5-(3-Aminopropylphosphanyloxy)-2-(hydroxymethyl)pyran-4-one (BioDeep_00000183615)
human metabolite blood metabolite
代谢物信息卡片
5-((3-Aminopropyl)phosphinooxy)-2-(hydroxymethyl)-4H-pyran-4-one
化学式: C9H14NO4P (231.0660414)
中文名称:
谱图信息:
最多检出来源 Homo sapiens(blood) 95.45%
分子结构信息
SMILES: C1=C(OC=C(C1=O)OPCCCN)CO
InChI: InChI=1S/C9H14NO4P/c10-2-1-3-15-14-9-6-13-7(5-11)4-8(9)12/h4,6,11,15H,1-3,5,10H2
描述信息
D020011 - Protective Agents > D000975 - Antioxidants
同义名列表
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)
1 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。
文献列表
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International journal of biological macromolecules.
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Dalton transactions (Cambridge, England : 2003).
2022 Apr; 51(16):6254-6263. doi:
10.1039/d2dt00111j. [PMID: 35373808] - Xiang Liu, Jinqiu Rao, Kai Wang, Meijun Wang, Tie Yao, Feng Qiu. Highly Potent Inhibition of Tyrosinase by Mulberrosides and the Inhibitory Mechanism in Vitro.
Chemistry & biodiversity.
2022 Jan; 19(1):e202100740. doi:
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Current pharmaceutical biotechnology.
2022; 23(4):486-494. doi:
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European journal of medicinal chemistry.
2021 Dec; 226(?):113850. doi:
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Artificial cells, nanomedicine, and biotechnology.
2021 Dec; 49(1):38-47. doi:
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Pigment cell & melanoma research.
2021 11; 34(6):1000-1014. doi:
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Molecular neurobiology.
2021 Oct; 58(10):5127-5140. doi:
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Molecules (Basel, Switzerland).
2021 Jul; 26(15):. doi:
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BMC biotechnology.
2020 10; 20(1):52. doi:
10.1186/s12896-020-00644-9. [PMID: 33008398] - Sameh S M Soliman, Rania Hamdy, Samia A Elseginy, Teclegiorgis Gebremariam, Alshaimaa M Hamoda, Mohamed Madkour, Thenmozhi Venkatachalam, Mai N Ershaid, Mohammad G Mohammad, Georgios Chamilos, Ashraf S Ibrahim. Selective inhibition of Rhizopus eumelanin biosynthesis by novel natural product scaffold-based designs caused significant inhibition of fungal pathogenesis.
The Biochemical journal.
2020 07; 477(13):2489-2507. doi:
10.1042/bcj20200310. [PMID: 32538426] - Chie Miyabe, Yupeng Dong, Kazumasa Wakamatsu, Shosuke Ito, Tamihiro Kawakami. Kojic acid alters pheomelanin content in human induced pluripotent stem cell-derived melanocytes.
The Journal of dermatology.
2020 Apr; 47(4):435-436. doi:
10.1111/1346-8138.15260. [PMID: 32067265] - Weike Shaoyong, Qian Li, Zhiqiang Ren, Junying Xiao, Zhaoxi Diao, Gongshe Yang, Weijun Pang. Effects of kojic acid on boar sperm quality and anti-bacterial activity during liquid preservation at 17 C.
Theriogenology.
2019 Dec; 140(?):124-135. doi:
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Molecules (Basel, Switzerland).
2019 Nov; 24(22):. doi:
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Journal of drugs in dermatology : JDD.
2019 May; 18(5):454-459. doi:
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Experimental parasitology.
2019 May; 200(?):7-12. doi:
10.1016/j.exppara.2019.03.009. [PMID: 30904693] - Weimeng Feng, Jinrui Liang, Bingbing Wang, Jianhua Chen. Improvement of kojic acid production in Aspergillus oryzae AR-47 mutant strain by combined mutagenesis.
Bioprocess and biosystems engineering.
2019 May; 42(5):753-761. doi:
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Bulletin of entomological research.
2019 Apr; 109(2):236-247. doi:
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Bioorganic & medicinal chemistry.
2018 11; 26(21):5654-5663. doi:
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Analytical biochemistry.
2017 05; 525(?):54-59. doi:
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Fitoterapia.
2016 Jun; 111(?):95-101. doi:
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Clinical and experimental dermatology.
2016 Mar; 41(2):196-201. doi:
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Insect science.
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Phytochemical analysis : PCA.
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Food chemistry.
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Fungal genetics and biology : FG & B.
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BMC microbiology.
2014 Apr; 14(?):95. doi:
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Journal of dermatological science.
2014 Mar; 73(3):241-50. doi:
10.1016/j.jdermsci.2013.11.002. [PMID: 24296160] - Noureddin El-Boulifi, Siti Efliza Ashari, Marta Serrano, Jose Aracil, Mercedes Martínez. Solvent-free lipase-catalyzed synthesis of a novel hydroxyl-fatty acid derivative of kojic acid.
Enzyme and microbial technology.
2014 Feb; 55(?):128-32. doi:
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Phytochemistry.
2013 Dec; 96(?):305-11. doi:
10.1016/j.phytochem.2013.08.014. [PMID: 24070617] - Biswapriya B Misra, Satyahari Dey. TLC-bioautographic evaluation of in vitro anti-tyrosinase and anti-cholinesterase potentials of sandalwood oil.
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2013 Feb; 8(2):253-6. doi:
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International journal of molecular sciences.
2012 Oct; 13(11):13867-80. doi:
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2012 Sep; 63(5):311-20. doi:
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2012 Sep; 83(6):1008-13. doi:
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Bioscience, biotechnology, and biochemistry.
2012; 76(5):863-9. doi:
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Journal of peptide science : an official publication of the European Peptide Society.
2011 Dec; 17(12):791-7. doi:
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Molecules (Basel, Switzerland).
2011 Nov; 16(11):9331-9. doi:
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Journal of the European Academy of Dermatology and Venereology : JEADV.
2011 Oct; 25(10):1140-5. doi:
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Journal of the American Academy of Dermatology.
2011 Oct; 65(4):699-714. doi:
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Journal of inorganic biochemistry.
2011 Aug; 105(8):1081-5. doi:
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Clinics in plastic surgery.
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Cutis.
2010 Sep; 86(3):153-8. doi:
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Clinical and experimental dermatology.
2010 Jun; 35(4):e103-5. doi:
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Biological & pharmaceutical bulletin.
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Journal of ethnopharmacology.
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The Journal of toxicological sciences.
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Bioorganic & medicinal chemistry.
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Pigment cell research.
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Biological & pharmaceutical bulletin.
2006 Apr; 29(4):655-69. doi:
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International journal of pharmaceutics.
2005 Jul; 298(1):13-25. doi:
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Central European journal of public health.
2004 Mar; 12 Suppl(?):S41-4. doi:
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Polish journal of pathology : official journal of the Polish Society of Pathologists.
2004; 55(3):15-21. doi:
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Toxicological sciences : an official journal of the Society of Toxicology.
2003 Jun; 73(2):287-93. doi:
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Planta medica.
2003 Jun; 69(6):559-61. doi:
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Planta medica.
2003 May; 69(5):457-9. doi:
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The Journal of toxicological sciences.
2002 Dec; 27(5):423-31. doi:
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The Journal of biological chemistry.
2002 May; 277(18):16340-4. doi:
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