Adenosine diphosphate

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Adenosine diphosphate
Skeletal formula o ADP
Baw-an-stick model o ADP (shawn here as a 3- ion)
Names
IUPAC name
[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphono hydrogen phosphate
Ither names
adenosine 5′-diphosphate
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.000.356
EC Nummer 218-249-0
KEGG
RTECS nummer AU7467000
Properties
C10H15N5O10P2
Molar mass 427.201 g/mol
Appearance white powder
Density 2.49 g/mL
Bylin pynt 877.7 °C (1,611.9 °F; 1,150.8 K)
log P -2.640
Hazards
Safety data sheet MSDS
Except whaur itherwise notit, data are gien for materials in thair staundart state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Adenosine diphosphate (ADP) (Adenosine pyrophosphate (APP)) is an important organic compoond in metabolism an is essential tae the flow o energy in livin cells. A molecule o ADP conseests o three important structural components: a succar backbane attached tae a molecule o adenine an twa phosphate groups bondit tae the 5 carbon atom o ribose. The carbon molecules that mak up the raing structur o a succar can be named in a way that mair specifically designates the location o the phosphate an adenosine attachments: The succar backbane o ADP is kent as a pentose succar an conseests o five carbon molecules. The twa phosphate groups o ADP are addit in series tae the 5’ carbon o the succar backbane, while the adenosine molecule attaches tae the 1’ carbon.[1]

References[eedit | eedit soorce]

  1. Cox, Michael; Nelson, David R.; Lehninger, Albert L (2008). Lehninger principles of biochemistry. San Francisco: W.H. Freeman. ISBN 0-7167-7108-X.