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N<sup>6</sup>-Benzyladenosine, 99%|411372|4294-16-0

N6-Benzyladenosine, 99%

Cat. No JK411372_250_MG
J&K Chemical

Product Information

Product Name
N6-Benzyladenosine, 99%
Brand Name
J&K
Product Number
411372
CAS
4294-16-0
Molecular Formula
C17H19N5O4
Molecular Weight
357.36
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
6-Benzylaminopurine riboside
PubChem CID
92208
IUPAC Name
(2R,3R,4S,5R)-2-6-(benzylamino)purin-9-yl-5-(hydroxymethyl)oxolane-3,4-diol
InChI Key
MRPKNNSABYPGBF-LSCFUAHRSA-N
SMILES
C1=CC=C(C=C1)CNC2=C3C(=NC=N2)N(C=N3)C@H4C@@H(C@@H(C@H(O4)CO)O)O

Properties

Melting Point
184-186

Safety Information

Precautionary Statement
P262
Storage Condition
Store at 2-8℃

References Data Source From Pubchem

Hsa_circ_0038737 promotes PARPi resistance in castration-resistant prostate cancer via IGF2BP3-mediated DNPH1 mRNA stabilization
Publication Name: Molecular Cancer
Publication Date: 2025-10-02
DOI: 10.1186/s12943-025-02447-y

Elongation of N6-benzyladenosine scaffold via Pd-catalyzed C–C bond formation leads to derivatives with antiflaviviral activity
Publication Name: Bioorganic & Medicinal Chemistry
Publication Date: 2024-01-15
DOI: 10.1016/j.bmc.2023.117552

Toxic interactions between dopamine, α-synuclein, monoamine oxidase, and genes in mitochondria of Parkinson’s disease
Publication Name: Journal of neural transmission (Vienna, Austria : 1996)
Publication Date: 2024-01-09
DOI: 10.1007/s00702-023-02730-6

Insights into enterovirus a-71 antiviral development: from natural sources to synthetic nanoparticles
Publication Name: Archives of Microbiology
Publication Date: 2023-09-21
DOI: 10.1007/s00203-023-03660-3

PINK1-Dependent Mitophagy Inhibits Elevated Ubiquitin Phosphorylation Caused by Mitochondrial Damage
Publication Name: Journal of Medicinal Chemistry
Publication Date: 2023-05-30
DOI: 10.1021/acs.jmedchem.3c00555

N6-Benzyladenosine, 99%

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