Evidence map›Paper›PMID 31330911›Full record

ArticleMolecules (Basel, Switzerland)2019

Novel Derivatives of Deoxycholic Acid Bearing Linear Aliphatic Diamine and Aminoalcohol Moieties and their Cyclic Analogs at the C3 Position: Synthesis and Evaluation of Their In Vitro Antitumor Potential.

Andrey V Markov, Valeriya O Babich, Irina I Popadyuk, Oksana V Salomatina, Evgeniya B Logashenko, Nariman F Salakhutdinov, Marina A Zenkova

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 52% of its field
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

4 citing papers in PubMed, 6 citations in OpenAlex.

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

7 authors at 3 institutions in 1 country.

Andrey V MarkovInstitute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, Lavrent'ev ave., 8, 630090 Novosibirsk, Russia. andmrkv@gmail.com.
Valeriya O BabichInstitute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, Lavrent'ev ave., 8, 630090 Novosibirsk, Russia.
Irina I PopadyukN.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Lavrent'ev ave., 9, 630090 Novosibirsk, Russia.
Oksana V SalomatinaInstitute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, Lavrent'ev ave., 8, 630090 Novosibirsk, Russia.
Evgeniya B LogashenkoInstitute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, Lavrent'ev ave., 8, 630090 Novosibirsk, Russia.
Nariman F SalakhutdinovNovosibirsk State University, Pirogova str. 2, 630090 Novosibirsk, Russia.
Marina A ZenkovaInstitute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, Lavrent'ev ave., 8, 630090 Novosibirsk, Russia.
Institute of Chemical Biology and Fundamental Medicine · RUNovosibirsk State University · RUNovosibirsk Institute of Organic Chemistry · RU

Funding

Russian Science Foundation 17-75-20120State funded budget project of ICBFM SB RAS AAAA-A17-117020210024-8
6 · The paper itself

Abstract

A series of novel deoxycholic acid (DCA) derivatives containing aliphatic diamine and aminoalcohol or morpholine moieties at the C3 position were synthesized by 3,26-epoxide ring-opening reactions. These compounds were investigated for their cytotoxicity in four human tumor cell lines and murine macrophages and for inhibitory activity against macrophage-mediated NO synthesis in vitro. Obtained data revealed that: (i) all amine-containing substituents significantly increased the cytotoxicity of the novel compounds (IC

Indexed as

Amino AlcoholsAnimalsAntineoplastic AgentsCell Line, TumorDeoxycholic AcidDiaminesDose-Response Relationship, DrugHumansMembrane Potential, MitochondrialMiceModels, MolecularMolecular ConformationMolecular StructureStructure-Activity RelationshipAmino AlcoholsAntineoplastic AgentsDeoxycholic AcidDiaminesaminoalcoholsapoptosisautophagydeoxycholic acid derivativesdiaminesVDR

Identifiers

PMID31330911
PMCPMC6681416
OpenAlexW2963950227

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.