• Corpus ID: 89514960

Three New Clerodane Diterpenes from Polyalthia longifolia var. pendula

  title={Three New Clerodane Diterpenes from Polyalthia longifolia var. pendula},
  author={陳朝榮 and 黃麗嬌 and 郭盛助 and 吳永昌},

A Review on Therapeutic Benefits of Active Chemical Moieties Present in Polyalthia longifolia

This paper presents the results of a two-year study conducted at the National Institute of Medical Microbiology and Parasitology, Da Nang, Vietnam, aiming at determining the carrier and removal of canine coronavirus from human faeces.

Clerodane Diterpenoids from an Edible Plant Justicia insularis: Discovery, Cytotoxicity, and Apoptosis Induction in Human Ovarian Cancer Cells

Clerodane diterpenoids (1 and 2) in J. insularis were identified as cytotoxic to ovarian cancer cells via the induction of apoptosis, providing an abundant and valuable source of hit compounds for the treatment of ovarian cancer.

Phytochemicals from Polyalthia Species: Potential and Implication on Anti-Oxidant, Anti-Inflammatory, Anti-Cancer, and Chemoprevention Activities

This review is an attempt to collect current available phytochemicals from Polyalthia species, which exhibit anti-cancer potentials for chemoprevention purposes, providing directions for further research on the interesting agents and possible clinical applications.

16-Hydroxycleroda-3,13-Dien-15,16-Olide Induces Apoptosis in Human Bladder Cancer Cells through Cell Cycle Arrest, Mitochondria ROS Overproduction, and Inactivation of EGFR-Related Signalling Pathways

CD induces apoptosis in T24 bladder cancer cells through targeting multiple intracellular signaling pathways as a result of oxidative stress and cell cycle arrest as well as inhibition of the cell cycle-related genes.

Polyalthia Clerodane Diterpene Potentiates Hypoglycemia via Inhibition of Dipeptidyl Peptidase 4

Serine protease dipeptidyl peptidase 4 (DPP-4) is involved in self/non-self-recognition and insulin sensitivity. DPP-4 inhibitors are conventional choices for diabetic treatment; however, side

The autophagic inhibition oral squamous cell carcinoma cancer growth of 16-hydroxycleroda-3,13-dien-15,16-olide.

An in vivo assay indicated that HCD could treat oral cancer by deferring tumor growth, and provided a favorable assessment for further elucidating the role of HCD that targets autophagic cell death pathways as a potential agent for cancer therapy.

Agelamasines A and B, diterpene alkaloids from an Okinawan marine sponge Agelas sp.

Two new diterpene alkaloids having an N-methyladenine moiety, agelamasines A and B, were isolated from an Okinawan marine sponge and elucidated on the basis of spectroscopic analyses.

Annonaceae: Breaking the Wall of Inflammation

This review is an effort to abridge the ethnobotany, morphology, phytochemistry, toxicity, and particularly focusing on the anti-inflammatory activity of the Annonaceae species.

A new sesquiterpenoid from Polyalthia petelotii

The isolates were assessed for their cytotoxicity against five human tumour lines, and the result showed that only 2 displayed weak inhibitory activity.