Dayani Senadeera Sarath Parakumge

Dr. Dayani Senadeera Sarath Parakumge

orcid

Research Focus & Metrics

Academic Career Length

9Years (2018-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
3 July 2018 in Journal of Natural Products
Verified
Journal Article
Closed access
DPDayani Senadeera Sarath Parakumge
Dayani Senadeera Sarath Parakumge
LLLeonardo Lucantoni
Leonardo Lucantoni
SDSandra Duffy
Sandra Duffy
VAVicky Avery
Vicky Avery
ACAnthony Carroll
Anthony Carroll

13 June 2022 in Journal of Natural Products
Verified
Journal Article
Closed access
DPDayani Senadeera Sarath Parakumge
Dayani Senadeera Sarath Parakumge
Dongdong WangDongdong Wang
Dongdong Wang
CKChang-Kwon Kim
Chang-Kwon Kim
ESEmily Smith
Emily Smith
DDDavid E. Durrant
David E. Durrant
John BeutlerJohn Beutler
John Beutler

28 July 2023 in Molecules
Verified
Journal Article
Open access
PDF file
FEFatma Memnune Eruçar
Fatma Memnune Eruçar
DPDayani Senadeera Sarath Parakumge
Dayani Senadeera Sarath Parakumge
JWJennifer Wilson
Jennifer Wilson
EGEkaterina Goncharova
Ekaterina Goncharova
John BeutlerJohn Beutler
John Beutler
Mahmut MiskiMahmut Miski
Mahmut Miski
Six new sesquiterpene coumarin ethers, namely turcicanol A (1), turcicanol A acetate (2), turcicanol B (3), turcica ketone (4), 11′-dehydrokaratavicinol (5), and galbanaldehyde (6), and one new sulfur-containing compound, namely turcicasulphide (7), along with thirty-two known secondary metabolites were isolated from the root of the endemic species Ferula turcica Akalın, Miski, & Tuncay through a bioassay-guided isolation approach. The structures of the new compounds were elucidated by spectroscopic analysis and comparison with the literature. Cell growth inhibition of colon cancer cell lines (COLO205 and HCT116) and kidney cancer cell lines (UO31 and A498) was used to guide isolation. Seventeen of the compounds showed significant activity against the cell lines.

25 April 2025 in Molecules
Verified
Journal Article
Open access
PDF file
F. Kaan KuranF. Kaan Kuran
F. Kaan Kuran
DPDayani Senadeera Sarath Parakumge
Dayani Senadeera Sarath Parakumge
Dongdong WangDongdong Wang
Dongdong Wang
JHJiyeon Hwang
Jiyeon Hwang
EGEkaterina Goncharova
Ekaterina Goncharova
Mahmut MiskiMahmut Miski
Mahmut Miski
Four new sesquiterpene coumarin ethers (1–4) and a new phenylpropanoid compound (5) were isolated from a hexane extract of the roots of Ferula drudeana, the putative Anatolian ecotype of the silphion plant, in addition to nineteen previously described sesquiterpene coumarins (6–24) and four known phenylpropanoid derivatives (25–28). The structures of these compounds were elucidated by extensive spectroscopic analysis and computational studies. The cytotoxic activities of all isolated compounds were evaluated on renal, malignant pleural mesothelioma (MPM) and colon cancer cell lines. While 11 sesquiterpene coumarin derivatives showed strong-to-moderate cytotoxic activity against the UO31 renal cancer cell line, 13 compounds showed strong cytotoxic activity against the MPM cell line, and four sesquiterpene coumarin derivatives displayed moderate cytotoxic activity against the colon cancer cell line.