NCBI Taxonomy: 56621
Pseudomyrmex (ncbi_taxid: 56621)
found 8 associated metabolites at genus taxonomy rank level.
Ancestor: Pseudomyrmecinae
Child Taxonomies: Pseudomyrmex ita, Pseudomyrmex oki, Pseudomyrmex pallidus, Pseudomyrmex pupa, Pseudomyrmex major, Pseudomyrmex lisus, Pseudomyrmex faber, Pseudomyrmex niger, Pseudomyrmex ferox, Pseudomyrmex ultrix, Pseudomyrmex evitus, Pseudomyrmex micans, Pseudomyrmex apache, Pseudomyrmex boopis, Pseudomyrmex pazosi, Pseudomyrmex tenuis, Pseudomyrmex viduus, Pseudomyrmex peperi, Pseudomyrmex lizeri, Pseudomyrmex longus, Pseudomyrmex cretus, Pseudomyrmex duckei, Pseudomyrmex osurus, Pseudomyrmex fortis, Pseudomyrmex mordax, Pseudomyrmex feralis, Pseudomyrmex obtusus, Pseudomyrmex cordiae, Pseudomyrmex godmani, Pseudomyrmex pallens, Pseudomyrmex simplex, Pseudomyrmex subater, Pseudomyrmex salvini, Pseudomyrmex atripes, Pseudomyrmex eduardi, Pseudomyrmex ejectus, Pseudomyrmex ethicus, Pseudomyrmex goeldii, Pseudomyrmex janzeni, Pseudomyrmex lynceus, Pseudomyrmex schuppi, Pseudomyrmex urbanus, Pseudomyrmex eculeus, Pseudomyrmex concolor, Pseudomyrmex oculatus, Pseudomyrmex sericeus, Pseudomyrmex spiculus, Pseudomyrmex mixtecus, Pseudomyrmex beccarii, Pseudomyrmex fervidus, Pseudomyrmex gebellii, Pseudomyrmex malignus, Pseudomyrmex gracilis, Pseudomyrmex seminole, Pseudomyrmex unicolor, Pseudomyrmex venustus, Pseudomyrmex crudelis, Pseudomyrmex insuavis, Pseudomyrmex kuenckeli, Pseudomyrmex cubaensis, Pseudomyrmex haytianus, Pseudomyrmex holmgreni, Pseudomyrmex perboscii, Pseudomyrmex satanicus, Pseudomyrmex spinicola, Pseudomyrmex caeciliae, Pseudomyrmex championi, Pseudomyrmex depressus, Pseudomyrmex elongatus, Pseudomyrmex maculatus, Pseudomyrmex opaciceps, Pseudomyrmex particeps, Pseudomyrmex santschii, Pseudomyrmex veneficus, Pseudomyrmex dendroicus, Pseudomyrmex filiformis, Pseudomyrmex euryblemma, Pseudomyrmex laevifrons, Pseudomyrmex laevigatus, Pseudomyrmex rufomedius, Pseudomyrmex flavidulus, Pseudomyrmex hospitalis, Pseudomyrmex inquilinus, Pseudomyrmex penetrator, Pseudomyrmex rubiginosus, Pseudomyrmex denticollis, Pseudomyrmex elongatulus, Pseudomyrmex flavicornis, Pseudomyrmex tachigaliae, Pseudomyrmex tenuissimus, Pseudomyrmex acanthobius, Pseudomyrmex curacaensis, Pseudomyrmex laevivertex, Pseudomyrmex ferrugineus, Pseudomyrmex termitarius, Pseudomyrmex rufiventris, Pseudomyrmex triplaridis, Pseudomyrmex triplarinus, Pseudomyrmex nigrocinctus, Pseudomyrmex nigropilosus, Pseudomyrmex phyllophilus, unclassified Pseudomyrmex, Pseudomyrmex cf. cocae PSW-2015, Pseudomyrmex cf. pallens PSW-2015, Pseudomyrmex cf. simplex PSW-2015, Pseudomyrmex cf. gracilis PSW-2015, Pseudomyrmex cf. sericeus PSW-2015, Pseudomyrmex nr. spiculus PSW-2015, Pseudomyrmex nr. championi PSW-2015, Pseudomyrmex nr. cladoicus PSW-2015, Pseudomyrmex nr. peruvianus PSW-2015, Pseudomyrmex aff. flavicornis-a MAS-2013, Pseudomyrmex aff. flavicornis-b MAS-2013, Pseudomyrmex aff. flavicornis-c MAS-2013
Adenosine
C10H13N5O4 (267.09674980000005)
Adenosine is a ribonucleoside composed of a molecule of adenine attached to a ribofuranose moiety via a beta-N(9)-glycosidic bond. It has a role as an anti-arrhythmia drug, a vasodilator agent, an analgesic, a human metabolite and a fundamental metabolite. It is a purines D-ribonucleoside and a member of adenosines. It is functionally related to an adenine. The structure of adenosine was first described in 1931, though the vasodilating effects were not described in literature until the 1940s. Adenosine is indicated as an adjunct to thallium-201 in myocardial perfusion scintigraphy, though it is rarely used in this indication, having largely been replaced by [dipyridamole] and [regadenson]. Adenosine is also indicated in the treatment of supraventricular tachycardia. Adenosine was granted FDA approval on 30 October 1989. Adenosine is a metabolite found in or produced by Escherichia coli (strain K12, MG1655). Adenosine is an Adenosine Receptor Agonist. The mechanism of action of adenosine is as an Adenosine Receptor Agonist. Adenosine is a natural product found in Smilax bracteata, Mikania laevigata, and other organisms with data available. Adenosine is a ribonucleoside comprised of adenine bound to ribose, with vasodilatory, antiarrhythmic and analgesic activities. Phosphorylated forms of adenosine play roles in cellular energy transfer, signal transduction and the synthesis of RNA. Adenosine is a nucleoside that is composed of adenine and d-ribose. Adenosine or adenosine derivatives play many important biological roles in addition to being components of DNA and RNA. For instance, adenosine plays an important role in energy transfer - as adenosine triphosphate (ATP) and adenosine diphosphate (ADP). It also plays a role in signal transduction as cyclic adenosine monophosphate, cAMP. Adenosine itself is both a neurotransmitter and potent vasodilator. When administered intravenously, adenosine causes transient heart block in the AV node. Because of the effects of adenosine on AV node-dependent supraventricular tachycardia, adenosine is considered a class V antiarrhythmic agent. Adenosine is a metabolite found in or produced by Saccharomyces cerevisiae. A nucleoside that is composed of adenine and d-ribose. Adenosine or adenosine derivatives play many important biological roles in addition to being components of DNA and RNA. Adenosine