Evidence map›Paper›PMID 34830456›Full record

ArticleInternational journal of molecular sciences2021

Manipulating Estrogenic/Anti-Estrogenic Activity of Triphenylethylenes towards Development of Novel Anti-Neoplastic SERMs.

Heba E Elnakib, Marian M Ramsis, Nouran O Albably, Merna A Vector, Jan J Weigand, Kai Schwedtmann, Jannette Wober, Oliver Zierau, Günter Vollmer, Ashraf H Abadi and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 28% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. 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

11 authors at 2 institutions in 2 countries.

Heba E ElnakibDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy and Biotechnology, German University in Cairo, Cairo 11835, Egypt.
Marian M RamsisDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy and Biotechnology, German University in Cairo, Cairo 11835, Egypt.
Nouran O AlbablyDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy and Biotechnology, German University in Cairo, Cairo 11835, Egypt.
Merna A VectorDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy and Biotechnology, German University in Cairo, Cairo 11835, Egypt.
Jan J WeigandFaculty of Chemistry and Food Chemistry, Institute of Inorganic Molecular Chemistry, Technische Universität Dresden, 01062 Dresden, Germany.ORCID 0000-0001-7323-7816
Kai SchwedtmannFaculty of Chemistry and Food Chemistry, Institute of Inorganic Molecular Chemistry, Technische Universität Dresden, 01062 Dresden, Germany.ORCID 0000-0002-7965-2647
Jannette WoberFaculty of Biology, Institute of Zoology, Technische Universität Dresden, 01062 Dresden, Germany.
Oliver ZierauFaculty of Biology, Institute of Zoology, Technische Universität Dresden, 01062 Dresden, Germany.
Günter VollmerFaculty of Biology, Institute of Zoology, Technische Universität Dresden, 01062 Dresden, Germany.
Ashraf H AbadiDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy and Biotechnology, German University in Cairo, Cairo 11835, Egypt.ORCID 0000-0002-7433-261X
Nermin S AhmedDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy and Biotechnology, German University in Cairo, Cairo 11835, Egypt.ORCID 0000-0002-8869-3387
German University in Cairo · EGTechnische Universität Dresden · DE

Funding

German Academic Exchange Service ERAScience and Technology Development Fund 30298Science and Technology Development Fund 5386
6 · The paper itself

Abstract

Selective estrogen receptor modulators (SERMs) act as estrogen receptor (ERα) agonists or antagonists depending on the target issue. Tamoxifen (TAM) (a non-steroidal triphenylethylene derivative) was the first SERM approved as anti-estrogen for the treatment of metastatic breast cancer. On the hunt for novel SERMs with potential growth inhibitory activity on breast cancer cell lines yet no potential to induce endometrial carcinoma, we designed and synthesized 28 novel TAM analogs. The novel analogs bear a triphenylethylene scaffold. Modifications on rings

Indexed as

AnimalsBreast NeoplasmsEndometrial NeoplasmsEstrogen AntagonistsEstrogen Receptor alphaFemaleHumansMCF-7 CellsRatsReceptors, EstrogenSelective Estrogen Receptor ModulatorsStilbenesTamoxifenEstrogen AntagonistsEstrogen Receptor alphaReceptors, EstrogenSelective Estrogen Receptor ModulatorsStilbenesTamoxifentriphenylethyleneCYP2D6Ishikawa cellsMCF-7SERMtamoxifenTNBCuterotrophic

Identifiers

PMID34830456
PMCPMC8621172
OpenAlexW3216514479

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.