Academic Journal

ADMET and Druglikeness Calculations of Sarin, Soman, and Their Hypothetical Derivatives

التفاصيل البيبلوغرافية
العنوان: ADMET and Druglikeness Calculations of Sarin, Soman, and Their Hypothetical Derivatives
المؤلفون: Kafa Khalaf Hammud
المصدر: Iraqi Journal of Industrial Research, Vol 9, Iss 3 (2022)
بيانات النشر: Corporation of Research and Industrial Development, 2022.
سنة النشر: 2022
المجموعة: LCC:Special industries and trades
LCC:Industrial engineering. Management engineering
مصطلحات موضوعية: ADMET, Druglikeness, Sarin, Soman, Hypothetical derivative, Special industries and trades, HD9000-9999, Industrial engineering. Management engineering, T55.4-60.8
الوصف: Absorption, Distribution, Metabolism, Excretion, and Toxicity (ADMET) represents a numerical classification of any chemical to be a drug candidate with promising therapeutic efficacy with minimum toxicity or sensitivity depending on its chemical structures and its physicochemical properties. Sarin (GB) and Soman (GD) are nerve agents classified as chemical warfare agent containing phosphorous atom. Acetylcholine (ACh) as a neurotransmitter esterifies by acetyl cholinesterase enzyme (AChE) that can be irreversibly inhibited by (GB and GD) meaning termination of muscle function. Here, new in Silico predication of two nerve agents (Sarin and Soman) was done. These organophosphorous agents were hypothetically subjected to a reaction with lactic acid and various amino acids. New P-O with lactic acid and P-N linkage was between Sarin or Soman and different amino acids. Both reactions were through fluorine atom with hydroxyl group (P-O formation) and with amine (P-N). The ADMET and Druglikeness properties of the parent chemical warfare agents and their hypothetical products were subjected to MarvinSketch program and preadmet website. Sarin and Soman and their hypothetical products showed many noticeable characters such as: all 20 tested compounds were with non- inhibition character of Pgp and CYp-2D6; substrate character with CYP-3A4, negative values to skin permeability, negative to Carcino-Mouse, low risk to hERG inhibition. Other calculated predictors were varied in response between all calculated compounds.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2788-712X
Relation: http://ijoir.gov.iq/ijoir/index.php/jou/article/view/260; https://doaj.org/toc/2788-712X
DOI: 10.53523/ijoirVol9I3ID260
URL الوصول: https://doaj.org/article/b4273eb790174f17a83b2a890fba4b1d
رقم الانضمام: edsdoj.b4273eb790174f17a83b2a890fba4b1d
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:2788712X
DOI:10.53523/ijoirVol9I3ID260