DL-Glutamate (BioDeep_00000014820)

Main id: BioDeep_00000000342

Secondary id: BioDeep_00001868016

human metabolite PANOMIX_OTCML-2023 blood metabolite


代谢物信息卡片


Glutamic Acid, (D)-Isomer

化学式: C5H9NO4 (147.0532)
中文名称: 谷氨酸, DL-谷氨酸, D-谷氨酸
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C(=O)(CC[C@H](C(=O)O)N)O
InChI: InChI=1S/C5H9NO4/c6-3(5(9)10)1-2-4(7)8/h3H,1-2,6H2,(H,7,8)(H,9,10)

描述信息

DL-Glutamate, also known as E or DL-glutamic acid, belongs to the class of organic compounds known as glutamic acid and derivatives. Glutamic acid and derivatives are compounds containing glutamic acid or a derivative thereof resulting from reaction of glutamic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). DL-Glutamate exists in all living organisms, ranging from bacteria to humans. DL-Glutamate is found, on average, in the highest concentration within a few different foods, such as red bell peppers, milk (cow), and wheats and in a lower concentration in eggplants, romaine lettuces, and nanking cherries. DL-Glutamate has also been detected, but not quantified, in a few different foods, such as apples, broccoli, and lettuces.
Glutamic acid (abbreviated as Glu or E) is one of the 20 proteinogenic amino acids. It is a non-essential amino acid. Glutamic acid is found in many foods, some of which are garden onion, orange bell pepper, oat, and cucumber.
D018377 - Neurotransmitter Agents > D018846 - Excitatory Amino Acids
DL-Glutamic acid is the conjugate acid of Glutamic acid, which acts as a fundamental metabolite. Comparing with the second phase of polymorphs α and β L-Glutamic acid, DL-Glutamic acid presents better stability[1].
DL-Glutamic acid is the conjugate acid of Glutamic acid, which acts as a fundamental metabolite. Comparing with the second phase of polymorphs α and β L-Glutamic acid, DL-Glutamic acid presents better stability[1].

同义名列表

34 个代谢物同义名

Glutamic Acid, (D)-Isomer; 2-aminopentanedioic acid; D-2-Aminoglutaric acid; L-Glutamate, Aluminum; 2-Aminoglutaric acid; Aluminum L Glutamate; Glutamate, Potassium; Aluminum L-Glutamate; Potassium Glutamate; DL-Glutaminic acid; D(-)-Glutamic acid; D-Glutaminic acid; 2-Aminoglutarate; DL-Glutamic acid; L-glutamic acid; glutaminic acid; L Glutamic Acid; D-Glutamic acid; DL-Glutaminate; Glutaminsaeure; Glutamic Acid; DL-Glutamate; L Glutamate; Glutaminate; L-glutamate; D Glutamate; D-Glutamate; glutamate; glu; E; D-Glutamate; Glutamate; Glutamic acid; DL-Glutamic acid



数据库引用编号

29 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)

