TETRABENAZINE (BioDeep_00000858452)

Main id: BioDeep_00000008526

 


代谢物信息卡片


TETRABENAZINE

化学式: C19H27NO3 (317.1991)
中文名称: 丁苯那嗪
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC(C)CC1CN2CCC3=CC(=C(C=C3C2CC1=O)OC)OC
InChI: InChI=1S/C19H27NO3/c1-12(2)7-14-11-20-6-5-13-8-18(22-3)19(23-4)9-15(13)16(20)10-17(14)21/h8-9,12,14,16H,5-7,10-11H2,1-4H3

描述信息

D018377 - Neurotransmitter Agents > D014179 - Neurotransmitter Uptake Inhibitors > D018759 - Adrenergic Uptake Inhibitors
D018377 - Neurotransmitter Agents > D018663 - Adrenergic Agents
D049990 - Membrane Transport Modulators
N - Nervous system
Same as: D08575

同义名列表

2 个代谢物同义名

TETRABENAZINE; Tetrabenazine



数据库引用编号

13 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)

0 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 8 BDNF, CYP2D6, DBH, DDC, HTT, PPP1R1B, SLC6A3, TH
Peripheral membrane protein 1 ACHE
Endosome membrane 2 HTT, SLC6A4
Endoplasmic reticulum membrane 3 CYP2D6, DRD1, SLC18A1
Mitochondrion membrane 1 MAOA
Nucleus 6 ACHE, DRD1, HTT, NKX2-1, PPP1R1B, TH
autophagosome 1 HTT
cytosol 5 DDC, HTT, MAOA, PPP1R1B, TH
dendrite 6 BDNF, DRD2, HTR1A, HTT, SLC18A2, TH
centrosome 1 SLC18A2
nucleoplasm 2 HTT, NKX2-1
Cell membrane 8 ACHE, DRD1, DRD2, GRID1, HTR1A, HTT, SLC6A3, SLC6A4
Cytoplasmic side 1 MAOA
Cell projection, axon 3 SLC18A2, SLC6A3, TH
Multi-pass membrane protein 9 DRD1, DRD2, GRID1, HTR1A, HTT, SLC18A1, SLC18A2, SLC6A3, SLC6A4
Golgi apparatus membrane 1 DRD2
Synapse 6 ACHE, DBH, DRD2, HTR1A, HTT, SLC6A4
cell surface 2 ACHE, SLC6A3
glutamatergic synapse 3 DRD1, DRD2, GRID1
Golgi apparatus 2 ACHE, HTT
Golgi membrane 2 DRD2, INS
neuromuscular junction 1 ACHE
neuronal cell body 2 PPP1R1B, SLC6A3
presynaptic membrane 5 DRD1, DRD2, HTT, SLC6A3, SLC6A4
smooth endoplasmic reticulum 1 TH
synaptic vesicle 3 BDNF, SLC18A2, TH
Presynapse 2 SLC18A1, SLC6A4
acrosomal vesicle 1 DRD2
plasma membrane 9 ACHE, DRD1, DRD2, GRID1, HTR1A, HTT, SLC18A2, SLC6A3, SLC6A4
synaptic vesicle membrane 3 DRD2, SLC18A1, SLC18A2
terminal bouton 3 SLC18A1, SLC18A2, TH
Membrane 9 ACHE, BDNF, CYP2D6, DBH, MAOA, SLC18A1, SLC18A2, SLC6A3, SLC6A4
axon 6 BDNF, DRD2, HTT, SLC18A2, SLC6A3, TH
extracellular exosome 2 DDC, GRID1
endoplasmic reticulum 3 CYP2D6, DBH, HTT
extracellular space 4 ACHE, BDNF, DBH, INS
perinuclear region of cytoplasm 4 ACHE, BDNF, HTT, TH
mitochondrion 3 CYP2D6, MAOA, TH
protein-containing complex 1 HTT
intracellular membrane-bounded organelle 3 CYP2D6, DBH, SLC18A2
Microsome membrane 1 CYP2D6
Secreted 5 ACHE, BDNF, DBH, INS, TRH
extracellular region 5 ACHE, BDNF, DBH, INS, TRH
cytoplasmic side of plasma membrane 1 TH
Mitochondrion outer membrane 1 MAOA
Single-pass membrane protein 2 CYP2D6, MAOA
mitochondrial outer membrane 1 MAOA
