Synthesis of bis-indolylmethanes as new potential inhibitors of β-glucuronidase and their molecular docking studies.

Taha M, Ullah H, Al Muqarrabun LMR, Khan MN, Rahim F, Ahmat N, Ali M, Perveen S.

Open source

DOI
10.1016/j.ejmech.2017.10.071
Published
2017-10-26
Container
Eur J Med Chem
Publisher
Not recorded
Open access
no

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BibTeX

@article{allodium:10.1016/j.ejmech.2017.10.071,
  title = {Synthesis of bis-indolylmethanes as new potential inhibitors of β-glucuronidase and their molecular docking studies.},
  author = {Taha M and  Ullah H and  Al Muqarrabun LMR and  Khan MN and  Rahim F and  Ahmat N and  Ali M and  Perveen S.},
  year = {2018},
  journal = {Eur J Med Chem},
  doi = {10.1016/j.ejmech.2017.10.071},
  url = {https://doi.org/10.1016/j.ejmech.2017.10.071}
}

RIS

TY  - JOUR
TI  - Synthesis of bis-indolylmethanes as new potential inhibitors of β-glucuronidase and their molecular docking studies.
AU  - Taha M
AU  -  Ullah H
AU  -  Al Muqarrabun LMR
AU  -  Khan MN
AU  -  Rahim F
AU  -  Ahmat N
AU  -  Ali M
AU  -  Perveen S.
PY  - 2018
JO  - Eur J Med Chem
DO  - 10.1016/j.ejmech.2017.10.071
UR  - https://doi.org/10.1016/j.ejmech.2017.10.071
ER  - 

APA

M, T., H, U., LMR, A. M., MN, K., F, R., N, A., M, A., & S., P. (2018). Synthesis of bis-indolylmethanes as new potential inhibitors of β-glucuronidase and their molecular docking studies.. Eur J Med Chem. https://doi.org/10.1016/j.ejmech.2017.10.071

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