2 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 5 CHAT, ITPR3, MTOR, NOS1, PC
Peripheral membrane protein 2 MTOR, NOS1
Endoplasmic reticulum membrane 2 ITPR3, MTOR
Nucleus 4 CHAT, GRM1, MTOR, NOS1
cytosol 5 CHAT, MTOR, NOS1, PC, SST
dendrite 4 DRD2, GRM1, GRM7, MTOR
phagocytic vesicle 1 MTOR
nucleoplasm 5 ATP2B1, GRIK2, ITPR3, MTOR, NOS1
Cell membrane 11 ATP2B1, DRD2, GRIA3, GRIK2, GRM1, GRM3, GRM4, GRM7, GRM8, OPRD1, SLC17A8
Cytoplasmic side 1 MTOR
Multi-pass membrane protein 12 ATP2B1, DRD2, GRIA3, GRIK2, GRM1, GRM3, GRM4, GRM7, GRM8, ITPR3, OPRD1, SLC17A8
Golgi apparatus membrane 2 DRD2, MTOR
Synapse 6 ATP2B1, CHAT, CRH, DRD2, NOS1, TAC1
cell cortex 1 GRM7
dendritic shaft 1 GRM7
glutamatergic synapse 6 ATP2B1, DRD2, GRIK2, GRM1, GRM3, SLC17A8
Golgi apparatus 1 NPY
Golgi membrane 2 DRD2, MTOR
lysosomal membrane 1 MTOR
neuronal cell body 3 ITPR3, SST, TAC1
presynaptic membrane 5 ATP2B1, DRD2, GRIK2, GRM3, OPRD1
sarcolemma 1 NOS1
Lysosome 1 MTOR
Presynapse 1 GRM4
acrosomal vesicle 1 DRD2
plasma membrane 13 ATP2B1, DRD2, GRIA3, GRIK2, GRM1, GRM3, GRM4, GRM7, GRM8, ITPR3, NOS1, OPRD1, SLC17A8
presynaptic active zone 1 GRM7
synaptic vesicle membrane 4 ATP2B1, DRD2, OPRD1, SLC17A8
terminal bouton 1 GRIK2
Membrane 9 ATP2B1, GRIK2, GRM3, GRM4, GRM7, GRM8, ITPR3, MTOR, OPRD1
axon 4 DRD2, GRM3, GRM7, TAC1
basolateral plasma membrane 1 ATP2B1
brush border 1 ITPR3
extracellular exosome 1 ATP2B1
Lysosome membrane 1 MTOR
endoplasmic reticulum 2 GRIK2, ITPR3
extracellular space 4 CRH, NPY, SST, TAC1
perinuclear region of cytoplasm 1 NOS1
Schaffer collateral - CA1 synapse 1 GRM1
mitochondrion 2 NOS1, PC
protein-containing complex 1 NOS1
intracellular membrane-bounded organelle 1 ATP2B1
Microsome membrane 1 MTOR
postsynaptic density 3 GRIK2, GRM3, NOS1
TORC1 complex 1 MTOR
TORC2 complex 1 MTOR
Secreted 3 CRH, NPY, SST
extracellular region 4 CRH, NPY, SST, TAC1
Mitochondrion outer membrane 1 MTOR
mitochondrial outer membrane 1 MTOR
excitatory synapse 1 SLC17A8
hippocampal mossy fiber to CA3 synapse 1 GRIK2
Mitochondrion matrix 1 PC
mitochondrial matrix 1 PC
ciliary membrane 1 DRD2
photoreceptor inner segment 1 NOS1
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane 2 ATP2B1, SLC17A8
varicosity 1 CRH
