HETEROCYCLES 40. THE LIPOPHILICITY EVALUATION OF SOME NEW PYRIDIN-3/4-YL-THIAZOLO [3,2-B] [1,2,4]TRIAZOLE COMPOUNDS WITH ANTI-INFLAMMATORY ACTIVITY BY RP-TLC AND COMPUTATIONAL METHODS
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Toma, Alexandra
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Iuliu Hatieganu Univ Med & Pharm, Dept Organ Chem, 41 Victor Babes St, Cluj Napoca 400012, RomaniaIuliu Hatieganu Univ Med & Pharm, Dept Organ Chem, 41 Victor Babes St, Cluj Napoca 400012, Romania
Toma, Alexandra
[1
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Leonte, Denisa
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Iuliu Hatieganu Univ Med & Pharm, Dept Organ Chem, 41 Victor Babes St, Cluj Napoca 400012, RomaniaIuliu Hatieganu Univ Med & Pharm, Dept Organ Chem, 41 Victor Babes St, Cluj Napoca 400012, Romania
Leonte, Denisa
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Zaharia, Valentin
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Iuliu Hatieganu Univ Med & Pharm, Dept Organ Chem, 41 Victor Babes St, Cluj Napoca 400012, RomaniaIuliu Hatieganu Univ Med & Pharm, Dept Organ Chem, 41 Victor Babes St, Cluj Napoca 400012, Romania
Zaharia, Valentin
[1
]
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[1] Iuliu Hatieganu Univ Med & Pharm, Dept Organ Chem, 41 Victor Babes St, Cluj Napoca 400012, Romania
A series of new pyridin-3/4-yl-thiazolo[3,2-b][1,2,4]triazole compounds and their corresponding thioetheric intermediates with anti-inflammatory activity were evaluated in order to establish their lipophilic profile by reversed phase thin layer chromatography (RP-TLC). The lipophilicity parameters were determined experimentally, based on the chromatographic data (R-M, R-mo, b, mRM, phi(0), PC1/R-M). A series of theoretical lipophilicity indices were estimated with different computational methods. A good correlation was observed between the experimental lipophilicity parameters and the computed logP values (R-2 >+/- 0.83). The scores obtained by applying the principal components analysis (PCA) classify the investigated compounds into three groups, their repartition being correlated with the chemical structure and the anti-inflammatory activity.
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Islamic Azad Univ, Pharmaceut Sci Branch, Dept Med Chem, Tehran 19419, IranIslamic Azad Univ, Pharmaceut Sci Branch, Dept Med Chem, Tehran 19419, Iran
Assarzadeh, Mohammad Javad
Almasirad, Ali
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Islamic Azad Univ, Pharmaceut Sci Branch, Dept Med Chem, Tehran 19419, IranIslamic Azad Univ, Pharmaceut Sci Branch, Dept Med Chem, Tehran 19419, Iran
Almasirad, Ali
Shafiee, Abbas
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Univ Tehran Med Sci, Fac Pharm, Dept Med Chem, Tehran 14174, Iran
Univ Tehran Med Sci, Pharmaceut Sci Res Ctr, Tehran 14174, IranIslamic Azad Univ, Pharmaceut Sci Branch, Dept Med Chem, Tehran 19419, Iran
Shafiee, Abbas
Koopaei, Mansur Nassiri
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Islamic Azad Univ, Pharmaceut Sci Branch, Dept Med Chem, Tehran 19419, IranIslamic Azad Univ, Pharmaceut Sci Branch, Dept Med Chem, Tehran 19419, Iran
Koopaei, Mansur Nassiri
Abdollahi, Mohammad
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Univ Tehran Med Sci, Pharmaceut Sci Res Ctr, Tehran 14174, Iran
Univ Tehran Med Sci, Fac Pharm, Dept Pharmacol & Toxicol, Tehran 14174, IranIslamic Azad Univ, Pharmaceut Sci Branch, Dept Med Chem, Tehran 19419, Iran
机构:
Islamic Azad Univ, Pharmaceut Sci Branch, Dept Med Chem, Tehran 19419, IranIslamic Azad Univ, Pharmaceut Sci Branch, Dept Med Chem, Tehran 19419, Iran
Assarzadeh, Mohammad Javad
Almasirad, Ali
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Islamic Azad Univ, Pharmaceut Sci Branch, Dept Med Chem, Tehran 19419, IranIslamic Azad Univ, Pharmaceut Sci Branch, Dept Med Chem, Tehran 19419, Iran
Almasirad, Ali
Shafiee, Abbas
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Univ Tehran Med Sci, Fac Pharm, Dept Med Chem, Tehran 14174, Iran
Univ Tehran Med Sci, Pharmaceut Sci Res Ctr, Tehran 14174, IranIslamic Azad Univ, Pharmaceut Sci Branch, Dept Med Chem, Tehran 19419, Iran
Shafiee, Abbas
Koopaei, Mansur Nassiri
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机构:
Islamic Azad Univ, Pharmaceut Sci Branch, Dept Med Chem, Tehran 19419, IranIslamic Azad Univ, Pharmaceut Sci Branch, Dept Med Chem, Tehran 19419, Iran
Koopaei, Mansur Nassiri
Abdollahi, Mohammad
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Univ Tehran Med Sci, Pharmaceut Sci Res Ctr, Tehran 14174, Iran
Univ Tehran Med Sci, Fac Pharm, Dept Pharmacol & Toxicol, Tehran 14174, IranIslamic Azad Univ, Pharmaceut Sci Branch, Dept Med Chem, Tehran 19419, Iran