Arecolin (BioDeep_00000868533)

Main id: BioDeep_00000002582

 

PANOMIX_OTCML-2023


代谢物信息卡片


3-Pyridinecarboxylic acid, 1,2,5,6-tetrahydro-1-methyl-, methyl ester

化学式: C8H13NO2 (155.0946)
中文名称: 槟榔碱
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CN1CCC=C(C1)C(=O)OC
InChI: InChI=1S/C8H13NO2/c1-9-5-3-4-7(6-9)8(10)11-2/h4H,3,5-6H2,1-2H3

描述信息

D018377 - Neurotransmitter Agents > D018678 - Cholinergic Agents > D018679 - Cholinergic Agonists
C78272 - Agent Affecting Nervous System > C47796 - Cholinergic Agonist

同义名列表

72 个代谢物同义名

3-Pyridinecarboxylic acid, 1,2,5,6-tetrahydro-1-methyl-, methyl ester; 1,2,5,6-Tetrahydro-1-methyl-3-pyridinecarboxylic acid, methyl ester; 1,2,5,6-Tetrahydro-1-methyl-3-pyridinecarboxylic acid methyl ester; 1-methyl-5,6-dihydro-2H-pyridine-3-carboxylic acid methyl ester; N-Methyltetrahydropyridine-.beta.-carboxylic acid methyl ester; InChI=1\C8H13NO2\c1-9-5-3-4-7(6-9)8(10)11-2\h4H,3,5-6H2,1-2H; N-Methyltetrahydropyridine-beta-carboxylic acid methyl ester; NICOTINIC ACID, 1,2,5,6-TETRAHYDRO-1-METHYL-, METHYL ESTER; methyl 1-methyl-1,2,5,6-tetrahydropyridine-3-carboxylate; 1,2,5,6-Tetrahydro-1-methylnicotinic acid, methyl ester; 1-Methyl-delta(sup 3,4)tetrahydro-3-pyridinecarboxylate; N-Methyl-.delta.-tetrahydronicotinic acid methyl ester; methyl 1-methyl-5,6-dihydro-2H-pyridine-3-carboxylate; N-Methyltetrahydronicotinic acid, methyl ester; Methyl N-methyl-1,2,5,6-tetrahydronicotinate; 5-22-01-00322 (Beilstein Handbook Reference); Methyl 1,2,5,6-tetrahydro-1-methylnicotinate; Methyl N-methyltetrahydronicotinate; Arecaidine methyl ester; WLN: T6N CUTJ A1 CVO1; SDCCGMLS-0066647.P001; Prestwick1_000402; Prestwick2_000402; Prestwick0_000402; Prestwick3_000402; Spectrum4_000810; Spectrum5_001316; Spectrum3_001387; EINECS 200-565-5; Spectrum2_000051; NCGC00162053-02; Spectrum_000055; NCGC00015075-02; NCGC00015075-01; Methylarecaidin; Methylarecaiden; Arecoline base; MEGxp0_001891; KBioSS_000435; BSPBio_002974; BSPBio_000324; DivK1c_000810; Lopac0_000049; KBioGR_001299; BPBio1_000358; ACon1_002372; KBio3_002194; KBio2_000435; KBio2_003003; SPBio_000201; Lopac-A-6134; NINDS_000810; CAS-300-08-3; KBio1_000810; SPBio_002263; KBio2_005571; BRN 0123045; AIDS-002686; IDI1_000810; Arecholine; AIDS002686; CCRIS 7688; Arecaline; Arecoline; NSC 56321; Arecolin; NSC56321; Arekolin; 63-75-2; C10129; Arecoline; Arecoline



数据库引用编号

9 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)