itself is a neurotransmitter. See also: Adenosine; Niacinamide (component of); Adenosine; Glycerin (component of); Adenosine; ginsenosides (component of) ... View More ... Adenosine is a nucleoside that is composed of adenine and D-ribose. Adenosine or adenosine derivatives play many important biological roles in addition to being components of DNA and RNA. For instance, adenosine plays an important role in energy transfer as adenosine triphosphate (ATP) and adenosine diphosphate (ADP). It also plays a role in signal transduction as cyclic adenosine monophosphate (cAMP). Adenosine itself is both a neurotransmitter and potent vasodilator. When administered intravenously adenosine causes transient heart block in the AV node. Due to the effects of adenosine on AV node-dependent supraventricular tachycardia, adenosine is considered a class V antiarrhythmic agent. Overdoses of adenosine intake (as a drug) can lead to several side effects including chest pain, feeling faint, shortness of breath, and tingling of the senses. Serious side effects include a worsening dysrhythmia and low blood pressure. When present in sufficiently high levels, adenosine can act as an immunotoxin and a metabotoxin. An immunotoxin disrupts, limits the function, or destroys immune cells. A metabotoxin is an endogenous metabolite that causes adverse health effects at chronically high levels. Chronically high levels of adenosine are associated with adenosine deaminase deficiency. Adenosine is a precursor to deoxyadenosine, which is a precursor to dATP. A buildup of dATP in cells inhibits ribonucleotide reductase and prevents DNA synthesis, so cells are unable to divide. Since developing T cells and B cells are some of the most mitotically active cells, they are unable to divide and propagate to respond to immune challenges. High levels of deoxyadenosine also lead to an increase in S-adenosylhomocysteine, which is toxic to immature lymphocytes. Adenosine is a nucleoside composed of a molecule of adenine attached to a ribose sugar molecule (ribofuranose) moiety via a beta-N9-glycosidic bond. [Wikipedia]. Adenosine is found in many foods, some of which are borage, japanese persimmon, nuts, and barley. COVID info from PDB, Protein Data Bank, COVID-19 Disease Map, clinicaltrial, clinicaltrials, clinical trial, clinical trials A ribonucleoside composed of a molecule of adenine attached to a ribofuranose moiety via a beta-N(9)-glycosidic bond. Adenosine. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=58-61-7 (retrieved 2024-06-29) (CAS RN: 58-61-7). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Adenosine (Adenine riboside), a ubiquitous endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physiology, including neuronal activity, vascular function, platelet aggregation, and blood cell regulation[1][2]. Adenosine (Adenine riboside), a ubiquitous endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physiology, including neuronal activity, vascular function, platelet aggregation, and blood cell regulation[1][2]. Adenosine (Adenine riboside), a ubiquitous endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physiology, including neuronal activity, vascular function, platelet aggregation, and blood cell regulation[1][2].
Adenosine
C10H13N5O4 (267.09674980000005)
COVID info from PDB, Protein Data Bank, COVID-19 Disease Map, clinicaltrial, clinicaltrials, clinical trial, clinical trials D018377 - Neurotransmitter Agents > D058905 - Purinergic Agents > D058913 - Purinergic Agonists D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002317 - Cardiovascular Agents > D000889 - Anti-Arrhythmia Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D002317 - Cardiovascular Agents > D014665 - Vasodilator Agents C - Cardiovascular system > C01 - Cardiac therapy Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Formula(Parent): C10H13N5O4; Bottle Name:Adenosine; PRIME Parent Name:Adenosine; PRIME in-house No.:0040 R0018, Purines MS2 deconvoluted using MS2Dec from all ion fragmentation data, MetaboLights identifier MTBLS1040; OIRDTQYFTABQOQ_STSL_0143_Adenosine_0500fmol_180430_S2_LC02_MS02_33; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. MS2 deconvoluted using CorrDec from all ion fragmentation data, MetaboLights identifier MTBLS1040; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. relative retention time with respect to 9-anthracene Carboxylic Acid is 0.113 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.109 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.097 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.096 Acquisition and generation of the data is financially supported by the Max-Planck-Society IPB_RECORD: 2621; CONFIDENCE confident structure Adenosine (Adenine riboside), a ubiquitous endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physiology, including neuronal activity, vascular function, platelet aggregation, and blood cell regulation[1][2]. Adenosine (Adenine riboside), a ubiquitous endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physiology, including neuronal activity, vascular function, platelet aggregation, and blood cell regulation[1][2]. Adenosine (Adenine riboside), a ubiquitous endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physiology, including neuronal activity, vascular function, platelet aggregation, and blood cell regulation[1][2].