From Wikipedia, the free encyclopedia
EHNA
Identifiers
  • 3-(6-aminopurin-9-yl)nonan-2-ol
CAS Number
PubChem CID
ChemSpider
ChEMBL
CompTox Dashboard ( EPA)
Chemical and physical data
FormulaC14H23N5O
Molar mass277.372 g·mol−1
3D model ( JSmol)
  • CCCCCCC(C(C)O)n1cnc2c1ncnc2N
  • InChI=1S/C14H23N5O/c1-3-4-5-6-7-11(10(2)20)19-9-18-12-13(15)16-8-17-14(12)19/h8-11,20H,3-7H2,1-2H3,(H2,15,16,17)
  • Key:IOSAAWHGJUZBOG-UHFFFAOYSA-N
   (verify)

EHNA (erythro-9-(2-hydroxy-3-nonly)adenine) is a potent adenosine deaminase inhibitor, [1] which also acts as a phosphodiesterase inhibitor that selectively inhibits phosphodiesterase type 2 (PDE2). [2] [3]

References

  1. ^ "Sigma Aldrich". Retrieved 16 January 2013.
  2. ^ Podzuweit T, Nennstiel P, Müller A (September 1995). "Isozyme selective inhibition of cGMP-stimulated cyclic nucleotide phosphodiesterases by erythro-9-(2-hydroxy-3-nonyl) adenine". Cellular Signalling. 7 (7): 733–8. doi: 10.1016/0898-6568(95)00042-N. PMID  8519602.
  3. ^ Méry PF, Pavoine C, Pecker F, Fischmeister R (July 1995). "Erythro-9-(2-hydroxy-3-nonyl)adenine inhibits cyclic GMP-stimulated phosphodiesterase in isolated cardiac myocytes". Molecular Pharmacology. 48 (1): 121–30. PMID  7623766.


From Wikipedia, the free encyclopedia
EHNA
Identifiers
  • 3-(6-aminopurin-9-yl)nonan-2-ol
CAS Number
PubChem CID
ChemSpider
ChEMBL
CompTox Dashboard ( EPA)
Chemical and physical data
FormulaC14H23N5O
Molar mass277.372 g·mol−1
3D model ( JSmol)
  • CCCCCCC(C(C)O)n1cnc2c1ncnc2N
  • InChI=1S/C14H23N5O/c1-3-4-5-6-7-11(10(2)20)19-9-18-12-13(15)16-8-17-14(12)19/h8-11,20H,3-7H2,1-2H3,(H2,15,16,17)
  • Key:IOSAAWHGJUZBOG-UHFFFAOYSA-N
   (verify)

EHNA (erythro-9-(2-hydroxy-3-nonly)adenine) is a potent adenosine deaminase inhibitor, [1] which also acts as a phosphodiesterase inhibitor that selectively inhibits phosphodiesterase type 2 (PDE2). [2] [3]

References

  1. ^ "Sigma Aldrich". Retrieved 16 January 2013.
  2. ^ Podzuweit T, Nennstiel P, Müller A (September 1995). "Isozyme selective inhibition of cGMP-stimulated cyclic nucleotide phosphodiesterases by erythro-9-(2-hydroxy-3-nonyl) adenine". Cellular Signalling. 7 (7): 733–8. doi: 10.1016/0898-6568(95)00042-N. PMID  8519602.
  3. ^ Méry PF, Pavoine C, Pecker F, Fischmeister R (July 1995). "Erythro-9-(2-hydroxy-3-nonyl)adenine inhibits cyclic GMP-stimulated phosphodiesterase in isolated cardiac myocytes". Molecular Pharmacology. 48 (1): 121–30. PMID  7623766.



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