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

Details

Stereochemistry ABSOLUTE
Molecular Formula C10H12N4O5
Molecular Weight 268.2261
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of INOSINE

SMILES

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

InChI

InChIKey=UGQMRVRMYYASKQ-KQYNXXCUSA-N
InChI=1S/C10H12N4O5/c15-1-4-6(16)7(17)10(19-4)14-3-13-5-8(14)11-2-12-9(5)18/h2-4,6-7,10,15-17H,1H2,(H,11,12,18)/t4-,6-,7-,10-/m1/s1

HIDE SMILES / InChI

Molecular Formula C10H12N4O5
Molecular Weight 268.2261
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 17:32:52 UTC 2023
Edited
by admin
on Sat Dec 16 17:32:52 UTC 2023
Record UNII
5A614L51CT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
INOSINE
INCI   INN   JAN   MART.   MI   WHO-DD   WHO-IP  
INN   INCI  
Official Name English
HYPOXANTHINE RIBOSIDE
Common Name English
INOSINE [MART.]
Common Name English
9-.BETA.-D-RIBOFURANOSYL-1,9-DIHYDRO-6H-PURIN-6-ONE
Systematic Name English
inosine [INN]
Common Name English
9-.BETA.-D-RIBOFURANOSYLHYPOXANTHINE
Common Name English
INOSINE [MI]
Common Name English
DIDANOSINE IMPURITY B [EP IMPURITY]
Common Name English
INOSINE [WHO-IP]
Common Name English
INOSINE [JAN]
Common Name English
INOSINE [INCI]
Common Name English
NSC-20262
Code English
INOTIN
Brand Name English
9-.BETA.-D-RIBOFURANOSYL-1,9-DIHYDRO-6H-PURIN-6-ONE [WHO-IP]
Common Name English
HYPOXANTHOSINE
Common Name English
INOSINE [USP IMPURITY]
Common Name English
ADENOSINE IMPURITY G [EP IMPURITY]
Common Name English
DIDANOSINE IMPURITY B [WHO-IP]
Common Name English
Inosine [WHO-DD]
Common Name English
Classification Tree Code System Code
WHO-VATC QG01AX02
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
WHO-ATC G01AX02
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
LOINC 59210-5
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
WHO-ATC S01XA10
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
WHO-ATC D06BB05
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
WHO-VATC QS01XA10
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
LOINC 75154-5
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
LOINC 75150-3
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
WHO-VATC QD06BB05
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
LOINC 2479-4
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
DSLD 1774 (Number of products:41)
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
Code System Code Type Description
FDA UNII
5A614L51CT
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
PRIMARY
DAILYMED
5A614L51CT
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
PRIMARY
EVMPD
SUB08191MIG
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
PRIMARY
WIKIPEDIA
Inosine
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
PRIMARY
DRUG CENTRAL
3301
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
PRIMARY
RXCUI
1483575
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
PRIMARY RxNorm
ECHA (EC/EINECS)
200-390-4
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
PRIMARY
CAS
58-63-9
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
PRIMARY
DRUG BANK
DB04335
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
PRIMARY
INN
4687
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
PRIMARY
MERCK INDEX
m6288
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
PRIMARY Merck Index
NCI_THESAURUS
C166836
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
PRIMARY
ChEMBL
CHEMBL1556
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
PRIMARY
PUBCHEM
135398641
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
PRIMARY
CHEBI
17596
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
PRIMARY
SMS_ID
100000083399
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
PRIMARY
NSC
20262
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
PRIMARY
MESH
D007288
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
PRIMARY
EPA CompTox
DTXSID2045993
Created by admin on Sat Dec 16 17:32:53 UTC 2023 , Edited by admin on Sat Dec 16 17:32:53 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
PARENT -> METABOLITE
Adenosine is broken down by adenosine deaminase, which is present in red cells and the vessel wall.
MAJOR
Related Record Type Details
PARENT -> IMPURITY
The area of any individual peak corresponding to impurity B is not greater than 0.2 times the area of the principal peak obtained with solution (4) (0.2%).
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
PARENT -> IMPURITY
correction factors: for the calculation of content, multiply the peak areas of the following impurities by the corresponding correction factor: impurity A = 0.6; impurity G = 1.4
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
ACTIVE MOIETY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP