The chemical substance N-(N-Formyl-L-Val-)cyclo[L-Thr*-4-methoxy-D-Phe-D-Ala-N-methyl-L-Ile-[(3S)-3-hydroxy-L-Nva-]-5-methoxy-N-methyl-L-Trp-] is a complex peptide derivative characterized by its cyclic structure and the presence of various amino acid residues, including both natural and modified forms. The inclusion of methoxy groups and N-methylation suggests enhanced stability and potential bioactivity, which may influence its interaction with biological targets. The presence of a formyl group indicates that it may participate in specific biochemical pathways or reactions. This compound is likely to exhibit properties typical of peptides, such as solubility in polar solvents and potential biological activity, including antimicrobial or anticancer effects, depending on its specific structure and conformation. Its CAS number, 30270-78-1, allows for precise identification in chemical databases, facilitating research and application in fields such as medicinal chemistry and pharmacology. Further studies would be necessary to elucidate its full range of characteristics and potential applications.

N-(N-Formyl-L-Val-)cyclo[L-Thr*-4-methoxy-D-Phe-D-Ala-N-methyl-L-aIle-[(3S)-3-hydroxy-L-Nva-]-5-methoxy-N-methyl-L-Trp-]

30270-78-1: The chemical substance N-(N-Formyl-L-Val-)cyclo[L-Thr*-4-methoxy-D-Phe-D-Ala-N-methyl-L-Ile-[(3S)-3-hydroxy-L-Nva-]-5-methoxy-N-methyl-L-Trp-] is a complex peptide derivative characterized by its cyclic structure and the presence of various amino acid residues, including both natural and modified forms. The inclusion of methoxy groups and N-methylation suggests enhanced stability and potential bioactivity, which may influence its interaction with biological targets. The presence of a formyl group indicates that it may participate in specific biochemical pathways or reactions. This compound is likely to exhibit properties typical of peptides, such as solubility in polar solvents and potential biological activity, including antimicrobial or anticancer effects, depending on its specific structure and conformation. Its CAS number, 30270-78-1, allows for precise identification in chemical databases, facilitating research and application in fields such as medicinal chemistry and pharmacology. Further studies would be necessary to elucidate its full range of characteristics and potential applications.

<p>Cycloheptamycin exhibits activity against Gram-positive bacteria and mycobacteria.</p>

CAS 30270-78-1

N-(N-Formyl-L-Val-)cyclo[L-Thr*-4-methoxy-D-Phe-D-Ala-N-methyl-L-aIle-[(3S)-3-hydroxy-L-Nva-]-5-methoxy-N-methyl-L-Trp-]

Cycloheptamycin

Ref: TM-TN10293