2016
DOI: 10.1002/asia.201601138
|View full text |Cite
|
Sign up to set email alerts
|

RA‐dimer B, a New Dimeric RA‐series Cyclopeptide Incorporating Two Different Types of Cycloisodityrosine Units, from Rubia cordifolia L.

Abstract: RA-dimer B, a new cytotoxic RA-series peptide, was isolated from the roots of Rubia cordifolia L. Its structure was elucidated on the basis of spectroscopic analysis to be a dimeric cyclopeptide composed of deoxybouvardin and allo-RA-V. Those two cyclopeptide units are connected by an ether linkage between the phenolic oxygen atom of deoxybouvardin and the ϵa carbon atom of Tyr-6 of allo-RA-V. RA-dimer B was synthesized by the coupling reaction of deoxybouvardin with the boronic acid derivative of allo-RA-V, a… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2018
2018
2023
2023

Publication Types

Select...
5

Relationship

2
3

Authors

Journals

citations
Cited by 8 publications
(2 citation statements)
references
References 28 publications
(30 reference statements)
0
2
0
Order By: Relevance
“…The absolute structure of RA‐XXV ( 4 ) was established by the total synthesis of this peptide with d ‐alanine at residue 1, l ‐alanines at residues 2 and 4, and modified l ‐tyrosines at residues 3, 5, and 6. We synthesized peptide 4 on the basis our previous synthesis of allo‐RA‐V, a related compound but with a structurally different cycloisodityrosine unit in which a diphenyl ether bond was formed between the carbon atom at the ϵ position of Tyr‐5 and the phenolic oxygen at the ζ position of Tyr‐6. This synthesis was characterized by the diaryl ether formation of the core cycloisodityrosine unit by copper(II) acetate‐mediated intramolecular phenol/arylboronic acid coupling and the macrocyclization of the linear hexapeptide between the Tyr‐6 and d ‐Ala‐1 residues to construct the 18‐membered cyclopeptide ring.…”
Section: Resultsmentioning
confidence: 99%
“…The absolute structure of RA‐XXV ( 4 ) was established by the total synthesis of this peptide with d ‐alanine at residue 1, l ‐alanines at residues 2 and 4, and modified l ‐tyrosines at residues 3, 5, and 6. We synthesized peptide 4 on the basis our previous synthesis of allo‐RA‐V, a related compound but with a structurally different cycloisodityrosine unit in which a diphenyl ether bond was formed between the carbon atom at the ϵ position of Tyr‐5 and the phenolic oxygen at the ζ position of Tyr‐6. This synthesis was characterized by the diaryl ether formation of the core cycloisodityrosine unit by copper(II) acetate‐mediated intramolecular phenol/arylboronic acid coupling and the macrocyclization of the linear hexapeptide between the Tyr‐6 and d ‐Ala‐1 residues to construct the 18‐membered cyclopeptide ring.…”
Section: Resultsmentioning
confidence: 99%
“…RA-dimer B ( 39 ), the second dimeric RA-series peptide, is composed of deoxybouvardin ( 3 ) and allo-RA-V ( 20 ), and those two cyclopeptides are connected between the phenolic oxygen atom of deoxybouvardin and the εa-carbon atom of the Tyr-6 residue of allo-RA-V ( 20 ) (Fig. 13 ) [ 39 ]. The structure of RA-dimer B ( 39 ) was elucidated on the basis of spectroscopic data, and the synthesis of 39 confirmed the relative stereochemistry and established the absolute configuration of this peptide.…”
Section: Synthesis Of Natural Compoundsmentioning
confidence: 99%