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102029-87-8

102029-87-8 Structure

102029-87-8 Structure
IdentificationBack Directory
[Name]

ADENOSINE 5'-DIPHOSPHATE DI(MONOCYCLOHEXYLAMMONIUM) SALT
[CAS]

102029-87-8
[Synonyms]

methyl hydrogendiphosphate
Cyclohexanaminium ((2R,3S,4R,5R)
ADP DI(MONOCYCLOHEXYLAMMONIUM) SALT
adenosine 5'-diphosphate*di(monocyclohexylammoniu
ADENOSINE 5'-DIPHOSPHATEDI(MONOCYCLOHEXY LAMMONIUM)
Adenosine 5`-diphosphate di(dicyclohexyl)aMine salt
adenosine 5'-diphosphate bis(cyclohexylammonium) salt
ADENOSINE 5'-DIPHOSPHATE DI(MONOCYCLOHEXYLAMMONIUM) SALT
Adenosine 5′-diphosphate bis(cyclohexylammonium) salt,ADP
Adenosine 5'-(trihydrogen diphosphate) cyclohexanamine salt
Adenosine 5'-(trihydrogen diphosphate), compd. with cyclohexanamine (1:2) (9CI)
Adenosine 5'-diphosphate bis(cyclohexylammonium) salt >=95% (HPLC), crystalline, bacterial
Cyclohexanaminium ((2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)m
Cyclohexanaminium ((2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)meth
[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphono hydrogen phosphate cyclohexanamine
CyclohexanaMiniuM ((2R,3S,4R,5R)-5-(6-aMino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)Methyl hydrogendiphosphate
[Molecular Formula]

C22H41N7O10P2
[MDL Number]

MFCD00058338
[MOL File]

102029-87-8.mol
[Molecular Weight]

625.55
Chemical PropertiesBack Directory
[storage temp. ]

-20°C
[solubility ]

H2O: soluble, clear to slightly hazy, colorless to faintly yellow
[form ]

crystalline
[color ]

clear to slightly hazycolorless to faint yellowH2O
[biological source]

bacterial
[Water Solubility ]

H2O: soluble, clear to slightly hazy, colorless to faintly yellow
[InChIKey]

SCOUEIPNDLFPCX-IDIVVRGQSA-N
[SMILES]

NC1CCCCC1.NC2CCCCC2.Nc3ncnc4n(cnc34)[C@@H]5O[C@H](COP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]5O
Safety DataBack Directory
[WGK Germany ]

3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

Adenosine 5′-diphosphate (ADP) is an adenine nucleotide involved in energy storage and nucleic acid metabolism via its conversion into ATP by ATP synthases. ADP affects platelet activation through its interaction with ADP receptors P2Y1, P2Y12 and P2X1. Upon its conversion to adenosine by ecto-ADPases, platelet activation is inhibited via adenosine receptors.
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