multivesicular body 1 SLC17A8
dendritic spine 4 DRD2, GRIA3, GRM3, NOS1
neuronal dense core vesicle lumen 1 CRH
perikaryon 4 CRH, DRD2, GRIK2, SLC17A8
cytoplasmic vesicle 1 GRM4
nucleolus 1 ITPR3
apical part of cell 1 ITPR3
postsynaptic membrane 5 DRD2, GRIA3, GRIK2, GRM3, GRM7
Cell membrane, sarcolemma 1 NOS1
Cytoplasm, perinuclear region 1 NOS1
Membrane raft 1 NOS1
GABA-ergic synapse 3 DRD2, NPY, SST
sarcoplasmic reticulum 2 ITPR3, NOS1
Cell projection, dendritic spine 1 NOS1
Nucleus, PML body 1 MTOR
PML body 1 MTOR
lateral plasma membrane 2 ATP2B1, DRD2
nuclear outer membrane 1 ITPR3
Postsynaptic cell membrane 3 GRIA3, GRIK2, GRM1
dendrite cytoplasm 1 GRIK2
kainate selective glutamate receptor complex 1 GRIK2
mossy fiber rosette 1 GRIK2
receptor complex 2 GRM7, ITPR3
neuron projection 2 CHAT, OPRD1
cilium 1 DRD2
cell projection 2 ATP2B1, GRIK2
cell periphery 1 NOS1
cytoskeleton 1 NOS1
non-motile cilium 1 DRD2
Basolateral cell membrane 1 ATP2B1
sperm flagellum 1 DRD2
nuclear envelope 1 MTOR
Endomembrane system 1 MTOR
chloride channel complex 1 SLC17A8
AMPA glutamate receptor complex 1 GRIA3
Presynaptic cell membrane 2 ATP2B1, GRIK2
secretory granule membrane 1 ITPR3
axon terminus 3 DRD2, OPRD1, SLC17A8
endocytic vesicle membrane 1 GRIA3
endocytic vesicle 1 DRD2
postsynaptic density membrane 4 GRIA3, GRIK2, GRM1, OPRD1
immunological synapse 1 ATP2B1
neuronal dense core vesicle 3 NPY, OPRD1, SST
parallel fiber to Purkinje cell synapse 1 GRIA3
platelet dense tubular network membrane 1 ITPR3
Synapse, synaptosome 1 SLC17A8
apical dendrite 1 SLC17A8
basal dendrite 1 SLC17A8
dopaminergic synapse 1 DRD2
dendrite membrane 1 OPRD1
Cytoplasmic vesicle, secretory vesicle membrane 1 ITPR3
Cytoplasmic vesicle, phagosome 1 MTOR
astrocyte projection 1 GRM3
Cytoplasmic vesicle, secretory vesicle, neuronal dense core vesicle 1 NPY
transport vesicle membrane 1 ITPR3
glial limiting end-foot 1 SLC17A8
asymmetric synapse 1 GRM7
photoreceptor ribbon synapse 1 ATP2B1
G protein-coupled receptor complex 1 DRD2
cytoplasmic side of endoplasmic reticulum membrane 1 ITPR3
spine apparatus 1 OPRD1
G protein-coupled receptor dimeric complex 1 GRM1
G protein-coupled receptor homodimeric complex 1 GRM1
pericellular basket 1 SLC17A8


