121263-19-2 | Carbonic acid,(1R)-2-[12-[(2R)-2-(benzoyloxy)propyl]-3,10-dihydro-4,9-dihydroxy-2,6,7,11-tetramethoxy-3,10-dioxo-1-perylenyl]-1-methylethyl4-hydroxyphenyl ester, stereoisomer

Packsize	Purity	Availability	Price	Discounted Price
1mg	95%	1 week	$2,128.00	$1,490.00

Description

• Catalog Number: AD35520
• Chemical Name: Carbonic acid,(1R)-2-[12-[(2R)-2-(benzoyloxy)propyl]-3,10-dihydro-4,9-dihydroxy-2,6,7,11-tetramethoxy-3,10-dioxo-1-perylenyl]-1-methylethyl4-hydroxyphenyl ester, stereoisomer
• CAS Number: 121263-19-2
• Molecular Formula: C44H38O14
• Molecular Weight: 790.7641
• MDL Number: MFCD00133155
• SMILES: COC1=CC(=O)c2c3c1c1C(=CC(=O)c4c1c(c3c(c(c2O)OC)CC(OC(=O)Oc1ccc(cc1)O)C)c(CC(OC(=O)c1ccccc1)C)c(c4O)OC)OC

Upstream Synthesis Route

Calphostin C, a natural compound derived from a bacterium, has gained significant attention in the field of chemical synthesis due to its unique properties. This potent inhibitor of protein kinase C (PKC) plays a crucial role in regulating various cellular processes, making it a valuable tool in chemical research and development.In chemical synthesis, Calphostin C is utilized as a key reagent for studying signal transduction pathways and elucidating the mechanisms of PKC activation. By effectively blocking the activity of PKC, Calphostin C enables researchers to investigate the role of this enzyme in cellular signaling and to understand its impact on biological systems.Moreover, Calphostin C has been employed in the synthesis of bioactive molecules and pharmaceutical compounds. Its ability to modulate PKC activity makes it a versatile compound for designing novel drugs targeting specific signaling pathways. Researchers have also leveraged Calphostin C in the development of new synthetic methodologies, utilizing its unique structure and reactivity to achieve complex molecular transformations.Overall, the application of Calphostin C in chemical synthesis underscores its importance as a powerful tool for exploring cellular signaling pathways, designing therapeutic agents, and advancing the field of organic chemistry.