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Details

Stereochemistry ABSOLUTE
Molecular Formula C10H10N4O3
Molecular Weight 234.2114
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2',3'-DIDEOXY-2',3'-DIDEHYDROINOSINE

SMILES

OC[C@H]1O[C@H](C=C1)N2C=NC3=C2N=CNC3=O

InChI

InChIKey=TYQPBHYPIRLWKU-NKWVEPMBSA-N
InChI=1S/C10H10N4O3/c15-3-6-1-2-7(17-6)14-5-13-8-9(14)11-4-12-10(8)16/h1-2,4-7,15H,3H2,(H,11,12,16)/t6-,7+/m0/s1

HIDE SMILES / InChI

Molecular Formula C10H10N4O3
Molecular Weight 234.2114
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 03:27:57 GMT 2023
Edited
by admin
on Sat Dec 16 03:27:57 GMT 2023
Record UNII
849Y7EQ734
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2',3'-DIDEOXY-2',3'-DIDEHYDROINOSINE
Systematic Name English
DIDANOSINE IMPURITY F [WHO-IP]
Common Name English
INOSINE, 2',3'-DIDEHYDRO-2',3'-DIDEOXY-
Systematic Name English
DIDANOSINE IMPURITY, DIDEOXYDIDEHYDROINOSINE- [USP IMPURITY]
Common Name English
DIDANOSINE IMPURITY F [EP IMPURITY]
Common Name English
DIDANOSINE IMPURITY F
EP   WHO-IP  
Common Name English
9-(2,3-DIDEOXY-.BETA.-D-GLYCERO-PENT-2-ENOFURANOSYL)-1,9-DIHYDRO-6H-PURIN-6-ONE [WHO-IP]
Systematic Name English
DIDEOXYDIDEHYDROINOSINE
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID80195544
Created by admin on Sat Dec 16 03:27:57 GMT 2023 , Edited by admin on Sat Dec 16 03:27:57 GMT 2023
PRIMARY
PUBCHEM
135418295
Created by admin on Sat Dec 16 03:27:57 GMT 2023 , Edited by admin on Sat Dec 16 03:27:57 GMT 2023
PRIMARY
FDA UNII
849Y7EQ734
Created by admin on Sat Dec 16 03:27:57 GMT 2023 , Edited by admin on Sat Dec 16 03:27:57 GMT 2023
PRIMARY
CAS
42867-68-5
Created by admin on Sat Dec 16 03:27:57 GMT 2023 , Edited by admin on Sat Dec 16 03:27:57 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 F about 0.8. The area of any individual peak corresponding to impurity F is not greater than 0.2 times the area of the principal peak obtained with solution (4) (0.2%).
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP