Evidence map›Paper›PMID 39716766›Full record

ArticleThe New phytologist2025

Unique bibenzyl cannabinoids in the liverwort Radula marginata: parallels with Cannabis chemistry.

Christelle M Andre, Catherine E Sansom, Blue J Plunkett, Cyril Hamiaux, Lenhy Massey, Andrew Chan, Manu Caddie, Richard V Espley, Nigel B Perry

Abstract read
In one paragraph

Article in The New phytologist, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Christelle M AndreThe New Zealand Institute for Plant and Food Research Limited (PFR), Mt Albert Research Centre, Auckland, 1142, New Zealand.ORCID https://orcid.org/0000-0001-9056-160X
Catherine E SansomPFR, Chemistry Department, University of Otago, Dunedin, 9016, New Zealand.ORCID https://orcid.org/0000-0002-0034-524X
Blue J PlunkettThe New Zealand Institute for Plant and Food Research Limited (PFR), Mt Albert Research Centre, Auckland, 1142, New Zealand.ORCID https://orcid.org/0000-0003-3793-9495
Cyril HamiauxThe New Zealand Institute for Plant and Food Research Limited (PFR), Mt Albert Research Centre, Auckland, 1142, New Zealand.ORCID https://orcid.org/0000-0001-9198-3441
Lenhy MasseyThe New Zealand Institute for Plant and Food Research Limited (PFR), Mt Albert Research Centre, Auckland, 1142, New Zealand.
Andrew ChanThe New Zealand Institute for Plant and Food Research Limited (PFR), Mt Albert Research Centre, Auckland, 1142, New Zealand.ORCID https://orcid.org/0000-0002-8128-1021
Manu CaddieTe Kotahi Research Institute, University of Waikato, Hamilton, 3240, New Zealand.ORCID https://orcid.org/0000-0003-4141-4085
Richard V EspleyThe New Zealand Institute for Plant and Food Research Limited (PFR), Mt Albert Research Centre, Auckland, 1142, New Zealand.ORCID https://orcid.org/0000-0002-1732-3688
Nigel B PerryPFR, Chemistry Department, University of Otago, Dunedin, 9016, New Zealand.ORCID https://orcid.org/0000-0003-3196-3945

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The potential of cannabinoids to address public health challenges has stimulated exploration into alternative sources and production technologies. Radula marginata, an endemic Aotearoa/New Zealand liverwort, produces the bibenzyl cannabinoid perrottetinene (PET), analogous to Cannabis psychoactive tetrahydrocannabinol (THC). Structural differences between PET and THC could alter therapeutic interactions and mitigate adverse side effects. To understand the cannabinoid production potential of R. marginata, we analyzed 75 collections from three locations across several seasons, collaborating with kaitiaki Māori (indigenous guardians). Metabolic plasticity of the phytocannabinoids and plant growth was assessed under controlled growth conditions, and in in vitro culture. Perrottetinene diol (trans-PTD), analogous to cannabidiol (trans-CBD), and its acid precursor (PTDA), were identified and fully characterized from nature for the first time. Bibenzyl-4-geranyl (BB4G), analogous to cannabigerol (CBG), and its corresponding acid (BB4GA), were also isolated. Radula marginata showed chemotypes dominated by PET, PTD, or BB4G, in striking analogy to the main Cannabis chemotypes. These site-selective chemotypes persisted after growth under artificial lighting and in in vitro progeny, suggesting genetic control. These results expand phytocannabinoid knowledge through the discovery of PTD analogous to CBD. They add a new dimension to liverwort cannabinoids and suggest convergent evolution of biosynthesis in two distant plant lineages.

Indexed as

BibenzylsCannabinoidsCannabisHepatophytaBibenzylsCannabinoids1H NMR spectroscopybibenzylcannabinoidGC‐MSintraspecific variationlight treatmentliverwortRadula marginata

Identifiers

PMID39716766
PMCPMC12095976

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.