文献列表

  • Jingbin Chen, Yali Liu, Yonggui Song, Huihui Liang, Genhua Zhu, Bike Zhang, Liangliang Liao, Jian Luo, Ming Yang, Dan Su. Neuro-stimulating effect of Citri Reticulata Pericarpium Viride essential oil through regulating Glu/NMDAR on olfactory bulb to improve anxiety-like behavior. Journal of ethnopharmacology. 2024 Sep; 331(?):118332. doi: 10.1016/j.jep.2024.118332. [PMID: 38735421]
  • Parham Khoshbakht Marvi, Syed Rahin Ahmed, Poushali Das, Raja Ghosh, Seshasai Srinivasan, Amin Reza Rajabzadeh. Prunella vulgaris-phytosynthesized platinum nanoparticles: Insights into nanozymatic activity for H2O2 and glutamate detection and antioxidant capacity. Talanta. 2024 Jul; 274(?):125998. doi: 10.1016/j.talanta.2024.125998. [PMID: 38574541]
  • Cheng-Wei Lu, Tzu-Yu Lin, Kuan-Ming Chiu, Ming-Yi Lee, Su-Jane Wang. Gypenoside XVII Reduces Synaptic Glutamate Release and Protects against Excitotoxic Injury in Rats. Biomolecules. 2024 May; 14(5):. doi: 10.3390/biom14050589. [PMID: 38785996]
  • Giulia Leni, Gabriele Rocchetti, Terenzio Bertuzzi, Alessio Abate, Alessandra Scansani, Federico Froldi, Aldo Prandini. Volatile compounds, gamma-glutamyl-peptides and free amino acids as biomarkers of long-ripened protected designation of origin Coppa Piacentina. Food chemistry. 2024 May; 440(?):138225. doi: 10.1016/j.foodchem.2023.138225. [PMID: 38134826]
  • Tenghan Ling, Aiping Yin, Yan Cao, Jiali Li, Hengxi Li, Ying Zhou, Xiaobing Guo, Jinghui Li, Ruilin Zhang, Haiying Wu, Ping Li. Purinergic Astrocyte Signaling Driven by TNF-α After Cannabidiol Administration Restores Normal Synaptic Remodeling Following Traumatic Brain Injury. Neuroscience. 2024 May; 545(?):31-46. doi: 10.1016/j.neuroscience.2024.03.002. [PMID: 38460903]
  • Fuming He, Baojun Gao, Xin Cheng, Jiao Zhai, Xinqing Zhang, Chuanlun Yang, Tian Jiewei. High-level production of poly-γ-glutamic acid by a newly isolated Bacillus sp. YJY-8 and potential use in increasing the production of tomato. Preparative biochemistry & biotechnology. 2024 May; 54(5):637-646. doi: 10.1080/10826068.2023.2261058. [PMID: 37768129]
  • Stanislav Jabinski, Wesley D M Rangel, Marek Kopáček, Veronika Jílková, Jan Jansa, Travis B Meador. Constraining activity and growth substrate of fungal decomposers via assimilation patterns of inorganic carbon and water into lipid biomarkers. Applied and environmental microbiology. 2024 Apr; 90(4):e0206523. doi: 10.1128/aem.02065-23. [PMID: 38527003]
  • Jinpeng Li, Xingbei Liu, Shumin Chang, Wei Chu, Jingchen Lin, Hui Zhou, Zhuoran Hu, Mancang Zhang, Mingming Xin, Yingyin Yao, Weilong Guo, Xiaodong Xie, Huiru Peng, Zhongfu Ni, Qixin Sun, Yu Long, Zhaorong Hu. The potassium transporter TaNHX2 interacts with TaGAD1 to promote drought tolerance via modulating stomatal aperture in wheat. Science advances. 2024 Apr; 10(15):eadk4027. doi: 10.1126/sciadv.adk4027. [PMID: 38608020]
  • František Sedlák, Aleš Kvasnička, Barbora Marešová, Radana Brumarová, Dana Dobešová, Kateřina Dostálová, Karolína Šrámková, Martin Pehr, Pavel Šácha, David Friedecký, Jan Konvalinka. Parallel Metabolomics and Lipidomics of a PSMA/GCPII Deficient Mouse Model Reveal Alteration of NAAG Levels and Brain Lipid Composition. ACS chemical neuroscience. 2024 Apr; 15(7):1342-1355. doi: 10.1021/acschemneuro.3c00494. [PMID: 38377674]