3 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 15 BCL2, CASP3, CCND1, CDH1, CDK1, CDKN1A, EGFR, MAPK14, MTOR, PIK3C3, PTGS2, SMAD2, STAT3, TP53, VIM
Peripheral membrane protein 3 ACHE, MTOR, PTGS2
Endosome membrane 1 EGFR
Endoplasmic reticulum membrane 5 BCL2, CDK1, EGFR, MTOR, PTGS2
Cytoplasmic vesicle, autophagosome 1 PIK3C3
Nucleus 14 ACHE, BCL2, CASP3, CCND1, CDH1, CDK1, CDKN1A, EGFR, FOS, MAPK14, MTOR, SMAD2, STAT3, TP53
autophagosome 1 PIK3C3
cytosol 14 BCL2, CASP3, CCND1, CDH1, CDK1, CDKN1A, FOS, MAPK14, MTOR, PIK3C3, SMAD2, STAT3, TP53, VIM
dendrite 1 MTOR
nuclear body 1 CDKN1A
phagocytic vesicle 2 MTOR, VIM
phosphatidylinositol 3-kinase complex, class III 1 PIK3C3
trans-Golgi network 1 CDH1
centrosome 3 CCND1, CDK1, TP53
nucleoplasm 11 CASP3, CCND1, CDH1, CDK1, CDKN1A, FOS, MAPK14, MTOR, SMAD2, STAT3, TP53
RNA polymerase II transcription regulator complex 2 FOS, STAT3
Cell membrane 4 ACHE, CDH1, EGFR, VIM
Cytoplasmic side 1 MTOR
lamellipodium 1 CDH1
ruffle membrane 1 EGFR
Early endosome membrane 1 EGFR
Golgi apparatus membrane 1 MTOR
Synapse 1 ACHE
cell junction 2 CDH1, EGFR
cell surface 2 ACHE, EGFR
glutamatergic synapse 5 CASP3, CDH1, EGFR, MAPK14, PIK3C3
Golgi apparatus 3 ACHE, CCN2, CDH1
Golgi membrane 3 EGFR, INS, MTOR
lysosomal membrane 1 MTOR
neuromuscular junction 1 ACHE
neuronal cell body 1 CASP3
postsynapse 1 CDH1
Lysosome 1 MTOR
endosome 3 CDH1, EGFR, PIK3C3
plasma membrane 6 ACHE, CCN2, CDH1, EGFR, STAT3, VIM
Membrane 9 ACHE, BCL2, CDH1, CDK1, EGFR, MTOR, PIK3C3, SMAD2, TP53
apical plasma membrane 1 EGFR
axon 1 VIM
basolateral plasma membrane 1 EGFR
caveola 1 PTGS2
extracellular exosome 3 CDH1, CDK1, VIM
Lysosome membrane 1 MTOR
endoplasmic reticulum 4 BCL2, FOS, PTGS2, TP53
extracellular space 5 ACHE, CCN2, EGFR, IL6, INS
perinuclear region of cytoplasm 4 ACHE, CDH1, CDKN1A, EGFR
adherens junction 1 CDH1
bicellular tight junction 1 CCND1
mitochondrion 4 BCL2, CDK1, MAPK14, TP53
protein-containing complex 6 BCL2, CDKN1A, EGFR, PTGS2, SMAD2, TP53
intracellular membrane-bounded organelle 1 CCN2
Microsome membrane 2 MTOR, PTGS2
postsynaptic density 1 CASP3
TORC1 complex 1 MTOR
TORC2 complex 1 MTOR
Single-pass type I membrane protein 2 CDH1, EGFR
Secreted 4 ACHE, CCN2, IL6, INS
extracellular region 6 ACHE, CCN2, CDH1, IL6, INS, MAPK14
cytoplasmic side of plasma membrane 1 CDH1
Mitochondrion outer membrane 2 BCL2, MTOR
Single-pass membrane protein 1 BCL2
mitochondrial outer membrane 2 BCL2, MTOR
Mitochondrion matrix 1 TP53
mitochondrial matrix 2 CDK1, TP53
Extracellular side 1 ACHE
transcription regulator complex 3 SMAD2, STAT3, TP53
Cytoplasm, cytoskeleton, microtubule organizing center, centrosome 2 CDK1, TP53
Nucleus membrane 2 BCL2, CCND1
Bcl-2 family protein complex 1 BCL2
nuclear membrane 4 BCL2, CCND1, CDH1, EGFR
Secreted, extracellular space, extracellular matrix 1 CCN2
actin cytoskeleton 1 CDH1
