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Discovery of Novel Soluble Epoxide Hydrolase Inhibitors as Potent Vasodilators.
Tripathi, Neetika; Paliwal, Sarvesh; Sharma, Swapnil; Verma, Kanika; Gururani, Ritika; Tiwari, Akanksha; Verma, Amrita; Chauhan, Monika; Singh, Aarti; Kumar, Dipak; Pant, Aditya.
Affiliation
  • Tripathi N; Department of Pharmacy, Banasthali University, P. O. Banasthali, 304022, Rajasthan, India.
  • Paliwal S; Department of Pharmacy, Banasthali University, P. O. Banasthali, 304022, Rajasthan, India. paliwalsarvesh@yahoo.com.
  • Sharma S; Department of Pharmacy, Banasthali University, P. O. Banasthali, 304022, Rajasthan, India.
  • Verma K; Department of Pharmacy, Banasthali University, P. O. Banasthali, 304022, Rajasthan, India.
  • Gururani R; Department of Pharmacy, Banasthali University, P. O. Banasthali, 304022, Rajasthan, India.
  • Tiwari A; Department of Pharmacy, Banasthali University, P. O. Banasthali, 304022, Rajasthan, India.
  • Verma A; Department of Pharmacy, Banasthali University, P. O. Banasthali, 304022, Rajasthan, India.
  • Chauhan M; Department of Pharmacy, Banasthali University, P. O. Banasthali, 304022, Rajasthan, India.
  • Singh A; Department of Pharmacy, Banasthali University, P. O. Banasthali, 304022, Rajasthan, India.
  • Kumar D; Indian Institute of Toxicology Research, Mahatma Gandhi Marg, Post Box No- 80, Lucknow, 226001, UP, India.
  • Pant A; Indian Institute of Toxicology Research, Mahatma Gandhi Marg, Post Box No- 80, Lucknow, 226001, UP, India.
Sci Rep ; 8(1): 14604, 2018 10 02.
Article in En | MEDLINE | ID: mdl-30279487
ABSTRACT
In view of the role of sEH (soluble epoxide hydrolase) in hypertension, we have developed a rigorously validated pharmacophore model containing one HBA (Hydrogen Bond Acceptor), two HY (Hydrophobic) and one RA (Ring Aromatic) features. The model was used as a query to search the NCI (National Cancer Institute) and Maybridge database leading to retrieval of many compounds which were sorted on the basis of predicted activity, fit value and Lipinski's violation. The selected compounds were docked into the active site of enzyme soluble epoxide hydrolase. Potential interactions were observed between the features of the identified hits and the amino acids present in the docking site. The three selected compounds were subjected to in vitro evaluation using enzyme- based assay and the isolated rat aortic model followed by cytotoxicity studies. The results demonstrate that the identified compounds are potent, safe and novel soluble epoxide hydrolase inhibitors.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Aorta / Vasodilation / Vasodilator Agents / Enzyme Inhibitors / Epoxide Hydrolases Type of study: Prognostic_studies Limits: Animals / Humans / Male Language: En Journal: Sci Rep Year: 2018 Document type: Article Affiliation country: India

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Aorta / Vasodilation / Vasodilator Agents / Enzyme Inhibitors / Epoxide Hydrolases Type of study: Prognostic_studies Limits: Animals / Humans / Male Language: En Journal: Sci Rep Year: 2018 Document type: Article Affiliation country: India