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

Details

Stereochemistry ABSOLUTE
Molecular Formula C10H14N5O8P
Molecular Weight 363.2206
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3'-GUANYLIC ACID

SMILES

NC1=NC2=C(N=CN2[C@@H]3O[C@H](CO)[C@@H](OP(O)(O)=O)[C@H]3O)C(=O)N1

InChI

InChIKey=ZDPUTNZENXVHJC-UUOKFMHZSA-N
InChI=1S/C10H14N5O8P/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-5(17)6(3(1-16)22-9)23-24(19,20)21/h2-3,5-6,9,16-17H,1H2,(H2,19,20,21)(H3,11,13,14,18)/t3-,5-,6-,9-/m1/s1

HIDE SMILES / InChI

Molecular Formula C10H14N5O8P
Molecular Weight 363.2206
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
The salt-dependence of a protein-ligand interaction: ion-protein binding energetics.
2005-02-25
Inhibition of herpes simplex virus DNA polymerase by purine ribonucleoside monophosphates.
1986-02-05
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 17:47:45 GMT 2025
Edited
by admin
on Mon Mar 31 17:47:45 GMT 2025
Record UNII
839SG0O89X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3'-GUANYLIC ACID
MI  
Common Name English
3'-GMP
Preferred Name English
Guanylic acid [WHO-DD]
Common Name English
GUANOSINE 3'-MONOPHOSPHATE
Systematic Name English
3'-GUANYLIC ACID [MI]
Common Name English
Code System Code Type Description
MERCK INDEX
m5874
Created by admin on Mon Mar 31 17:47:45 GMT 2025 , Edited by admin on Mon Mar 31 17:47:45 GMT 2025
PRIMARY Merck Index
ECHA (EC/EINECS)
204-202-1
Created by admin on Mon Mar 31 17:47:45 GMT 2025 , Edited by admin on Mon Mar 31 17:47:45 GMT 2025
PRIMARY
CHEBI
28072
Created by admin on Mon Mar 31 17:47:45 GMT 2025 , Edited by admin on Mon Mar 31 17:47:45 GMT 2025
PRIMARY
DRUG BANK
DB03315
Created by admin on Mon Mar 31 17:47:45 GMT 2025 , Edited by admin on Mon Mar 31 17:47:45 GMT 2025
PRIMARY
EPA CompTox
DTXSID70904627
Created by admin on Mon Mar 31 17:47:45 GMT 2025 , Edited by admin on Mon Mar 31 17:47:45 GMT 2025
PRIMARY
PUBCHEM
135398727
Created by admin on Mon Mar 31 17:47:45 GMT 2025 , Edited by admin on Mon Mar 31 17:47:45 GMT 2025
PRIMARY
CHEBI
60732
Created by admin on Mon Mar 31 17:47:45 GMT 2025 , Edited by admin on Mon Mar 31 17:47:45 GMT 2025
PRIMARY
CAS
117-68-0
Created by admin on Mon Mar 31 17:47:45 GMT 2025 , Edited by admin on Mon Mar 31 17:47:45 GMT 2025
PRIMARY
FDA UNII
839SG0O89X
Created by admin on Mon Mar 31 17:47:45 GMT 2025 , Edited by admin on Mon Mar 31 17:47:45 GMT 2025
PRIMARY