Phosphocreatine (BioDeep_00000002691)
Secondary id: BioDeep_00000399955
human metabolite Endogenous natural product BioNovoGene_Lab2019
代谢物信息卡片
化学式: C4H10N3O5P (211.0358)
中文名称: 磷酸肌酸 二钠盐 水合物, 肌酸磷酸氢二钠四水合物, 磷酸肌酸
谱图信息:
最多检出来源 Homo sapiens(blood) 14.79%
Last reviewed on 2024-09-14.
Cite this Page
Phosphocreatine. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China.
https://query.biodeep.cn/s/phosphocreatine (retrieved
2024-12-22) (BioDeep RN: BioDeep_00000002691). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
分子结构信息
SMILES: CN(CC(=O)O)C(=N)NP(=O)(O)O
InChI: InChI=1S/C4H10N3O5P/c1-7(2-3(8)9)4(5)6-13(10,11)12/h2H2,1H3,(H,8,9)(H4,5,6,10,11,12)
描述信息
Phosphocreatine, also known as creatine phosphate (CP) or PCr (Pcr), is a phosphorylated creatine molecule that serves as a rapidly mobilizable reserve of high-energy phosphates in skeletal muscle, myocardium and the brain to recycle adenosine triphosphate, the energy currency of the cell. Phosphocreatine undergoes irreversible cyclization and dehydration to form creatinine at a fractional rate of 0.026 per day, thus forming approximately 2 g creatinine/day in an adult male. This is the amount of creatine that must be provided either from dietary sources or by endogenous synthesis to maintain the body pool of (creatine and) phosphocreatine. Creatine is an amino acid that plays a vital role as phosphocreatine in regenerating adenosine triphosphate in skeletal muscle to energize muscle contraction. Creatine is phosphorylated to phosphocreatine in muscle in a reaction that is catalyzed by the enzyme creatine kinase. This enzyme is in highest concentration in muscle and nerve. Oral administration increases muscle stores. During the past decade, creatine has assumed prominence as an ergogenic (and legal) aid for professional and elite athletes. Most (~ 95\\%) of the total body creatine-phosphocreatine pool is in muscle (more in skeletal muscle than in smooth muscle) and amounts to 120 g (or 925 mmol) in a 70 kg adult male. Approximately 60-67\\% of the content in resting muscle is in the phosphorylated form. This generates enough ATP at the myofibrillar apparatus to power about 4 seconds of muscle contraction in exercise. Phosphocreatine reacts with ADP to yield ATP and creatine; the reversible reaction is catalyzed by creatine kinase. phosphocreatine is the chief store of high-energy phosphates in muscle. Thus, this reaction, which permits the rephosphorylation of ADP to ATP, is the immediate source of energy in muscle contraction. During rest, metabolic processes regenerate phosphocreatine stores. In normal muscle, ATP that is broken down to ADP is immediately rephosphorylated to ATP. Thus, phosphocreatine serves as a reservoir of ATP-synthesizing potential. phosphocreatine is the only fuel available to precipitously regenerate ATP during episodes of rapid fluctuations in demand. The availability of phosphocreatine likely limits muscle performance during brief, high-power exercise, i.e., maximal exercise of short duration. With near maximal isometric contraction, the rate of utilization of phosphocreatine declines after 1-2 seconds of contraction, prior to the glycolysis peak at approximately 3 seconds (PMID:10079702).