nucleolus 2 CDKN1A, TP53
midbody 2 CDK1, PIK3C3
Membrane raft 1 EGFR
pore complex 1 BCL2
Cytoplasm, cytoskeleton 2 TP53, VIM
focal adhesion 2 EGFR, VIM
GABA-ergic synapse 1 PIK3C3
Cell junction, adherens junction 1 CDH1
flotillin complex 1 CDH1
extracellular matrix 1 CCN2
Peroxisome 2 PIK3C3, VIM
basement membrane 1 ACHE
intracellular vesicle 1 EGFR
Nucleus, PML body 2 MTOR, TP53
PML body 2 MTOR, TP53
intermediate filament 1 VIM
lateral plasma membrane 1 CDH1
axoneme 1 PIK3C3
nuclear speck 1 MAPK14
Nucleus inner membrane 1 PTGS2
Nucleus outer membrane 1 PTGS2
nuclear inner membrane 1 PTGS2
nuclear outer membrane 1 PTGS2
Late endosome 1 PIK3C3
receptor complex 1 EGFR
neuron projection 2 PTGS2, VIM
chromatin 4 FOS, SMAD2, STAT3, TP53
cell leading edge 1 VIM
phagocytic vesicle membrane 1 PIK3C3
mitotic spindle 1 CDK1
cytoskeleton 1 VIM
Golgi apparatus, trans-Golgi network 1 CDH1
spindle pole 1 MAPK14
chromosome, telomeric region 1 CDK1
Lipid-anchor, GPI-anchor 1 ACHE
site of double-strand break 1 TP53
nuclear envelope 1 MTOR
Endomembrane system 1 MTOR
endosome lumen 1 INS
microtubule organizing center 1 VIM
phagophore assembly site 1 PIK3C3
phosphatidylinositol 3-kinase complex, class III, type I 1 PIK3C3
phosphatidylinositol 3-kinase complex, class III, type II 1 PIK3C3
side of membrane 1 ACHE
germ cell nucleus 1 TP53
replication fork 1 TP53
myelin sheath 1 BCL2
intermediate filament cytoskeleton 1 VIM
basal plasma membrane 1 EGFR
synaptic membrane 1 EGFR
ficolin-1-rich granule lumen 1 MAPK14
secretory granule lumen 2 INS, MAPK14
Golgi lumen 1 INS
endoplasmic reticulum lumen 3 IL6, INS, PTGS2
nuclear matrix 3 FOS, TP53, VIM
transcription repressor complex 2 CCND1, TP53
transport vesicle 1 INS
anaphase-promoting complex 1 CDH1
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
presynaptic endosome 1 PIK3C3
Nucleus matrix 1 VIM
clathrin-coated endocytic vesicle membrane 1 EGFR
[Isoform 2]: Nucleus 1 CDH1
[Isoform 1]: Nucleus 1 TP53
heteromeric SMAD protein complex 1 SMAD2
SMAD protein complex 1 SMAD2
synaptic cleft 1 ACHE
protein-DNA complex 1 FOS
spindle microtubule 1 CDK1
death-inducing signaling complex 1 CASP3
apical junction complex 1 CDH1
Cell junction, desmosome 1 CDH1
desmosome 1 CDH1
Cytoplasmic vesicle, phagosome 1 MTOR
catenin complex 1 CDH1
activin responsive factor complex 1 SMAD2
cyclin-dependent protein kinase holoenzyme complex 3 CCND1, CDK1, CDKN1A
postsynaptic endosome 1 PIK3C3
multivesicular body, internal vesicle lumen 1 EGFR
Shc-EGFR complex 1 EGFR
transcription factor AP-1 complex 1 FOS
Autolysosome 1 PIK3C3
interleukin-6 receptor complex 1 IL6
cyclin A1-CDK1 complex 1 CDK1
cyclin A2-CDK1 complex 1 CDK1
cyclin B1-CDK1 complex 1 CDK1
BAD-BCL-2 complex 1 BCL2
cyclin D1-CDK4 complex 1 CCND1
PCNA-p21 complex 1 CDKN1A
[Isoform H]: Cell membrane 1 ACHE
cyclin D1-CDK6 complex 1 CCND1
homomeric SMAD protein complex 1 SMAD2


