Evidence map›Paper›PMID 39543237›Full record

ArticleScientific reports2024

Synthesis and preliminary cytotoxicity evaluation of water soluble pentacyclic triterpenoid phosphonates.

Jevgeņija Lugiņina, Vladislavs Kroškins, Rihards Lācis, Elza Fedorovska, Öznur Demir, Arita Dubnika, Dagnija Loca, Māris Turks

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

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

8 authors.

Jevgeņija LugiņinaInstitute of Chemistry and Chemical Technology, Faculty of Natural Sciences and Technology, Riga Technical University, 3 P.Valdena Street, Riga, LV-1048, Latvia.
Vladislavs KroškinsInstitute of Chemistry and Chemical Technology, Faculty of Natural Sciences and Technology, Riga Technical University, 3 P.Valdena Street, Riga, LV-1048, Latvia.
Rihards LācisInstitute of Chemistry and Chemical Technology, Faculty of Natural Sciences and Technology, Riga Technical University, 3 P.Valdena Street, Riga, LV-1048, Latvia.
Elza FedorovskaInstitute of Chemistry and Chemical Technology, Faculty of Natural Sciences and Technology, Riga Technical University, 3 P.Valdena Street, Riga, LV-1048, Latvia.
Öznur DemirInstitute of Biomaterials and Bioengineering, Faculty of Natural Sciences and Technology, Riga Technical University, 3 Pulka Street, Riga, LV-1048, Latvia.
Arita DubnikaInstitute of Biomaterials and Bioengineering, Faculty of Natural Sciences and Technology, Riga Technical University, 3 Pulka Street, Riga, LV-1048, Latvia.
Dagnija LocaInstitute of Biomaterials and Bioengineering, Faculty of Natural Sciences and Technology, Riga Technical University, 3 Pulka Street, Riga, LV-1048, Latvia.
Māris TurksInstitute of Chemistry and Chemical Technology, Faculty of Natural Sciences and Technology, Riga Technical University, 3 P.Valdena Street, Riga, LV-1048, Latvia. maris.turks@rtu.lv.

Funding

European Union's Horizon 2020 857287Ministry of Economics Republic of Latvia VPP-EM-BIOMEDICINA-2022/1-0001
6 · The paper itself

Abstract

Synthesis, solubility and cytotoxicity evaluation of anionic phosphonates derived from betulin, betulinic acid, oleanolic acid and ursolic acid is reported. Phosphonate moieties were successfully installed at terpenoid C28 by carboxylic acid deprotonation/alkylation sequence using (dimethoxyphosphoryl)methyl trifluoromethanesulfonate as alkylation reagent. Also, betulin-derived and ether-linked bis-phosphonate is obtained and characterized. After demethylation in the presence of TMSI the resulting phosphonic acids were transformed into their disodium salts. All target compounds display excellent water solubility, which was determined by qNMR in D

Indexed as

OrganophosphonatesPentacyclic TriterpenesSolubilityTriterpenesWaterAnimalsBetulinic AcidCell Line, TumorCell SurvivalHumansMicebetulinBetulinic AcidOrganophosphonatesPentacyclic TriterpenesTriterpenesWaterAqueous solubilityCytotoxicityPentacyclic triterpenoidsPhosphonates

Identifiers

PMID39543237
PMCPMC11564732

What OpenQuestion holds

Textmetadata
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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.