neuronal cell body membrane 1 SLC6A3
Extracellular side 1 ACHE
transcription regulator complex 1 NKX2-1
centriolar satellite 1 DBH
ciliary membrane 2 DRD1, DRD2
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane 2 SLC18A1, SLC18A2
dendritic spine 2 DRD1, DRD2
perikaryon 2 DRD2, TH
cytoplasmic vesicle 1 TH
Melanosome membrane 1 TH
Early endosome 1 HTT
Single-pass type II membrane protein 1 DBH
postsynaptic membrane 6 DRD1, DRD2, GRID1, HTT, SLC6A3, SLC6A4
Cytoplasm, perinuclear region 1 TH
Membrane raft 3 HTT, SLC6A3, SLC6A4
Cell junction, focal adhesion 2 HTT, SLC6A4
focal adhesion 2 HTT, SLC6A4
GABA-ergic synapse 3 DRD1, DRD2, GRID1
flotillin complex 1 SLC6A3
basement membrane 1 ACHE
Cell projection, dendritic spine 1 DRD1
secretory granule 1 TRH
lateral plasma membrane 1 DRD2
Postsynaptic cell membrane 1 GRID1
Late endosome 1 HTT
Cell projection, neuron projection 3 HTT, SLC6A3, SLC6A4
neuron projection 4 HTT, SLC6A3, SLC6A4, TH
cilium 2 DRD1, DRD2
chromatin 1 NKX2-1
centriole 1 HTT
non-motile cilium 2 DRD1, DRD2
Lipid-anchor, GPI-anchor 1 ACHE
sperm flagellum 1 DRD2
Endomembrane system 2 HTT, SLC6A4
endosome lumen 1 INS
Cytoplasmic vesicle membrane 1 HTT
Cell projection, dendrite 3 DRD1, HTR1A, SLC18A2
side of membrane 1 ACHE
secretory granule lumen 2 DBH, INS
secretory granule membrane 3 DBH, SLC18A1, SLC18A2
Golgi lumen 1 INS
endoplasmic reticulum lumen 2 BDNF, INS
axon terminus 2 DRD2, SLC6A3
endocytic vesicle 1 DRD2
transport vesicle 1 INS
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
postsynaptic density membrane 1 GRID1
Single-pass type IV membrane protein 1 MAOA
synaptic cleft 1 ACHE
dopaminergic synapse 3 DRD2, SLC18A2, SLC6A3
Cytoplasmic vesicle, secretory vesicle membrane 3 DBH, SLC18A1, SLC18A2
postsynaptic cytosol 1 HTT
[Isoform 2]: Endoplasmic reticulum membrane 1 SLC18A1
Cell projection, cilium membrane 1 DRD1
presynaptic cytosol 1 HTT
Cytoplasmic vesicle, secretory vesicle, chromaffin granule lumen 1 DBH
chromaffin granule lumen 1 DBH
transport vesicle membrane 1 DBH
inclusion body 1 HTT
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle 1 TH
[Soluble dopamine beta-hydroxylase]: Cytoplasmic vesicle, secretory vesicle lumen 1 DBH
Cytoplasmic vesicle, secretory vesicle, chromaffin granule membrane 1 DBH
chromaffin granule membrane 1 DBH
G protein-coupled receptor complex 2 DRD1, DRD2
clathrin-sculpted monoamine transport vesicle membrane 2 SLC18A1, SLC18A2
[Isoform H]: Cell membrane 1 ACHE
[Neurotrophic factor BDNF precursor form]: Secreted 1 BDNF
serotonergic synapse 2 HTT, SLC6A4
[Huntingtin]: Cytoplasm 1 HTT
[Huntingtin, myristoylated N-terminal fragment]: Cytoplasmic vesicle, autophagosome 1 HTT
[Isoform 1]: Cytoplasmic vesicle, secretory vesicle membrane 1 SLC18A1