Phosphocreatine undergoes irreversible cyclization and dehydration to form creatinine at a fractional rate of 0.026 per day, thus forming approximately 2 g creatinine/day in an adult male. This is the amount of creatine that must be provided either from dietary sources or by endogenous synthesis to maintain the body pool of (creatine and) phosphocreatine. Creatine is an amino acid that plays a vital role as phosphocreatine in regenerating adenosine triphosphate in skeletal muscle to energize muscle contraction. Creatine is phosphorylated to phosphocreatine in muscle in a reaction that is catalyzed by the enzyme creatine kinase. This enzyme is in highest concentration in muscle and nerve. Oral administration increases muscle stores. During the past decade, creatine has assumed prominence as an ergogenic (and legal) aid for professional and elite athletes. Most (~ 95\\%) of the total body creatine-phosphocreatine pool is in muscle (more in skeletal muscle than in smooth muscle) and amounts to 120 g (or 925 mmol) in a 70 kg adult male. Approximately 60-67\\% of the content in resting muscle is in the phosphorylated form. This generates enough ATP at the myofibrillar apparatus to power about 4 seconds of muscle contraction in exercise. Phosphocreatine reacts with ADP to yield ATP and creatine; the reversible reaction is catalyzed by creatine kinase. phosphocreatine is the chief store of high-energy phosphates in muscle. Thus, this reaction, which permits the rephosphorylation of ADP to ATP, is the immediate source of energy in muscle contraction. During rest, metabolic processes regenerate phosphocreatine stores. In normal muscle, ATP that is broken down to ADP is immediately rephosphorylated to ATP. Thus, phosphocreatine serves as a reservoir of ATP-synthesizing potential. phosphocreatine is the only fuel available to precipitously regenerate ATP during episodes of rapid fluctuations in demand. The availability of phosphocreatine likely limits muscle performance during brief, high-power exercise, i.e., maximal exercise of short duration. With near maximal isometric contraction, the rate of utilization of phosphocreatine declines after 1-2 seconds of contraction, prior to the glycolysis peak at approximately 3 seconds. (PMID: 10079702, Nutr Rev. 1999 Feb;57(2):45-50.) [HMDB]
D020011 - Protective Agents > D002316 - Cardiotonic Agents
C - Cardiovascular system > C01 - Cardiac therapy
D002317 - Cardiovascular Agents
KEIO_ID P084; [MS2] KO009218
KEIO_ID P084
同义名列表
22 个代谢物同义名
{[imino(phosphonoamino)methyl](methyl)amino}acetic acid; {[imino(phosphonoamino)methyl](methyl)amino}acetate; 2-(N-methyl-N-phosphonocarbamimidamido)acetic acid; N-[Imino(phosphonoamino)methyl]-N-methyl-glycine; N-(Phosphonoamidino)-sarcosine; N-(N-Phosphonoamido)sarcosine; N-(Phosphonoamidino)sarcosine; N(Omega)-phosphonocreatine; Creatine phosphoric acid; Creatinephosphoric acid; Creatine phosphic acid; N-Phosphorylcreatine; N-Phosphorocreatine; Creatine phosphate; Creatine-phosphate; Phosphorylcreatine; N-Phosphocreatine; Phosphocreatine; Creatine-p; p-Creatine; Neo-ton; Phosphocreatine
数据库引用编号
31 个数据库交叉引用编号
- ChEBI: CHEBI:17287
- KEGG: C02305
- PubChem: 9548602
- PubChem: 587
- HMDB: HMDB0001511
- Metlin: METLIN326
- DrugBank: DB13191
- ChEMBL: CHEMBL1204644
- Wikipedia: Phosphocreatine
- MeSH: Phosphocreatine
- MetaCyc: CREATINE-P
- foodb: FDB022665
- chemspider: 567
- CAS: 67-07-2
- MoNA: KO003849
- MoNA: KO003852
- MoNA: KO009218
- MoNA: KO009220
- MoNA: KO003848
- MoNA: KO003850
- MoNA: KO003851
- MoNA: KO009219
- PMhub: MS000004528
- PubChem: 5359
- 3DMET: B00422
- NIKKAJI: J4.848H
- RefMet: Phosphocreatine
- LOTUS: LTS0104544
- BioNovoGene_Lab2019: BioNovoGene_Lab2019-257
- BioNovoGene_Lab2019: BioNovoGene_Lab2019-340
- KNApSAcK: 17287
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
45 个相关的代谢反应过程信息。
Reactome(4)
- Metabolism:
1-3-oxo-THA-CoA + CoA-SH ⟶ DHA-CoA + propionyl CoA
- Amino acid and derivative metabolism:
2MACA-CoA + CoA ⟶ Ac-CoA + PROP-CoA
- Metabolism of polyamines:
GAA + SAM ⟶ CRET + H+ + SAH
- Creatine metabolism:
GAA + SAM ⟶ CRET + H+ + SAH
BioCyc(0)
Plant Reactome(0)
INOH(2)
- Arginine and Proline metabolism ( Arginine and Proline metabolism ):
ATP + Creatine ⟶ ADP + N-Phospho-creatine
- ATP + Creatine = ADP + N-Phospho-creatine ( Arginine and Proline metabolism ):
ATP + Creatine ⟶ ADP + N-Phospho-creatine
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(38)
- Arginine and Proline Metabolism:
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Prolidase Deficiency (PD):
