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

Details

Stereochemistry ABSOLUTE
Molecular Formula C10H13N5O
Molecular Weight 219.2431
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2',3',5'-TRIDEOXYADENOSINE

SMILES

C[C@@H]1CC[C@@H](O1)N2C=NC3=C2N=CN=C3N

InChI

InChIKey=PSPPXRNUZVTTON-RNFRBKRXSA-N
InChI=1S/C10H13N5O/c1-6-2-3-7(16-6)15-5-14-8-9(11)12-4-13-10(8)15/h4-7H,2-3H2,1H3,(H2,11,12,13)/t6-,7-/m1/s1

HIDE SMILES / InChI

Molecular Formula C10H13N5O
Molecular Weight 219.2431
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 03:31:15 GMT 2023
Edited
by admin
on Sat Dec 16 03:31:15 GMT 2023
Record UNII
43XPX901BB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2',3',5'-TRIDEOXYADENOSINE
Systematic Name English
9-(TETRAHYDRO-5-METHYL-2-FURYL)ADENINE
Systematic Name English
SQ-22538
Code English
ADENOSINE, 2',3',5'-TRIDEOXY-
Systematic Name English
DIDANOSINE IMPURITY, 5'-DEOXYDIDEOXYADENOSINE- [USP IMPURITY]
Common Name English
DIDANOSINE IMPURITY H [EP IMPURITY]
Common Name English
DIDANOSINE IMPURITY H
EP  
Common Name English
SQ 22538
Code English
Code System Code Type Description
CAS
6612-70-0
Created by admin on Sat Dec 16 03:31:15 GMT 2023 , Edited by admin on Sat Dec 16 03:31:15 GMT 2023
PRIMARY
FDA UNII
43XPX901BB
Created by admin on Sat Dec 16 03:31:15 GMT 2023 , Edited by admin on Sat Dec 16 03:31:15 GMT 2023
PRIMARY
PUBCHEM
65165
Created by admin on Sat Dec 16 03:31:15 GMT 2023 , Edited by admin on Sat Dec 16 03:31:15 GMT 2023
PRIMARY
EPA CompTox
DTXSID40216320
Created by admin on Sat Dec 16 03:31:15 GMT 2023 , Edited by admin on Sat Dec 16 03:31:15 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
In the chromatogram obtained with solution (2), the following peaks are eluted at the following relative retention with reference to didanosine (retention time about 13-15 min): impurity H about 2.0.
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP