Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C17H22N2O4 |
Molecular Weight | 318.3676 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOC(=O)CNC(=O)[C@@H]1CCCN1C(=O)CC2=CC=CC=C2
InChI
InChIKey=PJNSMUBMSNAEEN-AWEZNQCLSA-N
InChI=1S/C17H22N2O4/c1-2-23-16(21)12-18-17(22)14-9-6-10-19(14)15(20)11-13-7-4-3-5-8-13/h3-5,7-8,14H,2,6,9-12H2,1H3,(H,18,22)/t14-/m0/s1
DescriptionCurator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/12596521
https://examine.com/supplements/noopept/
Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/12596521
https://examine.com/supplements/noopept/
Noopept (DVD-111) is a peptide promoted and prescribed in Russia and neighbouring countries as a nootropic. Noopept was patented by Russian-based pharmaceutical company JSC LEKKO Pharmaceuticals in the 1996. Research shows Noopept has similar effects, but works differently than other nootropics in the racetam-family. The compound is patented in both the US and Russia with patent of Russian Federation number 2119496, U.S. Patent 5,439,930 issued 8/8/1995. Noopept exhibits a combined neuroprotector effect both in vitro and in vivo. Noopept decreases the extent of necrotic damage caused by photoinduced thrombosis of cortical blood vessels. It was established that the neuroprotector effect of noopept is related to its action upon the well-known "triad", whereby the drug reduces neurotoxic effects of excess extracellular calcium, glutamate, and free radicals. Two additional components of the neuroprotector action of noopept are related to the antiinflammatory and antithrombotic activity.
CNS Activity
Sources: http://nootropicsexpert.com/noopept/
Curator's Comment: Noopept is very bioavailable and easily crosses the blood-brain barrier.
Originator
Sources: http://nootropicsexpert.com/noopept/
Curator's Comment: Noopept was patented by Russian-based pharmaceutical company JSC LEKKO Pharmaceuticals in the 1996.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: GO:0051402 Sources: https://www.ncbi.nlm.nih.gov/pubmed/12711349 |
1.21 µM [IC50] | ||
Target ID: GO:0007215 |
|||
Target ID: P23560|||Q9BYY7 Gene ID: 627.0 Gene Symbol: BDNF Target Organism: Homo sapiens (Human) |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Noopept Approved UseNoopept used for the treatment of patients of different age groups of adults and elderly patients suffering from cognitive impairment and emotional lability of various origins. In particular, the drug can be assigned Noopept after craniocerebral injury and coma, as well as patients with cerebral circulatory insufficiency of various etiologies including encephalopathy and asthenic disorders.
Noopept can be assigned to improve the cognitive functions of memory, concentration and learning ability in patients with increased physical, intellectual and emotional loads. |
Sample Use Guides
In Vivo Use Guide
Sources: http://nootropicsexpert.com/noopept/
Curator's Comment: Noopept is primarily water-soluble nootropic, but won’t easily dissolve in water or juice. So it may help if you take it with a meal containing healthy fats. Or with a tablespoon of extra virgin, expeller cold-pressed coconut or olive oil. Or other similar healthy fat to ensure quick absorption.
For even quicker absorption you can use Noopept sublingually. Let the tablet or powder dissolve under your tongue so it can go straight into your blood-stream, and into your brain. Bypassing your digestive system completely.
Recommended Noopept dosage is 10 – 30 mg per day. Noopept is sold in tablet, capsule and powder form. Tablets and capsules are usually 10 mg each.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/12711349
Noopept (GVS-111) significantly increased neuronal survival after H(2)O(2)-treatment displaying a dose-dependent neuroprotective activity from 10nM to 100 microM, and an IC(50) value of 1.21+/-0.07 microM.
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DSLD |
3380 (Number of products:17)
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N-Phenylacetyl-L-prolylglycine ethyl ester
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100000154968
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180496
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DTXSID80166214
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10682
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SUB128773
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4QBJ98683M
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C166777
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ACTIVE MOIETY
METABOLITE ACTIVE (PARENT)