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      Investigation of anti-nociceptive, anti-inflammatory potential and ADMET studies of pure compounds isolated from Isodon rugosus Wall. ex Benth

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          Abstract

          The strong ethnopharmacological utilization of Isodon rugosus Wall. Ex. Benth is evident in the treatment of several types of pain and inflammation, including toothache, earache, abdominal pain, gastric pain, and generalized body pain and inflammation. Based on this background, the antinociceptive effects of the crude extract, various fractions, and essential oil have been reported previously. In this research work, we isolate and characterize pure bioactive compounds from I. rugosus and evaluate possible mechanisms using various in vivo and in vitro models. The pure compounds were analyzed for analgesic and anti-inflammatory activities through various assays. The column chromatography of the chloroform fraction of I. rugosus led to the identification of two pure compounds, i.e., 1 and 2. Compound 1 demonstrated notable inhibition (62% writhing inhibition, 72.77% COX-2 inhibition, and 76.97% 5-LOX inhibition) and anti-inflammatory potential (>50% paw edema inhibition at various intervals). The possible mechanism involved in antinociception was considered primarily, a concept that has already been elucidated through the application of naloxone (an antagonist of opioid receptors). The involvement of adrenergic receptors was investigated using a hot plate model (an adrenergic receptor antagonist). The strong ethnomedicinal analgesic background of I. rugosus, supported by previous reports and current observations, leads to the conclusion that I. rugosus is a potential source of antinociceptive and anti-inflammatory bioactive compounds. It may be concluded from the results that the isolated analgesic compounds of I. rugosus may be a possible alternative remedy for pain and inflammation management with admirable efficacy and safety profiles.

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          SwissADME: a free web tool to evaluate pharmacokinetics, drug-likeness and medicinal chemistry friendliness of small molecules

          To be effective as a drug, a potent molecule must reach its target in the body in sufficient concentration, and stay there in a bioactive form long enough for the expected biologic events to occur. Drug development involves assessment of absorption, distribution, metabolism and excretion (ADME) increasingly earlier in the discovery process, at a stage when considered compounds are numerous but access to the physical samples is limited. In that context, computer models constitute valid alternatives to experiments. Here, we present the new SwissADME web tool that gives free access to a pool of fast yet robust predictive models for physicochemical properties, pharmacokinetics, drug-likeness and medicinal chemistry friendliness, among which in-house proficient methods such as the BOILED-Egg, iLOGP and Bioavailability Radar. Easy efficient input and interpretation are ensured thanks to a user-friendly interface through the login-free website http://www.swissadme.ch. Specialists, but also nonexpert in cheminformatics or computational chemistry can predict rapidly key parameters for a collection of molecules to support their drug discovery endeavours.
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            Lead- and drug-like compounds: the rule-of-five revolution.

            Citations in CAS SciFinder to the rule-of-five (RO5) publication will exceed 1000 by year-end 2004. Trends in the RO5 literature explosion that can be discerned are the further definitions of drug-like. This topic is explored in terms of drug-like physicochemical features, drug-like structural features, a comparison of drug-like and non-drug-like in drug discovery and a discussion of how drug-like features relate to clinical success. Physicochemical features of CNS drugs and features related to CNS blood-brain transporter affinity are briefly reviewed. Recent literature on features of non-oral drugs is reviewed and how features of lead-like compounds differ from those of drug-like compounds is discussed. Most recently, partly driven by NIH roadmap initiatives, considerations have arisen as to what tool-like means in the search for chemical tools to probe biology space. All these topics frame the scope of this short review/perspective.: © 2004 Elsevier Ltd . All rights reserved.
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              A bioavailability score.

              Responding to a demonstrated need for scientists to forecast the permeability and bioavailability (F) properties of compounds before their purchase, synthesis, or advanced testing, we have developed a score that assigns the probability that a compound will have F > 10% in the rat. Neither the rule-of-five, log P, log D, nor the combination of the number of rotatable bonds and polar surface area successfully categorized compounds. Instead, different properties govern the bioavailability of compounds depending on their predominant charge at biological pH. The fraction of anions with >10% F falls from 85% if the polar surface area (PSA) is or = 150 A(2). On the other hand, whereas 55% of the neutral, zwitterionic, or cationic compounds that pass the rule-of-five have >10% F, only 17% of those that fail have > 10% F. This same categorization distinguishes compounds that are poorly permeable from those that are permeable in Caco-2 cells. Further validation is provided with human bioavailability values from the literature.
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                Author and article information

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                Journal
                Front Pharmacol
                Front Pharmacol
                Front. Pharmacol.
                Frontiers in Pharmacology
                Frontiers Media S.A.
                1663-9812
                13 February 2024
                2024
                : 15
                : 1328128
                Affiliations
                [1] 1 Department of Clinical Laboratory Sciences , College of Applied Medical Sciences , Najran University , Najran, Saudi Arabia
                [2] 2 Department of Pharmacy , University of Swabi , Swabi, Pakistan
                [3] 3 Department of pharmaceutical chemistry , College of pharmacy , Najran University , Najran, Saudi Arabia
                [4] 4 Department of Clinical Laboratory Sciences , Faculty of Applied Medical Sciences , Najran University , Najran, Saudi Arabia
                [5] 5 Department of Pharmacognosy , College of Pharmacy , Najran University , Najran, Saudi Arabia
                [6] 6 Department of Pharmacy , Univeristy of Malakand , Chakdara, Pakistan
                [7] 7 Department of Pharmacy , Bacha Khan University , Charsadda, Pakistan
                Author notes

                Edited by: Gokhan Zengin, Selcuk University, Science Faculty, Türkiye

                Reviewed by: Shahnaz Rahim, Cardiff University, United Kingdom

                Fabrício Souza Silva, Federal University of São Francisco Valley, Brazil

                Inamullah Hakeem Said, Jacobs University, Germany

                *Correspondence: Muhammad Saeed Jan, saeedjan@ 123456bkuc.edu.pk ; Saleh Alshamrani, saalshamrani@ 123456nu.edu.sa
                Article
                1328128
                10.3389/fphar.2024.1328128
                10897015
                38414736
                1e71d8ae-685e-4321-92a7-b764e07402d2
                Copyright © 2024 Alshehri, Zeb, Mukarram Shah, Mahnashi, Asiri, Alqahtani, Sadiq, Ibrar, Alshamrani and Jan.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 26 October 2023
                : 22 January 2024
                Funding
                The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.
                Categories
                Pharmacology
                Original Research
                Custom metadata
                Experimental Pharmacology and Drug Discovery

                Pharmacology & Pharmaceutical medicine
                isodon rugosus,antinociception,anti-inflammatory,opioid receptors,adrenergic receptors

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