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Arginine: Glycine Amidinotransferase Deficiency (AGAT Deficiency):
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Hyperprolinemia Type II:
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Hyperprolinemia Type I:
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Prolinemia Type II:
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency):
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Ornithine Aminotransferase Deficiency (OAT Deficiency):
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Creatine Deficiency, Guanidinoacetate Methyltransferase Deficiency:
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Hyperornithinemia with Gyrate Atrophy (HOGA):
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Hyperornithinemia-Hyperammonemia-Homocitrullinuria [HHH-syndrome]:
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- L-Arginine:Glycine Amidinotransferase Deficiency:
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Arginine and Proline Metabolism:
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Arginine and Proline Metabolism:
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Arginine: Glycine Amidinotransferase Deficiency (AGAT Deficiency):
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency):
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Hyperprolinemia Type I:
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Hyperprolinemia Type II:
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Ornithine Aminotransferase Deficiency (OAT Deficiency):
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Prolinemia Type II:
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Prolidase Deficiency (PD):
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Creatine Deficiency, Guanidinoacetate Methyltransferase Deficiency:
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Hyperornithinemia with Gyrate Atrophy (HOGA):
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Hyperornithinemia-Hyperammonemia-Homocitrullinuria [HHH-syndrome]:
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- L-Arginine:Glycine Amidinotransferase Deficiency:
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Arginine and Proline Metabolism:
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Arginine and Proline Metabolism:
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Arginine: Glycine Amidinotransferase Deficiency (AGAT Deficiency):
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency):
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Hyperprolinemia Type I:
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Hyperprolinemia Type II:
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Ornithine Aminotransferase Deficiency (OAT Deficiency):
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Prolinemia Type II:
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Prolidase Deficiency (PD):
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Creatine Deficiency, Guanidinoacetate Methyltransferase Deficiency:
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Hyperornithinemia with Gyrate Atrophy (HOGA):
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- Hyperornithinemia-Hyperammonemia-Homocitrullinuria [HHH-syndrome]:
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
- L-Arginine:Glycine Amidinotransferase Deficiency:
Guanidoacetic acid + S-Adenosylmethionine ⟶ Creatine + S-Adenosylhomocysteine
PharmGKB(0)
25 个相关的物种来源信息
- 186623 - Actinopteri: LTS0104544
- 7898 - Actinopterygii: LTS0104544
- 7458 - Apidae: LTS0104544
- 7459 - Apis: LTS0104544
- 7461 - Apis cerana: 10.1371/JOURNAL.PONE.0175573
- 7461 - Apis cerana: LTS0104544
- 6656 - Arthropoda: LTS0104544
- 4890 - Ascomycota: LTS0104544
- 8184 - Centropomidae: LTS0104544
- 7711 - Chordata: LTS0104544
- 2759 - Eukaryota: LTS0104544
- 4751 - Fungi: LTS0104544
- 9606 - Homo sapiens: -
- 9606 - Homo sapiens: 10.1007/S11306-016-1051-4
- 50557 - Insecta: LTS0104544
- 8186 - Lates: LTS0104544
- 8187 - Lates calcarifer: 10.3389/FPHYS.2020.00205
- 8187 - Lates calcarifer: LTS0104544
- 33208 - Metazoa: LTS0104544
- 4895 - Schizosaccharomyces: LTS0104544
- 4896 - Schizosaccharomyces pombe: 10.1039/C4MB00346B
- 4896 - Schizosaccharomyces pombe: LTS0104544
- 4894 - Schizosaccharomycetaceae: LTS0104544
- 147554 - Schizosaccharomycetes: LTS0104544
- 32443 - Teleostei: LTS0104544
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。
文献列表
- Ming-Wei Liu, Chun-Hai Zhang, Qiu-Juan Zhang, Bing-Ran Zhang. Rhabdomyolysis caused by Botrychium ternatum intoxication: Case report and literature review.
