Evidence map›Paper›PMID 40289985›Full record

ReviewCurrent drug discovery technologies2025

Darunavir: A Versatile Protease Inhibitor against Microbial Infections.

Mridul Singh Sengar, Kalpana Rahate, Megha Verma

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current drug discovery technologies, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Mridul Singh SengarDepartment of Pharmacy, School of Medical and Allied Sciences, Galgotias University, Greater Noida, 203201, Uttar Pradesh, India.ORCID 0009-0006-4817-3543
Kalpana RahateDepartment of Pharmacy, School of Medical and Allied Sciences, Galgotias University, Greater Noida, 203201, Uttar Pradesh, India.ORCID 0000-0003-1033-7814
Megha VermaDepartment of Pharmacy, School of Medical and Allied Sciences, Galgotias University, Greater Noida, 203201, Uttar Pradesh, India.ORCID 0009-0003-2856-9055

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microbial infections continue to pose significant threats to global health, necessitating the development of innovative therapeutic strategies. One promising avenue is the use of protease inhibitors, with darunavir (DRV) emerging as a potent candidate in the field. Designed to combat resistance to standard HIV therapy, DRV is a second-generation protease inhibitor. Regarding microbial infections, this study sheds light on the internal processes behind the impact of DRV within cells. Novel protease inhibitor DRV targets essential proteolytic enzymes that are essential for microbial survival and growth in order to achieve its antimicrobial actions. By interfering with the proteolytic digestion of important microbial proteins, its inhibitory effect prevents infectious particles from being assembled and maturing. DRV is a viable treatment option for microbial infections as its selective suppression reduces the possibility of off-target consequences. DRV efficiently penetrates the intracellular milieu of host cells, where it prevents the proteolytic cleavage of vital viral and bacterial proteins, hence combating pathogenic infections. Microbial infections may be treated in a variety of ways using DRV as it disrupts the cycle of pathogen reproduction. The present review explores the molecular principles behind the effectiveness of DRV against microbial infections, emphasizing the drug's ability to fight a wide range of pathogens. The comprehension of the intracellular activity of DRV is promising for the creation of novel treatment approaches, providing encouragement in the continuous fight against microbial diseases.

Indexed as

Bacterial InfectionsDarunavirHIV Protease InhibitorsProtease InhibitorsAnimalsHumansDarunavirHIV Protease InhibitorsProtease Inhibitorsdarunavirmicrobial infectionsPathogensprotease inhibitorsproteolytic cleavage.therapeutic approaches

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.