文献列表

  • Sangram Nag, Mahabuba Jahan, Miklós Tóth, Ryuji Nakao, Andrea Varrone, Christer Halldin. PET Imaging of VMAT2 with the Novel Radioligand [18F]FE-DTBZ-d4 in Nonhuman Primates: Comparison with [11C]DTBZ and [18F]FE-DTBZ. ACS chemical neuroscience. 2021 12; 12(24):4580-4586. doi: 10.1021/acschemneuro.1c00651. [PMID: 34813272]
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  • Xianying Wu, Xue Zhou, Shuxian Zhang, Yan Zhang, Aifang Deng, Jie Han, Lin Zhu, Hank F Kung, Jinping Qiao. Brain uptake of a non-radioactive pseudo-carrier and its effect on the biodistribution of [(18)F]AV-133 in mouse brain. Nuclear medicine and biology. 2015 Jul; 42(7):630-6. doi: 10.1016/j.nucmedbio.2015.03.009. [PMID: 25910857]
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  • Francisco Molinet-Dronda, Belén Gago, Ana Quiroga-Varela, Carlos Juri, María Collantes, Mercedes Delgado, Elena Prieto, Margarita Ecay, Elena Iglesias, Concepció Marín, Iván Peñuelas, José A Obeso. Monoaminergic PET imaging and histopathological correlation in unilateral and bilateral 6-hydroxydopamine lesioned rat models of Parkinson's disease: a longitudinal in-vivo study. Neurobiology of disease. 2015 May; 77(?):165-72. doi: 10.1016/j.nbd.2015.01.007. [PMID: 25681534]
  • Aifang Deng, Xianying Wu, Xue Zhou, Yan Zhang, Wei Yin, Jinping Qiao, Lin Zhu. Mapping the target localization and biodistribution of non-radiolabeled VMAT2 ligands in rat brain. The AAPS journal. 2014 May; 16(3):592-9. doi: 10.1208/s12248-014-9584-9. [PMID: 24706374]
  • Surbhi Gupta, Bhupesh Sharma. Pharmacological benefit of I(1)-imidazoline receptors activation and nuclear factor kappa-B (NF-κB) modulation in experimental Huntington's disease. Brain research bulletin. 2014 Mar; 102(?):57-68. doi: 10.1016/j.brainresbull.2014.02.007. [PMID: 24582883]
  • Chung Chan, Xiao Jin, Edward K Fung, Mika Naganawa, Tim Mulnix, Richard E Carson, Chi Liu. Event-by-event respiratory motion correction for PET with 3D internal-1D external motion correlation. Medical physics. 2013 Nov; 40(11):112507. doi: 10.1118/1.4826165. [PMID: 24320466]
  • Venkata Ramu Derangula, Nageswara Rao Pilli, Siva Kumar Nadavala, Vinayender Adireddy, Jaswanth Kumar Inamadugu, Venkateswarlu Ponneri. Liquid chromatography-tandem mass spectrometric assay for the determination of tetrabenazine and its active metabolites in human plasma: a pharmacokinetic study. Biomedical chromatography : BMC. 2013 Jun; 27(6):792-801. doi: 10.1002/bmc.2862. [PMID: 23339053]
  • Ryuji Nakao, Christer Halldin. 'Mixed' anionic and non-ionic micellar liquid chromatography for high-speed radiometabolite analysis of positron emission tomography radioligands. Journal of chromatography. A. 2013 Mar; 1281(?):54-9. doi: 10.1016/j.chroma.2013.01.071. [PMID: 23399000]
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  • Alison I Bernstein, Kristen A Stout, Gary W Miller. A fluorescent-based assay for live cell, spatially resolved assessment of vesicular monoamine transporter 2-mediated neurotransmitter transport. Journal of neuroscience methods. 2012 Aug; 209(2):357-66. doi: 10.1016/j.jneumeth.2012.06.002. [PMID: 22698664]
  • Carlos Singer. Comprehensive treatment of Huntington disease and other choreic disorders. Cleveland Clinic journal of medicine. 2012 Jul; 79 Suppl 2(?):S30-4. doi: 10.3949/ccjm.79.s2a.06. [PMID: 22761268]
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  • Catarina A Owesson-White, Mitchell F Roitman, Leslie A Sombers, Anna M Belle, Richard B Keithley, Jessica L Peele, Regina M Carelli, R Mark Wightman. Sources contributing to the average extracellular concentration of dopamine in the nucleus accumbens. Journal of neurochemistry. 2012 Apr; 121(2):252-62. doi: 10.1111/j.1471-4159.2012.07677.x. [PMID: 22296263]
  • Erik G Puffenberger, Robert N Jinks, Carrie Sougnez, Kristian Cibulskis, Rebecca A Willert, Nathan P Achilly, Ryan P Cassidy, Christopher J Fiorentini, Kory F Heiken, Johnny J Lawrence, Molly H Mahoney, Christopher J Miller, Devika T Nair, Kristin A Politi, Kimberly N Worcester, Roni A Setton, Rosa Dipiazza, Eric A Sherman, James T Eastman, Christopher Francklyn, Susan Robey-Bond, Nicholas L Rider, Stacey Gabriel, D Holmes Morton, Kevin A Strauss. Genetic mapping and exome sequencing identify variants associated with five novel diseases. PloS one. 2012; 7(1):e28936. doi: 10.1371/journal.pone.0028936. [PMID: 22279524]
  • LinLin Tian, Morvarid Karimi, Susan K Loftin, Chris A Brown, HuChuan Xia, JinBin Xu, Robert H Mach, Joel S Perlmutter. No differential regulation of dopamine transporter (DAT) and vesicular monoamine transporter 2 (VMAT2) binding in a primate model of Parkinson disease. PloS one. 2012; 7(2):e31439. doi: 10.1371/journal.pone.0031439. [PMID: 22359591]
  • Mélanie Bourque, Bin Liu, Dean E Dluzen, Thérèse Di Paolo. Sex differences in methamphetamine toxicity in mice: effect on brain dopamine signaling pathways. Psychoneuroendocrinology. 2011 Aug; 36(7):955-69. doi: 10.1016/j.psyneuen.2010.12.007. [PMID: 21236583]
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  • Raúl de la Fuente-Fernández, Michael Schulzer, Lisa Kuramoto, Jacquelyn Cragg, Nandhagopal Ramachandiran, Wing L Au, Edwin Mak, Jess McKenzie, Siobhan McCormick, Vesna Sossi, Thomas J Ruth, Chong S Lee, Donald B Calne, A Jon Stoessl. Age-specific progression of nigrostriatal dysfunction in Parkinson's disease. Annals of neurology. 2011 May; 69(5):803-10. doi: 10.1002/ana.22284. [PMID: 21246604]
  • Xue Zhou, Jinping Qiao, Wei Yin, Lin Zhu, Hank F Kung. Study the effect of a pseudo-carrier on pharmacokinetics of 9-fluoropropyl-(+)-dihydrotetrabenazine in rat plasma by ultra-performance liquid chromatography-tandem mass spectrometry. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2011 Mar; 879(7-8):505-10. doi: 10.1016/j.jchromb.2011.01.011. [PMID: 21277842]
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