Medicine.
2024 Mar; 103(9):e37304. doi:
10.1097/md.0000000000037304
. [PMID: 38428852] - Xiangyu Liu, Bo Zhang, Junsheng Tian, Yumei Han. Plasma metabolomics reveals the intervention mechanism of different types of exercise on chronic unpredictable mild stress-induced depression rat model.
Metabolic brain disease.
2024 Jan; 39(1):1-13. doi:
10.1007/s11011-023-01310-7
. [PMID: 37999885] - Shveta Monga, Ladislav Valkovič, Saul G Myerson, Stefan Neubauer, Masliza Mahmod, Oliver J Rider. Role of Cardiac Energetics in Aortic Stenosis Disease Progression: Identifying the High-risk Metabolic Phenotype.
Circulation. Cardiovascular imaging.
2023 10; 16(10):e014863. doi:
10.1161/circimaging.122.014863
. [PMID: 37847766] - Hechuan Wang, Minghui Guo, Tianfeng Li, Han Zhang, Qian Wang, Qun Zhang, Yulun Song, Heze Feng, Yanbing Li, Guosheng Wei, Jingchun Li. Phosphocreatine addition to extender enhances the quality and antioxidant capacity of cryopreserved boar sperm.
Reproduction in domestic animals = Zuchthygiene.
2023 Jun; ?(?):. doi:
10.1111/rda.14404
. [PMID: 37313775] - Ping-An Yao, Ke-Zhao Wei, Jia-Hua Feng, Xiao-Ning Liu, Xu Xu, Hong-Yan Cui, Xiao-Chen Zhang, Jian-Ping Gao. Sodium houttuyfonate protects against cardiac injury by regulating cardiac energy metabolism in diabetic rats.
European journal of pharmacology.
2022 Oct; 932(?):175236. doi:
10.1016/j.ejphar.2022.175236
. [PMID: 36044971] - Ming-Ying Ling, Yi-Ping Song, Chun Liu, Zhi-Hao Wang, Yan Wang, Xue-Hui Li, Zhen Zhang, Rong-Xiang Zhou, Liang-Yi Qie, Man Li, Yun-Ling Xiao, Huan-Qin Chen, Yan-Qiu Xing. Protection of Exogenous Phosphocreatine for Myocardium in Percutaneous Coronary Intervention Related to Inflammation.
Reviews in cardiovascular medicine.
2022 Mar; 23(3):89. doi:
10.31083/j.rcm2303089
. [PMID: 35345256] - Salwan Maqdasy, Simon Lecoutre, Gianluca Renzi, Scott Frendo-Cumbo, David Rizo-Roca, Thomas Moritz, Marta Juvany, Ondrej Hodek, Hui Gao, Morgane Couchet, Michael Witting, Alastair Kerr, Martin O Bergo, Robin P Choudhury, Myriam Aouadi, Juleen R Zierath, Anna Krook, Niklas Mejhert, Mikael Rydén. Impaired phosphocreatine metabolism in white adipocytes promotes inflammation.
Nature metabolism.
2022 02; 4(2):190-202. doi:
10.1038/s42255-022-00525-9
. [PMID: 35165448] - Shu Yang, Lei Guo, Duozi Wang, Yanwei Yang, Jianhong Wang. Research on Mechanism of miR-106a Nanoparticles Carrying Dexmedetomidine in Regulating Recovery and Metabolism of Nerve Cells in Hypoxia-Reoxygenation Injury.
Journal of biomedical nanotechnology.