文献列表

  • Mingyu Pan, Wenfeng Geng, Yuanxiao Wang, Makoto Tsunoda, Jiatong Liu, Yingxia Zhang, Haimei Yang, Lu-Shuang Li, Shiwen Song, Jinqiang Liang, Yanting Song. Simultaneous determination of five constituents of areca nut extract in rat plasma using UPLC-MS/MS and its application in a pharmacokinetic study. Journal of pharmaceutical and biomedical analysis. 2024 Aug; 245(?):116158. doi: 10.1016/j.jpba.2024.116158. [PMID: 38643703]
  • Sineenart Sanpinit, Julalak Chokpaisarn, Pinanong Na-Phatthalung, Dennapa Saeloh Sotthibandhu, Kanyatorn Yincharoen, Palika Wetchakul, Surasak Limsuwan, Sasitorn Chusri. Effectiveness of Ya-Samarn-Phlae in diabetic wound healing: Evidence from in vitro studies and a multicenter randomized controlled clinical trial. Journal of ethnopharmacology. 2024 May; 326(?):117929. doi: 10.1016/j.jep.2024.117929. [PMID: 38373661]
  • Soumya Ranjan Mishra, Bishnu Prasad Behera, Vineet Kumar Singh, Kewal Kumar Mahapatra, Deepak Mundkinajeddu, Deeksha Bhat, Aruna Mukti Minz, Gautam Sethi, Thomas Efferth, Surajit Das, Sujit Kumar Bhutia. Anticancer activity of Bacopa monnieri through apoptosis induction and mitophagy-dependent NLRP3 inflammasome inhibition in oral squamous cell carcinoma. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2024 Jan; 123(?):155157. doi: 10.1016/j.phymed.2023.155157. [PMID: 37951147]
  • Baile Ning, Zhifang Wang, Jiangshan He, Qian Wu, Qiyue Deng, Qing Yang, Jing Gao, Wen Fu, Ying Deng, Bingxin Wu, Xichang Huang, Jilin Mei, Fan Jiang, Wenbin Fu. The rapid antidepressant effect of acupuncture on two animal models of depression by inhibiting M1-Ach receptors regulates synaptic plasticity in the prefrontal cortex. Brain research. 2023 Sep; 1822(?):148609. doi: 10.1016/j.brainres.2023.148609. [PMID: 37783259]
  • Lin Zhang, Jin Tan, Yiping Liu, Mang Luo. Curcumin relieves arecoline-induced oral submucous fibrosis via inhibiting the LTBP2/NF-κB axis. Oral diseases. 2023 Jun; ?(?):. doi: 10.1111/odi.14656. [PMID: 37382472]
  • Ming Li, Zhiyuan Deng, Changqin Xie, Juan Chen, Zhenying Yuan, Omar Rahhal, Zhangui Tang. Fibroblast activating protein promotes the proliferation, migration, and activation of fibroblasts in oral submucous fibrosis. Oral diseases. 2023 Jun; ?(?):. doi: 10.1111/odi.14602. [PMID: 37357365]
  • Meng Xu, Shunyong Su, Shuaiming Jiang, Wanggao Li, Zeng Zhang, Jiachao Zhang, Xiaosong Hu. Short-term arecoline exposure affected the systemic health state of mice, in which gut microbes played an important role. Ecotoxicology and environmental safety. 2023 May; 259(?):115055. doi: 10.1016/j.ecoenv.2023.115055. [PMID: 37224782]
  • Shuhan Yi, Keyu Chen, Kozue Sakao, Makoto Ikenaga, Yuanliang Wang, De-Xing Hou. Assessment of Areca Nut Bioactivities in Western Diet-Induced Mice NAFLD Model. Nutrients. 2023 May; 15(10):. doi: 10.3390/nu15102403. [PMID: 37242285]
