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

Details

Stereochemistry RACEMIC
Molecular Formula C9H13N5O4
Molecular Weight 255.2306
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ISOGANCICLOVIR

SMILES

NC1=NC2=C(N=CN2COCC(O)CO)C(=O)N1

InChI

InChIKey=YMJRISBBXAOKCD-UHFFFAOYSA-N
InChI=1S/C9H13N5O4/c10-9-12-7-6(8(17)13-9)11-3-14(7)4-18-2-5(16)1-15/h3,5,15-16H,1-2,4H2,(H3,10,12,13,17)

HIDE SMILES / InChI

Molecular Formula C9H13N5O4
Molecular Weight 255.2306
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Treatment of cytomegalovirus infections in renal transplant recipients with 9-(1,3-dihydroxy-2-propoxymethyl) guanine.
1988-06
Responses of neurologic complications of AIDS to 3'-azido-3'-deoxythymidine and 9-(1,3-dihydroxy-2-propoxymethyl) guanine. I. Clinical features.
1988-03-01
Successful treatment of cytomegalovirus disease with 9-(1,3-dihydroxy-2-propoxymethyl guanine).
1988-02
[Treatment of cytomegalovirus retinitis with dihydroxypropoxymethylguanine in a patient with acquired immunodeficiency syndrome].
1987-10-03
Synthesis of cytomegalovirus DNA is an antiviral target late in virus growth.
1987-06
Fine structure of cells infected with human cytomegalovirus after treatment with 9-(1,3-dihydroxy-2-propoxymethyl)guanine.
1987-06
Selection of a derivative of the antiviral agent 9-[(1,3-dihydroxy-2-propoxy)-methyl]guanine (DHPG) with improved oral absorption.
1987-04
Synthesis and antiviral activity of various esters of 9-[(1,3-dihydroxy-2-propoxy)methyl]guanine.
1987-02
Respiratory pharmacology. Antiviral agents.
1986-09
Synthesis and anti-herpes-virus activity of acyclic 2'-deoxyguanosine analogues related to 9-[(1,3-dihydroxy-2-propoxy)methyl]guanine.
1986-08
Successful treatment of murine cytomegalovirus disease does not prevent latent virus infection.
1986-08
Enzymatic phosphorylation of the antiherpetic agent 9-[(2,3-dihydroxy-1-propoxy)methyl]guanine.
1986-05
Synthesis and antiherpes virus activity of phosphate and phosphonate derivatives of 9-[(1,3-dihydroxy-2-propoxy)methyl]guanine.
1986-05
Treatment of serious cytomegalovirus infections with 9-(1,3-dihydroxy-2-propoxymethyl)guanine in patients with AIDS and other immunodeficiencies.
1986-03-27
Life-threatening cytomegalovirus infection treated with dihydropropoxymethylguanine.
1986-03-22
The ophthalmological features of AIDS and AIDS related disorders.
1986
Synthesis and antiherpetic activity of (S)-, (R)-, and (+/-)-9-[(2,3-dihydroxy-1-propoxy)methyl]guanine, linear isomers of 2'-nor-2'-deoxyguanosine.
1985-07
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 21:23:11 GMT 2025
Edited
by admin
on Mon Mar 31 21:23:11 GMT 2025
Record UNII
NNJ00018WY
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ISOGANCICLOVIR
Common Name English
GANCICLOVIR RELATED COMPOUND A
USP  
Preferred Name English
(±)-2-AMINO-9-((2,3-DIHYDROXYPROPOXY)METHYL)-1,9-DIHYDRO-6H-PURIN-6-ONE
Systematic Name English
GANCICLOVIR IMPURITY E [EP IMPURITY]
Common Name English
GANCICLOVIR RELATED COMPOUND A [USP-RS]
Common Name English
6H-PURIN-6-ONE, 2-AMINO-9-((2,3-DIHYDROXYPROPOXY)METHYL)-1,9-DIHYDRO-
Systematic Name English
(RS)-2-AMINO-9-(2,3-DIHYDROXY-PROPOXYMETHYL)-1,9-DIHYDRO-PURIN-6-ONE
Systematic Name English
2-AMINO-9-((2,3-DIHYDROXYPROPOXY)METHYL)-1,9-DIHYDRO-6H-PURIN-6-ONE
Systematic Name English
GANCICLOVIR RELATED COMPOUND A [USP IMPURITY]
Common Name English
2-AMINO-9-(((2RS)-2,3-DIHYDROXYPROPOXY)METHYL)-1,9-DIHYDRO-6H-PURIN-6-ONE
Systematic Name English
3-((2-AMINO-6-HYDROXY-9H-PURIN-9-YL)METHOXY)-1,2-PROPANEDIOL
Systematic Name English
Code System Code Type Description
RS_ITEM_NUM
1288317
Created by admin on Mon Mar 31 21:23:11 GMT 2025 , Edited by admin on Mon Mar 31 21:23:11 GMT 2025
PRIMARY
FDA UNII
NNJ00018WY
Created by admin on Mon Mar 31 21:23:11 GMT 2025 , Edited by admin on Mon Mar 31 21:23:11 GMT 2025
PRIMARY
CAS
86357-09-7
Created by admin on Mon Mar 31 21:23:11 GMT 2025 , Edited by admin on Mon Mar 31 21:23:11 GMT 2025
PRIMARY
PUBCHEM
135446919
Created by admin on Mon Mar 31 21:23:11 GMT 2025 , Edited by admin on Mon Mar 31 21:23:11 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> IMPURITY