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EHNA hydrochloride (Synonyms: erythro-9-(2-Hydroxy-3-nonyl)adenine)

Katalog-Nr.GC10935

EHNA-Hydrochlorid ist ein potenter und selektiver dualer Inhibitor der zyklischen Nukleotid-Phosphodiesterase 2 (PDE2) (IC50=4 μM) und der Adenosindeaminase (ADA).

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EHNA hydrochloride Chemische Struktur

Cas No.: 58337-38-5

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5mg
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10mg
82,00 $
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25mg
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Sample solution is provided at 25 µL, 10mM.

Description of EHNA hydrochloride

EHNA is a reversible adenosine deaminase inhibitor (IC50 = 1.2 μM in human red blood cells) that also selectively inhibits the cGMP-specific phosphodiesterase (PDE2) (IC50s = 0.8 and 2 μM from human and porcine myocardium, respectively, 3.5 μM in rat hepatocyte, and 5.5 μM in human platelet).[1],[2] Comparatively, EHNA is much less potent at inhibiting PDE1, PDE3, or PDE4 (IC50s > 100 μM).1 EHNA has been used to evaluate cardioprotective and neuroprotective effects during ischemia, to study the role of cAMP/cGMP signaling, and to maintain pluripotency/prevent differentiation of human embryonic stem cells.[3],[4][5]

Reference
[1]. Podzuweit, T., Nennstiel, P., and Müller, A. Isozyme selective inhibition of cGMP-stimulated cyclic nucleotide phosphodiesterases by erythro-9-(2-hydroxy-3-nonyl) adenine. Cell. Signal. 7(7), 733-738 (1995).[
[2]. Michie, A.M., Lobban, M., Müller, T., et al. Rapid regulation of PDE-2 and PDE-4 cyclic AMP phosphodiesterase activity following ligation of the T cell antigen receptor on thymocytes: Analysis using the selective inhibitors erythro-9-(2-hydroxy-3-nonyl)-adenine (EHNA) and rolipram. Cell. Signal. 8(2), 97-110 (1996).
[3]. Barankiewicz, J., Danks, A.M., Abushanab, E., et al. Regulation of adenosine concentration and cytoprotective effects of novel reversible adenosine deaminase inhibitors. J. Pharmacol. Exp. Ther. 283(3), 1230-1238 (1997).
[4]. Dickinson, N.T., Jang, E.K., and Haslam, R.J. Activation of cGMP-stimulated phosphodiesterase by nitroprusside limits cAMP accumulation in human platelets: Effects on platelet aggregation. Biochem. J. 323(Pt. 2), 371-377 (1997).
[5]. Burton, P., Adams, D.R., Abraham, A., et al. Erythro-9-(2-hydroxy-3-nonyl)adenine (EHNA) blocks differentiation and maintains the expression of pluripotency markers in human embryonic stem cells. Biochem. J. 432(3), 575-584 (2010).

Chemical Properties of EHNA hydrochloride

Cas No. 58337-38-5 SDF
Überlieferungen erythro-9-(2-Hydroxy-3-nonyl)adenine
Chemical Name (2R,3S)-3-(6-amino-9H-purin-9-yl)nonan-2-ol hydrochloride
Canonical SMILES O[C@H](C)[C@H](CCCCCC)N1C2=NC=NC(N)=C2N=C1.Cl
Formula C14H23N5O.HCl M.Wt 313.83
Löslichkeit 30mg/mL in DMSO, 30mg/mL in DMF, 20mg/mL in Ethanol, 10mg/mL in Water Storage Store at -20°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of EHNA hydrochloride

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1 mg 5 mg 10 mg
1 mM 3.1864 mL 15.9322 mL 31.8644 mL
5 mM 0.6373 mL 3.1864 mL 6.3729 mL
10 mM 0.3186 mL 1.5932 mL 3.1864 mL
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Average Rating: 5 ★★★★★ (Based on Reviews and 37 reference(s) in Google Scholar.)

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