Cyperquat (BioDeep_00000008596)

   


代谢物信息卡片


1-Methyl-4-phenylpyridinium

化学式: C12H12N+ (170.097)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C[N+]1=CC=C(C=C1)C2=CC=CC=C2
InChI: InChI=1S/C12H12N/c1-13-9-7-12(8-10-13)11-5-3-2-4-6-11/h2-10H,1H3/q+1

描述信息

D010575 - Pesticides > D006540 - Herbicides
D016573 - Agrochemicals

同义名列表

4 个代谢物同义名

1-Methyl-4-phenylpyridinium; N-Methyl-4-phenylpyridine; Cyperquat; 1-Methyl-4-phenylpyridinium



数据库引用编号

12 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 10 ABCB1, CASP1, CAT, LRRK2, MTOR, NLRP3, PARK7, PINK1, SLC6A3, SQSTM1
Peripheral membrane protein 3 CYP1B1, LRRK2, MTOR
Endoplasmic reticulum membrane 3 CYP1B1, LRRK2, MTOR
Mitochondrion membrane 1 SLC22A3
Cytoplasmic vesicle, autophagosome 1 SQSTM1
Nucleus 8 JUN, MTOR, NLRP3, PARK7, PINK1, PPARGC1A, SQSTM1, TFAM
autophagosome 2 MAP1LC3A, SQSTM1
cytosol 11 CASP1, CAT, LRRK2, MAP1LC3A, MTOR, NLRP3, PARK7, PINK1, PPARGC1A, SQSTM1, TFAM
dendrite 4 DRD2, LRRK2, MTOR, SLC18A2
mitochondrial membrane 2 LRRK2, SLC22A3
phagocytic vesicle 2 LRRK2, MTOR
trans-Golgi network 1 LRRK2
centrosome 1 SLC18A2
nucleoplasm 5 JUN, MTOR, PARK7, PPARGC1A, SQSTM1
RNA polymerase II transcription regulator complex 1 JUN
Cell membrane 8 ABCB1, CASP1, DRD2, PARK7, SLC22A1, SLC22A3, SLC6A3, TNF
Lipid-anchor 2 MAP1LC3A, PARK7
Cytoplasmic side 1 MTOR
Cell projection, axon 3 LRRK2, SLC18A2, SLC6A3
Multi-pass membrane protein 6 ABCB1, DRD2, SLC18A2, SLC22A1, SLC22A3, SLC6A3
Golgi apparatus membrane 4 DRD2, LRRK2, MTOR, NLRP3
Synapse 1 DRD2
cell surface 3 ABCB1, SLC6A3, TNF
glutamatergic synapse 4 DRD2, LRRK2, MAP1LC3A, SQSTM1
Golgi apparatus 1 LRRK2
Golgi membrane 4 DRD2, LRRK2, MTOR, NLRP3
growth cone 2 LRRK2, PINK1
lysosomal membrane 1 MTOR
mitochondrial inner membrane 2 LRRK2, PINK1
neuronal cell body 4 LRRK2, SLC22A3, SLC6A3, TNF
postsynapse 1 LRRK2
presynaptic membrane 2 DRD2, SLC6A3
synaptic vesicle 2 PARK7, SLC18A2
Cytoplasm, cytosol 3 NLRP3, PINK1, SQSTM1
Lysosome 3 LRRK2, MTOR, SQSTM1
Presynapse 2 SLC22A1, SLC22A3
acrosomal vesicle 1 DRD2
endosome 1 LRRK2
plasma membrane 10 ABCB1, CASP1, DRD2, LRRK2, PARK7, SLC18A2, SLC22A1, SLC22A3, SLC6A3, TNF
synaptic vesicle membrane 3 DRD2, LRRK2, SLC18A2
terminal bouton 2 LRRK2, SLC18A2
Membrane 11 ABCB1, CAT, CYP1B1, MTOR, NLRP3, PARK7, PINK1, SLC18A2, SLC22A1, SLC22A3, SLC6A3