  • Lei Zhang, Xin Yue Bai, Ke Yao Sun, Xuan Li, Zhao Qi Zhang, Yi Ding Liu, Yang Xiang, Xiao Long Liu. A New Perspective in the Treatment of Ischemic Stroke: Ferroptosis. Neurochemical research. 2024 Apr; 49(4):815-833. doi: 10.1007/s11064-023-04096-3. [PMID: 38170383]
  • Giuseppe Forlani, Giuseppe Sabbioni, Simone Barera, Dietmar Funck. A complex array of factors regulate the activity of Arabidopsis thaliana δ1 -pyrroline-5-carboxylate synthetase isoenzymes to ensure their specific role in plant cell metabolism. Plant, cell & environment. 2024 Apr; 47(4):1348-1362. doi: 10.1111/pce.14817. [PMID: 38223941]
  • Raul Sanchez-Muñoz. Highway to cell: Unravelling the main player in Arabidopsis chloroplast glutamate export. The Plant cell. 2024 Mar; 36(4):805-806. doi: 10.1093/plcell/koad322. [PMID: 38134387]
  • Samantha Vivia The, James P Santiago, Clara Pappenberger, Ulrich Z Hammes, Mechthild Tegeder. UMAMIT44 is a key player in glutamate export from Arabidopsis chloroplasts. The Plant cell. 2024 Mar; 36(4):1119-1139. doi: 10.1093/plcell/koad310. [PMID: 38092462]
  • Siyu Zhang, Dong Wang, Yawen Ding, Fuyang Song, Yong Li, Jin Zeng, Yujiong Wang. Injury of Macrophages Induced by Clostridium perfringens Type C Exotoxins. International journal of molecular sciences. 2024 Mar; 25(7):. doi: 10.3390/ijms25073718. [PMID: 38612529]
  • Zhen Guo, Jian Wang, Tianqing Chen, Haiou Zhang, Xiandong Hou, Juan Li. Effects of γ-polyglutamic acid supplementation on alfalfa growth and rhizosphere soil microorganisms in sandy soil. Scientific reports. 2024 03; 14(1):6440. doi: 10.1038/s41598-024-57197-6. [PMID: 38499631]
  • Hongqian Zhang, Xue Gao, Qian Sun, Xiaoxue Dong, Zongwei Zhu, Chuanxu Yang. Incorporation of poly(γ-glutamic acid) in lipid nanoparticles for enhanced mRNA delivery efficiency in vitro and in vivo. Acta biomaterialia. 2024 Mar; 177(?):361-376. doi: 10.1016/j.actbio.2024.02.004. [PMID: 38342193]
  • Namita Nabar, Tamara G Dacoba, Gil Covarrubias, Denisse Romero-Cruz, Paula T Hammond. Electrostatic adsorption of polyanions onto lipid nanoparticles controls uptake, trafficking, and transfection of RNA and DNA therapies. Proceedings of the National Academy of Sciences of the United States of America. 2024 Mar; 121(11):e2307809121. doi: 10.1073/pnas.2307809121. [PMID: 38437543]
  • Ju-Bin Kang, Hyun-Kyoung Son, Dong-Ju Park, Yeung-Bae Jin, Fawad-Ali Shah, Phil-Ok Koh. Modulation of thioredoxin by chlorogenic acid in an ischemic stroke model and glutamate-exposed neurons. Neuroscience letters. 2024 Mar; 825(?):137701. doi: 10.1016/j.neulet.2024.137701. [PMID: 38395190]
  • Ying Li, Weijie Zhang, Chao Tang, Chen Wang, Changhui Liu, Qian Chen, Kai Yang, Yian Gu, Peng Lei, Hong Xu, Rui Wang. Antidiabetic effects and mechanism of γ-polyglutamic acid on type II diabetes mice. International journal of biological macromolecules. 2024 Mar; 261(Pt 1):129809. doi: 10.1016/j.ijbiomac.2024.129809. [PMID: 38290633]
  • Yueruxin Jin, Canying Li, Shuran Zhang, Jiaqi Liu, Miao Wang, Yan Guo, Hengping Xu, Yonghong Ge. Sucrose, cell wall, and polyamine metabolisms involve in preserving postharvest quality of 'Zaosu' pear fruit by L-glutamate treatment. Plant physiology and biochemistry : PPB. 2024 Mar; 208(?):108455. doi: 10.1016/j.plaphy.2024.108455. [PMID: 38428157]
