Evidence map›Paper›PMID 35382311›Full record

ArticleACS omega2022

Effective Synthesis and Biological Evaluation of Natural and Designed Bis(indolyl)methanes via Taurine-Catalyzed Green Approach.

Kailas A Chavan, Manjari Shukla, Amar Nath Singh Chauhan, Sushobhan Maji, Ghanshyam Mali, Sudipta Bhattacharyya, Rohan D Erande

Open access · goldAbstract read
In one paragraph

Article in ACS omega, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
6.7field-weighted citation impact, top 2% 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

18 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Kinesin Spindle Protein (KIF11) in Mitosis and Cancer.International journal of molecular sciences · 2025
    Review
  3. FeClRSC advances · 2025
    Article
  4. Review
  5. Bisindole Compounds-Synthesis and Medicinal Properties.Antibiotics (Basel, Switzerland) · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. PolyaromaticMolecules (Basel, Switzerland) · 2023
    Article
  15. [RhCp*ClACS omega · 2023
    Review
  16. Article
  17. Article
  18. 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

7 authors at 1 institution in 1 country.

Kailas A ChavanDepartment of Chemistry, Indian Institute of Technology Jodhpur, Jodhpur 342037, India.
Manjari ShuklaDepartment of Bioscience and Bioengineering, Indian Institute of Technology Jodhpur, Jodhpur 342037, India.
Amar Nath Singh ChauhanDepartment of Chemistry, Indian Institute of Technology Jodhpur, Jodhpur 342037, India.
Sushobhan MajiDepartment of Bioscience and Bioengineering, Indian Institute of Technology Jodhpur, Jodhpur 342037, India.
Ghanshyam MaliDepartment of Chemistry, Indian Institute of Technology Jodhpur, Jodhpur 342037, India.
Sudipta BhattacharyyaDepartment of Bioscience and Bioengineering, Indian Institute of Technology Jodhpur, Jodhpur 342037, India.
Rohan D ErandeDepartment of Chemistry, Indian Institute of Technology Jodhpur, Jodhpur 342037, India.ORCID https://orcid.org/0000-0002-8763-5353
Indian Institute of Technology Jodhpur · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An ecofriendly, inexpensive, and efficient route for synthesizing 3,3'-bis(indolyl)methanes (BIMs) and their derivatives was carried out by an electrophilic substitution reaction of indole with structurally divergent aldehydes and ketones using taurine and water as a green catalyst and solvent, respectively, under sonication conditions. Using water as the only solvent, the catalytic process demonstrated outstanding activity, productivity, and broad functional group tolerance, affording the required BIM natural products and derivatives in excellent yields (59-90%). Furthermore, in silico based structure activity analysis of the synthesized BIM derivatives divulges their potential ability to bind antineoplastic drug target and spindle motor protein kinesin Eg5. The precise binding mode of BIM derivatives with the ATPase motor domain of Eg5 is structurally reminiscent with previously reported allosteric inhibitor Arry520, which is under phase III clinical trials. Nevertheless, detailed analysis of the binding poses indicates that BIM derivatives bind the allosteric pocket of the Eg5 motor domain more robustly than Arry520; moreover, unlike Arry520, BIM binding is found to be resistant to drug-resistant mutations of Eg5. Accordingly, a structure-guided mechanism of Eg5 inhibition by synthesized BIM derivatives is proposed.

Identifiers

PMID35382311
PMCPMC8973083
OpenAlexW4226090513

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.