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586846

N-Benzoyladenosine

Name: <I>N</I>-Benzoyladenosine
Brand: ALDRICH

96%

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About This Item

Empirical Formula (Hill Notation):

C₁₇H₁₇N₅O₅

CAS Number:

4546-55-8

Molecular Weight:

371.35

UNSPSC Code:

12352200

NACRES:

NA.22

PubChem Substance ID:

24881135

MDL number:

MFCD00056988

Beilstein/REAXYS Number:

632501

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Properties

Quality Level

100

assay

96%

form

solid

optical activity

[α]20/D -49°, c = 1% in DMSO

mp

141-145 °C (lit.)

SMILES string

OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n2cnc3c(NC(=O)c4ccccc4)ncnc23

InChI

1S/C17H17N5O5/c23-6-10-12(24)13(25)17(27-10)22-8-20-11-14(18-7-19-15(11)22)21-16(26)9-4-2-1-3-5-9/h1-5,7-8,10,12-13,17,23-25H,6H2,(H,18,19,21,26)/t10-,12-,13-,17-/m1/s1

InChI key

NZDWTKFDAUOODA-CNEMSGBDSA-N

Description

pictograms

GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Classical and systems genetics have identified wide networks of genes associated with cognitive and neurodevelopmental diseases. In parallel to deciphering the role of each of these genes in neuronal or synaptic function, evaluating the response of neuronal and molecular networks

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Kevin W-H Lo et al.

Journal of tissue engineering and regenerative medicine, 10(10), 867-875 (2014-02-05)

Small molecule-based regenerative engineering is emerging as a promising strategy for regenerating bone tissue. Small molecule cAMP analogues have been proposed as novel biofactors for bone repair and regeneration and, while promising, the effect that these small molecules have on

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Estelle R Simo-Cheyou et al.

Canadian journal of physiology and pharmacology, 95(8), 928-937 (2017-05-02)

cAMP has been shown to inhibit vascular smooth muscle cell proliferation and exerts a vasculoprotective effect. An upregulation of the early growth response protein-1 (Egr-1) expression has been linked with the development of atherosclerosis and intimal hyperplasia. We have recently

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