  • Tomasz Skalski, Ewelina Zając, Elżbieta Jędrszczyk, Katarzyna Papaj, Joanna Kohyt, Artur Góra, Anna Kasprzycka, Divine Shytum, Barbara Skowera, Agnieszka Ziernicka-Wojtaszek. Effects of γ-polyglutamic acid on grassland sandy soil properties and plant functional traits exposed to drought stress. Scientific reports. 2024 02; 14(1):3769. doi: 10.1038/s41598-024-54459-1. [PMID: 38355917]
  • Li Ren. The mechanistic basis for the rapid antidepressant-like effects of ketamine: From neural circuits to molecular pathways. Progress in neuro-psychopharmacology & biological psychiatry. 2024 Feb; 129(?):110910. doi: 10.1016/j.pnpbp.2023.110910. [PMID: 38061484]
  • Sarathadevi Rajendran, Patrick Silcock, Phil Bremer. Volatile Organic Compounds (VOCs) Produced by Levilactobacillus brevis WLP672 Fermentation in Defined Media Supplemented with Different Amino Acids. Molecules (Basel, Switzerland). 2024 Feb; 29(4):. doi: 10.3390/molecules29040753. [PMID: 38398505]
  • Yangxia Han, Manchang Kou, Kaijun Quan, Juanjuan Wang, Haixia Zhang, Hirotaka Ihara, Makoto Takafuji, Hongdeng Qiu. Enantioselective Glutamic Acid Discrimination and Nanobiological Imaging by Chiral Fluorescent Silicon Nanoparticles. Analytical chemistry. 2024 02; 96(5):2173-2182. doi: 10.1021/acs.analchem.3c05150. [PMID: 38261544]
  • Ji-Yun Kang, Ji-Yeon Gu, Dong-Cheol Baek, Chang-Gue Son, Jin-Seok Lee. A Capsicum annuum L. seed extract exerts anti-neuroexcitotoxicity in HT22 hippocampal neurons. Food & function. 2024 Feb; ?(?):. doi: 10.1039/d3fo04501c. [PMID: 38305768]
  • Yoichiro Kasuga, Ailing Hu, Zenji Kawakami, Masahiro Tabuchi, Takuji Yamaguchi, Hiroyuki Kobayashi, Shigaku Ikeda. Suppressive effect of Yokukansan on glutamate released from canine keratinocytes. Open veterinary journal. 2024 Feb; 14(2):683-691. doi: 10.5455/ovj.2024.v14.i2.8. [PMID: 38549576]
  • Delin Yan, Lei Huang, Zhiqing Mei, Han Bao, Yaman Xie, Cunyi Yang, Xiangyang Gao. Untargeted metabolomics revealed the effect of soybean metabolites on poly(γ-glutamic acid) production in fermented natto and its metabolic pathway. Journal of the science of food and agriculture. 2024 Feb; 104(3):1298-1307. doi: 10.1002/jsfa.13011. [PMID: 37782527]
  • Fengqing Wang, Yanmei Chen, Jia Zheng, Can Yang, Li Li, Rong Li, Meilin Shi, Zhongxuan Li. Preparation of potential organic fertilizer rich in γ-polyglutamic acid via microbial fermentation using brewer's spent grain as basic substrate. Bioresource technology. 2024 Feb; 394(?):130216. doi: 10.1016/j.biortech.2023.130216. [PMID: 38122994]
  • Xi Zhang, Hong Zheng, Zhitao Ni, Yuyin Shen, Die Wang, Wenqing Li, Liangcai Zhao, Chen Li, Hongchang Gao. Fibroblast growth factor 21 alleviates diabetes-induced cognitive decline. Cerebral cortex (New York, N.Y. : 1991). 2024 01; 34(2):. doi: 10.1093/cercor/bhad502. [PMID: 38220573]
  • Xiaorui Xing, Qin Sun, Ruwen Wang, Yibing Wang, Ru Wang. Impacts of glutamate, an exercise-responsive metabolite on insulin signaling. Life sciences. 2024 Jan; ?(?):122471. doi: 10.1016/j.lfs.2024.122471. [PMID: 38301875]
  • Ruyan Gao, Tahir Ali, Zizhen Liu, Axiang Li, Liangliang Hao, Liufang He, Xiaoming Yu, Shupeng Li. Ceftriaxone averts neuroinflammation and relieves depressive-like behaviors via GLT-1/TrkB signaling. Biochemical and biophysical research communications. 2024 Jan; 701(?):149550. doi: 10.1016/j.bbrc.2024.149550. [PMID: 38310688]
