Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C16H21NO2S |
| Molecular Weight | 291.408 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1CN(CCCOCCC2=CC=C3SC=CC3=C2)C1
InChI
InChIKey=HQNACSFBDBYLJP-UHFFFAOYSA-N
InChI=1S/C16H21NO2S/c18-15-11-17(12-15)6-1-7-19-8-4-13-2-3-16-14(10-13)5-9-20-16/h2-3,5,9-10,15,18H,1,4,6-8,11-12H2
| Molecular Formula | C16H21NO2S |
| Molecular Weight | 291.408 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
T-817 is a thiophenylalkyl derivative patented by Toyama Chemical Co., Ltd. as a neuroprotectant for the treatment of Alzheimer's disease. T-817MA protects neurons against amyloid-b peptide- and hydrogen peroxide-induced neurotoxicity and promoted neurite outgrowth in hippocampal slice cultures and neuronal reaggregation culture. T-817MA protected against nitric oxide-induced neurotoxicity in cultured primary neurons. In a preclinical model of Alzheimer's disease, T-817 increases decreased dopamine levels and tyrosine hydroxylase immunostaining in mice's substantia nigra (SNc) and striatum. Systemic administration of T-817 rescues tau-induced synaptic abnormalities.
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: O08553 Gene ID: 12934.0 Gene Symbol: Dpysl2 Target Organism: Mus musculus (Mouse) Sources: https://www.ncbi.nlm.nih.gov/pubmed/29622647 |
PubMed
| Title | Date | PubMed |
|---|---|---|
| CRMP2-binding compound, edonerpic maleate, accelerates motor function recovery from brain damage. | 2018-04-06 |
|
| Blocking Effects of Human Tau on Squid Giant Synapse Transmission and Its Prevention by T-817 MA. | 2011 |
|
| A neuroprotective agent, T-817MA (1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl} azetidin-3-ol maleate), prevents 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced neurotoxicity in mice. | 2008-10 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/18573265
mice 30mg/kg
Route of Administration:
Oral
| Substance Class |
Chemical
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ACTIVE MOIETY |