  • Pei-Feng Liu, Yung-Fu Chang. The Controversial Roles of Areca Nut: Medicine or Toxin?. International journal of molecular sciences. 2023 May; 24(10):. doi: 10.3390/ijms24108996. [PMID: 37240342]
  • Sarita Pal, Disha Sharma, Narayan Prasad Yadav. Plant leads for mitigation of oral submucous fibrosis: Current scenario and future prospect. Oral diseases. 2022 Dec; ?(?):. doi: 10.1111/odi.14485. [PMID: 36565439]
  • Dandan Kong, Gaofeng Wang, Yang Tang, Mengyue Guo, Zia Ul Haq Khan, Yifei Guo, Wei Gu, Yonggui Ma, Ming Sui, Jinping Li, Meihua Yang. Potential health risk of areca nut consumption: Hazardous effect of toxic alkaloids and aflatoxins on human digestive system. Food research international (Ottawa, Ont.). 2022 12; 162(Pt A):112012. doi: 10.1016/j.foodres.2022.112012. [PMID: 36461237]
  • Feng-Mei Qi, Xiao-Yong Rao, Tong-Tong Han, Ling-Yun Zhong, Xiao-Jian Luo, Yan He, Rui-Lin Shen. [Water migration and kinetics of Arecae Semen during moistening process]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica. 2022 Apr; 47(7):1871-1880. doi: 10.19540/j.cnki.cjcmm.20211123.301. [PMID: 35534257]
  • Tsung-Jung Ho, Bruce Chi-Kang Tsai, Chia-Hua Kuo, Hsiang-Ning Luk, Cecilia Hsuan Day, Dennis Jine-Yuan Hsieh, Ray-Jade Chen, Wei-Wen Kuo, V Bharath Kumar, Chun-Hsu Yao, Chih-Yang Huang. Arecoline induces cardiotoxicity by upregulating and activating cardiac hypertrophy-related pathways in Sprague-Dawley rats. Chemico-biological interactions. 2022 Feb; 354(?):109810. doi: 10.1016/j.cbi.2022.109810. [PMID: 34999050]
  • Pangzhen Zhang, Nathaniel Quan En Chua, Simon Dang, Ashleigh Davis, Kah Wee Chong, Stephen S Prime, Nicola Cirillo. Molecular Mechanisms of Malignant Transformation of Oral Submucous Fibrosis by Different Betel Quid Constituents-Does Fibroblast Senescence Play a Role?. International journal of molecular sciences. 2022 Jan; 23(3):. doi: 10.3390/ijms23031637. [PMID: 35163557]
  • Jiao Wu, Chuang Cui, He Zhang, Dongjun Liu, Lukas Schreiber, Weiquan Qin, Yinglang Wan. Identifying new compounds with potential pharmaceutical and physiological activity in Areca catechu and Areca triandra via a non-targeted metabolomic approach. Phytochemical analysis : PCA. 2021 Nov; 32(6):970-981. doi: 10.1002/pca.3039. [PMID: 33619832]
  • Wen-Yuan Lin, Bruce Chi-Kang Tsai, Cecilia Hsuan Day, Ping-Ling Chiu, Ray-Jade Chen, Michael Yu-Chih Chen, V Vijaya Padma, Hsiang-Ning Luk, Hsiang-Chen Lee, Chih-Yang Huang. Arecoline induces heart injure via Fas/Fas ligand apoptotic pathway in heart of Sprague-Dawley rat. Environmental toxicology. 2021 Aug; 36(8):1567-1575. doi: 10.1002/tox.23153. [PMID: 33929070]
  • Q Chen, Z Jiang, J Zhang, L Cao, Z Chen. Arecoline hydrobromide enhances jejunum smooth muscle contractility via voltage-dependent potassium channels in W/Wv mice. Physiological research. 2021 07; 70(3):437-446. doi: 10.33549/physiolres.934557. [PMID: 33982580]
