Alcimaterpenoids A and B, Two Enantiomeric Pairs of Bis-Denudaquinol-Monoterpenoid Meroterpenoids from the Endangered Plant Alcimandra cathcartii

Abstract Alcimaterpenoids A (1) and B (2), two pairs of racemic bis-denudaquinol-monoterpenoid meroterpenoids, were isolated and identified from Alcimandra cathcartii. Electronic circular dichroism (ECD) computations, GIAO 13C{1H} NMR (in conjunction with DP4+ probability analysis), and extensive 2D-NMR spectroscopic analysis techniques were used to determine their structures and absolute configurations. Structurally, compounds 1 and 2 are the first enantiomeric bis-denudaquinol-monoterpenoid meroterpenoids. Plausible biosynthetic pathways were briefly proposed. Compound (±)–1 exhibited moderate cytotoxic activity against the human PLC/PRF/5 cell line (IC50: 20.6 μM).

Authors

Institutions

Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-11-03
DOI
https://doi.org/10.1021/acs.joc.6c01752
Primary Topic
Molecular spectroscopy and chirality
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Alcimaterpenoids A and B, Two Enantiomeric Pairs of Bis-Denudaquinol-Monoterpenoid Meroterpenoids from the Endangered Plant Alcimandra cathcartii

Jin‐Feng Hu, Chuan-Yun Xiao, Yingpeng Tong, Yeun‐Mun Choo et al.
The Journal of Organic Chemistry
Molecular spectroscopy and chirality
article

Alcimaterpenoids A and B, Two Enantiomeric Pairs of Bis-Denudaquinol-Monoterpenoid Meroterpenoids from the Endangered Plant Alcimandra cathcartii

Jin‐Feng Hu, Chuan-Yun Xiao, Yingpeng Tong, Yeun‐Mun Choo, Can Wang, Chun‐Xiao Jiang, Dong Huang, Jiang Wan
article en

Abstract

Abstract Alcimaterpenoids A (1) and B (2), two pairs of racemic bis-denudaquinol-monoterpenoid meroterpenoids, were isolated and identified from Alcimandra cathcartii. Electronic circular dichroism (ECD) computations, GIAO 13C{1H} NMR (in conjunction with DP4+ probability analysis), and extensive 2D-NMR spectroscopic analysis techniques were used to determine their structures and absolute configurations. Structurally, compounds 1 and 2 are the first enantiomeric bis-denudaquinol-monoterpenoid meroterpenoids. Plausible biosynthetic pathways were briefly proposed. Compound (±)–1 exhibited moderate cytotoxic activity against the human PLC/PRF/5 cell line (IC50: 20.6 μM).

The Journal of Organic Chemistry
Jiangxi University of Traditional Chinese Medicine (CN), Peking University (CN), University of Malaya (MY), Zhejiang Hisun Pharmaceutical (China) (CN), Taizhou University (CN), Taizhou University (CN)
Openalex Percentile: Top 29%
Molecular spectroscopy and chirality
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Laika access coming soon