Adenosine N1-oxide

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C10H13N5O5
Molecular Weight	283.2407
Optical Activity	UNSPECIFIED
Defined Stereocenters	4 / 4
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

NC1=[N+]([O-])C=NC2=C1N=CN2[C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O

InChI

InChIKey=VYSCKHGOLQAMAT-KQYNXXCUSA-N

InChI=1S/C10H13N5O5/c11-8-5-9(13-3-15(8)19)14(2-12-5)10-7(18)6(17)4(1-16)20-10/h2-4,6-7,10,16-18H,1,11H2/t4-,6-,7-,10-/m1/s1

HIDE SMILES / InChI

Molecular Formula	C10H13N5O5
Molecular Weight	283.2407
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	4 / 4
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Targets

Primary Target	Pharmacology	Condition	Potency
viral gene expression 1 Target ID: GO:0019080 Sources: https://www.ncbi.nlm.nih.gov/pubmed/7666536	Inhibitor 8504

Substance Class	Chemical Created by `admin` on `Wed Apr 02 12:47:23 GMT 2025` Edited by `admin` on `Wed Apr 02 12:47:23 GMT 2025`
Record UNII	2K3CSJ5RMU
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

NSC-128561

Preferred Name

English

Adenosine N1-oxide

Common Name

English

1-Oxoadenosine

Common Name

English

Adenosine-1-N-oxide

Common Name

English

6-Amino-9-?-D-ribofuranosyl-9H-purine 1-oxide

Systematic Name

English

6-amino-9-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-9H-purine 1-oxide

Systematic Name

English

ADENOSINE N(1)-OXIDE

Common Name

English

Adenosine N-oxide

Common Name

English

Adenosine, 1-oxide

Common Name

English

Code System Code Type Description

FDA UNII

2K3CSJ5RMU

Created by admin on Wed Apr 02 12:47:23 GMT 2025 , Edited by admin on Wed Apr 02 12:47:23 GMT 2025

PRIMARY

EPA CompTox

DTXSID901019902

Created by admin on Wed Apr 02 12:47:23 GMT 2025 , Edited by admin on Wed Apr 02 12:47:23 GMT 2025

PRIMARY

NSC

128561

Created by admin on Wed Apr 02 12:47:23 GMT 2025 , Edited by admin on Wed Apr 02 12:47:23 GMT 2025

PRIMARY

CAS

146-92-9

Created by admin on Wed Apr 02 12:47:23 GMT 2025 , Edited by admin on Wed Apr 02 12:47:23 GMT 2025

PRIMARY