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Details

Stereochemistry ABSOLUTE
Molecular Formula C18H18ClIN6O4
Molecular Weight 544.731
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NAMODENOSON

SMILES

CNC(=O)[C@H]1O[C@H]([C@H](O)[C@@H]1O)N2C=NC3=C2N=C(Cl)N=C3NCC4=CC=CC(I)=C4

InChI

InChIKey=IPSYPUKKXMNCNQ-PFHKOEEOSA-N
InChI=1S/C18H18ClIN6O4/c1-21-16(29)13-11(27)12(28)17(30-13)26-7-23-10-14(24-18(19)25-15(10)26)22-6-8-3-2-4-9(20)5-8/h2-5,7,11-13,17,27-28H,6H2,1H3,(H,21,29)(H,22,24,25)/t11-,12+,13-,17+/m0/s1

HIDE SMILES / InChI

Molecular Formula C18H18ClIN6O4
Molecular Weight 544.731
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 Fri Dec 15 18:10:38 UTC 2023
Edited
by admin
on Fri Dec 15 18:10:38 UTC 2023
Record UNII
Z07JR07J6C
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NAMODENOSON
USAN   INN  
Official Name English
2-CHLORO-N6-(3-IODOBENZYL)ADENOSINE-5'-N-METHYLURONAMIDE
Common Name English
CF-102
Code English
CF102
Code English
2-CHLORO-N(6)-(3-IODOBENZYL)ADENOSINE-5'-N-METHYLURONAMIDE
Common Name English
.BETA.-D-RIBOFURANURONAMIDE, 1-(2-CHLORO-6-(((3-IODOPHENYL)METHYL)AMINO)-9H-PURIN-9-YL)-1-DEOXY-N-METHYL-
Systematic Name English
1-(2-CHLORO-6-(((3-IODOPHENYL)METHYL)AMINO)-9H-PURIN-9-YL)-1-DEOXY-N-METHYL-.BETA.-D-RIBOFURANURONAMIDE
Systematic Name English
Namodenoson [WHO-DD]
Common Name English
CHLORO-IB-MECA
Common Name English
NAMODENOSON [USAN]
Common Name English
namodenoson [INN]
Common Name English
CL-IB-MECA
Code English
Classification Tree Code System Code
EU-Orphan Drug EU/3/15/1565
Created by admin on Fri Dec 15 18:10:39 UTC 2023 , Edited by admin on Fri Dec 15 18:10:39 UTC 2023
NCI_THESAURUS C274
Created by admin on Fri Dec 15 18:10:39 UTC 2023 , Edited by admin on Fri Dec 15 18:10:39 UTC 2023
FDA ORPHAN DRUG 363512
Created by admin on Fri Dec 15 18:10:39 UTC 2023 , Edited by admin on Fri Dec 15 18:10:39 UTC 2023
Code System Code Type Description
EPA CompTox
DTXSID80167504
Created by admin on Fri Dec 15 18:10:39 UTC 2023 , Edited by admin on Fri Dec 15 18:10:39 UTC 2023
PRIMARY
FDA UNII
Z07JR07J6C
Created by admin on Fri Dec 15 18:10:39 UTC 2023 , Edited by admin on Fri Dec 15 18:10:39 UTC 2023
PRIMARY
INN
10651
Created by admin on Fri Dec 15 18:10:39 UTC 2023 , Edited by admin on Fri Dec 15 18:10:39 UTC 2023
PRIMARY
SMS_ID
100000181845
Created by admin on Fri Dec 15 18:10:39 UTC 2023 , Edited by admin on Fri Dec 15 18:10:39 UTC 2023
PRIMARY
DRUG BANK
DB12885
Created by admin on Fri Dec 15 18:10:39 UTC 2023 , Edited by admin on Fri Dec 15 18:10:39 UTC 2023
PRIMARY
CAS
163042-96-4
Created by admin on Fri Dec 15 18:10:39 UTC 2023 , Edited by admin on Fri Dec 15 18:10:39 UTC 2023
PRIMARY
ChEMBL
CHEMBL431733
Created by admin on Fri Dec 15 18:10:39 UTC 2023 , Edited by admin on Fri Dec 15 18:10:39 UTC 2023
PRIMARY
USAN
DE-95
Created by admin on Fri Dec 15 18:10:39 UTC 2023 , Edited by admin on Fri Dec 15 18:10:39 UTC 2023
PRIMARY
PUBCHEM
3035850
Created by admin on Fri Dec 15 18:10:39 UTC 2023 , Edited by admin on Fri Dec 15 18:10:39 UTC 2023
PRIMARY
NCI_THESAURUS
C79826
Created by admin on Fri Dec 15 18:10:39 UTC 2023 , Edited by admin on Fri Dec 15 18:10:39 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Related Record Type Details
ACTIVE MOIETY