Adenosine 2′-phosphate
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Adenosine 2′-phosphate
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CAS No:
130-49-4
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Formula:
C10H14N5O7P
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Chemical Name:
Adenosine 2′-phosphate
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Synonyms:
2′-Adenylic acid;2′-AMP;Adenosine 2′-phosphate;Adenosine 2′-monophosphate;Adenosine 2′-(dihydrogen phosphate);27082-34-4;293738-05-3
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CAS No:
Description
Adenosine-2'-monophosphate (2'-AMP) is converted by extracellular 2’,3'-CAMP. Adenosine-2'-monophosphate is further metabolized to extracellular adenosine (a mechanism called the extracellular 2’,3’-cAMP-adenosine pathway). Adenosine-2'-monophosphate inhibits LPS-induced TNF-α and CXCL10 production via A2A receptor activation[1][2].
Adenosine 2'-phosphate is a purine ribonucleoside 2'-monophosphate. It has a role as a Saccharomyces cerevisiae metabolite. It is a conjugate acid of an adenosine 2'-phosphate(2-).|Adenine nucleotide containing one phosphate group esterified to the sugar moiety in the 2'-, 3'-, or 5'-position.
Characteristics
195.88000
-1.74
2.3±0.1 g/cm3
183 °C
815.5±75.0 °C at 760 mmHg
447.0±37.1 °C
1.905
−20°C
Computed Properties
Molecular Weight:347.22
XLogP3:-2.1
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:11
Rotatable Bond Count:4
Exact Mass:347.06308480
Monoisotopic Mass:347.06308480
Topological Polar Surface Area:186
Heavy Atom Count:23
Complexity:481
Defined Atom Stereocenter Count:4
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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