2022 Feb; 18(2):343-351. doi:
10.1166/jbn.2022.3244
. [PMID: 35484744] - John Paul V Anders, Tyler J Neltner, Robert W Smith, Joshua L Keller, Terry J Housh, F Joseph Daugherty, Michael S Tempesta, Alekha K Dash, Daniel J Munt, Richard J Schmidt, Glen O Johnson. The effects of phosphocreatine disodium salts plus blueberry extract supplementation on muscular strength, power, and endurance.
Journal of the International Society of Sports Nutrition.
2021 Sep; 18(1):60. doi:
10.1186/s12970-021-00456-y
. [PMID: 34503541] - P G Wibowo, S J Charman, N C Okwose, L Velicki, D Popovic, K G Hollingsworth, G A Macgowan, D G Jakovljevic. Association between cardiac high-energy phosphate metabolism and whole body metabolism in healthy female adults.
Physiological research.
2021 07; 70(3):393-399. doi:
10.33549/physiolres.934627
. [PMID: 33982584] - Salwa A Elgebaly, Robert Todd, Donald L Kreutzer, Robert Christenson, Nashwa El-Khazragy, Reem K Arafa, Mostafa A Rabie, Ahmed F Mohamed, Lamiaa A Ahmed, Nesrine S El Sayed. Nourin-Associated miRNAs: Novel Inflammatory Monitoring Markers for Cyclocreatine Phosphate Therapy in Heart Failure.
International journal of molecular sciences.
2021 Mar; 22(7):. doi:
10.3390/ijms22073575
. [PMID: 33808213] - Lisha Joshi, Ioanna Plastira, Eva Bernhart, Helga Reicher, Chintan N Koyani, Tobias Madl, Corina Madreiter-Sokolowski, Zhanat Koshenov, Wolfgang F Graier, Seth Hallström, Wolfgang Sattler. Lysophosphatidic Acid Induces Aerobic Glycolysis, Lipogenesis, and Increased Amino Acid Uptake in BV-2 Microglia.
International journal of molecular sciences.
2021 Feb; 22(4):. doi:
10.3390/ijms22041968
. [PMID: 33671212] - Yi Wang, Jin-Fang Chen, Pengyu Li, Jia-Hong Gao. Quantifying the fractional concentrations and exchange rates of small-linewidth CEST agents using the QUCESOP method under multi-solute conditions in MRI signals.
Magnetic resonance in medicine.
2021 01; 85(1):268-280. doi:
10.1002/mrm.28436
. [PMID: 32726502] - Guillaume Chazot, Sandrine Lemoine, Gabriel Kocevar, Emilie Kalbacher, Dominique Sappey-Marinier, Olivier Rouvière, Laurent Juillard. Intracellular Phosphate and ATP Depletion Measured by Magnetic Resonance Spectroscopy in Patients Receiving Maintenance Hemodialysis.
Journal of the American Society of Nephrology : JASN.
2021 01; 32(1):229-237. doi:
10.1681/asn.2020050716
. [PMID: 33093193] - William D Watson, Kerstin N Timm, Andrew J Lewis, Jack J J Miller, Yaso Emmanuel, Kieran Clarke, Stefan Neubauer, Damian J Tyler, Oliver J Rider. Nicotinic acid receptor agonists impair myocardial contractility by energy starvation.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
2020 11; 34(11):14878-14891. doi:
10.1096/fj.202000084rr
. [PMID: 32954525] - Alessandra Palma, Sveva Grande, Lucia Ricci-Vitiani, Anna Maria Luciani, Mariachiara Buccarelli, Mauro Biffoni, Valentina Dini, Giuseppe A P Cirrone, Mario Ciocca, Laura Guidoni, Roberto Pallini, Vincenza Viti, Antonella Rosi. Different Mechanisms Underlie the Metabolic Response of GBM Stem-Like Cells to Ionizing Radiation: Biological and MRS Studies on Effects of Photons and Carbon Ions.
International journal of molecular sciences.
2020 Jul; 21(14):. doi:
10.3390/ijms21145167
. [PMID: 32708312] - Jorge L Gamboa, Baback Roshanravan, Theodore Towse, Chad A Keller, Aaron M Falck, Chang Yu, Walter R Frontera, Nancy J Brown, T Alp Ikizler. Skeletal Muscle Mitochondrial Dysfunction Is Present in Patients with CKD before Initiation of Maintenance Hemodialysis.
