Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C8H10N2OS |
| Molecular Weight | 182.243 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C1NCCNC1C2=CC=CS2
InChI
InChIKey=BBACKDMGYMXYLE-UHFFFAOYSA-N
InChI=1S/C8H10N2OS/c11-8-7(9-3-4-10-8)6-2-1-5-12-6/h1-2,5,7,9H,3-4H2,(H,10,11)
| Molecular Formula | C8H10N2OS |
| Molecular Weight | 182.243 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Tenilsetam (CAS 997: ( /-)-3-(2-thienyl)-2-piperazinone), a cognition-enhancing drug successfully used for the treatment of patients suffering from Alzheimer's disease. According to the mechanism proposed, it inhibits advanced glycation end-product (AGE) formation. The beneficial effect of tenilsetam in Alzheimer's disease could come from the interference with AGE-derived crosslinking of amyloid plaques and a decreased inflammatory response to diminished activation of phagocytosing microglia. In addition was shown, that the long-term treatment with tenilsetam inhibited the formation of acellular capillaries without correcting pericyte loss. Was suggested that tenilsetam could be useful for the treatment of early diabetic retinopathy, but then these studies were discontinued.
CNS Activity
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: Advanced glycation end-product Sources: https://www.ncbi.nlm.nih.gov/pubmed/7748463 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Unknown Approved UseUnknown |
|||
| Primary | Unknown Approved UseUnknown |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
2.03 μg/mL EXPERIMENT https://doi.org/10.1002/ddr.430090203 |
75 mg single, oral dose: 75 mg route of administration: Oral experiment type: SINGLE co-administered: |
TENILSETAM plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
4.33 μg/mL EXPERIMENT https://doi.org/10.1002/ddr.430090203 |
150 mg single, oral dose: 150 mg route of administration: Oral experiment type: SINGLE co-administered: |
TENILSETAM plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
9.03 μg/mL EXPERIMENT https://doi.org/10.1002/ddr.430090203 |
300 mg single, oral dose: 300 mg route of administration: Oral experiment type: SINGLE co-administered: |
TENILSETAM plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
31.97 μg × h/mL EXPERIMENT https://doi.org/10.1002/ddr.430090203 |
75 mg single, oral dose: 75 mg route of administration: Oral experiment type: SINGLE co-administered: |
TENILSETAM plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
65.98 μg × h/mL EXPERIMENT https://doi.org/10.1002/ddr.430090203 |
150 mg single, oral dose: 150 mg route of administration: Oral experiment type: SINGLE co-administered: |
TENILSETAM plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
146.99 μg × h/mL EXPERIMENT https://doi.org/10.1002/ddr.430090203 |
300 mg single, oral dose: 300 mg route of administration: Oral experiment type: SINGLE co-administered: |
TENILSETAM plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
18.31 h EXPERIMENT https://doi.org/10.1002/ddr.430090203 |
75 mg single, oral dose: 75 mg route of administration: Oral experiment type: SINGLE co-administered: |
TENILSETAM plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
18.39 h EXPERIMENT https://doi.org/10.1002/ddr.430090203 |
150 mg single, oral dose: 150 mg route of administration: Oral experiment type: SINGLE co-administered: |
TENILSETAM plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
|
21.84 h EXPERIMENT https://doi.org/10.1002/ddr.430090203 |
300 mg single, oral dose: 300 mg route of administration: Oral experiment type: SINGLE co-administered: |
TENILSETAM plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: UNKNOWN food status: UNKNOWN |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/25025046
a pilot trial for Alzheimer's disease (AD) patients. Over a 3-month period at 150 mg/day doses, AD patients showed significant improvements in the favorability judgment task (FJT) and reaction time
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/15639802/
In the experiments with human neuroblastoma SH-SY5Y cells, incubated with methylglyoxal which was preincubated with tenilsetam for 2 or 24 hours, tenilsetam completely nullified the toxicity of methylglyoxal at both time points.
| Substance Class |
Chemical
Created
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Edited
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| Record UNII |
O4Q7XM74N6
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Validated (UNII)
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C1509
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C059511
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