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Noopept

HCID 180496
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Grundinformationen

CAS
157115-85-0
Standard-SMILES
CCOC(=O)CNC(=O)[C@@H]1CCCN1C(=O)Cc1ccccc1
InChIKey
PJNSMUBMSNAEEN-AWEZNQCLSA-N
Summenformel
C17H22N2O4
Durchschnittliche Molmasse
318,373 g/mol
Monoisotopische Masse
318,15795718

Namen und Bezeichner

Bevorzugter Name
Noopept
IUPAC
Ethyl 1-(phenylacetyl)-L-prolylglycinate
Englischer Name
Noopept
Summenformel
C17H22N2O4
Molmasse
318.37

Namen und Synonyme

Omberacetamnoopept powderNPEP12N-(1-(Phenylacetyl)-L-prolyl)glycine ethyl esterskypeSGS111SGS-111NoopeptSGS 111CS-1723

Datenbank-Bezeichner

CAS
157115-85-0
PubChem CID
180496
DTXSID
DTXSID80166214
ChEMBL
CHEMBL4303687
UNII
4QBJ98683M
EC Number
839-170-3
Nikkaji
J759.455K

Eigenschaften

Physikochemische Eigenschaften

Schmelzpunkt
94 to · 94.0 to 98.0 °C
Siedepunkt
547.3 · 547.3±50.0 °C(Predicted)
Dichte
1.202 · 1.202±0.06 g/cm3(Predicted)
storage temp.
-20 °C · -20°C
Löslichkeit
Soluble in DMSO (up to 25 mg/ml)
pka
13.41 · 13.41±0.20(Predicted)
Aggregatzustand
powder
Farbe
white to beige
Stabilität
1 year · Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 2 months.
InChI
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
InChIKey
PJNSMUBMSNAEEN-AWEZNQCLSA-N
SMILES
C(OCC)(=O)CNC(=O)[C@@H]1CCCN1C(CC1=CC=CC=C1)=O
CAS Datenbank
157115 · 157115-85-0

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

Sicherheitsdaten

wgk
WGK 3
hs_code
29339900
RTECS-Nr.
MC0814400
Speicherklasse
11 - Combustible Solids

Chemie und Industrie

Anwendungen · 3 Einträge

BeschreibungNoopept is the brand name for N-phenylacetyl-L-prolylglycine ethyl ester , a synthetic nootropic molecule. It has a similar effect to piracetam, in that it provides a mild cognitive boost after supplementation. It also provides a subtle psychostimulatory effect. Noopept is up to 1000-times more potent than the original racetam, Piracetam.

HistoryNoopept (previously GVS-111) is a nootropic developed at the Zakusov Institute of Pharmacology (Russian Academy of Medical Sciences) by T. A. Gudasheva. It is one of several nootropics developed based on the structure of piracetam. Its advantage over piracetam is that it can be taken at a lower dose.Noopept is a popular cognitive-enhancing supplement in the nootropic community. Proposed mechanism of actions based on preclinical studies include increasing acetylcholine signaling, increasing the expression of BDNF and NGF, protecting from glutamate toxicity, and increasing inhibitory neurotransmission in the brain.www.alzdiscovery.org

VerwendenNoopept is a well-known nootropic that is often suggested as a first nootropic.Noopept is over 500 times more potentthan Piracetam.Like piracetam,it is capable of enhancing memory,learning,andfocus. Noopept is also a powerful antioxidant that prevents neurological disorders andhelps the brain grow.Because of this, it is thought to improve long-term memory. The human studies have shown promising results, with potential application in the treatment of Alzheimer's disease.

Darstellung · 1 Eintrag

synthetischeNoopept (ethyl ester of N-phenylacetyl-L-prolylglycine) was designed as a drug at State Zakusov Institute of Pharmacology. The synthesis of the drug is based on the original hypothesis of peptide design, according to which structures similar to known psychotropic agents are reproduced using appropriate amino acids. The non-peptide prototype of Noopept is the nootropic drug Piracetam.1. Perform the carboxylation of N-phenylacetyl-L-proline and ethyl glycine in the presence of isobutyl chloroformate. 2. Add slowly isobutyl chloroformate (1.17 g, 8.6 mmol) to a solution of N-phenylacetyl-L-proline (2.0 g, 8.6 mmol) dissolved in a mixed solvent of THF and dichloromethane (1:1; THF/dichloromethane (v/v)).3.Stir the mixture for 4 h at 0 ~5 °CMolecular Mechanism Underlying the Action of Substituted Pro-Gly Dipeptide Noopept

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Vorgelagerte Rohstoffe

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