U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C12H17N5O4
Molecular Weight 295.2945
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N6,N6-DIMETHYLADENOSINE

SMILES

CN(C)C1=NC=NC2=C1N=CN2[C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O

InChI

InChIKey=WVGPGNPCZPYCLK-WOUKDFQISA-N
InChI=1S/C12H17N5O4/c1-16(2)10-7-11(14-4-13-10)17(5-15-7)12-9(20)8(19)6(3-18)21-12/h4-6,8-9,12,18-20H,3H2,1-2H3/t6-,8-,9-,12-/m1/s1

HIDE SMILES / InChI

Molecular Formula C12H17N5O4
Molecular Weight 295.2945
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Ribosome structure: localization of N6,N6-dimethyladenosine by electron microscopy of a ribosome-antibody complex.
1977 Apr
Analogs of 3'-amino-3'-deoxyadenosine inhibit HIV-1 replication.
1989 Dec
Synthesis of pyrrolo[2,3-d]pyrimidine nucleoside derivatives as potential anti-HCV agents.
2007 Feb
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:13:28 GMT 2023
Edited
by admin
on Sat Dec 16 08:13:28 GMT 2023
Record UNII
0L9766EW9W
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N6,N6-DIMETHYLADENOSINE
Systematic Name English
(2R,3R,4S,5R)-2-(6-(DIMETHYLAMINO)PURIN-9-YL)-5-(HYDROXYMETHYL)OXOLANE-3,4-DIOL
Systematic Name English
6-DIMETHYLAMINOPURINE D-RIBOSIDE
Common Name English
N,N-DIMETHYLADENOSINE
Systematic Name English
NSC-627046
Code English
C03416
Code English
N6-DIMETHYLADENOSINE
Common Name English
J108.278G
Code English
N,N-DIMETHYL-9-.BETA.-D-RIBOFURANOSYL-9H-PURINE-6-AMINE
Code English
Code System Code Type Description
CAS
2620-62-4
Created by admin on Sat Dec 16 08:13:28 GMT 2023 , Edited by admin on Sat Dec 16 08:13:28 GMT 2023
PRIMARY
CHEBI
28284
Created by admin on Sat Dec 16 08:13:28 GMT 2023 , Edited by admin on Sat Dec 16 08:13:28 GMT 2023
PRIMARY
NSC
627046
Created by admin on Sat Dec 16 08:13:28 GMT 2023 , Edited by admin on Sat Dec 16 08:13:28 GMT 2023
PRIMARY
EPA CompTox
DTXSID90949075
Created by admin on Sat Dec 16 08:13:28 GMT 2023 , Edited by admin on Sat Dec 16 08:13:28 GMT 2023
PRIMARY
ECHA (EC/EINECS)
220-057-7
Created by admin on Sat Dec 16 08:13:28 GMT 2023 , Edited by admin on Sat Dec 16 08:13:28 GMT 2023
PRIMARY
FDA UNII
0L9766EW9W
Created by admin on Sat Dec 16 08:13:28 GMT 2023 , Edited by admin on Sat Dec 16 08:13:28 GMT 2023
PRIMARY
PUBCHEM
440004
Created by admin on Sat Dec 16 08:13:28 GMT 2023 , Edited by admin on Sat Dec 16 08:13:28 GMT 2023
PRIMARY