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Details

Stereochemistry ACHIRAL
Molecular Formula C7H11N3
Molecular Weight 137.1823
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ISAXONINE

SMILES

CC(C)NC1=NC=CC=N1

InChI

InChIKey=FTCYIGBVOHNHCD-UHFFFAOYSA-N
InChI=1S/C7H11N3/c1-6(2)10-7-8-4-3-5-9-7/h3-6H,1-2H3,(H,8,9,10)

HIDE SMILES / InChI

Molecular Formula C7H11N3
Molecular Weight 137.1823
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Isaxonine (N-isopropyl-amino-2-pyrimidine orthophosphate) is able to accelerate nerve regeneration and functional recovery. Isaxonine has specific affinity for peripheral nerves. It acts directly on the neuron or indirectly by stimulating the production of a growth factor remains unknown. It demonstrates activity in the treatment of neuropathies of various etiology. Isaxonine treatment may be associated with hepatotoxicity.

Approval Year

PubMed

PubMed

TitleDatePubMed
Presence of covalently bound metabolites on rat hepatocyte plasma membrane proteins after administration of isaxonine, a drug leading to immunoallergic hepatitis in man.
1989-05
Drug-induced hepatitis associated with anticytoplasmic organelle autoantibodies.
1985-09-01
[Protective effect of isaxonine against vincristine-induced neuropathy (author's transl)].
1982-04-08
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:33:26 GMT 2025
Edited
by admin
on Mon Mar 31 18:33:26 GMT 2025
Record UNII
883G6DMT63
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ISAXONINE [MI]
Preferred Name English
ISAXONINE
INN   MI   WHO-DD  
INN  
Official Name English
isaxonine [INN]
Common Name English
Isaxonine [WHO-DD]
Common Name English
2-(ISOPROPYLAMINO)PYRIMIDINE
Systematic Name English
NSC-760406
Code English
Classification Tree Code System Code
NCI_THESAURUS C542
Created by admin on Mon Mar 31 18:33:26 GMT 2025 , Edited by admin on Mon Mar 31 18:33:26 GMT 2025
Code System Code Type Description
PUBCHEM
71169
Created by admin on Mon Mar 31 18:33:26 GMT 2025 , Edited by admin on Mon Mar 31 18:33:26 GMT 2025
PRIMARY
MESH
C020375
Created by admin on Mon Mar 31 18:33:26 GMT 2025 , Edited by admin on Mon Mar 31 18:33:26 GMT 2025
PRIMARY
EVMPD
SUB08306MIG
Created by admin on Mon Mar 31 18:33:26 GMT 2025 , Edited by admin on Mon Mar 31 18:33:26 GMT 2025
PRIMARY
FDA UNII
883G6DMT63
Created by admin on Mon Mar 31 18:33:26 GMT 2025 , Edited by admin on Mon Mar 31 18:33:26 GMT 2025
PRIMARY
SMS_ID
100000083360
Created by admin on Mon Mar 31 18:33:26 GMT 2025 , Edited by admin on Mon Mar 31 18:33:26 GMT 2025
PRIMARY
CAS
4214-72-6
Created by admin on Mon Mar 31 18:33:26 GMT 2025 , Edited by admin on Mon Mar 31 18:33:26 GMT 2025
PRIMARY
NCI_THESAURUS
C65969
Created by admin on Mon Mar 31 18:33:26 GMT 2025 , Edited by admin on Mon Mar 31 18:33:26 GMT 2025
PRIMARY
MERCK INDEX
m249
Created by admin on Mon Mar 31 18:33:26 GMT 2025 , Edited by admin on Mon Mar 31 18:33:26 GMT 2025
PRIMARY Merck Index
DRUG CENTRAL
1485
Created by admin on Mon Mar 31 18:33:26 GMT 2025 , Edited by admin on Mon Mar 31 18:33:26 GMT 2025
PRIMARY
EPA CompTox
DTXSID20194975
Created by admin on Mon Mar 31 18:33:26 GMT 2025 , Edited by admin on Mon Mar 31 18:33:26 GMT 2025
PRIMARY
ChEMBL
CHEMBL1740513
Created by admin on Mon Mar 31 18:33:26 GMT 2025 , Edited by admin on Mon Mar 31 18:33:26 GMT 2025
PRIMARY
NSC
760406
Created by admin on Mon Mar 31 18:33:26 GMT 2025 , Edited by admin on Mon Mar 31 18:33:26 GMT 2025
PRIMARY
INN
4501
Created by admin on Mon Mar 31 18:33:26 GMT 2025 , Edited by admin on Mon Mar 31 18:33:26 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY