First Total Synthesis and Pharmacological Potential of a Plant Based Hexacyclopeptide

AuthorRajiv Dahiyaen
AuthorSunil Singhen
AuthorSheeba Varghese Guptaen
AuthorVijaykumar B. Sutariyaen
AuthorDeepak Bhatiaen
AuthorRita Mouryaen
AuthorSuresh V. Chennupatien
AuthorAjay Sharmaen
Issued Date2019-04-30en
AbstractA new bioactive proline-rich cyclohexapeptide - diandrine C (6), previously isolated from whole plant of Drymaria diandra (Caryophyllaceae), was synthesized through coupling reactions of tetrapeptide unit Boc-Gly--Pro--Tyr--Trp-OH with dipeptide unit -Pro-Gly-OMe using N,N-diisopropylcarbodiimide (DIPC) as the coupling agent, followed by cyclization of linear hexapeptide unit under alkaline condition. Structure of cyclohexapeptide was confirmed by means of chemical, and spectroscopic analyses and also was screened for its antimicrobial and anthelmintic properties. Bioevaluation results indicated that the newly synthesized hexacyclopeptide exhibited potent antimicrobial activity against Gram-negative bacteria Pseudomonas aeruginosa, Klebsiella pneumoniae and pathogenic Candida albicans at 6 μg/mL. Moderate to good level of antihelmintic activity against three earthworm species Megascoplex konkanensis, Pontoscotex corethruses and Eudrilus eugeniae was also observed at concentration of 2 mg/mL.en
DOIhttps://doi.org/10.22037/ijpr.2019.1100643en
KeywordDiandrine Cen
KeywordProline-rich cyclic peptideen
KeywordSolution-phase peptide synthesisen
KeywordDrymaria diandraen
KeywordAntimicrobial activityen
KeywordAntihelmintic activityen
PublisherBrieflandsen
TitleFirst Total Synthesis and Pharmacological Potential of a Plant Based Hexacyclopeptideen
TypeOriginal Articleen

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
ijpr-18-938.pdf
Size:
539.78 KB
Format:
Adobe Portable Document Format
Description:
Article/s PDF