Synthesis, in vitro, and in silico study of novel pyridine based 1,3-diphenylurea derivatives as tyrosinase inhibitors.

1,3-diphenylurea Docking MD simulation Pyridine Tyrosinase

Journal

Bioorganic chemistry
ISSN: 1090-2120
Titre abrégé: Bioorg Chem
Pays: United States
ID NLM: 1303703

Informations de publication

Date de publication:
13 Aug 2024
Historique:
received: 22 07 2024
revised: 11 08 2024
accepted: 12 08 2024
medline: 22 8 2024
pubmed: 22 8 2024
entrez: 21 8 2024
Statut: aheadofprint

Résumé

Tyrosinase inhibitors are studied in the cosmetics and pharmaceutical sectors as tyrosinase enzyme is involved in the biosynthesis and regulation of melanin, hence these inhibitors are beneficial for the management of melanogenesis and hyperpigmentation-related disorders. In the current work, a novel series of diphenyl urea derivatives containing a halo-pyridine moiety (5a-t) was synthesized via a multi-step synthesis. In vitro, tyrosinase inhibitory assay results showed that, except for two compounds, the derivatives were excellent inhibitors of human tyrosinase. The average IC

Identifiants

pubmed: 39167873
pii: S0045-2068(24)00629-1
doi: 10.1016/j.bioorg.2024.107724
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

107724

Informations de copyright

Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Anam Rubbab Pasha (A)

Institute of Chemical Sciences, Bahauddin Zakariya University, Multan 60800, Pakistan; Natural and Medical Sciences Research Centre, University of Nizwa, P.O. Box 33, PC 616, Birkat Al Mauz, Nizwa, Oman.

Majid Khan (M)

Natural and Medical Sciences Research Centre, University of Nizwa, P.O. Box 33, PC 616, Birkat Al Mauz, Nizwa, Oman; Department of Biochemistry, Hazara University, Mansehra, Pakistan.

Ajmal Khan (A)

Natural and Medical Sciences Research Centre, University of Nizwa, P.O. Box 33, PC 616, Birkat Al Mauz, Nizwa, Oman.

Javid Hussain (J)

Department of Biological Sciences and Chemistry, University of Nizwa, Oman.

Mariya Al-Rashida (M)

Department of Chemistry, Forman Christian College (A Chartered University), Lahore, Pakistan.

Talha Islam (T)

Department of Chemistry, Forman Christian College (A Chartered University), Lahore, Pakistan.

Zahra Batool (Z)

Institute of Chemical Sciences, Bahauddin Zakariya University, Multan 60800, Pakistan.

Hamdy Kashtoh (H)

Department of Biotechnology, Yeungnam University, Gyeongsan 38541, Gyeongbuk, Republic of Korea. Electronic address: hamdy_kashtoh@ynu.ac.kr.

Magda H Abdellattif (MH)

Chemistry Department, College of Sciences, University College of Taraba, Taif University, Taif 21944, Saudi Arabia.

Ahmed Al-Harrasi (A)

Natural and Medical Sciences Research Centre, University of Nizwa, P.O. Box 33, PC 616, Birkat Al Mauz, Nizwa, Oman. Electronic address: aharrasi@unizwa.edu.om.

Zahid Shafiq (Z)

Institute of Chemical Sciences, Bahauddin Zakariya University, Multan 60800, Pakistan.

Silvia Schenone (S)

Department of Pharmacy, University of Genoa, Viale Benedetto XV, 3, Genoa 16132, Italy. Electronic address: silvia.schenone@unige.it.

Classifications MeSH