Wang W, He L, Lin T, Xiang F, Wu Y, Zhou F
Front Oncol. 2025; 15:1522273.
PMID: 39949739
PMC: 11821653.
DOI: 10.3389/fonc.2025.1522273.
Retsas S
Biomolecules. 2024; 14(11).
PMID: 39595560
PMC: 11591967.
DOI: 10.3390/biom14111383.
Qiu X, Zhang H, Tang Z, Fan Y, Yuan W, Feng C
Chin Med J (Engl). 2023; 137(12):1453-1464.
PMID: 37962205
PMC: 11188914.
DOI: 10.1097/CM9.0000000000002813.
Temaj G, Chichiarelli S, Eufemi M, Altieri F, Hadziselimovic R, Farooqi A
Biomedicines. 2022; 10(9).
PMID: 36140189
PMC: 9495564.
DOI: 10.3390/biomedicines10092088.
Yu G, Wu J, Shi B, Bao M, Cai X
Nat Prod Bioprospect. 2022; 12(1):24.
PMID: 35778536
PMC: 9249953.
DOI: 10.1007/s13659-022-00344-1.
An Update on Pharmacological Relevance and Chemical Synthesis of Natural Products and Derivatives with Anti SARS-CoV-2 Activity.
Shagufta , Ahmad I
ChemistrySelect. 2021; 6(42):11502-11527.
PMID: 34909460
PMC: 8661826.
DOI: 10.1002/slct.202103301.
Harringtonine Inhibits Herpes Simplex Virus Type 1 Infection by Reducing Herpes Virus Entry Mediator Expression.
Liu Y, You Q, Zhang F, Chen D, Huang Z, Wu Z
Front Microbiol. 2021; 12:722748.
PMID: 34531841
PMC: 8438530.
DOI: 10.3389/fmicb.2021.722748.
A modular and divergent approach to spirocyclic pyrrolidines.
Shennan B, Smith P, Ogura Y, Dixon D
Chem Sci. 2021; 11(38):10354-10360.
PMID: 34094297
PMC: 8162384.
DOI: 10.1039/d0sc03676e.
Protein synthesis inhibitor omacetaxine is effective against hepatocellular carcinoma.
Li L, Halpert G, Lerner M, Hu H, Dimitrion P, Weiss M
JCI Insight. 2021; 6(12).
PMID: 34003798
PMC: 8262474.
DOI: 10.1172/jci.insight.138197.
Harringtonine Inhibits Zika Virus Infection through Multiple Mechanisms.
Lai Z, Ho Y, Lu J
Molecules. 2020; 25(18).
PMID: 32906689
PMC: 7570876.
DOI: 10.3390/molecules25184082.
Turning the Tide: Natural Products and Natural-Product-Inspired Chemicals as Potential Counters to SARS-CoV-2 Infection.
Wang Z, Yang L
Front Pharmacol. 2020; 11:1013.
PMID: 32714193
PMC: 7343773.
DOI: 10.3389/fphar.2020.01013.
Targeting the Human 80S Ribosome in Cancer: From Structure to Function and Drug Design for Innovative Adjuvant Therapeutic Strategies.
Gilles A, Frechin L, Natchiar K, Biondani G, von Loeffelholz O, Holvec S
Cells. 2020; 9(3).
PMID: 32151059
PMC: 7140421.
DOI: 10.3390/cells9030629.
Cytostatic and Cytotoxic Natural Products against Cancer Cell Models.
Ling T, Lang W, Maier J, Quintana Centurion M, Rivas F
Molecules. 2019; 24(10).
PMID: 31130671
PMC: 6571673.
DOI: 10.3390/molecules24102012.
Isolation and identification of two new compounds from the twigs and leaves of Cephalotaxus fortunei.
Feng Q, Li B, Feng Y, Li X, Ma X, Wang H
J Nat Med. 2019; 73(3):653-660.
PMID: 30976949
DOI: 10.1007/s11418-019-01308-5.
Homoharringtonine is a safe and effective substitute for anthracyclines in children younger than 2 years old with acute myeloid leukemia.
Chen X, Tang Y, Chen J, Chen R, Gu L, Xue H
Front Med. 2019; 13(3):378-387.
PMID: 30635781
DOI: 10.1007/s11684-018-0658-4.
The Search for Anticancer Agents from Tropical Plants.
Henkin J, Ren Y, Soejarto D, Kinghorn A
Prog Chem Org Nat Prod. 2018; 107:1-94.
PMID: 30178270
PMC: 11840880.
DOI: 10.1007/978-3-319-93506-5_1.
HAG (Homoharringtonine, Cytarabine, G-CSF) Regimen for the Treatment of Acute Myeloid Leukemia and Myelodysplastic Syndrome: A Meta-Analysis with 2,314 Participants.
Xie M, Jiang Q, Li L, Zhu J, Zhu L, Zhou D
PLoS One. 2016; 11(10):e0164238.
PMID: 27706258
PMC: 5051946.
DOI: 10.1371/journal.pone.0164238.
Five New Alkaloids from Cephalotaxus lanceolata and C. fortunei var. alpina.
Ni L, Zhong X, Cai J, Bao M, Zhang B, Wu J
Nat Prod Bioprospect. 2016; 6(3):149-54.
PMID: 27016921
PMC: 5385657.
DOI: 10.1007/s13659-016-0093-7.
Acyl flavonoids, biflavones, and flavonoids from Cephalotaxus harringtonia var. nana.
Komoto N, Nakane T, Matsumoto S, Hashimoto S, Shirota O, Sekita S
J Nat Med. 2015; 69(4):479-86.
PMID: 25905687
DOI: 10.1007/s11418-015-0912-x.
Cancer wars: natural products strike back.
Basmadjian C, Zhao Q, Bentouhami E, Djehal A, Nebigil C, Johnson R
Front Chem. 2014; 2:20.
PMID: 24822174
PMC: 4013484.
DOI: 10.3389/fchem.2014.00020.