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

Details

Stereochemistry ACHIRAL
Molecular Formula C15H13N5O4
Molecular Weight 327.2948
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LETEPRINIM

SMILES

OC(=O)C1=CC=C(NC(=O)CCN2C=NC3=C2N=CNC3=O)C=C1

InChI

InChIKey=JMPOIZCOJJMTHI-UHFFFAOYSA-N
InChI=1S/C15H13N5O4/c21-11(19-10-3-1-9(2-4-10)15(23)24)5-6-20-8-18-12-13(20)16-7-17-14(12)22/h1-4,7-8H,5-6H2,(H,19,21)(H,23,24)(H,16,17,22)

HIDE SMILES / InChI
Leteprinim is the synthetic purine. It has both anti-excitotoxic neuroprotective properties and enhances the regenerative response of surviving neurons within the central nervous system. Moreover, the experiments in vitro and in vivo reveal that leteprinim can be administered after an excitotoxic event and still produce neuroprotection. This is clearly crucial for any drug designed to treat stroke or any acute central nervous system injury. Therefore, leteprinim has the pharmacological properties required by a drug intended to treat acute stroke as well as a spinal injury. It may be useful in reducing brain injury; it possesses clinical relevance for the treatment of hypoxic-ischemic encephalopathy in the newborn. Leteprinim has the therapeutic potential for use in clinical trials in the treatment of neuronal deterioration in depression.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P01138
Gene ID: 4803.0
Gene Symbol: NGF
Target Organism: Homo sapiens (Human)
PubMed

PubMed

TitleDatePubMed
AIT-082 as a potential neuroprotective and regenerative agent in stroke and central nervous system injury.
1999 Aug
Drugs in development for Parkinson's disease.
2004 Jul

Sample Use Guides

In Vivo Use Guide
Curator's Comment: Rat data
60 mg/kg daily
Route of Administration: Intraperitoneal
Name Type Language
LETEPRINIM
INN   MI   WHO-DD  
INN  
Official Name English
P-(3-(1,6-DIHYDRO-6-OXO-9H-PURIN-9-YL)PROPIONAMIDO)BENZOIC ACID
Common Name English
LETEPRINIM [MI]
Common Name English
leteprinim [INN]
Common Name English
Leteprinim [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C1509
Created by admin on Fri Dec 15 16:03:55 GMT 2023 , Edited by admin on Fri Dec 15 16:03:55 GMT 2023
Code System Code Type Description
FDA UNII
NBY3IU407M
Created by admin on Fri Dec 15 16:03:55 GMT 2023 , Edited by admin on Fri Dec 15 16:03:55 GMT 2023
PRIMARY
MERCK INDEX
m1203
Created by admin on Fri Dec 15 16:03:55 GMT 2023 , Edited by admin on Fri Dec 15 16:03:55 GMT 2023
PRIMARY Merck Index
WIKIPEDIA
Leteprinim
Created by admin on Fri Dec 15 16:03:55 GMT 2023 , Edited by admin on Fri Dec 15 16:03:55 GMT 2023
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EPA CompTox
DTXSID00160496
Created by admin on Fri Dec 15 16:03:55 GMT 2023 , Edited by admin on Fri Dec 15 16:03:55 GMT 2023
PRIMARY
SMS_ID
100000086646
Created by admin on Fri Dec 15 16:03:55 GMT 2023 , Edited by admin on Fri Dec 15 16:03:55 GMT 2023
PRIMARY
NCI_THESAURUS
C80995
Created by admin on Fri Dec 15 16:03:55 GMT 2023 , Edited by admin on Fri Dec 15 16:03:55 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104345
Created by admin on Fri Dec 15 16:03:55 GMT 2023 , Edited by admin on Fri Dec 15 16:03:55 GMT 2023
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EVMPD
SUB02897MIG
Created by admin on Fri Dec 15 16:03:55 GMT 2023 , Edited by admin on Fri Dec 15 16:03:55 GMT 2023
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CAS
138117-50-7
Created by admin on Fri Dec 15 16:03:55 GMT 2023 , Edited by admin on Fri Dec 15 16:03:55 GMT 2023
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DRUG CENTRAL
3318
Created by admin on Fri Dec 15 16:03:55 GMT 2023 , Edited by admin on Fri Dec 15 16:03:55 GMT 2023
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PUBCHEM
135409548
Created by admin on Fri Dec 15 16:03:55 GMT 2023 , Edited by admin on Fri Dec 15 16:03:55 GMT 2023
PRIMARY
INN
7814
Created by admin on Fri Dec 15 16:03:55 GMT 2023 , Edited by admin on Fri Dec 15 16:03:55 GMT 2023
PRIMARY