apical plasma membrane 3 ABCB1, SLC22A1, SLC22A3
axon 6 DRD2, LRRK2, PARK7, PINK1, SLC18A2, SLC6A3
basolateral plasma membrane 2 SLC22A1, SLC22A3
extracellular exosome 5 ABCB1, CAT, LRRK2, PARK7, SQSTM1
Lysosome membrane 1 MTOR
endoplasmic reticulum 5 LRRK2, NLRP3, PARK7, PINK1, SQSTM1
extracellular space 2 LRRK2, TNF
perinuclear region of cytoplasm 2 PARK7, PINK1
adherens junction 1 PARK7
mitochondrion 8 CAT, CYP1B1, LRRK2, NLRP3, PARK7, PINK1, SQSTM1, TFAM
protein-containing complex 3 CASP1, CAT, TFAM
intracellular membrane-bounded organelle 6 CAT, CYP1B1, LRRK2, MAP1LC3A, SLC18A2, SQSTM1
Microsome membrane 2 CYP1B1, MTOR
TORC1 complex 1 MTOR
TORC2 complex 1 MTOR
Secreted 1 NLRP3
extracellular region 3 CAT, NLRP3, TNF
Mitochondrion outer membrane 3 LRRK2, MTOR, PINK1
Single-pass membrane protein 1 PINK1
mitochondrial outer membrane 3 LRRK2, MTOR, PINK1
neuronal cell body membrane 1 SLC6A3
mitochondrial matrix 4 CAT, LRRK2, PARK7, TFAM
transcription regulator complex 1 JUN
ciliary membrane 1 DRD2
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane 2 LRRK2, SLC18A2
Nucleus membrane 1 SLC22A3
external side of plasma membrane 1 TNF
dendritic spine 1 DRD2
perikaryon 2 DRD2, LRRK2
cytoplasmic vesicle 2 LRRK2, SQSTM1
nucleolus 1 CASP1
Wnt signalosome 1 LRRK2
P-body 1 SQSTM1
Golgi-associated vesicle 1 LRRK2
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
postsynaptic membrane 2 DRD2, SLC6A3
Apical cell membrane 3 ABCB1, SLC22A1, SLC22A3
Mitochondrion inner membrane 1 PINK1
Membrane raft 3 PARK7, SLC6A3, TNF
Cytoplasm, cytoskeleton 2 LRRK2, MAP1LC3A
focal adhesion 1 CAT
microtubule 2 CASP1, MAP1LC3A
GABA-ergic synapse 1 DRD2
flotillin complex 1 SLC6A3
mitochondrial nucleoid 1 TFAM
Peroxisome 1 CAT
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
Nucleus, PML body 3 MTOR, PPARGC1A, SQSTM1
PML body 4 MTOR, PARK7, PPARGC1A, SQSTM1
mitochondrial intermembrane space 2 PARK7, PINK1
lateral plasma membrane 2 DRD2, SLC22A1
Cytoplasm, cytoskeleton, microtubule organizing center 1 NLRP3
Inflammasome 1 NLRP3
interphase microtubule organizing center 1 NLRP3
NLRP3 inflammasome complex 2 CASP1, NLRP3
Nucleus outer membrane 1 SLC22A3
nuclear outer membrane 1 SLC22A3
dendrite cytoplasm 1 LRRK2
Cytoplasm, myofibril, sarcomere 1 SQSTM1
Late endosome 2 MAP1LC3A, SQSTM1