  • Hui Ren, Guoqin He, Zhiyuan Lu, Qianting He, Shuai Li, Zhexun Huang, Zheng Chen, Congyuan Cao, Anxun Wang. Arecoline induces epithelial-mesenchymal transformation and promotes metastasis of oral cancer by SAA1 expression. Cancer science. 2021 Jun; 112(6):2173-2184. doi: 10.1111/cas.14866. [PMID: 33626219]
  • Sachin C Sarode, Gargi S Sarode. Comment on 'Genetic toxicology and toxicokinetics of arecoline and related areca nut compounds: an updated review'. Archives of toxicology. 2021 05; 95(5):1859-1860. doi: 10.1007/s00204-021-03027-x. [PMID: 33738546]
  • Nuno G Oliveira, Daniela L Ramos, Ricardo Jorge Dinis-Oliveira. Reply to the commentary by Sarode and Sarode on 'Genetic toxicology and toxicokinetics of arecoline and related areca nut compounds: an updated review'. Archives of toxicology. 2021 05; 95(5):1861-1862. doi: 10.1007/s00204-021-03039-7. [PMID: 33846819]
  • Mark J Henderson, Kathleen A Trychta, Shyh-Ming Yang, Susanne Bäck, Adam Yasgar, Emily S Wires, Carina Danchik, Xiaokang Yan, Hideaki Yano, Lei Shi, Kuo-Jen Wu, Amy Q Wang, Dingyin Tao, Gergely Zahoránszky-Kőhalmi, Xin Hu, Xin Xu, David Maloney, Alexey V Zakharov, Ganesha Rai, Fumihiko Urano, Mikko Airavaara, Oksana Gavrilova, Ajit Jadhav, Yun Wang, Anton Simeonov, Brandon K Harvey. A target-agnostic screen identifies approved drugs to stabilize the endoplasmic reticulum-resident proteome. Cell reports. 2021 04; 35(4):109040. doi: 10.1016/j.celrep.2021.109040. [PMID: 33910017]
  • Xiaojian Yin, Yunxie Wei, Wei Song, He Zhang, Guoyin Liu, Yan Chen, Lan-Zhu Li, Raphael N Alolga, Gaoxiang Ma, Russel J Reiter, Jia Li, Haitao Shi. Melatonin as an inducer of arecoline and their coordinated roles in anti-oxidative activity and immune responses. Food & function. 2020 Oct; 11(10):8788-8799. doi: 10.1039/d0fo01841d. [PMID: 32955540]
  • Yi-Hsien Hsieh, Ru-Jiang Syu, Chu-Che Lee, Shin-Huey Lin, Chien-Hsing Lee, Chun-Wen Cheng, Jen-Pi Tsai. Arecoline induces epithelial mesenchymal transition in HK2 cells by upregulating the ERK-mediated signaling pathway. Environmental toxicology. 2020 Sep; 35(9):1007-1014. doi: 10.1002/tox.22937. [PMID: 32441858]
  • Romi Dasgupta, Indraneel Saha, Prajna Paramita Ray, Aniruddha Maity, Debajoyti Pradhan, Hari Prasad Sarkar, B R Maiti. Arecoline plays dual role on adrenal function and glucose-glycogen homeostasis under thermal stress in mice. Archives of physiology and biochemistry. 2020 Jul; 126(3):214-224. doi: 10.1080/13813455.2018.1508238. [PMID: 30318934]
  • Mei-Chi Chang, Yu-Hwa Pan, Hsyueh-Liang Wu, Yi-Jie Lu, Wan-Chuen Liao, Chien-Yang Yeh, Jang-Jaer Lee, Jiiang-Huei Jeng. Stimulation of MMP-9 of oral epithelial cells by areca nut extract is related to TGF-β/Smad2-dependent and -independent pathways and prevented by betel leaf extract, hydroxychavicol and melatonin. Aging. 2019 12; 11(23):11624-11639. doi: 10.18632/aging.102565. [PMID: 31831717]
