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Details

Stereochemistry ACHIRAL
Molecular Formula C6H6N4O.CH4O3S
Molecular Weight 246.244
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DEZAGUANINE MESYLATE

SMILES

CS(O)(=O)=O.NC1=CC2=C(N=CN2)C(=O)N1

InChI

InChIKey=ZNTIXVYOBQDFFV-UHFFFAOYSA-N
InChI=1S/C6H6N4O.CH4O3S/c7-4-1-3-5(6(11)10-4)9-2-8-3;1-5(2,3)4/h1-2H,(H,8,9)(H3,7,10,11);1H3,(H,2,3,4)

HIDE SMILES / InChI

Molecular Formula C6H6N4O
Molecular Weight 150.138
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula CH4O3S
Molecular Weight 96.106
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Dezaguanine is a broad spectrum guanine antimetabolite. This compound differs from guanine only in the substitution of a carbon for the 3-nitrogen of guanine. Dezaguanine must be converted to its nucleotides to be active. Dezaguanine nucleotides inhibit synthesis of guanine nucleotides, and can be incorporated into nucleic acids in place of guanine nucleotides; incorporation into DNA may be particularly important in the cytotoxicity of this compound. Addition of certain purines or purine nucleosides can prevent dezaguanine cytotoxicity in vitro. It has exhibited sufficient preclinical antitumor activity, particularly against rat and mouse mammary adenocarcinomas, slow and fast growing mammary tumors in mice and the human breast xenograft subrenal capsule implant system. It has completed one phase I trial.

Approval Year

PubMed

PubMed

TitleDatePubMed
Expression and prognostic significance of IAP-family genes in human cancers and myeloid leukemias.
2000-05
Antiviral and immunomodulating inhibitors of experimentally-induced Punta Toro virus infections.
1994-10
Low molecular weight human T-cell response immunopotentiator: alpha-2'-deoxy-3-deazaguanosine.
1990
Inhibitory effect of selected antiviral compounds on measles (SSPE) virus replication in vitro.
1989-09
Inhibitory effects of antiviral compounds on respiratory syncytial virus replication in vitro.
1987-08
Selective inhibitory effect of (S)-9-(3-hydroxy-2-phosphonylmethoxypropyl)adenine and 2'-nor-cyclic GMP on adenovirus replication in vitro.
1987-02
Synthesis and antiviral/antitumor activities of certain 3-deazaguanine nucleosides and nucleotides.
1984-11
Inhibition of rotaviruses by selected antiviral substances: mechanisms of viral inhibition and in vivo activity.
1982-01
Synthesis and antiviral and enzymatic studies of certain 3-deazaguanines and their imidazolecarboxamide precursors.
1978-12
Antiviral activity of 3-deazaguanine, 3-deazaguanosine, and 3-deazaguanylic acid.
1977-07
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: Rat data
Dose - 140 mg/kg once daily for 9 days.
Route of Administration: Intraperitoneal
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:50:37 GMT 2025
Edited
by admin
on Mon Mar 31 17:50:37 GMT 2025
Record UNII
H56TJ4554M
Record Status Validated (UNII)
Record Version
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Name Type Language
DEZAGUANINE MESYLATE
USAN  
USAN  
Official Name English
DEZAGUANINE MESILATE
WHO-DD  
Preferred Name English
6-AMINO-1,5-DIHYDRO-4H-IMIDAZO(4,5-C)PYRIDINE-4-ONE MESILATE
Systematic Name English
CI-908 MESILATE
Common Name English
6-AMINO-1,5-DIHYDRO-4H-IMIDAZO(4,5-C)PYRIDIN-4-ONE MONOMETHANESULPHONATE
Systematic Name English
4H-IMIDAZO(4,5-C)PYRIDIN-4-ONE, 6-AMINO-1,5-DIHYDRO-, MONOMETHANESULPHONATE
Systematic Name English
DEZAGUANINE MESYLATE [USAN]
Common Name English
Dezaguanine mesilate [WHO-DD]
Common Name English
4H-IMIDAZO(4,5-C)PYRIDIN-4-ONE, 6-AMINO-1,5-DIHYDRO-, MONOMETHANESULFONATE
Systematic Name English
PD-90695-73
Code English
CI-908 MESYLATE
Code English
6-Amino-1,5-dihydro-4H-imidazo[4,5-c]pyridin-4-one monomethanesulfonate
Systematic Name English
6-AMINO-1,5-DIHYDRO-4H-IMIDAZO(4,5-C)PYRIDINE-4-ONE MESYLATE
Systematic Name English
PD 90,695-73
Code English
Classification Tree Code System Code
NCI_THESAURUS C1556
Created by admin on Mon Mar 31 17:50:37 GMT 2025 , Edited by admin on Mon Mar 31 17:50:37 GMT 2025
Code System Code Type Description
SMS_ID
300000055421
Created by admin on Mon Mar 31 17:50:37 GMT 2025 , Edited by admin on Mon Mar 31 17:50:37 GMT 2025
PRIMARY
CAS
87434-82-0
Created by admin on Mon Mar 31 17:50:37 GMT 2025 , Edited by admin on Mon Mar 31 17:50:37 GMT 2025
PRIMARY
PUBCHEM
55709
Created by admin on Mon Mar 31 17:50:37 GMT 2025 , Edited by admin on Mon Mar 31 17:50:37 GMT 2025
PRIMARY
USAN
W-21
Created by admin on Mon Mar 31 17:50:37 GMT 2025 , Edited by admin on Mon Mar 31 17:50:37 GMT 2025
PRIMARY
ChEMBL
CHEMBL31882
Created by admin on Mon Mar 31 17:50:37 GMT 2025 , Edited by admin on Mon Mar 31 17:50:37 GMT 2025
PRIMARY
EPA CompTox
DTXSID001007560
Created by admin on Mon Mar 31 17:50:37 GMT 2025 , Edited by admin on Mon Mar 31 17:50:37 GMT 2025
PRIMARY
FDA UNII
H56TJ4554M
Created by admin on Mon Mar 31 17:50:37 GMT 2025 , Edited by admin on Mon Mar 31 17:50:37 GMT 2025
PRIMARY
NCI_THESAURUS
C80635
Created by admin on Mon Mar 31 17:50:37 GMT 2025 , Edited by admin on Mon Mar 31 17:50:37 GMT 2025
PRIMARY
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