Dihydroconiferyl alcohol (BioDeep_00000008095)
Secondary id: BioDeep_00000397413
human metabolite PANOMIX_OTCML-2023
代谢物信息卡片
化学式: C10H14O3 (182.0942894)
中文名称: 3-(4-羟基-3-甲氧基苯)-1-丙醇, 二氢松柏醇
谱图信息:
最多检出来源 Viridiplantae(plant) 1.52%
分子结构信息
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
描述信息
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].
同义名列表
21 个代谢物同义名
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
数据库引用编号
16 个数据库交叉引用编号
- ChEBI: CHEBI:4559
- KEGG: C10448
- PubChem: 16822
- HMDB: HMDB0303757
- Metlin: METLIN68331
- ChEMBL: CHEMBL4207816
- MetaCyc: CPD-94
- KNApSAcK: C00002736
- foodb: FDB020694
- chemspider: 15941
- CAS: 2305-13-7
- PMhub: MS000021644
- PubChem: 12631
- 3DMET: B03854
- NIKKAJI: J305.428D
- medchemexpress: HY-W016393
分类词条
相关代谢途径
Reactome(0)
代谢反应
48 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(3)
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapaldehyde ⟶ H+ + UDP + sinapaldehyde glucoside
- dihydroconiferyl alcohol biosynthesis:
H+ + NADPH + coniferaldehyde ⟶ NADP+ + dihydroconiferyl aldehyde
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapaldehyde ⟶ H+ + UDP + sinapaldehyde glucoside
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(45)
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapaldehyde ⟶ H+ + UDP + sinapaldehyde glucoside
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapaldehyde ⟶ H+ + UDP + sinapaldehyde glucoside
- dihydroconiferyl alcohol biosynthesis:
H+ + NADPH + coniferaldehyde ⟶ NADP+ + dihydroconiferyl aldehyde
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapaldehyde ⟶ H+ + UDP + sinapaldehyde glucoside
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
- monolignol glucosides biosynthesis:
UDP-α-D-glucose + sinapyl alcohol ⟶ H+ + UDP + syringin
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
38 个相关的物种来源信息
- 3330 Picea glauca: 10.1016/S0031-9422(96)00388-3
- 93694 Tsuga chinensis: 10.1002/JCCS.198500075
- 39279 Bongardia chrysogonum: 10.1021/NP50064A024
- 3355 Pseudolarix amabilis: 10.5246/JCPS.2012.05.057
- 54800 Larix kaempferi: 10.5246/JCPS.2012.05.057
- 172644 Broussonetia papyrifera: 10.1080/10286020.2010.481260
- 342581 Abies spectabilis: 10.1248/CPB.58.1646
- 115466 Euterpe oleracea: 10.1021/JF801792N
- 2487474 Bulbophyllum protractum: 10.1016/S0031-9422(96)00402-5
- 257357 Dendrobium longicornu: 10.1055/S-2008-1074492
- 3349 Pinus sylvestris: 10.1021/JF048948Q
- 50863 Aconitum baicalense: 10.1007/BF00630592
- 25629 Taxus baccata:
- 67778 Picea jezoensis: 10.1021/NP070104O
- 597316 Licaria chrysophylla: 10.1016/0031-9422(89)80368-1
- 99806 Taxus cuspidata: 10.1016/0031-9422(93)85117-A
- 3339 Pinus contorta: 10.1016/S0031-9422(00)81488-0
- 77912 Pinus densiflora: 10.3186/JJPHYTOPATH.50.166
- 3330 Picea glauca: 10.1016/S0031-9422(96)00388-3
- 93694 Tsuga chinensis: 10.1002/JCCS.198500075
- 39279 Bongardia chrysogonum: 10.1021/NP50064A024
- 3355 Pseudolarix amabilis: 10.5246/JCPS.2012.05.057
- 54800 Larix kaempferi: 10.5246/JCPS.2012.05.057
- 172644 Broussonetia papyrifera: 10.1080/10286020.2010.481260
- 342581 Abies spectabilis: 10.1248/CPB.58.1646
- 115466 Euterpe oleracea: 10.1021/JF801792N
- 2487474 Bulbophyllum protractum: 10.1016/S0031-9422(96)00402-5
- 257357 Dendrobium longicornu: 10.1055/S-2008-1074492
- 3349 Pinus sylvestris: 10.1021/JF048948Q
- 50863 Aconitum baicalense: 10.1007/BF00630592
- 25629 Taxus baccata:
- 67778 Picea jezoensis: 10.1021/NP070104O
- 597316 Licaria chrysophylla: 10.1016/0031-9422(89)80368-1
- 99806 Taxus cuspidata: 10.1016/0031-9422(93)85117-A
- 3339 Pinus contorta: 10.1016/S0031-9422(00)81488-0
- 77912 Pinus densiflora: 10.3186/JJPHYTOPATH.50.166
- 9606 Homo sapiens: -
- 33090 Plants: -
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
- 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]