
Catalog Number	AR01CCJM
Chemical Name	4-Thiazolecarboxamide,N-[1-(aminocarbonyl)ethenyl]-2-[(11S,14Z,21S,23S,29S)-14-ethylidene-9,10,11,12,13,14,19,20,21,22,23,24,26,33,35,36-hexadecahydro-3,23-dihydroxy-11-[(1R)-1-hydroxyethyl]-31-methyl-9,12,19,24,33,43-hexaoxo-30,32-imino-8,5:18,15:40,37-trinitrilo-21,36-([2,4]-endo-thiazolomethanimino)-5H,15H,37H-pyrido[3,2-w][2
CAS Number	56377-79-8
Molecular Formula	C51H43N13O12S6
Molecular Weight	1222.357
MDL Number	MFCD00867479
SMILES	C/C=C/1NC(=O)[C@@H](NC(=O)c2csc(-c3cc(O)c(nc3-c3csc(n3)[C@H]3NC(=O)c4nc([C@@H](NC(=O)c5nc1sc5)C[C@H](O)C(=O)OCc1cccc5c1c(C)c([nH]5)C(=O)SC3)sc4)c1scc(n1)C(=O)NC(=C)C(=O)N)n2)[C@@H](O)C
NSC Number	307240

Nosiheptide, a naturally occurring antibiotic, holds great significance in chemical synthesis as a powerful tool for peptide bond formation. This potent compound displays exceptional bioactivity and selectivity, making it a valuable asset in the creation of complex peptide structures. In chemical synthesis, Nosiheptide serves as a catalyst, enabling the efficient assembly of peptides by facilitating the formation of peptide bonds between amino acids. Its unique mechanism of action and high specificity contribute to the precision and yield of peptide synthesis reactions. Furthermore, the use of Nosiheptide in chemical synthesis allows for the development of novel peptide-based drugs, pharmaceuticals, and biomolecules with enhanced therapeutic potential.