Adenosine (symbol A) is an organic compound that occurs widely in nature in the form of diverse derivatives. The molecule consists of an adenine attached to a ribose via a β-N9-glycosidic bond. Adenosine is one of the four nucleoside building blocks of RNA (and its derivative deoxyadenosine is a building block of DNA), which are essential for all life on Earth. Its derivatives include the energy carriers adenosine mono-, di-, and triphosphate, also known as AMP/ADP/ATP. Cyclic adenosine monophosphate (cAMP) is pervasive in signal transduction. Adenosine is used as an intravenous medication for some cardiac arrhythmias.
Adenosyl (abbreviated Ado or 5'-dAdo) is the chemical group formed by removal of the 5′-hydroxy (OH) group. It is found in adenosylcobalamin (an active form of vitamin B12) and as a radical in the radical SAM enzymes. |
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InChI=1S/C5H9NO4/c1-6-3(5(9)10)2-4(7)8/h3,6H,2H2,1H3,(H,7,8)(H,9,10)/t3-/m1/s1 |
HOKKHZGPKSLGJE-GSVOUGTGSA-N |
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Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
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neurotransmitter agent
A substance used for its pharmacological action on any aspect of neurotransmitter systems. Neurotransmitter agents include agonists, antagonists, degradation inhibitors, uptake inhibitors, depleters, precursors, and modulators of receptor function.
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neurotransmitter agent
A substance used for its pharmacological action on any aspect of neurotransmitter systems. Neurotransmitter agents include agonists, antagonists, degradation inhibitors, uptake inhibitors, depleters, precursors, and modulators of receptor function.
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View more via ChEBI Ontology
(R)-2-Methylamino-succinic acid
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ChEMBL
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2-Methylamino-succinic acid
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ChEMBL
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Methyl aspartic acid
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ChemIDplus
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N-Methyl aspartic acid
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ChemIDplus
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N-Methyl-D-aspartate
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KEGG COMPOUND
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N-Methyl-D-aspartic acid
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KEGG COMPOUND
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N-Methylaspartate
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ChemIDplus
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NMDA
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KEGG COMPOUND
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1724431
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Reaxys Registry Number
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Reaxys
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6384-92-5
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CAS Registry Number
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ChemIDplus
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10514280
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PubMed citation
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ChEMBL
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10893301
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PubMed citation
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ChEMBL
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1967316
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PubMed citation
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ChEMBL
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2170646
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PubMed citation
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ChEMBL
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3351864
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PubMed citation
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ChEMBL
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8568805
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PubMed citation
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ChEMBL
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9572889
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PubMed citation
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ChEMBL
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