Clinical journal of the American Society of Nephrology : CJASN.
2020 07; 15(7):926-936. doi:
10.2215/cjn.10320819
. [PMID: 32591419] - Margarida Souto-Carneiro, Lilla Tóth, Rouven Behnisch, Konstantin Urbach, Karel D Klika, Rui A Carvalho, Hanns-Martin Lorenz. Differences in the serum metabolome and lipidome identify potential biomarkers for seronegative rheumatoid arthritis versus psoriatic arthritis.
Annals of the rheumatic diseases.
2020 04; 79(4):499-506. doi:
10.1136/annrheumdis-2019-216374
. [PMID: 32079570] - KowsalyaDevi Pavuluri, Jens T Rosenberg, Shannon Helsper, Shaowei Bo, Michael T McMahon. Amplified detection of phosphocreatine and creatine after supplementation using CEST MRI at high and ultrahigh magnetic fields.
Journal of magnetic resonance (San Diego, Calif. : 1997).
2020 04; 313(?):106703. doi:
10.1016/j.jmr.2020.106703
. [PMID: 32179431] - Dong-Min Cao, Qin-Xiao Guan, Ya-Li Liu, Shu-Mei Wang. [Effect of ginsenosides on serous metabonomic profiles in cerebral ischemia-reperfusion rats based on ~1H-NMR].
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2020 Mar; 45(5):1142-1148. doi:
10.19540/j.cnki.cjcmm.20190619.505
. [PMID: 32237458] - Abdullah Shopit, Mengyue Niu, Hongyan Wang, Zhongyuan Tang, Xiaodong Li, Tsehaye Tesfaldet, Jie Ai, Nisar Ahmad, Mahmoud Al-Azab, Zeyao Tang. Protection of diabetes-induced kidney injury by phosphocreatine via the regulation of ERK/Nrf2/HO-1 signaling pathway.
Life sciences.
2020 Feb; 242(?):117248. doi:
10.1016/j.lfs.2019.117248
. [PMID: 31899224] - Kirill Gorshkov, Amy Q Wang, Wei Sun, Ethan Fisher, Marta Frigeni, Marc Singleton, Natasha Thorne, Bradley Class, Wenwei Huang, Nicola Longo, Minh-Ha T Do, Elizabeth A Ottinger, Xin Xu, Wei Zheng. Phosphocyclocreatine is the dominant form of cyclocreatine in control and creatine transporter deficiency patient fibroblasts.
Pharmacology research & perspectives.
2019 12; 7(6):e00525. doi:
10.1002/prp2.525
. [PMID: 31859463] - Heng Xi, Ailin Zhang, Guozhu Han, Chuanxun Li, Li Lv. Pharmacokinetics and hemorheology of phosphocreatine and creatine in rabbits: A directly comparative study between parent drug and active metabolite.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.
2019 Oct; 138(?):105033. doi:
10.1016/j.ejps.2019.105033
. [PMID: 31382031] - Ning Sun, Qirui Li, Libo Zhao, Huan He, Meng Zhang, Xiaoling Wang. Simultaneous quantitative analysis of phosphocreatine, creatine and creatinine in plasma of children by HPLC-MS/MS method: Application to a pharmacokinetic study in children with viral myocarditis.
Biomedical chromatography : BMC.
2019 Aug; 33(8):e4558. doi:
10.1002/bmc.4558
. [PMID: 31013362] - Gessica Perin, Matheus D Baldissera, Antonise M Jaguezeski, Regiane B Crecencio, Lenita M Stefani, Anderson Gris, Ricardo E Mendes, Carine F Souza, Vanessa Dalzuk, Aleksandro S da Silva. Involvement of the phosphoryl transfer network on cardiac energetic metabolism during Staphylococcus aureus infection and its association to disease pathophysiology.
Microbial pathogenesis.
2019 Jan; 126(?):318-322. doi:
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