sarcomere 1 SQSTM1
Cell projection, neuron projection 1 SLC6A3
neuron projection 2 LRRK2, SLC6A3
cilium 1 DRD2
chromatin 4 JUN, PARK7, PINK1, PPARGC1A
Cytoplasmic vesicle, autophagosome membrane 1 MAP1LC3A
autophagosome membrane 1 MAP1LC3A
phagocytic cup 1 TNF
cytoskeleton 2 LRRK2, PINK1
nuclear chromosome 1 JUN
non-motile cilium 1 DRD2
sperm midpiece 1 SQSTM1
Basolateral cell membrane 2 SLC22A1, SLC22A3
organelle membrane 1 MAP1LC3A
sperm flagellum 1 DRD2
nuclear envelope 1 MTOR
Endomembrane system 4 MAP1LC3A, MTOR, NLRP3, SLC22A3
microvillus 1 LRRK2
microtubule organizing center 1 NLRP3
phagophore assembly site 1 SQSTM1
Cell projection, dendrite 2 LRRK2, SLC18A2
euchromatin 1 JUN
cell body 2 PARK7, PINK1
basal plasma membrane 2 SLC22A1, SLC22A3
ficolin-1-rich granule lumen 1 CAT
secretory granule lumen 1 CAT
secretory granule membrane 1 SLC18A2
axon terminus 2 DRD2, SLC6A3
endocytic vesicle 1 DRD2
endoplasmic reticulum exit site 1 LRRK2
aggresome 1 SQSTM1
AIM2 inflammasome complex 1 CASP1
ribonucleoprotein complex 1 LRRK2
[Isoform 1]: Nucleus 1 PPARGC1A
Basal cell membrane 1 SLC22A1
Lateral cell membrane 1 SLC22A1
external side of apical plasma membrane 1 ABCB1
canonical inflammasome complex 1 CASP1
dopaminergic synapse 3 DRD2, SLC18A2, SLC6A3
intracellular non-membrane-bounded organelle 1 SQSTM1
Cytoplasmic vesicle, secretory vesicle membrane 1 SLC18A2
Lewy body 2 PINK1, SQSTM1
Cytoplasmic vesicle, phagosome 2 LRRK2, MTOR
Preautophagosomal structure 1 SQSTM1
presynaptic cytosol 1 LRRK2
astrocyte projection 1 PINK1
transcription factor AP-1 complex 1 JUN
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
multivesicular body, internal vesicle 1 LRRK2
Autolysosome 3 LRRK2, MAP1LC3A, SQSTM1
catalase complex 1 CAT
inclusion body 1 SQSTM1
G protein-coupled receptor complex 1 DRD2
clathrin-sculpted monoamine transport vesicle membrane 1 SLC18A2
cytoplasmic side of mitochondrial outer membrane 1 LRRK2
Mitochondrion matrix, mitochondrion nucleoid 1 TFAM
IPAF inflammasome complex 1 CASP1
NLRP1 inflammasome complex 1 CASP1
protease inhibitor complex 1 CASP1
amphisome 2 LRRK2, SQSTM1
caveola neck 1 LRRK2
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF
[Isoform B4]: Nucleus 1 PPARGC1A
[Isoform B4-8a]: Cytoplasm 1 PPARGC1A
[Isoform B5]: Nucleus 1 PPARGC1A
[Isoform 9]: Nucleus 1 PPARGC1A


