Dihydroconiferyl alcohol (BioDeep_00000008095)

 

Secondary id: BioDeep_00000397413

human metabolite PANOMIX_OTCML-2023 natural product PANOMIX_OTCML-2025


Metabolite Card


3-(4-hydroxy-3-methoxyphenyl)-propan-1-ol

  Formula: C10H14O3 (182.0943)
Chinese Names: 3-(4-羟基-3-甲氧基苯)-1-丙醇, 二氢松柏醇
  Spectrum Hits: Top Source Viridiplantae(plant) 14.64%

Molecular Structure

SMILES: c1(c(ccc(c1)CCCO)O)OC
InChI: InChI=1S/C10H14O3/c1-13-10-7-8(3-2-6-11)4-5-9(10)12/h4-5,7,11-12H,2-3,6H2,1H3


Description

Dihydroconiferyl alcohol, also known as 3-(4-guaiacyl)propanol or 3-(4-hydroxy-3-methoxyphenyl)-propan-1-ol, is a member of the class of compounds known as methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety. Dihydroconiferyl alcohol is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Dihydroconiferyl alcohol can be found in lettuce and romaine lettuce, which makes dihydroconiferyl alcohol a potential biomarker for the consumption of these food products.
Dihydroconiferyl alcohol is a cell division factor that can be found in pring sap of Acer pseudoplatanus L. Dihydroconiferyl alcohol can stimulate growth of soybean callus[1].

Synonyms

23 synonym names

3-(4-hydroxy-3-methoxyphenyl)-propan-1-ol; 3-(3-METHOXY-4-HYDROXYPHENYL)-1-PROPANOL; 3-(4-HYDROXY-3-METHOXYPHENYL)-1-PROPANOL; 3-(p-Hydroxy-m-methoxyphenyl)-1-propanol; 4-(gamma-Hydroxypropyl)-2-methoxyphenol; 3-(4-Hydroxy-3-methoxyphenyl)propanol; 3-(3-Methoxy-4-hydroxyphenyl)propanol; 4-Hydroxy-3-methoxy-benzenepropanol; 4-(γ-Hydroxypropyl)-2-methoxyphenol; 4-(3-hydroxypropyl)-2-methoxyphenol; 4-hydroxy-3-methoxybenzenepropanol; 4-(3-Hydroxypropyl)guaiacol; Dihydroconiferyl alcohol; 3-(4-guaiacyl)propanol; Hydroconiferyl Alcohol; 3-Guaiacyl-1-propanol; 1-GUAIACYL-3-PROPANOL; GUAIACYL-3-PROPANOL; 4-Propanolguaiacol; guaiacyl propanol; DHCA; Dihydroconiferyl alcohol; Dihydroconiferyl alcohol



Cross Reference

18 cross reference id

Classification Terms

Related Pathways

Reactome(0)

BioCyc(1)

PlantCyc(1)

Biological Process

48 related biological process reactions.

Reactome(0)

BioCyc(3)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(45)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

76 organism taxonomy source information

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。

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Literature Reference

  • Masatoshi Kondo, Naomi Oyama-Okubo, Masanori Sagae, Toshio Ando, Eduardo Marchesi, Masayoshi Nakayama. Metabolic regulation of floral scent in Petunia axillaris lines: biosynthetic relationship between dihydroconiferyl acetate and iso-eugenol. Bioscience, biotechnology, and biochemistry. 2007 Feb; 71(2):458-63. doi: 10.1271/bbb.60507. [PMID: 17284848]
  • Ralf Möller, Diane Steward, Lorelle Phillips, Heather Flint, Armin Wagner. Gene silencing of cinnamyl alcohol dehydrogenase in Pinus radiata callus cultures. Plant physiology and biochemistry : PPB. 2005 Dec; 43(12):1061-6. doi: 10.1016/j.plaphy.2005.11.001. [PMID: 16386427]
  • R R Sederoff, J J MacKay, J Ralph, R D Hatfield. Unexpected variation in lignin. Current opinion in plant biology. 1999 Apr; 2(2):145-52. doi: 10.1016/s1369-5266(99)80029-6. [PMID: 10322194]
  • . . . . doi: . [PMID: 9211851]