  • Tzu-Kang Lin, Kun-Chieh Yeh, Ming-Shang Pai, Pei-Wen Hsieh, Su-Jane Wang. Ursolic acid inhibits the synaptic release of glutamate and prevents glutamate excitotoxicity in rats. European journal of pharmacology. 2024 Jan; 963(?):176280. doi: 10.1016/j.ejphar.2023.176280. [PMID: 38113967]
  • Huizhen Sun, Shanshan Wei, Yanchun Gong, Kaizhi Ding, Shan Tang, Wei Sun, Chunhua Yuan, Liping Huang, Zhibing Liu, Chong Chen, Lihua Yao. Neuroprotective effects of cordycepin inhibit glutamate-induced apoptosis in hippocampal neurons. Cell stress & chaperones. 2024 Jan; ?(?):. doi: 10.1016/j.cstres.2024.01.001. [PMID: 38219840]
  • Shreya Banerjee, Rakesh Sarkar, Arpita Mukherjee, Suvrotoa Mitra, Animesh Gope, Mamta Chawla-Sarkar. Rotavirus-induced lncRNA SLC7A11-AS1 promotes ferroptosis by targeting cystine/glutamate antiporter xCT (SLC7A11) to facilitate virus infection. Virus research. 2024 01; 339(?):199261. doi: 10.1016/j.virusres.2023.199261. [PMID: 37923170]
  • Lenka Vlasatikova, Michal Zeman, Magdalena Crhanova, Jitka Matiasovicova, Daniela Karasova, Marcela Faldynova, Hana Prikrylova, Alena Sebkova, Ivan Rychlik. Colonization of chickens with competitive exclusion products results in extensive differences in metabolite composition in cecal digesta. Poultry science. 2024 Jan; 103(1):103217. doi: 10.1016/j.psj.2023.103217. [PMID: 37980752]
  • Xin Jin, Hangyi Wu, Jie Yu, Yanni Cao, Lanyi Zhang, Zhenhai Zhang, Huixia Lv. Glutamate affects self-assembly, protein corona, and anti-4 T1 tumor effects of melittin/vitamin E-succinic acid-(glutamate)n nanoparticles. Journal of controlled release : official journal of the Controlled Release Society. 2024 Jan; 365(?):802-817. doi: 10.1016/j.jconrel.2023.12.013. [PMID: 38092255]
  • Anqi Ge, Qi He, Da Zhao, Yuwei Li, Junpeng Chen, Ying Deng, Wang Xiang, Hongqiao Fan, Shiting Wu, Yan Li, Lifang Liu, Yue Wang. Mechanism of ferroptosis in breast cancer and research progress of natural compounds regulating ferroptosis. Journal of cellular and molecular medicine. 2024 01; 28(1):e18044. doi: 10.1111/jcmm.18044. [PMID: 38140764]
  • Bei Zhang, Lei Qi, Xinhua Xie, Yue Shen, Jiahui Li, Bobo Zhang, Hongshuai Zhu. Emulsifying properties of O/W emulsion stabilized by soy protein isolate and γ-polyglutamic acid electrostatic complex. Journal of food science. 2024 Jan; 89(1):174-185. doi: 10.1111/1750-3841.16873. [PMID: 38051023]
  • Mengran Wang, Tingting Xuan, Haining Li, Jing An, Tianhui Hao, Jiang Cheng. Protective effect of FXN overexpression on ferroptosis in L-Glu-induced SH-SY5Y cells. Acta histochemica. 2024 Jan; 126(1):152135. doi: 10.1016/j.acthis.2024.152135. [PMID: 38266318]
  • Danuta Jantas, Piotr Warszyński, Władysław Lasoń. Carnosic Acid Shows Higher Neuroprotective Efficiency than Edaravone or Ebselen in In Vitro Models of Neuronal Cell Damage. Molecules (Basel, Switzerland). 2023 Dec; 29(1):. doi: 10.3390/molecules29010119. [PMID: 38202702]
  • Kim-Teng Lee, Hong-Sheng Liao, Ming-Hsiun Hsieh. Glutamine Metabolism, Sensing and Signaling in Plants. Plant & cell physiology. 2023 Dec; 64(12):1466-1481. doi: 10.1093/pcp/pcad054. [PMID: 37243703]
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