CAS 22155-91-5
:(2S)-N-2-Naphthalenyl-5-oxo-2-pyrrolidinecarboxamide
Description:
(2S)-N-2-Naphthalenyl-5-oxo-2-pyrrolidinecarboxamide, with the CAS number 22155-91-5, is a chemical compound characterized by its unique structural features. It contains a pyrrolidine ring, which is a five-membered nitrogen-containing heterocycle, and is substituted with a naphthalenyl group, contributing to its aromatic properties. The presence of a carbonyl group (5-oxo) indicates that it has ketone functionality, which can influence its reactivity and interactions with other molecules. This compound is likely to exhibit specific biological activities due to its structural characteristics, making it of interest in medicinal chemistry and drug development. Its stereochemistry, indicated by the (2S) designation, suggests that it has a specific spatial arrangement that may affect its pharmacological properties. Overall, this compound's unique combination of functional groups and stereochemistry positions it as a potentially valuable substance in various chemical and pharmaceutical applications.
Formula:C15H14N2O2
InChI:InChI=1S/C15H14N2O2/c18-14-8-7-13(17-14)15(19)16-12-6-5-10-3-1-2-4-11(10)9-12/h1-6,9,13H,7-8H2,(H,16,19)(H,17,18)/t13-/m0/s1
InChI key:InChIKey=BZEPQNMASTUAMY-ZDUSSCGKSA-N
SMILES:N(C(=O)[C@H]1NC(=O)CC1)C2=CC3=C(C=C2)C=CC=C3
Synonyms:- (2S)-N-2-Naphthalenyl-5-oxo-2-pyrrolidinecarboxamide
- (2S)-N-Naphthalen-2-yl-5-oxopyrrolidine-2-carboxamide
- (S)-N-(2-Naphthyl)-5-oxopyrrolidine-2-carboxamide
- 2-Pyrrolidinecarboxamide, N-2-naphthalenyl-5-oxo-, (2S)-
- 2-Pyrrolidinecarboxamide, N-2-naphthalenyl-5-oxo-, (S)-
- 2-Pyrrolidinecarboxamide, N-2-naphthyl-5-oxo-, <span class="text-smallcaps">L</span>-
- <span class="text-smallcaps">L</span>-N-β-Naphthyl-5-oxo-2-pyrrolidinecarboxamide
- <span class="text-smallcaps">L</span>-Pyrrolidonecarboxy-β-naphthylamide
- L-Pyroglutamic Acid Beta-Naphthylamide
- L-Pyrrolidonyl-?-naphthylamide L-Pyroglutamic acid-2-naphthylamide
- N-naphthalen-1-yl-5-oxo-L-prolinamide
- N-naphthalen-2-yl-5-oxoprolinamide
- Pyr-.beta.NA
- L-Pyrrolidonecarboxy-β-naphthylamide
- See more synonyms
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Found 9 products.
Pyr-βNA
CAS:Substrate for the assay of pyroglutamyl peptidase I.Formula:C15H14N2O2Purity:> 99%Color and Shape:White PowderMolecular weight:254.28L-PYROGLUTAMIC ACID β-NAPHTHYLAMIDE
CAS:Formula:C15H14N2O2Purity:98%Color and Shape:SolidMolecular weight:254.2839L-Pyroglutamic acid β-naphthylamide
CAS:L-Pyroglutamic acid β-naphthylamideFormula:C15H14N2O2Purity:By hplc: 99.9% by area (Typical Value in Batch COA)Color and Shape: gray solidMolecular weight:254.28g/molL-Pyroglutamic acid β-naphthylamide
CAS:L-Pyroglutamic acid β-naphthylamide (PYR) is a derivative of glutamic acid.Formula:C15H14N2O2Color and Shape:SolidMolecular weight:254.28L-Pyroglutamic acid β-naphthylamide
CAS:Formula:C15H14N2O2Purity:≥ 99.0%Color and Shape:White to off-white powderMolecular weight:254.28(S)-N-(Naphthalen-2-yl)-5-oxopyrrolidine-2-carboxamide
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:254.28900146484375L-Pyroglutamic Acid β-Naphthylamide
CAS:Controlled Product<p>Applications A substrate for pyroglutamate aminopeptidase. Used for colorimetric determination of pyrrolidonyl peptidase activity in bacteria.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Szewczuk, A., et al.: Eur. J. Biochem., 8, 63 (1969), Szewczuk, A., et al.: Anal. Biochem., 39, 268 (1971)<br></p>Formula:C15H14N2O2Color and Shape:NeatMolecular weight:254.28L-Pyroglutamic acid β-naphthylamide
CAS:<p>Substrate for proglutamyl peptidase 1. 2-naphthylamide is released upon hydrolysation. By simultainous coupling with a diazonium salt, the corresponding azo dye is formed. Naphthylamide can also be detected by fluorescence analysis. Used in identification of Enterococcus spp. and group A streptococci (Streptococcus pyogenes).</p>Formula:C15H14N2O2Purity:Min. 99 Area-%Molecular weight:254.29 g/molL-Pyroglutamic acid-beta-naphthylamide
CAS:<p>L-Pyroglutamic acid-beta-naphthylamide is a cell nucleus pressor that has been shown to stimulate locomotor activity in rats. It is a highly selective agonist at the 5-HT2 receptor, which is involved in the regulation of energy metabolism and feeding behaviour. L-Pyroglutamic acid-beta-naphthylamide also stimulates cholinergic and serotonergic systems. This drug also inhibits bacterial growth by binding to the receptor site on bacterial cell nuclei, thereby preventing DNA synthesis and locomotor activity. L-Pyroglutamic acid-beta-naphthylamide is an antimicrobial agent that can be used to treat infections caused by bacteria resistant to erythromycin. The antimicrobial effect of this drug is due to its ability to bind to the receptor site on bacterial cell nuclei, thereby preventing DNA synthesis and locomotor activity.</p>Formula:C15H14N2O2Purity:Min. 98 Area-%Color and Shape:White PowderMolecular weight:254.28 g/mol







