8CI); n-Dodecyl aldehyde; 1-Dodecyl aldehyde; Dodecyl aldehyde; Lauryl aldehyde; UNII-C42O120SEF; Lauric aldehyde; Dodecanaldehyde; Dodecylaldehyde; n-Lauraldehyde; Laurylaldehyde; Laurinaldehyde; Lauraldehyde; Aldehyde C12; C12 aldehyde; 1-Dodecanal; n-Dodecanal; C42O120SEF; FEMA 2615; AI3-02459; Dodecanal; WLN: VH11; FAL 12:0; Dodecylaldehyde; Dodecanal
数据库引用编号
23 个数据库交叉引用编号
- ChEBI: CHEBI:27836
- KEGG: C02278
- KEGGdrug: D77654
- PubChem: 8194
- HMDB: HMDB0033933
- Metlin: METLIN36591
- ChEMBL: CHEMBL2228373
- Wikipedia: Dodecanal
- LipidMAPS: LMFA06000071
- ChemIDplus: 0000112549
- MetaCyc: CPD-7880
- KNApSAcK: C00030644
- foodb: FDB012137
- chemspider: 7902
- CAS: 112-54-9
- medchemexpress: HY-W004301
- PMhub: MS000017522
- MetaboLights: MTBLC27836
- PubChem: 5336
- 3DMET: B01555
- NIKKAJI: J22.116C
- RefMet: Laurylaldehyde
- KNApSAcK: 27836
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)
26 个相关的物种来源信息
- 155124 - Aspalathus linearis: 10.1021/JF00062A024
- 3483 - Cannabis sativa: 10.1021/NP50008A001
- 2706 - Citrus: 10.1080/10412905.1993.9698179
- 79217 - Citrus iyo: 10.1271/BBB1961.47.1841
- 332445 - Clinopodium gilliesii: 10.1080/10412905.1993.9698276
- 4047 - Coriandrum sativum:
- 4039 - Daucus carota:
- 477864 - Eryngium foetidum: 10.1080/10412905.1992.9698097
- 188493 - Etlingera elatior: 10.1080/10412905.1993.9698191
- 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
- 9606 - Homo sapiens: -
- 16752 - Houttuynia cordata:
- 225107 - Karenia mikimotoi: 10.1016/0031-9422(92)80160-G
- 1231670 - Leiocarpa semicalva: 10.1055/S-2006-957552
- 2689076 - Ligusticum chuanxiong: 10.1016/J.JEP.2012.10.010
- 1508160 - Ligusticum striatum: 10.1016/J.JEP.2012.10.010
- 1127086 - Mikania cordifolia: 10.1016/S0031-9422(00)80558-0
- 580473 - Persicaria odorata: 10.1080/10412905.1995.9698534
- 37565 - Ruta graveolens: 10.1080/10412905.1989.9697787
- 27967 - Scytosiphon lomentaria: 10.1016/0031-9422(91)85017-T
- 13727 - Thujopsis dolabrata: 10.1016/0031-9422(82)83156-7
- 13750 - Vaccinium macrocarpon: 10.3891/ACTA.CHEM.SCAND.21-2076
- 4577 - Zea mays: 10.1021/JF60218A022
- 136225 - Zingiber mioga: 10.1271/BBB1961.55.1655
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
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Chemical communications (Cambridge, England).
2009 Oct; ?(40):6092-4. doi:
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Biochemistry.
2009 Oct; 48(40):9627-40. doi:
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Journal of experimental & clinical cancer research : CR.
2009 Aug; 28(?):121. doi:
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. [PMID: 19715603] - Jana Collatz, Till Tolasch, Johannes L M Steidle. Mate finding in the parasitic wasp Cephalonomia tarsalis (Ashmead): more than one way to a female's heart.
Journal of chemical ecology.
2009 Jul; 35(7):761-8. doi:
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BMC genomics.
2009 Jun; 10(?):288. doi:
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Journal of experimental & clinical cancer research : CR.
2009 Jun; 28(?):79. doi:
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Animal reproduction science.
2009 Jun; 112(3-4):362-70. doi:
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Insect molecular biology.
2009 Jun; 18(3):405-17. doi:
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Chemical reviews.
2009 May; 109(5):1793-899. doi:
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Parazitologiia.
2009 May; 43(3):206-24. doi:
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Nature cell biology.
2009 Feb; 11(2):183-9. doi:
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The Journal of parasitology.
2009 Feb; 95(1):113-9. doi:
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Zhongguo Zhong xi yi jie he za zhi Zhongguo Zhongxiyi jiehe zazhi = Chinese journal of integrated traditional and Western medicine.
2008 Nov; 28(11):1031-3. doi:
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BMC developmental biology.
2008 Oct; 8(?):96. doi:
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The FEBS journal.
2008 Oct; 275(20):5201-14. doi:
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Journal of nematology.
2008 Sep; 40(3):179-89. doi:
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Journal of agricultural and food chemistry.
2008 Aug; 56(16):7316-20. doi:
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Journal of insect physiology.
2008 Jul; 54(7):1184-92. doi:
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International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists.
2008 Jul; 27(3):447-52. doi:
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The EMBO journal.
2008 Jun; 27(12):1647-57. doi:
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Contact dermatitis.
2008 Jun; 58(6):364-5. doi:
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BMC developmental biology.
2008 May; 8(?):54. doi:
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The journal of the Royal Society for the Promotion of Health.
2008 Jan; 128(1):41-6. doi:
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The journals of gerontology. Series A, Biological sciences and medical sciences.
2007 Dec; 62(12):1337-45. doi:
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Traffic (Copenhagen, Denmark).
2007 Nov; 8(11):1568-89. doi:
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DNA research : an international journal for rapid publication of reports on genes and genomes.
2007 Oct; 14(5):207-16. doi:
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The British journal of dermatology.
2007 Sep; 157(3):622-4. doi:
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Biochimica et biophysica acta.
2007 Sep; 1768(9):2205-12. doi:
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Journal of colloid and interface science.
2007 Sep; 313(1):363-8. doi:
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BMC biotechnology.
2007 Aug; 7(?):53. doi:
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Journal of natural products.
2007 Jun; 70(6):974-8. doi:
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. [PMID: 17511505] - Mohammad Najlah, Sally Freeman, David Attwood, Antony D'Emanuele. In vitro evaluation of dendrimer prodrugs for oral drug delivery.
International journal of pharmaceutics.
2007 May; 336(1):183-90. doi:
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The Veterinary record.
2007 Mar; 160(9):293-6. doi:
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American journal of obstetrics and gynecology.
2007 Mar; 196(3):e9-e10. doi:
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Journal of AOAC International.
2007 Jan; 90(1):60-7. doi:
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Animal reproduction science.
2007 Jan; 97(1-2):165-74. doi:
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Genome biology.
2007; 8(10):R211. doi:
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Molecular pharmaceutics.
2006 Nov; 3(6):737-44. doi:
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PLoS biology.
2006 Nov; 4(11):e362. doi:
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European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology.
2006 Oct; 32(8):818-24. doi:
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Tijdschrift voor diergeneeskunde.
2006 Oct; 131(19):686-91. doi:
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The EMBO journal.
2006 Jun; 25(11):2347-57. doi:
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BMC public health.
2006 Apr; 6(?):106. doi:
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Journal of agricultural and food chemistry.
2006 Apr; 54(8):3067-71. doi:
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