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{{Unreferenced|date=October 2006}}
{{Chembox
{{Chembox
| verifiedrevid = 400825361
| verifiedrevid = 447288275
|ImageFile=DAMP chemical structure.png
| ImageFile=DAMP chemical structure.png
| ImageAlt = Skeletal formula of deoxyadenosine monophosphate
|ImageSize=
| ImageFile1 = Deoxyadenosine-monophosphate-anion-3D-balls.png
|IUPACName=
| ImageSize1 = 220
|OtherNames=
| ImageAlt1 = Ball-and-stick model of the deoxyadenosine monophosphate anion
|Section1= {{Chembox Identifiers
| IUPACName=2′-Deoxyadenylic acid
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| SystematicName=[(2''R'',3''S'',5''R'')-5-(6-Amino-9''H''-purin-9-yl)-3-hydroxyoxolan-2-yl]methyl dihydrogen phosphate
| OtherNames=
|Section1={{Chembox Identifiers
| IUPHAR_ligand = 5120
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 12079
| ChemSpiderID = 12079
| InChI = 1/C10H14N5O6P/c11-9-8-10(13-3-12-9)15(4-14-8)7-1-5(16)6(21-7)2-20-22(17,18)19/h3-7,16H,1-2H2,(H2,11,12,13)(H2,17,18,19)/t5-,6+,7+/m0/s1
| InChI = 1/C10H14N5O6P/c11-9-8-10(13-3-12-9)15(4-14-8)7-1-5(16)6(21-7)2-20-22(17,18)19/h3-7,16H,1-2H2,(H2,11,12,13)(H2,17,18,19)/t5-,6+,7+/m0/s1
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| CASNo_Ref = {{cascite|correct|CAS}}
| CASNo_Ref = {{cascite|correct|CAS}}
| CASNo=653-63-4
| CASNo=653-63-4
| UNII_Ref = {{fdacite|correct|FDA}}
| PubChem=621
| ChEBI = 17713
| UNII = VFR8I97ORM
| PubChem=621
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI = 17713
| SMILES = c1nc(c2c(n1)n(cn2)[C@H]3C[C@@H]([C@H](O3)COP(=O)(O)O)O)N
| SMILES = c1nc(c2c(n1)n(cn2)[C@H]3C[C@@H]([C@H](O3)COP(=O)(O)O)O)N
| MeSHName=Deoxyadenosine+monophosphate
| MeSHName=Deoxyadenosine+monophosphate
}}
}}
|Section2= {{Chembox Properties
|Section2={{Chembox Properties
| Formula=C<sub>10</sub>H<sub>14</sub>N<sub>5</sub>O<sub>6</sub>P
| Formula=C<sub>10</sub>H<sub>14</sub>N<sub>5</sub>O<sub>6</sub>P
| MolarMass=331.222 g/mol
| MolarMass=331.222 g/mol
| Appearance=
| Appearance=
| Density=
| Density=
| MeltingPt=
| MeltingPt=
| BoilingPt=
| BoilingPt=
| Solubility=
| Solubility=
}}
}}
|Section3= {{Chembox Hazards
|Section3={{Chembox Hazards
| MainHazards=
| MainHazards=
| FlashPt=
| FlashPt=
| AutoignitionPt =
| Autoignition=
}}
}}
}}
}}

{{Context|article|date=October 2009}}
'''Deoxyadenosine monophosphate''', also known as '''deoxyadenylate''', or '''dAMP''', is a derivative of the common [[nucleic acid]] AMP, or [[adenosine monophosphate]], in which the -OH ([[hydroxyl]]) group on the 2' carbon on the nucleotide's [[pentose]] has been reduced to just a hydrogen atom (hence the "deoxy-" part of the name). The monophosphate of the name indicates that two of the [[phosphoryl]] groups of ATP have been removed, most likely by [[hydrolysis]].
'''Deoxyadenosine monophosphate''' ('''dAMP'''), also known as '''deoxyadenylic acid''' or '''deoxyadenylate''' in its [[conjugate acid]] and conjugate base forms, respectively, is a derivative of the common [[nucleotide]] AMP, or [[adenosine monophosphate]], in which the -OH ([[hydroxyl]]) group on the 2' carbon on the nucleotide's [[pentose]] has been reduced to just a hydrogen atom (hence the "deoxy-" part of the name). Deoxyadenosine monophosphate is abbreviated dAMP. It is a [[monomer]] used in [[DNA]].
Deoxyadenosine monophosphate is abbreviated dAMP.


==See also==
==See also==
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*[[Cyclic AMP]] (cAMP)
*[[Cyclic AMP]] (cAMP)
*[[Adenosine Triphosphate|ATP]]
*[[Adenosine Triphosphate|ATP]]

==Sources==
* {{cite HMDB|author1-link=David S. Wishart|url=http://www.hmdb.ca/metabolites/HMDB00905|title=Showing metabocard for Deoxyadenosine monophosphate (HMDB0000905)}}


{{Nucleobases, nucleosides, and nucleotides}}
{{Nucleobases, nucleosides, and nucleotides}}
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{{DEFAULTSORT:Deoxyadenosine Monophosphate}}
{{DEFAULTSORT:Deoxyadenosine Monophosphate}}
[[Category:Nucleotides]]
[[Category:Nucleotides]]



{{Biochemistry-stub}}
{{Biochemistry-stub}}

[[ca:Monofosfat de desoxiadenosina]]
[[fr:Désoxyadénosine monophosphate]]
[[gl:Desoxiadenosina monofosfato]]
[[nl:Deoxyadenosinemonofosfaat]]
[[ja:デオキシアデノシン一リン酸]]
[[sr:Dezoksiadenozin-monofosfat]]
[[zh:脫氧腺苷單磷酸]]