文献列表

  • Yonghui Wang, Zhuo Li, Jiwen Li, Chao Sun. LncRNA NEAT1 promotes MPP+ induced injury of PC12 cells and accelerates the progression of Parkinson's disease in mice through FUS mediated inhibition of PI3K/AKT/mTOR signalling pathway. Experimental gerontology. 2024 Jun; 191(?):112436. doi: 10.1016/j.exger.2024.112436. [PMID: 38636570]
  • Jiahua Huang, Xinyue Zhang, Xueping Yang, Qingyun Yv, Fanlong Ye, Sheng Chen, Ying Cui, Linting Gu, Min Zhu, Wenwei Li. Baicalin exerts neuroprotective actions by regulating the Nrf2-NLRP3 axis in toxin-induced models of Parkinson's disease. Chemico-biological interactions. 2024 Jan; 387(?):110820. doi: 10.1016/j.cbi.2023.110820. [PMID: 38016618]
  • Wenbo Fan, Jianwu Zhou. Icariside II suppresses ferroptosis to protect against MPP+-Induced Parkinson's disease through Keap1/Nrf2/GPX4 signaling. The Chinese journal of physiology. 2023 Nov; 66(6):437-445. doi: 10.4103/cjop.cjop-d-23-00107. [PMID: 38149556]
  • Yanyan Jiang, Guangming Xie, Aydos Alimujiang, Hongrong Xie, Weiting Yang, Feng Yin, Dongya Huang. Protective Effects of Querectin against MPP+-Induced Dopaminergic Neurons Injury via the Nrf2 Signaling Pathway. Frontiers in bioscience (Landmark edition). 2023 03; 28(3):42. doi: 10.31083/j.fbl2803042. [PMID: 37005755]
  • Belinda Fouché, Stephanie Turner, Rebecca Gorham, Eloise J Stephenson, Simon Gutbier, Joanna L Elson, Olimpo García-Beltrán, Francois H Van Der Westhuizen, Ilse S Pienaar. A Novel Mitochondria-Targeting Iron Chelator Neuroprotects Multimodally via HIF-1 Modulation Against a Mitochondrial Toxin in a Dopaminergic Cell Model of Parkinson's Disease. Molecular neurobiology. 2023 Feb; 60(2):749-767. doi: 10.1007/s12035-022-03107-8. [PMID: 36357615]
  • M E Arslan, A Yılmaz. Neuroprotective effects of Geranium Robertianum L. Aqueous extract on the cellular Parkinson's disease model. European review for medical and pharmacological sciences. 2023 01; 27(2):570-579. doi: 10.26355/eurrev_202301_31058. [PMID: 36734700]
  • Li-Kung Wu, Surbhi Agarwal, Chia-Hua Kuo, Yen-Lun Kung, Cecilia Hsuan Day, Pi-Yu Lin, Shinn-Zong Lin, Dennis Jine-Yuan Hsieh, Chih-Yang Huang, Chien-Yi Chiang. Artemisia Leaf Extract protects against neuron toxicity by TRPML1 activation and promoting autophagy/mitophagy clearance in both in vitro and in vivo models of MPP+/MPTP-induced Parkinson's disease. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2022 Sep; 104(?):154250. doi: 10.1016/j.phymed.2022.154250. [PMID: 35752074]
  • Jianhu Fan, Dahua Wu, Yuxing Guo, Zhongbao Yang. SOS1-IT1 silencing alleviates MPP+-induced neuronal cell injury through regulating the miR-124-3p/PTEN/AKT/mTOR pathway. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. 2022 May; 99(?):137-146. doi: 10.1016/j.jocn.2022.01.003. [PMID: 35279586]
  • Zhijiang Zhuang, Lihong Zhang, Chongchong Liu. SNHG14 Upregulation Was a Molecular Mechanism Underlying MPP+ Neurotoxicity in Dopaminergic SK-N-SH Cells via SNHG14-miR-519a-3p-ATG10 ceRNA Pathway. Neurotoxicity research. 2022 Apr; 40(2):553-563. doi: 10.1007/s12640-022-00488-5. [PMID: 35349097]
