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Details

Stereochemistry ACHIRAL
Molecular Formula C10H13N5O4
Molecular Weight 267.2413
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 9-(2-ACETOXYETHOXYMETHYL)GUANINE

SMILES

CC(=O)OCCOCN1C=NC2=C1N=C(N)NC2=O

InChI

InChIKey=DMHAXLGAKQREIL-UHFFFAOYSA-N
InChI=1S/C10H13N5O4/c1-6(16)19-3-2-18-5-15-4-12-7-8(15)13-10(11)14-9(7)17/h4H,2-3,5H2,1H3,(H3,11,13,14,17)

HIDE SMILES / InChI

Molecular Formula C10H13N5O4
Molecular Weight 267.2413
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis and biological evaluation of iodinated and fluorinated 9-(2-hydroxypropyl) and 9-(2-hydroxyethoxy)methyl purine nucleoside analogues.
2003 Dec 18
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 21:43:19 GMT 2025
Edited
by admin
on Mon Mar 31 21:43:19 GMT 2025
Record UNII
Y16CE349S3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-((2-AMINO-6-OXO-1,6-DIHYDRO-9H-PURIN-9-YL)METHOXY)ETHYL ACETATE
WHO-IP  
Preferred Name English
9-(2-ACETOXYETHOXYMETHYL)GUANINE
Systematic Name English
ACYCLOVIR RELATED COMPOUND A [USP IMPURITY]
Common Name English
6H-PURIN-6-ONE, 9-((2-(ACETYLOXY)ETHOXY)METHYL)-2-AMINO-1,9-DIHYDRO-
Systematic Name English
ACICLOVIR IMPURITY A [WHO-IP]
Common Name English
ACYCLOVIR RELATED COMPOUND A [USP-RS]
Common Name English
VALACICLOVIR HYDROCHLORIDE HYDRATE IMPURITY I [EP IMPURITY]
Common Name English
VALACYCLOVIR RELATED COMPOUND A [USP IMPURITY]
Common Name English
ACYCLOVIR ACETATE
Common Name English
ACICLOVIR IMPURITY A [EP IMPURITY]
Common Name English
VALACICLOVIR HYDROCHLORIDE IMPURITY I [EP IMPURITY]
Common Name English
Code System Code Type Description
PUBCHEM
135446930
Created by admin on Mon Mar 31 21:43:19 GMT 2025 , Edited by admin on Mon Mar 31 21:43:19 GMT 2025
PRIMARY
RS_ITEM_NUM
1012076
Created by admin on Mon Mar 31 21:43:19 GMT 2025 , Edited by admin on Mon Mar 31 21:43:19 GMT 2025
PRIMARY
CAS
102728-64-3
Created by admin on Mon Mar 31 21:43:19 GMT 2025 , Edited by admin on Mon Mar 31 21:43:19 GMT 2025
PRIMARY
FDA UNII
Y16CE349S3
Created by admin on Mon Mar 31 21:43:19 GMT 2025 , Edited by admin on Mon Mar 31 21:43:19 GMT 2025
PRIMARY
EPA CompTox
DTXSID50145470
Created by admin on Mon Mar 31 21:43:19 GMT 2025 , Edited by admin on Mon Mar 31 21:43:19 GMT 2025
PRIMARY
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EP
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