Gnetol (BioDeep_00000000687)

   

PANOMIX_OTCML-2023 Antitumor activity


代谢物信息卡片


2-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]benzene-1,3-diol

化学式: C14H12O4 (244.0736)
中文名称: 买麻藤醇, 2,6,3',5'-四羟基二苯乙烯
谱图信息: 最多检出来源 Chinese Herbal Medicine(otcml) 78.57%

Reviewed

Last reviewed on 2024-12-11.

Cite this Page

Gnetol. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/gnetol (retrieved 2024-12-22) (BioDeep RN: BioDeep_00000000687). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

分子结构信息

SMILES: C1=CC(=C(C(=C1)O)C=CC2=CC(=CC(=C2)O)O)O
InChI: InChI=1S/C14H12O4/c15-10-6-9(7-11(16)8-10)4-5-12-13(17)2-1-3-14(12)18/h1-8,15-18H/b5-4+

描述信息

Gnetol is a natural product found in Gnetum edule, Gnetum hainanense, and other organisms with data available.
Gnetol is a phenolic compound isolated from the root of Gnetum montanum . Gnetol potently inhibits COX-1 (IC50 of 0.78 μM) and HDAC. Gnetol is a potent tyrosinase inhibitor with an IC50 of 4.5 μM for murine tyrosinase and suppresses melanin biosynthesis. Gnetol has antioxidant, antiproliferative, anticancer and hepatoprotective activity. Gnetol also possesses concentration-dependent α-Amylase, α-glucosidase, and adipogenesis activities[1][2][3].

Gnetol. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=86361-55-9 (retrieved 2024-12-11) (CAS RN: 86361-55-9). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

同义名列表

8 个代谢物同义名

1,3-Benzenediol, 2-[(1E)-2-(3,5-dihydroxyphenyl)ethenyl]-; 2-[(1E)-2-(3,5-Dihydroxyphenyl)ethenyl]-1,3-benzenediol; 5-[(1E)-2-(2,6-dihydroxyphenyl)ethenyl]benzene-1,3-diol; 2-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]benzene-1,3-diol; 2-[2-(3,5-dihydroxyphenyl)vinyl]benzene-1,3-diol; (E)-2-(3,5-Dihydroxystyryl)benzene-1,3-diol; 2,3,5,6-tetrahydroxy-trans-stilbene; Gnetol



数据库引用编号

7 个数据库交叉引用编号

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)

7 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。

亚细胞结构定位 关联基因列表
Cytoplasm 7 DLG4, EDN1, NOS1, PRKAA2, PTGS1, PTGS2, TYR
Golgi apparatus, trans-Golgi network membrane 1 DLG4
Peripheral membrane protein 4 ACHE, NOS1, PTGS1, PTGS2
Endoplasmic reticulum membrane 2 PTGS1, PTGS2
Nucleus 4 ACHE, NOS1, PPARA, PRKAA2
cytosol 3 DLG4, NOS1, PRKAA2
dendrite 1 PRKAA2
nucleoplasm 3 NOS1, PPARA, PRKAA2
Cell membrane 2 ACHE, DLG4
Lipid-anchor 1 DLG4
Cytoplasmic side 1 DLG4
Cell projection, axon 1 DLG4
Early endosome membrane 1 DLG4
Golgi apparatus membrane 1 DLG4
Synapse 3 ACHE, DLG4, NOS1
cell junction 1 DLG4
cell surface 1 ACHE
glutamatergic synapse 1 DLG4
Golgi apparatus 3 ACHE, PRKAA2, PTGS1
Golgi membrane 1 DLG4
lysosomal membrane 1 GAA
neuromuscular junction 2 ACHE, DLG4
neuronal cell body 1 PRKAA2
sarcolemma 1 NOS1
synaptic vesicle 1 DLG4
Lysosome 2 GAA, TYR
Presynapse 1 DLG4
plasma membrane 6 ACHE, BCHE, DLG4, F2, GAA, NOS1
Membrane 3 ACHE, GAA, PRKAA2
axon 2 DLG4, PRKAA2
basolateral plasma membrane 1 DLG4
caveola 1 PTGS2
extracellular exosome 3 F2, GAA, PTGS1
Lysosome membrane 1 GAA
endoplasmic reticulum 2 DLG4, PTGS2
extracellular space 4 ACHE, BCHE, EDN1, F2
lysosomal lumen 1 GAA
perinuclear region of cytoplasm 3 ACHE, NOS1, TYR
adherens junction 1 DLG4
mitochondrion 1 NOS1
protein-containing complex 2 NOS1, PTGS2
intracellular membrane-bounded organelle 3 GAA, PTGS1, TYR
Microsome membrane 2 PTGS1, PTGS2
postsynaptic density 2 DLG4, NOS1
Single-pass type I membrane protein 1 TYR
Secreted 5 ACHE, BCHE, EDN1, F2, GAA
extracellular region 5 ACHE, BCHE, EDN1, F2, GAA
basal part of cell 1 EDN1
excitatory synapse 1 DLG4
Extracellular side 1 ACHE
photoreceptor inner segment 1 NOS1
photoreceptor outer segment 1 PTGS1
dendritic spine 2 DLG4, NOS1
Melanosome membrane 1 TYR
neuron spine 1 DLG4
Golgi-associated vesicle 1 TYR
postsynaptic membrane 1 DLG4
Cell membrane, sarcolemma 1 NOS1
Cytoplasm, perinuclear region 1 NOS1
Membrane raft 1 NOS1
Cytoplasm, cytoskeleton 1 DLG4
basement membrane 1 ACHE
sarcoplasmic reticulum 1 NOS1
Cell projection, dendritic spine 2 DLG4, NOS1
collagen-containing extracellular matrix 1 F2
nuclear speck 1 PRKAA2
Nucleus inner membrane 1 PTGS2
Nucleus outer membrane 1 PTGS2
nuclear inner membrane 1 PTGS2
nuclear outer membrane 1 PTGS2
dendrite cytoplasm 1 DLG4
neuron projection 3 DLG4, PTGS1, PTGS2
chromatin 1 PPARA
cell periphery 1 NOS1
cytoskeleton 2 DLG4, NOS1
blood microparticle 2 BCHE, F2
Lipid-anchor, GPI-anchor 1 ACHE
Endomembrane system 1 PTGS1
AMPA glutamate receptor complex 1 DLG4
Cell projection, dendrite 1 DLG4
tertiary granule membrane 1 GAA
Melanosome 1 TYR
cytoplasmic stress granule 1 PRKAA2
side of membrane 1 ACHE
synaptic membrane 1 DLG4
trans-Golgi network membrane 1 DLG4
Golgi lumen 1 F2
endoplasmic reticulum lumen 3 BCHE, F2, PTGS2
cortical actin cytoskeleton 1 DLG4
endocytic vesicle membrane 1 DLG4
transport vesicle 1 EDN1
azurophil granule membrane 1 GAA
cerebellar mossy fiber 1 DLG4
postsynaptic density membrane 1 DLG4
nuclear envelope lumen 1 BCHE
synaptic cleft 1 ACHE
ficolin-1-rich granule membrane 1 GAA
nucleotide-activated protein kinase complex 1 PRKAA2
cortical cytoskeleton 1 DLG4
rough endoplasmic reticulum lumen 1 EDN1
Weibel-Palade body 1 EDN1
neuron projection terminus 1 DLG4
autolysosome lumen 1 GAA
juxtaparanode region of axon 1 DLG4
[Isoform H]: Cell membrane 1 ACHE
Golgi cis cisterna 1 DLG4


文献列表

  • Kei Shimoda, Naoji Kubota, Daisuke Uesugi, Yusuke Kobayashi, Hatsuyuki Hamada, Hiroki Hamada. Glycosylation of Stilbene Compounds by Cultured Plant Cells. Molecules (Basel, Switzerland). 2020 Mar; 25(6):. doi: 10.3390/molecules25061437. [PMID: 32235774]
  • Bolanle C Akinwumi, Kimberly-Ann M Bordun, Hope D Anderson. Biological Activities of Stilbenoids. International journal of molecular sciences. 2018 Mar; 19(3):. doi: 10.3390/ijms19030792. [PMID: 29522491]
  • Connie M Remsberg, Stephanie E Martinez, Bolanle C Akinwumi, Hope D Anderson, Jody K Takemoto, Casey L Sayre, Neal M Davies. Preclinical Pharmacokinetics and Pharmacodynamics and Content Analysis of Gnetol in Foodstuffs. Phytotherapy research : PTR. 2015 Aug; 29(8):1168-79. doi: 10.1002/ptr.5363. [PMID: 25939395]
  • Thiendanai Sermboonpaisarn, Pattara Sawasdee. Potent and selective butyrylcholinesterase inhibitors from Ficus foveolata. Fitoterapia. 2012 Jun; 83(4):780-4. doi: 10.1016/j.fitote.2012.03.009. [PMID: 22450264]
  • Connie M Remsberg, Jody K Takemoto, Rebecca M Bertram, Neal M Davies. High-performance liquid chromatography assay of gnetol in rat serum and application to pre-clinical pharmacokinetic studies. Journal of pharmaceutical and biomedical analysis. 2011 Mar; 54(4):878-81. doi: 10.1016/j.jpba.2010.10.028. [PMID: 21126844]