Evidence map›Paper›PMID 40488850›Full record

ReviewNaunyn-Schmiedeberg's archives of pharmacology2025

Formononetin: pharmacological properties and therapeutic potential.

Navneet Sharma, Atul Kabra

Abstract readReview
PubMed Publisher
In one paragraph

Review in Naunyn-Schmiedeberg's archives of pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. 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

2 authors.

Navneet SharmaUniversity Institute of Pharma Sciences, Chandigarh University, Gharuan, Mohali, Punjab, 140413, India.
Atul KabraUniversity Institute of Pharma Sciences, Chandigarh University, Gharuan, Mohali, Punjab, 140413, India. atul.kbr@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Formononetin (FMN) is a naturally occurring isoflavonoid. It has been extensively researched for its therapeutic properties in neurological disorders, cancer, renal dysfunction, and inflammatory diseases, as demonstrated by both in vivo and in vitro studies. The compound is primarily obtained from plants such as Trifolium pratense (red clover) and Astragalus membranaceus. A number of clinical trials have also emphasized its function in enhancing vascular health, bone mineral content, and glucose metabolism. Formononetin has good pharmacokinetics, with rapid oral absorption, a maximum plasma concentration between 30 and 60 min, and a half-life of approximately 2 h. It is regulated by the liver through cytochrome P450 enzymes and phase II conjugation. In addition, the therapeutic action of formononetin has been found to be improved in various models when either its derivatives are formed or when it is combined with other drugs. This review article aims to comprehensively examine the pharmacological potential of formononetin across disease models while highlighting recent advances in its pharmacokinetics and safety profile. Recent developments in nanoformulation and chemical modification have been encouraging in improving its bioavailability and therapeutic efficacy. Further exploration into next-generation delivery systems such as nanoparticles and phospholipid complexes, along with combination therapies and derivative synthesis, may significantly enhance formononetin's clinical applicability. Additionally, comprehensive toxicological evaluations to establish its long-term safety in diverse patient populations are warranted.

Indexed as

IsoflavonesAnimalsBiological AvailabilityHumansformononetinIsoflavonesDerivatives of formononetinFormononetinHerbal sources of formononetinIn vitro and in vivo studies of formononetinIsoflavonoidSAR of formononetin

Identifiers

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.