  • Jeny Laskar, Mahuya Sengupta, Yashmin Choudhury. Treatment with the anti-diabetic drug metformin ameliorates betel-nut induced carcinogenesis in a murine model. Pharmacological reports : PR. 2019 Dec; 71(6):1115-1124. doi: 10.1016/j.pharep.2019.06.011. [PMID: 31645006]
  • Tobie D Lee, Olivia W Lee, Kyle R Brimacombe, Lu Chen, Rajarshi Guha, Sabrina Lusvarghi, Bethilehem G Tebase, Carleen Klumpp-Thomas, Robert W Robey, Suresh V Ambudkar, Min Shen, Michael M Gottesman, Matthew D Hall. A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. Molecular pharmacology. 2019 11; 96(5):629-640. doi: 10.1124/mol.119.115964. [PMID: 31515284]
  • Jiao Wu, He Zhang, Shijie Wang, Langxing Yuan, Paul Grünhofer, Lukas Schreiber, Yinglang Wan. Tissue-specific and maturity-dependent distribution of pyridine alkaloids in Areca triandra. Journal of plant research. 2019 Jul; 132(4):531-540. doi: 10.1007/s10265-019-01115-9. [PMID: 31127431]
  • Yu-Ping Hsieh, King-Jean Wu, Hsin-Ming Chen, Yi-Ting Deng. Arecoline activates latent transforming growth factor β1 via mitochondrial reactive oxygen species in buccal fibroblasts: Suppression by epigallocatechin-3-gallate. Journal of the Formosan Medical Association = Taiwan yi zhi. 2018 Jun; 117(6):527-534. doi: 10.1016/j.jfma.2017.07.003. [PMID: 28720506]
  • Hong Pan, Yi Li, Linyan Huang, Xumei Zhou, Yuanfu Lu, Fuguo Shi. Development and validation of a rapid LC-MS/MS method for simultaneous quantification of arecoline and its two active metabolites in rat plasma and its application to a pharmacokinetic study. Journal of pharmaceutical and biomedical analysis. 2018 May; 154(?):397-403. doi: 10.1016/j.jpba.2018.03.033. [PMID: 29573735]
  • Saeeda Baig, Zile Rubab, Wasfa Farooq. Molecular Pathogenesis of Chewable Tobacco. Journal of the College of Physicians and Surgeons--Pakistan : JCPSP. 2018 May; 28(5):381-385. doi: 10.29271/jcpsp.2018.05.381. [PMID: 29690969]
  • Lian Zheng, Zhen-Jie Guan, Wen-Ting Pan, Tian-Feng Du, Yu-Jia Zhai, Jia Guo. Tanshinone Suppresses Arecoline-Induced Epithelial-Mesenchymal Transition in Oral Submucous Fibrosis by Epigenetically Reactivating the p53 Pathway. Oncology research. 2018 Apr; 26(3):483-494. doi: 10.3727/096504017x14941825760362. [PMID: 28550687]
  • Ghulam Abbas, Muhammad Kashif, - Mudassar, Taseer Ahmed Khan, Huma Aslam Bhatti, Sayedul Haque, Sabira Naqvi, Ahsana Dar Farooq. Cytotoxic, embryotoxic, insecticidal and anti-microbial activities of standardized Areca catechu nut. Pakistan journal of pharmaceutical sciences. 2018 Mar; 31(2):385-392. doi: ". [PMID: 29618425]
  • Hong Pan, Linyan Huang, Yi Li, Xumei Zhou, Yuanfu Lu, Fuguo Shi. Liquid chromatography-tandem mass spectrometric assay for determination of unstable arecoline in rat plasma and its application. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2017 Dec; 1070(?):112-116. doi: 10.1016/j.jchromb.2017.10.026. [PMID: 29107731]
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