CAS 41447-18-1
:N-Methyl-L-pipecolic acid
Description:
N-Methyl-L-pipecolic acid is an amino acid derivative characterized by its unique cyclic structure, which includes a six-membered piperidine ring. This compound features a methyl group attached to the nitrogen atom of the pipecolic acid backbone, contributing to its distinct properties. It is a chiral molecule, existing in two enantiomeric forms, with the L-form being biologically relevant. N-Methyl-L-pipecolic acid is soluble in water and polar organic solvents, making it suitable for various biochemical applications. It is often studied for its potential role in metabolic pathways and its implications in neurobiology, particularly in relation to neurotransmitter systems. Additionally, this compound may serve as a building block in the synthesis of pharmaceuticals and other bioactive molecules. Its stability under standard laboratory conditions and its reactivity with various functional groups further enhance its utility in organic synthesis and medicinal chemistry. Overall, N-Methyl-L-pipecolic acid is a significant compound in both research and potential therapeutic applications.
Formula:C7H13NO2
InChI:InChI=1S/C7H13NO2/c1-8-5-3-2-4-6(8)7(9)10/h6H,2-5H2,1H3,(H,9,10)/t6-/m0/s1
InChI key:InChIKey=BPSLZWSRHTULGU-LURJTMIESA-N
SMILES:C(O)(=O)[C@H]1N(C)CCCC1
Synonyms:- (2S)-1-Methyl-2-piperidinecarboxylic acid
- (-)-(S)-N-Methylpipecolic acid
- 2-Piperidinecarboxylic acid, 1-methyl-, (2S)-
- 2-Piperidinecarboxylic acid, 1-methyl-, (S)-
- N-Methyl-L-pipecolic acid
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Found 4 products.
(S)-1-Methylpiperidine-2-carboxylic acid
CAS:Formula:C7H13NO2Purity:97%Color and Shape:SolidMolecular weight:143.1836(S)-1-Methylpiperidine-2-carboxylic acid
CAS:<p>(S)-1-Methylpiperidine-2-carboxylic acid</p>Purity:97%Molecular weight:143.18g/mol(S)-1-Methylpiperidine-2-carboxylic acid
CAS:<p>(S)-1-Methylpiperidine-2-carboxylic acid is an antibiotic that inhibits the growth of bacteria by binding to bacterial ribosomes. It has been shown to have antitumor effects in mice and has been found to be effective against Escherichia coli, methicillin-resistant Staphylococcus aureus, and Mycobacterium tuberculosis. (S)-1-Methylpiperidine-2-carboxylic acid has also shown antibacterial activity in cell culture experiments. This drug binds to the P site of the ribosome, which blocks the binding site for aminoacyl tRNA, preventing protein synthesis. The protonation state of (S)-1-methylpiperidine-2-carboxylic acid is important for its antibacterial activity because it affects its ability to bind to the ribosome. (S)-1-Methylpiperidine-2-carboxy</p>Formula:C7H13NO2Purity:Min. 95%Molecular weight:143.18 g/mol



