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
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)
Molecular Formula | C15H13N5O4 |
Molecular Weight | 327.2948 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
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
Primary Target | Pharmacology | Condition | Potency |
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Target ID: P01138 Gene ID: 4803.0 Gene Symbol: NGF Target Organism: Homo sapiens (Human) Sources: https://www.ncbi.nlm.nih.gov/pubmed/18465624 |
PubMed
Title | Date | PubMed |
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AIT-082 as a potential neuroprotective and regenerative agent in stroke and central nervous system injury. | 1999 Aug |
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Drugs in development for Parkinson's disease. | 2004 Jul |
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AIT-082 and methylprednisolone singly, but not in combination, enhance functional and histological improvement after acute spinal cord injury in rats. | 2004 Sep-Dec |
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Protection of sensory function in diabetic rats by Neotrofin. | 2006 Mar 18 |
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Small molecule activators of the Trk receptors for neuroprotection. | 2008 Dec 3 |
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Integrative emphases on intimate, intrinsic propensity/pathological processes--causes of self recovery limits and also, subtle related targets for neuroprotectionl pleiotropicity/multimodal actions, by accessible therapeutic approaches--in spinal cord injuries. | 2010 Jul-Sep |
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Effects of neotrofin on neonatal hypoxic ischemic brain injury. | 2011 Nov 14 |
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Neuroprotective effect of neotrofin in a neonatal rat model of periventricular leukomalacia. | 2012 Jun 27 |
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Neotrofin reverses the effects of chronic unpredictable mild stress on behavior via regulating BDNF, PSD-95 and synaptophysin expression in rat. | 2013 Sep 15 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/15992149
Curator's Comment: Rat data
60 mg/kg daily
Route of Administration:
Intraperitoneal
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:03:55 GMT 2023
by
admin
on
Fri Dec 15 16:03:55 GMT 2023
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Record UNII |
NBY3IU407M
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Record Status |
Validated (UNII)
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Record Version |
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C1509
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NBY3IU407M
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m1203
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Leteprinim
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C80995
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Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
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ACTIVE MOIETY |