  • Lina Li, Hongjuan Wang, Huicang Li, Xin Lu, Yanxiang Gao, Xiaofeng Guo. Long noncoding RNA BACE1-antisense transcript plays a critical role in Parkinson's disease via microRNA-214-3p/Cell death-inducing p53-target protein 1 axis. Bioengineered. 2022 04; 13(4):10889-10901. doi: 10.1080/21655979.2022.2066750. [PMID: 35481549]
  • Qingxin Song, Shanxin Peng, Xiaosong Zhu. Baicalein protects against MPP+/MPTP-induced neurotoxicity by ameliorating oxidative stress in SH-SY5Y cells and mouse model of Parkinson's disease. Neurotoxicology. 2021 12; 87(?):188-194. doi: 10.1016/j.neuro.2021.10.003. [PMID: 34666128]
  • Hongyan Yang, Libo Li, Yu Jiao, Yuanliang Zhang, Yuhua Wang, Kunjie Zhu, Chao Sun. Thioredoxin-1 mediates neuroprotection of Schisanhenol against MPP+-induced apoptosis via suppression of ASK1-P38-NF-κB pathway in SH-SY5Y cells. Scientific reports. 2021 11; 11(1):21604. doi: 10.1038/s41598-021-01000-3. [PMID: 34732784]
  • Gabriela Pérez-Barrón, Sergio Montes, Yoshajandith Aguirre-Vidal, Marti Santiago, Elena Gallardo, José Luis Espartero, Camilo Ríos, Antonio Monroy-Noyola. Antioxidant Effect of Hydroxytyrosol, Hydroxytyrosol Acetate and Nitrohydroxytyrosol in a Rat MPP+ Model of Parkinson's Disease. Neurochemical research. 2021 Nov; 46(11):2923-2935. doi: 10.1007/s11064-021-03379-x. [PMID: 34260002]
  • Qi Xu, Ziyu Chen, Borong Zhu, Yiming Li, Manju B Reddy, Huilin Liu, Guodong Dang, Qi Jia, Xiaojun Wu. Neuroprotective Effects of B-Type Cinnamon Procyanidin Oligomers on MPP+-Induced Apoptosis in a Cell Culture Model of Parkinson's Disease. Molecules (Basel, Switzerland). 2021 Oct; 26(21):. doi: 10.3390/molecules26216422. [PMID: 34770830]
  • Adaze Bijou Enogieru, William Haylett, Donavon Hiss, Okobi Ekpo. Inhibition of γH2AX, COX-2 and regulation of antioxidant enzymes in MPP+-exposed SH-SY5Y cells pre-treated with rutin. Metabolic brain disease. 2021 10; 36(7):2119-2130. doi: 10.1007/s11011-021-00746-z. [PMID: 33978902]
  • B S Cagle, M L Sturgeon, J B O'Brien, J C Wilkinson, R A Cornell, D L Roman, J A Doorn. Stable expression of the human dopamine transporter in N27 cells as an in vitro model for dopamine cell trafficking and metabolism. Toxicology in vitro : an international journal published in association with BIBRA. 2021 Oct; 76(?):105210. doi: 10.1016/j.tiv.2021.105210. [PMID: 34252731]
  • Jie Cao, Baojian Guo, Sai Li, Xaojing Zhang, Xiaoqi Zhang, Gaoxiao Zhang, Yewei Sun, Yuqiang Wang, Xiubao Song, Zaijun Zhang. Neuroprotection against 1-Methyl-4-phenylpyridinium-induced cytotoxicity by naturally occurring polydatin through activation of transcription factor MEF2D. Neuroreport. 2021 08; 32(12):1065-1072. doi: 10.1097/wnr.0000000000001696. [PMID: 34232128]
  • Liping Bai, Fang Yan, Ruhua Deng, Rou Gu, Xianwen Zhang, Jie Bai. Thioredoxin-1 Rescues MPP+/MPTP-Induced Ferroptosis by Increasing Glutathione Peroxidase 4. Molecular neurobiology. 2021 Jul; 58(7):3187-3197. doi: 10.1007/s12035-021-02320-1. [PMID: 33634378]
  • Ratchaneekorn Reudhabibadh, Thunwa Binlateh, Pennapa Chonpathompikunlert, Nongyao Nonpanya, Peerada Prommeenate, Pithi Chanvorachote, Pilaiwanwadee Hutamekalin. Suppressing Cdk5 Activity by Luteolin Inhibits MPP+-Induced Apoptotic of Neuroblastoma through Erk/Drp1 and Fak/Akt/GSK3β Pathways. Molecules (Basel, Switzerland). 2021 Feb; 26(5):. doi: 10.3390/molecules26051307. [PMID: 33671094]
  • Gaurav Bhatia, Jatinder Singh, Bimla Nehru. Neuroprotective effects of hydro-alcoholic extract of Eclipta alba against 1-methyl-4-phenylpyridinium-induced in vitro and in vivo models of Parkinson's disease. Environmental science and pollution research international. 2021 Feb; 28(8):9390-9406. doi: 10.1007/s11356-020-11452-1. [PMID: 33145730]
  • Dajing Jiang, Yang Peng. The protective effect of decoction of Rehmanniae via PI3K/Akt/mTOR pathway in MPP+-induced Parkinson's disease model cells. Journal of receptor and signal transduction research. 2021 Feb; 41(1):74-84. doi: 10.1080/10799893.2020.1787445. [PMID: 32611232]
  • Asami Saito, Naoki Ishiguro, Masahito Takatani, Bojan Bister, Hiroyuki Kusuhara. Impact of Direction of Transport on the Evaluation of Inhibition Potencies of Multidrug and Toxin Extrusion Protein 1 Inhibitors. Drug metabolism and disposition: the biological fate of chemicals. 2021 02; 49(2):152-158. doi: 10.1124/dmd.120.000136. [PMID: 33262224]
  • Xu Li, Tian-Jiao Xu, Li-Kun Liu, Miao-Xian Dong. [Antioxidant mechanism of gastrodin combined with isorhynchophylline in inhibiting MPP~+-induced apoptosis of PC12 cells]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2021 Jan; 46(2):420-425. doi: 10.19540/j.cnki.cjcmm.20201009.401. [PMID: 33645131]
  • Juliann D Jaumotte, Mart Saarma, Michael J Zigmond. Protection of dopamine neurons by CDNF and neurturin variant N4 against MPP+ in dissociated cultures from rat mesencephalon. PloS one. 2021; 16(2):e0245663. doi: 10.1371/journal.pone.0245663. [PMID: 33534843]
  • Yoshajandith Aguirre-Vidal, Jorge Morales-Montor, Carmen T Gómez de León, Pedro Ostoa-Saloma, Mariana Díaz-Zaragoza, Sergio Montes, Marcela Arteaga-Silva, Antonio Monroy-Noyola. Protection induced by estradiol benzoate in the MPP+ rat model of Parkinson's disease is associated with the regulation of the inflammatory cytokine profile in the nigro striatum. Journal of neuroimmunology. 2020 12; 349(?):577426. doi: 10.1016/j.jneuroim.2020.577426. [PMID: 33096292]
  • Fang Zhang, Xia Zhang, Sheng Guo, Funing Cao, Xiaofei Zhang, Yaqi Wang, Jiazheng Liu, Bowen Qian, Yichao Yan, Peidong Chen, Chunlei Xu, Chunmei Liu, Dawei Qian, Jin-Ao Duan. An acidic heteropolysaccharide from Lycii fructus: Purification, characterization, neurotrophic and neuroprotective activities in vitro. Carbohydrate polymers. 2020 Dec; 249(?):116894. doi: 10.1016/j.carbpol.2020.116894. [PMID: 32933702]
  • Abobaker S Ibrakaw, Sylvester I Omoruyi, Okobi E Ekpo, Ahmed A Hussein. Neuroprotective Activities of Boophone haemanthoides (Amaryllidaceae) Extract and Its Chemical Constituents. Molecules (Basel, Switzerland). 2020 Nov; 25(22):. doi: 10.3390/molecules25225376. [PMID: 33212961]
  • Xiaoli Chang, Zegang Ma, Limin Shi, Junxia Xie. Effects of ghrelin on the electrical activities of substantia nigra dopaminergic neurons treated with MPP. Neurochemistry international. 2020 09; 138(?):104780. doi: 10.1016/j.neuint.2020.104780. [PMID: 32569790]
  • Im-Sook Song, Hyeon-Uk Jeong, Min-Koo Choi, Mihwa Kwon, Yongho Shin, Jeong Han Kim, Hye-Suk Lee. Interactions between cyazofamid and human drug transporters. Journal of biochemical and molecular toxicology. 2020 Apr; 34(4):e22459. doi: 10.1002/jbt.22459. [PMID: 32003934]
  • Tanapol Limboonreung, Patoomratana Tuchinda, Sukumal Chongthammakun. Chrysoeriol mediates mitochondrial protection via PI3K/Akt pathway in MPP+ treated SH-SY5Y cells. Neuroscience letters. 2020 01; 714(?):134545. doi: 10.1016/j.neulet.2019.134545. [PMID: 31622648]
  • Severin Hörmann, Zhibo Gai, Gerd A Kullak-Ublick, Michele Visentin. Plasma Membrane Cholesterol Regulates the Allosteric Binding of 1-Methyl-4-Phenylpyridinium to Organic Cation Transporter 2 (SLC22A2). The Journal of pharmacology and experimental therapeutics. 2020 01; 372(1):46-53. doi: 10.1124/jpet.119.260877. [PMID: 31624079]
  • Adaze Bijou Enogieru, William Lloyd Haylett, Hayley Christy Miller, Francois Hendrikus van der Westhuizen, Donavon Charles Hiss, Okobi Eko Ekpo. Attenuation of Endoplasmic Reticulum Stress, Impaired Calcium Homeostasis, and Altered Bioenergetic Functions in MPP+-Exposed SH-SY5Y Cells Pretreated with Rutin. Neurotoxicity research. 2019 Nov; 36(4):764-776. doi: 10.1007/s12640-019-00048-4. [PMID: 31055769]
  • Jian-Liang Zhu, Yu-Ying Wu, Di Wu, Wei-Feng Luo, Zhi-Qing Zhang, Chun-Feng Liu. SC79, a novel Akt activator, protects dopaminergic neuronal cells from MPP+ and rotenone. Molecular and cellular biochemistry. 2019 Nov; 461(1-2):81-89. doi: 10.1007/s11010-019-03592-x. [PMID: 31342299]
  • Kuan-Ho Lin, Chien-Yu Li, Yuan-Man Hsu, Chang-Hai Tsai, Fuu-Jen Tsai, Chih-Hsin Tang, Jai-Sing Yang, Zhi-Hong Wang, Mei-Chin Yin. Oridonin, A natural diterpenoid, protected NGF-differentiated PC12 cells against MPP+- and kainic acid-induced injury. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2019 Nov; 133(?):110765. doi: 10.1016/j.fct.2019.110765. [PMID: 31430510]
  • Liyue Qin, Ziyu Chen, Liu Yang, Hailian Shi, Hui Wu, Beibei Zhang, Weiqi Zhang, Qi Xu, Fei Huang, Xiaojun Wu. Luteolin-7-O-glucoside protects dopaminergic neurons by activating estrogen-receptor-mediated signaling pathway in MPTP-induced mice. Toxicology. 2019 10; 426(?):152256. doi: 10.1016/j.tox.2019.152256. [PMID: 31381935]
  • Wassamon Boonying, Alvin Joselin, En Huang, Dianbo Qu, Farzaneh Safarpour, Grace O Iyirhiaro, Yasmilde Rodriguez Gonzalez, Steve M Callaghan, Ruth S Slack, Daniel Figeys, Young-Hwa Chung, David S Park. Pink1 regulates FKBP5 interaction with AKT/PHLPP and protects neurons from neurotoxin stress induced by MPP. Journal of neurochemistry. 2019 08; 150(3):312-329. doi: 10.1111/jnc.14683. [PMID: 30734931]
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